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depmap_mutation_cancer_type

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The gene AADACL4 has a mutation status of WRDAI263del, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF5 has a mutation status of P432A, The gene IFNLR1 has a mutation status of G337G, The gene SNRNP40 has a mutation status of L24W, The gene POU3F1 has a mutation status of G93R, The gene MAST2 has a mutation status of R1122R, The gene GBP4 has a mutation status of R253R, The gene NBPF10 has a mutation status of L891V, The gene NBPF11 has a mutation status of Q55H, The gene FLG2 has a mutation status of E24K, The gene FCRL5 has a mutation status of L570H, The gene SPTA1 has a mutation status of K601N, The gene DUSP12 has a mutation status of V80A, The gene QSOX1 has a mutation status of L269L, The gene OR2T4 has a mutation status of V109L, The gene MATN3 has a mutation status of T175P, The gene APOB has a mutation status of T4560T, The gene APOB has a mutation status of E1517A, The gene KLHL29 has a mutation status of D308E, The gene NLRC4 has a mutation status of A524T, The gene EML6 has a mutation status of E659D, The gene AL845331.2 has a mutation status of L268L, The gene AL845331.2 has a mutation status of A335D, The gene ARID5A has a mutation status of T444I, The gene CFAP221 has a mutation status of P756P, The gene GPR39 has a mutation status of N434I, The gene SP9 has a mutation status of R328S, The gene SGO2 has a mutation status of S125N, The gene AOX1 has a mutation status of S1330S, The gene UNC80 has a mutation status of H397Y, The gene UNC80 has a mutation status of K2323R, The gene FN1 has a mutation status of V923V, The gene TRIP12 has a mutation status of R1428C, The gene SPATA3 has a mutation status of S114L, The gene PRRT3 has a mutation status of R107G, The gene DLEC1 has a mutation status of V1308G, The gene XIRP1 has a mutation status of L1803L, The gene CACNA1D has a mutation status of N1520T, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene C3orf67 has a mutation status of M676T, The gene STX19 has a mutation status of F149L, The gene SLC9C1 has a mutation status of Y329S, The gene CD200R1 has a mutation status of H346R, The gene ESYT3 has a mutation status of P457P, The gene BCHE has a mutation status of L123L, The gene CCDC39 has a mutation status of S67L, The gene ATP13A4 has a mutation status of A10T, The gene UBXN7 has a mutation status of N190N, The gene ZNF721 has a mutation status of D897E, The gene TLR1 has a mutation status of L302S, The gene TMPRSS11E has a mutation status of L280L, The gene PTPN13 has a mutation status of F1296S, The gene ANK2 has a mutation status of H2307H, The gene RAPGEF2 has a mutation status of E406G, The gene ADAM29 has a mutation status of T800M, The gene TARS1 has a mutation status of N726N, The gene RXFP3 has a mutation status of Y287Y, The gene POLK has a mutation status of S514fs, The gene YTHDC2 has a mutation status of E1419D, The gene CSNK1G3 has a mutation status of L116L, The gene JADE2 has a mutation status of E376V, The gene TGFBI has a mutation status of A323A, The gene HSPA9 has a mutation status of G61G, The gene PROB1 has a mutation status of P559fs, The gene PROB1 has a mutation status of E558fs, The gene PCDHA6 has a mutation status of L56L, The gene PCDHB12 has a mutation status of F615F, The gene PCDH1 has a mutation status of A1047T, The gene TMEM14B has a mutation status of 140_141CA>SP, The gene ATAT1 has a mutation status of H265fs, The gene MUC22 has a mutation status of T273E, The gene PBX2 has a mutation status of P32P, The gene C6orf132 has a mutation status of P183P, The gene RARS2 has a mutation status of R456C, The gene USP42 has a mutation status of L1187V, The gene DNAH11 has a mutation status of R1445R, The gene DNAH11 has a mutation status of K4463K, The gene NOD1 has a mutation status of E172K, The gene VPS41 has a mutation status of K762E, The gene PCLO has a mutation status of T115A, The gene SRI has a mutation status of A9fs, The gene FZD1 has a mutation status of E149K, The gene ERVW-1 has a mutation status of L333*, The gene MCM7 has a mutation status of R532W, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S558T, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene COL26A1 has a mutation status of D428N, The gene KCP has a mutation status of R801fs, The gene KCP has a mutation status of R801*, The gene COPG2 has a mutation status of I125V, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PRSS1 has a mutation status of N77N, The gene ASB10 has a mutation status of R90S, The gene ACTR3B has a mutation status of I238V, The gene CSMD1 has a mutation status of S721S, The gene MTMR9 has a mutation status of P403A, The gene FGF17 has a mutation status of A3A, The gene SLC25A37 has a mutation status of G245G, The gene NEFM has a mutation status of E578V, The gene FNTA has a mutation status of K185R, The gene SNTG1 has a mutation status of T165A, The gene RDH10 has a mutation status of F52F, The gene CA1 has a mutation status of H97Y, The gene RUNX1T1 has a mutation status of D398G, The gene FER1L6 has a mutation status of R319W, The gene AC100868.1 has a mutation status of K146K, The gene DENND3 has a mutation status of T879T, The gene EPPK1 has a mutation status of A2633del, The gene CNTNAP3B has a mutation status of L968L, The gene AUH has a mutation status of Q314H, The gene ROR2 has a mutation status of V149I, The gene FBP2 has a mutation status of A190V, The gene FRRS1L has a mutation status of R51A, The gene TRIM32 has a mutation status of K627E, The gene OR1B1 has a mutation status of R124H, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene CLIC3 has a mutation status of A209T, The gene PCBD1 has a mutation status of K41K, The gene ZNF503 has a mutation status of P128P, The gene GFRA1 has a mutation status of G24R, The gene CPXM2 has a mutation status of Y610C, The gene TCERG1L has a mutation status of P442S, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of N1458N, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of I1961I, The gene MUC5AC has a mutation status of STTSASTA4496del, The gene BRSK2 has a mutation status of K152K, The gene SYT8 has a mutation status of Q357R, The gene OSBPL5 has a mutation status of V166V, The gene MMP26 has a mutation status of C82F, The gene BBOX1 has a mutation status of W116L, The gene KBTBD4 has a mutation status of T362S, The gene OR4C12 has a mutation status of M134I, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MTA2 has a mutation status of R341W, The gene RELT has a mutation status of G154D, The gene PAFAH1B2 has a mutation status of P65P, The gene SMIM35 has a mutation status of G75G, The gene OR8G5 has a mutation status of A119V, The gene CACNA2D4 has a mutation status of R33L, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene PTHLH has a mutation status of P118L, The gene AAAS has a mutation status of M1I, The gene PIP4K2C has a mutation status of P7S, The gene ANKS1B has a mutation status of L348V, The gene NR1H4 has a mutation status of I286I, The gene POU4F1 has a mutation status of G338G, The gene ABCC4 has a mutation status of R52H, The gene FANCM has a mutation status of A1016T, The gene ACOT4 has a mutation status of A83A, The gene RPS6KL1 has a mutation status of A130V, The gene WDR25 has a mutation status of P208R, The gene JAG2 has a mutation status of S963S, The gene GOLGA6L6 has a mutation status of R460R, The gene GOLGA6L6 has a mutation status of R460fs, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene GOLGA6L7 has a mutation status of A185A, The gene RYR3 has a mutation status of R1556Q, The gene KNL1 has a mutation status of N618S, The gene ADAM10 has a mutation status of A568T, The gene USP3 has a mutation status of S284F, The gene ANKDD1A has a mutation status of P238R, The gene ANKDD1A has a mutation status of L516L, The gene DPP8 has a mutation status of A269T, The gene UACA has a mutation status of N880K, The gene HEXA has a mutation status of L417L, The gene NEIL1 has a mutation status of R52G, The gene CSPG4 has a mutation status of Q2299Q, The gene GOLGA6L10 has a mutation status of I73V, The gene AC245033.1 has a mutation status of F560F, The gene BRICD5 has a mutation status of A179T, The gene DNAJA3 has a mutation status of Y427Y, The gene ZNF764 has a mutation status of G199D, The gene NDRG4 has a mutation status of R48H, The gene PDP2 has a mutation status of R25C, The gene HYDIN has a mutation status of F4675L, The gene BCO1 has a mutation status of V166I, The gene JPH3 has a mutation status of R98R, The gene CLUH has a mutation status of T363T, The gene OR1A2 has a mutation status of L32fs, The gene AIPL1 has a mutation status of R209R, The gene TP53 has a mutation status of R248Q, The gene EVPLL has a mutation status of I259N, The gene SLC47A2 has a mutation status of T335P, The gene CCL4L2 has a mutation status of P67R, The gene GGNBP2 has a mutation status of Q66Q, The gene KRT25 has a mutation status of K222N, The gene KRTAP1-1 has a mutation status of R117K, The gene KRTAP1-1 has a mutation status of T78T, The gene ITGA2B has a mutation status of G367G, The gene LRRC46 has a mutation status of M244V, The gene CCDC182 has a mutation status of R131P, The gene KCNH6 has a mutation status of V267A, The gene CD79B has a mutation status of L21L, The gene SOX9 has a mutation status of L3L, The gene SLC25A10 has a mutation status of D130N, The gene EPG5 has a mutation status of H1384Q, The gene SKOR2 has a mutation status of D146N, The gene DCC has a mutation status of N176D, The gene MUC16 has a mutation status of G13530S, The gene DNMT1 has a mutation status of R114K, The gene OR10H2 has a mutation status of T74T, The gene AC008397.1 has a mutation status of G164C, The gene SUGP1 has a mutation status of R44Q, The gene SLC7A9 has a mutation status of I44V, The gene PROSER3 has a mutation status of K104*, The gene WDR62 has a mutation status of R1512W, The gene WDR87 has a mutation status of D359fs, The gene DLL3 has a mutation status of S198S, The gene DYRK1B has a mutation status of R593W, The gene CEACAM4 has a mutation status of A169T, The gene PRR19 has a mutation status of V7I, The gene FCGRT has a mutation status of H258H, The gene KLK7 has a mutation status of K197R, The gene ZNF600 has a mutation status of L666P, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of S395T, The gene LILRA1 has a mutation status of R296T, The gene LILRA1 has a mutation status of S392A, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of V111V, The gene KIR2DL1 has a mutation status of P175T, The gene KIR2DL1 has a mutation status of K271N, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene SNRPB has a mutation status of A101A, The gene CENPB has a mutation status of R291W, The gene PAX1 has a mutation status of S213L, The gene XKR7 has a mutation status of R524W, The gene ZNF341 has a mutation status of S284S, The gene HNF4A has a mutation status of L340L, The gene FAM217B has a mutation status of R156*, The gene ZDHHC8 has a mutation status of K752T, The gene MRTFA has a mutation status of P767S, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene GTSE1 has a mutation status of S594F, The gene PLXNB2 has a mutation status of R1535Q, The gene CPT1B has a mutation status of G668E, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene TBL1X has a mutation status of G231D, The gene CXorf21 has a mutation status of S197R, The gene GCNA has a mutation status of G479S, The gene CXCR3 has a mutation status of G70G, The gene HMGN5 has a mutation status of R4*, The gene TBC1D8B has a mutation status of L28L, The gene SLC25A5 has a mutation status of G121C, The gene C1GALT1C1 has a mutation status of N236N, The gene HMGB3 has a mutation status of T51A, The gene AC236972.4 has a mutation status of S1611S, The gene MT-ND1 has a mutation status of T164A, The gene MT-ND5 has a mutation status of F85L, The gene MT-CYB has a mutation status of T241M, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene IFNLR1 has a mutation status of G337G, The gene SNRNP40 has a mutation status of L24W, The gene PPCS has a mutation status of R25P, The gene PPCS has a mutation status of F26L, The gene MAST2 has a mutation status of R1122R, The gene RABGGTB has a mutation status of E274K, The gene GBP4 has a mutation status of R253R, The gene GCLM has a mutation status of P244R, The gene SLC6A17 has a mutation status of G42G, The gene NBPF11 has a mutation status of Q55H, The gene FLG2 has a mutation status of E24K, The gene PEAR1 has a mutation status of D1020Y, The gene FCRL5 has a mutation status of L570H, The gene DUSP12 has a mutation status of V80A, The gene QSOX1 has a mutation status of L269L, The gene TPR has a mutation status of A1704G, The gene CAMK1G has a mutation status of S129S, The gene RD3 has a mutation status of T28M, The gene EPRS1 has a mutation status of A1098A, The gene EPHX1 has a mutation status of N256K, The gene URB2 has a mutation status of K652R, The gene GREM2 has a mutation status of V152A, The gene ZBTB18 has a mutation status of S136G, The gene GEN1 has a mutation status of Q906K, The gene MATN3 has a mutation status of T175P, The gene APOB has a mutation status of T4560T, The gene APOB has a mutation status of E1517A, The gene NLRC4 has a mutation status of A524T, The gene AL845331.2 has a mutation status of L268L, The gene AL845331.2 has a mutation status of A335D, The gene CREG2 has a mutation status of Q237K, The gene CFAP221 has a mutation status of P756P, The gene GPR39 has a mutation status of N434I, The gene SP9 has a mutation status of R328S, The gene OSBPL6 has a mutation status of A809A, The gene TTN has a mutation status of D30397H, The gene COL5A2 has a mutation status of P926L, The gene SGO2 has a mutation status of S125N, The gene AOX1 has a mutation status of S1330S, The gene ZDBF2 has a mutation status of I1346V, The gene FN1 has a mutation status of V923V, The gene TRIP12 has a mutation status of R1428C, The gene PRRT3 has a mutation status of R107G, The gene FGD5 has a mutation status of S458S, The gene TRANK1 has a mutation status of D1226Y, The gene XIRP1 has a mutation status of L1803L, The gene ZKSCAN7 has a mutation status of K418K, The gene ATRIP has a mutation status of T766M, The gene RBM5 has a mutation status of D660fs, The gene CACNA1D has a mutation status of N1520T, The gene DNAH12 has a mutation status of R402R, The gene C3orf67 has a mutation status of M676T, The gene STX19 has a mutation status of F149L, The gene SLC9C1 has a mutation status of Y329S, The gene CD200R1 has a mutation status of H346R, The gene ESYT3 has a mutation status of P457P, The gene BCHE has a mutation status of L123L, The gene CCDC39 has a mutation status of S67L, The gene IL1RAP has a mutation status of G363G, The gene UBXN7 has a mutation status of N190N, The gene ZNF721 has a mutation status of D897E, The gene TLR1 has a mutation status of L302S, The gene TMPRSS11E has a mutation status of L280L, The gene MOB1B has a mutation status of V147A, The gene PTPN13 has a mutation status of F1296S, The gene ANK2 has a mutation status of H2307H, The gene KIAA1109 has a mutation status of R4674C, The gene HSPA4L has a mutation status of N96S, The gene PRDM9 has a mutation status of I31I, The gene TARS1 has a mutation status of N726N, The gene RXFP3 has a mutation status of Y287Y, The gene FGF10 has a mutation status of K81E, The gene POLK has a mutation status of S514fs, The gene YTHDC2 has a mutation status of E1419D, The gene CSNK1G3 has a mutation status of L116L, The gene JADE2 has a mutation status of E376V, The gene TGFBI has a mutation status of A323A, The gene HSPA9 has a mutation status of G61G, The gene PCDHA6 has a mutation status of L56L, The gene PCDH1 has a mutation status of A1047T, The gene PDE6A has a mutation status of V685M, The gene ADAMTS2 has a mutation status of D263D, The gene FOXC1 has a mutation status of L518F, The gene OR12D3 has a mutation status of S205S, The gene CDSN has a mutation status of Q162Q, The gene HLA-DQA2 has a mutation status of A16T, The gene COL9A1 has a mutation status of P540P, The gene RARS2 has a mutation status of R456C, The gene TBC1D32 has a mutation status of I751V, The gene SOGA3 has a mutation status of E699Q, The gene BRAT1 has a mutation status of A642G, The gene IQCE has a mutation status of A426A, The gene USP42 has a mutation status of L1187V, The gene ICA1 has a mutation status of T245T, The gene AC019117.4 has a mutation status of K346R, The gene DNAH11 has a mutation status of R1445R, The gene DNAH11 has a mutation status of K4463K, The gene JAZF1 has a mutation status of F229L, The gene NOD1 has a mutation status of E172K, The gene VPS41 has a mutation status of K762E, The gene YKT6 has a mutation status of Y64C, The gene ADCY1 has a mutation status of A17V, The gene CCDC201 has a mutation status of Q122fs, The gene FZD9 has a mutation status of C111*, The gene PCLO has a mutation status of T115A, The gene FZD1 has a mutation status of E149K, The gene LMTK2 has a mutation status of R1470Q, The gene MCM7 has a mutation status of R532W, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene COL26A1 has a mutation status of D428N, The gene KMT2E has a mutation status of L349F, The gene CPED1 has a mutation status of N494N, The gene COPG2 has a mutation status of I125V, The gene ACTR3B has a mutation status of I238V, The gene CSMD1 has a mutation status of S721S, The gene MTMR9 has a mutation status of P403A, The gene FGF17 has a mutation status of A3A, The gene SLC25A37 has a mutation status of G245G, The gene NEFL has a mutation status of E469D, The gene FNTA has a mutation status of K185R, The gene SNTG1 has a mutation status of T165A, The gene CA1 has a mutation status of H97Y, The gene RUNX1T1 has a mutation status of D398G, The gene CBWD6 has a mutation status of D159N, The gene FBP2 has a mutation status of A190V, The gene ECPAS has a mutation status of Q915K, The gene TRIM32 has a mutation status of K627E, The gene OR1B1 has a mutation status of R124H, The gene COL5A1 has a mutation status of N176K, The gene PCBD1 has a mutation status of K41K, The gene TCF7L2 has a mutation status of G582G, The gene GFRA1 has a mutation status of G24R, The gene WDR11 has a mutation status of T1001I, The gene CPXM2 has a mutation status of Y610C, The gene MUC5B has a mutation status of GTTWILTELTTAATTTAATGPTATPSSTP4387del, The gene BRSK2 has a mutation status of K152K, The gene DUSP8 has a mutation status of D12E, The gene SYT8 has a mutation status of Q357R, The gene OSBPL5 has a mutation status of V166V, The gene MMP26 has a mutation status of C82F, The gene BBOX1 has a mutation status of W116L, The gene KCNA4 has a mutation status of G59G, The gene EIF3M has a mutation status of Q302*, The gene KBTBD4 has a mutation status of T362S, The gene OR4C12 has a mutation status of M134I, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MTA2 has a mutation status of R341W, The gene MAP3K11 has a mutation status of H186P, The gene RIN1 has a mutation status of S13P, The gene IGHMBP2 has a mutation status of G801S, The gene RELT has a mutation status of G154D, The gene POU2AF1 has a mutation status of L237*, The gene HTR3B has a mutation status of V407G, The gene PAFAH1B2 has a mutation status of P65P, The gene OR8G5 has a mutation status of A119V, The gene CHD4 has a mutation status of Q1442H, The gene SLC2A14 has a mutation status of E243*, The gene PTHLH has a mutation status of P118L, The gene KRT85 has a mutation status of S460T, The gene NXPH4 has a mutation status of P95P, The gene PIP4K2C has a mutation status of P7S, The gene LRRIQ1 has a mutation status of S1208R, The gene CDK17 has a mutation status of R131C, The gene ANKS1B has a mutation status of L348V, The gene NR1H4 has a mutation status of I286I, The gene POLR3B has a mutation status of T462T, The gene RNFT2 has a mutation status of A93T, The gene ABCC4 has a mutation status of R52H, The gene ACOT4 has a mutation status of A83A, The gene RPS6KL1 has a mutation status of A130V, The gene NEK9 has a mutation status of Q276H, The gene ADCK1 has a mutation status of K362E, The gene DGLUCY has a mutation status of A372T, The gene WDR25 has a mutation status of P208R, The gene JAG2 has a mutation status of S963S, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L7 has a mutation status of A185A, The gene KNL1 has a mutation status of N618S, The gene SORD has a mutation status of P124P, The gene SORD has a mutation status of D126D, The gene ADAM10 has a mutation status of A568T, The gene VPS13C has a mutation status of P2254H, The gene USP3 has a mutation status of S284F, The gene DPP8 has a mutation status of A269T, The gene UACA has a mutation status of N880K, The gene HEXA has a mutation status of L417L, The gene NEIL1 has a mutation status of R52G, The gene CSPG4 has a mutation status of Q2299Q, The gene AC245033.1 has a mutation status of F560F, The gene BRICD5 has a mutation status of A179T, The gene DNAJA3 has a mutation status of Y427Y, The gene GTF3C1 has a mutation status of R1089C, The gene ZNF764 has a mutation status of G199D, The gene NDRG4 has a mutation status of R48H, The gene PDP2 has a mutation status of R25C, The gene AARS1 has a mutation status of M255I, The gene BCO1 has a mutation status of V166I, The gene JPH3 has a mutation status of R98R, The gene CLUH has a mutation status of T363T, The gene OR1A2 has a mutation status of L32fs, The gene AIPL1 has a mutation status of R209R, The gene TP53 has a mutation status of R248Q, The gene EVPLL has a mutation status of I259N, The gene SLC47A2 has a mutation status of T335P, The gene CCL4L2 has a mutation status of P67R, The gene GGNBP2 has a mutation status of Q66Q, The gene KRT25 has a mutation status of K222N, The gene KRTAP1-1 has a mutation status of R117K, The gene KRTAP1-1 has a mutation status of T78T, The gene ITGA2B has a mutation status of G367G, The gene LRRC46 has a mutation status of M244V, The gene KCNH6 has a mutation status of V267A, The gene CD79B has a mutation status of L21L, The gene ABCA9 has a mutation status of W174R, The gene FBF1 has a mutation status of A919A, The gene INO80C has a mutation status of A22V, The gene EPG5 has a mutation status of H1384Q, The gene SKOR2 has a mutation status of D146N, The gene DCC has a mutation status of N176D, The gene SALL3 has a mutation status of A819A, The gene ATP9B has a mutation status of E683Q, The gene DNMT1 has a mutation status of R114K, The gene OR10H2 has a mutation status of T74T, The gene C19orf44 has a mutation status of D346E, The gene SLC7A9 has a mutation status of I44V, The gene LSM14A has a mutation status of G115S, The gene ARHGAP33 has a mutation status of P966P, The gene PRODH2 has a mutation status of P90fs, The gene WDR62 has a mutation status of R1512W, The gene ZNF585A has a mutation status of M56L, The gene DLL3 has a mutation status of S198S, The gene DYRK1B has a mutation status of R593W, The gene CEACAM4 has a mutation status of A169T, The gene PRR19 has a mutation status of V7I, The gene GEMIN7 has a mutation status of F129L, The gene FCGRT has a mutation status of H258H, The gene KLK7 has a mutation status of K197R, The gene ZNF600 has a mutation status of L666P, The gene NLRP12 has a mutation status of T260M, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA2 has a mutation status of W163S, The gene LILRA1 has a mutation status of R296T, The gene LILRB1 has a mutation status of R30S, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of H203R, The gene KIR2DL1 has a mutation status of K271N, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene SNRPB has a mutation status of A101A, The gene CENPB has a mutation status of R291W, The gene BMP2 has a mutation status of P187T, The gene PAX1 has a mutation status of S213L, The gene XKR7 has a mutation status of R524W, The gene ZNF341 has a mutation status of S284S, The gene HNF4A has a mutation status of L340L, The gene PLTP has a mutation status of F19L, The gene ZNF335 has a mutation status of Q1251H, The gene FAM217B has a mutation status of R156*, The gene LAMA5 has a mutation status of Q741R, The gene PPDPF has a mutation status of A93V, The gene PRPF6 has a mutation status of Y658Y, The gene GART has a mutation status of G377A, The gene COL6A1 has a mutation status of F250F, The gene ZDHHC8 has a mutation status of K752T, The gene APOBEC3H has a mutation status of R171G, The gene MEI1 has a mutation status of T40P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene GTSE1 has a mutation status of S594F, The gene PLXNB2 has a mutation status of R1535Q, The gene CPT1B has a mutation status of G668E, The gene OPHN1 has a mutation status of T235T, The gene CXCR3 has a mutation status of G70G, The gene HMGN5 has a mutation status of R4*, The gene SRPX2 has a mutation status of G172G, The gene HMGB3 has a mutation status of T51A, The gene MT-ND1 has a mutation status of T164A, The gene MT-ND5 has a mutation status of F85L, The gene MT-CYB has a mutation status of T241M
OV
The gene FNDC10 has a mutation status of H225P, The gene TNFRSF8 has a mutation status of T471P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene EPHA2 has a mutation status of V904G, The gene HSPG2 has a mutation status of T3909P, The gene AHDC1 has a mutation status of R72Q, The gene PPCS has a mutation status of V37G, The gene CPT2 has a mutation status of L651S, The gene CYP2J2 has a mutation status of R435S, The gene CELSR2 has a mutation status of V433M, The gene CELSR2 has a mutation status of R2015K, The gene AMPD2 has a mutation status of G34G, The gene NRAS has a mutation status of Q61L, The gene ACP6 has a mutation status of V29G, The gene MEX3A has a mutation status of H426P, The gene LAMC1 has a mutation status of N345S, The gene HMCN1 has a mutation status of T5004F, The gene FMOD has a mutation status of W133C, The gene TRIM11 has a mutation status of R252H, The gene GREM2 has a mutation status of E113E, The gene OR2C3 has a mutation status of A203G, The gene PXDN has a mutation status of C42F, The gene PXDN has a mutation status of R39L, The gene MYT1L has a mutation status of Y110D, The gene GMCL1 has a mutation status of V8G, The gene C2orf81 has a mutation status of T247P, The gene KRCC1 has a mutation status of T55T, The gene PSD4 has a mutation status of T819P, The gene ZRANB3 has a mutation status of V57G, The gene CSRNP3 has a mutation status of S383N, The gene HOXD9 has a mutation status of H97P, The gene CCDC150 has a mutation status of Q411H, The gene BARD1 has a mutation status of R155R, The gene ABCB6 has a mutation status of E731G, The gene SLC16A14 has a mutation status of C99G, The gene ARMC9 has a mutation status of D90V, The gene SSUH2 has a mutation status of R108W, The gene IL17RE has a mutation status of I603T, The gene ALS2CL has a mutation status of H155P, The gene NBEAL2 has a mutation status of P2251P, The gene DOCK3 has a mutation status of P1659L, The gene GRM2 has a mutation status of S489S, The gene IL17RB has a mutation status of V16V, The gene PROS1 has a mutation status of L236L, The gene MYH15 has a mutation status of T1899K, The gene GATA2 has a mutation status of H460P, The gene FOXL2 has a mutation status of A283A, The gene FOXL2 has a mutation status of G38G, The gene ZIC4 has a mutation status of R12Q, The gene SLC7A14 has a mutation status of V131L, The gene FXR1 has a mutation status of G588C, The gene SLC26A1 has a mutation status of T697I, The gene IDUA has a mutation status of T374P, The gene OTOP1 has a mutation status of V69M, The gene SORCS2 has a mutation status of S1125R, The gene CLNK has a mutation status of V211I, The gene SLC9B2 has a mutation status of T310T, The gene PLEKHG4B has a mutation status of R810C, The gene IQGAP2 has a mutation status of L65L, The gene SLF1 has a mutation status of A620G, The gene SLF1 has a mutation status of T999N, The gene HSD17B4 has a mutation status of T597T, The gene PRDM6 has a mutation status of G160G, The gene SLC12A2 has a mutation status of D176G, The gene ACSL6 has a mutation status of A70G, The gene TGFBI has a mutation status of V497V, The gene HNRNPA0 has a mutation status of G296G, The gene PCDHA8 has a mutation status of E94E, The gene FBLL1 has a mutation status of G21I, The gene MAML1 has a mutation status of Q769H, The gene DHX16 has a mutation status of S263S, The gene NRM has a mutation status of W149*, The gene MUC22 has a mutation status of A123S, The gene HLA-DRB5 has a mutation status of L246L, The gene HLA-DRB5 has a mutation status of D40G, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DRB1 has a mutation status of L265L, The gene ARMC12 has a mutation status of A22Y, The gene RNF8 has a mutation status of M25G, The gene GTPBP2 has a mutation status of V5G, The gene PTCHD4 has a mutation status of N566S, The gene RWDD1 has a mutation status of Y19S, The gene TRDN has a mutation status of T604K, The gene TAAR5 has a mutation status of C118C, The gene TXLNB has a mutation status of G117E, The gene RAB32 has a mutation status of G3G, The gene RAB32 has a mutation status of G4G, The gene PPP1R14C has a mutation status of V59G, The gene INTS1 has a mutation status of L2164P, The gene AMZ1 has a mutation status of T343P, The gene FOXK1 has a mutation status of T683P, The gene SLC29A4 has a mutation status of A69T, The gene SLC29A4 has a mutation status of G414G, The gene DGKB has a mutation status of S293S, The gene WIPF3 has a mutation status of I145T, The gene ADCYAP1R1 has a mutation status of Q336Q, The gene ELMO1 has a mutation status of E306Q, The gene IGFBP1 has a mutation status of A31A, The gene POM121L12 has a mutation status of D85A, The gene CLDN4 has a mutation status of V124G, The gene LMTK2 has a mutation status of Q348K, The gene TMEM130 has a mutation status of E204D, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S1242N, The gene MUC3A has a mutation status of S1250T, The gene MUC3A has a mutation status of T1510I, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene CUX1 has a mutation status of L960L, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene KRBA1 has a mutation status of A316V, The gene TMEM176A has a mutation status of L196F, The gene ATG9B has a mutation status of T96P, The gene GALNT11 has a mutation status of R291C, The gene SHH has a mutation status of D405G, The gene USP17L7 has a mutation status of D11E, The gene NEFM has a mutation status of F35F, The gene ADGRA2 has a mutation status of T397P, The gene ADRB3 has a mutation status of D117N, The gene OPRK1 has a mutation status of T55S, The gene CHMP4C has a mutation status of S21G, The gene RAD54B has a mutation status of E510K, The gene LAPTM4B has a mutation status of L16P, The gene FER1L6 has a mutation status of I506V, The gene MROH1 has a mutation status of C804R, The gene BOP1 has a mutation status of P188L, The gene SCRT1 has a mutation status of A133S, The gene SLC39A4 has a mutation status of R251W, The gene DMRT2 has a mutation status of G36R, The gene TTC39B has a mutation status of K492Q, The gene CDKN2A has a mutation status of R29*, The gene CEMIP2 has a mutation status of N914S, The gene GOLM1 has a mutation status of L42V, The gene ZNF484 has a mutation status of L511F, The gene TBC1D2 has a mutation status of V376G, The gene OR1N2 has a mutation status of L143P, The gene NUP188 has a mutation status of I966V, The gene PRRX2 has a mutation status of A194S, The gene UCK1 has a mutation status of *278W, The gene CFAP77 has a mutation status of T282P, The gene CAMSAP1 has a mutation status of L569F, The gene CCDC187 has a mutation status of E1017E, The gene NOTCH1 has a mutation status of T701P, The gene TUBAL3 has a mutation status of M405V, The gene ITGA8 has a mutation status of V446I, The gene ANXA8L1 has a mutation status of I116I, The gene WDFY4 has a mutation status of T885P, The gene ECD has a mutation status of N447N, The gene TLL2 has a mutation status of R221*, The gene TWNK has a mutation status of D584D, The gene AFAP1L2 has a mutation status of T756T, The gene C10orf143 has a mutation status of D22D, The gene PNPLA2 has a mutation status of A463A, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of R1283R, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4396A, The gene KCNQ1 has a mutation status of P7S, The gene DNHD1 has a mutation status of S4518P, The gene CAT has a mutation status of A251T, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene RTN4RL2 has a mutation status of A339A, The gene PRPF19 has a mutation status of E203L, The gene CSKMT has a mutation status of Q191*, The gene VEGFB has a mutation status of T156P, The gene CTSF has a mutation status of S76A, The gene CTTN has a mutation status of V536G, The gene DHCR7 has a mutation status of G147S, The gene B3GNT6 has a mutation status of A172G, The gene CREBZF has a mutation status of T293P, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene BHLHE41 has a mutation status of A402P, The gene KRT5 has a mutation status of G570G, The gene ESPL1 has a mutation status of A1527A, The gene HOXC11 has a mutation status of D164A, The gene GPR84 has a mutation status of R20H, The gene NAB2 has a mutation status of D439A, The gene CCDC59 has a mutation status of Y27D, The gene CCER1 has a mutation status of P73R, The gene ANKS1B has a mutation status of L245L, The gene ISCU has a mutation status of M1K, The gene NOS1 has a mutation status of V316A, The gene TMEM132C has a mutation status of L21M, The gene AMER2 has a mutation status of D274A, The gene MYCBP2 has a mutation status of S15S, The gene FARP1 has a mutation status of A446A, The gene FARP1 has a mutation status of H702P, The gene FARP1 has a mutation status of H703P, The gene GPR135 has a mutation status of D456G, The gene PLEKHG3 has a mutation status of H388Y, The gene RIOX1 has a mutation status of T307S, The gene GOLGA5 has a mutation status of K220T, The gene CEP170B has a mutation status of P1511P, The gene TMEM121 has a mutation status of P286P, The gene UBE3A has a mutation status of F785F, The gene MNS1 has a mutation status of D422E, The gene NOX5 has a mutation status of R671Q, The gene CHRNA3 has a mutation status of A461T, The gene IL16 has a mutation status of R1189G, The gene GOLGA6L10 has a mutation status of 387_388insDRLREL, The gene KLHL25 has a mutation status of M306I, The gene LRRK1 has a mutation status of H559H, The gene JPT2 has a mutation status of D61D, The gene NTN3 has a mutation status of T345P, The gene OR1F1 has a mutation status of V150V, The gene SEPTIN12 has a mutation status of D356N, The gene ITGAM has a mutation status of T1124P, The gene ATMIN has a mutation status of E67G, The gene CDT1 has a mutation status of T402P, The gene GALNS has a mutation status of G66V, The gene CBFA2T3 has a mutation status of T76T, The gene ZNF778 has a mutation status of G231A, The gene AC092143.1 has a mutation status of V122M, The gene SCGB1C2 has a mutation status of T22T, The gene CLDN7 has a mutation status of G179G, The gene CLDN7 has a mutation status of S172A, The gene SPEM2 has a mutation status of R125D, The gene SPEM3 has a mutation status of S88L, The gene DNAH9 has a mutation status of S237P, The gene CCL4L2 has a mutation status of P67R, The gene SPPL2C has a mutation status of A135A, The gene COL1A1 has a mutation status of A1075T, The gene SGSH has a mutation status of T47P, The gene DCC has a mutation status of P280P, The gene ZCCHC2 has a mutation status of A946V, The gene PHLPP1 has a mutation status of W312G, The gene CDH7 has a mutation status of P375P, The gene DIPK1C has a mutation status of L406P, The gene ZNF516 has a mutation status of D486A, The gene MISP has a mutation status of P421P, The gene GRIN3B has a mutation status of D391G, The gene ABCA7 has a mutation status of H1498P, The gene APC2 has a mutation status of G1962G, The gene PCSK4 has a mutation status of V111G, The gene TBXA2R has a mutation status of G56G, The gene CACTIN has a mutation status of R261R, The gene STAP2 has a mutation status of T150T, The gene RANBP3 has a mutation status of V227L, The gene TIMM44 has a mutation status of C11F, The gene MUC16 has a mutation status of H4357N, The gene S1PR2 has a mutation status of V310G, The gene FBXW9 has a mutation status of R338Q, The gene MAP1S has a mutation status of T410P, The gene TMEM59L has a mutation status of G264G, The gene PROSER3 has a mutation status of E340K, The gene ARHGAP33 has a mutation status of S964S, The gene WDR62 has a mutation status of G24G, The gene WDR62 has a mutation status of V25G, The gene PPP1R14A has a mutation status of L124P, The gene PSMD8 has a mutation status of K131N, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene MAP3K10 has a mutation status of D805A, The gene LTBP4 has a mutation status of T1556P, The gene VASP has a mutation status of D57A, The gene DMWD has a mutation status of H453P, The gene NOP53 has a mutation status of R36R, The gene RASIP1 has a mutation status of D489A, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene ZNF579 has a mutation status of V291G, The gene USP29 has a mutation status of A750E, The gene MZF1 has a mutation status of T702P, The gene TCF15 has a mutation status of R159P, The gene TCF15 has a mutation status of G158P, The gene CENPB has a mutation status of A153A, The gene RASSF2 has a mutation status of I58V, The gene PAX1 has a mutation status of Y386S, The gene CCM2L has a mutation status of D52N, The gene ZNF335 has a mutation status of L1161R, The gene TMPRSS3 has a mutation status of I320I, The gene PFKL has a mutation status of T770P, The gene TRPM2 has a mutation status of A553A, The gene RTN4R has a mutation status of V23G, The gene GSTT4 has a mutation status of Q197R, The gene KIAA1671 has a mutation status of P818L, The gene SEC14L3 has a mutation status of E204G, The gene SFI1 has a mutation status of E695G, The gene SSTR3 has a mutation status of T190P, The gene Z83844.3 has a mutation status of Y301fs, The gene MICALL1 has a mutation status of T313P, The gene MEI1 has a mutation status of T40P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of Q151R, The gene CYP2D6 has a mutation status of V136V, The gene TTC38 has a mutation status of V292M, The gene CCDC22 has a mutation status of E378D, The gene CCNB3 has a mutation status of T219T, The gene FAM120C has a mutation status of V138G, The gene AMER1 has a mutation status of G820G, The gene PWWP3B has a mutation status of P515S, The gene COL4A6 has a mutation status of R630H, The gene ALG13 has a mutation status of *1138Y, The gene GPC4 has a mutation status of F108F, The gene MT-ND3 has a mutation status of E38E, The gene MT-ND4 has a mutation status of F438L, The gene MT-ND5 has a mutation status of V92V, The gene MT-CYB has a mutation status of D171N, The gene MT-CYB has a mutation status of V356M
LAML
The gene RNF207 has a mutation status of E593Q, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF5 has a mutation status of P432A, The gene PRAMEF15 has a mutation status of L407L, The gene PDPN has a mutation status of I137V, The gene NBPF1 has a mutation status of E362Q, The gene RAP1GAP has a mutation status of S714T, The gene C1QC has a mutation status of A172A, The gene COL16A1 has a mutation status of G1105G, The gene EIF3I has a mutation status of S94L, The gene CSMD2 has a mutation status of H217H, The gene KLF18 has a mutation status of K992N, The gene SLC44A3 has a mutation status of V416G, The gene SPAG17 has a mutation status of V1266fs, The gene NBPF20 has a mutation status of L3357L, The gene NBPF11 has a mutation status of Q55H, The gene AC242842.3 has a mutation status of V503L, The gene ADAM15 has a mutation status of V271V, The gene CD244 has a mutation status of A52L, The gene NAV1 has a mutation status of T786K, The gene IPO9 has a mutation status of Y363N, The gene PTPN7 has a mutation status of G44G, The gene PLEKHA6 has a mutation status of N812N, The gene DSTYK has a mutation status of G20G, The gene INTS7 has a mutation status of L123V, The gene USH2A has a mutation status of Y4318F, The gene PYCR2 has a mutation status of V92M, The gene CDC42BPA has a mutation status of A19S, The gene OBSCN has a mutation status of T5745T, The gene TRIM17 has a mutation status of P451P, The gene LYST has a mutation status of R988Q, The gene HNRNPU has a mutation status of G703G, The gene TFB2M has a mutation status of T372I, The gene HPCAL1 has a mutation status of G95G, The gene OTOF has a mutation status of Y345Y, The gene C2orf16 has a mutation status of E4236A, The gene PRKCE has a mutation status of P507A, The gene BCL11A has a mutation status of R572R, The gene TIA1 has a mutation status of G284fs, The gene FBXO41 has a mutation status of 179_180insGP, The gene DCTN1 has a mutation status of K262K, The gene SULT1C2 has a mutation status of 140_141FL>LI, The gene EDAR has a mutation status of G226A, The gene SMPD4 has a mutation status of K404T, The gene UBXN4 has a mutation status of E193Q, The gene LRP2 has a mutation status of T2086S, The gene HOXD11 has a mutation status of G221W, The gene OSBPL6 has a mutation status of S912A, The gene TTN has a mutation status of V24147A, The gene DUSP19 has a mutation status of G101G, The gene FN1 has a mutation status of P620P, The gene COL4A3 has a mutation status of A413T, The gene MAB21L4 has a mutation status of R115W, The gene SNED1 has a mutation status of N630N, The gene PASK has a mutation status of E1305fs, The gene STK25 has a mutation status of P348P, The gene CHL1 has a mutation status of L427V, The gene ITPR1 has a mutation status of I2428I, The gene RPL32 has a mutation status of A3S, The gene SLC4A7 has a mutation status of R318H, The gene CLASP2 has a mutation status of K1305K, The gene DLEC1 has a mutation status of F510F, The gene SCN11A has a mutation status of T795T, The gene CCDC12 has a mutation status of A93T, The gene NBEAL2 has a mutation status of T2446M, The gene COL7A1 has a mutation status of P1795P, The gene DALRD3 has a mutation status of C385C, The gene DNAH1 has a mutation status of R1087C, The gene NISCH has a mutation status of E663K, The gene EOGT has a mutation status of F391F, The gene CLDND1 has a mutation status of R80W, The gene SENP7 has a mutation status of M511V, The gene HHLA2 has a mutation status of G387G, The gene BOC has a mutation status of N349D, The gene PLA1A has a mutation status of G111G, The gene HGD has a mutation status of E27A, The gene TXNRD3 has a mutation status of R370C, The gene PRR20G has a mutation status of P42T, The gene MGLL has a mutation status of T270T, The gene EEFSEC has a mutation status of A460A, The gene IFT122 has a mutation status of L562L, The gene ESYT3 has a mutation status of E4Q, The gene PXYLP1 has a mutation status of T44M, The gene DIPK2A has a mutation status of K182E, The gene EIF2A has a mutation status of H466R, The gene IGSF10 has a mutation status of S1873N, The gene ACTRT3 has a mutation status of P7A, The gene YEATS2 has a mutation status of I1226I, The gene AC131160.1 has a mutation status of L79L, The gene TP63 has a mutation status of E636Q, The gene OPA1 has a mutation status of I24T, The gene MUC4 has a mutation status of F279N, The gene FGFR3 has a mutation status of M432V, The gene OTOP1 has a mutation status of M495L, The gene MAN2B2 has a mutation status of N260S, The gene FAM90A26 has a mutation status of P382S, The gene SEL1L3 has a mutation status of I349V, The gene DTHD1 has a mutation status of L393V, The gene CORIN has a mutation status of S683R, The gene NFXL1 has a mutation status of A58A, The gene FRYL has a mutation status of P1902P, The gene OCIAD1 has a mutation status of P125R, The gene UGT2B28 has a mutation status of A346T, The gene SLC4A4 has a mutation status of K229K, The gene ARHGAP24 has a mutation status of T481M, The gene RAB33B has a mutation status of L86L, The gene FSTL5 has a mutation status of Y645C, The gene MSMO1 has a mutation status of N236S, The gene SPEF2 has a mutation status of L5R, The gene RICTOR has a mutation status of T144T, The gene ERBIN has a mutation status of A1141V, The gene CERT1 has a mutation status of A245A, The gene VCAN has a mutation status of V955D, The gene FBXL17 has a mutation status of C20S, The gene APC has a mutation status of N862K, The gene ETF1 has a mutation status of T329T, The gene PCDHB4 has a mutation status of V662E, The gene DCTN4 has a mutation status of S274S, The gene SLC36A3 has a mutation status of A158V, The gene FAT2 has a mutation status of R368K, The gene ADAM19 has a mutation status of P315R, The gene HIVEP1 has a mutation status of N272K, The gene MRS2 has a mutation status of G397A, The gene CARMIL1 has a mutation status of D533D, The gene AL031777.2 has a mutation status of P81L, The gene LY6G6F-LY6G6D has a mutation status of V334V, The gene STK19 has a mutation status of P101T, The gene TNXB has a mutation status of R847Q, The gene AL669918.1 has a mutation status of S289S, The gene TEAD3 has a mutation status of G33G, The gene TULP1 has a mutation status of A496T, The gene CLPS has a mutation status of S64S, The gene BTBD9 has a mutation status of E112E, The gene CUL9 has a mutation status of V1430M, The gene PHF3 has a mutation status of N99S, The gene MAP3K7 has a mutation status of S328T, The gene MAP3K5 has a mutation status of T1308I, The gene HEBP2 has a mutation status of P99P, The gene CCDC170 has a mutation status of S658L, The gene SYNE1 has a mutation status of S545S, The gene SYNJ2 has a mutation status of T1390A, The gene INTS1 has a mutation status of P847L, The gene ELFN1 has a mutation status of S74S, The gene FOXK1 has a mutation status of A33D, The gene FOXK1 has a mutation status of P214L, The gene YAE1 has a mutation status of P113T, The gene GLI3 has a mutation status of C1363C, The gene CAMK2B has a mutation status of P354S, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of R2339P, The gene MUC3A has a mutation status of P3166P, The gene MUC17 has a mutation status of L2358I, The gene CDHR3 has a mutation status of T631P, The gene SLC26A3 has a mutation status of N748N, The gene DLD has a mutation status of S10F, The gene ANKRD7 has a mutation status of H247H, The gene RBM28 has a mutation status of C44C, The gene KCP has a mutation status of W1164C, The gene PRSS2 has a mutation status of V118I, The gene MYOM2 has a mutation status of P811L, The gene CSMD1 has a mutation status of K2461K, The gene C8orf74 has a mutation status of L129L, The gene USP17L7 has a mutation status of G388C, The gene PCM1 has a mutation status of S2002C, The gene PSD3 has a mutation status of Q444R, The gene TNFRSF10A has a mutation status of *469L, The gene NEFL has a mutation status of A486A, The gene AC083977.1 has a mutation status of V50M, The gene UNC5D has a mutation status of S226A, The gene ZNF703 has a mutation status of G558S, The gene RPL7 has a mutation status of N40Y, The gene JPH1 has a mutation status of G215V, The gene VPS13B has a mutation status of Y1164H, The gene VPS13B has a mutation status of P2176P, The gene SLA has a mutation status of S219S, The gene FAM135B has a mutation status of I554T, The gene TSTA3 has a mutation status of P125L, The gene EXOSC4 has a mutation status of E238Q, The gene ZNF251 has a mutation status of T456A, The gene JAK2 has a mutation status of V617F, The gene TRIM14 has a mutation status of G113E, The gene FRRS1L has a mutation status of R51A, The gene C5 has a mutation status of L571V, The gene GARNL3 has a mutation status of P637S, The gene ENG has a mutation status of H108Y, The gene COL5A1 has a mutation status of P996P, The gene DIP2C has a mutation status of P1351P, The gene AKR1C3 has a mutation status of A52G, The gene CDC123 has a mutation status of D278D, The gene OPTN has a mutation status of S263R, The gene ANKRD30A has a mutation status of D1406Y, The gene TIMM23 has a mutation status of T64T, The gene WASHC2A has a mutation status of G444fs, The gene DKK1 has a mutation status of M178L, The gene PRF1 has a mutation status of G413G, The gene UNC5B has a mutation status of A924A, The gene DLG5 has a mutation status of H381R, The gene ENTPD1 has a mutation status of H428N, The gene LZTS2 has a mutation status of R121R, The gene STN1 has a mutation status of I327T, The gene TACC2 has a mutation status of E1109E, The gene PTPRE has a mutation status of P670S, The gene EPS8L2 has a mutation status of K221Q, The gene MUC5AC has a mutation status of T3668P, The gene DNHD1 has a mutation status of L764W, The gene C11orf16 has a mutation status of E2D, The gene MADD has a mutation status of S700C, The gene OR5I1 has a mutation status of I276fs, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene ZDHHC5 has a mutation status of V181I, The gene FAM111A has a mutation status of E267Q, The gene TMEM132A has a mutation status of A953G, The gene CAPN1 has a mutation status of P533S, The gene CTSW has a mutation status of T261T, The gene ACTN3 has a mutation status of R728H, The gene TCIRG1 has a mutation status of P390S, The gene MYEOV has a mutation status of C313S, The gene NUMA1 has a mutation status of V652V, The gene PRCP has a mutation status of D377N, The gene CCDC90B has a mutation status of N171K, The gene TRIM77 has a mutation status of K232K, The gene SRSF8 has a mutation status of G113S, The gene EXPH5 has a mutation status of Q1700R, The gene TTC12 has a mutation status of L613V, The gene ZPR1 has a mutation status of R226Q, The gene SIK3 has a mutation status of R500R, The gene CEP164 has a mutation status of K318*, The gene UBE4A has a mutation status of Q39L, The gene ARHGEF12 has a mutation status of D308Y, The gene TECTA has a mutation status of C305C, The gene VWF has a mutation status of T2023M, The gene ACSM4 has a mutation status of C253C, The gene GDF3 has a mutation status of T160T, The gene A2M has a mutation status of R1031Q, The gene OLR1 has a mutation status of L173F, The gene TAS2R13 has a mutation status of L109H, The gene PTPRO has a mutation status of S251S, The gene DERA has a mutation status of G252A, The gene MUC19 has a mutation status of Q259K, The gene KMT2D has a mutation status of T2524M, The gene SLC39A5 has a mutation status of L447P, The gene MYO1A has a mutation status of G674D, The gene GLI1 has a mutation status of G600C, The gene MARS1 has a mutation status of L773P, The gene KIF5A has a mutation status of T976I, The gene CYP27B1 has a mutation status of I198V, The gene IRAK3 has a mutation status of E494K, The gene PTPRB has a mutation status of T968I, The gene CEP83 has a mutation status of C221R, The gene WASHC4 has a mutation status of E4D, The gene ACAD10 has a mutation status of R834H, The gene P2RX7 has a mutation status of I568N, The gene AACS has a mutation status of G610D, The gene TMEM132C has a mutation status of V695L, The gene POLE has a mutation status of I634V, The gene SOHLH2 has a mutation status of T314M, The gene FREM2 has a mutation status of R53R, The gene NUFIP1 has a mutation status of K402E, The gene COG3 has a mutation status of P739S, The gene ATP7B has a mutation status of G869E, The gene ALG11 has a mutation status of L266L, The gene SLITRK5 has a mutation status of V620I, The gene SLITRK5 has a mutation status of C882S, The gene ERCC5 has a mutation status of N1566N, The gene ZFHX2 has a mutation status of D2061N, The gene L3HYPDH has a mutation status of R109Q, The gene EIF2S1 has a mutation status of P224P, The gene CEP170B has a mutation status of L742S, The gene NPAP1 has a mutation status of D304N, The gene TYRO3 has a mutation status of V233fs, The gene TYRO3 has a mutation status of D555fs, The gene STARD9 has a mutation status of S4482F, The gene TUBGCP4 has a mutation status of E367E, The gene SQOR has a mutation status of G50G, The gene MYO1E has a mutation status of R362Q, The gene SNX22 has a mutation status of N118S, The gene ANKDD1A has a mutation status of L516L, The gene THAP10 has a mutation status of R132H, The gene STRA6 has a mutation status of S112N, The gene GOLGA6C has a mutation status of N364N, The gene WHAMM has a mutation status of F41F, The gene AKAP13 has a mutation status of T605T, The gene KIF7 has a mutation status of I464V, The gene UNC45A has a mutation status of A642A, The gene ST8SIA2 has a mutation status of Y313Y, The gene RAB11FIP3 has a mutation status of E445K, The gene ABCA3 has a mutation status of S608S, The gene MEFV has a mutation status of M500I, The gene TNRC6A has a mutation status of S1100S, The gene APOBR has a mutation status of T882T, The gene CD19 has a mutation status of L285P, The gene SETD1A has a mutation status of R1288C, The gene NDRG4 has a mutation status of R12Q, The gene CES3 has a mutation status of F216L, The gene FA2H has a mutation status of R113W, The gene SPATA33 has a mutation status of V99V, The gene HIC1 has a mutation status of A675E, The gene SGSM2 has a mutation status of G411R, The gene ACADVL has a mutation status of R538R, The gene SPEM2 has a mutation status of R126H, The gene TP53 has a mutation status of M133K, The gene NCOR1 has a mutation status of Y311Y, The gene RSKR has a mutation status of L368R, The gene CCL4L2 has a mutation status of P67R, The gene SYNRG has a mutation status of D1224G, The gene CASC3 has a mutation status of R350Q, The gene CDC6 has a mutation status of E487E, The gene KRT39 has a mutation status of L72V, The gene KRT40 has a mutation status of R159T, The gene PTGES3L-AARSD1 has a mutation status of D353D, The gene CRHR1 has a mutation status of Q43Q, The gene HOXB7 has a mutation status of G64R, The gene LRRC37A3 has a mutation status of G1530E, The gene AMZ2 has a mutation status of F209L, The gene LLGL2 has a mutation status of R667Q, The gene SEPTIN9 has a mutation status of T200T, The gene DNAH17 has a mutation status of Q1891Q, The gene TBC1D16 has a mutation status of D655D, The gene SGSH has a mutation status of R169W, The gene RNF213 has a mutation status of S2483S, The gene P4HB has a mutation status of K342K, The gene TMEM200C has a mutation status of D528E, The gene CIDEA has a mutation status of E88D, The gene DSG4 has a mutation status of G400fs, The gene C18orf54 has a mutation status of S149N, The gene ATP9B has a mutation status of T1120T, The gene POLRMT has a mutation status of G327E, The gene PWWP3A has a mutation status of K581K, The gene TCF3 has a mutation status of P27P, The gene DUS3L has a mutation status of S563L, The gene MBD3L2B has a mutation status of R201Q, The gene FBN3 has a mutation status of R166C, The gene HNRNPM has a mutation status of P331H, The gene NIBAN3 has a mutation status of V326M, The gene MAST3 has a mutation status of D80D, The gene ZNF737 has a mutation status of T523S, The gene SBSN has a mutation status of T220T, The gene KMT2B has a mutation status of P174A, The gene TBCB has a mutation status of G131S, The gene ZNF568 has a mutation status of S204N, The gene PPP1R14A has a mutation status of R65C, The gene RYR1 has a mutation status of I1571V, The gene RYR1 has a mutation status of R3366H, The gene RYR1 has a mutation status of Y3933C, The gene CAPN12 has a mutation status of R518L, The gene RINL has a mutation status of R401G, The gene IFNL2 has a mutation status of R161W, The gene FCGBP has a mutation status of D617D, The gene PLD3 has a mutation status of A123T, The gene CYP2A6 has a mutation status of Y351H, The gene B3GNT8 has a mutation status of F70L, The gene MEGF8 has a mutation status of R2065Q, The gene PSG7 has a mutation status of W67S, The gene ZNF229 has a mutation status of T791N, The gene FCGRT has a mutation status of A294G, The gene KLK3 has a mutation status of R201L, The gene CNOT3 has a mutation status of E220K, The gene CNOT3 has a mutation status of A621A, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene TTYH1 has a mutation status of D427D, The gene LILRB1 has a mutation status of E34E, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene NLRP7 has a mutation status of F523F, The gene TMEM238 has a mutation status of A6A, The gene SSC5D has a mutation status of H215H, The gene FIZ1 has a mutation status of G410G, The gene ZNF324 has a mutation status of T508T, The gene MZF1 has a mutation status of A498A, The gene C20orf194 has a mutation status of L117fs, The gene ADAM33 has a mutation status of P592del, The gene BMP2 has a mutation status of G88A, The gene PAK5 has a mutation status of M338L, The gene PCSK2 has a mutation status of R605W, The gene NKX2-4 has a mutation status of 185_186insA, The gene PYGB has a mutation status of G23G, The gene BPIFB1 has a mutation status of V203M, The gene C20orf144 has a mutation status of E109E, The gene NCOA6 has a mutation status of E1844del, The gene EPB41L1 has a mutation status of R572C, The gene SOGA1 has a mutation status of S381S, The gene SNX21 has a mutation status of P224P, The gene CDH4 has a mutation status of G523S, The gene LAMA5 has a mutation status of Q1456Q, The gene NCAM2 has a mutation status of P240P, The gene KRTAP26-1 has a mutation status of S8L, The gene TTC3 has a mutation status of T357I, The gene RIPK4 has a mutation status of N328N, The gene MCM3AP has a mutation status of S493N, The gene ZNRF3 has a mutation status of R4H, The gene MIEF1 has a mutation status of L415L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene EFCAB6 has a mutation status of C1102C, The gene TUBGCP6 has a mutation status of N1186S, The gene IL3RA has a mutation status of Q69H, The gene BCOR has a mutation status of Y1350Y, The gene ZXDA has a mutation status of Q138L, The gene SLC6A8 has a mutation status of M560V, The gene HCFC1 has a mutation status of A1173A, The gene UTY has a mutation status of S451S, The gene NLGN4Y has a mutation status of T213T, The gene MT-ND2 has a mutation status of Y208Y, The gene MT-CO2 has a mutation status of Q59Q, The gene MT-ND5 has a mutation status of T533A, The gene MT-CYB has a mutation status of T158A, The gene RNF207 has a mutation status of E593Q, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF15 has a mutation status of L407L, The gene PDPN has a mutation status of I137V, The gene CASP9 has a mutation status of G402A, The gene NBPF1 has a mutation status of E362Q, The gene RAP1GAP has a mutation status of S714T, The gene C1QC has a mutation status of A172A, The gene COL16A1 has a mutation status of G1105G, The gene EIF3I has a mutation status of S94L, The gene CSMD2 has a mutation status of H217H, The gene SLC44A3 has a mutation status of V416G, The gene SPAG17 has a mutation status of V1266fs, The gene NBPF20 has a mutation status of L3357L, The gene NBPF11 has a mutation status of Q55H, The gene CD244 has a mutation status of A52L, The gene NAV1 has a mutation status of T786K, The gene IPO9 has a mutation status of Y363N, The gene PTPN7 has a mutation status of G44G, The gene PLEKHA6 has a mutation status of N812N, The gene INTS7 has a mutation status of L123V, The gene USH2A has a mutation status of Y4318F, The gene DEGS1 has a mutation status of P266T, The gene CDC42BPA has a mutation status of A19S, The gene TFB2M has a mutation status of T372I, The gene HPCAL1 has a mutation status of G95G, The gene C2orf16 has a mutation status of E4236A, The gene PRKCE has a mutation status of P507A, The gene AFTPH has a mutation status of R599Q, The gene TIA1 has a mutation status of G284fs, The gene DCTN1 has a mutation status of K262K, The gene SULT1C2 has a mutation status of 140_141FL>LI, The gene EDAR has a mutation status of G226A, The gene SMPD4 has a mutation status of K404T, The gene OSBPL6 has a mutation status of S912A, The gene TTN has a mutation status of V24147A, The gene DUSP19 has a mutation status of G101G, The gene COL4A3 has a mutation status of A413T, The gene MAB21L4 has a mutation status of R115W, The gene PASK has a mutation status of E1305fs, The gene CHL1 has a mutation status of L427V, The gene ITPR1 has a mutation status of I2428I, The gene RPL32 has a mutation status of A3S, The gene SLC4A7 has a mutation status of R318H, The gene CLASP2 has a mutation status of K1305K, The gene DLEC1 has a mutation status of F510F, The gene SCN11A has a mutation status of T795T, The gene DALRD3 has a mutation status of C385C, The gene NISCH has a mutation status of E663K, The gene DNAH12 has a mutation status of S3174S, The gene DNAH12 has a mutation status of E2938E, The gene EOGT has a mutation status of F391F, The gene CLDND1 has a mutation status of R80W, The gene SENP7 has a mutation status of M511V, The gene BOC has a mutation status of N349D, The gene PLA1A has a mutation status of G111G, The gene HGD has a mutation status of E27A, The gene MGLL has a mutation status of T270T, The gene EEFSEC has a mutation status of A460A, The gene IFT122 has a mutation status of L562L, The gene ESYT3 has a mutation status of E4Q, The gene EIF2A has a mutation status of H466R, The gene IGSF10 has a mutation status of S1873N, The gene YEATS2 has a mutation status of I1226I, The gene TP63 has a mutation status of E636Q, The gene OPA1 has a mutation status of I24T, The gene MUC4 has a mutation status of F279N, The gene FGFR3 has a mutation status of M432V, The gene OTOP1 has a mutation status of M495L, The gene MAN2B2 has a mutation status of N260S, The gene SEL1L3 has a mutation status of I349V, The gene CORIN has a mutation status of S683R, The gene FRYL has a mutation status of P1902P, The gene SLC4A4 has a mutation status of K229K, The gene ARHGAP24 has a mutation status of T481M, The gene DSPP has a mutation status of D1155D, The gene RAB33B has a mutation status of L86L, The gene FSTL5 has a mutation status of Y645C, The gene SPEF2 has a mutation status of L5R, The gene ERBIN has a mutation status of A1141V, The gene CERT1 has a mutation status of A245A, The gene VCAN has a mutation status of V955D, The gene FBXL17 has a mutation status of C20S, The gene APC has a mutation status of N862K, The gene ETF1 has a mutation status of T329T, The gene PCDHB4 has a mutation status of V662E, The gene DCTN4 has a mutation status of S274S, The gene SLC36A3 has a mutation status of A158V, The gene FAT2 has a mutation status of R368K, The gene ADAM19 has a mutation status of P315R, The gene HIVEP1 has a mutation status of N272K, The gene MRS2 has a mutation status of G397A, The gene CARMIL1 has a mutation status of D533D, The gene AL031777.2 has a mutation status of P81L, The gene OR2I1P has a mutation status of R130S, The gene MUC22 has a mutation status of G1102fs, The gene LY6G6F-LY6G6D has a mutation status of V334V, The gene STK19 has a mutation status of P101T, The gene HLA-DRB5 has a mutation status of L246L, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DRB1 has a mutation status of I248L, The gene TULP1 has a mutation status of A496T, The gene CLPS has a mutation status of S64S, The gene BTBD9 has a mutation status of E112E, The gene PGM3 has a mutation status of T78K, The gene MAP3K7 has a mutation status of S328T, The gene MAP3K5 has a mutation status of T1308I, The gene CCDC170 has a mutation status of S658L, The gene SYNE1 has a mutation status of S545S, The gene SYNJ2 has a mutation status of T1390A, The gene INTS1 has a mutation status of P847L, The gene ELFN1 has a mutation status of S74S, The gene FOXK1 has a mutation status of P214L, The gene YAE1 has a mutation status of P113T, The gene GLI3 has a mutation status of C1363C, The gene CAMK2B has a mutation status of P354S, The gene ZNF727 has a mutation status of K275E, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of V2475S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene MUC17 has a mutation status of L2358I, The gene CDHR3 has a mutation status of T631P, The gene SLC26A3 has a mutation status of N748N, The gene DLD has a mutation status of S10F, The gene ANKRD7 has a mutation status of H247H, The gene RBM28 has a mutation status of C44C, The gene KCP has a mutation status of W1164C, The gene COPG2 has a mutation status of T552T, The gene PRSS2 has a mutation status of V118I, The gene IQCA1L has a mutation status of 588_589insL, The gene CSMD1 has a mutation status of K2461K, The gene C8orf74 has a mutation status of L129L, The gene PCM1 has a mutation status of S2002C, The gene AC083977.1 has a mutation status of V50M, The gene UNC5D has a mutation status of S226A, The gene ZNF703 has a mutation status of G558S, The gene RPL7 has a mutation status of N40Y, The gene JPH1 has a mutation status of G215V, The gene VPS13B has a mutation status of Y1164H, The gene SLA has a mutation status of S219S, The gene FAM135B has a mutation status of I554T, The gene TSTA3 has a mutation status of P125L, The gene EXOSC4 has a mutation status of E238Q, The gene ZNF251 has a mutation status of T456A, The gene JAK2 has a mutation status of V617F, The gene TRIM14 has a mutation status of G113E, The gene C5 has a mutation status of L571V, The gene GARNL3 has a mutation status of P637S, The gene ENG has a mutation status of H108Y, The gene COL5A1 has a mutation status of P996P, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene DIP2C has a mutation status of P1351P, The gene OPTN has a mutation status of S263R, The gene ANKRD30A has a mutation status of D1406Y, The gene AGAP4 has a mutation status of Q20Q, The gene TIMM23 has a mutation status of T64T, The gene TIMM23 has a mutation status of S139S, The gene AGAP9 has a mutation status of S611A, The gene PARG has a mutation status of Q192Q, The gene DKK1 has a mutation status of M178L, The gene PRF1 has a mutation status of G413G, The gene UNC5B has a mutation status of A924A, The gene DLG5 has a mutation status of H381R, The gene ENTPD1 has a mutation status of H428N, The gene STN1 has a mutation status of I327T, The gene TACC2 has a mutation status of E1109E, The gene PTPRE has a mutation status of P670S, The gene EPS8L2 has a mutation status of K221Q, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of R3590R, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4396A, The gene MUC5AC has a mutation status of P4427S, The gene MUC5AC has a mutation status of STTSASTA4496del, The gene DNHD1 has a mutation status of L764W, The gene C11orf16 has a mutation status of E2D, The gene MADD has a mutation status of S700C, The gene OR5I1 has a mutation status of I276fs, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene ZDHHC5 has a mutation status of V181I, The gene FAM111A has a mutation status of E267Q, The gene TMEM132A has a mutation status of A953G, The gene CTSW has a mutation status of T261T, The gene TCIRG1 has a mutation status of P390S, The gene MYEOV has a mutation status of C313S, The gene NUMA1 has a mutation status of V652V, The gene PRCP has a mutation status of D377N, The gene CCDC90B has a mutation status of N171K, The gene TRIM77 has a mutation status of K232K, The gene SRSF8 has a mutation status of G113S, The gene EXPH5 has a mutation status of Q1700R, The gene CEP164 has a mutation status of K318*, The gene UBE4A has a mutation status of Q39L, The gene ARHGEF12 has a mutation status of D308Y, The gene TAS2R46 has a mutation status of 296_297HV>QM, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene PTPRO has a mutation status of S251S, The gene DERA has a mutation status of G252A, The gene MUC19 has a mutation status of Q259K, The gene GXYLT1 has a mutation status of C414H, The gene KMT2D has a mutation status of T2524M, The gene DAZAP2 has a mutation status of L130A, The gene SLC39A5 has a mutation status of L447P, The gene CYP27B1 has a mutation status of I198V, The gene IRAK3 has a mutation status of E494K, The gene WASHC4 has a mutation status of E4D, The gene P2RX7 has a mutation status of I568N, The gene TMEM132C has a mutation status of V695L, The gene POLE has a mutation status of I634V, The gene SOHLH2 has a mutation status of T314M, The gene FREM2 has a mutation status of R53R, The gene ATP7B has a mutation status of G869E, The gene ALG11 has a mutation status of L266L, The gene SLITRK5 has a mutation status of V620I, The gene SLITRK5 has a mutation status of C882S, The gene ZFHX2 has a mutation status of D2061N, The gene L3HYPDH has a mutation status of R109Q, The gene EIF2S1 has a mutation status of P224P, The gene CEP170B has a mutation status of L742S, The gene NPAP1 has a mutation status of D304N, The gene TMEM87A has a mutation status of F426fs, The gene TMEM87A has a mutation status of M424fs, The gene STARD9 has a mutation status of S4482F, The gene TUBGCP4 has a mutation status of E367E, The gene MYO1E has a mutation status of R362Q, The gene ANKDD1A has a mutation status of L516L, The gene THAP10 has a mutation status of R132H, The gene STRA6 has a mutation status of S112N, The gene GOLGA6L10 has a mutation status of C286R, The gene GOLGA6L9 has a mutation status of R6H, The gene WHAMM has a mutation status of F41F, The gene UNC45A has a mutation status of A642A, The gene RAB11FIP3 has a mutation status of E445K, The gene ABCA3 has a mutation status of S608S, The gene MEFV has a mutation status of M500I, The gene REXO5 has a mutation status of L436fs, The gene TNRC6A has a mutation status of S1100S, The gene APOBR has a mutation status of T882T, The gene CD19 has a mutation status of L285P, The gene SETD1A has a mutation status of R1288C, The gene NDRG4 has a mutation status of R12Q, The gene CES3 has a mutation status of F216L, The gene HYDIN has a mutation status of V189V, The gene FA2H has a mutation status of R113W, The gene SPATA33 has a mutation status of V99V, The gene HIC1 has a mutation status of A675E, The gene SGSM2 has a mutation status of G411R, The gene ACADVL has a mutation status of R538R, The gene SPEM2 has a mutation status of R126H, The gene TP53 has a mutation status of M133K, The gene NCOR1 has a mutation status of Y311Y, The gene TBC1D3B has a mutation status of S510G, The gene CCL4L2 has a mutation status of P67R, The gene CASC3 has a mutation status of R350Q, The gene CDC6 has a mutation status of E487E, The gene KRT39 has a mutation status of L72V, The gene KRTAP9-6 has a mutation status of G106C, The gene PTGES3L-AARSD1 has a mutation status of D353D, The gene AMZ2 has a mutation status of F209L, The gene GRIN2C has a mutation status of R997C, The gene MYO15B has a mutation status of G470D, The gene MYO15B has a mutation status of G474A, The gene MYO15B has a mutation status of S620H, The gene DNAH17 has a mutation status of Q1891Q, The gene SGSH has a mutation status of R169W, The gene TMEM200C has a mutation status of D528E, The gene CIDEA has a mutation status of E88D, The gene DSG4 has a mutation status of G400fs, The gene ATP9B has a mutation status of T1120T, The gene POLRMT has a mutation status of G327E, The gene PWWP3A has a mutation status of K581K, The gene TCF3 has a mutation status of P27P, The gene DUS3L has a mutation status of S563L, The gene HNRNPM has a mutation status of P331H, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of H12873R, The gene MUC16 has a mutation status of T12336L, The gene NIBAN3 has a mutation status of V326M, The gene ZNF737 has a mutation status of T523S, The gene ZNF66 has a mutation status of F97F, The gene KMT2B has a mutation status of P174A, The gene TBCB has a mutation status of G131S, The gene RYR1 has a mutation status of R3366H, The gene CAPN12 has a mutation status of R518L, The gene PLD3 has a mutation status of A123T, The gene ZNF229 has a mutation status of T791N, The gene FCGRT has a mutation status of A294G, The gene KLK3 has a mutation status of R201L, The gene CNOT3 has a mutation status of E220K, The gene CNOT3 has a mutation status of A621A, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene TTYH1 has a mutation status of D427D, The gene LILRA2 has a mutation status of H13P, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene TMEM238 has a mutation status of A6A, The gene C20orf194 has a mutation status of L117fs, The gene ADAM33 has a mutation status of P592del, The gene BMP2 has a mutation status of G88A, The gene PAK5 has a mutation status of M338L, The gene PCSK2 has a mutation status of R605W, The gene PYGB has a mutation status of G23G, The gene NCOA6 has a mutation status of E1844del, The gene SNX21 has a mutation status of P224P, The gene LAMA5 has a mutation status of Q1456Q, The gene NCAM2 has a mutation status of P240P, The gene TTC3 has a mutation status of T357I, The gene RIPK4 has a mutation status of N328N, The gene MCM3AP has a mutation status of S493N, The gene CLTCL1 has a mutation status of V652F, The gene GSTT4 has a mutation status of P89L, The gene MIEF1 has a mutation status of L415L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene EFCAB6 has a mutation status of C1102C, The gene TUBGCP6 has a mutation status of N1186S, The gene GTPBP6 has a mutation status of G61R, The gene BCOR has a mutation status of Y1350Y, The gene SLC25A5 has a mutation status of T221R, The gene SLC6A8 has a mutation status of M560V, The gene HCFC1 has a mutation status of A1173A, The gene UTY has a mutation status of S451S, The gene NLGN4Y has a mutation status of T213T, The gene MT-CO1 has a mutation status of H52H, The gene MT-ND5 has a mutation status of T533A, The gene MT-CYB has a mutation status of T158A
LAML
The gene RERE has a mutation status of A793A, The gene MTHFR has a mutation status of D163D, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene TMEM51 has a mutation status of H102P, The gene TMCO4 has a mutation status of G453E, The gene TMCO4 has a mutation status of E75G, The gene CLIC4 has a mutation status of R250R, The gene TMEM39B has a mutation status of D210A, The gene MACF1 has a mutation status of A6494T, The gene UROD has a mutation status of L234L, The gene DMRTA2 has a mutation status of A396V, The gene CTBS has a mutation status of A117fs, The gene ARHGAP29 has a mutation status of L878R, The gene POLR3C has a mutation status of M394T, The gene SLC27A3 has a mutation status of S216S, The gene SLC25A44 has a mutation status of E253E, The gene PAQR6 has a mutation status of A314V, The gene USH2A has a mutation status of K1986R, The gene ZNF695 has a mutation status of A360T, The gene OR1C1 has a mutation status of A67S, The gene ALLC has a mutation status of P257P, The gene TDRD15 has a mutation status of G1784A, The gene BIRC6 has a mutation status of N3138S, The gene OXER1 has a mutation status of S325P, The gene PPP4R3B has a mutation status of P253R, The gene ADD2 has a mutation status of E301G, The gene CD207 has a mutation status of H229Q, The gene MRPL19 has a mutation status of L26P, The gene NCKAP5 has a mutation status of P1829L, The gene LRP1B has a mutation status of Y4006Y, The gene FSIP2 has a mutation status of T4430S, The gene IDH1 has a mutation status of L288L, The gene SCYGR2 has a mutation status of C31R, The gene ALPI has a mutation status of M229L, The gene USP40 has a mutation status of H665L, The gene MROH2A has a mutation status of P1243P, The gene PASK has a mutation status of V178L, The gene TTC14 has a mutation status of F265L, The gene ETV5 has a mutation status of F131L, The gene TMEM175 has a mutation status of H484P, The gene HTT has a mutation status of D2796D, The gene MED28 has a mutation status of T68A, The gene TLR10 has a mutation status of D362N, The gene MCUB has a mutation status of I141T, The gene AC126283.2 has a mutation status of C266R, The gene FGF2 has a mutation status of R42R, The gene FAT4 has a mutation status of Y4219*, The gene SH3RF1 has a mutation status of Q566K, The gene DNAH5 has a mutation status of E2558D, The gene CPLANE1 has a mutation status of P3084P, The gene MAP3K1 has a mutation status of V936L, The gene MAP1B has a mutation status of G800S, The gene ADGRV1 has a mutation status of A4147P, The gene FBN2 has a mutation status of K1759Q, The gene SAR1B has a mutation status of L168L, The gene LECT2 has a mutation status of Y81S, The gene SGCD has a mutation status of E262K, The gene HIVEP1 has a mutation status of P2620P, The gene HLA-C has a mutation status of S140L, The gene HLA-B has a mutation status of Y140L, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q38W, The gene COL11A2 has a mutation status of P1261L, The gene ITPR3 has a mutation status of L1811R, The gene AARS2 has a mutation status of S71R, The gene ADGRF1 has a mutation status of T564I, The gene SMPD2 has a mutation status of T135S, The gene FAM184A has a mutation status of V107A, The gene TCF21 has a mutation status of K66K, The gene FAM220A has a mutation status of T138S, The gene STK31 has a mutation status of H379H, The gene NPC1L1 has a mutation status of A165A, The gene ELN has a mutation status of G514G, The gene PCLO has a mutation status of P872P, The gene ASB4 has a mutation status of R318Q, The gene PDK4 has a mutation status of S337F, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2042S, The gene MUC3A has a mutation status of D2269G, The gene MUC3A has a mutation status of K2298E, The gene ST7 has a mutation status of A355S, The gene KLF14 has a mutation status of P58S, The gene EPHA1 has a mutation status of T230A, The gene VIPR2 has a mutation status of T396P, The gene DOCK5 has a mutation status of R1540Q, The gene KIF13B has a mutation status of K1749E, The gene TCEA1 has a mutation status of S128*, The gene TGS1 has a mutation status of E330G, The gene HNF4G has a mutation status of S142A, The gene KCNQ3 has a mutation status of V406I, The gene SLC39A4 has a mutation status of R251W, The gene KANK1 has a mutation status of K1179N, The gene SPATA31A6 has a mutation status of C398F, The gene PCSK5 has a mutation status of S87R, The gene OLFML2A has a mutation status of S57R, The gene TTC16 has a mutation status of A550A, The gene UCK1 has a mutation status of *278W, The gene ADAMTS13 has a mutation status of G861R, The gene MRPS2 has a mutation status of T30P, The gene ABCA2 has a mutation status of V1665G, The gene NDOR1 has a mutation status of K504E, The gene ITIH2 has a mutation status of P88L, The gene WASHC2A has a mutation status of A761V, The gene LRRTM3 has a mutation status of F153F, The gene RNLS has a mutation status of Q53R, The gene LIPJ has a mutation status of Y295H, The gene ACSM6 has a mutation status of Q340H, The gene INA has a mutation status of A27P, The gene JAKMIP3 has a mutation status of A556V, The gene CFAP46 has a mutation status of A550S, The gene MUC6 has a mutation status of T1071P, The gene MUC5AC has a mutation status of R2899S, The gene MUC5AC has a mutation status of T4991P, The gene PHLDA2 has a mutation status of A121A, The gene PHLDA2 has a mutation status of A118A, The gene OR5D14 has a mutation status of I53S, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene GLYAT has a mutation status of P23P, The gene DDB1 has a mutation status of V364M, The gene MAP3K11 has a mutation status of H186P, The gene DHCR7 has a mutation status of V402G, The gene DHCR7 has a mutation status of G401G, The gene ACAT1 has a mutation status of C126C, The gene ZW10 has a mutation status of R76K, The gene PTPN6 has a mutation status of V453M, The gene FOXJ2 has a mutation status of P295P, The gene AICDA has a mutation status of Y144F, The gene RERG has a mutation status of I105I, The gene PLCZ1 has a mutation status of E74G, The gene ASB8 has a mutation status of I183T, The gene NCKAP5L has a mutation status of G253S, The gene MAP3K12 has a mutation status of E421G, The gene CCER1 has a mutation status of L250fs, The gene ACTR6 has a mutation status of V24F, The gene HVCN1 has a mutation status of M71T, The gene DNAH10 has a mutation status of T3545P, The gene BRI3BP has a mutation status of E228E, The gene FLT3 has a mutation status of V592A, The gene FAM124A has a mutation status of P342L, The gene WDFY2 has a mutation status of D285fs, The gene NDRG2 has a mutation status of Q8*, The gene SALL2 has a mutation status of P46R, The gene OR10G3 has a mutation status of G153G, The gene MYH6 has a mutation status of T1284T, The gene NUBPL has a mutation status of A214T, The gene ATP6V1D has a mutation status of E55K, The gene ACOT6 has a mutation status of V94G, The gene SLC24A4 has a mutation status of T592T, The gene PPP4R4 has a mutation status of G71E, The gene MARK3 has a mutation status of P580P, The gene HERC2 has a mutation status of A4555A, The gene HERC2 has a mutation status of S3111S, The gene PLCB2 has a mutation status of T111P, The gene SEMA7A has a mutation status of N533N, The gene PKMYT1 has a mutation status of V82G, The gene XYLT1 has a mutation status of D796N, The gene UMOD has a mutation status of S324G, The gene ATXN2L has a mutation status of P41S, The gene ZNF747 has a mutation status of R298P, The gene SRCAP has a mutation status of P3019S, The gene CCDC102A has a mutation status of V446G, The gene PLEKHG4 has a mutation status of F759Y, The gene BCO1 has a mutation status of D176E, The gene NECAB2 has a mutation status of T212P, The gene MBTPS1 has a mutation status of V814I, The gene PIEZO1 has a mutation status of R1955R, The gene MYBBP1A has a mutation status of P1258P, The gene SMTNL2 has a mutation status of T130T, The gene TP53 has a mutation status of R273H, The gene DNAH2 has a mutation status of S2076P, The gene PIK3R5 has a mutation status of H199H, The gene NLK has a mutation status of S257*, The gene CCL4L2 has a mutation status of P67R, The gene ARHGAP23 has a mutation status of V1409G, The gene KRTAP29-1 has a mutation status of H88H, The gene MAPT has a mutation status of R5H, The gene CDK5RAP3 has a mutation status of E148K, The gene ABI3 has a mutation status of V86G, The gene XYLT2 has a mutation status of F520L, The gene WFIKKN2 has a mutation status of E420K, The gene COIL has a mutation status of E62G, The gene TACO1 has a mutation status of P32P, The gene DDX5 has a mutation status of V323I, The gene GNA13 has a mutation status of S9S, The gene KIF19 has a mutation status of L585L, The gene TMEM104 has a mutation status of A47E, The gene SEPTIN9 has a mutation status of Q118P, The gene USP36 has a mutation status of A1051V, The gene BAIAP2 has a mutation status of P190L, The gene ACTG1 has a mutation status of Y218Y, The gene FOXK2 has a mutation status of V474I, The gene DSG1 has a mutation status of E708K, The gene HCN2 has a mutation status of A141L, The gene DAZAP1 has a mutation status of S381W, The gene PEX11G has a mutation status of P210P, The gene CAMSAP3 has a mutation status of M600T, The gene XAB2 has a mutation status of P518P, The gene ZNF558 has a mutation status of A10A, The gene ZNF675 has a mutation status of F95S, The gene CHST8 has a mutation status of D67N, The gene LSR has a mutation status of V173I, The gene RYR1 has a mutation status of S1489N, The gene LGALS16 has a mutation status of G86S, The gene IRGC has a mutation status of S141P, The gene EXOC3L2 has a mutation status of Q84K, The gene VASP has a mutation status of P185P, The gene AKT1S1 has a mutation status of E114G, The gene SHANK1 has a mutation status of G1814G, The gene FPR3 has a mutation status of I284I, The gene LILRA2 has a mutation status of W163S, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of T333A, The gene DNAAF3 has a mutation status of D323D, The gene SIRPA has a mutation status of L44S, The gene VPS16 has a mutation status of T323N, The gene CENPB has a mutation status of T150P, The gene RRBP1 has a mutation status of H666P, The gene KAT14 has a mutation status of P740P, The gene TTLL9 has a mutation status of R228S, The gene RPRD1B has a mutation status of L269L, The gene BPI has a mutation status of P424L, The gene RALGAPB has a mutation status of P914S, The gene AL031681.3 has a mutation status of S361R, The gene UBE2C has a mutation status of R78S, The gene ZSWIM1 has a mutation status of H391P, The gene CD40 has a mutation status of V218G, The gene STAU1 has a mutation status of M82V, The gene PHACTR3 has a mutation status of S19S, The gene TCFL5 has a mutation status of G3G, The gene MYT1 has a mutation status of V227V, The gene GART has a mutation status of T828T, The gene RUNX1 has a mutation status of A107V, The gene KRTAP10-9 has a mutation status of P29T, The gene MRPL40 has a mutation status of Q103Q, The gene CABIN1 has a mutation status of D927G, The gene KIAA1671 has a mutation status of A488A, The gene SEZ6L has a mutation status of H659H, The gene CCDC157 has a mutation status of V395G, The gene MYH9 has a mutation status of I414I, The gene IFT27 has a mutation status of R107W, The gene MICALL1 has a mutation status of S640S, The gene KCNJ4 has a mutation status of G102G, The gene ZC3H7B has a mutation status of P781L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PNPLA5 has a mutation status of G288R, The gene TUBGCP6 has a mutation status of H1647Y, The gene SBF1 has a mutation status of V1122V, The gene CCDC120 has a mutation status of T355P, The gene ZNF711 has a mutation status of R306R, The gene ARMCX4 has a mutation status of G1300C, The gene BCORL1 has a mutation status of L1132P, The gene NSDHL has a mutation status of V363M, The gene L1CAM has a mutation status of V364V, The gene L1CAM has a mutation status of Q361K, The gene MT-ND2 has a mutation status of T226T, The gene MT-ND4 has a mutation status of L351L, The gene RERE has a mutation status of A793A, The gene MTHFR has a mutation status of D163D, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene CLIC4 has a mutation status of R250R, The gene UROD has a mutation status of L234L, The gene CTBS has a mutation status of A117fs, The gene OLFM3 has a mutation status of L308L, The gene POLR3C has a mutation status of M394T, The gene KCNN3 has a mutation status of L66Q, The gene SLC25A44 has a mutation status of E253E, The gene PAQR6 has a mutation status of A314V, The gene USH2A has a mutation status of K1986R, The gene ZNF695 has a mutation status of A360T, The gene ALLC has a mutation status of P257P, The gene TDRD15 has a mutation status of G1784A, The gene PPP4R3B has a mutation status of P253R, The gene ADD2 has a mutation status of E301G, The gene CD207 has a mutation status of H229Q, The gene NCKAP5 has a mutation status of P1829L, The gene COBLL1 has a mutation status of R894Q, The gene FSIP2 has a mutation status of C3645R, The gene IDH1 has a mutation status of L288L, The gene RETREG2 has a mutation status of G8G, The gene ALPI has a mutation status of M229L, The gene USP40 has a mutation status of H665L, The gene MROH2A has a mutation status of P1243P, The gene PASK has a mutation status of V178L, The gene RFT1 has a mutation status of P422S, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene H1-8 has a mutation status of V78G, The gene TTC14 has a mutation status of F265L, The gene FBXL5 has a mutation status of E104*, The gene MED28 has a mutation status of T68A, The gene ARAP2 has a mutation status of T628fs, The gene TLR10 has a mutation status of D362N, The gene MCUB has a mutation status of I141T, The gene AC126283.2 has a mutation status of C266R, The gene FGF2 has a mutation status of R42R, The gene SH3RF1 has a mutation status of Q566K, The gene MAP3K1 has a mutation status of V936L, The gene ADGRV1 has a mutation status of A4147P, The gene SAR1B has a mutation status of L168L, The gene LECT2 has a mutation status of Y81S, The gene FAT2 has a mutation status of R3719W, The gene HIVEP1 has a mutation status of P2620P, The gene HLA-B has a mutation status of Y140L, The gene COL11A2 has a mutation status of P1261L, The gene ADGRF1 has a mutation status of T564I, The gene COX7A2 has a mutation status of G47G, The gene FAM184A has a mutation status of V107A, The gene ENPP1 has a mutation status of E57D, The gene FAM220A has a mutation status of T138S, The gene STK31 has a mutation status of H379H, The gene NPC1L1 has a mutation status of A165A, The gene ELN has a mutation status of G514G, The gene PCLO has a mutation status of P872P, The gene ERVW-1 has a mutation status of L333*, The gene ASB4 has a mutation status of R318Q, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S558T, The gene MUC3A has a mutation status of S2042S, The gene MUC3A has a mutation status of D2269G, The gene MUC3A has a mutation status of K2298E, The gene MUC3A has a mutation status of V2475S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene ST7 has a mutation status of A355S, The gene SLC7A2 has a mutation status of S269P, The gene DOCK5 has a mutation status of R1540Q, The gene TCEA1 has a mutation status of S128*, The gene TGS1 has a mutation status of E330G, The gene HNF4G has a mutation status of S142A, The gene STK3 has a mutation status of R366W, The gene KCNQ3 has a mutation status of V406I, The gene KCNK9 has a mutation status of Y220Y, The gene MROH6 has a mutation status of C254C, The gene EPPK1 has a mutation status of A2633del, The gene SCRT1 has a mutation status of A133S, The gene SLC39A4 has a mutation status of R251W, The gene KANK1 has a mutation status of K1179N, The gene CNTNAP3 has a mutation status of A1204T, The gene OLFML2A has a mutation status of S57R, The gene TTC16 has a mutation status of A550A, The gene CCDC187 has a mutation status of L747L, The gene NDOR1 has a mutation status of K504E, The gene ANKRD30A has a mutation status of R485V, The gene WASHC2A has a mutation status of A761V, The gene PRKG1 has a mutation status of R407C, The gene LRRTM3 has a mutation status of F153F, The gene RNLS has a mutation status of Q53R, The gene LIPJ has a mutation status of Y295H, The gene RBM20 has a mutation status of I1090fs, The gene GRK5 has a mutation status of R399H, The gene JAKMIP3 has a mutation status of A556V, The gene MUC5AC has a mutation status of R2899S, The gene OR4A16 has a mutation status of K22Q, The gene OR4A16 has a mutation status of N132T, The gene OR4A16 has a mutation status of I319A, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene RTN4RL2 has a mutation status of R349R, The gene GLYAT has a mutation status of P23P, The gene DDB1 has a mutation status of V364M, The gene CCDC85B has a mutation status of E31G, The gene MAP6 has a mutation status of P106P, The gene ACAT1 has a mutation status of C126C, The gene ZW10 has a mutation status of R76K, The gene KCNA5 has a mutation status of V407L, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R31 has a mutation status of 150_151KE>NQ, The gene TAS2R46 has a mutation status of 296_297HV>QM, The gene TAS2R46 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of N76C, The gene TAS2R45 has a mutation status of I33T, The gene LRP6 has a mutation status of Q1254H, The gene LRMP has a mutation status of A714S, The gene GXYLT1 has a mutation status of V28K, The gene ASB8 has a mutation status of I183T, The gene NCKAP5L has a mutation status of G253S, The gene CCER1 has a mutation status of L250fs, The gene ACTR6 has a mutation status of V24F, The gene HVCN1 has a mutation status of M71T, The gene BRI3BP has a mutation status of E228E, The gene FLT3 has a mutation status of V592A, The gene FAM124A has a mutation status of P342L, The gene NDRG2 has a mutation status of Q8*, The gene SALL2 has a mutation status of P46R, The gene OR10G3 has a mutation status of G153G, The gene MYH6 has a mutation status of T1284T, The gene NUBPL has a mutation status of A214T, The gene ATP6V1D has a mutation status of E55K, The gene SLC24A4 has a mutation status of T592T, The gene PPP4R4 has a mutation status of G71E, The gene GOLGA6L22 has a mutation status of E575K, The gene HERC2 has a mutation status of S3111S, The gene ANKDD1A has a mutation status of L516L, The gene XYLT1 has a mutation status of D796N, The gene UMOD has a mutation status of S324G, The gene ATXN2L has a mutation status of P41S, The gene ZNF747 has a mutation status of R298P, The gene SRCAP has a mutation status of P3019S, The gene PLEKHG4 has a mutation status of F759Y, The gene PKD1L3 has a mutation status of W717S, The gene MBTPS1 has a mutation status of V814I, The gene SPIRE2 has a mutation status of L101L, The gene TP53 has a mutation status of R273H, The gene ALOX12B has a mutation status of S439N, The gene PIK3R5 has a mutation status of H199H, The gene TEKT3 has a mutation status of I153fs, The gene NLK has a mutation status of S257*, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP4-7 has a mutation status of P117R, The gene CDK5RAP3 has a mutation status of E148K, The gene XYLT2 has a mutation status of F520L, The gene GNA13 has a mutation status of S9S, The gene KIF19 has a mutation status of L585L, The gene SEPTIN9 has a mutation status of Q118P, The gene BAIAP2 has a mutation status of P190L, The gene FOXK2 has a mutation status of V474I, The gene PEX11G has a mutation status of P210P, The gene XAB2 has a mutation status of P518P, The gene ZNF558 has a mutation status of A10A, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T12336L, The gene CC2D1A has a mutation status of E943K, The gene ADGRL1 has a mutation status of G1413R, The gene ZNF66 has a mutation status of F97F, The gene ZNF675 has a mutation status of F95S, The gene CHST8 has a mutation status of D67N, The gene RYR1 has a mutation status of S1489N, The gene ERCC2 has a mutation status of R299R, The gene AKT1S1 has a mutation status of E114G, The gene FPR3 has a mutation status of I284I, The gene LILRB3 has a mutation status of Q270R, The gene LILRA2 has a mutation status of S395T, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Y99I, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of P224S, The gene KIR2DL3 has a mutation status of N274fs, The gene KIR2DL1 has a mutation status of T91K, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene DNAAF3 has a mutation status of D323D, The gene TRIM28 has a mutation status of P347L, The gene SIRPA has a mutation status of L44S, The gene VPS16 has a mutation status of T323N, The gene PLCB4 has a mutation status of V126V, The gene KAT14 has a mutation status of P740P, The gene TTLL9 has a mutation status of R228S, The gene ASXL1 has a mutation status of L1393fs, The gene RALGAPB has a mutation status of P914S, The gene MYBL2 has a mutation status of P284R, The gene JPH2 has a mutation status of T618A, The gene GDAP1L1 has a mutation status of I65I, The gene UBE2C has a mutation status of R78S, The gene COL9A3 has a mutation status of P111S, The gene COL9A3 has a mutation status of S521S, The gene GART has a mutation status of T828T, The gene RUNX1 has a mutation status of A107V, The gene U2AF1 has a mutation status of Q157P, The gene KRTAP10-9 has a mutation status of P29T, The gene MRPL40 has a mutation status of Q103Q, The gene GSTT4 has a mutation status of Q197R, The gene CABIN1 has a mutation status of D927G, The gene KIAA1671 has a mutation status of A488A, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PNPLA5 has a mutation status of G288R, The gene SBF1 has a mutation status of V1122V, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene PWWP3B has a mutation status of S324T, The gene SLC25A5 has a mutation status of T221R, The gene NSDHL has a mutation status of V363M, The gene MT-ND2 has a mutation status of T226T, The gene MT-ND4 has a mutation status of A226T, The gene MT-ND4 has a mutation status of L351L
LAML
The gene PER3 has a mutation status of R1118W, The gene CASZ1 has a mutation status of S951S, The gene FBXO44 has a mutation status of E59K, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF15 has a mutation status of E284K, The gene PRAMEF20 has a mutation status of S294S, The gene KLHDC7A has a mutation status of V544M, The gene GRIK3 has a mutation status of R228C, The gene USP1 has a mutation status of Q332E, The gene ROR1 has a mutation status of G358D, The gene PDE4B has a mutation status of S128N, The gene IL23R has a mutation status of V338A, The gene MSH4 has a mutation status of A802V, The gene MFSD14A has a mutation status of A342A, The gene KCND3 has a mutation status of S319S, The gene AP4B1 has a mutation status of F405fs, The gene NBPF26 has a mutation status of K1096K, The gene NBPF9 has a mutation status of N855D, The gene NBPF9 has a mutation status of Q804L, The gene MRPL9 has a mutation status of R72L, The gene FLG has a mutation status of R2953H, The gene HCN3 has a mutation status of R250H, The gene NTRK1 has a mutation status of S146S, The gene VANGL2 has a mutation status of H230H, The gene UFC1 has a mutation status of L142V, The gene FCGR3A has a mutation status of A176V, The gene F5 has a mutation status of R534Q, The gene GORAB has a mutation status of Q62*, The gene FMO4 has a mutation status of G196R, The gene PAPPA2 has a mutation status of T174T, The gene CACNA1E has a mutation status of M791I, The gene SHCBP1L has a mutation status of D120D, The gene SHCBP1L has a mutation status of A75T, The gene ARPC5 has a mutation status of A75E, The gene HMCN1 has a mutation status of S580G, The gene TPR has a mutation status of S1824G, The gene RAB7B has a mutation status of I17T, The gene IRF6 has a mutation status of G170S, The gene NENF has a mutation status of R45R, The gene CENPF has a mutation status of S1954S, The gene KCNK2 has a mutation status of T49M, The gene USH2A has a mutation status of R4092I, The gene BPNT1 has a mutation status of I254V, The gene OBSCN has a mutation status of R3109H, The gene NUP133 has a mutation status of L935H, The gene RYR2 has a mutation status of P1307P, The gene RYR2 has a mutation status of A2346E, The gene RYR2 has a mutation status of E4074E, The gene KIF26B has a mutation status of P223P, The gene CPSF3 has a mutation status of L605S, The gene WDR35 has a mutation status of L925fs, The gene APOB has a mutation status of E2740*, The gene FAM228B has a mutation status of Q303fs, The gene PPM1G has a mutation status of M386T, The gene IFT172 has a mutation status of F53L, The gene MAP4K3 has a mutation status of V46V, The gene BCL11A has a mutation status of E91*, The gene IL1R1 has a mutation status of I493I, The gene RANBP2 has a mutation status of D2673G, The gene HS6ST1 has a mutation status of T294T, The gene ARHGEF4 has a mutation status of A816D, The gene ACVR2A has a mutation status of K437fs, The gene RIF1 has a mutation status of A1996A, The gene FIGN has a mutation status of F18L, The gene HNRNPA3 has a mutation status of Y323C, The gene TTC30A has a mutation status of R45S, The gene TTN has a mutation status of A32695F, The gene TTN has a mutation status of L17076I, The gene TTN has a mutation status of S8372Y, The gene ZNF804A has a mutation status of W725C, The gene BMPR2 has a mutation status of R491Q, The gene ABCA12 has a mutation status of Y643*, The gene OBSL1 has a mutation status of V817M, The gene SCYGR2 has a mutation status of GGGCGGGCGGGCGGGC20del, The gene ECEL1 has a mutation status of L247L, The gene ASB18 has a mutation status of A144T, The gene COL6A3 has a mutation status of V2778M, The gene HDAC4 has a mutation status of Q125E, The gene KIF1A has a mutation status of S1099L, The gene SEPTIN2 has a mutation status of I153V, The gene IRAK2 has a mutation status of I182I, The gene RAF1 has a mutation status of E478K, The gene NEK10 has a mutation status of L1048F, The gene SUSD5 has a mutation status of G573S, The gene BSN has a mutation status of T3581M, The gene MST1 has a mutation status of V598A, The gene ITIH4 has a mutation status of D387N, The gene SFMBT1 has a mutation status of H344Y, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene CADPS has a mutation status of V1229M, The gene ZNF717 has a mutation status of V22A, The gene TBC1D23 has a mutation status of K510Q, The gene GAP43 has a mutation status of L37F, The gene PLXND1 has a mutation status of R831R, The gene NMNAT3 has a mutation status of D42H, The gene RASA2 has a mutation status of Y194*, The gene MECOM has a mutation status of T408I, The gene FAM43A has a mutation status of Y70C, The gene ACAP2 has a mutation status of A363D, The gene NRROS has a mutation status of A127S, The gene ZFYVE28 has a mutation status of E123*, The gene NOP14 has a mutation status of P17P, The gene HTT has a mutation status of Q1621H, The gene ADRA2C has a mutation status of R166C, The gene TRMT44 has a mutation status of R629S, The gene SLIT2 has a mutation status of C436F, The gene NWD2 has a mutation status of F775L, The gene SLC4A4 has a mutation status of D1060N, The gene SEC31A has a mutation status of E583V, The gene DSPP has a mutation status of D849D, The gene MEPE has a mutation status of D412Y, The gene ENPEP has a mutation status of W868L, The gene ZGRF1 has a mutation status of K1690N, The gene PCDH10 has a mutation status of A351S, The gene CPE has a mutation status of A266V, The gene ADAMTS16 has a mutation status of K901R, The gene DNAH5 has a mutation status of V1672M, The gene PRDM9 has a mutation status of D787Y, The gene PDZD2 has a mutation status of Q777P, The gene NPR3 has a mutation status of G32G, The gene CWC27 has a mutation status of A351S, The gene ADAMTS6 has a mutation status of D351N, The gene MAST4 has a mutation status of D977G, The gene ZBED3 has a mutation status of L155A, The gene ADGRV1 has a mutation status of G3138C, The gene FBN2 has a mutation status of R509C, The gene PCDHB10 has a mutation status of T573T, The gene HK3 has a mutation status of E858K, The gene FLT4 has a mutation status of Y109Y, The gene FOXF2 has a mutation status of S49L, The gene NRN1 has a mutation status of A33A, The gene ERVFRD-1 has a mutation status of G366D, The gene H1-2 has a mutation status of K17K, The gene ZKSCAN4 has a mutation status of E132K, The gene TNXB has a mutation status of T4265I, The gene KIFC1 has a mutation status of D514D, The gene SYNGAP1 has a mutation status of S52L, The gene PGK2 has a mutation status of I265I, The gene EYS has a mutation status of Y563C, The gene EYS has a mutation status of G484V, The gene ADGRB3 has a mutation status of D60Y, The gene CASP8AP2 has a mutation status of V189I, The gene AMD1 has a mutation status of T57T, The gene TBC1D32 has a mutation status of H487Y, The gene PTPRK has a mutation status of L561V, The gene SLC18B1 has a mutation status of N218H, The gene TAB2 has a mutation status of G526G, The gene MAP3K4 has a mutation status of S524F, The gene CARD11 has a mutation status of S772S, The gene SDK1 has a mutation status of N1762N, The gene USP42 has a mutation status of P857R, The gene NXPH1 has a mutation status of S270S, The gene STK31 has a mutation status of Y194D, The gene SFRP4 has a mutation status of S122G, The gene AMPH has a mutation status of L191V, The gene POU6F2 has a mutation status of H311N, The gene CDK13 has a mutation status of R405Q, The gene HECW1 has a mutation status of E586K, The gene SPDYE1 has a mutation status of A210P, The gene ABCA13 has a mutation status of L4668R, The gene SEPTIN14 has a mutation status of F356V, The gene PSPH has a mutation status of L68P, The gene TYW1 has a mutation status of I662fs, The gene CASTOR2 has a mutation status of T195M, The gene PTPN12 has a mutation status of K141R, The gene ZAN has a mutation status of S713P, The gene ZAN has a mutation status of T2778fs, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T303V, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene FOXP2 has a mutation status of S442R, The gene MET has a mutation status of E34K, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene BRAF has a mutation status of E204L, The gene CLCN1 has a mutation status of D19G, The gene CTAGE8 has a mutation status of R768R, The gene DPP6 has a mutation status of V165V, The gene SHH has a mutation status of G221R, The gene DLC1 has a mutation status of V920V, The gene ENTPD4 has a mutation status of Y105*, The gene PREX2 has a mutation status of Q898H, The gene EPPK1 has a mutation status of A2633del, The gene GRINA has a mutation status of A257V, The gene ACO1 has a mutation status of L24L, The gene DDX58 has a mutation status of P885S, The gene TLN1 has a mutation status of E1816K, The gene GBA2 has a mutation status of D280D, The gene CNTNAP3 has a mutation status of A1204T, The gene CNTNAP3 has a mutation status of A1182A, The gene SMC5 has a mutation status of Y560H, The gene TGFBR1 has a mutation status of D333H, The gene TGFBR1 has a mutation status of R413*, The gene TRIM32 has a mutation status of A585V, The gene SPOUT1 has a mutation status of R352H, The gene HMCN2 has a mutation status of G833R, The gene AL162417.1 has a mutation status of S740S, The gene COL5A1 has a mutation status of P599P, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of T90M, The gene ANAPC2 has a mutation status of K405K, The gene RBP3 has a mutation status of H633Y, The gene ASAH2 has a mutation status of A346S, The gene CDH23 has a mutation status of R2304W, The gene KAT6B has a mutation status of V1748I, The gene HECTD2 has a mutation status of L156I, The gene PPRC1 has a mutation status of T844N, The gene SH3PXD2A has a mutation status of G336S, The gene ATRNL1 has a mutation status of T1362A, The gene HSPA12A has a mutation status of P227P, The gene DOCK1 has a mutation status of R958T, The gene CFAP46 has a mutation status of N1367N, The gene RIC8A has a mutation status of L507L, The gene SIRT3 has a mutation status of L312I, The gene MUC5AC has a mutation status of T2408P, The gene FAM160A2 has a mutation status of S214A, The gene ANO5 has a mutation status of S506G, The gene PAX6 has a mutation status of S110F, The gene HARBI1 has a mutation status of E246E, The gene PTPMT1 has a mutation status of V143M, The gene OR5L1 has a mutation status of I192V, The gene OR8H3 has a mutation status of L130V, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene CCDC85B has a mutation status of R96S, The gene PC has a mutation status of L747M, The gene FGF4 has a mutation status of N36N, The gene TRIM64 has a mutation status of T292R, The gene MMP20 has a mutation status of V325V, The gene TRAPPC4 has a mutation status of V6M, The gene OR4D5 has a mutation status of G95D, The gene OR10G8 has a mutation status of C249F, The gene GLB1L3 has a mutation status of G91R, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R46 has a mutation status of 296_297HV>QM, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PRB3 has a mutation status of R242fs, The gene ABCC9 has a mutation status of F112F, The gene KRAS has a mutation status of G12D, The gene IPO8 has a mutation status of E162Q, The gene PKP2 has a mutation status of E478K, The gene PKP2 has a mutation status of S172T, The gene GXYLT1 has a mutation status of V28K, The gene ZCRB1 has a mutation status of E153Q, The gene KRT18 has a mutation status of T103N, The gene OR6C65 has a mutation status of T72T, The gene TMTC2 has a mutation status of H126P, The gene WSCD2 has a mutation status of A413T, The gene UBE3B has a mutation status of G314G, The gene MVK has a mutation status of C173C, The gene TMEM132C has a mutation status of S19I, The gene TMEM132D has a mutation status of A449A, The gene LATS2 has a mutation status of N1012N, The gene KBTBD7 has a mutation status of V287M, The gene FAM124A has a mutation status of R127Q, The gene WDFY2 has a mutation status of E94*, The gene SUGT1 has a mutation status of F18C, The gene PCDH17 has a mutation status of G393R, The gene EDNRB has a mutation status of V415I, The gene SLITRK5 has a mutation status of H780H, The gene STK24 has a mutation status of S299N, The gene MCF2L has a mutation status of G385G, The gene CHAMP1 has a mutation status of H756Y, The gene OR4K17 has a mutation status of *313Y, The gene SUPT16H has a mutation status of R317R, The gene FBXO33 has a mutation status of H348P, The gene TBPL2 has a mutation status of T259T, The gene ZNF410 has a mutation status of G377R, The gene NRXN3 has a mutation status of L1100I, The gene SERPINA4 has a mutation status of D116N, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene GOLGA6L1 has a mutation status of Q428Q, The gene GOLGA6L2 has a mutation status of R427L, The gene NPAP1 has a mutation status of R13H, The gene GABRA5 has a mutation status of L24V, The gene FMN1 has a mutation status of S272A, The gene ITPKA has a mutation status of A278A, The gene MGA has a mutation status of S276I, The gene UNC13C has a mutation status of G2123R, The gene ANKDD1A has a mutation status of L516L, The gene FEM1B has a mutation status of N56S, The gene TLNRD1 has a mutation status of A310V, The gene GOLGA6L9 has a mutation status of R6H, The gene ADAMTSL3 has a mutation status of T1412N, The gene SLCO3A1 has a mutation status of A91A, The gene PIGQ has a mutation status of A164A, The gene CRAMP1 has a mutation status of R53L, The gene SRRM2 has a mutation status of S421I, The gene CARHSP1 has a mutation status of P81P, The gene CES3 has a mutation status of P286L, The gene AARS1 has a mutation status of R333P, The gene KARS1 has a mutation status of E260A, The gene ZCCHC14 has a mutation status of P632P, The gene BANP has a mutation status of R67W, The gene SPIRE2 has a mutation status of R505W, The gene TRPV3 has a mutation status of A269E, The gene CHRNE has a mutation status of P333fs, The gene ALOX15B has a mutation status of S334I, The gene KIAA0100 has a mutation status of R1831W, The gene CCL4L2 has a mutation status of P67R, The gene TTC25 has a mutation status of L394L, The gene MLX has a mutation status of V289I, The gene TOM1L1 has a mutation status of S383S, The gene SOX9 has a mutation status of R120L, The gene KCTD2 has a mutation status of Q53L, The gene UBE2O has a mutation status of E723A, The gene ENPP7 has a mutation status of D60D, The gene ZNF521 has a mutation status of L1118L, The gene ZNF521 has a mutation status of T896T, The gene MEP1B has a mutation status of R516W, The gene FHOD3 has a mutation status of P1038P, The gene ATP8B1 has a mutation status of G777G, The gene SERPINB5 has a mutation status of I341I, The gene MBP has a mutation status of K5R, The gene SALL3 has a mutation status of R239W, The gene PRSS57 has a mutation status of A90T, The gene CELF5 has a mutation status of A2A, The gene UHRF1 has a mutation status of A476A, The gene KHSRP has a mutation status of G18C, The gene C3 has a mutation status of Q417K, The gene TRAPPC5 has a mutation status of I146N, The gene OR2Z1 has a mutation status of C241*, The gene MUC16 has a mutation status of L13880C, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T10831T, The gene OR7G2 has a mutation status of I260M, The gene YIPF2 has a mutation status of G107fs, The gene SMARCA4 has a mutation status of R973W, The gene CASP14 has a mutation status of R121*, The gene NOTCH3 has a mutation status of S2096L, The gene ABHD8 has a mutation status of S423E, The gene ZNF486 has a mutation status of P349A, The gene ZNF43 has a mutation status of E473*, The gene ZNF536 has a mutation status of S407S, The gene TSHZ3 has a mutation status of A736S, The gene SLC7A9 has a mutation status of E282K, The gene ZNF790 has a mutation status of H461R, The gene ARHGAP35 has a mutation status of A1414A, The gene SYT3 has a mutation status of Y523Y, The gene SHANK1 has a mutation status of D10D, The gene ZNF816 has a mutation status of D109N, The gene ZNF845 has a mutation status of G949C, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB3 has a mutation status of A4A, The gene LILRA6 has a mutation status of H290H, The gene LILRA6 has a mutation status of H290N, The gene LILRA6 has a mutation status of P130P, The gene LILRA2 has a mutation status of W163S, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of T91K, The gene KIR2DL1 has a mutation status of D184N, The gene KIR2DL1 has a mutation status of G283G, The gene NLRP2 has a mutation status of R431H, The gene ZNF805 has a mutation status of T244K, The gene ZSCAN18 has a mutation status of E213K, The gene SIRPA has a mutation status of L44S, The gene KAT14 has a mutation status of P740P, The gene NINL has a mutation status of G232*, The gene PPP1R16B has a mutation status of C302Y, The gene ZMYND8 has a mutation status of E560D, The gene TAF4 has a mutation status of A143S, The gene MTG2 has a mutation status of A235T, The gene MYT1 has a mutation status of A709T, The gene CHODL has a mutation status of S6L, The gene MRAP has a mutation status of V26G, The gene KRTAP10-5 has a mutation status of A249P, The gene CABIN1 has a mutation status of S11S, The gene KIAA1671 has a mutation status of P1729P, The gene PDGFB has a mutation status of R3L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene EFCAB6 has a mutation status of K630K, The gene MAPK8IP2 has a mutation status of P432P, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene DCAF8L1 has a mutation status of A31V, The gene RPS6KA6 has a mutation status of R310S, The gene DCX has a mutation status of K112N, The gene SLC25A5 has a mutation status of G121C, The gene SLC25A5 has a mutation status of T221R, The gene SLITRK2 has a mutation status of C220F, The gene AC236972.4 has a mutation status of S1611S, The gene MT-ND2 has a mutation status of A164T, The gene MT-ND5 has a mutation status of V92V, The gene MT-ND5 has a mutation status of T533M, The gene MT-CYB has a mutation status of F18L
COAD
The gene MAD2L2 has a mutation status of Q43Q, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PUM1 has a mutation status of L942F, The gene PHC2 has a mutation status of A251A, The gene TEKT2 has a mutation status of D332E, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene SLC5A9 has a mutation status of G108fs, The gene PARS2 has a mutation status of L73L, The gene ADGRL2 has a mutation status of V56V, The gene PLPPR5 has a mutation status of R299*, The gene COL11A1 has a mutation status of E335*, The gene CELSR2 has a mutation status of R2015K, The gene PHTF1 has a mutation status of Y470Y, The gene HIPK1 has a mutation status of S98S, The gene NBPF12 has a mutation status of R1042R, The gene NBPF14 has a mutation status of P2677R, The gene PI4KB has a mutation status of E170K, The gene FLG2 has a mutation status of Y350H, The gene MEF2D has a mutation status of A32A, The gene USF1 has a mutation status of V140I, The gene FMO4 has a mutation status of R258fs, The gene TNR has a mutation status of I751I, The gene CACNA1S has a mutation status of G1436G, The gene IGFN1 has a mutation status of R126Q, The gene CD46 has a mutation status of W216*, The gene ANGEL2 has a mutation status of V16M, The gene FMN2 has a mutation status of P971S, The gene BECN2 has a mutation status of R311*, The gene APOB has a mutation status of F1193F, The gene DNAJC5G has a mutation status of R75R, The gene CAPN14 has a mutation status of W586G, The gene THUMPD2 has a mutation status of K343K, The gene TLX2 has a mutation status of P16P, The gene SNRNP200 has a mutation status of L1868L, The gene FER1L5 has a mutation status of R1166R, The gene ZAP70 has a mutation status of V470F, The gene SULT1C4 has a mutation status of H299Y, The gene GCC2 has a mutation status of R1580Q, The gene CYTIP has a mutation status of I42S, The gene SCN3A has a mutation status of S665L, The gene SCN1A has a mutation status of R568Q, The gene TTN has a mutation status of L21404fs, The gene TTN has a mutation status of W7540*, The gene ZNF804A has a mutation status of P1193S, The gene HECW2 has a mutation status of G216E, The gene AOX1 has a mutation status of H1071H, The gene CTDSP1 has a mutation status of C92C, The gene DOCK10 has a mutation status of S1461S, The gene SCYGR2 has a mutation status of H97S, The gene INPP5D has a mutation status of H753Y, The gene TRPM8 has a mutation status of D231N, The gene OR6B3 has a mutation status of T282T, The gene BTD has a mutation status of R128C, The gene CNOT10 has a mutation status of G694S, The gene SCN10A has a mutation status of F843F, The gene CDC25A has a mutation status of R10H, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene DNAH12 has a mutation status of L1060S, The gene STXBP5L has a mutation status of G299E, The gene SLC35G2 has a mutation status of L353L, The gene MED12L has a mutation status of E1502V, The gene PPM1L has a mutation status of R338S, The gene CHRD has a mutation status of E500K, The gene ATP13A5 has a mutation status of W57*, The gene DGKQ has a mutation status of C218H, The gene DTHD1 has a mutation status of C772F, The gene TLR10 has a mutation status of S72S, The gene CCDC158 has a mutation status of E206K, The gene ADH1A has a mutation status of S342L, The gene CAMK2D has a mutation status of F17F, The gene MARCHF1 has a mutation status of S35S, The gene TLL1 has a mutation status of S932F, The gene FBXO8 has a mutation status of R219C, The gene ICE1 has a mutation status of Q2043E, The gene MYO10 has a mutation status of L1851fs, The gene NIPBL has a mutation status of T2731S, The gene NUP155 has a mutation status of E536*, The gene DDX4 has a mutation status of P165S, The gene IPO11 has a mutation status of G712V, The gene MAST4 has a mutation status of E2267K, The gene ZBED3 has a mutation status of L155A, The gene PCDHB13 has a mutation status of L726F, The gene TCERG1 has a mutation status of A179S, The gene ARHGEF37 has a mutation status of R472H, The gene CD74 has a mutation status of D150A, The gene GRM6 has a mutation status of P431L, The gene RIPK1 has a mutation status of A569V, The gene TMEM14B has a mutation status of 140_141CA>SP, The gene KIF13A has a mutation status of L752L, The gene H2BC12 has a mutation status of T53A, The gene DDX39B has a mutation status of I399I, The gene DDAH2 has a mutation status of R173H, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene COL11A2 has a mutation status of P1026H, The gene SPDEF has a mutation status of P20P, The gene ADGRF5 has a mutation status of P413L, The gene IMPG1 has a mutation status of F228F, The gene PHIP has a mutation status of T667I, The gene BCKDHB has a mutation status of Q267*, The gene DSE has a mutation status of V351V, The gene SLC22A3 has a mutation status of G442R, The gene NUDT1 has a mutation status of G36V, The gene PRPS1L1 has a mutation status of M127V, The gene TMEM196 has a mutation status of L17L, The gene NPSR1 has a mutation status of V113I, The gene YKT6 has a mutation status of S58S, The gene ABCA13 has a mutation status of I3759N, The gene ATP5MF-PTCD1 has a mutation status of L559L, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of ITTTENATHSTPNFTSS2131del, The gene MUC3A has a mutation status of P2711S, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene KIAA1549 has a mutation status of K615E, The gene BRAF has a mutation status of V600E, The gene KRBA1 has a mutation status of D119N, The gene GIMAP8 has a mutation status of S21L, The gene POLB has a mutation status of F200V, The gene RRM2B has a mutation status of A83A, The gene RAD21 has a mutation status of L229S, The gene MROH6 has a mutation status of G462G, The gene DMRT2 has a mutation status of L250L, The gene MPDZ has a mutation status of E702M, The gene IFNA7 has a mutation status of D25Y, The gene PLAA has a mutation status of P470P, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene SIT1 has a mutation status of V84G, The gene CNTNAP3 has a mutation status of A1204T, The gene OR13C2 has a mutation status of H20P, The gene ABCA1 has a mutation status of I1749V, The gene FRRS1L has a mutation status of R51A, The gene ECPAS has a mutation status of R1265*, The gene OR1N2 has a mutation status of G32G, The gene NR5A1 has a mutation status of T327T, The gene TTC16 has a mutation status of M1I, The gene ADAMTSL2 has a mutation status of A840A, The gene GPSM1 has a mutation status of L255L, The gene SEC16A has a mutation status of T521T, The gene CUBN has a mutation status of P672P, The gene KIAA1217 has a mutation status of S743L, The gene ZEB1 has a mutation status of M1093I, The gene LRRC18 has a mutation status of I163L, The gene ASAH2 has a mutation status of F203F, The gene CTNNA3 has a mutation status of V731V, The gene PRF1 has a mutation status of N252N, The gene ANXA11 has a mutation status of S387N, The gene TACC2 has a mutation status of D218Y, The gene B4GALNT4 has a mutation status of A799A, The gene OR51B2 has a mutation status of S165L, The gene OR51B5 has a mutation status of E109K, The gene USH1C has a mutation status of S267F, The gene ANO3 has a mutation status of D111N, The gene BBOX1 has a mutation status of T255I, The gene OR8H3 has a mutation status of F63F, The gene OR8J3 has a mutation status of S110L, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene SLC22A25 has a mutation status of R277K, The gene DSCAML1 has a mutation status of T1654T, The gene MFRP has a mutation status of E472E, The gene NECTIN1 has a mutation status of E98K, The gene SORL1 has a mutation status of D315N, The gene OR10G4 has a mutation status of V49V, The gene OR8D2 has a mutation status of I282F, The gene NCAPD2 has a mutation status of G667E, The gene ZNF384 has a mutation status of Q367*, The gene CLEC12A has a mutation status of R40L, The gene TAS2R46 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene GXYLT1 has a mutation status of K440R, The gene GXYLT1 has a mutation status of C414H, The gene NELL2 has a mutation status of H235Y, The gene MON2 has a mutation status of P258S, The gene OTOGL has a mutation status of E1902K, The gene LIN7A has a mutation status of A206S, The gene MGAT4C has a mutation status of D327N, The gene ASCL1 has a mutation status of L133V, The gene ACAD10 has a mutation status of D48N, The gene CAMKK2 has a mutation status of N247N, The gene HIP1R has a mutation status of A327fs, The gene PITPNM2 has a mutation status of R534Q, The gene EP400 has a mutation status of A471T, The gene ZNF605 has a mutation status of R176R, The gene ATP8A2 has a mutation status of I126N, The gene AKAP11 has a mutation status of V884L, The gene LRRC63 has a mutation status of P159L, The gene CDH24 has a mutation status of A603T, The gene TTC6 has a mutation status of P62P, The gene LTBP2 has a mutation status of S267L, The gene YLPM1 has a mutation status of E29A, The gene CIPC has a mutation status of T380I, The gene KIF26A has a mutation status of A869P, The gene ADSS1 has a mutation status of H244H, The gene CEP170B has a mutation status of R1198C, The gene GOLGA6L22 has a mutation status of *811Q, The gene GOLGA8S has a mutation status of I439V, The gene HERC2 has a mutation status of P2391P, The gene MAP1A has a mutation status of E1098Q, The gene GTF2A2 has a mutation status of V55M, The gene ANKDD1A has a mutation status of L516L, The gene SLC24A1 has a mutation status of E320E, The gene IDH3A has a mutation status of A187A, The gene ABHD2 has a mutation status of S316S, The gene WDR93 has a mutation status of P257L, The gene BAIAP3 has a mutation status of L601I, The gene SCNN1G has a mutation status of T259N, The gene PRSS36 has a mutation status of G179G, The gene LRRC36 has a mutation status of S346L, The gene NQO1 has a mutation status of Q234*, The gene LDHD has a mutation status of G458C, The gene WWOX has a mutation status of D58H, The gene ADAD2 has a mutation status of P31P, The gene ANKRD11 has a mutation status of I433R, The gene HIC1 has a mutation status of Y168H, The gene HIC1 has a mutation status of R176L, The gene SPNS3 has a mutation status of S150L, The gene ZFP3 has a mutation status of H104Y, The gene TEKT1 has a mutation status of R244Q, The gene SLC16A13 has a mutation status of F122F, The gene NEURL4 has a mutation status of K478Q, The gene SPEM2 has a mutation status of H131R, The gene BORCS6 has a mutation status of V207V, The gene MYH4 has a mutation status of K1056K, The gene KIAA0100 has a mutation status of G1388E, The gene EFCAB5 has a mutation status of Q496Q, The gene MMP28 has a mutation status of P453S, The gene CCL4L2 has a mutation status of P67R, The gene KRT25 has a mutation status of R4*, The gene KRT34 has a mutation status of G53G, The gene KRT37 has a mutation status of R396W, The gene HSF5 has a mutation status of T75S, The gene ABCA8 has a mutation status of M62I, The gene CANT1 has a mutation status of A84A, The gene ENDOV has a mutation status of P163L, The gene ASPSCR1 has a mutation status of E331V, The gene EPB41L3 has a mutation status of L528L, The gene PTPRM has a mutation status of Q872E, The gene ANKRD12 has a mutation status of L1009S, The gene ANKRD12 has a mutation status of D1013Y, The gene GAREM1 has a mutation status of S779F, The gene SETBP1 has a mutation status of P558L, The gene ONECUT2 has a mutation status of E216K, The gene SMIM21 has a mutation status of R86Q, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T12336L, The gene DOCK6 has a mutation status of L1578F, The gene ZNF44 has a mutation status of P531P, The gene USHBP1 has a mutation status of G467E, The gene ZNF66 has a mutation status of F97F, The gene ZNF723 has a mutation status of C371S, The gene CCER2 has a mutation status of G259R, The gene PLEKHG2 has a mutation status of E275E, The gene FGF21 has a mutation status of S191P, The gene CGB7 has a mutation status of C54W, The gene RCN3 has a mutation status of A121A, The gene KLK7 has a mutation status of K197N, The gene ZNF415 has a mutation status of L511C, The gene TARM1 has a mutation status of K177K, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of W163S, The gene LILRB1 has a mutation status of R30S, The gene LILRB1 has a mutation status of Y99I, The gene LILRB1 has a mutation status of R487Q, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene ZIM2 has a mutation status of R404R, The gene RNF225 has a mutation status of P260L, The gene CD93 has a mutation status of A611G, The gene BPIFB3 has a mutation status of H430R, The gene EPB41L1 has a mutation status of G549S, The gene MYL9 has a mutation status of I49T, The gene HNF4A has a mutation status of S162S, The gene CDH22 has a mutation status of P497del, The gene CDH22 has a mutation status of N493fs, The gene CABLES2 has a mutation status of Q101R, The gene KRTAP10-7 has a mutation status of V237I, The gene COL18A1 has a mutation status of L1494L, The gene COL6A2 has a mutation status of D751N, The gene PCNT has a mutation status of K1308K, The gene CECR2 has a mutation status of S273F, The gene GGT1 has a mutation status of E432K, The gene IL2RB has a mutation status of A397A, The gene SREBF2 has a mutation status of T275T, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene LMF2 has a mutation status of A253V, The gene GTPBP6 has a mutation status of G61R, The gene NHS has a mutation status of R484Q, The gene MED12 has a mutation status of E33K, The gene SERPINA7 has a mutation status of P383L, The gene COL4A5 has a mutation status of L1352I, The gene SLC25A5 has a mutation status of T221R, The gene SPANXD has a mutation status of L80D, The gene SLITRK4 has a mutation status of G515W, The gene FLNA has a mutation status of T1603T, The gene PLXNA3 has a mutation status of D1639N
SKCM
The gene CCNL2 has a mutation status of R234Q, The gene MEGF6 has a mutation status of C628C, The gene RERE has a mutation status of D662Y, The gene MTOR has a mutation status of Y1151C, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of L121P, The gene PRAMEF18 has a mutation status of L28L, The gene PRAMEF18 has a mutation status of V27I, The gene SLC66A1 has a mutation status of L137S, The gene CSMD2 has a mutation status of S183F, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene ZYG11A has a mutation status of A650A, The gene JAK1 has a mutation status of I375V, The gene SLC44A5 has a mutation status of K157K, The gene TSPAN2 has a mutation status of A213P, The gene IGSF3 has a mutation status of 1038_1039insE, The gene WDR3 has a mutation status of R930R, The gene NBPF20 has a mutation status of L4577L, The gene ANKRD35 has a mutation status of K43K, The gene HJV has a mutation status of E302Q, The gene AC242842.3 has a mutation status of Y3806C, The gene SLC27A3 has a mutation status of R748Q, The gene TRIM46 has a mutation status of Q134H, The gene NES has a mutation status of Q408K, The gene RRNAD1 has a mutation status of R251C, The gene KIRREL1 has a mutation status of V302V, The gene ATF6 has a mutation status of S222N, The gene SLC9C2 has a mutation status of F667S, The gene IER5 has a mutation status of R194G, The gene HMCN1 has a mutation status of V2976V, The gene KCNT2 has a mutation status of R698R, The gene ZC3H11A has a mutation status of V657V, The gene PIK3C2B has a mutation status of R751W, The gene NFASC has a mutation status of S680S, The gene RBBP5 has a mutation status of E523*, The gene PLXNA2 has a mutation status of V779M, The gene PLXNA2 has a mutation status of R484W, The gene CDC42BPA has a mutation status of G1108E, The gene GUK1 has a mutation status of Y54*, The gene OBSCN has a mutation status of N5342N, The gene OR2T4 has a mutation status of V109L, The gene MYT1L has a mutation status of D198N, The gene LRATD1 has a mutation status of E190Q, The gene KCNS3 has a mutation status of T85P, The gene NRXN1 has a mutation status of A1461E, The gene USP34 has a mutation status of S1873S, The gene ARHGAP25 has a mutation status of S494I, The gene MRPS9 has a mutation status of V241M, The gene DPP10 has a mutation status of V730G, The gene MARCO has a mutation status of D84Y, The gene LRP1B has a mutation status of S4007C, The gene SLC4A10 has a mutation status of E878*, The gene DPP4 has a mutation status of I590I, The gene CDCA7 has a mutation status of I201M, The gene TTN has a mutation status of P12112A, The gene TTN has a mutation status of D7086fs, The gene TTN has a mutation status of C6437S, The gene MARS2 has a mutation status of R592W, The gene ZDBF2 has a mutation status of S1716C, The gene MAP2 has a mutation status of L578F, The gene USP37 has a mutation status of F852L, The gene USP37 has a mutation status of N184N, The gene ACSL3 has a mutation status of S45S, The gene COL6A3 has a mutation status of A1790A, The gene ANKMY1 has a mutation status of T547T, The gene SLC6A11 has a mutation status of A34V, The gene SYN2 has a mutation status of P105A, The gene FYCO1 has a mutation status of R731W, The gene ZNF589 has a mutation status of L92L, The gene DNAH12 has a mutation status of E2938E, The gene SENP7 has a mutation status of D578H, The gene CD47 has a mutation status of A261A, The gene COL6A5 has a mutation status of G1698R, The gene PHC3 has a mutation status of D791E, The gene PCGF3 has a mutation status of N124S, The gene NSD2 has a mutation status of D560H, The gene BOD1L1 has a mutation status of R2385W, The gene FAM200B has a mutation status of E551K, The gene TMEM165 has a mutation status of T220S, The gene CLOCK has a mutation status of L467L, The gene TMPRSS11D has a mutation status of A267S, The gene CABS1 has a mutation status of S296S, The gene SPARCL1 has a mutation status of S31S, The gene SMARCAD1 has a mutation status of E237E, The gene DCHS2 has a mutation status of L1439L, The gene NPY2R has a mutation status of I194I, The gene F11 has a mutation status of T179T, The gene NSUN2 has a mutation status of R185C, The gene SPEF2 has a mutation status of K442E, The gene TTC33 has a mutation status of I100L, The gene ERCC8 has a mutation status of Q326H, The gene NSA2 has a mutation status of V224E, The gene APC has a mutation status of Q1367*, The gene TSSK1B has a mutation status of M66V, The gene ANKHD1 has a mutation status of T1954I, The gene PCDHB3 has a mutation status of P245L, The gene PCDHB9 has a mutation status of R652C, The gene PCDHB15 has a mutation status of V123V, The gene SOX30 has a mutation status of P340P, The gene EBF1 has a mutation status of V436M, The gene NKX2-5 has a mutation status of G232G, The gene HRH2 has a mutation status of A253V, The gene CPLX2 has a mutation status of E114K, The gene NOP16 has a mutation status of Y130C, The gene CDHR2 has a mutation status of E1115K, The gene RIPK1 has a mutation status of A569V, The gene SNRNP48 has a mutation status of S107S, The gene H2BC4 has a mutation status of A8A, The gene HLA-A has a mutation status of K292E, The gene TNXB has a mutation status of Y4433Y, The gene HLA-DRB5 has a mutation status of Q220W, The gene CMTR1 has a mutation status of L389F, The gene TNFRSF21 has a mutation status of T291I, The gene MMUT has a mutation status of R31*, The gene DST has a mutation status of N6493S, The gene SLC17A5 has a mutation status of V459M, The gene IMPG1 has a mutation status of L214L, The gene EPHA7 has a mutation status of E884A, The gene AKAP12 has a mutation status of G67S, The gene VIP has a mutation status of Q8H, The gene CNKSR3 has a mutation status of N387N, The gene LPA has a mutation status of R1283R, The gene INTS1 has a mutation status of A1847A, The gene HDAC9 has a mutation status of E1066E, The gene MACC1 has a mutation status of D231D, The gene SP8 has a mutation status of T101P, The gene INMT has a mutation status of L235L, The gene PKD1L1 has a mutation status of P1809P, The gene ABCA13 has a mutation status of R3589I, The gene STEAP4 has a mutation status of D233H, The gene COL1A2 has a mutation status of R216H, The gene MUC3A has a mutation status of S2112S, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene RELN has a mutation status of L411I, The gene KMT2E has a mutation status of T1383R, The gene DOCK4 has a mutation status of L150F, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene MKLN1 has a mutation status of D493H, The gene KIAA1549 has a mutation status of G1278G, The gene PARP12 has a mutation status of R636H, The gene MGAM has a mutation status of Y2390Y, The gene KEL has a mutation status of L705L, The gene CUL1 has a mutation status of Y228C, The gene ZNF425 has a mutation status of T732M, The gene KRBA1 has a mutation status of P690P, The gene KMT2C has a mutation status of G2579D, The gene KMT2C has a mutation status of S2472G, The gene MYOM2 has a mutation status of V1376M, The gene CSMD1 has a mutation status of T2T, The gene XKR6 has a mutation status of A530V, The gene PCM1 has a mutation status of R1310R, The gene LZTS1 has a mutation status of K416K, The gene SCARA3 has a mutation status of P110P, The gene SLC20A2 has a mutation status of T297T, The gene PXDNL has a mutation status of W1233L, The gene PXDNL has a mutation status of N401N, The gene ALKAL1 has a mutation status of A108A, The gene TRPA1 has a mutation status of E223*, The gene FZD6 has a mutation status of T661T, The gene PLEC has a mutation status of A2007A, The gene PPP1R16A has a mutation status of F90F, The gene CEP78 has a mutation status of G717E, The gene OR13D1 has a mutation status of G138E, The gene AMBP has a mutation status of E187E, The gene PAPPA has a mutation status of E1202V, The gene GSN has a mutation status of S411P, The gene GSN has a mutation status of V606M, The gene CRB2 has a mutation status of S374R, The gene NR6A1 has a mutation status of E427K, The gene WDR38 has a mutation status of T86I, The gene GOLGA1 has a mutation status of R411R, The gene SLC2A8 has a mutation status of S270S, The gene USP20 has a mutation status of T258T, The gene HMCN2 has a mutation status of S1138S, The gene LAMC3 has a mutation status of A1137P, The gene NUP214 has a mutation status of R854Q, The gene SARDH has a mutation status of V826V, The gene PPP1R26 has a mutation status of L571L, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of T90M, The gene CCDC187 has a mutation status of A52T, The gene MCM10 has a mutation status of L320L, The gene RBP3 has a mutation status of P308A, The gene WDFY4 has a mutation status of L2974F, The gene CSTF2T has a mutation status of A450A, The gene IPMK has a mutation status of R41R, The gene LRRTM3 has a mutation status of E492D, The gene PSAP has a mutation status of S112F, The gene ZNF503 has a mutation status of S321F, The gene SEC31B has a mutation status of V881I, The gene C10orf120 has a mutation status of C48F, The gene DPYSL4 has a mutation status of S147R, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of R3590R, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4396A, The gene MUC5AC has a mutation status of P4427S, The gene MUC5AC has a mutation status of STTSASTA4496del, The gene MTCH2 has a mutation status of T294fs, The gene OR8U1 has a mutation status of Y149H, The gene OR5M8 has a mutation status of S263fs, The gene OR9G1 has a mutation status of T62V, The gene NUMA1 has a mutation status of G1461G, The gene USP35 has a mutation status of G52G, The gene TRIM77 has a mutation status of L110del, The gene C11orf54 has a mutation status of R314*, The gene GPR83 has a mutation status of T121T, The gene DDX10 has a mutation status of R331Q, The gene NXPE2 has a mutation status of M335fs, The gene TECTA has a mutation status of V683V, The gene ROBO3 has a mutation status of Q433L, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PRB4 has a mutation status of P237H, The gene EPS8 has a mutation status of P366S, The gene LMO3 has a mutation status of A101A, The gene CAPZA3 has a mutation status of R188T, The gene SLCO1A2 has a mutation status of L269L, The gene RESF1 has a mutation status of K1349N, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of E249R, The gene ADAMTS20 has a mutation status of F1887F, The gene ADAMTS20 has a mutation status of R1126K, The gene TMEM117 has a mutation status of G61E, The gene DBX2 has a mutation status of P50S, The gene ZNF641 has a mutation status of R35L, The gene FIGNL2 has a mutation status of F477L, The gene NR4A1 has a mutation status of L26L, The gene HOXC11 has a mutation status of G196G, The gene NABP2 has a mutation status of I62I, The gene TPH2 has a mutation status of K429R, The gene METTL25 has a mutation status of R495W, The gene OAS1 has a mutation status of R295S, The gene NUP58 has a mutation status of G31A, The gene DCLK1 has a mutation status of N315N, The gene RCBTB2 has a mutation status of N151D, The gene PCDH17 has a mutation status of A31A, The gene IPO5 has a mutation status of D171H, The gene CLYBL has a mutation status of L72L, The gene MYO16 has a mutation status of S387S, The gene COL4A1 has a mutation status of P96L, The gene MCF2L has a mutation status of L255F, The gene RPGRIP1 has a mutation status of E489K, The gene TOX4 has a mutation status of L400L, The gene DHRS4 has a mutation status of G250F, The gene NFATC4 has a mutation status of S217L, The gene FOXG1 has a mutation status of G125C, The gene SCFD1 has a mutation status of A131G, The gene FBXO34 has a mutation status of A223P, The gene ZFYVE26 has a mutation status of T799T, The gene ATG2B has a mutation status of E232D, The gene GOLGA6L1 has a mutation status of W616G, The gene FAM189A1 has a mutation status of A503A, The gene MGA has a mutation status of D2557fs, The gene PLA2G4E has a mutation status of L540M, The gene COPS2 has a mutation status of S26C, The gene RNF111 has a mutation status of S267C, The gene ANKDD1A has a mutation status of L516L, The gene UACA has a mutation status of T434M, The gene GOLGA6L10 has a mutation status of E224K, The gene ADAMTS17 has a mutation status of G420A, The gene FLYWCH1 has a mutation status of L189L, The gene NPIPB5 has a mutation status of P472L, The gene ZNF629 has a mutation status of H684H, The gene KCTD19 has a mutation status of R124K, The gene PDPR has a mutation status of Q111K, The gene HYDIN has a mutation status of I1535del, The gene HYDIN has a mutation status of R197G, The gene ZFHX3 has a mutation status of G1925V, The gene GLG1 has a mutation status of S453S, The gene KARS1 has a mutation status of T56T, The gene ZNF469 has a mutation status of R2617Q, The gene TRPV1 has a mutation status of T699M, The gene PELP1 has a mutation status of P684P, The gene TP53 has a mutation status of E204*, The gene PER1 has a mutation status of S1053S, The gene CCDC42 has a mutation status of E52Q, The gene ERAL1 has a mutation status of T251T, The gene TBC1D3B has a mutation status of S510G, The gene CCL4L2 has a mutation status of P67R, The gene ABCC3 has a mutation status of A86A, The gene ABCC3 has a mutation status of N1181D, The gene APCDD1 has a mutation status of E393K, The gene DSC3 has a mutation status of I577R, The gene SMAD4 has a mutation status of D255H, The gene CCBE1 has a mutation status of A147S, The gene CNN2 has a mutation status of M249T, The gene TCF3 has a mutation status of R550R, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of V13007G, The gene ZNF709 has a mutation status of R464Q, The gene OR10H4 has a mutation status of P59P, The gene UPF1 has a mutation status of P48S, The gene ZNF66 has a mutation status of F97F, The gene TSHZ3 has a mutation status of H168N, The gene GRAMD1A has a mutation status of T670T, The gene LGI4 has a mutation status of *538*, The gene NFKBID has a mutation status of S14P, The gene ZNF568 has a mutation status of V404L, The gene WDR87 has a mutation status of Q1458E, The gene SIPA1L3 has a mutation status of G435R, The gene DACT3 has a mutation status of K606K, The gene SLC8A2 has a mutation status of E332Q, The gene ZNF600 has a mutation status of R579K, The gene LILRA6 has a mutation status of 350_351insGY, The gene LILRA1 has a mutation status of T30T, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL1 has a mutation status of G283G, The gene ZSCAN18 has a mutation status of S349S, The gene CDS2 has a mutation status of R331Q, The gene CCM2L has a mutation status of S408S, The gene C20orf144 has a mutation status of R106R, The gene LBP has a mutation status of A384T, The gene PPP1R16B has a mutation status of H284D, The gene CHD6 has a mutation status of P2693P, The gene CHD6 has a mutation status of R2035T, The gene AL031681.3 has a mutation status of L75L, The gene OCSTAMP has a mutation status of F254fs, The gene GNAS has a mutation status of G50E, The gene OGFR has a mutation status of P646L, The gene SRMS has a mutation status of S172fs, The gene GABPA has a mutation status of R336G, The gene SCAF4 has a mutation status of Q942E, The gene RCAN1 has a mutation status of T237M, The gene ERG has a mutation status of G337R, The gene TRPM2 has a mutation status of R1407W, The gene MICAL3 has a mutation status of S1797S, The gene CYP2D6 has a mutation status of S486T, The gene PNPLA3 has a mutation status of E467Q, The gene PLXNB2 has a mutation status of F1319F, The gene GTPBP6 has a mutation status of G61R, The gene NUDT11 has a mutation status of P42L, The gene SPANXN5 has a mutation status of L67L, The gene BX276092.9 has a mutation status of V364M, The gene HDX has a mutation status of W98*, The gene RAB40AL has a mutation status of G26R, The gene ATG4A has a mutation status of V241A, The gene SMIM10L2B has a mutation status of Q74Q, The gene SOX3 has a mutation status of S380S, The gene MAGEC3 has a mutation status of V159I, The gene PLXNA3 has a mutation status of T432T, The gene CLIC2 has a mutation status of M38R, The gene MT-CO1 has a mutation status of S187S, The gene MT-CO1 has a mutation status of T217T, The gene MT-CO2 has a mutation status of G131A, The gene MT-ND4 has a mutation status of F411L, The gene MT-ND4 has a mutation status of G456G, The gene MT-ND5 has a mutation status of V92V, The gene MT-ND5 has a mutation status of T449A, The gene MT-CYB has a mutation status of F18L, The gene MT-CYB has a mutation status of R71R
COAD
The gene CALML6 has a mutation status of M1V, The gene PER3 has a mutation status of C510Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene AHDC1 has a mutation status of R73P, The gene FGR has a mutation status of D353N, The gene ZMPSTE24 has a mutation status of E231E, The gene ZNF684 has a mutation status of S368S, The gene MPL has a mutation status of T428I, The gene ZFYVE9 has a mutation status of S314N, The gene SLC35D1 has a mutation status of L101F, The gene FNBP1L has a mutation status of K52K, The gene ABCD3 has a mutation status of G41E, The gene DENND2D has a mutation status of 108_109WA>*T, The gene SPAG17 has a mutation status of T1392S, The gene NOTCH2 has a mutation status of G1076G, The gene FMO5 has a mutation status of D492G, The gene CHD1L has a mutation status of L294F, The gene VPS45 has a mutation status of N289fs, The gene TCHHL1 has a mutation status of V516L, The gene AL691442.2 has a mutation status of K120T, The gene IFI16 has a mutation status of H701N, The gene AIM2 has a mutation status of K39Q, The gene GPA33 has a mutation status of W72C, The gene PAPPA2 has a mutation status of K319N, The gene QSOX1 has a mutation status of G140G, The gene LAMC2 has a mutation status of L269L, The gene LAMC2 has a mutation status of D1037Y, The gene HMCN1 has a mutation status of G4042D, The gene RGS2 has a mutation status of Y47C, The gene RGS2 has a mutation status of F48Y, The gene CFHR4 has a mutation status of E244A, The gene LMOD1 has a mutation status of R370G, The gene PTPN7 has a mutation status of D283N, The gene USH2A has a mutation status of Y3701H, The gene TMEM63A has a mutation status of C315G, The gene GNPAT has a mutation status of L169R, The gene MTR has a mutation status of L646F, The gene OR2L5 has a mutation status of M139I, The gene SNTG2 has a mutation status of E245Q, The gene NBAS has a mutation status of N1936N, The gene GEN1 has a mutation status of I789M, The gene WDR35 has a mutation status of M99fs, The gene APOB has a mutation status of S1162T, The gene ADGRF3 has a mutation status of R440S, The gene ABHD1 has a mutation status of A220A, The gene PCARE has a mutation status of V463I, The gene ALK has a mutation status of G1202G, The gene MEMO1 has a mutation status of A178A, The gene ARHGEF33 has a mutation status of R548R, The gene EHBP1 has a mutation status of R862C, The gene PLEK has a mutation status of R293G, The gene DYSF has a mutation status of D1958E, The gene RNF103 has a mutation status of R407fs, The gene SNRNP200 has a mutation status of I993M, The gene MAP4K4 has a mutation status of K41M, The gene TGFBRAP1 has a mutation status of F361L, The gene ST6GAL2 has a mutation status of S44Y, The gene SH3RF3 has a mutation status of I324N, The gene SCTR has a mutation status of D129N, The gene MAP3K19 has a mutation status of L903fs, The gene ZRANB3 has a mutation status of S159L, The gene LY75-CD302 has a mutation status of R1522R, The gene SCN9A has a mutation status of L75P, The gene SCN7A has a mutation status of P828P, The gene DYNC1I2 has a mutation status of A431P, The gene NFE2L2 has a mutation status of G65S, The gene TTN has a mutation status of V20469V, The gene TTN has a mutation status of V4268V, The gene FN1 has a mutation status of R1479R, The gene SPEG has a mutation status of E120D, The gene INPP5D has a mutation status of R167*, The gene LRRFIP1 has a mutation status of M3L, The gene GPC1 has a mutation status of Q351K, The gene ANO7 has a mutation status of T518T, The gene CAND2 has a mutation status of V839F, The gene NUP210 has a mutation status of T419M, The gene KCNH8 has a mutation status of A463V, The gene PDCD6IP has a mutation status of P816L, The gene SETD2 has a mutation status of D1537fs, The gene SETD2 has a mutation status of N1535K, The gene COL7A1 has a mutation status of A1397D, The gene ARIH2OS has a mutation status of A153G, The gene AMT has a mutation status of H91Y, The gene CCDC66 has a mutation status of S56T, The gene LRIG1 has a mutation status of R982T, The gene DCBLD2 has a mutation status of Y732F, The gene CCDC54 has a mutation status of M112L, The gene TEX55 has a mutation status of T114A, The gene ARHGAP31 has a mutation status of T467T, The gene TIMMDC1 has a mutation status of R86S, The gene CD80 has a mutation status of F93C, The gene SLC15A2 has a mutation status of K110Q, The gene CASR has a mutation status of R752H, The gene SLC49A4 has a mutation status of S6S, The gene SLC41A3 has a mutation status of I370S, The gene MCM2 has a mutation status of K691E, The gene AMOTL2 has a mutation status of G139V, The gene ATR has a mutation status of T2641I, The gene IGSF10 has a mutation status of T1062T, The gene SMC4 has a mutation status of E292V, The gene NMD3 has a mutation status of V96L, The gene PIK3CA has a mutation status of E545G, The gene APOD has a mutation status of K176E, The gene LMLN has a mutation status of R88G, The gene NSD2 has a mutation status of A965P, The gene CC2D2A has a mutation status of E241V, The gene DHX15 has a mutation status of K132R, The gene RASL11B has a mutation status of I116I, The gene AFF1 has a mutation status of D1024H, The gene INTS12 has a mutation status of P244S, The gene PRDM5 has a mutation status of T222P, The gene INPP4B has a mutation status of P789L, The gene FGG has a mutation status of I262M, The gene ICE1 has a mutation status of K209M, The gene TRIO has a mutation status of A47A, The gene SPEF2 has a mutation status of S1662G, The gene NIPBL has a mutation status of Q2311L, The gene CPLANE1 has a mutation status of P2839L, The gene IQGAP2 has a mutation status of C439Y, The gene AC022414.1 has a mutation status of D18Y, The gene PCSK1 has a mutation status of G236A, The gene TRIM36 has a mutation status of L64L, The gene SLC22A4 has a mutation status of I89P, The gene SLC22A4 has a mutation status of P476P, The gene CDKL3 has a mutation status of R101Q, The gene PKD2L2 has a mutation status of I172N, The gene PCDHA2 has a mutation status of A437V, The gene PCDHA13 has a mutation status of P756R, The gene PCDHB15 has a mutation status of G665V, The gene PCDHGA2 has a mutation status of E282K, The gene SPRY4 has a mutation status of G145D, The gene DOCK2 has a mutation status of S1528S, The gene THOC3 has a mutation status of T155S, The gene RASGEF1C has a mutation status of D94E, The gene NQO2 has a mutation status of G3D, The gene H4C2 has a mutation status of R96L, The gene MUC22 has a mutation status of G44V, The gene AGER has a mutation status of R77P, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene BRD2 has a mutation status of Y737C, The gene ANKS1A has a mutation status of A488V, The gene DEFB113 has a mutation status of T25P, The gene DST has a mutation status of R6837C, The gene RIMS1 has a mutation status of R363R, The gene IMPG1 has a mutation status of L268I, The gene ZNF292 has a mutation status of F1944L, The gene HACE1 has a mutation status of N74I, The gene SOBP has a mutation status of D811N, The gene WASF1 has a mutation status of H524P, The gene L3MBTL3 has a mutation status of Q255Q, The gene SLC2A12 has a mutation status of P550R, The gene NHSL1 has a mutation status of V924V, The gene UTRN has a mutation status of D1781D, The gene UTRN has a mutation status of K2159N, The gene FBXO30 has a mutation status of I467M, The gene AGPAT4 has a mutation status of S340R, The gene AFDN has a mutation status of T405T, The gene ACTB has a mutation status of V54G, The gene RNF216 has a mutation status of M558V, The gene BZW2 has a mutation status of E281G, The gene NT5C3A has a mutation status of V244L, The gene TNS3 has a mutation status of G535G, The gene COBL has a mutation status of L368P, The gene RSBN1L has a mutation status of G386R, The gene PCLO has a mutation status of Q951Q, The gene SEMA3E has a mutation status of I436G, The gene TRRAP has a mutation status of F1411C, The gene ATP5MF-PTCD1 has a mutation status of R350W, The gene PPP1R35 has a mutation status of A119V, The gene ZAN has a mutation status of A2272A, The gene MUC3A has a mutation status of S123L, The gene MUC17 has a mutation status of S2003N, The gene TRIM56 has a mutation status of G448E, The gene RELN has a mutation status of Y886Y, The gene DOCK4 has a mutation status of P172P, The gene CTTNBP2 has a mutation status of S475P, The gene ZC3HAV1L has a mutation status of A68A, The gene PRSS2 has a mutation status of R68C, The gene CNTNAP2 has a mutation status of F497I, The gene CUL1 has a mutation status of K93N, The gene ZNF862 has a mutation status of T459T, The gene NOS3 has a mutation status of R202K, The gene AGAP3 has a mutation status of T243T, The gene ABCF2 has a mutation status of L616L, The gene CLDN23 has a mutation status of S87*, The gene MTMR7 has a mutation status of Y582Y, The gene DOCK5 has a mutation status of G134V, The gene KCTD9 has a mutation status of A373T, The gene DDHD2 has a mutation status of P210T, The gene PRKDC has a mutation status of R4082*, The gene PXDNL has a mutation status of T514I, The gene RB1CC1 has a mutation status of V1264L, The gene CHD7 has a mutation status of N2518T, The gene PSKH2 has a mutation status of G170G, The gene GEM has a mutation status of S69S, The gene KLF10 has a mutation status of R391G, The gene NRBP2 has a mutation status of V445E, The gene EPPK1 has a mutation status of F465S, The gene OPLAH has a mutation status of A1213V, The gene RANBP6 has a mutation status of D221G, The gene DENND4C has a mutation status of F1867L, The gene RPS6 has a mutation status of R198H, The gene SLC24A2 has a mutation status of V646M, The gene CLTA has a mutation status of G16G, The gene FRMPD1 has a mutation status of S690N, The gene CARNMT1 has a mutation status of S44S, The gene VPS13A has a mutation status of T1844T, The gene TLE4 has a mutation status of Y370*, The gene PAPPA has a mutation status of N1141Y, The gene GARNL3 has a mutation status of N202H, The gene ENDOG has a mutation status of R25R, The gene HMCN2 has a mutation status of G833R, The gene SURF6 has a mutation status of R339H, The gene KLF6 has a mutation status of V210fs, The gene SFMBT2 has a mutation status of V491L, The gene TAF3 has a mutation status of Q222*, The gene ANKRD26 has a mutation status of I1360V, The gene ANKRD26 has a mutation status of K7*, The gene FZD8 has a mutation status of G343G, The gene ZNF32 has a mutation status of Y161Y, The gene JMJD1C has a mutation status of N1181S, The gene SLC29A3 has a mutation status of F146V, The gene VCL has a mutation status of I384T, The gene SFTPA1 has a mutation status of E237E, The gene LDB3 has a mutation status of A422P, The gene NUTM2D has a mutation status of V6L, The gene CHUK has a mutation status of Q616R, The gene ADRA2A has a mutation status of P270L, The gene TDRD1 has a mutation status of D717H, The gene SEC23IP has a mutation status of N612S, The gene PLEKHA1 has a mutation status of S398R, The gene SIRT3 has a mutation status of S178S, The gene MUC6 has a mutation status of T1854I, The gene HBD has a mutation status of V136I, The gene DNHD1 has a mutation status of R3978P, The gene MRGPRX1 has a mutation status of R207G, The gene AGBL2 has a mutation status of P137P, The gene OR8K5 has a mutation status of L166L, The gene OR9G1 has a mutation status of T62V, The gene TKFC has a mutation status of V49V, The gene VEGFB has a mutation status of T156P, The gene DDX10 has a mutation status of Q528K, The gene KDM5A has a mutation status of L236L, The gene DCP1B has a mutation status of I515N, The gene PRH1 has a mutation status of P186T, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene AEBP2 has a mutation status of L315L, The gene SLCO1B3 has a mutation status of V349I, The gene SLCO1B3-SLCO1B7 has a mutation status of V708D, The gene DDX11 has a mutation status of P559S, The gene LRRK2 has a mutation status of S1345I, The gene SLC38A4 has a mutation status of E179Q, The gene COL2A1 has a mutation status of G324G, The gene HIGD1C has a mutation status of I31V, The gene KRT80 has a mutation status of I175T, The gene ZNF740 has a mutation status of L144P, The gene ITGB7 has a mutation status of C654Y, The gene ZNF385A has a mutation status of P275T, The gene LRP1 has a mutation status of V1561M, The gene AVIL has a mutation status of E240G, The gene POC1B-GALNT4 has a mutation status of Y102N, The gene CHST11 has a mutation status of T95K, The gene CUX2 has a mutation status of A1186T, The gene RPL6 has a mutation status of M1T, The gene RNF10 has a mutation status of G665W, The gene TMEM132B has a mutation status of R571H, The gene SLC15A4 has a mutation status of V233V, The gene TMEM132D has a mutation status of I383I, The gene NOC4L has a mutation status of P488P, The gene LATS2 has a mutation status of A773T, The gene PARP4 has a mutation status of F1350F, The gene PABPC3 has a mutation status of L38H, The gene WASF3 has a mutation status of F371V, The gene ELF1 has a mutation status of G339G, The gene PIBF1 has a mutation status of R469H, The gene RBM26 has a mutation status of P540H, The gene SLITRK5 has a mutation status of K742N, The gene MBNL2 has a mutation status of H249N, The gene IRS2 has a mutation status of L1182L, The gene MCF2L has a mutation status of P49P, The gene GAS6 has a mutation status of L611L, The gene RASA3 has a mutation status of T395A, The gene SALL2 has a mutation status of P758T, The gene HECTD1 has a mutation status of R1058K, The gene DLGAP5 has a mutation status of Q635*, The gene SYNE2 has a mutation status of E4598Q, The gene HSPA2 has a mutation status of T422M, The gene LTBP2 has a mutation status of N421I, The gene ADCK1 has a mutation status of D403H, The gene TTC8 has a mutation status of W12*, The gene CATSPERB has a mutation status of A34A, The gene COX8C has a mutation status of P38S, The gene DYNC1H1 has a mutation status of M2779V, The gene GABRG3 has a mutation status of M381T, The gene OCA2 has a mutation status of N465D, The gene HERC2 has a mutation status of A199T, The gene DISP2 has a mutation status of I180V, The gene IVD has a mutation status of G279W, The gene BAHD1 has a mutation status of P410R, The gene PLA2G4D has a mutation status of T767A, The gene TLE3 has a mutation status of I584I, The gene HCN4 has a mutation status of P166P, The gene TBC1D21 has a mutation status of S160N, The gene CYP11A1 has a mutation status of G336S, The gene SCAPER has a mutation status of Q866P, The gene PEAK1 has a mutation status of L1519L, The gene MINAR1 has a mutation status of E822K, The gene BTBD1 has a mutation status of A451A, The gene ADAMTSL3 has a mutation status of Y58F, The gene AC013489.1 has a mutation status of K433T, The gene PCSK6 has a mutation status of P133P, The gene CLCN7 has a mutation status of M349I, The gene NMRAL1 has a mutation status of G294R, The gene LITAF has a mutation status of T49M, The gene ACSM2B has a mutation status of G405fs, The gene ERN2 has a mutation status of L499L, The gene SLC5A11 has a mutation status of D14H, The gene CLN3 has a mutation status of L426Q, The gene RABEP2 has a mutation status of T347S, The gene GNAO1 has a mutation status of F336I, The gene SLC12A3 has a mutation status of Q1030K, The gene CES2 has a mutation status of G180S, The gene CARMIL2 has a mutation status of A414S, The gene MTSS2 has a mutation status of R745H, The gene HSDL1 has a mutation status of G29A, The gene COTL1 has a mutation status of T80A, The gene ABR has a mutation status of H507R, The gene SPNS2 has a mutation status of A52T, The gene CTC1 has a mutation status of L633L, The gene DNAH9 has a mutation status of E2983K, The gene DNAH9 has a mutation status of D4224N, The gene ZNF18 has a mutation status of E110D, The gene TOP3A has a mutation status of T194T, The gene SPECC1 has a mutation status of E638K, The gene PROCA1 has a mutation status of K238T, The gene MYO18A has a mutation status of A1897G, The gene MYO1D has a mutation status of A486A, The gene CCL4L2 has a mutation status of P67R, The gene MRM1 has a mutation status of G194W, The gene CWC25 has a mutation status of L400M, The gene FBXO47 has a mutation status of L59F, The gene GJD3 has a mutation status of H175Y, The gene KRT28 has a mutation status of C342Y, The gene KRTAP4-7 has a mutation status of L148V, The gene KRTAP4-7 has a mutation status of C150C, The gene CNTD1 has a mutation status of R17K, The gene BRCA1 has a mutation status of V1708F, The gene MRPL27 has a mutation status of V59V, The gene EPN3 has a mutation status of D344E, The gene NME2 has a mutation status of E152E, The gene UTP18 has a mutation status of G16G, The gene OR4D2 has a mutation status of I273I, The gene RAD51C has a mutation status of F229L, The gene HEATR6 has a mutation status of S531A, The gene TANC2 has a mutation status of L225F, The gene MAP3K3 has a mutation status of Q256R, The gene LLGL2 has a mutation status of R728R, The gene DNAH17 has a mutation status of E597D, The gene CCDC40 has a mutation status of K438Q, The gene RAC3 has a mutation status of I33I, The gene FN3KRP has a mutation status of G152R, The gene ASXL3 has a mutation status of V171I, The gene ATP8B1 has a mutation status of D12E, The gene SERPINB8 has a mutation status of A89G, The gene ZNF516 has a mutation status of H767L, The gene SALL3 has a mutation status of S914N, The gene RPS15 has a mutation status of P80S, The gene REXO1 has a mutation status of P657P, The gene CTXN1 has a mutation status of L42L, The gene NOTCH3 has a mutation status of A1948P, The gene MED26 has a mutation status of P448R, The gene HAUS8 has a mutation status of M149I, The gene UNC13A has a mutation status of G484S, The gene IL12RB1 has a mutation status of G353E, The gene ISYNA1 has a mutation status of T434A, The gene SLC25A42 has a mutation status of G237G, The gene ZNF708 has a mutation status of C506S, The gene ZNF536 has a mutation status of A465E, The gene KCTD15 has a mutation status of L133L, The gene HNRNPL has a mutation status of H339Y, The gene ACP7 has a mutation status of R152fs, The gene CYP2A7 has a mutation status of R485*, The gene ZNF225 has a mutation status of K328K, The gene PNMA8A has a mutation status of F86F, The gene CCDC114 has a mutation status of R363H, The gene FUZ has a mutation status of P274P, The gene KLK1 has a mutation status of V92A, The gene KLK10 has a mutation status of M213V, The gene ZNF808 has a mutation status of H306L, The gene ZNF28 has a mutation status of H565H, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene NLRP5 has a mutation status of R456C, The gene ZFP28 has a mutation status of 39_40LA>FS, The gene ZNF71 has a mutation status of T290fs, The gene ZNF71 has a mutation status of L289L, The gene VN1R1 has a mutation status of L173F, The gene MRPS26 has a mutation status of R155R, The gene FASTKD5 has a mutation status of Q159H, The gene ZNF133 has a mutation status of G361V, The gene XRN2 has a mutation status of Y14Y, The gene TM9SF4 has a mutation status of I551I, The gene SPAG4 has a mutation status of H275H, The gene HNF4A has a mutation status of G440S, The gene DDX27 has a mutation status of A688T, The gene CASS4 has a mutation status of A18G, The gene HELZ2 has a mutation status of W1062*, The gene TNFRSF6B has a mutation status of C126F, The gene NRIP1 has a mutation status of A635A, The gene BACH1 has a mutation status of F130I, The gene TIAM1 has a mutation status of K579N, The gene DONSON has a mutation status of A183S, The gene DONSON has a mutation status of R88R, The gene UBASH3A has a mutation status of D428E, The gene CSTB has a mutation status of A14S, The gene FTCD has a mutation status of A486A, The gene RTL10 has a mutation status of V58V, The gene LZTR1 has a mutation status of Q319fs, The gene ZNF280B has a mutation status of D275E, The gene EMID1 has a mutation status of G217S, The gene CDC42EP1 has a mutation status of G72R, The gene H1-0 has a mutation status of L70L, The gene TNRC6B has a mutation status of T274S, The gene MCHR1 has a mutation status of A203T, The gene FBLN1 has a mutation status of D30G, The gene TUBGCP6 has a mutation status of L1171L, The gene ADM2 has a mutation status of C115C, The gene MAPK8IP2 has a mutation status of S690S, The gene MAPK8IP2 has a mutation status of V693V, The gene PPP2R3B has a mutation status of S24I, The gene PPP2R3B has a mutation status of Y21N, The gene SLC25A6 has a mutation status of G172S, The gene RAB9A has a mutation status of A168A, The gene REPS2 has a mutation status of P414A, The gene APOO has a mutation status of L103P, The gene POLA1 has a mutation status of P3P, The gene CYBB has a mutation status of C369F, The gene SSX5 has a mutation status of D31D, The gene SSX4 has a mutation status of K60Q, The gene PRICKLE3 has a mutation status of M325I, The gene HUWE1 has a mutation status of G3295C, The gene DLG3 has a mutation status of T577N, The gene MAGEE1 has a mutation status of I884T, The gene DACH2 has a mutation status of L560F, The gene KIAA1210 has a mutation status of H432H, The gene BCORL1 has a mutation status of L1132P, The gene SLITRK4 has a mutation status of P610T, The gene DDX3Y has a mutation status of T242T, The gene MT-ND1 has a mutation status of G203G, The gene MT-CO3 has a mutation status of W58W, The gene MT-ND5 has a mutation status of F478L, The gene MT-ND6 has a mutation status of N174fs, The gene AGRN has a mutation status of S330fs, The gene AGRN has a mutation status of S330I, The gene ESPN has a mutation status of P275A, The gene PER3 has a mutation status of C510Y, The gene PRAMEF13 has a mutation status of L464L, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene SDHB has a mutation status of A262fs, The gene FGR has a mutation status of D353N, The gene ZMPSTE24 has a mutation status of E231E, The gene ZNF684 has a mutation status of S368S, The gene PPCS has a mutation status of R25P, The gene MPL has a mutation status of T428I, The gene PTPRF has a mutation status of L431M, The gene ZFYVE9 has a mutation status of S314N, The gene SLC35D1 has a mutation status of L101F, The gene FNBP1L has a mutation status of K52K, The gene ABCD3 has a mutation status of G41E, The gene DENND2D has a mutation status of 108_109WA>*T, The gene SPAG17 has a mutation status of T1392S, The gene NOTCH2 has a mutation status of G1076G, The gene FMO5 has a mutation status of D492G, The gene CHD1L has a mutation status of L294F, The gene VPS45 has a mutation status of N289fs, The gene TCHHL1 has a mutation status of V516L, The gene FLG2 has a mutation status of GQTSGFGQHRSSSGQYSGFGQHGSGSGQSSGFGQHGTGSGQYSGFGQHESRSHQSSYGQHGSGSSQSSGYGQHGSSS866del, The gene AL691442.2 has a mutation status of K120T, The gene IFI16 has a mutation status of H701N, The gene AIM2 has a mutation status of K39Q, The gene GPA33 has a mutation status of W72C, The gene PRRX1 has a mutation status of V175M, The gene SLC9C2 has a mutation status of L512L, The gene PAPPA2 has a mutation status of K319N, The gene LAMC2 has a mutation status of L269L, The gene LAMC2 has a mutation status of D1037Y, The gene SMG7 has a mutation status of D21D, The gene RGS2 has a mutation status of Y47C, The gene RGS2 has a mutation status of F48Y, The gene CFHR4 has a mutation status of E244A, The gene CFHR4 has a mutation status of Q360H, The gene PTPN7 has a mutation status of D283N, The gene ZC3H11A has a mutation status of R373H, The gene SRGAP2 has a mutation status of A744A, The gene USH2A has a mutation status of Y3701H, The gene USH2A has a mutation status of L2443R, The gene AIDA has a mutation status of D264H, The gene TMEM63A has a mutation status of C315G, The gene LEFTY1 has a mutation status of G156D, The gene STUM has a mutation status of R23R, The gene FAM89A has a mutation status of R75Q, The gene GNPAT has a mutation status of L169R, The gene TBCE has a mutation status of R386R, The gene MTR has a mutation status of L646F, The gene RYR2 has a mutation status of A118S, The gene AL451007.3 has a mutation status of G62D, The gene OR2C3 has a mutation status of M186I, The gene OR2L5 has a mutation status of M139I, The gene SNTG2 has a mutation status of E245Q, The gene NBAS has a mutation status of N1936N, The gene GEN1 has a mutation status of I789M, The gene WDR35 has a mutation status of M99fs, The gene APOB has a mutation status of S1162T, The gene ADGRF3 has a mutation status of L284I, The gene ABHD1 has a mutation status of A220A, The gene PCARE has a mutation status of V463I, The gene MEMO1 has a mutation status of A178A, The gene BIRC6 has a mutation status of Q1158L, The gene BIRC6 has a mutation status of H1159P, The gene CYP1B1 has a mutation status of V178L, The gene EHBP1 has a mutation status of R862C, The gene DYSF has a mutation status of D1958E, The gene SNRNP200 has a mutation status of I993M, The gene MAP4K4 has a mutation status of K41M, The gene TGFBRAP1 has a mutation status of F361L, The gene ST6GAL2 has a mutation status of S44Y, The gene SCTR has a mutation status of D129N, The gene MAP3K19 has a mutation status of L903fs, The gene LRP1B has a mutation status of D2962fs, The gene LRP1B has a mutation status of D2961VL*EVSPFFALH, The gene ZEB2 has a mutation status of S61R, The gene KIF5C has a mutation status of E659G, The gene LY75-CD302 has a mutation status of R1522R, The gene SCN9A has a mutation status of L75P, The gene SCN7A has a mutation status of P828P, The gene DYNC1I2 has a mutation status of A431P, The gene NFE2L2 has a mutation status of G65S, The gene TTN has a mutation status of V20469V, The gene ABI2 has a mutation status of R219R, The gene CCNYL1 has a mutation status of D193Y, The gene CPS1 has a mutation status of V1073V, The gene FN1 has a mutation status of R1479R, The gene COPS7B has a mutation status of T216T, The gene INPP5D has a mutation status of R167*, The gene SNED1 has a mutation status of P61Q, The gene ANO7 has a mutation status of T518T, The gene IL17RE has a mutation status of L492L, The gene CAND2 has a mutation status of V839F, The gene NUP210 has a mutation status of T419M, The gene PDCD6IP has a mutation status of P816L, The gene SETD2 has a mutation status of D1537fs, The gene SETD2 has a mutation status of N1535K, The gene COL7A1 has a mutation status of E27D, The gene AMT has a mutation status of H91Y, The gene LRTM1 has a mutation status of Q98H, The gene CCDC66 has a mutation status of S56T, The gene LRIG1 has a mutation status of R982T, The gene ZNF717 has a mutation status of S56fs, The gene CHMP2B has a mutation status of D107G, The gene DCBLD2 has a mutation status of Y732F, The gene CCDC54 has a mutation status of M112L, The gene NECTIN3 has a mutation status of G121V, The gene CCDC191 has a mutation status of L450fs, The gene ARHGAP31 has a mutation status of T467T, The gene TIMMDC1 has a mutation status of R86S, The gene CD80 has a mutation status of F93C, The gene SLC15A2 has a mutation status of K110Q, The gene CASR has a mutation status of R752H, The gene SLC41A3 has a mutation status of I370S, The gene MCM2 has a mutation status of K691E, The gene NPHP3 has a mutation status of E192K, The gene AMOTL2 has a mutation status of G139V, The gene ATR has a mutation status of T2641I, The gene IGSF10 has a mutation status of T1062T, The gene MFSD1 has a mutation status of T221T, The gene SMC4 has a mutation status of E292V, The gene PIK3CA has a mutation status of E545G, The gene NDUFB5 has a mutation status of Q141H, The gene AP2M1 has a mutation status of S236G, The gene APOD has a mutation status of K176E, The gene LMLN has a mutation status of R88G, The gene IDUA has a mutation status of R5R, The gene NSD2 has a mutation status of A965P, The gene FAM90A26 has a mutation status of P346L, The gene CC2D2A has a mutation status of E241V, The gene DHX15 has a mutation status of K132R, The gene NWD2 has a mutation status of D1376H, The gene RFC1 has a mutation status of D111V, The gene RASL11B has a mutation status of I116I, The gene AFF1 has a mutation status of D1024H, The gene INTS12 has a mutation status of P244S, The gene PRDM5 has a mutation status of T222P, The gene MAML3 has a mutation status of Q493Q, The gene MAML3 has a mutation status of Q491Q, The gene ELMOD2 has a mutation status of N82fs, The gene INPP4B has a mutation status of P789L, The gene FGG has a mutation status of I262M, The gene ADAMTS16 has a mutation status of Q148*, The gene ICE1 has a mutation status of K209M, The gene SPEF2 has a mutation status of S1662G, The gene NIPBL has a mutation status of Q2311L, The gene CPLANE1 has a mutation status of P2839L, The gene TTC33 has a mutation status of S235S, The gene IQGAP2 has a mutation status of C439Y, The gene NR2F1 has a mutation status of G21G, The gene PCSK1 has a mutation status of G236A, The gene TRIM36 has a mutation status of L64L, The gene FBN2 has a mutation status of I534I, The gene ADAMTS19 has a mutation status of F192F, The gene TCF7 has a mutation status of H140H, The gene CDKL3 has a mutation status of R101Q, The gene PKD2L2 has a mutation status of I172N, The gene PCDHA2 has a mutation status of A437V, The gene PCDHB15 has a mutation status of G665V, The gene PCDHGA2 has a mutation status of E282K, The gene DOCK2 has a mutation status of S1528S, The gene PDLIM7 has a mutation status of Q131*, The gene H4C2 has a mutation status of R96L, The gene HLA-B has a mutation status of G131G, The gene HLA-DRB5 has a mutation status of T262R, The gene BRD2 has a mutation status of Y737C, The gene UQCC2 has a mutation status of R5Q, The gene CUL9 has a mutation status of N1627K, The gene DEFB113 has a mutation status of T25P, The gene DST has a mutation status of R6837C, The gene IMPG1 has a mutation status of L268I, The gene ZNF292 has a mutation status of F1944L, The gene FHL5 has a mutation status of P47Q, The gene HACE1 has a mutation status of N74I, The gene SOBP has a mutation status of D811N, The gene FOXO3 has a mutation status of L407fs, The gene RSPH4A has a mutation status of R354C, The gene SLC35F1 has a mutation status of R53R, The gene L3MBTL3 has a mutation status of Q255Q, The gene SLC2A12 has a mutation status of P550R, The gene UTRN has a mutation status of D1781D, The gene FBXO30 has a mutation status of I467M, The gene AGPAT4 has a mutation status of S340R, The gene AFDN has a mutation status of T405T, The gene SUN1 has a mutation status of V550V, The gene ACTB has a mutation status of V54G, The gene RNF216 has a mutation status of M558V, The gene RNF216 has a mutation status of S418F, The gene BZW2 has a mutation status of E281G, The gene NT5C3A has a mutation status of V244L, The gene TNS3 has a mutation status of G535G, The gene RSBN1L has a mutation status of G386R, The gene MAGI2 has a mutation status of L304L, The gene SEMA3E has a mutation status of I436G, The gene TRRAP has a mutation status of F1411C, The gene ATP5MF-PTCD1 has a mutation status of R350W, The gene PPP1R35 has a mutation status of A119V, The gene ZAN has a mutation status of A2272A, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene MUC3A has a mutation status of T1218T, The gene MUC17 has a mutation status of S2003N, The gene TRIM56 has a mutation status of G448E, The gene DOCK4 has a mutation status of P172P, The gene CTTNBP2 has a mutation status of S475P, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene STRA8 has a mutation status of S244fs, The gene STRA8 has a mutation status of A243A, The gene PRSS1 has a mutation status of N77N, The gene CNTNAP2 has a mutation status of F497I, The gene CUL1 has a mutation status of K93N, The gene NOS3 has a mutation status of R202K, The gene CLDN23 has a mutation status of S87*, The gene MTMR7 has a mutation status of Y582Y, The gene DOCK5 has a mutation status of G134V, The gene KCTD9 has a mutation status of A373T, The gene DDHD2 has a mutation status of P210T, The gene PRKDC has a mutation status of R4082*, The gene RGS20 has a mutation status of S65L, The gene CHD7 has a mutation status of N2518T, The gene PSKH2 has a mutation status of G170G, The gene GEM has a mutation status of S69S, The gene VIRMA has a mutation status of P1449R, The gene KLF10 has a mutation status of R391G, The gene OPLAH has a mutation status of A1213V, The gene C8orf33 has a mutation status of R247R, The gene AK3 has a mutation status of G17G, The gene RANBP6 has a mutation status of D221G, The gene DENND4C has a mutation status of F1867L, The gene RPS6 has a mutation status of R198H, The gene SLC24A2 has a mutation status of V646M, The gene CLTA has a mutation status of G16G, The gene FRMPD1 has a mutation status of S690N, The gene CARNMT1 has a mutation status of S44S, The gene VPS13A has a mutation status of T1844T, The gene TLE4 has a mutation status of Y370*, The gene DENND1A has a mutation status of L871M, The gene GARNL3 has a mutation status of N202H, The gene SURF6 has a mutation status of R339H, The gene CCDC187 has a mutation status of A321T, The gene ABCA2 has a mutation status of K18R, The gene ENTPD2 has a mutation status of R387R, The gene KLF6 has a mutation status of V210fs, The gene SFMBT2 has a mutation status of V491L, The gene ANKRD30A has a mutation status of A585S, The gene ZNF32 has a mutation status of Y161Y, The gene JMJD1C has a mutation status of N1181S, The gene CCAR1 has a mutation status of D944H, The gene SLC29A3 has a mutation status of F146V, The gene ECD has a mutation status of C146Y, The gene ZSWIM8 has a mutation status of R1666H, The gene VCL has a mutation status of I384T, The gene SFTPA1 has a mutation status of E237E, The gene LDB3 has a mutation status of A422P, The gene SORBS1 has a mutation status of D248N, The gene CHUK has a mutation status of Q616R, The gene ADRA2A has a mutation status of A354E, The gene TDRD1 has a mutation status of D717H, The gene PLEKHA1 has a mutation status of S398R, The gene SIRT3 has a mutation status of S178S, The gene HBD has a mutation status of V136I, The gene DNHD1 has a mutation status of S1100I, The gene MRGPRX1 has a mutation status of R207G, The gene RAPSN has a mutation status of D158G, The gene C1QTNF4 has a mutation status of A325A, The gene AGBL2 has a mutation status of P137P, The gene OR8K5 has a mutation status of L166L, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene GLYATL1 has a mutation status of N274S, The gene TKFC has a mutation status of V49V, The gene KLC2 has a mutation status of Y346F, The gene USP35 has a mutation status of S901C, The gene GAB2 has a mutation status of M438fs, The gene ARHGAP32 has a mutation status of R1252R, The gene IQSEC3 has a mutation status of Q714R, The gene KDM5A has a mutation status of L236L, The gene DCP1B has a mutation status of I515N, The gene CACNA1C has a mutation status of H2078Y, The gene PRH1 has a mutation status of P186T, The gene TAS2R13 has a mutation status of E61K, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene AEBP2 has a mutation status of L315L, The gene SLCO1B3 has a mutation status of V349I, The gene LRRK2 has a mutation status of S1345I, The gene SLC38A4 has a mutation status of E179Q, The gene HDAC7 has a mutation status of L489L, The gene COL2A1 has a mutation status of G324G, The gene HIGD1C has a mutation status of I31V, The gene KRT80 has a mutation status of I175T, The gene ITGB7 has a mutation status of C654Y, The gene LRP1 has a mutation status of V1561M, The gene MBD6 has a mutation status of A224S, The gene AVIL has a mutation status of E240G, The gene PTPRB has a mutation status of Q1261*, The gene POC1B-GALNT4 has a mutation status of Y102N, The gene CUX2 has a mutation status of A1186T, The gene RPL6 has a mutation status of M1T, The gene FBXW8 has a mutation status of A201A, The gene RNF10 has a mutation status of G665W, The gene TMEM132B has a mutation status of R571H, The gene SLC15A4 has a mutation status of V233V, The gene TMEM132D has a mutation status of I383I, The gene ADGRD1 has a mutation status of K354R, The gene LATS2 has a mutation status of A773T, The gene PARP4 has a mutation status of F1350F, The gene NBEA has a mutation status of K1275*, The gene NBEA has a mutation status of W2286*, The gene PIBF1 has a mutation status of R469H, The gene RBM26 has a mutation status of P540H, The gene MYO16 has a mutation status of L1120V, The gene IRS2 has a mutation status of L1182L, The gene MCF2L has a mutation status of P49P, The gene GAS6 has a mutation status of L611L, The gene RASA3 has a mutation status of T395A, The gene SALL2 has a mutation status of P758T, The gene HECTD1 has a mutation status of R1058K, The gene DLGAP5 has a mutation status of Q635*, The gene SYNE2 has a mutation status of E4598Q, The gene HSPA2 has a mutation status of T422M, The gene ZFYVE1 has a mutation status of P393L, The gene ADCK1 has a mutation status of D403H, The gene TTC8 has a mutation status of W12*, The gene COX8C has a mutation status of P38S, The gene UNC79 has a mutation status of D1479N, The gene BCL11B has a mutation status of P268T, The gene DYNC1H1 has a mutation status of M2779V, The gene OCA2 has a mutation status of N465D, The gene HERC2 has a mutation status of A199T, The gene DISP2 has a mutation status of I180V, The gene IVD has a mutation status of G279W, The gene BAHD1 has a mutation status of P410R, The gene PLA2G4D has a mutation status of T767A, The gene ITGA11 has a mutation status of H275Q, The gene TLE3 has a mutation status of I584I, The gene HCN4 has a mutation status of I48M, The gene CYP11A1 has a mutation status of G336S, The gene SCAPER has a mutation status of Q866P, The gene PEAK1 has a mutation status of L1519L, The gene MINAR1 has a mutation status of E822K, The gene BTBD1 has a mutation status of A451A, The gene ADAMTSL3 has a mutation status of Y58F, The gene AC013489.1 has a mutation status of K433T, The gene PCSK6 has a mutation status of P133P, The gene PCSK6 has a mutation status of P66P, The gene RHBDL1 has a mutation status of F350L, The gene CACNA1H has a mutation status of Q2051R, The gene NMRAL1 has a mutation status of G294R, The gene LITAF has a mutation status of T49M, The gene NOMO3 has a mutation status of Y634*, The gene ACSM2B has a mutation status of G405fs, The gene ERN2 has a mutation status of L499L, The gene SLC5A11 has a mutation status of D14H, The gene CLN3 has a mutation status of L426Q, The gene PAGR1 has a mutation status of R135R, The gene PAGR1 has a mutation status of P137H, The gene GNAO1 has a mutation status of F336I, The gene SLC12A3 has a mutation status of Q1030K, The gene CES2 has a mutation status of G180S, The gene CDYL2 has a mutation status of M1I, The gene HSDL1 has a mutation status of G29A, The gene COTL1 has a mutation status of T80A, The gene KLHDC4 has a mutation status of S175A, The gene ZNF276 has a mutation status of L38L, The gene ABR has a mutation status of H507R, The gene CNTROB has a mutation status of A530A, The gene CTC1 has a mutation status of L633L, The gene DNAH9 has a mutation status of E2983K, The gene DNAH9 has a mutation status of D4224N, The gene ZNF18 has a mutation status of E110D, The gene TOP3A has a mutation status of T194T, The gene SPECC1 has a mutation status of E638K, The gene MYO1D has a mutation status of A486A, The gene CCL4L2 has a mutation status of P67R, The gene MRM1 has a mutation status of G194W, The gene CWC25 has a mutation status of L400M, The gene FBXO47 has a mutation status of L59F, The gene GJD3 has a mutation status of H175Y, The gene GJD3 has a mutation status of F70I, The gene KRT28 has a mutation status of C342Y, The gene FKBP10 has a mutation status of L430fs, The gene CNTD1 has a mutation status of R17K, The gene BRCA1 has a mutation status of V1708F, The gene MRPL27 has a mutation status of V59V, The gene EPN3 has a mutation status of D344E, The gene NME2 has a mutation status of E152E, The gene UTP18 has a mutation status of G16G, The gene OR4D2 has a mutation status of I273I, The gene RAD51C has a mutation status of F229L, The gene SMG8 has a mutation status of V317V, The gene HEATR6 has a mutation status of S531A, The gene BRIP1 has a mutation status of E1104Q, The gene MAP3K3 has a mutation status of Q256R, The gene ABCA6 has a mutation status of T1581I, The gene LLGL2 has a mutation status of R728R, The gene DNAH17 has a mutation status of A3287A, The gene DNAH17 has a mutation status of E597D, The gene ENGASE has a mutation status of L390L, The gene CCDC40 has a mutation status of K438Q, The gene RNF213 has a mutation status of N2376D, The gene RAC3 has a mutation status of I33I, The gene GPS1 has a mutation status of S81C, The gene RMC1 has a mutation status of G172E, The gene ASXL3 has a mutation status of V171I, The gene SERPINB8 has a mutation status of A89G, The gene ZNF516 has a mutation status of H767L, The gene SALL3 has a mutation status of A185L, The gene SALL3 has a mutation status of S914N, The gene ABCA7 has a mutation status of K411N, The gene ZFR2 has a mutation status of C328*, The gene PEX11G has a mutation status of W205C, The gene FCER2 has a mutation status of E249D, The gene TGFBR3L has a mutation status of Q92K, The gene PRKCSH has a mutation status of A380S, The gene PRKCSH has a mutation status of E381*, The gene CACNA1A has a mutation status of E2347K, The gene SYDE1 has a mutation status of L292L, The gene NOTCH3 has a mutation status of A1948P, The gene NOTCH3 has a mutation status of S310T, The gene MED26 has a mutation status of P448R, The gene HAUS8 has a mutation status of M149I, The gene UNC13A has a mutation status of G484S, The gene IL12RB1 has a mutation status of G353E, The gene ISYNA1 has a mutation status of T434A, The gene ZNF708 has a mutation status of C506S, The gene ZNF728 has a mutation status of P395P, The gene GPI has a mutation status of P201T, The gene CATSPERG has a mutation status of T321T, The gene HNRNPL has a mutation status of H339Y, The gene LTBP4 has a mutation status of P522A, The gene CYP2A7 has a mutation status of R485*, The gene ZNF225 has a mutation status of K328K, The gene BCL3 has a mutation status of G86*, The gene PNMA8A has a mutation status of F86F, The gene CCDC114 has a mutation status of R363H, The gene SCAF1 has a mutation status of A1061V, The gene KLK1 has a mutation status of V92A, The gene ZNF808 has a mutation status of H306L, The gene ZNF28 has a mutation status of H565H, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q50Q, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene NLRP5 has a mutation status of R456C, The gene ZFP28 has a mutation status of 39_40LA>FS, The gene VN1R1 has a mutation status of L173F, The gene FASTKD5 has a mutation status of Q159H, The gene ZNF133 has a mutation status of G361V, The gene DZANK1 has a mutation status of P244L, The gene SPAG4 has a mutation status of H275H, The gene RBL1 has a mutation status of T713I, The gene HNF4A has a mutation status of G440S, The gene DDX27 has a mutation status of A688T, The gene NPEPL1 has a mutation status of A287A, The gene COL20A1 has a mutation status of H598N, The gene HELZ2 has a mutation status of W1062*, The gene BACH1 has a mutation status of F130I, The gene TIAM1 has a mutation status of K579N, The gene DONSON has a mutation status of A183S, The gene DONSON has a mutation status of R88R, The gene BRWD1 has a mutation status of S2070T, The gene UBASH3A has a mutation status of D428E, The gene SLC19A1 has a mutation status of R243Q, The gene FTCD has a mutation status of A486A, The gene RTL10 has a mutation status of V58V, The gene LZTR1 has a mutation status of Q319fs, The gene ZNF280B has a mutation status of D275E, The gene TMPRSS6 has a mutation status of S343G, The gene CDC42EP1 has a mutation status of G72R, The gene H1-0 has a mutation status of L70L, The gene SLC16A8 has a mutation status of L89M, The gene TNRC6B has a mutation status of T274S, The gene MCHR1 has a mutation status of A203T, The gene MEI1 has a mutation status of T81T, The gene EFCAB6 has a mutation status of P365S, The gene FBLN1 has a mutation status of D30G, The gene TUBGCP6 has a mutation status of L1171L, The gene DENND6B has a mutation status of S444N, The gene SBF1 has a mutation status of E366D, The gene ADM2 has a mutation status of C115C, The gene SLC25A6 has a mutation status of G172S, The gene ARHGAP6 has a mutation status of G745E, The gene RAB9A has a mutation status of A168A, The gene BMX has a mutation status of T353T, The gene REPS2 has a mutation status of P414A, The gene APOO has a mutation status of L103P, The gene POLA1 has a mutation status of P3P, The gene USP9X has a mutation status of Q51E, The gene SSX4 has a mutation status of K60Q, The gene HUWE1 has a mutation status of G3295C, The gene STARD8 has a mutation status of G662A, The gene DLG3 has a mutation status of T577N, The gene MAGEE1 has a mutation status of I884T, The gene SATL1 has a mutation status of F598L, The gene DACH2 has a mutation status of L560F, The gene KIAA1210 has a mutation status of H432H, The gene BCORL1 has a mutation status of L1132P, The gene SLITRK4 has a mutation status of P610T, The gene DUSP9 has a mutation status of G107S, The gene MT-ND1 has a mutation status of N5N, The gene MT-ND1 has a mutation status of G203G, The gene MT-ND4L has a mutation status of L40L, The gene MT-ND5 has a mutation status of F478L, The gene MT-ND5 has a mutation status of I537I, The gene MT-ND6 has a mutation status of N174fs
BLCA
The gene PERM1 has a mutation status of G75C, The gene MXRA8 has a mutation status of I430I, The gene CASZ1 has a mutation status of E1606Q, The gene TNFRSF1B has a mutation status of A127S, The gene PRAMEF9 has a mutation status of R48R, The gene PRAMEF9 has a mutation status of Q261K, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of L121P, The gene PRAMEF18 has a mutation status of W98R, The gene IGSF21 has a mutation status of R272H, The gene TAS1R2 has a mutation status of L688L, The gene ALPL has a mutation status of F327F, The gene FGR has a mutation status of A239T, The gene EPB41 has a mutation status of H16Y, The gene CSMD2 has a mutation status of D845N, The gene CAP1 has a mutation status of E335V, The gene SLC2A1 has a mutation status of L231L, The gene LDLRAD1 has a mutation status of W196*, The gene PARS2 has a mutation status of A13T, The gene DAB1 has a mutation status of A294D, The gene KANK4 has a mutation status of Y801H, The gene FPGT-TNNI3K has a mutation status of L487fs, The gene TTLL7 has a mutation status of R449Q, The gene GBP6 has a mutation status of R48C, The gene LRRC8D has a mutation status of R112G, The gene FNBP1L has a mutation status of S364*, The gene DPYD has a mutation status of G681C, The gene S1PR1 has a mutation status of N21K, The gene PPIAL4H has a mutation status of N102I, The gene NBPF12 has a mutation status of E826E, The gene CELF3 has a mutation status of G302G, The gene FLG has a mutation status of G3587C, The gene FLG has a mutation status of S3282S, The gene FLG has a mutation status of S2619S, The gene FCRL2 has a mutation status of Y332*, The gene FCRLA has a mutation status of Q193K, The gene F5 has a mutation status of R534Q, The gene KDM5B has a mutation status of F1077L, The gene NFASC has a mutation status of L1120P, The gene CR1 has a mutation status of S1498P, The gene OBSCN has a mutation status of A2212L, The gene TAF5L has a mutation status of P225L, The gene RYR2 has a mutation status of L3519M, The gene NLRP3 has a mutation status of R270M, The gene OR11L1 has a mutation status of F104F, The gene OR2L13 has a mutation status of P286H, The gene OR2T4 has a mutation status of V109L, The gene RNF144A has a mutation status of P289P, The gene CAPN14 has a mutation status of Y182*, The gene CRIM1 has a mutation status of D1000E, The gene EML4 has a mutation status of K406R, The gene NRXN1 has a mutation status of N554S, The gene PTCD3 has a mutation status of I375N, The gene ITPRIPL1 has a mutation status of L134L, The gene FER1L5 has a mutation status of G246R, The gene SLC9A2 has a mutation status of I376T, The gene SLC5A7 has a mutation status of T176T, The gene SH3RF3 has a mutation status of N537I, The gene SFT2D3 has a mutation status of R50L, The gene LRP2 has a mutation status of L732I, The gene TTN has a mutation status of D20753N, The gene TTN has a mutation status of E13260Q, The gene FSIP2 has a mutation status of S2796F, The gene CFLAR has a mutation status of C345C, The gene DOCK10 has a mutation status of V839L, The gene AGAP1 has a mutation status of P467R, The gene SSUH2 has a mutation status of E52G, The gene TATDN2 has a mutation status of E550K, The gene CAPN7 has a mutation status of T668T, The gene GALNT15 has a mutation status of W487C, The gene SATB1 has a mutation status of V511M, The gene VILL has a mutation status of R95R, The gene SCN5A has a mutation status of F1292S, The gene TTC21A has a mutation status of Y284C, The gene SEC22C has a mutation status of H172Y, The gene CDCP1 has a mutation status of T251T, The gene SCAP has a mutation status of D1211G, The gene SCAP has a mutation status of 1209_1210insLAHCNLCLPS, The gene ARIH2 has a mutation status of E57E, The gene DNAH1 has a mutation status of F1738F, The gene TASOR has a mutation status of I1032V, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene ARL13B has a mutation status of Q217Q, The gene LSAMP has a mutation status of Q114H, The gene CASR has a mutation status of I235N, The gene TMCC1 has a mutation status of Q59H, The gene LEKR1 has a mutation status of I547I, The gene SLITRK3 has a mutation status of R777H, The gene SLITRK3 has a mutation status of A112E, The gene LRRIQ4 has a mutation status of E461K, The gene PIGX has a mutation status of G17R, The gene IDUA has a mutation status of P357A, The gene TBC1D1 has a mutation status of I197I, The gene N4BP2 has a mutation status of E620A, The gene SCFD2 has a mutation status of R195W, The gene UGT2B11 has a mutation status of A327D, The gene UGT2A1 has a mutation status of P282L, The gene GK2 has a mutation status of G320C, The gene WDFY3 has a mutation status of WCTDSG3322del, The gene FHDC1 has a mutation status of R577W, The gene TRIM75P has a mutation status of R348R, The gene TENM3 has a mutation status of V1648V, The gene SPEF2 has a mutation status of P1443S, The gene ZBED3 has a mutation status of L155A, The gene SOWAHA has a mutation status of K69del, The gene SHROOM1 has a mutation status of G194G, The gene HARS2 has a mutation status of R170G, The gene GRIA1 has a mutation status of G915V, The gene UNC5A has a mutation status of A677T, The gene GRM6 has a mutation status of V842I, The gene GPX5 has a mutation status of A77V, The gene HLA-C has a mutation status of V272V, The gene HLA-C has a mutation status of R132H, The gene HLA-B has a mutation status of I308I, The gene PHF3 has a mutation status of G758S, The gene REV3L has a mutation status of T2983I, The gene PTPRK has a mutation status of E64G, The gene ENPP1 has a mutation status of D701D, The gene ENPP1 has a mutation status of F703L, The gene MYB has a mutation status of L300F, The gene MAP7 has a mutation status of R488Q, The gene ARFGEF3 has a mutation status of V1898V, The gene GRM1 has a mutation status of G861S, The gene TIAM2 has a mutation status of T807M, The gene SMOC2 has a mutation status of A303P, The gene PGAM2 has a mutation status of Y92Y, The gene ZMIZ2 has a mutation status of L550Q, The gene PKD1L1 has a mutation status of P272S, The gene EGFR has a mutation status of ELREA701del, The gene ZSCAN25 has a mutation status of A100T, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of V2475S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene FLNC has a mutation status of V2661I, The gene KCP has a mutation status of P883P, The gene COPG2 has a mutation status of T552T, The gene PODXL has a mutation status of D373E, The gene GBX1 has a mutation status of A361P, The gene DPP6 has a mutation status of E295*, The gene CSMD1 has a mutation status of W1349C, The gene SOX7 has a mutation status of L103M, The gene DLC1 has a mutation status of Q917H, The gene NEFM has a mutation status of L381L, The gene UNC5D has a mutation status of A596P, The gene ADGRA2 has a mutation status of N650N, The gene ADAM32 has a mutation status of P452P, The gene RGS20 has a mutation status of S117S, The gene EYA1 has a mutation status of I333I, The gene MMP16 has a mutation status of A72A, The gene LRRC69 has a mutation status of D205V, The gene UQCRB has a mutation status of P110S, The gene RIMS2 has a mutation status of K986E, The gene RAD21 has a mutation status of P245P, The gene ADGRB1 has a mutation status of A1314V, The gene LY6L has a mutation status of L138F, The gene MROH1 has a mutation status of R1180W, The gene MPDZ has a mutation status of E1827A, The gene PRSS3 has a mutation status of G208R, The gene RUSC2 has a mutation status of IS986del, The gene CNTNAP3 has a mutation status of A1204T, The gene APBA1 has a mutation status of T442A, The gene CENPP has a mutation status of T257A, The gene PTCH1 has a mutation status of T314N, The gene NUTM2G has a mutation status of P42T, The gene OR13C4 has a mutation status of M219R, The gene FRRS1L has a mutation status of R51A, The gene PAPPA has a mutation status of V375V, The gene BRINP1 has a mutation status of I617V, The gene RC3H2 has a mutation status of L350L, The gene HMCN2 has a mutation status of A3161V, The gene COL5A1 has a mutation status of P1355P, The gene CCDC187 has a mutation status of L747L, The gene CACNB2 has a mutation status of S45L, The gene WDFY4 has a mutation status of Y2417H, The gene GRID1 has a mutation status of L851V, The gene RBP4 has a mutation status of C88C, The gene HELLS has a mutation status of E743G, The gene INA has a mutation status of E185D, The gene ZDHHC6 has a mutation status of E288G, The gene ATRNL1 has a mutation status of R814H, The gene ADGRA1 has a mutation status of A28V, The gene IRF7 has a mutation status of L179L, The gene MUC6 has a mutation status of I1653V, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of Y1116Y, The gene MUC5AC has a mutation status of I1311I, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1569L, The gene MUC5AC has a mutation status of T1570T, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of R3590R, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of E4005K, The gene CYB5R2 has a mutation status of T244M, The gene NLRP10 has a mutation status of S527S, The gene FJX1 has a mutation status of R266R, The gene HSD17B12 has a mutation status of L49L, The gene OR5M10 has a mutation status of I49M, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR9I1 has a mutation status of C107F, The gene CCDC88B has a mutation status of P244S, The gene PYGM has a mutation status of L653V, The gene CDCA5 has a mutation status of E190K, The gene FGF4 has a mutation status of R192Q, The gene KCTD21 has a mutation status of A106A, The gene FAT3 has a mutation status of S2917T, The gene GPR83 has a mutation status of F97C, The gene PIWIL4 has a mutation status of L300L, The gene KDM4D has a mutation status of L497V, The gene OR10S1 has a mutation status of V300L, The gene KCNJ5 has a mutation status of G164R, The gene LAG3 has a mutation status of V251I, The gene TAS2R46 has a mutation status of 296_297HV>QM, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene LRP6 has a mutation status of P1413F, The gene SLCO1B1 has a mutation status of R57Q, The gene DDX11 has a mutation status of T675M, The gene RESF1 has a mutation status of S1352Y, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of V28K, The gene IRAK4 has a mutation status of A97A, The gene AMIGO2 has a mutation status of I29V, The gene SCN8A has a mutation status of E1804K, The gene KRT18 has a mutation status of T103N, The gene OR6C4 has a mutation status of M83V, The gene MDM1 has a mutation status of P86S, The gene PHLDA1 has a mutation status of P87R, The gene CEP290 has a mutation status of E1841K, The gene GLT8D2 has a mutation status of N254D, The gene GALNT9 has a mutation status of L271L, The gene FBRSL1 has a mutation status of A482V, The gene AC026786.1 has a mutation status of Q135L, The gene CDX2 has a mutation status of T310T, The gene ELF1 has a mutation status of S310S, The gene AKAP11 has a mutation status of P336L, The gene PCDH17 has a mutation status of P241S, The gene SLC39A2 has a mutation status of S221*, The gene CHD8 has a mutation status of H2215Y, The gene SALL2 has a mutation status of A461A, The gene INSM2 has a mutation status of A92T, The gene IFI27L1 has a mutation status of G24G, The gene SLC25A47 has a mutation status of R54W, The gene INF2 has a mutation status of T170T, The gene UBE3A has a mutation status of L735F, The gene OCA2 has a mutation status of V767I, The gene FMN1 has a mutation status of S272A, The gene FAM98B has a mutation status of G3E, The gene INO80 has a mutation status of M315V, The gene SPTBN5 has a mutation status of R2089C, The gene WDR76 has a mutation status of S71S, The gene MYO5C has a mutation status of T643M, The gene ANKDD1A has a mutation status of L516L, The gene GOLGA6L9 has a mutation status of R6H, The gene GOLGA6L9 has a mutation status of V377F, The gene ALPK3 has a mutation status of T81M, The gene PDE8A has a mutation status of L422L, The gene AKAP13 has a mutation status of T412T, The gene TICRR has a mutation status of Q1399E, The gene SEMA4B has a mutation status of D462N, The gene SOX8 has a mutation status of V252M, The gene UNKL has a mutation status of P551P, The gene PTX4 has a mutation status of R42R, The gene CIITA has a mutation status of L597L, The gene AC138811.2 has a mutation status of S144P, The gene HSF4 has a mutation status of L309V, The gene SLC7A6OS has a mutation status of N127S, The gene NFAT5 has a mutation status of A614E, The gene HYDIN has a mutation status of T744A, The gene MLYCD has a mutation status of G193R, The gene SLC38A8 has a mutation status of I296F, The gene PITPNM3 has a mutation status of A305A, The gene SPEM3 has a mutation status of P787P, The gene TP53 has a mutation status of V218del, The gene PFAS has a mutation status of G847G, The gene CCDC42 has a mutation status of D211N, The gene MYH3 has a mutation status of E1057K, The gene ELAC2 has a mutation status of S490A, The gene SLC47A1 has a mutation status of H337Y, The gene ALDH3A2 has a mutation status of D40G, The gene KIAA0100 has a mutation status of E1788E, The gene SLFN12L has a mutation status of R309C, The gene CCL4L2 has a mutation status of P67R, The gene KRT16 has a mutation status of A180V, The gene AOC2 has a mutation status of H438H, The gene AOC2 has a mutation status of G698G, The gene HOXB1 has a mutation status of G201G, The gene HID1 has a mutation status of D295N, The gene MYO15B has a mutation status of G470D, The gene MYO15B has a mutation status of G474A, The gene MYO15B has a mutation status of S620H, The gene DNAH17 has a mutation status of A332V, The gene ASXL3 has a mutation status of T531A, The gene TCF4 has a mutation status of D142D, The gene NFATC1 has a mutation status of S512F, The gene MKNK2 has a mutation status of P57P, The gene RFX2 has a mutation status of G360S, The gene TNFSF14 has a mutation status of S4I, The gene CAMSAP3 has a mutation status of A237A, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of L12947L, The gene MUC16 has a mutation status of T12336L, The gene DNM2 has a mutation status of F94F, The gene ZNF433 has a mutation status of L605L, The gene ZNF844 has a mutation status of F6F, The gene MYO9B has a mutation status of G1379R, The gene CCDC194 has a mutation status of S205L, The gene GATAD2A has a mutation status of Q401P, The gene ZNF99 has a mutation status of T355N, The gene ANKRD27 has a mutation status of A757A, The gene GPI has a mutation status of N329N, The gene CD22 has a mutation status of S401S, The gene WDR62 has a mutation status of D843D, The gene ZNF146 has a mutation status of H282H, The gene ZNF850 has a mutation status of P805A, The gene WDR87 has a mutation status of R2534*, The gene SIPA1L3 has a mutation status of P1595P, The gene PLD3 has a mutation status of G452E, The gene CYP2F1 has a mutation status of V175R, The gene PSG7 has a mutation status of T259I, The gene DKKL1 has a mutation status of L52L, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of W163S, The gene LILRA2 has a mutation status of S395T, The gene LILRA1 has a mutation status of L268R, The gene LILRA1 has a mutation status of P271R, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Y99I, The gene LILRB1 has a mutation status of 171_172QP>HS, The gene NLRP11 has a mutation status of E987G, The gene SIRPA has a mutation status of L44S, The gene ITPA has a mutation status of N78S, The gene SIGLEC1 has a mutation status of V1220V, The gene PLCB1 has a mutation status of D206Y, The gene LAMP5 has a mutation status of T56T, The gene RRBP1 has a mutation status of E851K, The gene RALGAPA2 has a mutation status of L1357R, The gene SLC32A1 has a mutation status of A35V, The gene PCIF1 has a mutation status of R113Q, The gene SLC12A5 has a mutation status of 74_75insGG, The gene HELZ2 has a mutation status of R1639H, The gene LIPI has a mutation status of L423L, The gene C21orf91 has a mutation status of K93K, The gene ADAMTS1 has a mutation status of S134R, The gene GART has a mutation status of C93I, The gene TTC3 has a mutation status of R277C, The gene VPS26C has a mutation status of L246L, The gene UMODL1 has a mutation status of A1416A, The gene FAM207A has a mutation status of P189Q, The gene LSS has a mutation status of V662I, The gene LRRC74B has a mutation status of E44G, The gene IGLL1 has a mutation status of T146T, The gene CABIN1 has a mutation status of F413C, The gene SPECC1L has a mutation status of R157Q, The gene MYO18B has a mutation status of K1826R, The gene MRTFA has a mutation status of A619P, The gene MEI1 has a mutation status of H1145H, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ARFGAP3 has a mutation status of M431T, The gene SBF1 has a mutation status of R567H, The gene CRLF2 has a mutation status of S323F, The gene NLGN4X has a mutation status of P111H, The gene ARX has a mutation status of P38S, The gene AC231657.3 has a mutation status of T167P, The gene UBQLN2 has a mutation status of A469S, The gene FAM236C has a mutation status of T34T, The gene POF1B has a mutation status of H34Y, The gene NXF3 has a mutation status of R76W, The gene MORC4 has a mutation status of N639K, The gene KLHL13 has a mutation status of E476E, The gene WDR44 has a mutation status of P142L, The gene WDR44 has a mutation status of S143F, The gene AL772284.2 has a mutation status of K293N, The gene SLC25A5 has a mutation status of T221R, The gene SEPTIN6 has a mutation status of R370C, The gene ATP1B4 has a mutation status of T46T, The gene LAMP2 has a mutation status of S113S, The gene ZNF75D has a mutation status of Q312*, The gene MAGEC3 has a mutation status of S119S, The gene MAGEC1 has a mutation status of P197P, The gene AFF2 has a mutation status of R927H, The gene AC236972.4 has a mutation status of S1611S, The gene MT-ND2 has a mutation status of T89N, The gene MT-ND2 has a mutation status of T334T, The gene MT-CO2 has a mutation status of G222G, The gene MT-ATP8 has a mutation status of P36L, The gene MT-ND4 has a mutation status of N390S, The gene MT-ND4 has a mutation status of L445F, The gene MT-ND5 has a mutation status of M55M, The gene MT-ND5 has a mutation status of A162A, The gene MT-ND5 has a mutation status of A219V, The gene MT-ND5 has a mutation status of P265S, The gene MT-ND5 has a mutation status of G433G, The gene MT-ND5 has a mutation status of A458A, The gene MT-ND6 has a mutation status of V31V, The gene PERM1 has a mutation status of G75C, The gene MXRA8 has a mutation status of I430I, The gene CASZ1 has a mutation status of E1606Q, The gene TNFRSF1B has a mutation status of A127S, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene PADI2 has a mutation status of R157Q, The gene TAS1R2 has a mutation status of L688L, The gene FGR has a mutation status of A239T, The gene EPB41 has a mutation status of H16Y, The gene CSMD2 has a mutation status of D845N, The gene FHL3 has a mutation status of T189T, The gene CAP1 has a mutation status of E335V, The gene SLC2A1 has a mutation status of L231L, The gene ARTN has a mutation status of L133L, The gene PLK3 has a mutation status of R34L, The gene FAAH has a mutation status of P424L, The gene FOXD2 has a mutation status of A294fs, The gene FOXD2 has a mutation status of F295fs, The gene BTF3L4 has a mutation status of D134H, The gene LDLRAD1 has a mutation status of W196*, The gene PARS2 has a mutation status of A13T, The gene C8A has a mutation status of Y172C, The gene DAB1 has a mutation status of A294D, The gene PATJ has a mutation status of D552Y, The gene KANK4 has a mutation status of Y801H, The gene FPGT-TNNI3K has a mutation status of L487fs, The gene ADGRL2 has a mutation status of T510K, The gene TTLL7 has a mutation status of R449Q, The gene CTBS has a mutation status of I302N, The gene GBP6 has a mutation status of R48C, The gene LRRC8D has a mutation status of R112G, The gene BRDT has a mutation status of A405T, The gene FNBP1L has a mutation status of S364*, The gene DPYD has a mutation status of G681C, The gene S1PR1 has a mutation status of N21K, The gene DDX20 has a mutation status of Q145Q, The gene ADAM30 has a mutation status of S384L, The gene NBPF14 has a mutation status of V1509V, The gene BOLA1 has a mutation status of K39K, The gene VPS45 has a mutation status of S399R, The gene CELF3 has a mutation status of G302G, The gene FLG has a mutation status of S3282S, The gene FLG has a mutation status of S2619S, The gene S100A16 has a mutation status of I90I, The gene SLC27A3 has a mutation status of D670D, The gene UBAP2L has a mutation status of S707*, The gene CHRNB2 has a mutation status of W464*, The gene NAXE has a mutation status of A98A, The gene FCRL2 has a mutation status of Y332*, The gene FCRL1 has a mutation status of S287N, The gene FCRLA has a mutation status of Q193K, The gene ALDH9A1 has a mutation status of G160D, The gene DPT has a mutation status of A98P, The gene F5 has a mutation status of R534Q, The gene SCYL3 has a mutation status of F467L, The gene FMO3 has a mutation status of M402V, The gene SLC9C2 has a mutation status of R526H, The gene TOR1AIP1 has a mutation status of S143F, The gene CACNA1E has a mutation status of Y1512*, The gene LAMC1 has a mutation status of A1160A, The gene NR5A2 has a mutation status of V449V, The gene KDM5B has a mutation status of F1077L, The gene NFASC has a mutation status of L1120P, The gene SLC26A9 has a mutation status of D21N, The gene CR1 has a mutation status of S1498P, The gene TATDN3 has a mutation status of L85I, The gene USH2A has a mutation status of R1870Q, The gene OBSCN has a mutation status of A2212L, The gene TAF5L has a mutation status of P225L, The gene NID1 has a mutation status of L1058F, The gene RYR2 has a mutation status of L3519M, The gene FMN2 has a mutation status of P1156P, The gene NLRP3 has a mutation status of R270M, The gene OR11L1 has a mutation status of F104F, The gene OR2AJ1 has a mutation status of I209M, The gene OR2L5 has a mutation status of I68T, The gene OR2L13 has a mutation status of P286H, The gene SH3YL1 has a mutation status of K76N, The gene TPO has a mutation status of L274L, The gene SOX11 has a mutation status of A150T, The gene TP53I3 has a mutation status of D84N, The gene ASXL2 has a mutation status of Q958*, The gene DRC1 has a mutation status of A473V, The gene CAPN14 has a mutation status of Y182*, The gene CRIM1 has a mutation status of D1000E, The gene EML4 has a mutation status of K406R, The gene NRXN1 has a mutation status of N554S, The gene PPP4R3B has a mutation status of S29F, The gene PAPOLG has a mutation status of A448A, The gene PTCD3 has a mutation status of I375N, The gene SMYD1 has a mutation status of E324K, The gene ITPRIPL1 has a mutation status of L134L, The gene FAHD2B has a mutation status of R200H, The gene SLC9A2 has a mutation status of I376T, The gene RGPD3 has a mutation status of Y7Y, The gene SLC5A7 has a mutation status of T176T, The gene SH3RF3 has a mutation status of W501L, The gene SH3RF3 has a mutation status of N537I, The gene IL36G has a mutation status of Y87H, The gene IL36G has a mutation status of V114M, The gene SFT2D3 has a mutation status of R50L, The gene LCT has a mutation status of E490K, The gene TNFAIP6 has a mutation status of 276_277HL>Q, The gene NEB has a mutation status of E3803D, The gene CCDC148 has a mutation status of C257R, The gene SCN1A has a mutation status of I1200T, The gene LRP2 has a mutation status of G2802V, The gene LRP2 has a mutation status of L732I, The gene PJVK has a mutation status of D29G, The gene TTN has a mutation status of D20753N, The gene TTN has a mutation status of D2655N, The gene CFLAR has a mutation status of C345C, The gene CASP10 has a mutation status of P501L, The gene SLC4A3 has a mutation status of I405I, The gene UGT1A7 has a mutation status of S80A, The gene TRPM8 has a mutation status of E356Q, The gene AGAP1 has a mutation status of P467R, The gene CROCC2 has a mutation status of V855M, The gene GRM7 has a mutation status of P40K, The gene SSUH2 has a mutation status of E52G, The gene TATDN2 has a mutation status of E550K, The gene GRIP2 has a mutation status of S671L, The gene GALNT15 has a mutation status of W487C, The gene SATB1 has a mutation status of V511M, The gene VILL has a mutation status of R95R, The gene SCN5A has a mutation status of F1292S, The gene TTC21A has a mutation status of Y284C, The gene SEC22C has a mutation status of H172Y, The gene ZBTB47 has a mutation status of H725P, The gene ARIH2 has a mutation status of E57E, The gene DNAH1 has a mutation status of F1738F, The gene TASOR has a mutation status of I1032V, The gene ARL13B has a mutation status of Q217Q, The gene LSAMP has a mutation status of Q114H, The gene EAF2 has a mutation status of H263Y, The gene CASR has a mutation status of I235N, The gene TMCC1 has a mutation status of Q59H, The gene AADACL2 has a mutation status of L128M, The gene ARHGEF26 has a mutation status of E295D, The gene LEKR1 has a mutation status of I547I, The gene SLITRK3 has a mutation status of R777H, The gene SLITRK3 has a mutation status of A112E, The gene LRRIQ4 has a mutation status of E461K, The gene IDUA has a mutation status of P357A, The gene CRMP1 has a mutation status of I111T, The gene SLIT2 has a mutation status of A1247V, The gene DHX15 has a mutation status of E328Q, The gene TBC1D1 has a mutation status of I197I, The gene UGT2B11 has a mutation status of G186R, The gene UGT2A1 has a mutation status of P282L, The gene ADAMTS3 has a mutation status of R270C, The gene GK2 has a mutation status of G320C, The gene PDE5A has a mutation status of L309V, The gene ELF2 has a mutation status of M159K, The gene FHDC1 has a mutation status of R577W, The gene TRIM75P has a mutation status of R348R, The gene DUX4 has a mutation status of P6P, The gene SLC6A3 has a mutation status of V464I, The gene DNAH5 has a mutation status of D3992H, The gene SPEF2 has a mutation status of P1443S, The gene EGFLAM has a mutation status of Y619Y, The gene GZMK has a mutation status of S34L, The gene ZSWIM6 has a mutation status of E671E, The gene ZBED3 has a mutation status of L155A, The gene LYSMD3 has a mutation status of L98L, The gene SOWAHA has a mutation status of K69del, The gene JADE2 has a mutation status of R596G, The gene WDR55 has a mutation status of V64V, The gene ARHGAP26 has a mutation status of T602T, The gene GRIA1 has a mutation status of G915V, The gene GABRP has a mutation status of C11C, The gene UNC5A has a mutation status of A677T, The gene GRM6 has a mutation status of V842I, The gene FOXC1 has a mutation status of A28A, The gene BLOC1S5 has a mutation status of V105I, The gene NUP153 has a mutation status of D341F, The gene ABT1 has a mutation status of R214H, The gene GPX5 has a mutation status of A77V, The gene HLA-C has a mutation status of R132H, The gene HLA-B has a mutation status of I308I, The gene USP49 has a mutation status of R225C, The gene TRERF1 has a mutation status of P272Q, The gene PHF3 has a mutation status of G758S, The gene CYB5R4 has a mutation status of F78Y, The gene ASF1A has a mutation status of F28fs, The gene SERINC1 has a mutation status of Y219S, The gene PTPRK has a mutation status of E64G, The gene MAP7 has a mutation status of R488Q, The gene GRM1 has a mutation status of G861S, The gene ADGB has a mutation status of G164R, The gene TIAM2 has a mutation status of T807M, The gene THBS2 has a mutation status of T507I, The gene SDK1 has a mutation status of I642I, The gene TNRC18 has a mutation status of S2664S, The gene ABCB5 has a mutation status of N864K, The gene ABCB5 has a mutation status of V1020V, The gene TBX20 has a mutation status of R311C, The gene HECW1 has a mutation status of L1057R, The gene PGAM2 has a mutation status of Y92Y, The gene ZMIZ2 has a mutation status of L550Q, The gene NACAD has a mutation status of A1408T, The gene TNS3 has a mutation status of Q1166*, The gene PKD1L1 has a mutation status of P272S, The gene EGFR has a mutation status of ELREA701del, The gene ELN has a mutation status of APGVGVAPGVGVAPGVGL480del, The gene SEMA3D has a mutation status of A150E, The gene KIAA1324L has a mutation status of Q43H, The gene ZSCAN25 has a mutation status of A100T, The gene SRRT has a mutation status of Y175Y, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene RELN has a mutation status of H3445D, The gene RELN has a mutation status of S1773*, The gene LAMB1 has a mutation status of R255S, The gene ASB15 has a mutation status of R547fs, The gene FLNC has a mutation status of V2661I, The gene KCP has a mutation status of P883P, The gene PODXL has a mutation status of D373E, The gene PRSS1 has a mutation status of N77N, The gene ZNF777 has a mutation status of R720W, The gene AOC1 has a mutation status of A139E, The gene GBX1 has a mutation status of A361P, The gene DPP6 has a mutation status of C536C, The gene CSMD1 has a mutation status of W1349C, The gene SOX7 has a mutation status of L103M, The gene DLC1 has a mutation status of Q917H, The gene NEFM has a mutation status of L381L, The gene UNC5D has a mutation status of A596P, The gene UNC5D has a mutation status of P785P, The gene ADGRA2 has a mutation status of N650N, The gene ADAM32 has a mutation status of P452P, The gene PXDNL has a mutation status of T837N, The gene RGS20 has a mutation status of S117S, The gene EYA1 has a mutation status of I333I, The gene ZFHX4 has a mutation status of P595fs, The gene MMP16 has a mutation status of A72A, The gene LRRC69 has a mutation status of D205V, The gene RIMS2 has a mutation status of K986E, The gene RAD21 has a mutation status of P245P, The gene FER1L6 has a mutation status of F1837F, The gene ADGRB1 has a mutation status of A1314V, The gene LY6L has a mutation status of L138F, The gene MROH1 has a mutation status of Q705*, The gene MROH1 has a mutation status of R1180W, The gene MPDZ has a mutation status of E1827A, The gene RUSC2 has a mutation status of IS986del, The gene APBA1 has a mutation status of T442A, The gene APBA1 has a mutation status of Q394H, The gene ROR2 has a mutation status of F739L, The gene CENPP has a mutation status of T257A, The gene PTCH1 has a mutation status of T314N, The gene NUTM2G has a mutation status of P42T, The gene TMOD1 has a mutation status of L127M, The gene OR13C4 has a mutation status of M219R, The gene FRRS1L has a mutation status of R51A, The gene KIF12 has a mutation status of R642R, The gene PAPPA has a mutation status of V375V, The gene TLR4 has a mutation status of D60V, The gene BRINP1 has a mutation status of I617V, The gene RC3H2 has a mutation status of L350L, The gene COL5A1 has a mutation status of P1355P, The gene CCDC187 has a mutation status of L747L, The gene NOTCH1 has a mutation status of R1991C, The gene TPRN has a mutation status of G382G, The gene CACNB2 has a mutation status of S45L, The gene RET has a mutation status of N723S, The gene LRRTM3 has a mutation status of L540H, The gene TBATA has a mutation status of T241K, The gene GRID1 has a mutation status of L851V, The gene RBP4 has a mutation status of C88C, The gene HELLS has a mutation status of E743G, The gene INA has a mutation status of E185D, The gene ZDHHC6 has a mutation status of E288G, The gene VWA2 has a mutation status of R526R, The gene ATRNL1 has a mutation status of R814H, The gene HMX3 has a mutation status of K27Q, The gene ADGRA1 has a mutation status of A28V, The gene IRF7 has a mutation status of L179L, The gene MUC5AC has a mutation status of Y1116Y, The gene MUC5AC has a mutation status of G2219G, The gene MUC5AC has a mutation status of T3668P, The gene OR51A4 has a mutation status of F100Y, The gene OR51L1 has a mutation status of M42K, The gene OR52L1 has a mutation status of E109E, The gene DNHD1 has a mutation status of A550S, The gene ZNF214 has a mutation status of L109V, The gene CYB5R2 has a mutation status of T244M, The gene FJX1 has a mutation status of R266R, The gene HSD17B12 has a mutation status of L49L, The gene OR5M10 has a mutation status of I49M, The gene OR9G1 has a mutation status of I196F, The gene OR9I1 has a mutation status of C107F, The gene OSBP has a mutation status of S43P, The gene MS4A6E has a mutation status of A43E, The gene CCDC88B has a mutation status of P244S, The gene PYGM has a mutation status of L653V, The gene CDCA5 has a mutation status of E190K, The gene DPP3 has a mutation status of K629M, The gene FGF4 has a mutation status of R192Q, The gene C2CD3 has a mutation status of R1977*, The gene KCTD21 has a mutation status of A106A, The gene NAALAD2 has a mutation status of G324V, The gene FAT3 has a mutation status of S2917T, The gene HEPHL1 has a mutation status of K374T, The gene KDM4D has a mutation status of L497V, The gene DYNC2H1 has a mutation status of A2152G, The gene NXPE1 has a mutation status of L230H, The gene OR10S1 has a mutation status of V300L, The gene OR8G1 has a mutation status of 289_290insYIC, The gene KCNJ5 has a mutation status of G164R, The gene LAG3 has a mutation status of V251I, The gene LRP6 has a mutation status of P1413F, The gene SLCO1B1 has a mutation status of R57Q, The gene DDX11 has a mutation status of T675M, The gene RESF1 has a mutation status of S1352Y, The gene ADAMTS20 has a mutation status of T1579A, The gene IRAK4 has a mutation status of A97A, The gene AMIGO2 has a mutation status of I29V, The gene ATF1 has a mutation status of A19S, The gene SCN8A has a mutation status of K1352K, The gene SCN8A has a mutation status of E1804K, The gene ANKRD33 has a mutation status of R338Q, The gene SMIM41 has a mutation status of F53L, The gene OR6C4 has a mutation status of M83V, The gene ANKRD52 has a mutation status of G663G, The gene MDM1 has a mutation status of P517P, The gene MDM1 has a mutation status of P86S, The gene PHLDA1 has a mutation status of P87R, The gene CEP290 has a mutation status of E1841K, The gene EEA1 has a mutation status of V287L, The gene GLT8D2 has a mutation status of N254D, The gene PHETA1 has a mutation status of G43R, The gene RPH3A has a mutation status of Q289K, The gene GALNT9 has a mutation status of L271L, The gene FBRSL1 has a mutation status of A482V, The gene AC026786.1 has a mutation status of Q135L, The gene TUBA3C has a mutation status of G17S, The gene CDX2 has a mutation status of T310T, The gene AKAP11 has a mutation status of P336L, The gene PCDH17 has a mutation status of P241S, The gene GPC5 has a mutation status of I194I, The gene UPF3A has a mutation status of E227E, The gene SALL2 has a mutation status of A461A, The gene ACTR10 has a mutation status of K191R, The gene GPR135 has a mutation status of A50S, The gene ZNF410 has a mutation status of T274T, The gene ADCK1 has a mutation status of N228S, The gene IFI27L1 has a mutation status of G24G, The gene GOLGA6L6 has a mutation status of 548_549insHD, The gene GOLGA6L6 has a mutation status of R548M, The gene GOLGA6L1 has a mutation status of W616G, The gene UBE3A has a mutation status of L735F, The gene OCA2 has a mutation status of V767I, The gene FMN1 has a mutation status of S272A, The gene FAM98B has a mutation status of G3E, The gene INO80 has a mutation status of M315V, The gene SPTBN5 has a mutation status of R2089C, The gene WDR76 has a mutation status of S71S, The gene MYO5C has a mutation status of T643M, The gene C2CD4B has a mutation status of E46W, The gene ANKDD1A has a mutation status of L516L, The gene NEO1 has a mutation status of V930V, The gene ALPK3 has a mutation status of T81M, The gene PDE8A has a mutation status of L422L, The gene AKAP13 has a mutation status of T412T, The gene TICRR has a mutation status of Q1399E, The gene SEMA4B has a mutation status of D462N, The gene PRR35 has a mutation status of E488Q, The gene SOX8 has a mutation status of V252M, The gene CACNA1H has a mutation status of L936H, The gene UNKL has a mutation status of P551P, The gene PTX4 has a mutation status of R42R, The gene CIITA has a mutation status of L597L, The gene AC138811.2 has a mutation status of S144P, The gene DNAH3 has a mutation status of P2403fs, The gene IRX6 has a mutation status of G323V, The gene HSF4 has a mutation status of L309V, The gene SLC7A6OS has a mutation status of N127S, The gene NFAT5 has a mutation status of A614E, The gene AP1G1 has a mutation status of Y460C, The gene MLYCD has a mutation status of G193R, The gene SLC38A8 has a mutation status of I296F, The gene ZFPM1 has a mutation status of T78T, The gene PITPNM3 has a mutation status of A305A, The gene AC004706.3 has a mutation status of P512S, The gene TP53 has a mutation status of V218del, The gene PFAS has a mutation status of G847G, The gene MYH3 has a mutation status of E1057K, The gene ELAC2 has a mutation status of S490A, The gene SREBF1 has a mutation status of R678Q, The gene SLC47A1 has a mutation status of H337Y, The gene ALDH3A2 has a mutation status of D40G, The gene KIAA0100 has a mutation status of E1788E, The gene SLFN12L has a mutation status of R309C, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP9-6 has a mutation status of G106C, The gene KRT16 has a mutation status of A180V, The gene KRT16 has a mutation status of G63R, The gene KAT2A has a mutation status of I352I, The gene KAT2A has a mutation status of L351L, The gene KAT2A has a mutation status of H315N, The gene AOC2 has a mutation status of H438H, The gene AOC2 has a mutation status of G698G, The gene COPZ2 has a mutation status of A17A, The gene HOXB1 has a mutation status of G201G, The gene DLX3 has a mutation status of W251*, The gene APPBP2 has a mutation status of Y226*, The gene HID1 has a mutation status of D295N, The gene DNAH17 has a mutation status of A332V, The gene RAB40B has a mutation status of 84_85insPRPP, The gene ASXL3 has a mutation status of T531A, The gene TCF4 has a mutation status of D142D, The gene NFATC1 has a mutation status of S512F, The gene ABCA7 has a mutation status of G1827A, The gene DAZAP1 has a mutation status of F262del, The gene DAZAP1 has a mutation status of T263P, The gene DAZAP1 has a mutation status of A286D, The gene MKNK2 has a mutation status of P57P, The gene KDM4B has a mutation status of P511S, The gene RFX2 has a mutation status of G360S, The gene TNFSF14 has a mutation status of S4I, The gene CAMSAP3 has a mutation status of A237A, The gene ZNF433 has a mutation status of L605L, The gene ZNF844 has a mutation status of F6F, The gene RASAL3 has a mutation status of R611R, The gene MYO9B has a mutation status of G1379R, The gene GATAD2A has a mutation status of Q401P, The gene YJEFN3 has a mutation status of F269F, The gene ZNF90 has a mutation status of V98E, The gene ZNF66 has a mutation status of C539*, The gene ZNF99 has a mutation status of T355N, The gene ZNF723 has a mutation status of K332N, The gene ANKRD27 has a mutation status of A757A, The gene GPI has a mutation status of N329N, The gene CD22 has a mutation status of S401S, The gene WDR62 has a mutation status of D843D, The gene ZNF146 has a mutation status of H282H, The gene ZNF850 has a mutation status of P805A, The gene WDR87 has a mutation status of R2534*, The gene SIPA1L3 has a mutation status of P1595P, The gene PLD3 has a mutation status of G452E, The gene PSG7 has a mutation status of T259I, The gene DKKL1 has a mutation status of L52L, The gene ZNF615 has a mutation status of E157Q, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of H25P, The gene LILRB1 has a mutation status of E34E, The gene NLRP11 has a mutation status of E987G, The gene NLRP8 has a mutation status of R781S, The gene SIRPA has a mutation status of L44S, The gene ITPA has a mutation status of N78S, The gene SIGLEC1 has a mutation status of V1220V, The gene CENPB has a mutation status of Y261H, The gene PLCB1 has a mutation status of D206Y, The gene LAMP5 has a mutation status of T56T, The gene RRBP1 has a mutation status of E851K, The gene RALGAPA2 has a mutation status of L1357R, The gene SYNDIG1 has a mutation status of V242M, The gene CST7 has a mutation status of R106C, The gene SUN5 has a mutation status of A292T, The gene SLC32A1 has a mutation status of A35V, The gene PCIF1 has a mutation status of R113Q, The gene HELZ2 has a mutation status of R1639H, The gene LIPI has a mutation status of L423L, The gene C21orf91 has a mutation status of K93K, The gene ADAMTS1 has a mutation status of S134R, The gene GART has a mutation status of C93I, The gene TTC3 has a mutation status of R277C, The gene VPS26C has a mutation status of L246L, The gene UMODL1 has a mutation status of A1416A, The gene FAM207A has a mutation status of P189Q, The gene LSS has a mutation status of V662I, The gene LRRC74B has a mutation status of E44G, The gene ZNF280B has a mutation status of I538fs, The gene IGLL1 has a mutation status of T146T, The gene CABIN1 has a mutation status of F413C, The gene SPECC1L has a mutation status of R157Q, The gene MYO18B has a mutation status of K1826R, The gene MEI1 has a mutation status of H1145H, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ARFGAP3 has a mutation status of M431T, The gene SBF1 has a mutation status of R567H, The gene NLGN4X has a mutation status of P111H, The gene PIGA has a mutation status of C356fs, The gene PIGA has a mutation status of L355L, The gene ARX has a mutation status of P38S, The gene MAGEB6B has a mutation status of S38F, The gene MAGEB1 has a mutation status of P66L, The gene XK has a mutation status of E117D, The gene GRIPAP1 has a mutation status of R396Q, The gene CCNB3 has a mutation status of H1336R, The gene UBQLN2 has a mutation status of A469S, The gene NXF3 has a mutation status of R76W, The gene MORC4 has a mutation status of N639K, The gene FRMPD3 has a mutation status of P1789A, The gene LRCH2 has a mutation status of Q74K, The gene KLHL13 has a mutation status of E476E, The gene WDR44 has a mutation status of P142L, The gene WDR44 has a mutation status of S143F, The gene AL772284.2 has a mutation status of K293N, The gene SEPTIN6 has a mutation status of R370C, The gene ATP1B4 has a mutation status of T46T, The gene LAMP2 has a mutation status of S113S, The gene TENM1 has a mutation status of Y2238N, The gene TENM1 has a mutation status of Y1707*, The gene TEX13C has a mutation status of G11R, The gene ZNF75D has a mutation status of Q312*, The gene MAGEC3 has a mutation status of S119S, The gene AFF2 has a mutation status of R927H, The gene MAMLD1 has a mutation status of I166N, The gene GABRA3 has a mutation status of S442I, The gene NSDHL has a mutation status of G50G, The gene IL9R has a mutation status of A195S, The gene MT-ND2 has a mutation status of A164V, The gene MT-ND2 has a mutation status of T334T, The gene MT-CO2 has a mutation status of G222G, The gene MT-ATP8 has a mutation status of P36L, The gene MT-ND3 has a mutation status of I60I, The gene MT-ND4L has a mutation status of C69W, The gene MT-ND4 has a mutation status of N390S, The gene MT-ND4 has a mutation status of L445F, The gene MT-ND5 has a mutation status of M55M, The gene MT-ND5 has a mutation status of A162A, The gene MT-ND5 has a mutation status of A219V, The gene MT-ND5 has a mutation status of P265S, The gene MT-ND5 has a mutation status of G433G, The gene MT-ND5 has a mutation status of A458A, The gene MT-ND6 has a mutation status of V31V
LUAD
The gene PLEKHN1 has a mutation status of R154*, The gene PERM1 has a mutation status of S277S, The gene AGRN has a mutation status of P32S, The gene TNFRSF4 has a mutation status of R108R, The gene TTC34 has a mutation status of A493G, The gene ACTRT2 has a mutation status of S139*, The gene ACOT7 has a mutation status of A126S, The gene CASZ1 has a mutation status of A1273P, The gene C1orf127 has a mutation status of L239P, The gene MFN2 has a mutation status of R259C, The gene PRAMEF18 has a mutation status of A393G, The gene PRAMEF18 has a mutation status of P294P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene EPHA2 has a mutation status of V554F, The gene ATP13A2 has a mutation status of L437V, The gene EMC1 has a mutation status of R404R, The gene KIF17 has a mutation status of K194E, The gene ECE1 has a mutation status of A336P, The gene EPHB2 has a mutation status of Y49*, The gene E2F2 has a mutation status of G196G, The gene SLC30A2 has a mutation status of E26G, The gene CRYBG2 has a mutation status of T1396I, The gene ARID1A has a mutation status of R1616C, The gene AHDC1 has a mutation status of V712G, The gene LAPTM5 has a mutation status of R18C, The gene HDAC1 has a mutation status of F241L, The gene MTF1 has a mutation status of P430P, The gene MTF1 has a mutation status of E429D, The gene POU3F1 has a mutation status of G59G, The gene MACF1 has a mutation status of Q5047K, The gene TIE1 has a mutation status of R219H, The gene TIE1 has a mutation status of T772P, The gene PTCH2 has a mutation status of E295G, The gene NSUN4 has a mutation status of P207P, The gene ZFYVE9 has a mutation status of V864V, The gene IL23R has a mutation status of G599W, The gene FPGT-TNNI3K has a mutation status of R609*, The gene PLPPR5 has a mutation status of Y205N, The gene NTNG1 has a mutation status of D255G, The gene AMPD2 has a mutation status of G34G, The gene KCNA3 has a mutation status of L223V, The gene WNT2B has a mutation status of K327R, The gene TSPAN2 has a mutation status of R5R, The gene IGSF3 has a mutation status of P1107A, The gene WDR3 has a mutation status of T922I, The gene TCHHL1 has a mutation status of R156G, The gene GBA has a mutation status of E9D, The gene ASH1L has a mutation status of V2078V, The gene SYT11 has a mutation status of R251C, The gene SYT11 has a mutation status of R419R, The gene ARHGEF11 has a mutation status of P597H, The gene KIRREL1 has a mutation status of T732P, The gene SPTA1 has a mutation status of K2202K, The gene SPTA1 has a mutation status of G1402W, The gene SPTA1 has a mutation status of A221D, The gene USP21 has a mutation status of H314N, The gene F5 has a mutation status of R2044K, The gene F5 has a mutation status of L1629L, The gene F5 has a mutation status of R534Q, The gene CACNA1E has a mutation status of Y2129*, The gene ZNF648 has a mutation status of T215P, The gene RGSL1 has a mutation status of T730I, The gene CFH has a mutation status of Y1205*, The gene CRB1 has a mutation status of D168H, The gene INAVA has a mutation status of A335A, The gene KIF21B has a mutation status of Q965E, The gene PLEKHA6 has a mutation status of C1016*, The gene TMCC2 has a mutation status of E326G, The gene OBSCN has a mutation status of A6826P, The gene TRIM11 has a mutation status of P396A, The gene AGT has a mutation status of R196R, The gene RYR2 has a mutation status of I1268K, The gene SDCCAG8 has a mutation status of 371_372insGG, The gene AHCTF1 has a mutation status of S2261N, The gene ZNF496 has a mutation status of S388F, The gene OR2T1 has a mutation status of I220I, The gene MYT1L has a mutation status of A581A, The gene KIDINS220 has a mutation status of Q1249H, The gene NTSR2 has a mutation status of V361M, The gene RAD51AP2 has a mutation status of Q944H, The gene RDH14 has a mutation status of A232T, The gene NCOA1 has a mutation status of T73I, The gene TCF23 has a mutation status of G69C, The gene C2orf16 has a mutation status of S4850F, The gene EPAS1 has a mutation status of T766T, The gene SOCS5 has a mutation status of S425F, The gene MSH6 has a mutation status of T1085N, The gene FBXO11 has a mutation status of Y829C, The gene ATP6V1B1 has a mutation status of A508A, The gene DYSF has a mutation status of P1037T, The gene HK2 has a mutation status of I550I, The gene REG1A has a mutation status of R44L, The gene PROM2 has a mutation status of L705L, The gene TMEM131 has a mutation status of L1111L, The gene NCK2 has a mutation status of Y99S, The gene GLI2 has a mutation status of M1406L, The gene CNTNAP5 has a mutation status of A679A, The gene ACMSD has a mutation status of D284E, The gene RIF1 has a mutation status of P2294L, The gene TBR1 has a mutation status of S141R, The gene IFIH1 has a mutation status of A691G, The gene SCN2A has a mutation status of R524L, The gene TTC21B has a mutation status of A285S, The gene LRP2 has a mutation status of V4149V, The gene SLC25A12 has a mutation status of A675P, The gene TTN has a mutation status of R19720L, The gene TTN has a mutation status of W15751C, The gene TTN has a mutation status of N7140Y, The gene TTN has a mutation status of S3954Y, The gene ITGAV has a mutation status of A311P, The gene DNAH7 has a mutation status of V1608V, The gene PARD3B has a mutation status of P1090P, The gene FAM237A has a mutation status of R165S, The gene MAP2 has a mutation status of P524L, The gene ATIC has a mutation status of I259I, The gene AAMP has a mutation status of V416L, The gene CHPF has a mutation status of 691_693LAA>P, The gene SLC4A3 has a mutation status of R107S, The gene FAM124B has a mutation status of P225S, The gene COL4A4 has a mutation status of G834W, The gene PSMD1 has a mutation status of N525S, The gene TRPM8 has a mutation status of R278W, The gene PER2 has a mutation status of P171S, The gene KIF1A has a mutation status of Y384*, The gene MTMR14 has a mutation status of A508G, The gene PRRT3 has a mutation status of D957V, The gene ATG7 has a mutation status of Y51C, The gene ARPP21 has a mutation status of L84F, The gene GOLGA4 has a mutation status of K1493N, The gene ITGA9 has a mutation status of Q486H, The gene SLC26A6 has a mutation status of V239G, The gene WDR6 has a mutation status of A329G, The gene CCDC71 has a mutation status of L458P, The gene BSN has a mutation status of G1633G, The gene ITIH4 has a mutation status of Y258*, The gene CD47 has a mutation status of A261V, The gene CD47 has a mutation status of L256L, The gene CFAP44 has a mutation status of R692S, The gene POGLUT1 has a mutation status of E299K, The gene FBXO40 has a mutation status of C72W, The gene SLC49A4 has a mutation status of S300A, The gene H1-8 has a mutation status of Q99H, The gene AMOTL2 has a mutation status of P262L, The gene TRIM42 has a mutation status of S69P, The gene ERICH6 has a mutation status of P460T, The gene MLF1 has a mutation status of H38D, The gene KPNA4 has a mutation status of C191S, The gene VPS8 has a mutation status of V421I, The gene MYL5 has a mutation status of G98S, The gene ZFYVE28 has a mutation status of F127F, The gene MFSD10 has a mutation status of S94S, The gene HS3ST1 has a mutation status of A83A, The gene BOD1L1 has a mutation status of N2607Y, The gene BOD1L1 has a mutation status of V1134V, The gene FAM184B has a mutation status of T115A, The gene LCORL has a mutation status of D1501G, The gene PGM2 has a mutation status of Y474*, The gene DCAF4L1 has a mutation status of W341C, The gene ATP8A1 has a mutation status of A827P, The gene KIT has a mutation status of S123Y, The gene EXOC1 has a mutation status of V789M, The gene SHROOM3 has a mutation status of Q1325K, The gene HPSE has a mutation status of L87F, The gene MMRN1 has a mutation status of G852G, The gene SEC24B has a mutation status of Y710C, The gene JADE1 has a mutation status of Y530*, The gene PCDH10 has a mutation status of E186E, The gene TBC1D9 has a mutation status of G1081A, The gene INPP4B has a mutation status of W521L, The gene NR3C2 has a mutation status of A301V, The gene GRIA2 has a mutation status of Y388*, The gene GRIA2 has a mutation status of P425P, The gene FNIP2 has a mutation status of E835K, The gene ADAM29 has a mutation status of H28L, The gene PLEKHG4B has a mutation status of V1117L, The gene CCT5 has a mutation status of R126R, The gene DNAH5 has a mutation status of L861F, The gene H3Y1 has a mutation status of A89T, The gene ADAMTS12 has a mutation status of T428I, The gene EGFLAM has a mutation status of A408S, The gene TTC33 has a mutation status of R76W, The gene PRKAA1 has a mutation status of S494W, The gene HTR1A has a mutation status of F165F, The gene MAST4 has a mutation status of A2218T, The gene AGGF1 has a mutation status of G248S, The gene WDR41 has a mutation status of I91T, The gene ARSB has a mutation status of Y210F, The gene FAM151B has a mutation status of Q268K, The gene APC has a mutation status of A1107fs, The gene DMXL1 has a mutation status of L2867F, The gene LOX has a mutation status of Y334*, The gene PRDM6 has a mutation status of Q571K, The gene FBN2 has a mutation status of C1323S, The gene PKD2L2 has a mutation status of K302R, The gene GFRA3 has a mutation status of T317P, The gene NRG2 has a mutation status of S512P, The gene WDR55 has a mutation status of G60G, The gene PCDH12 has a mutation status of L598F, The gene FAT2 has a mutation status of F3114S, The gene PWWP2A has a mutation status of A104P, The gene EIF4E1B has a mutation status of V140G, The gene FLT4 has a mutation status of Y25*, The gene TRIM41 has a mutation status of D223Y, The gene FOXF2 has a mutation status of G236A, The gene TXNDC5 has a mutation status of Q96E, The gene SLC35B3 has a mutation status of V65F, The gene DCDC2 has a mutation status of P305T, The gene H3C11 has a mutation status of R54C, The gene H3C11 has a mutation status of R41P, The gene GABBR1 has a mutation status of R372R, The gene HLA-A has a mutation status of I121R, The gene HLA-A has a mutation status of K292E, The gene PPT2 has a mutation status of F26S, The gene BRD2 has a mutation status of A49C, The gene TBC1D22B has a mutation status of L442I, The gene SLC29A1 has a mutation status of L410P, The gene IL17F has a mutation status of P48P, The gene ADGRB3 has a mutation status of L234V, The gene BEND3 has a mutation status of G287V, The gene MICAL1 has a mutation status of P668R, The gene GJA1 has a mutation status of L347P, The gene SMPDL3A has a mutation status of P317P, The gene MOXD1 has a mutation status of E374D, The gene PERP has a mutation status of A79G, The gene SYNE1 has a mutation status of A4070E, The gene FNDC1 has a mutation status of V1787V, The gene IGF2R has a mutation status of C1695C, The gene DACT2 has a mutation status of Y719C, The gene MAD1L1 has a mutation status of L434P, The gene SDK1 has a mutation status of T2091T, The gene TNRC18 has a mutation status of T1189N, The gene TNRC18 has a mutation status of V688G, The gene NXPH1 has a mutation status of S270S, The gene ETV1 has a mutation status of R51S, The gene NOD1 has a mutation status of D770N, The gene MPLKIP has a mutation status of P121P, The gene SUGCT has a mutation status of A74T, The gene HECW1 has a mutation status of G665V, The gene POM121L12 has a mutation status of A87A, The gene PSPH has a mutation status of L68P, The gene AUTS2 has a mutation status of V1014M, The gene FKBP6 has a mutation status of F227F, The gene CLIP2 has a mutation status of V407V, The gene HIP1 has a mutation status of E731G, The gene ZP3 has a mutation status of D56D, The gene CCDC146 has a mutation status of E286G, The gene PCLO has a mutation status of E1936D, The gene SEMA3D has a mutation status of S709T, The gene KIAA1324L has a mutation status of D253G, The gene AKAP9 has a mutation status of Q2232Q, The gene TECPR1 has a mutation status of V226S, The gene PVRIG has a mutation status of P268L, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of S3095S, The gene SH2B2 has a mutation status of A368P, The gene RELN has a mutation status of G53S, The gene TMEM229A has a mutation status of V150G, The gene GPR37 has a mutation status of A263A, The gene FAM71F2 has a mutation status of L126L, The gene FLNC has a mutation status of P2535L, The gene KLF14 has a mutation status of P58S, The gene CALD1 has a mutation status of I431T, The gene CREB3L2 has a mutation status of S9S, The gene KCNH2 has a mutation status of L315F, The gene NOS3 has a mutation status of R234C, The gene SLC4A2 has a mutation status of Q386E, The gene ACTR3B has a mutation status of I358fs, The gene HTR5A has a mutation status of S331S, The gene C8orf74 has a mutation status of N93N, The gene FAM167A has a mutation status of Q90E, The gene LZTS1 has a mutation status of R176Q, The gene EGR3 has a mutation status of R348R, The gene ERLIN2 has a mutation status of D87N, The gene ERLIN2 has a mutation status of E90K, The gene PXDNL has a mutation status of C869F, The gene CA3 has a mutation status of D161N, The gene WWP1 has a mutation status of K740N, The gene TRPS1 has a mutation status of D512D, The gene EPPK1 has a mutation status of L795P, The gene PLEC has a mutation status of A761G, The gene OPLAH has a mutation status of H596P, The gene KIAA2026 has a mutation status of G462S, The gene MPDZ has a mutation status of R1150K, The gene UBAP2 has a mutation status of T414A, The gene RUSC2 has a mutation status of S213R, The gene FAM221B has a mutation status of C356W, The gene SHB has a mutation status of L395fs, The gene TRPM6 has a mutation status of T1311I, The gene WNK2 has a mutation status of G908G, The gene WNK2 has a mutation status of L1399L, The gene TMEM245 has a mutation status of L809F, The gene SHOC1 has a mutation status of R1184H, The gene KIAA1958 has a mutation status of A544G, The gene KIF12 has a mutation status of E16E, The gene LHX6 has a mutation status of Q77H, The gene DENND1A has a mutation status of Q766H, The gene DENND1A has a mutation status of Q528fs, The gene ST6GALNAC6 has a mutation status of C10G, The gene NUP188 has a mutation status of G1355G, The gene EXOSC2 has a mutation status of R11P, The gene PRRC2B has a mutation status of T228A, The gene AL162417.1 has a mutation status of H89Y, The gene SARDH has a mutation status of R691*, The gene KCNT1 has a mutation status of 762_763SS>RP, The gene AJM1 has a mutation status of G716G, The gene FBXW5 has a mutation status of F239V, The gene ABCA2 has a mutation status of E536G, The gene DIP2C has a mutation status of E961K, The gene AKR1C8P has a mutation status of N172K, The gene CDNF has a mutation status of A91T, The gene VIM has a mutation status of V161G, The gene ACBD5 has a mutation status of G345R, The gene RASGEF1A has a mutation status of V386F, The gene MAPK8 has a mutation status of I157V, The gene C10orf71 has a mutation status of N405K, The gene OGDHL has a mutation status of T865T, The gene PRF1 has a mutation status of R123P, The gene NRG3 has a mutation status of D608E, The gene PLCE1 has a mutation status of Q854K, The gene CYP2C9 has a mutation status of Q340K, The gene PAX2 has a mutation status of V129V, The gene PAX2 has a mutation status of D392A, The gene PSD has a mutation status of P168T, The gene PDCD11 has a mutation status of F1111F, The gene AFAP1L2 has a mutation status of R535*, The gene PNLIP has a mutation status of S405*, The gene DHX32 has a mutation status of I146V, The gene TCERG1L has a mutation status of R293R, The gene CFAP46 has a mutation status of V2593M, The gene TUBGCP2 has a mutation status of D220Y, The gene PTDSS2 has a mutation status of R62Q, The gene MUC5AC has a mutation status of C20*, The gene MUC5AC has a mutation status of V307A, The gene MUC5AC has a mutation status of T2729K, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4396A, The gene MUC5AC has a mutation status of G4925G, The gene MUC5B has a mutation status of L1772F, The gene OR52B6 has a mutation status of H200D, The gene DENND2B has a mutation status of K237E, The gene RASSF10 has a mutation status of F126F, The gene COPB1 has a mutation status of T591N, The gene ABCC8 has a mutation status of L175M, The gene OTOG has a mutation status of P910L, The gene MRGPRX2 has a mutation status of Q292H, The gene SLC6A5 has a mutation status of L658F, The gene KIAA1549L has a mutation status of N1516T, The gene NAT10 has a mutation status of N738S, The gene NUP160 has a mutation status of G75G, The gene OR4A16 has a mutation status of D20Y, The gene OR4C6 has a mutation status of T190N, The gene OR5W2 has a mutation status of M45I, The gene OR5T3 has a mutation status of K310K, The gene OR5R1 has a mutation status of H235Q, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene LRRC55 has a mutation status of C16Y, The gene MRPL16 has a mutation status of L97L, The gene MS4A4A has a mutation status of I71I, The gene MYRF has a mutation status of V604G, The gene C11orf95 has a mutation status of L622L, The gene AP006333.1 has a mutation status of S644T, The gene SF1 has a mutation status of A524P, The gene ATG2A has a mutation status of Q1734E, The gene ZNRD2 has a mutation status of Q116E, The gene PCNX3 has a mutation status of R769L, The gene PITPNM1 has a mutation status of A1196G, The gene PITPNM1 has a mutation status of L518L, The gene PITPNM1 has a mutation status of A517G, The gene ANO1 has a mutation status of Y30*, The gene C2CD3 has a mutation status of T90R, The gene C2CD3 has a mutation status of T44T, The gene USP35 has a mutation status of G839G, The gene FAT3 has a mutation status of A3793A, The gene HEPHL1 has a mutation status of F699Y, The gene MRE11 has a mutation status of I621I, The gene KDM4E has a mutation status of E215G, The gene MAML2 has a mutation status of Q598Q, The gene CCDC82 has a mutation status of R512R, The gene ARHGAP20 has a mutation status of S706fs, The gene OAF has a mutation status of V207G, The gene HEPACAM has a mutation status of L71V, The gene ADAMTS8 has a mutation status of Y703*, The gene NRIP2 has a mutation status of V175G, The gene TEX52 has a mutation status of Q248*, The gene PTPN6 has a mutation status of Y543Y, The gene APOBEC1 has a mutation status of W235L, The gene YBX3 has a mutation status of D208A, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene PIK3C2G has a mutation status of L547F, The gene SLCO1B3 has a mutation status of V221V, The gene SLCO1B1 has a mutation status of K285E, The gene MED21 has a mutation status of A41T, The gene TSPAN11 has a mutation status of Y48*, The gene ADAMTS20 has a mutation status of D1203E, The gene ARID2 has a mutation status of Q1678L, The gene KRT1 has a mutation status of T507K, The gene HOXC13 has a mutation status of H200P, The gene STAB2 has a mutation status of L1066I, The gene GLT8D2 has a mutation status of L135L, The gene SVOP has a mutation status of C497W, The gene GIT2 has a mutation status of S570L, The gene MED13L has a mutation status of L191F, The gene NOS1 has a mutation status of V887V, The gene PIWIL1 has a mutation status of T331T, The gene EP400 has a mutation status of Q2761Q, The gene P2RX2 has a mutation status of T135P, The gene LATS2 has a mutation status of G310W, The gene PDX1 has a mutation status of E69*, The gene RCBTB2 has a mutation status of T19N, The gene WDFY2 has a mutation status of R12R, The gene IPO5 has a mutation status of R59K, The gene MYO16 has a mutation status of P1529H, The gene METTL3 has a mutation status of R178W, The gene ZFHX2 has a mutation status of S1124S, The gene TTC6 has a mutation status of D1150H, The gene FANCM has a mutation status of R100R, The gene RTN1 has a mutation status of R375R, The gene RDH12 has a mutation status of T264P, The gene PLEKHD1 has a mutation status of S327P, The gene CEP128 has a mutation status of A624S, The gene PPP4R4 has a mutation status of A113G, The gene ATG2B has a mutation status of P757S, The gene SETD3 has a mutation status of A461S, The gene KIF26A has a mutation status of R644G, The gene CEP170B has a mutation status of D1315G, The gene SNRPN has a mutation status of P222Q, The gene GOLGA6L7 has a mutation status of R493Q, The gene DISP2 has a mutation status of L1014V, The gene INO80 has a mutation status of Y983*, The gene JMJD7-PLA2G4B has a mutation status of H398N, The gene UBR1 has a mutation status of S1075fs, The gene CEP152 has a mutation status of V12A, The gene MAPK6 has a mutation status of C440F, The gene C2CD4A has a mutation status of S92S, The gene THSD4 has a mutation status of R646G, The gene HCN4 has a mutation status of D329Y, The gene CLK3 has a mutation status of T484P, The gene ULK3 has a mutation status of G7G, The gene SCAPER has a mutation status of M476N, The gene TMC3 has a mutation status of G809E, The gene TICRR has a mutation status of D1170Y, The gene RHBDL1 has a mutation status of R218S, The gene PTX4 has a mutation status of A163P, The gene TMEM204 has a mutation status of V52G, The gene ZNF598 has a mutation status of S522L, The gene AMDHD2 has a mutation status of R192L, The gene DNAJA3 has a mutation status of G464A, The gene C16orf96 has a mutation status of L88L, The gene C16orf71 has a mutation status of D72D, The gene CLEC16A has a mutation status of L631L, The gene LITAF has a mutation status of P39P, The gene ABCC6 has a mutation status of N370D, The gene DNAH3 has a mutation status of Y3294*, The gene ZP2 has a mutation status of L516L, The gene USP31 has a mutation status of E1034E, The gene ERN2 has a mutation status of R843G, The gene TNRC6A has a mutation status of P115Q, The gene IL4R has a mutation status of S783S, The gene TBC1D10B has a mutation status of R329P, The gene PRR14 has a mutation status of E565G, The gene ABCC12 has a mutation status of G683R, The gene LPCAT2 has a mutation status of Q57H, The gene C16orf70 has a mutation status of W17*, The gene TSNAXIP1 has a mutation status of Q46Q, The gene TANGO6 has a mutation status of D386N, The gene TANGO6 has a mutation status of Q779Q, The gene IST1 has a mutation status of P280P, The gene CLEC18B has a mutation status of S245P, The gene FA2H has a mutation status of H146P, The gene USP10 has a mutation status of T105S, The gene CDT1 has a mutation status of P403P, The gene CBFA2T3 has a mutation status of S131P, The gene SCGB1C2 has a mutation status of T22T, The gene GLOD4 has a mutation status of A43T, The gene SGSM2 has a mutation status of S37T, The gene SPNS2 has a mutation status of V281A, The gene GGT6 has a mutation status of A63G, The gene ALOX15 has a mutation status of A155G, The gene TM4SF5 has a mutation status of G33G, The gene CHRNE has a mutation status of E432D, The gene SLC13A5 has a mutation status of L181L, The gene TP53 has a mutation status of Q144*, The gene WRAP53 has a mutation status of R282G, The gene PER1 has a mutation status of L496L, The gene PER1 has a mutation status of P474L, The gene CFAP52 has a mutation status of N23D, The gene MYH1 has a mutation status of 1337_1339LQS>P, The gene PIRT has a mutation status of G69S, The gene ARHGAP44 has a mutation status of R791H, The gene PLD6 has a mutation status of S171S, The gene FLII has a mutation status of H812P, The gene ANKRD13B has a mutation status of L532L, The gene ANKRD13B has a mutation status of P541T, The gene CCL3L1 has a mutation status of T30M, The gene CCL4L2 has a mutation status of P67R, The gene KRT12 has a mutation status of R414W, The gene KRT16 has a mutation status of S28P, The gene FMNL1 has a mutation status of Q734K, The gene ITGB3 has a mutation status of I370T, The gene MRPL10 has a mutation status of K31Q, The gene ABCC3 has a mutation status of L1441F, The gene USP32 has a mutation status of V566V, The gene COG1 has a mutation status of E408E, The gene UNC13D has a mutation status of A356G, The gene ACOX1 has a mutation status of R393Q, The gene CBX4 has a mutation status of E64G, The gene TBCD has a mutation status of S621S, The gene ROCK1 has a mutation status of V266V, The gene LOXHD1 has a mutation status of Y634D, The gene LOXHD1 has a mutation status of R587Q, The gene WDR7 has a mutation status of K801E, The gene CDH20 has a mutation status of R89K, The gene ZNF516 has a mutation status of Q417H, The gene CTDP1 has a mutation status of A390T, The gene MIER2 has a mutation status of Y96*, The gene POLRMT has a mutation status of A875A, The gene MED16 has a mutation status of P538S, The gene WDR18 has a mutation status of S133T, The gene KLF16 has a mutation status of D215E, The gene TJP3 has a mutation status of A903E, The gene FUT6 has a mutation status of P139Q, The gene FUT6 has a mutation status of S138P, The gene ALKBH7 has a mutation status of A95A, The gene OR1M1 has a mutation status of G170A, The gene TYK2 has a mutation status of S430P, The gene TYK2 has a mutation status of S350fs, The gene TYK2 has a mutation status of A349T, The gene SMARCA4 has a mutation status of E1310*, The gene DOCK6 has a mutation status of A1691G, The gene ZNF763 has a mutation status of V212F, The gene AKAP8L has a mutation status of I387V, The gene SIN3B has a mutation status of E583G, The gene LRRC25 has a mutation status of S280P, The gene CILP2 has a mutation status of S1068G, The gene GMIP has a mutation status of P390A, The gene ZNF85 has a mutation status of I553M, The gene SCN1B has a mutation status of S95R, The gene KCNK6 has a mutation status of V190G, The gene RASGRP4 has a mutation status of A501P, The gene CAPN12 has a mutation status of E162V, The gene NUMBL has a mutation status of Q514Q, The gene DMRTC2 has a mutation status of A130A, The gene MEGF8 has a mutation status of T183P, The gene ZNF229 has a mutation status of G764S, The gene PPP1R13L has a mutation status of G170G, The gene EML2 has a mutation status of A288A, The gene FKRP has a mutation status of R205G, The gene NPAS1 has a mutation status of E122D, The gene NPAS1 has a mutation status of H221N, The gene SLC8A2 has a mutation status of G712V, The gene NTN5 has a mutation status of P51P, The gene FGF21 has a mutation status of F164S, The gene GFY has a mutation status of P251P, The gene PRR12 has a mutation status of N2011T, The gene SCAF1 has a mutation status of P1167S, The gene AP2A1 has a mutation status of Y268S, The gene SIGLEC11 has a mutation status of S413S, The gene IGLON5 has a mutation status of G177V, The gene PRKCG has a mutation status of G612G, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene KIR2DL3 has a mutation status of G12A, The gene PTPRH has a mutation status of R704Q, The gene ZNF671 has a mutation status of Y479H, The gene ZNF497 has a mutation status of R350R, The gene VPS16 has a mutation status of R505P, The gene JAG1 has a mutation status of A833V, The gene RIN2 has a mutation status of V677V, The gene APMAP has a mutation status of D254Y, The gene PYGB has a mutation status of L500L, The gene COMMD7 has a mutation status of L25M, The gene SUN5 has a mutation status of R30*, The gene BPIFB1 has a mutation status of Q336K, The gene C20orf144 has a mutation status of L33P, The gene PXMP4 has a mutation status of A3G, The gene NCOA6 has a mutation status of A196T, The gene DLGAP4 has a mutation status of Y76C, The gene TGM2 has a mutation status of Q348L, The gene PLCG1 has a mutation status of E289G, The gene SERINC3 has a mutation status of P464P, The gene ZNF217 has a mutation status of C674S, The gene CTSZ has a mutation status of L273V, The gene DIDO1 has a mutation status of R1643P, The gene DIDO1 has a mutation status of G1641P, The gene NKAIN4 has a mutation status of V26G, The gene ARFGAP1 has a mutation status of V15M, The gene COL20A1 has a mutation status of R733H, The gene HELZ2 has a mutation status of T1019T, The gene PRPF6 has a mutation status of I491T, The gene RIPK4 has a mutation status of R317W, The gene TFF2 has a mutation status of Y93*, The gene SLC37A1 has a mutation status of P174A, The gene KRTAP10-10 has a mutation status of R232fs, The gene KRTAP12-2 has a mutation status of P17H, The gene COL18A1 has a mutation status of P1025L, The gene PCNT has a mutation status of A1816D, The gene GAB4 has a mutation status of A508D, The gene SEPTIN5 has a mutation status of G142S, The gene USP41 has a mutation status of Y168*, The gene THAP7 has a mutation status of P201A, The gene PPM1F has a mutation status of Q84E, The gene BCR has a mutation status of Y644*, The gene CABIN1 has a mutation status of T1381P, The gene KIAA1671 has a mutation status of A488A, The gene KIAA1671 has a mutation status of P1356T, The gene SEZ6L has a mutation status of P101R, The gene CCDC157 has a mutation status of K288R, The gene SLC35E4 has a mutation status of A59G, The gene BPIFC has a mutation status of L320I, The gene HMGXB4 has a mutation status of V7M, The gene RAC2 has a mutation status of P133L, The gene TOMM22 has a mutation status of A3G, The gene TNRC6B has a mutation status of K24K, The gene MRTFA has a mutation status of P238P, The gene CYP2D6 has a mutation status of V136V, The gene SULT4A1 has a mutation status of L210L, The gene BRD1 has a mutation status of P764P, The gene ALG12 has a mutation status of V20L, The gene PPP6R2 has a mutation status of S791F, The gene NCAPH2 has a mutation status of V185I, The gene CRLF2 has a mutation status of S323F, The gene CLTRN has a mutation status of L8L, The gene NHS has a mutation status of L215P, The gene RAI2 has a mutation status of P415H, The gene MAP3K15 has a mutation status of A1169P, The gene MAP3K15 has a mutation status of A860D, The gene DCAF8L2 has a mutation status of C283R, The gene TFE3 has a mutation status of V172V, The gene CCDC22 has a mutation status of L484L, The gene IQSEC2 has a mutation status of R917S, The gene TRO has a mutation status of R336W, The gene STARD8 has a mutation status of P752S, The gene SLC25A5 has a mutation status of T221R, The gene CUL4B has a mutation status of C637C, The gene CNGA2 has a mutation status of V225V, The gene AVPR2 has a mutation status of V51G, The gene VBP1 has a mutation status of K153M, The gene DDX3Y has a mutation status of V319L, The gene MT-ND1 has a mutation status of G203G, The gene MT-CO1 has a mutation status of P173L, The gene MT-CO3 has a mutation status of W58W, The gene MT-ND4L has a mutation status of L40L
LUAD
The gene AGRN has a mutation status of T1811T, The gene TTLL10 has a mutation status of H10L, The gene B3GALT6 has a mutation status of A60T, The gene B3GALT6 has a mutation status of K289K, The gene CDK11B has a mutation status of V539V, The gene PLCH2 has a mutation status of P1116P, The gene NPHP4 has a mutation status of E1376K, The gene SLC25A33 has a mutation status of R276H, The gene PRAMEF10 has a mutation status of L373L, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PADI4 has a mutation status of W296C, The gene AKR7A3 has a mutation status of F194L, The gene E2F2 has a mutation status of I169M, The gene HMGCL has a mutation status of M4T, The gene IFNLR1 has a mutation status of P304P, The gene MAP3K6 has a mutation status of S367S, The gene FNDC5 has a mutation status of R76Q, The gene SF3A3 has a mutation status of Q283H, The gene CFAP57 has a mutation status of L1186L, The gene SZT2 has a mutation status of A3117V, The gene SLC1A7 has a mutation status of F270F, The gene C8A has a mutation status of S449A, The gene CACHD1 has a mutation status of A1272fs, The gene RAVER2 has a mutation status of A548T, The gene LRRC7 has a mutation status of L484L, The gene GNG5 has a mutation status of V7V, The gene SYDE2 has a mutation status of N489S, The gene BTBD8 has a mutation status of S1512G, The gene AGL has a mutation status of T221I, The gene RNPC3 has a mutation status of L289W, The gene OLFML3 has a mutation status of L97L, The gene NBPF26 has a mutation status of A267A, The gene MTMR11 has a mutation status of S651*, The gene PLEKHO1 has a mutation status of K259K, The gene ZNF687 has a mutation status of L811L, The gene SELENBP1 has a mutation status of L417L, The gene HRNR has a mutation status of G931G, The gene AL162596.1 has a mutation status of Q73R, The gene NES has a mutation status of E996K, The gene PRCC has a mutation status of S222C, The gene SPTA1 has a mutation status of V2046M, The gene OR6K6 has a mutation status of F172F, The gene IGSF9 has a mutation status of Q103E, The gene GPR52 has a mutation status of V64V, The gene RGSL1 has a mutation status of L555L, The gene RGSL1 has a mutation status of L565L, The gene LAMC2 has a mutation status of R170Q, The gene NR5A2 has a mutation status of R446Q, The gene IGFN1 has a mutation status of K1635E, The gene PPP1R12B has a mutation status of E453*, The gene IKBKE has a mutation status of R706W, The gene PTPN14 has a mutation status of R163G, The gene SPATA17 has a mutation status of R275T, The gene CAPN2 has a mutation status of L600L, The gene PSEN2 has a mutation status of G103R, The gene OBSCN has a mutation status of A6554G, The gene TRIM67 has a mutation status of S674R, The gene OR2L5 has a mutation status of L221L, The gene PGBD2 has a mutation status of V431V, The gene DTNB has a mutation status of L426L, The gene PLB1 has a mutation status of V730V, The gene SULT6B1 has a mutation status of D18N, The gene SOS1 has a mutation status of E906Q, The gene PLEKHH2 has a mutation status of L1463L, The gene USP34 has a mutation status of S3332*, The gene USP34 has a mutation status of L3312V, The gene WDPCP has a mutation status of R728T, The gene AAK1 has a mutation status of P336P, The gene TMEM131 has a mutation status of Q1312*, The gene EPB41L5 has a mutation status of E296E, The gene INHBB has a mutation status of D311E, The gene TFCP2L1 has a mutation status of Q198H, The gene CLASP1 has a mutation status of D1071D, The gene NMI has a mutation status of E240V, The gene TBR1 has a mutation status of S620W, The gene IFIH1 has a mutation status of V988L, The gene SCN9A has a mutation status of E926K, The gene LRP2 has a mutation status of E1102K, The gene CCDC173 has a mutation status of Q528P, The gene PHOSPHO2 has a mutation status of D10H, The gene HNRNPA3 has a mutation status of Q213H, The gene NCKAP1 has a mutation status of I389I, The gene COL5A2 has a mutation status of R1283C, The gene ANKAR has a mutation status of I1035T, The gene TMEFF2 has a mutation status of R34L, The gene STK17B has a mutation status of P344R, The gene ALS2 has a mutation status of E1557Q, The gene CRYGD has a mutation status of R169K, The gene ABCA12 has a mutation status of T913I, The gene VIL1 has a mutation status of R630H, The gene ABCB6 has a mutation status of Y106C, The gene DOCK10 has a mutation status of T10T, The gene ARMC9 has a mutation status of A786fs, The gene NMUR1 has a mutation status of F100L, The gene RBM44 has a mutation status of S710*, The gene PASK has a mutation status of R224C, The gene FARP2 has a mutation status of T822T, The gene D2HGDH has a mutation status of C299Y, The gene LMCD1 has a mutation status of K139R, The gene JAGN1 has a mutation status of L90L, The gene IL17RC has a mutation status of Y247Y, The gene SYN2 has a mutation status of 67_68insPAPQPAPQ, The gene SYN2 has a mutation status of P105A, The gene RAB5A has a mutation status of R183T, The gene ZNF385D has a mutation status of S217L, The gene OSBPL10 has a mutation status of E78D, The gene TMEM158 has a mutation status of F197F, The gene CELSR3 has a mutation status of R1158R, The gene NCKIPSD has a mutation status of I71I, The gene MST1R has a mutation status of R983W, The gene DNAH1 has a mutation status of A3155T, The gene ITIH4 has a mutation status of E266K, The gene DNAH12 has a mutation status of L2786L, The gene SHQ1 has a mutation status of *550*, The gene CRYBG3 has a mutation status of A1200A, The gene CEP97 has a mutation status of R682I, The gene BBX has a mutation status of P423L, The gene UPK1B has a mutation status of W61*, The gene COL6A5 has a mutation status of S450S, The gene RASA2 has a mutation status of T634R, The gene TIPARP has a mutation status of M303I, The gene KLHL6 has a mutation status of L560L, The gene PSMD2 has a mutation status of G155C, The gene POLR2H has a mutation status of P77L, The gene PIGZ has a mutation status of N420N, The gene MELTF has a mutation status of E316Q, The gene HTT has a mutation status of F2449F, The gene HGFAC has a mutation status of S568S, The gene UGDH has a mutation status of E416Q, The gene PDS5A has a mutation status of H967H, The gene BEND4 has a mutation status of E272*, The gene ATP10D has a mutation status of G1075G, The gene CORIN has a mutation status of L60L, The gene KIT has a mutation status of N130D, The gene UGT2B7 has a mutation status of Q330*, The gene CCDC158 has a mutation status of D163N, The gene MTTP has a mutation status of R799C, The gene NEUROG2 has a mutation status of Y160Y, The gene PDE5A has a mutation status of I771T, The gene GAB1 has a mutation status of D614N, The gene TRIM2 has a mutation status of P64P, The gene FGG has a mutation status of D346H, The gene GK3P has a mutation status of R405L, The gene SLC12A7 has a mutation status of V324I, The gene SLC6A18 has a mutation status of Y302Y, The gene C5orf38 has a mutation status of R7Q, The gene ADAMTS12 has a mutation status of N1015K, The gene MAP3K1 has a mutation status of V647V, The gene ACTBL2 has a mutation status of R117R, The gene ZSWIM6 has a mutation status of D1071N, The gene MAP1B has a mutation status of F280F, The gene NSA2 has a mutation status of L90V, The gene ATP6AP1L has a mutation status of K26fs, The gene RASA1 has a mutation status of A29S, The gene WDR36 has a mutation status of L283L, The gene TGFBI has a mutation status of D483N, The gene PCDHA2 has a mutation status of E558K, The gene PDE6A has a mutation status of P308P, The gene LSM11 has a mutation status of R23W, The gene TENM2 has a mutation status of L1644M, The gene H4C4 has a mutation status of D69H, The gene ZSCAN12 has a mutation status of I400M, The gene HLA-F has a mutation status of D60H, The gene MUC22 has a mutation status of T273E, The gene BAG6 has a mutation status of S1058*, The gene MSH5 has a mutation status of S537T, The gene AL645922.1 has a mutation status of P670L, The gene EGFL8 has a mutation status of V236V, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DOA has a mutation status of F163L, The gene SRPK1 has a mutation status of E57Q, The gene TRERF1 has a mutation status of V28A, The gene CUL9 has a mutation status of E513Q, The gene DLK2 has a mutation status of H32H, The gene TNFRSF21 has a mutation status of T291I, The gene PKHD1 has a mutation status of W365*, The gene FAM83B has a mutation status of I20V, The gene COL21A1 has a mutation status of V86V, The gene AK9 has a mutation status of E198Q, The gene TRAF3IP2 has a mutation status of Q105K, The gene SAMD3 has a mutation status of T487I, The gene SHPRH has a mutation status of L402L, The gene SYNE1 has a mutation status of D4750H, The gene TULP4 has a mutation status of S676C, The gene SLC22A1 has a mutation status of L8V, The gene PACRG has a mutation status of T168I, The gene EIF3B has a mutation status of D171H, The gene PAPOLB has a mutation status of T573A, The gene VWDE has a mutation status of G1186G, The gene VWDE has a mutation status of N1028K, The gene DNAH11 has a mutation status of G4190D, The gene SKAP2 has a mutation status of L20V, The gene HOXA6 has a mutation status of E169A, The gene CDK13 has a mutation status of A484A, The gene GLI3 has a mutation status of M1312R, The gene TNS3 has a mutation status of S944C, The gene PKD1L1 has a mutation status of R874Q, The gene ABCA13 has a mutation status of A703G, The gene AUTS2 has a mutation status of S1233C, The gene MAGI2 has a mutation status of R109S, The gene PCLO has a mutation status of Q442*, The gene CLDN12 has a mutation status of L138M, The gene AKAP9 has a mutation status of A1006A, The gene VPS50 has a mutation status of M625I, The gene SEM1 has a mutation status of E93K, The gene NPTX2 has a mutation status of R103P, The gene ZAN has a mutation status of I1243T, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of S558T, The gene MUC3A has a mutation status of P3166P, The gene MUC17 has a mutation status of P753S, The gene RELN has a mutation status of V2238I, The gene KCP has a mutation status of R1474Q, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene MGAM has a mutation status of N1585N, The gene PRSS1 has a mutation status of N77N, The gene PIP has a mutation status of L143I, The gene GALNT11 has a mutation status of D275H, The gene KMT2C has a mutation status of Q2054E, The gene VIPR2 has a mutation status of L298F, The gene XKR5 has a mutation status of S368R, The gene RP1L1 has a mutation status of E1313fs, The gene TUSC3 has a mutation status of Q94K, The gene PSD3 has a mutation status of L211L, The gene ST18 has a mutation status of L814L, The gene LYPLA1 has a mutation status of R149Q, The gene PAG1 has a mutation status of E278Q, The gene KCNS2 has a mutation status of G17R, The gene VPS13B has a mutation status of D2797H, The gene SPAG1 has a mutation status of A368G, The gene UBR5 has a mutation status of H1579N, The gene CYP11B1 has a mutation status of E381E, The gene ZNF623 has a mutation status of R392Q, The gene IQANK1 has a mutation status of W467R, The gene EPPK1 has a mutation status of A2633del, The gene EPPK1 has a mutation status of Q532P, The gene PLEC has a mutation status of Y1412Y, The gene PLEC has a mutation status of Q649*, The gene FOXD4 has a mutation status of A284V, The gene SMARCA2 has a mutation status of R424K, The gene BNC2 has a mutation status of V559L, The gene KLHL9 has a mutation status of A409A, The gene TOPORS has a mutation status of L184V, The gene UBAP1 has a mutation status of I263M, The gene CD72 has a mutation status of T331S, The gene GRHPR has a mutation status of K134N, The gene FRMPD1 has a mutation status of P809P, The gene CEMIP2 has a mutation status of D969A, The gene CEP78 has a mutation status of F106L, The gene RASEF has a mutation status of S25L, The gene SLC28A3 has a mutation status of S466L, The gene ASPN has a mutation status of R153Q, The gene FRRS1L has a mutation status of R51A, The gene BRINP1 has a mutation status of V91I, The gene CNTRL has a mutation status of L1943R, The gene NR6A1 has a mutation status of A285S, The gene PRDM12 has a mutation status of A344T, The gene NTNG2 has a mutation status of P74P, The gene CCDC187 has a mutation status of E1017E, The gene CCDC187 has a mutation status of H128H, The gene SEC16A has a mutation status of R51S, The gene EGFL7 has a mutation status of R75C, The gene TRAF2 has a mutation status of K481N, The gene NMT2 has a mutation status of D186N, The gene MALRD1 has a mutation status of R676Q, The gene NEBL has a mutation status of D227D, The gene MYO3A has a mutation status of G44D, The gene ZNF239 has a mutation status of G7V, The gene ALOX5 has a mutation status of E173K, The gene VSTM4 has a mutation status of R92H, The gene ANK3 has a mutation status of S432L, The gene EGR2 has a mutation status of P252S, The gene CCAR1 has a mutation status of L105L, The gene CCAR1 has a mutation status of Q171E, The gene CRTAC1 has a mutation status of E383Q, The gene PSTK has a mutation status of G14R, The gene CTBP2 has a mutation status of T257N, The gene KNDC1 has a mutation status of A1360A, The gene UTF1 has a mutation status of E127Q, The gene IFITM1 has a mutation status of F100L, The gene CD151 has a mutation status of E211A, The gene MUC5AC has a mutation status of D3964D, The gene STIM1 has a mutation status of D100D, The gene TRIM5 has a mutation status of R124H, The gene MRVI1 has a mutation status of E526K, The gene IGSF22 has a mutation status of K101K, The gene MYBPC3 has a mutation status of I1021I, The gene OR4A15 has a mutation status of S27L, The gene OR9G1 has a mutation status of T62V, The gene TNKS1BP1 has a mutation status of S1503F, The gene SLC15A3 has a mutation status of D193H, The gene EHD1 has a mutation status of P247P, The gene PCNX3 has a mutation status of S1838L, The gene SPTBN2 has a mutation status of R1006Q, The gene SPTBN2 has a mutation status of F347F, The gene KRTAP5-7 has a mutation status of C146Y, The gene COA4 has a mutation status of D26H, The gene UVRAG has a mutation status of R323S, The gene GAB2 has a mutation status of E417Q, The gene CREBZF has a mutation status of L102V, The gene BIRC3 has a mutation status of G54G, The gene PCSK7 has a mutation status of Q393H, The gene TMPRSS13 has a mutation status of L175L, The gene SMIM35 has a mutation status of M1I, The gene VPS11 has a mutation status of L458L, The gene VPS11 has a mutation status of D789Y, The gene HINFP has a mutation status of R9*, The gene DDX25 has a mutation status of D482N, The gene CDON has a mutation status of R927H, The gene NTM has a mutation status of V47V, The gene IGSF9B has a mutation status of S633C, The gene DYRK4 has a mutation status of R271L, The gene AKAP3 has a mutation status of E570Q, The gene STYK1 has a mutation status of L206L, The gene PRB4 has a mutation status of R122G, The gene MANSC1 has a mutation status of A225A, The gene PLEKHA5 has a mutation status of R594T, The gene NCKAP5L has a mutation status of G680V, The gene ASIC1 has a mutation status of R145H, The gene TNS2 has a mutation status of D12Y, The gene CSAD has a mutation status of T349T, The gene ERBB3 has a mutation status of E952Q, The gene STAT2 has a mutation status of G825C, The gene XPOT has a mutation status of I315V, The gene TBC1D15 has a mutation status of V624V, The gene NUAK1 has a mutation status of N172N, The gene TMEM263 has a mutation status of A71S, The gene USP30 has a mutation status of K29K, The gene CIT has a mutation status of V576V, The gene FZD10 has a mutation status of R353H, The gene CCNA1 has a mutation status of P193S, The gene SPRY2 has a mutation status of D232H, The gene MCF2L has a mutation status of S19F, The gene F10 has a mutation status of *333R, The gene LAMP1 has a mutation status of P260P, The gene GAS6 has a mutation status of R414Q, The gene KLHL33 has a mutation status of E53G, The gene PABPN1 has a mutation status of M167I, The gene RIPK3 has a mutation status of V27V, The gene AKAP6 has a mutation status of A528V, The gene SRP54 has a mutation status of D190H, The gene FAM177A1 has a mutation status of E87D, The gene PSMA6 has a mutation status of E19K, The gene TRAPPC6B has a mutation status of D54V, The gene MGAT2 has a mutation status of E159D, The gene MGAT2 has a mutation status of E285Q, The gene MGAT2 has a mutation status of E333Q, The gene FERMT2 has a mutation status of S371F, The gene WDR89 has a mutation status of V369M, The gene SPTB has a mutation status of V364V, The gene VIPAS39 has a mutation status of N439fs, The gene GPR65 has a mutation status of V236F, The gene EFCAB11 has a mutation status of D140N, The gene DDX24 has a mutation status of P773L, The gene PACS2 has a mutation status of L360P, The gene GOLGA8S has a mutation status of I439V, The gene MAGEL2 has a mutation status of R295T, The gene MAGEL2 has a mutation status of P225A, The gene HERC2 has a mutation status of L3391Q, The gene BUB1B has a mutation status of A46G, The gene DUOX1 has a mutation status of Q451P, The gene MYO5A has a mutation status of E43K, The gene UNC13C has a mutation status of S1514S, The gene ANKDD1A has a mutation status of L516L, The gene DENND4A has a mutation status of I1437M, The gene THSD4 has a mutation status of G393G, The gene HCN4 has a mutation status of I1086M, The gene ULK3 has a mutation status of R421R, The gene ALPK3 has a mutation status of G1182A, The gene AC013489.1 has a mutation status of R117W, The gene TICRR has a mutation status of S1097S, The gene LMF1 has a mutation status of R559H, The gene PERCC1 has a mutation status of G140R, The gene C16orf96 has a mutation status of R822H, The gene UBN1 has a mutation status of A276V, The gene UBN1 has a mutation status of T712A, The gene SOCS1 has a mutation status of L73L, The gene AC099489.1 has a mutation status of M271L, The gene ABCC6 has a mutation status of I517I, The gene EEF2K has a mutation status of D24D, The gene GSG1L has a mutation status of N62N, The gene ZNF646 has a mutation status of D42N, The gene ABCC11 has a mutation status of F158F, The gene ADCY7 has a mutation status of N515N, The gene KLHL36 has a mutation status of A362T, The gene ZC3H18 has a mutation status of R575Q, The gene TLCD2 has a mutation status of Q65E, The gene SMYD4 has a mutation status of E74del, The gene RAP1GAP2 has a mutation status of T153T, The gene AC004706.3 has a mutation status of R1139G, The gene CLEC10A has a mutation status of I55I, The gene FGF11 has a mutation status of R186Q, The gene TP53 has a mutation status of R175H, The gene ALOX15B has a mutation status of R463*, The gene MYH4 has a mutation status of I1748I, The gene HS3ST3B1 has a mutation status of G107A, The gene SREBF1 has a mutation status of A1076V, The gene LLGL1 has a mutation status of A466V, The gene RAB34 has a mutation status of G124E, The gene TBC1D3B has a mutation status of M251V, The gene CCL4L2 has a mutation status of P67R, The gene ACACA has a mutation status of A52A, The gene ARHGAP23 has a mutation status of A1010A, The gene KRTAP9-6 has a mutation status of G106C, The gene KCNH4 has a mutation status of L218L, The gene STAT5B has a mutation status of E509K, The gene COA3 has a mutation status of E89K, The gene B4GALNT2 has a mutation status of V287V, The gene HSF5 has a mutation status of G34S, The gene HEATR6 has a mutation status of R778T, The gene ACE has a mutation status of P15P, The gene ACE has a mutation status of S660C, The gene STRADA has a mutation status of L58L, The gene CSHL1 has a mutation status of E160*, The gene ABCA6 has a mutation status of T942T, The gene AATK has a mutation status of G974R, The gene FASN has a mutation status of P1121S, The gene SS18 has a mutation status of F5F, The gene CDH20 has a mutation status of E688Q, The gene ZCCHC2 has a mutation status of S89W, The gene ZCCHC2 has a mutation status of L173L, The gene SERPINB8 has a mutation status of I13I, The gene CDH7 has a mutation status of P726A, The gene ATP9B has a mutation status of E675Q, The gene RNF126 has a mutation status of G123S, The gene DOT1L has a mutation status of E337E, The gene CACTIN has a mutation status of Q591H, The gene ZNRF4 has a mutation status of R149*, The gene MUC16 has a mutation status of W9392S, The gene ZNF441 has a mutation status of H50D, The gene DHPS has a mutation status of A341G, The gene SAMD1 has a mutation status of P250L, The gene CPAMD8 has a mutation status of F583C, The gene PLVAP has a mutation status of L77L, The gene JAK3 has a mutation status of P747P, The gene MAST3 has a mutation status of S1026S, The gene TMEM161A has a mutation status of L384L, The gene ZNF730 has a mutation status of E455Q, The gene CD22 has a mutation status of N400N, The gene CAPNS1 has a mutation status of L246F, The gene ZNF850 has a mutation status of S80L, The gene ZNF585B has a mutation status of L677F, The gene LRFN1 has a mutation status of R487S, The gene ZNF546 has a mutation status of R430*, The gene ZNF780A has a mutation status of T56T, The gene ZNF404 has a mutation status of R506H, The gene FKRP has a mutation status of S152R, The gene NOP53 has a mutation status of A394A, The gene TPRX1 has a mutation status of D342E, The gene GRWD1 has a mutation status of A195V, The gene FTL has a mutation status of L107L, The gene TEAD2 has a mutation status of A267A, The gene SCAF1 has a mutation status of E871D, The gene AKT1S1 has a mutation status of L28L, The gene HAS1 has a mutation status of S116S, The gene ERVV-1 has a mutation status of V427A, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of T25P, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL4 has a mutation status of P186S, The gene MZF1 has a mutation status of R345R, The gene ADRA1D has a mutation status of A466A, The gene XRN2 has a mutation status of P148L, The gene ID1 has a mutation status of P118L, The gene NCOA6 has a mutation status of S2038C, The gene ACSS2 has a mutation status of T628T, The gene MYH7B has a mutation status of E1823K, The gene PHF20 has a mutation status of E858Q, The gene BPI has a mutation status of G116R, The gene BPI has a mutation status of K334T, The gene HNF4A has a mutation status of R263R, The gene SLC12A5 has a mutation status of 74_75insGG, The gene ELMO2 has a mutation status of F555L, The gene ELMO2 has a mutation status of L549L, The gene ZNF334 has a mutation status of F581del, The gene PREX1 has a mutation status of N643K, The gene CSE1L has a mutation status of M352I, The gene CSE1L has a mutation status of E353VDLY*YTFAIITSK, The gene AURKA has a mutation status of R189R, The gene RTF2 has a mutation status of *231S, The gene TAF4 has a mutation status of S560S, The gene NCAM2 has a mutation status of E252K, The gene URB1 has a mutation status of L1014L, The gene SYNJ1 has a mutation status of P1304P, The gene DSCAM has a mutation status of R498*, The gene MX1 has a mutation status of R649Q, The gene UBASH3A has a mutation status of L57L, The gene CFAP410 has a mutation status of A168A, The gene COL18A1 has a mutation status of P1172L, The gene TBX1 has a mutation status of E87Q, The gene P2RX6 has a mutation status of KF208del, The gene BCR has a mutation status of E1161D, The gene DRICH1 has a mutation status of D117D, The gene MN1 has a mutation status of A612T, The gene MN1 has a mutation status of E415E, The gene GAS2L1 has a mutation status of E123Q, The gene SEC14L6 has a mutation status of G221E, The gene SMTN has a mutation status of E124Q, The gene PRR14L has a mutation status of R1864Q, The gene BPIFC has a mutation status of L476L, The gene FOXRED2 has a mutation status of S4C, The gene SSTR3 has a mutation status of I207I, The gene GCAT has a mutation status of I284I, The gene GCAT has a mutation status of S287C, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene DHRSX has a mutation status of L222L, The gene ZBED1 has a mutation status of L434F, The gene CA5B has a mutation status of I67I, The gene CYBB has a mutation status of K508N, The gene JADE3 has a mutation status of E42Q, The gene DGKK has a mutation status of F323F, The gene HEPH has a mutation status of P398R, The gene NAP1L2 has a mutation status of E217E, The gene ABCB7 has a mutation status of E732G, The gene RTL9 has a mutation status of L991L, The gene TRPC5 has a mutation status of E421K, The gene LUZP4 has a mutation status of H205Y, The gene AGTR2 has a mutation status of I135fs, The gene ADGRG4 has a mutation status of PTAAHSSATPV794del, The gene TMLHE has a mutation status of T406R, The gene MT-ND4 has a mutation status of I454I, The gene MT-ND5 has a mutation status of L10L, The gene TTLL10 has a mutation status of H10L, The gene B3GALT6 has a mutation status of K289K, The gene CDK11B has a mutation status of V539V, The gene NPHP4 has a mutation status of E1376K, The gene PLEKHG5 has a mutation status of S878S, The gene SLC25A33 has a mutation status of R276H, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PADI4 has a mutation status of W296C, The gene AKR7A3 has a mutation status of F194L, The gene E2F2 has a mutation status of I169M, The gene HMGCL has a mutation status of M4T, The gene IFNLR1 has a mutation status of P304P, The gene DHDDS has a mutation status of E264K, The gene MAP3K6 has a mutation status of S367S, The gene FNDC5 has a mutation status of R76Q, The gene SF3A3 has a mutation status of Q283H, The gene SZT2 has a mutation status of A3117V, The gene KLF17 has a mutation status of L205L, The gene CDCP2 has a mutation status of T157S, The gene C8A has a mutation status of S449A, The gene HOOK1 has a mutation status of A552A, The gene RAVER2 has a mutation status of A548T, The gene MIER1 has a mutation status of D266H, The gene LRRC7 has a mutation status of L484L, The gene GNG5 has a mutation status of V7V, The gene SYDE2 has a mutation status of N489S, The gene CLCA2 has a mutation status of V111V, The gene HFM1 has a mutation status of S593P, The gene AGL has a mutation status of T221I, The gene RNPC3 has a mutation status of L289W, The gene WNT2B has a mutation status of S26L, The gene OLFML3 has a mutation status of L97L, The gene NBPF26 has a mutation status of A267A, The gene NBPF15 has a mutation status of L515L, The gene MTMR11 has a mutation status of S651*, The gene PLEKHO1 has a mutation status of K259K, The gene ZNF687 has a mutation status of L811L, The gene SELENBP1 has a mutation status of L417L, The gene TCHH has a mutation status of R615fs, The gene HRNR has a mutation status of S1021C, The gene FLG has a mutation status of Q240Q, The gene PKLR has a mutation status of E75K, The gene SEMA4A has a mutation status of G441E, The gene NES has a mutation status of E996K, The gene PRCC has a mutation status of S222C, The gene FCRL5 has a mutation status of G608E, The gene FCRL1 has a mutation status of E116K, The gene SPTA1 has a mutation status of V2046M, The gene OR6K6 has a mutation status of F172F, The gene IGSF9 has a mutation status of Q103E, The gene RGSL1 has a mutation status of L555L, The gene RGSL1 has a mutation status of L565L, The gene LAMC2 has a mutation status of R170Q, The gene HMCN1 has a mutation status of E4445*, The gene CAMSAP2 has a mutation status of R1005R, The gene IGFN1 has a mutation status of M1630fs, The gene TIMM17A has a mutation status of K86E, The gene LGR6 has a mutation status of L740L, The gene PPP1R12B has a mutation status of E453*, The gene CNTN2 has a mutation status of R506P, The gene IKBKE has a mutation status of R706W, The gene PTPN14 has a mutation status of R163G, The gene SPATA17 has a mutation status of R275T, The gene MARK1 has a mutation status of A597A, The gene CAPN2 has a mutation status of S619C, The gene ACBD3 has a mutation status of E8K, The gene OBSCN has a mutation status of P2822P, The gene TRIM67 has a mutation status of S674R, The gene AHCTF1 has a mutation status of D1947H, The gene OR2C3 has a mutation status of L286L, The gene OR2L5 has a mutation status of L221L, The gene OR2T4 has a mutation status of V109L, The gene PGBD2 has a mutation status of E264Q, The gene PGBD2 has a mutation status of V431V, The gene FAM228B has a mutation status of L17L, The gene DTNB has a mutation status of L426L, The gene SLC5A6 has a mutation status of L439L, The gene PLB1 has a mutation status of V730V, The gene SULT6B1 has a mutation status of D18N, The gene SOS1 has a mutation status of E906Q, The gene MTA3 has a mutation status of K486N, The gene PLEKHH2 has a mutation status of L1463L, The gene ABCG5 has a mutation status of E452D, The gene MSH6 has a mutation status of S79L, The gene BCL11A has a mutation status of S608S, The gene USP34 has a mutation status of S3332*, The gene USP34 has a mutation status of L3312V, The gene WDPCP has a mutation status of R728T, The gene UGP2 has a mutation status of E77D, The gene AAK1 has a mutation status of P336P, The gene TMEM131 has a mutation status of Q1312*, The gene GCC2 has a mutation status of E250Q, The gene EPB41L5 has a mutation status of E296E, The gene INHBB has a mutation status of D311E, The gene GLI2 has a mutation status of L879L, The gene TFCP2L1 has a mutation status of Q198H, The gene CLASP1 has a mutation status of D1071D, The gene LIMS2 has a mutation status of V87V, The gene WDR33 has a mutation status of R828K, The gene ARHGEF4 has a mutation status of G598V, The gene GPR39 has a mutation status of C108W, The gene NMI has a mutation status of E240V, The gene TBR1 has a mutation status of S620W, The gene IFIH1 has a mutation status of V988L, The gene SCN9A has a mutation status of E926K, The gene LRP2 has a mutation status of E1102K, The gene CCDC173 has a mutation status of Q528P, The gene PHOSPHO2 has a mutation status of D10H, The gene HNRNPA3 has a mutation status of Q213H, The gene TTN has a mutation status of E8638K, The gene NCKAP1 has a mutation status of I389I, The gene COL5A2 has a mutation status of R1283C, The gene TMEFF2 has a mutation status of R34L, The gene STK17B has a mutation status of P344R, The gene ALS2 has a mutation status of E1557Q, The gene CRYGD has a mutation status of R169K, The gene ABCA12 has a mutation status of T913I, The gene ABCB6 has a mutation status of Y106C, The gene PTPRN has a mutation status of R872R, The gene DOCK10 has a mutation status of T10T, The gene NMUR1 has a mutation status of F100L, The gene DGKD has a mutation status of D97H, The gene RBM44 has a mutation status of S710*, The gene PASK has a mutation status of R224C, The gene FARP2 has a mutation status of T822T, The gene D2HGDH has a mutation status of C299Y, The gene LMCD1 has a mutation status of K139R, The gene MTMR14 has a mutation status of N218I, The gene JAGN1 has a mutation status of L90L, The gene IL17RC has a mutation status of Y247Y, The gene SYN2 has a mutation status of P105A, The gene NUP210 has a mutation status of G470G, The gene RAB5A has a mutation status of R183T, The gene ZNF385D has a mutation status of S217L, The gene OSBPL10 has a mutation status of E78D, The gene TMEM158 has a mutation status of F197F, The gene LARS2 has a mutation status of C467fs, The gene ALS2CL has a mutation status of G371E, The gene CELSR3 has a mutation status of R1158R, The gene NCKIPSD has a mutation status of I71I, The gene INKA1 has a mutation status of K246K, The gene UBA7 has a mutation status of L917V, The gene MST1R has a mutation status of R983W, The gene ITIH4 has a mutation status of E266K, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene DNAH12 has a mutation status of D2383E, The gene SHQ1 has a mutation status of *550*, The gene ROBO1 has a mutation status of V69V, The gene CSNKA2IP has a mutation status of R732W, The gene CRYBG3 has a mutation status of A1200A, The gene CEP97 has a mutation status of R682I, The gene BBX has a mutation status of P423L, The gene UPK1B has a mutation status of W61*, The gene PRR20G has a mutation status of L176F, The gene COPG1 has a mutation status of E100Q, The gene COL6A5 has a mutation status of S450S, The gene COL6A5 has a mutation status of G738R, The gene CPNE4 has a mutation status of D187N, The gene CLSTN2 has a mutation status of E162Q, The gene RASA2 has a mutation status of T634R, The gene GPR171 has a mutation status of K169R, The gene TIPARP has a mutation status of M303I, The gene TNIK has a mutation status of S77F, The gene KLHL6 has a mutation status of L560L, The gene PSMD2 has a mutation status of G155C, The gene POLR2H has a mutation status of P77L, The gene MB21D2 has a mutation status of I437I, The gene PCYT1A has a mutation status of P316P, The gene MELTF has a mutation status of E316Q, The gene MYL5 has a mutation status of E140K, The gene TMEM175 has a mutation status of L479L, The gene HTT has a mutation status of F2449F, The gene PROM1 has a mutation status of Q746K, The gene UGDH has a mutation status of E416Q, The gene PDS5A has a mutation status of H967H, The gene BEND4 has a mutation status of E272*, The gene GABRA4 has a mutation status of R466G, The gene ATP10D has a mutation status of G1075G, The gene CORIN has a mutation status of L60L, The gene KIT has a mutation status of N130D, The gene UGT2B7 has a mutation status of Q330*, The gene ENAM has a mutation status of R373C, The gene CCDC158 has a mutation status of D163N, The gene BMP2K has a mutation status of E233V, The gene PTPN13 has a mutation status of P1976L, The gene AFF1 has a mutation status of K973T, The gene MTTP has a mutation status of R799C, The gene TET2 has a mutation status of S348S, The gene MCUB has a mutation status of W7*, The gene NEUROG2 has a mutation status of Y160Y, The gene PDE5A has a mutation status of I771T, The gene GAB1 has a mutation status of D614N, The gene TRIM2 has a mutation status of P64P, The gene FGG has a mutation status of D346H, The gene TKTL2 has a mutation status of P67S, The gene GK3P has a mutation status of R405L, The gene SCRG1 has a mutation status of E66K, The gene FAT1 has a mutation status of G1604E, The gene NKD2 has a mutation status of E268D, The gene SLC12A7 has a mutation status of V324I, The gene SLC6A18 has a mutation status of Y302Y, The gene C5orf38 has a mutation status of R7Q, The gene IRX1 has a mutation status of D264N, The gene SEMA5A has a mutation status of Y1060N, The gene CDH18 has a mutation status of K52Q, The gene PDZD2 has a mutation status of Q2579E, The gene ADAMTS12 has a mutation status of N1015K, The gene MAP3K1 has a mutation status of V647V, The gene ACTBL2 has a mutation status of R117R, The gene ZSWIM6 has a mutation status of D1071N, The gene MCCC2 has a mutation status of V28V, The gene MAP1B has a mutation status of F280F, The gene NSA2 has a mutation status of L90V, The gene THBS4 has a mutation status of T356A, The gene ATP6AP1L has a mutation status of K26fs, The gene RASA1 has a mutation status of A29S, The gene ADGRV1 has a mutation status of L1141L, The gene ADGRV1 has a mutation status of R1142K, The gene WDR36 has a mutation status of L283L, The gene CEP120 has a mutation status of T209I, The gene PRRC1 has a mutation status of F277fs, The gene HARS1 has a mutation status of E439A, The gene PCDHA2 has a mutation status of E558K, The gene SH3TC2 has a mutation status of R828R, The gene PDE6A has a mutation status of P308P, The gene LSM11 has a mutation status of R23W, The gene TENM2 has a mutation status of L1644M, The gene GMCL2 has a mutation status of V468fs, The gene NRSN1 has a mutation status of M130T, The gene H2AC6 has a mutation status of R100R, The gene HLA-F has a mutation status of D60H, The gene MUC22 has a mutation status of T273E, The gene BAG6 has a mutation status of S1058*, The gene MSH5 has a mutation status of S537T, The gene AL645922.1 has a mutation status of P670L, The gene EGFL8 has a mutation status of V236V, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene HLA-DOA has a mutation status of F163L, The gene SRPK1 has a mutation status of E57Q, The gene DAAM2 has a mutation status of I917I, The gene TRERF1 has a mutation status of V28A, The gene CUL9 has a mutation status of E513Q, The gene DLK2 has a mutation status of H32H, The gene MEP1A has a mutation status of W567C, The gene PKHD1 has a mutation status of W365*, The gene KLHL31 has a mutation status of E201*, The gene FAM83B has a mutation status of I20V, The gene COL21A1 has a mutation status of V86V, The gene COL12A1 has a mutation status of S234C, The gene SLC35A1 has a mutation status of A30P, The gene CASP8AP2 has a mutation status of E1255G, The gene EPHA7 has a mutation status of R366T, The gene AK9 has a mutation status of E198Q, The gene TRAF3IP2 has a mutation status of Q105K, The gene SAMD3 has a mutation status of T487I, The gene IFNGR1 has a mutation status of D144N, The gene SHPRH has a mutation status of L402L, The gene SYNE1 has a mutation status of E7841*, The gene SYNE1 has a mutation status of D4750H, The gene SYNE1 has a mutation status of Q3063L, The gene NOX3 has a mutation status of S199S, The gene TULP4 has a mutation status of S676C, The gene SLC22A1 has a mutation status of L8V, The gene PACRG has a mutation status of T168I, The gene DNAAF5 has a mutation status of L492L, The gene EIF3B has a mutation status of D171H, The gene VWDE has a mutation status of G1186G, The gene ABCB5 has a mutation status of S1059T, The gene HOXA6 has a mutation status of E169A, The gene KIAA0895 has a mutation status of S367C, The gene CDK13 has a mutation status of A484A, The gene GLI3 has a mutation status of M1312R, The gene TNS3 has a mutation status of S944C, The gene ABCA13 has a mutation status of A703G, The gene IKZF1 has a mutation status of G106V, The gene AUTS2 has a mutation status of S1233C, The gene MAGI2 has a mutation status of R109S, The gene PCLO has a mutation status of G1764A, The gene PCLO has a mutation status of Q442*, The gene CLDN12 has a mutation status of L138M, The gene VPS50 has a mutation status of M625I, The gene SEM1 has a mutation status of E93K, The gene TECPR1 has a mutation status of G796V, The gene NPTX2 has a mutation status of R103P, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of V2475S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene MUC17 has a mutation status of P753S, The gene NAT16 has a mutation status of L327L, The gene SLC26A5 has a mutation status of A310P, The gene RELN has a mutation status of V2238I, The gene CPED1 has a mutation status of C697F, The gene AASS has a mutation status of G510E, The gene HYAL4 has a mutation status of R210*, The gene FLNC has a mutation status of F2024F, The gene KCP has a mutation status of R1474Q, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene EXOC4 has a mutation status of P750P, The gene PIP has a mutation status of L143I, The gene GALNT11 has a mutation status of D275H, The gene KMT2C has a mutation status of Q2054E, The gene SHH has a mutation status of T336S, The gene ESYT2 has a mutation status of V183V, The gene XKR5 has a mutation status of S368R, The gene TUSC3 has a mutation status of Q94K, The gene PSD3 has a mutation status of L211L, The gene XPO7 has a mutation status of E699Q, The gene ST18 has a mutation status of L814L, The gene LYPLA1 has a mutation status of R149Q, The gene RP1 has a mutation status of P387Q, The gene CYP7B1 has a mutation status of Y469C, The gene PAG1 has a mutation status of E278Q, The gene VPS13B has a mutation status of D2797H, The gene SPAG1 has a mutation status of A368G, The gene PABPC1 has a mutation status of Y140Y, The gene UBR5 has a mutation status of H1579N, The gene FZD6 has a mutation status of L176V, The gene CYP11B1 has a mutation status of E381E, The gene CYP11B1 has a mutation status of F239F, The gene ZNF623 has a mutation status of R392Q, The gene EPPK1 has a mutation status of Q532P, The gene PLEC has a mutation status of Y1412Y, The gene PLEC has a mutation status of Q649*, The gene VPS28 has a mutation status of Y36*, The gene FOXD4 has a mutation status of A284V, The gene SMARCA2 has a mutation status of R424K, The gene BNC2 has a mutation status of V559L, The gene KLHL9 has a mutation status of A409A, The gene TOPORS has a mutation status of L184V, The gene DNAJA1 has a mutation status of G166G, The gene UBAP1 has a mutation status of I263M, The gene CD72 has a mutation status of T331S, The gene GRHPR has a mutation status of K134N, The gene FRMPD1 has a mutation status of P809P, The gene SPATA31A6 has a mutation status of R282W, The gene CEP78 has a mutation status of F106L, The gene RASEF has a mutation status of S25L, The gene SLC28A3 has a mutation status of S466L, The gene ASPN has a mutation status of R153Q, The gene ZNF367 has a mutation status of R144P, The gene FRRS1L has a mutation status of R51A, The gene SHOC1 has a mutation status of R1184H, The gene BRINP1 has a mutation status of V91I, The gene CNTRL has a mutation status of L1943R, The gene NR6A1 has a mutation status of A285S, The gene RABEPK has a mutation status of T125M, The gene ASB6 has a mutation status of R278R, The gene LAMC3 has a mutation status of E509K, The gene RAPGEF1 has a mutation status of P82S, The gene NTNG2 has a mutation status of P74P, The gene STKLD1 has a mutation status of L387L, The gene NACC2 has a mutation status of L509L, The gene NACC2 has a mutation status of E281D, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene CCDC187 has a mutation status of E1017E, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of H128H, The gene SEC16A has a mutation status of R51S, The gene EGFL7 has a mutation status of R75C, The gene TRAF2 has a mutation status of K481N, The gene NOXA1 has a mutation status of R180fs, The gene ZMYND11 has a mutation status of T457I, The gene PRKCQ has a mutation status of E352K, The gene PRKCQ has a mutation status of P341L, The gene ITIH2 has a mutation status of E584K, The gene NMT2 has a mutation status of D186N, The gene MALRD1 has a mutation status of R676Q, The gene MLLT10 has a mutation status of Q997E, The gene MYO3A has a mutation status of G44D, The gene CSGALNACT2 has a mutation status of E50G, The gene ZNF239 has a mutation status of G7V, The gene ALOX5 has a mutation status of E173K, The gene VSTM4 has a mutation status of R92H, The gene JMJD1C has a mutation status of A90S, The gene SIRT1 has a mutation status of T177I, The gene CCAR1 has a mutation status of L105L, The gene CCAR1 has a mutation status of Q171E, The gene DDX21 has a mutation status of E446Q, The gene CRTAC1 has a mutation status of E383Q, The gene CHUK has a mutation status of N108N, The gene FGFR2 has a mutation status of G136E, The gene PSTK has a mutation status of G14R, The gene CTBP2 has a mutation status of T257N, The gene MKI67 has a mutation status of Q1497L, The gene KNDC1 has a mutation status of A1360A, The gene UTF1 has a mutation status of E127Q, The gene IFITM1 has a mutation status of F100L, The gene CD151 has a mutation status of E211A, The gene MUC5AC has a mutation status of D3964D, The gene MUC5B has a mutation status of P3887I, The gene MUC5B has a mutation status of I4642V, The gene MRGPRE has a mutation status of F215F, The gene TRIM5 has a mutation status of R124H, The gene OR52L1 has a mutation status of A215S, The gene IGSF22 has a mutation status of K101K, The gene TP53I11 has a mutation status of P102L, The gene MYBPC3 has a mutation status of I1021I, The gene NUP160 has a mutation status of L1321V, The gene FOLH1 has a mutation status of N51K, The gene OR4A15 has a mutation status of S27L, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TNKS1BP1 has a mutation status of S1503F, The gene SLC15A3 has a mutation status of D193H, The gene KCNK4 has a mutation status of A230V, The gene RASGRP2 has a mutation status of F338F, The gene EHD1 has a mutation status of P247P, The gene PCNX3 has a mutation status of S1838L, The gene SPTBN2 has a mutation status of R1006Q, The gene SPTBN2 has a mutation status of F347F, The gene CORO1B has a mutation status of A385V, The gene KRTAP5-7 has a mutation status of C146Y, The gene COA4 has a mutation status of D26H, The gene UVRAG has a mutation status of R323S, The gene GAB2 has a mutation status of E417Q, The gene CREBZF has a mutation status of L102V, The gene BIRC3 has a mutation status of G54G, The gene PCSK7 has a mutation status of Q393H, The gene TMPRSS13 has a mutation status of L175L, The gene VPS11 has a mutation status of L458L, The gene VPS11 has a mutation status of D789Y, The gene HINFP has a mutation status of R9*, The gene VWA5A has a mutation status of T564T, The gene PANX3 has a mutation status of S83A, The gene DDX25 has a mutation status of D482N, The gene CDON has a mutation status of R927H, The gene NTM has a mutation status of V47V, The gene IGSF9B has a mutation status of S633C, The gene GLB1L2 has a mutation status of E103*, The gene DCP1B has a mutation status of E540*, The gene DYRK4 has a mutation status of R271L, The gene AKAP3 has a mutation status of E570Q, The gene KCNA5 has a mutation status of F352L, The gene C1S has a mutation status of D55Y, The gene STYK1 has a mutation status of L206L, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PLEKHA5 has a mutation status of R594T, The gene GXYLT1 has a mutation status of E249R, The gene GXYLT1 has a mutation status of V28K, The gene ANO6 has a mutation status of R208K, The gene KMT2D has a mutation status of QAEGPHLSP791del, The gene NCKAP5L has a mutation status of G680V, The gene ASIC1 has a mutation status of R145H, The gene TNS2 has a mutation status of D12Y, The gene TNS2 has a mutation status of R374Q, The gene ERBB3 has a mutation status of E952Q, The gene STAT2 has a mutation status of G825C, The gene ZBTB39 has a mutation status of E534V, The gene GLI1 has a mutation status of I110M, The gene XPOT has a mutation status of I315V, The gene MYRFL has a mutation status of E478K, The gene TBC1D15 has a mutation status of V624V, The gene LUM has a mutation status of L139V, The gene APPL2 has a mutation status of A387V, The gene NUAK1 has a mutation status of N172N, The gene TMEM263 has a mutation status of A71S, The gene USP30 has a mutation status of K29K, The gene CIT has a mutation status of V576V, The gene FZD10 has a mutation status of R353H, The gene DDX51 has a mutation status of Y221N, The gene TEX26 has a mutation status of I188I, The gene PCDH8 has a mutation status of T703N, The gene SPRY2 has a mutation status of D232H, The gene SLC15A1 has a mutation status of Q324H, The gene MYO16 has a mutation status of A1690A, The gene MCF2L has a mutation status of S19F, The gene F10 has a mutation status of *333R, The gene LAMP1 has a mutation status of P260P, The gene ADPRHL1 has a mutation status of R1245I, The gene ADPRHL1 has a mutation status of A1043A, The gene TOX4 has a mutation status of P532P, The gene PABPN1 has a mutation status of M167I, The gene MYH6 has a mutation status of Y835N, The gene RIPK3 has a mutation status of V27V, The gene AKAP6 has a mutation status of A528V, The gene SRP54 has a mutation status of D190H, The gene PSMA6 has a mutation status of E19K, The gene TRAPPC6B has a mutation status of D54V, The gene MGAT2 has a mutation status of E159D, The gene MGAT2 has a mutation status of E285Q, The gene MGAT2 has a mutation status of E333Q, The gene FERMT2 has a mutation status of S371F, The gene KIAA0586 has a mutation status of S242T, The gene SPTB has a mutation status of V364V, The gene SPTB has a mutation status of D81N, The gene FLVCR2 has a mutation status of 178_181IMTL>M, The gene VIPAS39 has a mutation status of N439fs, The gene GPR65 has a mutation status of V236F, The gene EFCAB11 has a mutation status of D140N, The gene CCDC88C has a mutation status of E167Q, The gene DDX24 has a mutation status of P773L, The gene DIO3 has a mutation status of L32Q, The gene PACS2 has a mutation status of L360P, The gene LINC02203 has a mutation status of I259M, The gene GOLGA8S has a mutation status of I439V, The gene MAGEL2 has a mutation status of R295T, The gene MAGEL2 has a mutation status of P225A, The gene OCA2 has a mutation status of L710Q, The gene HERC2 has a mutation status of L3391Q, The gene GOLGA8G has a mutation status of R6H, The gene BUB1B has a mutation status of A46G, The gene DUOX1 has a mutation status of Q451P, The gene ATP8B4 has a mutation status of L1062L, The gene MYO5A has a mutation status of E43K, The gene UNC13C has a mutation status of S1514S, The gene MINDY2 has a mutation status of R445W, The gene ANKDD1A has a mutation status of L516L, The gene SLC24A1 has a mutation status of P284S, The gene DENND4A has a mutation status of I1437M, The gene HCN4 has a mutation status of I1086M, The gene HCN4 has a mutation status of S935Y, The gene CD276 has a mutation status of V425I, The gene CYP11A1 has a mutation status of L130F, The gene ULK3 has a mutation status of R421R, The gene GOLGA6L10 has a mutation status of T71A, The gene ADAMTSL3 has a mutation status of G1338R, The gene ALPK3 has a mutation status of G1182A, The gene ANPEP has a mutation status of E389D, The gene LMF1 has a mutation status of R559H, The gene UBN1 has a mutation status of A276V, The gene C16orf72 has a mutation status of A67D, The gene GRIN2A has a mutation status of G1258G, The gene SOCS1 has a mutation status of L73L, The gene ABCC6 has a mutation status of I517I, The gene DNAH3 has a mutation status of F664L, The gene OTOA has a mutation status of F15F, The gene UQCRC2 has a mutation status of V292F, The gene EEF2K has a mutation status of D24D, The gene GSG1L has a mutation status of N62N, The gene APOBR has a mutation status of E46*, The gene CCDC189 has a mutation status of E97E, The gene ZNF646 has a mutation status of D42N, The gene C16orf58 has a mutation status of D139N, The gene ABCC11 has a mutation status of F158F, The gene CDH8 has a mutation status of G170V, The gene PMFBP1 has a mutation status of E21Q, The gene PMFBP1 has a mutation status of G204E, The gene CHST5 has a mutation status of L217L, The gene GAN has a mutation status of L125F, The gene KLHL36 has a mutation status of A362T, The gene ZNF469 has a mutation status of A2512T, The gene ZC3H18 has a mutation status of R575Q, The gene TLCD2 has a mutation status of Q65E, The gene SMYD4 has a mutation status of E74del, The gene RAP1GAP2 has a mutation status of T153T, The gene SPNS2 has a mutation status of L114L, The gene ALOX15 has a mutation status of Q125H, The gene MINK1 has a mutation status of G925G, The gene GP1BA has a mutation status of L76L, The gene CLEC10A has a mutation status of I55I, The gene FGF11 has a mutation status of R186Q, The gene TP53 has a mutation status of R175H, The gene DNAH2 has a mutation status of E4369Q, The gene ALOX15B has a mutation status of R463*, The gene MYH4 has a mutation status of I1748I, The gene MYH3 has a mutation status of N898H, The gene DNAH9 has a mutation status of S208P, The gene HS3ST3B1 has a mutation status of G107A, The gene TEKT3 has a mutation status of I409S, The gene SREBF1 has a mutation status of A1076V, The gene LLGL1 has a mutation status of A466V, The gene RAB34 has a mutation status of G124E, The gene NEK8 has a mutation status of I252M, The gene NF1 has a mutation status of A502V, The gene CCL4L2 has a mutation status of P67R, The gene ACACA has a mutation status of A52A, The gene ARHGAP23 has a mutation status of A1010A, The gene RAPGEFL1 has a mutation status of E202*, The gene KCNH4 has a mutation status of L218L, The gene STAT5B has a mutation status of E509K, The gene COA3 has a mutation status of E89K, The gene SLC4A1 has a mutation status of S106G, The gene CDC27 has a mutation status of D558D, The gene CALCOCO2 has a mutation status of L257L, The gene B4GALNT2 has a mutation status of V287V, The gene HSF5 has a mutation status of G34S, The gene HEATR6 has a mutation status of R778T, The gene ACE has a mutation status of S824W, The gene CSHL1 has a mutation status of E160*, The gene AC015802.6 has a mutation status of P175P, The gene MGAT5B has a mutation status of E477del, The gene AATK has a mutation status of G974R, The gene FASN has a mutation status of P1121S, The gene L3MBTL4 has a mutation status of E551D, The gene SS18 has a mutation status of F5F, The gene MAPRE2 has a mutation status of S39Y, The gene SMAD4 has a mutation status of D259N, The gene CDH20 has a mutation status of E688Q, The gene ZCCHC2 has a mutation status of S89W, The gene SERPINB8 has a mutation status of I13I, The gene CDH7 has a mutation status of P726A, The gene DSEL has a mutation status of L929L, The gene ATP9B has a mutation status of E675Q, The gene RNF126 has a mutation status of G123S, The gene CFD has a mutation status of V78I, The gene CNN2 has a mutation status of M249T, The gene DOT1L has a mutation status of E337E, The gene ZNRF4 has a mutation status of R149*, The gene MUC16 has a mutation status of T13896S, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of T12336L, The gene ZNF441 has a mutation status of H50D, The gene DHPS has a mutation status of A341G, The gene SAMD1 has a mutation status of P250L, The gene CPAMD8 has a mutation status of F583C, The gene PLVAP has a mutation status of L77L, The gene UNC13A has a mutation status of L344L, The gene JAK3 has a mutation status of P747P, The gene MAST3 has a mutation status of S1026S, The gene TMEM161A has a mutation status of L384L, The gene TDRD12 has a mutation status of Q351H, The gene ZNF792 has a mutation status of F347F, The gene CD22 has a mutation status of N400N, The gene KMT2B has a mutation status of P587S, The gene CAPNS1 has a mutation status of L246F, The gene ZNF382 has a mutation status of I178T, The gene ZNF850 has a mutation status of G697C, The gene ZNF829 has a mutation status of G292D, The gene ZNF585B has a mutation status of L677F, The gene LRFN1 has a mutation status of R487S, The gene CBLC has a mutation status of S43L, The gene TPRX1 has a mutation status of D342E, The gene GRWD1 has a mutation status of A195V, The gene FTL has a mutation status of L107L, The gene TEAD2 has a mutation status of A267A, The gene SCAF1 has a mutation status of E871D, The gene AKT1S1 has a mutation status of L28L, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of T201M, The gene LILRB3 has a mutation status of M21V, The gene LENG9 has a mutation status of *479*, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL4 has a mutation status of P186S, The gene ZNF8 has a mutation status of C472Y, The gene MZF1 has a mutation status of R345R, The gene ADRA1D has a mutation status of A466A, The gene ESF1 has a mutation status of A500G, The gene DTD1 has a mutation status of D202Y, The gene XRN2 has a mutation status of P148L, The gene ID1 has a mutation status of P118L, The gene NCOA6 has a mutation status of S2038C, The gene ACSS2 has a mutation status of T628T, The gene PHF20 has a mutation status of E858Q, The gene PLCG1 has a mutation status of E822D, The gene HNF4A has a mutation status of R263R, The gene TOMM34 has a mutation status of E18Q, The gene CDH22 has a mutation status of V230A, The gene ELMO2 has a mutation status of F555L, The gene ELMO2 has a mutation status of L549L, The gene PREX1 has a mutation status of N643K, The gene RIPOR3 has a mutation status of V2M, The gene AURKA has a mutation status of R189R, The gene RTF2 has a mutation status of *231S, The gene TAF4 has a mutation status of S560S, The gene ZBTB46 has a mutation status of L433L, The gene NRIP1 has a mutation status of T970N, The gene CXADR has a mutation status of Q69E, The gene NCAM2 has a mutation status of E252K, The gene URB1 has a mutation status of L1014L, The gene SYNJ1 has a mutation status of P1304P, The gene DSCAM has a mutation status of R498*, The gene MX1 has a mutation status of R649Q, The gene UBASH3A has a mutation status of L57L, The gene CFAP410 has a mutation status of A168A, The gene PRMT2 has a mutation status of A229V, The gene TBX1 has a mutation status of E87Q, The gene PI4KA has a mutation status of E1829E, The gene BCR has a mutation status of E1161D, The gene DRICH1 has a mutation status of D117D, The gene MN1 has a mutation status of A612T, The gene MN1 has a mutation status of E415E, The gene GAS2L1 has a mutation status of E123Q, The gene SEC14L6 has a mutation status of G221E, The gene SMTN has a mutation status of E124Q, The gene PRR14L has a mutation status of R1864Q, The gene BPIFC has a mutation status of L476L, The gene FOXRED2 has a mutation status of S4C, The gene SSTR3 has a mutation status of I207I, The gene GCAT has a mutation status of I284I, The gene GCAT has a mutation status of S287C, The gene TNRC6B has a mutation status of L1144V, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene KIAA0930 has a mutation status of M230L, The gene PLXNB2 has a mutation status of E1269fs, The gene CRLF2 has a mutation status of V313V, The gene P2RY8 has a mutation status of L304V, The gene DHRSX has a mutation status of L222L, The gene ZBED1 has a mutation status of I436M, The gene ZBED1 has a mutation status of L434F, The gene TLR7 has a mutation status of K478E, The gene CA5B has a mutation status of I67I, The gene CYBB has a mutation status of K508N, The gene JADE3 has a mutation status of E42Q, The gene DGKK has a mutation status of F323F, The gene PAGE5 has a mutation status of N65N, The gene HEPH has a mutation status of P398R, The gene MED12 has a mutation status of S1400F, The gene ERCC6L has a mutation status of R527T, The gene NAP1L2 has a mutation status of E217E, The gene ABCB7 has a mutation status of E732G, The gene FGF16 has a mutation status of R63C, The gene ZNF711 has a mutation status of Q750H, The gene RTL9 has a mutation status of L991L, The gene HTR2C has a mutation status of A286S, The gene LUZP4 has a mutation status of H205Y, The gene SLC25A5 has a mutation status of T221R, The gene C1GALT1C1 has a mutation status of L2V, The gene ADGRG4 has a mutation status of PTAAHSSATPV794del, The gene MT-ND4 has a mutation status of I454I, The gene MT-ND5 has a mutation status of L10L, The gene MT-ND5 has a mutation status of G146S
BRCA
The gene C1QTNF12 has a mutation status of L12L, The gene PRAMEF9 has a mutation status of A352V, The gene PRAMEF13 has a mutation status of R138C, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF20 has a mutation status of R4R, The gene PLEKHM2 has a mutation status of I972I, The gene SPEN has a mutation status of E1962del, The gene TCEA3 has a mutation status of L27L, The gene GPATCH3 has a mutation status of E8*, The gene KIAA0319L has a mutation status of T901S, The gene NCDN has a mutation status of P613L, The gene NDUFS5 has a mutation status of T72M, The gene FOXO6 has a mutation status of E170K, The gene TTC22 has a mutation status of S276*, The gene TTLL7 has a mutation status of Q611Q, The gene MCOLN3 has a mutation status of D263D, The gene ZNHIT6 has a mutation status of E46D, The gene CD101 has a mutation status of R376K, The gene NBPF10 has a mutation status of V776A, The gene PPIAL4H has a mutation status of N102I, The gene LCE3C has a mutation status of C3C, The gene ARHGEF2 has a mutation status of R581Q, The gene HMCN1 has a mutation status of E5601K, The gene TMEM81 has a mutation status of R159C, The gene PROX1 has a mutation status of P728L, The gene DISP1 has a mutation status of L431L, The gene OBSCN has a mutation status of A2212L, The gene RYR2 has a mutation status of R739C, The gene RYR2 has a mutation status of R2401H, The gene SDCCAG8 has a mutation status of K261K, The gene OR2T4 has a mutation status of V109L, The gene PXDN has a mutation status of D1432H, The gene GDF7 has a mutation status of C414*, The gene APOB has a mutation status of N3977H, The gene CAD has a mutation status of V1294F, The gene FOSL2 has a mutation status of G197G, The gene ATL2 has a mutation status of E78A, The gene APLF has a mutation status of S267S, The gene FAM136A has a mutation status of E180E, The gene TET3 has a mutation status of R160T, The gene KCNIP3 has a mutation status of H164H, The gene TRIM43B has a mutation status of K71K, The gene IL1A has a mutation status of L204L, The gene GALNT5 has a mutation status of E564G, The gene IFIH1 has a mutation status of I441I, The gene WIPF1 has a mutation status of S344P, The gene FSIP2 has a mutation status of S3169P, The gene STAT1 has a mutation status of L466L, The gene ZNF142 has a mutation status of E216K, The gene SPEG has a mutation status of R1616W, The gene COL6A3 has a mutation status of G2344R, The gene CROCC2 has a mutation status of S622Y, The gene ANO7 has a mutation status of A44fs, The gene CRBN has a mutation status of S379N, The gene HYAL3 has a mutation status of L166L, The gene CCDC66 has a mutation status of Q74*, The gene ACKR4 has a mutation status of D10N, The gene AMOTL2 has a mutation status of R605*, The gene SHOX2 has a mutation status of GGGG70del, The gene SLITRK3 has a mutation status of T567N, The gene ATP13A5 has a mutation status of Q1212E, The gene HTT has a mutation status of P2912P, The gene CRACD has a mutation status of R517L, The gene CCDC158 has a mutation status of E509Q, The gene HSD17B11 has a mutation status of R283Q, The gene TBCK has a mutation status of S277*, The gene OTUD4 has a mutation status of E1071fs, The gene TKTL2 has a mutation status of F170S, The gene FAT1 has a mutation status of S2682*, The gene AGXT2 has a mutation status of E175K, The gene IL7R has a mutation status of D313G, The gene ARSB has a mutation status of R489K, The gene PCDHB6 has a mutation status of N553N, The gene PCDHB7 has a mutation status of F514I, The gene CPLX2 has a mutation status of V120V, The gene FLT4 has a mutation status of G755G, The gene NQO2 has a mutation status of R50G, The gene FAM8A1 has a mutation status of E253Q, The gene HLA-A has a mutation status of K292E, The gene HLA-B has a mutation status of L102L, The gene PRRC2A has a mutation status of E1800E, The gene DAXX has a mutation status of A368A, The gene PHF1 has a mutation status of D274N, The gene IRAK1BP1 has a mutation status of E147Q, The gene SNAP91 has a mutation status of E436K, The gene PREP has a mutation status of Q388R, The gene HIVEP2 has a mutation status of L2305F, The gene FNDC1 has a mutation status of P1258S, The gene EPDR1 has a mutation status of P41P, The gene CDK13 has a mutation status of E1019*, The gene ABCA13 has a mutation status of S294S, The gene ERV3-1 has a mutation status of Q539K, The gene TRIP6 has a mutation status of F363L, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene MYL10 has a mutation status of D167V, The gene LRWD1 has a mutation status of E340A, The gene RELN has a mutation status of D2171G, The gene SRPK2 has a mutation status of D54A, The gene SLC26A3 has a mutation status of L39L, The gene LAMB4 has a mutation status of A1699V, The gene DOCK4 has a mutation status of P449P, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene CUL1 has a mutation status of S114T, The gene NOS3 has a mutation status of S114F, The gene GPAT4 has a mutation status of A34V, The gene CNGB3 has a mutation status of R456R, The gene PABPC1 has a mutation status of Y140Y, The gene MAFA has a mutation status of G328R, The gene GSDMD has a mutation status of G347S, The gene MROH1 has a mutation status of S873G, The gene CNTLN has a mutation status of D217H, The gene RUSC2 has a mutation status of L231R, The gene ZBTB5 has a mutation status of D82N, The gene SPATA31A6 has a mutation status of W417*, The gene ASPN has a mutation status of K113T, The gene ERCC6L2 has a mutation status of P100A, The gene FRRS1L has a mutation status of R51A, The gene NR5A1 has a mutation status of E7K, The gene MVB12B has a mutation status of V53I, The gene GOLGA2 has a mutation status of L677L, The gene HMCN2 has a mutation status of R819H, The gene HMCN2 has a mutation status of G1098G, The gene PRDM12 has a mutation status of K319R, The gene REXO4 has a mutation status of L229L, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene CCDC187 has a mutation status of E1017E, The gene CCDC187 has a mutation status of T90M, The gene AJM1 has a mutation status of V387I, The gene AJM1 has a mutation status of L875P, The gene CACNA1B has a mutation status of R1062Q, The gene CUBN has a mutation status of H2366N, The gene ARHGAP22 has a mutation status of R472R, The gene C10orf71 has a mutation status of N1058K, The gene CDH23 has a mutation status of A356P, The gene IFIT3 has a mutation status of A179V, The gene FRG2B has a mutation status of R148C, The gene HRAS has a mutation status of G12V, The gene MUC5AC has a mutation status of A497V, The gene MUC5AC has a mutation status of A5353K, The gene ANO3 has a mutation status of K928N, The gene LGR4 has a mutation status of T709T, The gene FAM180B has a mutation status of A3V, The gene OR5D18 has a mutation status of A275V, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR6Q1 has a mutation status of F204F, The gene TEX54 has a mutation status of R37R, The gene CDC42BPG has a mutation status of T1095M, The gene NDUFS8 has a mutation status of C153C, The gene C2CD3 has a mutation status of R2252K, The gene HEPHL1 has a mutation status of D760D, The gene DRD2 has a mutation status of A420A, The gene HTR3B has a mutation status of R294W, The gene DSCAML1 has a mutation status of P1150L, The gene C2CD2L has a mutation status of D617N, The gene C2CD2L has a mutation status of E621K, The gene NECTIN1 has a mutation status of R210H, The gene GRAMD1B has a mutation status of R648R, The gene OR8G1 has a mutation status of 288_289insSYICF*I*SNL, The gene SLC37A2 has a mutation status of L124L, The gene CACNA2D4 has a mutation status of V298L, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene ALG10B has a mutation status of L165L, The gene ALG10B has a mutation status of D218N, The gene GXYLT1 has a mutation status of K440R, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of E249R, The gene GXYLT1 has a mutation status of V28K, The gene FAM186B has a mutation status of F616C, The gene GALNT6 has a mutation status of G518R, The gene KRT77 has a mutation status of L171L, The gene METTL7B has a mutation status of V169M, The gene MARS1 has a mutation status of P206L, The gene TBC1D30 has a mutation status of L45L, The gene WIF1 has a mutation status of A149E, The gene MYRFL has a mutation status of P659Q, The gene C12orf50 has a mutation status of K186N, The gene ANKS1B has a mutation status of R590Q, The gene PRDM4 has a mutation status of V277V, The gene ATXN2 has a mutation status of E141K, The gene TPCN1 has a mutation status of R348R, The gene TPCN1 has a mutation status of G428G, The gene DNAH10 has a mutation status of S3322S, The gene N4BP2L2 has a mutation status of R371I, The gene MYCBP2 has a mutation status of K3014N, The gene TM9SF2 has a mutation status of Q374Q, The gene NALCN has a mutation status of R1053I, The gene MAP3K9 has a mutation status of P795P, The gene RGS6 has a mutation status of S311N, The gene SERPINA12 has a mutation status of R294R, The gene GOLGA6L6 has a mutation status of QEQEEKM694del, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene APBA2 has a mutation status of A397V, The gene PHGR1 has a mutation status of G48H, The gene UNC13C has a mutation status of Q1582H, The gene NEDD4 has a mutation status of I1125V, The gene LACTB has a mutation status of K511R, The gene SNX22 has a mutation status of C149C, The gene ANKDD1A has a mutation status of L516L, The gene GOLGA6L10 has a mutation status of C314R, The gene GOLGA6L9 has a mutation status of R6H, The gene ALPK3 has a mutation status of D413N, The gene PDIA2 has a mutation status of E145K, The gene PRR35 has a mutation status of A113V, The gene MSLNL has a mutation status of R132R, The gene PGP has a mutation status of L16L, The gene PDILT has a mutation status of L457L, The gene ZNF768 has a mutation status of R337H, The gene HEATR3 has a mutation status of A436V, The gene NOD2 has a mutation status of P269L, The gene ADAD2 has a mutation status of S62L, The gene MYO1C has a mutation status of L146W, The gene SLC43A2 has a mutation status of R403H, The gene TSR1 has a mutation status of R737W, The gene MNT has a mutation status of A23V, The gene CLUH has a mutation status of I1211M, The gene SPNS3 has a mutation status of A276S, The gene TP53 has a mutation status of Y126*, The gene NTN1 has a mutation status of S67C, The gene RNF112 has a mutation status of E177K, The gene SLFN12 has a mutation status of T361M, The gene SLFN13 has a mutation status of I665I, The gene CCL4L2 has a mutation status of P67R, The gene MSL1 has a mutation status of V376V, The gene DHX8 has a mutation status of P811Q, The gene ITGA2B has a mutation status of L654F, The gene CDC27 has a mutation status of S553S, The gene OTOP2 has a mutation status of W170*, The gene ACOX1 has a mutation status of T155T, The gene CARD14 has a mutation status of I989I, The gene RNF213 has a mutation status of G3533S, The gene PIEZO2 has a mutation status of S2577*, The gene LAMA3 has a mutation status of C436Y, The gene EPG5 has a mutation status of L361fs, The gene CCDC68 has a mutation status of E80Q, The gene ZNF414 has a mutation status of P313G, The gene MUC16 has a mutation status of T12336L, The gene COL5A3 has a mutation status of V1162I, The gene DOCK6 has a mutation status of S439R, The gene CPAMD8 has a mutation status of H1834R, The gene FCHO1 has a mutation status of D478N, The gene DDX49 has a mutation status of L385L, The gene ZNF729 has a mutation status of C908S, The gene HAUS5 has a mutation status of A627S, The gene ZNF585A has a mutation status of R458G, The gene RASGRP4 has a mutation status of T418T, The gene ZNF155 has a mutation status of F411L, The gene ARHGAP35 has a mutation status of R1234R, The gene ZC3H4 has a mutation status of P990S, The gene NAPA has a mutation status of A161A, The gene RASIP1 has a mutation status of A951G, The gene MYH14 has a mutation status of R1735Q, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of T30T, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene NLRP8 has a mutation status of L451L, The gene PYGB has a mutation status of V788V, The gene BPIFA1 has a mutation status of G86D, The gene PCIF1 has a mutation status of A552G, The gene CDH22 has a mutation status of G712A, The gene STX16 has a mutation status of F10F, The gene DIDO1 has a mutation status of E140Q, The gene HELZ2 has a mutation status of M948V, The gene COL18A1 has a mutation status of W30C, The gene C21orf58 has a mutation status of A116P, The gene PI4KA has a mutation status of M889V, The gene TMEM191C has a mutation status of M213I, The gene TOP3B has a mutation status of R290K, The gene KIAA1671 has a mutation status of P818L, The gene TRIOBP has a mutation status of K189T, The gene EP300 has a mutation status of C1201Y, The gene CYB5R3 has a mutation status of S82L, The gene ZBED4 has a mutation status of M1036L, The gene PANX2 has a mutation status of R464H, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene PNPLA4 has a mutation status of E72Q, The gene DCAF8L2 has a mutation status of N310S, The gene FAM47C has a mutation status of A132V, The gene KDM6A has a mutation status of E895*, The gene SPANXN5 has a mutation status of L67L, The gene PHKA1 has a mutation status of G1001W, The gene XPNPEP2 has a mutation status of G453R, The gene AC236972.4 has a mutation status of S1611S, The gene HCFC1 has a mutation status of A1353S, The gene MT-ND1 has a mutation status of A147T, The gene MT-CO3 has a mutation status of A200T, The gene MT-CYB has a mutation status of L363L, The gene MEGF6 has a mutation status of Q117E, The gene PLOD1 has a mutation status of G156D, The gene PRAMEF13 has a mutation status of T257I, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PLEKHM2 has a mutation status of I972I, The gene SPEN has a mutation status of E1962del, The gene GPATCH3 has a mutation status of E8*, The gene HCRTR1 has a mutation status of V93I, The gene ZMYM4 has a mutation status of N788fs, The gene NCDN has a mutation status of P613L, The gene NDUFS5 has a mutation status of T72M, The gene P3H1 has a mutation status of L258fs, The gene B4GALT2 has a mutation status of F212V, The gene TTC22 has a mutation status of D362E, The gene L1TD1 has a mutation status of M171T, The gene KANK4 has a mutation status of E262*, The gene DNAJC6 has a mutation status of H549P, The gene LRRIQ3 has a mutation status of M588I, The gene ST6GALNAC3 has a mutation status of I48M, The gene ADGRL2 has a mutation status of I458V, The gene TTLL7 has a mutation status of Q611Q, The gene MCOLN3 has a mutation status of D263D, The gene CCN1 has a mutation status of G184E, The gene CLCA4 has a mutation status of H100Y, The gene RPAP2 has a mutation status of L587L, The gene STRIP1 has a mutation status of P21Q, The gene STRIP1 has a mutation status of F436F, The gene ST7L has a mutation status of P471P, The gene CD101 has a mutation status of R376K, The gene PHGDH has a mutation status of R236C, The gene PPIAL4H has a mutation status of N102I, The gene OTUD7B has a mutation status of G396V, The gene RPRD2 has a mutation status of S545N, The gene SETDB1 has a mutation status of M1151V, The gene BNIPL has a mutation status of E37E, The gene FLG has a mutation status of H2618N, The gene LCE3C has a mutation status of C3C, The gene LCE1A has a mutation status of K32E, The gene UBAP2L has a mutation status of S673*, The gene ASH1L has a mutation status of R1852L, The gene ARHGEF2 has a mutation status of R581Q, The gene ETV3L has a mutation status of E319D, The gene OR10T2 has a mutation status of S70fs, The gene DCAF8 has a mutation status of T193S, The gene CD244 has a mutation status of T193I, The gene XPR1 has a mutation status of F546F, The gene EDEM3 has a mutation status of S514L, The gene HMCN1 has a mutation status of E5601K, The gene UCHL5 has a mutation status of I286I, The gene TMEM81 has a mutation status of R159C, The gene PROX1 has a mutation status of P728L, The gene DISP1 has a mutation status of L431L, The gene DNAH14 has a mutation status of K3195N, The gene OBSCN has a mutation status of A2212L, The gene RYR2 has a mutation status of R2401H, The gene WDR64 has a mutation status of S721N, The gene OR2T4 has a mutation status of V109L, The gene PXDN has a mutation status of D1432H, The gene KIDINS220 has a mutation status of S1462L, The gene SMC6 has a mutation status of L216I, The gene GDF7 has a mutation status of C414*, The gene APOB has a mutation status of N3977H, The gene APOB has a mutation status of D2277E, The gene OTOF has a mutation status of T1904T, The gene CAD has a mutation status of V1294F, The gene FOSL2 has a mutation status of G197fs, The gene FOSL2 has a mutation status of G197G, The gene ATL2 has a mutation status of E78A, The gene USP34 has a mutation status of T3460T, The gene APLF has a mutation status of S267S, The gene FAM136A has a mutation status of E180E, The gene TET3 has a mutation status of R160T, The gene KRCC1 has a mutation status of V132V, The gene KCNIP3 has a mutation status of H164H, The gene CNNM3 has a mutation status of V431V, The gene ZAP70 has a mutation status of M549V, The gene LIPT1 has a mutation status of H239N, The gene FHL2 has a mutation status of R242W, The gene IL1A has a mutation status of L204L, The gene IL1F10 has a mutation status of Q62*, The gene SLC35F5 has a mutation status of I272V, The gene R3HDM1 has a mutation status of F1004I, The gene GALNT5 has a mutation status of E564G, The gene IFIH1 has a mutation status of I441I, The gene UBR3 has a mutation status of S325Y, The gene WIPF1 has a mutation status of S344P, The gene PDE11A has a mutation status of L662V, The gene FSIP2 has a mutation status of V2615V, The gene FSIP2 has a mutation status of S3169P, The gene STAT1 has a mutation status of L466L, The gene STAT4 has a mutation status of L272L, The gene SATB2 has a mutation status of S299Y, The gene STRADB has a mutation status of Y245C, The gene TMEM237 has a mutation status of R192H, The gene FASTKD2 has a mutation status of N263S, The gene IGFBP5 has a mutation status of S145F, The gene ZNF142 has a mutation status of E216K, The gene SPEG has a mutation status of R1616W, The gene INHA has a mutation status of R232C, The gene SP110 has a mutation status of R56R, The gene CROCC2 has a mutation status of S622Y, The gene MTERF4 has a mutation status of Q75fs, The gene ANO7 has a mutation status of A44fs, The gene CRBN has a mutation status of S379N, The gene TMEM40 has a mutation status of K49E, The gene CAPN7 has a mutation status of T312T, The gene COLQ has a mutation status of S187S, The gene RFTN1 has a mutation status of Q537L, The gene PLCD1 has a mutation status of R628Q, The gene CCR1 has a mutation status of L331H, The gene CSPG5 has a mutation status of L89L, The gene TCTA has a mutation status of H101D, The gene HYAL3 has a mutation status of L166L, The gene GPR62 has a mutation status of R82H, The gene CCDC66 has a mutation status of D856fs, The gene PTPRG has a mutation status of C751F, The gene CRYBG3 has a mutation status of R2360C, The gene CRYBG3 has a mutation status of E2763*, The gene PODXL2 has a mutation status of Q202R, The gene PODXL2 has a mutation status of P304L, The gene EFCC1 has a mutation status of V281M, The gene ACKR4 has a mutation status of D10N, The gene AMOTL2 has a mutation status of R605*, The gene TRIM42 has a mutation status of K620K, The gene XRN1 has a mutation status of P1658S, The gene SLITRK3 has a mutation status of T567N, The gene TNIK has a mutation status of R511R, The gene KLHL24 has a mutation status of Y584C, The gene BCL6 has a mutation status of F611F, The gene LPP has a mutation status of R246W, The gene LPP has a mutation status of C454*, The gene ATP13A5 has a mutation status of Q1212E, The gene ATP13A4 has a mutation status of R694Q, The gene TFRC has a mutation status of A54A, The gene TAPT1 has a mutation status of A9A, The gene LDB2 has a mutation status of G331N, The gene BEND4 has a mutation status of R165Q, The gene PDGFRA has a mutation status of A170A, The gene UGT2B15 has a mutation status of R419K, The gene CSN3 has a mutation status of P56T, The gene MAPK10 has a mutation status of P357P, The gene SLC9B2 has a mutation status of S241F, The gene TBCK has a mutation status of S277*, The gene MGAT4D has a mutation status of K328K, The gene RNF150 has a mutation status of P160L, The gene OTUD4 has a mutation status of S1072fs, The gene OTUD4 has a mutation status of E1071fs, The gene FHDC1 has a mutation status of A680S, The gene LRAT has a mutation status of S27W, The gene CEP44 has a mutation status of M213I, The gene ADAM29 has a mutation status of H333D, The gene FAT1 has a mutation status of S2682*, The gene SLC9A3 has a mutation status of S305S, The gene TRIO has a mutation status of D1310N, The gene AGXT2 has a mutation status of E175K, The gene IL7R has a mutation status of D313G, The gene UGT3A2 has a mutation status of L124I, The gene NIPBL has a mutation status of R808*, The gene NIPBL has a mutation status of E844Q, The gene NIPBL has a mutation status of A1308P, The gene DAB2 has a mutation status of D46N, The gene NIM1K has a mutation status of V139L, The gene ZBED3 has a mutation status of L155A, The gene AP3B1 has a mutation status of K874fs, The gene ARSB has a mutation status of R489K, The gene DMGDH has a mutation status of R510C, The gene ADGRV1 has a mutation status of G1829G, The gene PCDHA1 has a mutation status of A452A, The gene PCDHA12 has a mutation status of T400I, The gene PCDHB6 has a mutation status of N553N, The gene SLC25A2 has a mutation status of M293I, The gene SH3RF2 has a mutation status of E17G, The gene ARHGEF37 has a mutation status of L183M, The gene SLIT3 has a mutation status of T209I, The gene CPLX2 has a mutation status of V120V, The gene EIF4E1B has a mutation status of T158M, The gene PHYKPL has a mutation status of M415V, The gene NQO2 has a mutation status of R50G, The gene SNRNP48 has a mutation status of E88del, The gene FAM8A1 has a mutation status of E253Q, The gene H2BC4 has a mutation status of A75A, The gene HLA-C has a mutation status of H212H, The gene HLA-C has a mutation status of E207D, The gene PRRC2A has a mutation status of E1800E, The gene HLA-DRB1 has a mutation status of S66N, The gene HLA-DRB1 has a mutation status of W38E, The gene DAXX has a mutation status of A368A, The gene PHF1 has a mutation status of D274N, The gene RAB44 has a mutation status of V940V, The gene RAB44 has a mutation status of R995G, The gene XPO5 has a mutation status of A802A, The gene OPN5 has a mutation status of H368H, The gene DEFB112 has a mutation status of P18T, The gene BMP5 has a mutation status of K72I, The gene ADGRB3 has a mutation status of S129*, The gene IRAK1BP1 has a mutation status of E147Q, The gene SNAP91 has a mutation status of E436K, The gene HACE1 has a mutation status of S709Y, The gene SLC16A10 has a mutation status of A455A, The gene REV3L has a mutation status of I1994L, The gene RNF146 has a mutation status of S341T, The gene HIVEP2 has a mutation status of L2305F, The gene SCAF8 has a mutation status of I1027N, The gene CYTH3 has a mutation status of K82E, The gene ZNF316 has a mutation status of R702H, The gene HNRNPA2B1 has a mutation status of PG211del, The gene CDK13 has a mutation status of E1019*, The gene CCM2 has a mutation status of G377S, The gene ABCA13 has a mutation status of S294S, The gene ABCA13 has a mutation status of T1147T, The gene ZNF727 has a mutation status of M33I, The gene MLXIPL has a mutation status of P491L, The gene PCLO has a mutation status of Q462H, The gene TRIP6 has a mutation status of F363L, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MYL10 has a mutation status of D167V, The gene FBXL13 has a mutation status of N280K, The gene RELN has a mutation status of D2171G, The gene SRPK2 has a mutation status of D54A, The gene SLC26A3 has a mutation status of L39L, The gene LAMB4 has a mutation status of A1699V, The gene RNF148 has a mutation status of N33S, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene TBXAS1 has a mutation status of H165N, The gene MGAM2 has a mutation status of R1566I, The gene NOBOX has a mutation status of H447Y, The gene CUL1 has a mutation status of S114T, The gene REPIN1 has a mutation status of A370A, The gene KCNH2 has a mutation status of S959F, The gene NOS3 has a mutation status of S114F, The gene MNX1 has a mutation status of A124T, The gene MNX1 has a mutation status of G108R, The gene RP1L1 has a mutation status of D2375E, The gene GPAT4 has a mutation status of A34V, The gene CEBPD has a mutation status of M1I, The gene PI15 has a mutation status of C245Y, The gene CNGB3 has a mutation status of R456R, The gene PKHD1L1 has a mutation status of S3275S, The gene MAFA has a mutation status of G328R, The gene GSDMD has a mutation status of G347S, The gene EPPK1 has a mutation status of R2374R, The gene MROH1 has a mutation status of S873G, The gene SCRT1 has a mutation status of D13D, The gene DOCK8 has a mutation status of E1398D, The gene DOCK8 has a mutation status of D1464E, The gene CNTLN has a mutation status of D217H, The gene TAF1L has a mutation status of G979fs, The gene RUSC2 has a mutation status of L231R, The gene ZBTB5 has a mutation status of D82N, The gene ZNF658 has a mutation status of G408V, The gene PRUNE2 has a mutation status of D514E, The gene FOXB2 has a mutation status of P188L, The gene SEMA4D has a mutation status of P302L, The gene ERCC6L2 has a mutation status of P100A, The gene INVS has a mutation status of R909R, The gene PLPPR1 has a mutation status of E89D, The gene PPP3R2 has a mutation status of D16E, The gene AL160272.2 has a mutation status of R53L, The gene CNTRL has a mutation status of V656F, The gene TTC16 has a mutation status of T803A, The gene GOLGA2 has a mutation status of E702K, The gene COQ4 has a mutation status of L112V, The gene CERCAM has a mutation status of Q162K, The gene REXO4 has a mutation status of L229L, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene CCDC187 has a mutation status of E1017E, The gene INPP5E has a mutation status of G157W, The gene NOTCH1 has a mutation status of R1350L, The gene AJM1 has a mutation status of V387I, The gene FBXW5 has a mutation status of V234M, The gene CACNA1B has a mutation status of R1062Q, The gene CUBN has a mutation status of H2366N, The gene ENKUR has a mutation status of N77S, The gene GAD2 has a mutation status of A406V, The gene SVIL has a mutation status of R1766S, The gene C10orf71 has a mutation status of N1058K, The gene WASHC2A has a mutation status of G698R, The gene UNC5B has a mutation status of L909R, The gene IFIT3 has a mutation status of A179V, The gene TNKS2 has a mutation status of E914E, The gene SEC31B has a mutation status of W149L, The gene SORCS1 has a mutation status of A542A, The gene STK32C has a mutation status of R87fs, The gene CFAP46 has a mutation status of E1950D, The gene TUBGCP2 has a mutation status of G348fs, The gene HRAS has a mutation status of G12V, The gene PIDD1 has a mutation status of A308S, The gene MUC5AC has a mutation status of A497V, The gene MUC5AC has a mutation status of A5353K, The gene MUC5B has a mutation status of T301I, The gene MUC5B has a mutation status of E1350K, The gene MUC5B has a mutation status of P2250P, The gene MUC5B has a mutation status of V2505V, The gene OR52D1 has a mutation status of L225H, The gene LGR4 has a mutation status of T709T, The gene RAG1 has a mutation status of V65V, The gene HARBI1 has a mutation status of Y15H, The gene OR5D13 has a mutation status of Q198H, The gene OR5D18 has a mutation status of A275V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR1S2 has a mutation status of L114L, The gene MPEG1 has a mutation status of T206I, The gene OOSP4B has a mutation status of S62S, The gene POLA2 has a mutation status of L319L, The gene SPTBN2 has a mutation status of T700T, The gene SPTBN2 has a mutation status of T155T, The gene C2CD3 has a mutation status of R2252K, The gene TENM4 has a mutation status of P215P, The gene DLG2 has a mutation status of V353M, The gene DLG2 has a mutation status of I234V, The gene TRPC6 has a mutation status of K704K, The gene DDI1 has a mutation status of R393*, The gene CASP1 has a mutation status of A384V, The gene ATM has a mutation status of K2440R, The gene ZC3H12C has a mutation status of R311H, The gene DRD2 has a mutation status of A420A, The gene NECTIN1 has a mutation status of R210H, The gene SORL1 has a mutation status of D140N, The gene SORL1 has a mutation status of E746*, The gene SLC37A2 has a mutation status of L124L, The gene ADAMTS8 has a mutation status of T223A, The gene B4GALNT3 has a mutation status of R844R, The gene CACNA2D4 has a mutation status of V298L, The gene PRMT8 has a mutation status of Q35P, The gene FGF6 has a mutation status of D50E, The gene MFAP5 has a mutation status of Y95Y, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PDE3A has a mutation status of V3V, The gene C2CD5 has a mutation status of G201G, The gene ALG10B has a mutation status of L165L, The gene ALG10B has a mutation status of D218N, The gene LRRK2 has a mutation status of T2158I, The gene FAM186B has a mutation status of F616C, The gene GALNT6 has a mutation status of G518R, The gene KRT77 has a mutation status of L171L, The gene ESPL1 has a mutation status of A938A, The gene OR2AP1 has a mutation status of S36I, The gene METTL7B has a mutation status of V169M, The gene HSD17B6 has a mutation status of Y181*, The gene MARS1 has a mutation status of P206L, The gene TBC1D30 has a mutation status of L45L, The gene WIF1 has a mutation status of A149E, The gene LRRC10 has a mutation status of L103F, The gene MYRFL has a mutation status of P659Q, The gene E2F7 has a mutation status of Q138H, The gene C12orf50 has a mutation status of K186N, The gene FGD6 has a mutation status of S782C, The gene ANKS1B has a mutation status of R590Q, The gene SLC5A8 has a mutation status of G421D, The gene PRDM4 has a mutation status of V277V, The gene ATXN2 has a mutation status of E141K, The gene TPCN1 has a mutation status of R348R, The gene TPCN1 has a mutation status of G428G, The gene KSR2 has a mutation status of S731I, The gene KDM2B has a mutation status of T36S, The gene DNAH10 has a mutation status of S3322S, The gene ADGRD1 has a mutation status of C606F, The gene CRYL1 has a mutation status of T240I, The gene MTUS2 has a mutation status of G215A, The gene NAA16 has a mutation status of E304G, The gene SLAIN1 has a mutation status of G168A, The gene TTC5 has a mutation status of N141N, The gene ZNF219 has a mutation status of F20F, The gene ARHGAP5 has a mutation status of H1316H, The gene AKAP6 has a mutation status of E670*, The gene MAP3K9 has a mutation status of P795P, The gene PCNX1 has a mutation status of W2286fs, The gene RGS6 has a mutation status of S311N, The gene UNC79 has a mutation status of A1536A, The gene SERPINA12 has a mutation status of R294R, The gene RTL1 has a mutation status of L219L, The gene ADSS1 has a mutation status of V277M, The gene LINC02203 has a mutation status of I259M, The gene MKRN3 has a mutation status of E9D, The gene APBA2 has a mutation status of A397V, The gene RYR3 has a mutation status of R1028R, The gene TYRO3 has a mutation status of E509fs, The gene ATP8B4 has a mutation status of S259G, The gene GNB5 has a mutation status of I349F, The gene UNC13C has a mutation status of Q1582H, The gene NEDD4 has a mutation status of I1125V, The gene SNX22 has a mutation status of C149C, The gene ANKDD1A has a mutation status of L516L, The gene HIGD2B has a mutation status of Y65H, The gene EDC3 has a mutation status of G208E, The gene NEIL1 has a mutation status of R339W, The gene ADAMTS7 has a mutation status of P1569P, The gene TMED3 has a mutation status of A21A, The gene AP3B2 has a mutation status of A902S, The gene PDE8A has a mutation status of R655W, The gene ABHD2 has a mutation status of F46F, The gene ANPEP has a mutation status of S613R, The gene ANPEP has a mutation status of N527K, The gene CHD2 has a mutation status of T320T, The gene PDIA2 has a mutation status of E145K, The gene PRR35 has a mutation status of A113V, The gene MSLNL has a mutation status of R132R, The gene PKD1 has a mutation status of R2213Q, The gene PGP has a mutation status of L16L, The gene KREMEN2 has a mutation status of L137I, The gene SLX4 has a mutation status of K291K, The gene PDILT has a mutation status of L457L, The gene SEZ6L2 has a mutation status of H659N, The gene ZNF768 has a mutation status of R337H, The gene HEATR3 has a mutation status of A436V, The gene NOD2 has a mutation status of P269L, The gene KARS1 has a mutation status of L443L, The gene CPHXL has a mutation status of K64E, The gene CDYL2 has a mutation status of V135L, The gene PLCG2 has a mutation status of G654G, The gene ADAD2 has a mutation status of S62L, The gene ZFPM1 has a mutation status of P737P, The gene GAS8 has a mutation status of V159V, The gene SLC43A2 has a mutation status of R403H, The gene TSR1 has a mutation status of R737W, The gene CLUH has a mutation status of I1211M, The gene SPNS3 has a mutation status of A276S, The gene ALOX15 has a mutation status of T537S, The gene FGF11 has a mutation status of R166C, The gene TP53 has a mutation status of Y126*, The gene TRAPPC1 has a mutation status of L37V, The gene NTN1 has a mutation status of S67C, The gene MYH3 has a mutation status of E1788K, The gene SPECC1 has a mutation status of Y547Y, The gene SLFN12 has a mutation status of T361M, The gene SLFN13 has a mutation status of I665I, The gene CCL4L2 has a mutation status of P67R, The gene EPOP has a mutation status of E2*, The gene FBXO47 has a mutation status of L224F, The gene MED1 has a mutation status of A96T, The gene MSL1 has a mutation status of V376V, The gene KCNH4 has a mutation status of G213G, The gene HCRT has a mutation status of R79R, The gene ITGA2B has a mutation status of L654F, The gene TBKBP1 has a mutation status of S351P, The gene TTLL6 has a mutation status of K728*, The gene DHX40 has a mutation status of P87S, The gene POLG2 has a mutation status of H313N, The gene AXIN2 has a mutation status of R610fs, The gene ABCA10 has a mutation status of W270C, The gene MYO15B has a mutation status of P1150S, The gene ACOX1 has a mutation status of T155T, The gene CARD14 has a mutation status of I989I, The gene RNF213 has a mutation status of G3533S, The gene GPS1 has a mutation status of Y50*, The gene PIEZO2 has a mutation status of S2577*, The gene LAMA3 has a mutation status of C436Y, The gene ASXL3 has a mutation status of Q1897K, The gene ZNF396 has a mutation status of C312S, The gene EPG5 has a mutation status of L361fs, The gene CCDC68 has a mutation status of E80Q, The gene ST8SIA3 has a mutation status of P50P, The gene ONECUT2 has a mutation status of G45S, The gene CCDC102B has a mutation status of E377K, The gene ADNP2 has a mutation status of P354P, The gene MEX3D has a mutation status of A82V, The gene FZR1 has a mutation status of V14I, The gene ADGRE1 has a mutation status of A540V, The gene MAP2K7 has a mutation status of T190T, The gene MUC16 has a mutation status of G13062G, The gene MUC16 has a mutation status of Q8799E, The gene COL5A3 has a mutation status of V1162I, The gene TNPO2 has a mutation status of P431P, The gene STX10 has a mutation status of D196V, The gene CC2D1A has a mutation status of V449M, The gene ADGRL1 has a mutation status of A6fs, The gene PKN1 has a mutation status of P343T, The gene WIZ has a mutation status of H88Y, The gene CPAMD8 has a mutation status of H1834R, The gene DDX49 has a mutation status of L385L, The gene NCAN has a mutation status of R1299G, The gene ZNF66 has a mutation status of F97F, The gene ZNF729 has a mutation status of C908S, The gene CD22 has a mutation status of P341L, The gene FFAR2 has a mutation status of N293S, The gene HAUS5 has a mutation status of A627S, The gene RASGRP4 has a mutation status of T418T, The gene RASGRP4 has a mutation status of S194F, The gene MYPOP has a mutation status of P372P, The gene ARHGAP35 has a mutation status of R1234R, The gene ZC3H4 has a mutation status of P990S, The gene NAPA has a mutation status of A161A, The gene GRIN2D has a mutation status of A1092T, The gene RASIP1 has a mutation status of A951G, The gene IZUMO2 has a mutation status of M178I, The gene MYH14 has a mutation status of R1735Q, The gene ZNF845 has a mutation status of E884D, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene AURKC has a mutation status of R165K, The gene ZNF776 has a mutation status of T427A, The gene ADAM33 has a mutation status of S61S, The gene ZNF337 has a mutation status of Q619E, The gene TPX2 has a mutation status of S121C, The gene EFCAB8 has a mutation status of H313Y, The gene BPIFA1 has a mutation status of G86D, The gene MMP24 has a mutation status of A68E, The gene PCIF1 has a mutation status of A552G, The gene CDH22 has a mutation status of G712A, The gene STX16 has a mutation status of F10F, The gene CDH4 has a mutation status of I832I, The gene LAMA5 has a mutation status of H424H, The gene TCFL5 has a mutation status of R186H, The gene DIDO1 has a mutation status of E140Q, The gene HELZ2 has a mutation status of M948V, The gene NCAM2 has a mutation status of K806N, The gene ADAMTS5 has a mutation status of G171E, The gene UMODL1 has a mutation status of N652N, The gene KRTAP10-11 has a mutation status of G293A, The gene COL18A1 has a mutation status of W30C, The gene MCM3AP has a mutation status of C1561R, The gene C21orf58 has a mutation status of A116P, The gene PI4KA has a mutation status of M889V, The gene TOP3B has a mutation status of R290K, The gene GSTT4 has a mutation status of R208S, The gene KIAA1671 has a mutation status of P818L, The gene MTMR3 has a mutation status of H991Y, The gene SFI1 has a mutation status of Y152*, The gene SLC5A4 has a mutation status of D585Y, The gene TRIOBP has a mutation status of K189T, The gene EP300 has a mutation status of C1201Y, The gene CYB5R3 has a mutation status of S82L, The gene EFCAB6 has a mutation status of S27S, The gene ZBED4 has a mutation status of K292Q, The gene PNPLA4 has a mutation status of E72Q, The gene ARX has a mutation status of A111A, The gene KDM6A has a mutation status of E895*, The gene AKAP4 has a mutation status of N641K, The gene OPHN1 has a mutation status of S605S, The gene PHKA1 has a mutation status of G1001W, The gene PGAM4 has a mutation status of A28T, The gene TENM1 has a mutation status of L1600I, The gene XPNPEP2 has a mutation status of G453R, The gene MAGEA3 has a mutation status of K292T, The gene PNMA6E has a mutation status of A564A, The gene HCFC1 has a mutation status of A1353S, The gene EMD has a mutation status of G218R, The gene MT-ND1 has a mutation status of A147T, The gene MT-CO3 has a mutation status of A200T, The gene MT-CYB has a mutation status of L363L
BLCA
The gene PANK4 has a mutation status of F567F, The gene ESPN has a mutation status of P452T, The gene PEX14 has a mutation status of S265L, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of L28L, The gene PRAMEF18 has a mutation status of V27I, The gene SRRM1 has a mutation status of R520R, The gene RHD has a mutation status of V348V, The gene EYA3 has a mutation status of V366L, The gene ZMYM6 has a mutation status of D664G, The gene INPP5B has a mutation status of V662V, The gene NT5C1A has a mutation status of A352V, The gene SZT2 has a mutation status of A317G, The gene ADGRL2 has a mutation status of W159*, The gene SYCP1 has a mutation status of T531T, The gene FMO5 has a mutation status of I530T, The gene S100A10 has a mutation status of A77V, The gene SMCP has a mutation status of C65*, The gene MEX3A has a mutation status of L331L, The gene PRRC2C has a mutation status of K533R, The gene LAMC2 has a mutation status of R894H, The gene ASPM has a mutation status of R3392K, The gene PIK3C2B has a mutation status of S242S, The gene RAB7B has a mutation status of G65G, The gene PIGR has a mutation status of A639A, The gene PROX1 has a mutation status of A32E, The gene PGBD5 has a mutation status of H396Y, The gene MAP3K21 has a mutation status of P933P, The gene LYST has a mutation status of L2438Q, The gene WDR64 has a mutation status of H365Y, The gene OR2M3 has a mutation status of A119A, The gene RAD51AP2 has a mutation status of D698E, The gene TDRD15 has a mutation status of G1405R, The gene PPM1G has a mutation status of E451K, The gene PIGF has a mutation status of K76K, The gene EXOC6B has a mutation status of G4A, The gene ACTG2 has a mutation status of E199K, The gene KDM3A has a mutation status of A765V, The gene CKAP2L has a mutation status of P91Q, The gene TTN has a mutation status of C29309S, The gene TTN has a mutation status of A23795D, The gene KANSL1L has a mutation status of N615S, The gene ERBB4 has a mutation status of Y1242C, The gene ASIC4 has a mutation status of A143V, The gene IRS1 has a mutation status of R327C, The gene SCYGR2 has a mutation status of H97S, The gene INPP5D has a mutation status of S156S, The gene ESPNL has a mutation status of T17T, The gene BRPF1 has a mutation status of D852D, The gene VILL has a mutation status of R410H, The gene ZNF619 has a mutation status of Q596K, The gene ZNF619 has a mutation status of D597V, The gene CDCP1 has a mutation status of T778T, The gene RFT1 has a mutation status of V55M, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene UBA3 has a mutation status of A380G, The gene ZNF717 has a mutation status of T334T, The gene PROS1 has a mutation status of R41H, The gene NECTIN3 has a mutation status of P45fs, The gene NECTIN3 has a mutation status of P45T, The gene CD200 has a mutation status of Q102K, The gene MYLK has a mutation status of T151T, The gene HEG1 has a mutation status of T957T, The gene PLXNA1 has a mutation status of G36G, The gene HLTF has a mutation status of V287F, The gene KCNAB1 has a mutation status of G159D, The gene CCNL1 has a mutation status of R264R, The gene TNIK has a mutation status of G884V, The gene PIK3CA has a mutation status of E545K, The gene FAM131A has a mutation status of S119N, The gene MAP3K13 has a mutation status of D380N, The gene CLDN1 has a mutation status of Q163L, The gene ADD1 has a mutation status of S427L, The gene HTT has a mutation status of S3025S, The gene EVC has a mutation status of S665L, The gene HMX1 has a mutation status of P291T, The gene CD38 has a mutation status of P8P, The gene QDPR has a mutation status of L208L, The gene SLIT2 has a mutation status of E1104K, The gene ADGRA3 has a mutation status of P648L, The gene RFC1 has a mutation status of A247V, The gene LIAS has a mutation status of M180T, The gene GABRA2 has a mutation status of S412C, The gene ATP10D has a mutation status of Y81S, The gene EPHA5 has a mutation status of L1008P, The gene TMPRSS11B has a mutation status of V56G, The gene MRPL1 has a mutation status of G174G, The gene PRKG2 has a mutation status of R259*, The gene FAM13A has a mutation status of N217K, The gene DCHS2 has a mutation status of E1201A, The gene DDX60L has a mutation status of S1577S, The gene CLCN3 has a mutation status of W555*, The gene TENM3 has a mutation status of P1998H, The gene CASP3 has a mutation status of S29fs, The gene ZFP42 has a mutation status of G65E, The gene SEMA5A has a mutation status of P45H, The gene DNAH5 has a mutation status of D534D, The gene CDH18 has a mutation status of K339R, The gene ISL1 has a mutation status of R130P, The gene MAST4 has a mutation status of K2244Q, The gene ZBED3 has a mutation status of L155A, The gene AC022414.1 has a mutation status of R302Q, The gene ACOT12 has a mutation status of A403N, The gene XRCC4 has a mutation status of K197R, The gene VCAN has a mutation status of L2256P, The gene RGMB has a mutation status of G327S, The gene TSLP has a mutation status of S48S, The gene JAKMIP2 has a mutation status of I265V, The gene TENM2 has a mutation status of T856T, The gene SQSTM1 has a mutation status of E101D, The gene H2BC9 has a mutation status of P11P, The gene HLA-A has a mutation status of K292E, The gene PRR3 has a mutation status of P79L, The gene DHX16 has a mutation status of R525R, The gene MSH5 has a mutation status of S3F, The gene VWA7 has a mutation status of T26T, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene NUDT3 has a mutation status of H132H, The gene CLPSL1 has a mutation status of C57W, The gene SLC26A8 has a mutation status of G964C, The gene DNAH8 has a mutation status of I4199T, The gene EYS has a mutation status of K1077N, The gene COL9A1 has a mutation status of G364C, The gene COL12A1 has a mutation status of T1001T, The gene SNAP91 has a mutation status of A366S, The gene EPHA7 has a mutation status of V418L, The gene TRDN has a mutation status of E519K, The gene TAAR6 has a mutation status of Y311H, The gene ALDH8A1 has a mutation status of P269S, The gene RMND1 has a mutation status of F199L, The gene VWDE has a mutation status of I332N, The gene PDK4 has a mutation status of A144T, The gene TRIM4 has a mutation status of P104T, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S558T, The gene MUC3A has a mutation status of R931P, The gene MUC3A has a mutation status of G932A, The gene MUC3A has a mutation status of V2475S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene RELN has a mutation status of E2374K, The gene COPG2 has a mutation status of T552T, The gene PLXNA4 has a mutation status of W8C, The gene PRSS1 has a mutation status of N77N, The gene ZNF467 has a mutation status of V508M, The gene ZNF862 has a mutation status of V588M, The gene GIMAP7 has a mutation status of S73R, The gene ASB10 has a mutation status of G248V, The gene SH2D4A has a mutation status of P116T, The gene RP1 has a mutation status of G1355R, The gene LYN has a mutation status of K404K, The gene NBN has a mutation status of R43*, The gene ZFPM2 has a mutation status of E800Q, The gene ZNF572 has a mutation status of L179I, The gene HHLA1 has a mutation status of N121S, The gene JRK has a mutation status of K115R, The gene CYP11B2 has a mutation status of A414P, The gene EPPK1 has a mutation status of AA2632del, The gene MROH1 has a mutation status of S1272F, The gene CPSF1 has a mutation status of R63W, The gene GPT has a mutation status of P472S, The gene LRRC14 has a mutation status of R28R, The gene DOCK8 has a mutation status of N1195N, The gene KCNV2 has a mutation status of H26Q, The gene PTPRD has a mutation status of Q1597*, The gene CCDC171 has a mutation status of L413L, The gene CCDC171 has a mutation status of E551V, The gene PRSS3 has a mutation status of G208R, The gene CNTNAP3 has a mutation status of A1204T, The gene DAPK1 has a mutation status of I1065I, The gene SHC3 has a mutation status of M1I, The gene WNK2 has a mutation status of L312Q, The gene TDRD7 has a mutation status of E63D, The gene NCBP1 has a mutation status of K67K, The gene TRMO has a mutation status of S191Y, The gene COL15A1 has a mutation status of G664E, The gene STX17 has a mutation status of G241G, The gene STX17 has a mutation status of G245G, The gene NIPSNAP3B has a mutation status of N82K, The gene PTPN3 has a mutation status of M403I, The gene SVEP1 has a mutation status of A1142S, The gene INIP has a mutation status of A70A, The gene WDR31 has a mutation status of Q204*, The gene ADGRD2 has a mutation status of R656C, The gene TTC16 has a mutation status of D373N, The gene LRRC8A has a mutation status of T170M, The gene UCK1 has a mutation status of L62L, The gene PPP1R26 has a mutation status of A1185S, The gene CCDC187 has a mutation status of R945P, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of R294H, The gene MRC1 has a mutation status of Y719Y, The gene SLC39A12 has a mutation status of W446*, The gene ZNF22 has a mutation status of G27V, The gene WASHC2C has a mutation status of K1199R, The gene WDFY4 has a mutation status of V2122L, The gene ERCC6 has a mutation status of S1099R, The gene ERCC6 has a mutation status of V83I, The gene CSTF2T has a mutation status of Q167*, The gene SLC25A16 has a mutation status of G299A, The gene EIF4EBP2 has a mutation status of S14R, The gene MRPS16 has a mutation status of N69K, The gene CFAP70 has a mutation status of L451L, The gene NDST2 has a mutation status of R502G, The gene NRG3 has a mutation status of P122P, The gene LIPF has a mutation status of S134A, The gene TM9SF3 has a mutation status of T373A, The gene PIK3AP1 has a mutation status of E50K, The gene SMC3 has a mutation status of L1017L, The gene MUC6 has a mutation status of P1487L, The gene MUC5AC has a mutation status of D3964D, The gene DNHD1 has a mutation status of E4427K, The gene OR2D3 has a mutation status of Q12Q, The gene USH1C has a mutation status of K279K, The gene HTATIP2 has a mutation status of L170V, The gene NELL1 has a mutation status of E445V, The gene LUZP2 has a mutation status of P290L, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TNKS1BP1 has a mutation status of A104A, The gene PRG3 has a mutation status of C107*, The gene OR6Q1 has a mutation status of L27F, The gene GLYATL1B has a mutation status of R9W, The gene DAGLA has a mutation status of H471Y, The gene NRXN2 has a mutation status of Q1173K, The gene FOSL1 has a mutation status of R94Q, The gene TCIRG1 has a mutation status of G172G, The gene CLPB has a mutation status of K10NL, The gene C2CD3 has a mutation status of H2035L, The gene TPBGL has a mutation status of A247V, The gene FAM181B has a mutation status of G306S, The gene PIWIL4 has a mutation status of L551L, The gene CEP126 has a mutation status of H1081Y, The gene MMP13 has a mutation status of R458C, The gene DDX10 has a mutation status of H27R, The gene CD3E has a mutation status of K153T, The gene DPAGT1 has a mutation status of R156R, The gene NECTIN1 has a mutation status of A474A, The gene POU2F3 has a mutation status of P4A, The gene NCAPD3 has a mutation status of I691I, The gene NCAPD3 has a mutation status of A688D, The gene SLC6A12 has a mutation status of V59V, The gene C12orf4 has a mutation status of R335Q, The gene RIMKLB has a mutation status of M98V, The gene PZP has a mutation status of E152*, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R30 has a mutation status of I33T, The gene PRB4 has a mutation status of R122G, The gene LRMP has a mutation status of T107I, The gene LRMP has a mutation status of A714S, The gene PTHLH has a mutation status of T143T, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of I220G, The gene GXYLT1 has a mutation status of S212Y, The gene GXYLT1 has a mutation status of V28K, The gene FAM186B has a mutation status of W566C, The gene FAM186A has a mutation status of P1674A, The gene GALNT6 has a mutation status of S258S, The gene KRT2 has a mutation status of Q161H, The gene BAZ2A has a mutation status of E621*, The gene BBS10 has a mutation status of G401E, The gene EEA1 has a mutation status of L230L, The gene MYBPC1 has a mutation status of I86T, The gene ATP6V0A2 has a mutation status of S659C, The gene ADGRD1 has a mutation status of Q37H, The gene FBRSL1 has a mutation status of S752S, The gene MIPEP has a mutation status of S595*, The gene SPART has a mutation status of G386R, The gene SMAD9 has a mutation status of V42L, The gene NUDT15 has a mutation status of E151K, The gene TRIM13 has a mutation status of E165K, The gene DLEU7 has a mutation status of S129L, The gene JPH4 has a mutation status of R233C, The gene ADCY4 has a mutation status of L655L, The gene CNIH1 has a mutation status of F22F, The gene KIAA0586 has a mutation status of L1378I, The gene DACT1 has a mutation status of A590A, The gene GPR68 has a mutation status of Q95H, The gene COX8C has a mutation status of P38S, The gene PPP4R4 has a mutation status of D283Y, The gene SLC25A29 has a mutation status of P37L, The gene CEP170B has a mutation status of D1133G, The gene BTBD6 has a mutation status of G475R, The gene PAK6 has a mutation status of R637Q, The gene PPP1R14D has a mutation status of K135R, The gene VPS18 has a mutation status of L869F, The gene OIP5 has a mutation status of P5S, The gene LCMT2 has a mutation status of R8S, The gene TUBGCP4 has a mutation status of R647*, The gene SERF2 has a mutation status of T88T, The gene DMXL2 has a mutation status of I699T, The gene LEO1 has a mutation status of D68D, The gene ONECUT1 has a mutation status of C321Y, The gene ANKDD1A has a mutation status of L516L, The gene UBAP1L has a mutation status of A124V, The gene SMAD3 has a mutation status of V90F, The gene PKM has a mutation status of R383C, The gene ADPGK has a mutation status of E216K, The gene ULK3 has a mutation status of RR421del, The gene GOLGA6L9 has a mutation status of R6H, The gene GOLGA6L9 has a mutation status of A373P, The gene AGBL1 has a mutation status of E167D, The gene ARRDC4 has a mutation status of N169N, The gene FBXL16 has a mutation status of S398F, The gene CACNA1H has a mutation status of M611I, The gene RPL3L has a mutation status of R234L, The gene BICDL2 has a mutation status of E171E, The gene ZSCAN10 has a mutation status of E508K, The gene PPL has a mutation status of E1254K, The gene COG7 has a mutation status of K84K, The gene SLC9A5 has a mutation status of P466P, The gene AARS1 has a mutation status of P906P, The gene ZNF778 has a mutation status of T416fs, The gene VPS9D1 has a mutation status of A23S, The gene ITGAE has a mutation status of G103G, The gene NLRP1 has a mutation status of P242Q, The gene MYH3 has a mutation status of E1121E, The gene MPRIP has a mutation status of L858L, The gene CCL4L2 has a mutation status of P67R, The gene KRT32 has a mutation status of P427I, The gene NPEPPS has a mutation status of E857E, The gene HOXB7 has a mutation status of E216*, The gene KIF2B has a mutation status of D546N, The gene TBX2 has a mutation status of P4L, The gene ACE has a mutation status of S233F, The gene UNK has a mutation status of S517C, The gene QRICH2 has a mutation status of D262E, The gene CBX8 has a mutation status of S316Y, The gene PTPRM has a mutation status of D1063H, The gene SERPINB2 has a mutation status of E160*, The gene MIER2 has a mutation status of E97K, The gene PCSK4 has a mutation status of G302S, The gene THOP1 has a mutation status of V67V, The gene SH2D3A has a mutation status of L120L, The gene AC008878.3 has a mutation status of H233H, The gene MUC16 has a mutation status of D13719Y, The gene MUC16 has a mutation status of P13632fs, The gene MUC16 has a mutation status of V13007G, The gene TYK2 has a mutation status of P117S, The gene KEAP1 has a mutation status of V377V, The gene DNM2 has a mutation status of A796V, The gene PKN1 has a mutation status of T551T, The gene ILVBL has a mutation status of L126F, The gene NWD1 has a mutation status of T933T, The gene CPAMD8 has a mutation status of D684N, The gene ZNF66 has a mutation status of L102fs, The gene ZNF254 has a mutation status of H620N, The gene LSR has a mutation status of T196T, The gene RYR1 has a mutation status of A2141V, The gene KCNJ14 has a mutation status of G116S, The gene NUCB1 has a mutation status of L12P, The gene FUZ has a mutation status of V121M, The gene POLD1 has a mutation status of A916V, The gene ZNF610 has a mutation status of G210C, The gene ZNF610 has a mutation status of L387L, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of Y121Y, The gene LAIR1 has a mutation status of A266fs, The gene LAIR1 has a mutation status of R265G, The gene LILRA2 has a mutation status of W163S, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene KIR2DL1 has a mutation status of T91K, The gene KIR2DL1 has a mutation status of V111L, The gene KIR2DL1 has a mutation status of H203R, The gene USP29 has a mutation status of T709T, The gene SIRPA has a mutation status of L44S, The gene MKKS has a mutation status of N366Y, The gene MMP24 has a mutation status of R369R, The gene ATP9A has a mutation status of P369P, The gene SYCP2 has a mutation status of M477L, The gene BRWD1 has a mutation status of P621S, The gene MX2 has a mutation status of A686T, The gene TRPM2 has a mutation status of R634H, The gene KRTAP10-7 has a mutation status of A50fs, The gene KRTAP10-7 has a mutation status of C52fs, The gene POTEH has a mutation status of W34*, The gene CECR2 has a mutation status of E59K, The gene BCL2L13 has a mutation status of S5fs, The gene PI4KA has a mutation status of D584E, The gene SUSD2 has a mutation status of D77Y, The gene GGT5 has a mutation status of F302L, The gene KIAA1671 has a mutation status of Q1220*, The gene KIAA1671 has a mutation status of G1359E, The gene SLC5A1 has a mutation status of I397T, The gene CSDC2 has a mutation status of D111N, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CELSR1 has a mutation status of R2677R, The gene TUBGCP6 has a mutation status of L1171L, The gene PPP6R2 has a mutation status of G760S, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene SHROOM2 has a mutation status of A1523T, The gene FAM47A has a mutation status of W705*, The gene RBM3 has a mutation status of R145H, The gene TSPYL2 has a mutation status of I276I, The gene HUWE1 has a mutation status of L3620F, The gene PHF8 has a mutation status of H31P, The gene KIF4A has a mutation status of E125Q, The gene MAGEE1 has a mutation status of P154R, The gene NXF3 has a mutation status of R409W, The gene SLC25A5 has a mutation status of G121C, The gene SLC25A5 has a mutation status of T221R, The gene XIAP has a mutation status of F92F, The gene AC236972.4 has a mutation status of S1611S, The gene MT-CO1 has a mutation status of H291H, The gene MT-CO3 has a mutation status of V254I, The gene MT-ND5 has a mutation status of S308S, The gene MT-ND6 has a mutation status of N119D, The gene MT-CYB has a mutation status of T212A, The gene PANK4 has a mutation status of F567F, The gene HES5 has a mutation status of M64I, The gene PRDM16 has a mutation status of A835T, The gene ESPN has a mutation status of P452T, The gene PEX14 has a mutation status of S265L, The gene HNRNPCL2 has a mutation status of E207K, The gene PRAMEF18 has a mutation status of P294P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene RAP1GAP has a mutation status of T639T, The gene CDC42 has a mutation status of L165P, The gene SRRM1 has a mutation status of R520R, The gene RHD has a mutation status of V348V, The gene EYA3 has a mutation status of V366L, The gene YARS1 has a mutation status of I14I, The gene ZMYM6 has a mutation status of D664G, The gene INPP5B has a mutation status of V662V, The gene NT5C1A has a mutation status of A352V, The gene SZT2 has a mutation status of A317G, The gene USP33 has a mutation status of N230Y, The gene ADGRL2 has a mutation status of W159*, The gene SYCP1 has a mutation status of T531T, The gene FMO5 has a mutation status of I530T, The gene GOLPH3L has a mutation status of P189S, The gene S100A10 has a mutation status of A77V, The gene SMCP has a mutation status of C65*, The gene MEX3A has a mutation status of L331L, The gene IGSF9 has a mutation status of G939G, The gene MPZ has a mutation status of A83V, The gene GPA33 has a mutation status of I153I, The gene FMO3 has a mutation status of V127A, The gene PRRC2C has a mutation status of K533R, The gene LAMC2 has a mutation status of R894H, The gene BRINP3 has a mutation status of W20R, The gene KIF21B has a mutation status of A1367A, The gene IGFN1 has a mutation status of K1635E, The gene PIGR has a mutation status of A639A, The gene PROX1 has a mutation status of A32E, The gene OBSCN has a mutation status of R8618W, The gene PGBD5 has a mutation status of H396Y, The gene C1orf131 has a mutation status of A66V, The gene LYST has a mutation status of L2438Q, The gene RYR2 has a mutation status of P4534H, The gene CHRM3 has a mutation status of S319S, The gene OR2M3 has a mutation status of A119A, The gene RAD51AP2 has a mutation status of D698E, The gene TDRD15 has a mutation status of G1405R, The gene FAM228B has a mutation status of Q303fs, The gene BIRC6 has a mutation status of R2915K, The gene PIGF has a mutation status of K76K, The gene EXOC6B has a mutation status of G4A, The gene ACTG2 has a mutation status of E199K, The gene KDM3A has a mutation status of A765V, The gene SLC20A1 has a mutation status of S299S, The gene CKAP2L has a mutation status of P91Q, The gene CLASP1 has a mutation status of V1296L, The gene CERS6 has a mutation status of Q119E, The gene RAPGEF4 has a mutation status of Y986F, The gene TTN has a mutation status of C29309S, The gene TTN has a mutation status of E16950K, The gene TTN has a mutation status of E13174D, The gene ERBB4 has a mutation status of Y1242C, The gene ARPC2 has a mutation status of A268A, The gene ASIC4 has a mutation status of A143V, The gene IRS1 has a mutation status of R327C, The gene INPP5D has a mutation status of S156S, The gene UGT1A7 has a mutation status of M201T, The gene ESPNL has a mutation status of T17T, The gene BRPF1 has a mutation status of D852D, The gene VILL has a mutation status of R410H, The gene ZNF619 has a mutation status of Q596K, The gene ZNF619 has a mutation status of D597V, The gene CDCP1 has a mutation status of T778T, The gene UBA7 has a mutation status of L757L, The gene RFT1 has a mutation status of V55M, The gene UBA3 has a mutation status of A380G, The gene PROS1 has a mutation status of R41H, The gene CRYBG3 has a mutation status of I797I, The gene NECTIN3 has a mutation status of P45fs, The gene NECTIN3 has a mutation status of P45T, The gene SLC9C1 has a mutation status of L183S, The gene CD200 has a mutation status of Q102K, The gene FBXO40 has a mutation status of G337S, The gene MYLK has a mutation status of T151T, The gene HEG1 has a mutation status of T957T, The gene HLTF has a mutation status of V287F, The gene STRIT1 has a mutation status of I20T, The gene CCNL1 has a mutation status of R264R, The gene TRIM59 has a mutation status of E276K, The gene TNIK has a mutation status of G884V, The gene PIK3CA has a mutation status of E545K, The gene FAM131A has a mutation status of S119N, The gene MAP3K13 has a mutation status of D380N, The gene CLDN1 has a mutation status of Q163L, The gene ATP13A5 has a mutation status of S601S, The gene CPN2 has a mutation status of R541R, The gene WDR53 has a mutation status of A39D, The gene TMEM175 has a mutation status of A429fs, The gene DGKQ has a mutation status of P935T, The gene ADD1 has a mutation status of S427L, The gene HTT has a mutation status of S3025S, The gene EVC has a mutation status of S665L, The gene HMX1 has a mutation status of P291T, The gene C1QTNF7 has a mutation status of S157S, The gene QDPR has a mutation status of L208L, The gene SLIT2 has a mutation status of E1104K, The gene SLIT2 has a mutation status of T1221N, The gene ADGRA3 has a mutation status of P648L, The gene SEL1L3 has a mutation status of A343A, The gene RFC1 has a mutation status of V672L, The gene RFC1 has a mutation status of A247V, The gene LIAS has a mutation status of M180T, The gene GABRA2 has a mutation status of S412C, The gene ATP10D has a mutation status of Y81S, The gene EPHA5 has a mutation status of L1008P, The gene TMPRSS11B has a mutation status of V56G, The gene MRPL1 has a mutation status of G174G, The gene FAM13A has a mutation status of N217K, The gene DCHS2 has a mutation status of E1201A, The gene CLCN3 has a mutation status of W555*, The gene CASP3 has a mutation status of S29fs, The gene ZFP42 has a mutation status of G65E, The gene ADAMTS16 has a mutation status of L342L, The gene ADAMTS16 has a mutation status of R1158Q, The gene MARCHF6 has a mutation status of V317F, The gene DNAH5 has a mutation status of D534D, The gene CDH18 has a mutation status of K339R, The gene ERCC8 has a mutation status of K247K, The gene MAST4 has a mutation status of K2244Q, The gene BDP1 has a mutation status of N582N, The gene IQGAP2 has a mutation status of I640I, The gene ZBED3 has a mutation status of L155A, The gene AC022414.1 has a mutation status of R302Q, The gene ACOT12 has a mutation status of A403N, The gene XRCC4 has a mutation status of K197R, The gene VCAN has a mutation status of L2256P, The gene ADGRV1 has a mutation status of S2491P, The gene ADGRV1 has a mutation status of I3765I, The gene RGMB has a mutation status of G327S, The gene TSLP has a mutation status of S48S, The gene FTMT has a mutation status of G185D, The gene SLC22A4 has a mutation status of R227H, The gene SLC4A9 has a mutation status of F434I, The gene JAKMIP2 has a mutation status of I265V, The gene LARP1 has a mutation status of E189E, The gene TENM2 has a mutation status of T856T, The gene ADAMTS2 has a mutation status of Q915K, The gene SQSTM1 has a mutation status of E101D, The gene TBC1D9B has a mutation status of R982W, The gene RNF144B has a mutation status of E15G, The gene RIPOR2 has a mutation status of Q161R, The gene H2BC9 has a mutation status of P11P, The gene PRR3 has a mutation status of P79L, The gene HLA-C has a mutation status of H212H, The gene HLA-C has a mutation status of E207D, The gene MSH5 has a mutation status of S3F, The gene MSH5 has a mutation status of A488P, The gene VWA7 has a mutation status of T26T, The gene NUDT3 has a mutation status of H132H, The gene ANKS1A has a mutation status of S506fs, The gene SLC26A8 has a mutation status of G964C, The gene ZFAND3 has a mutation status of R17C, The gene DNAH8 has a mutation status of I4199T, The gene MOCS1 has a mutation status of P94P, The gene LRFN2 has a mutation status of R388H, The gene COL9A1 has a mutation status of G364C, The gene RIMS1 has a mutation status of G440G, The gene PHIP has a mutation status of E356E, The gene ZNF292 has a mutation status of I1115S, The gene EPHA7 has a mutation status of V418L, The gene TAAR6 has a mutation status of Y311H, The gene VNN2 has a mutation status of W320*, The gene ALDH8A1 has a mutation status of P269S, The gene ECT2L has a mutation status of T727T, The gene RMND1 has a mutation status of F199L, The gene SYNE1 has a mutation status of M6190I, The gene VWDE has a mutation status of I332N, The gene DPY19L1 has a mutation status of G84D, The gene NPC1L1 has a mutation status of R463H, The gene ZNF735 has a mutation status of K183N, The gene GTF2I has a mutation status of V309fs, The gene SSC4D has a mutation status of R97H, The gene CROT has a mutation status of T571A, The gene PDK4 has a mutation status of A144T, The gene TRIM4 has a mutation status of P104T, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC17 has a mutation status of T825N, The gene RELN has a mutation status of E2374K, The gene GRM8 has a mutation status of R258R, The gene GRM8 has a mutation status of I160I, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PLXNA4 has a mutation status of W8C, The gene MGAM has a mutation status of G818R, The gene PRSS1 has a mutation status of N77N, The gene KRBA1 has a mutation status of P979P, The gene ZNF467 has a mutation status of V508M, The gene ZNF862 has a mutation status of V588M, The gene GIMAP7 has a mutation status of S73R, The gene ASB10 has a mutation status of G248V, The gene MYOM2 has a mutation status of D348Y, The gene SH2D4A has a mutation status of P116T, The gene PTK2B has a mutation status of L58L, The gene ADGRA2 has a mutation status of P434L, The gene LYN has a mutation status of K404K, The gene NBN has a mutation status of R43*, The gene RNF19A has a mutation status of E95A, The gene FAM91A1 has a mutation status of S781S, The gene ZNF572 has a mutation status of L179I, The gene HHLA1 has a mutation status of N121S, The gene TRAPPC9 has a mutation status of L17I, The gene JRK has a mutation status of K115R, The gene CYP11B2 has a mutation status of A414P, The gene WDR97 has a mutation status of S227L, The gene MROH1 has a mutation status of S1272F, The gene LRRC14 has a mutation status of R28R, The gene DOCK8 has a mutation status of N1195N, The gene KCNV2 has a mutation status of H26Q, The gene CCDC171 has a mutation status of L413L, The gene CCDC171 has a mutation status of E551V, The gene C9orf131 has a mutation status of Q251Q, The gene DAPK1 has a mutation status of I1065I, The gene SHC3 has a mutation status of M1I, The gene WNK2 has a mutation status of L312Q, The gene TDRD7 has a mutation status of E63D, The gene TDRD7 has a mutation status of D962A, The gene NCBP1 has a mutation status of K67K, The gene TRMO has a mutation status of S191Y, The gene HEMGN has a mutation status of E59K, The gene COL15A1 has a mutation status of G664E, The gene NIPSNAP3B has a mutation status of N82K, The gene ELP1 has a mutation status of R1192I, The gene FRRS1L has a mutation status of R51A, The gene PTPN3 has a mutation status of M403I, The gene SVEP1 has a mutation status of A1142S, The gene INIP has a mutation status of A70A, The gene WDR31 has a mutation status of Q204*, The gene AKNA has a mutation status of S1184P, The gene AKNA has a mutation status of F845F, The gene OR1J2 has a mutation status of L110L, The gene ADGRD2 has a mutation status of R656C, The gene TTC16 has a mutation status of D373N, The gene LRRC8A has a mutation status of T170M, The gene HMCN2 has a mutation status of V2563I, The gene HMCN2 has a mutation status of I2567M, The gene UCK1 has a mutation status of L62L, The gene PPP1R26 has a mutation status of A1185S, The gene GATA3 has a mutation status of D335fs, The gene C1QL3 has a mutation status of P96S, The gene MRC1 has a mutation status of Y719Y, The gene SLC39A12 has a mutation status of W446*, The gene ZNF22 has a mutation status of G27V, The gene WASHC2C has a mutation status of K1199R, The gene FRMPD2 has a mutation status of P769L, The gene WDFY4 has a mutation status of V2122L, The gene ERCC6 has a mutation status of S1099R, The gene ERCC6 has a mutation status of V83I, The gene CSTF2T has a mutation status of Q167*, The gene ANK3 has a mutation status of F2979F, The gene SLC25A16 has a mutation status of G299A, The gene EIF4EBP2 has a mutation status of S14R, The gene MRPS16 has a mutation status of N69K, The gene CFAP70 has a mutation status of L451L, The gene NDST2 has a mutation status of R502G, The gene NRG3 has a mutation status of P122P, The gene LIPF has a mutation status of S134A, The gene HECTD2 has a mutation status of N86T, The gene TM9SF3 has a mutation status of T373A, The gene PIK3AP1 has a mutation status of E50K, The gene SMC3 has a mutation status of L1017L, The gene PLPP4 has a mutation status of T232A, The gene FOXI2 has a mutation status of Q17Q, The gene LRRC27 has a mutation status of E54*, The gene DNHD1 has a mutation status of E4427K, The gene OR2D3 has a mutation status of Q12Q, The gene USH1C has a mutation status of K279K, The gene NELL1 has a mutation status of E445V, The gene RAG2 has a mutation status of D105N, The gene LRP4 has a mutation status of P563P, The gene OR5D13 has a mutation status of V126E, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TNKS1BP1 has a mutation status of A104A, The gene OR6Q1 has a mutation status of L27F, The gene DAGLA has a mutation status of H471Y, The gene SLC22A9 has a mutation status of N107K, The gene NRXN2 has a mutation status of Q1173K, The gene FOSL1 has a mutation status of R94Q, The gene ANO1 has a mutation status of P724P, The gene CLPB has a mutation status of K10NL, The gene C2CD3 has a mutation status of H2035L, The gene TPBGL has a mutation status of A247V, The gene GDPD5 has a mutation status of A353fs, The gene FAM181B has a mutation status of G306S, The gene PRSS23 has a mutation status of N47S, The gene CEP295 has a mutation status of E179V, The gene PIWIL4 has a mutation status of L551L, The gene CNTN5 has a mutation status of L1035L, The gene CEP126 has a mutation status of H1081Y, The gene MMP13 has a mutation status of R458C, The gene DDX10 has a mutation status of H27R, The gene CD3E has a mutation status of K153T, The gene PHLDB1 has a mutation status of T643T, The gene VPS11 has a mutation status of G281D, The gene DPAGT1 has a mutation status of R156R, The gene ABCG4 has a mutation status of S69S, The gene NECTIN1 has a mutation status of A474A, The gene POU2F3 has a mutation status of P4A, The gene SLC6A12 has a mutation status of V59V, The gene C12orf4 has a mutation status of R335Q, The gene CHD4 has a mutation status of A525V, The gene ACRBP has a mutation status of F464L, The gene RIMKLB has a mutation status of M98V, The gene PZP has a mutation status of E152*, The gene PTHLH has a mutation status of T143T, The gene RAPGEF3 has a mutation status of C843C, The gene FAM186B has a mutation status of W566C, The gene GPD1 has a mutation status of M144T, The gene FAM186A has a mutation status of P1674A, The gene GALNT6 has a mutation status of S258S, The gene KRT2 has a mutation status of Q161H, The gene BAZ2A has a mutation status of E621*, The gene BBS10 has a mutation status of G401E, The gene EEA1 has a mutation status of L230L, The gene CFAP54 has a mutation status of L1087P, The gene MYBPC1 has a mutation status of I86T, The gene FICD has a mutation status of A147A, The gene DTX1 has a mutation status of G182G, The gene ATP6V0A2 has a mutation status of S659C, The gene DNAH10 has a mutation status of T1584T, The gene ADGRD1 has a mutation status of Q37H, The gene FBRSL1 has a mutation status of S752S, The gene ZMYM2 has a mutation status of S289L, The gene MIPEP has a mutation status of S595*, The gene SPART has a mutation status of G386R, The gene SMAD9 has a mutation status of V42L, The gene TRIM13 has a mutation status of E165K, The gene DLEU7 has a mutation status of S129L, The gene DACH1 has a mutation status of T69fs, The gene ZIC5 has a mutation status of P166P, The gene PABPN1 has a mutation status of A10A, The gene JPH4 has a mutation status of R233C, The gene ADCY4 has a mutation status of L655L, The gene COCH has a mutation status of F415fs, The gene DACT1 has a mutation status of N372S, The gene ZBTB1 has a mutation status of I447I, The gene TTC9 has a mutation status of P92P, The gene SIPA1L1 has a mutation status of N778D, The gene ZFYVE1 has a mutation status of P393P, The gene GPR68 has a mutation status of Q95H, The gene COX8C has a mutation status of P38S, The gene PPP4R4 has a mutation status of D283Y, The gene SLC25A29 has a mutation status of P37L, The gene INF2 has a mutation status of D1239A, The gene BTBD6 has a mutation status of G475R, The gene LINC02203 has a mutation status of I259M, The gene MAGEL2 has a mutation status of L642M, The gene UBE3A has a mutation status of T249M, The gene ATP10A has a mutation status of A1211V, The gene PAK6 has a mutation status of R637Q, The gene PPP1R14D has a mutation status of K135R, The gene VPS18 has a mutation status of L869F, The gene OIP5 has a mutation status of P5S, The gene LCMT2 has a mutation status of R8S, The gene TUBGCP4 has a mutation status of R647*, The gene SERF2 has a mutation status of T88T, The gene DMXL2 has a mutation status of I699T, The gene LEO1 has a mutation status of D68D, The gene ONECUT1 has a mutation status of C321Y, The gene ANKDD1A has a mutation status of L516L, The gene UBAP1L has a mutation status of A124V, The gene IGDCC3 has a mutation status of D731D, The gene INTS14 has a mutation status of G331G, The gene SKOR1 has a mutation status of G307S, The gene ITGA11 has a mutation status of T593R, The gene PML has a mutation status of A456T, The gene AGBL1 has a mutation status of E167D, The gene ARRDC4 has a mutation status of N169N, The gene STUB1 has a mutation status of S236G, The gene FBXL16 has a mutation status of S398F, The gene CACNA1H has a mutation status of M611I, The gene RPL3L has a mutation status of R234L, The gene BICDL2 has a mutation status of E171E, The gene ZSCAN10 has a mutation status of E508K, The gene CREBBP has a mutation status of Q1967P, The gene PPL has a mutation status of E1254K, The gene ERI2 has a mutation status of T386I, The gene COG7 has a mutation status of K84K, The gene SLC9A5 has a mutation status of P466P, The gene AARS1 has a mutation status of P906P, The gene WWOX has a mutation status of N269N, The gene ZNF778 has a mutation status of T416fs, The gene ITGAE has a mutation status of G103G, The gene FXR2 has a mutation status of E145K, The gene PIK3R6 has a mutation status of T145M, The gene DHRS7C has a mutation status of L9L, The gene MYH3 has a mutation status of E1121E, The gene MPRIP has a mutation status of L858L, The gene LGALS9 has a mutation status of S286Y, The gene FAM222B has a mutation status of R351H, The gene ANKRD13B has a mutation status of V22V, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP9-6 has a mutation status of G106C, The gene KRT32 has a mutation status of P427I, The gene HOXB7 has a mutation status of E216*, The gene B4GALNT2 has a mutation status of P109P, The gene KIF2B has a mutation status of D546N, The gene TBX2 has a mutation status of P4L, The gene ACE has a mutation status of S233F, The gene KCNJ2 has a mutation status of L109F, The gene UNK has a mutation status of S517C, The gene QRICH2 has a mutation status of D262E, The gene CBX8 has a mutation status of S316Y, The gene PTPRM has a mutation status of D1063H, The gene DSG3 has a mutation status of S454S, The gene SERPINB2 has a mutation status of E160*, The gene CDH7 has a mutation status of G198V, The gene PCSK4 has a mutation status of G302S, The gene THOP1 has a mutation status of V67V, The gene SH2D3A has a mutation status of L120L, The gene AC008878.3 has a mutation status of H233H, The gene MUC16 has a mutation status of D13719Y, The gene MUC16 has a mutation status of G1764A, The gene TYK2 has a mutation status of P117S, The gene KEAP1 has a mutation status of V377V, The gene DNM2 has a mutation status of A796V, The gene ZNF491 has a mutation status of S114Y, The gene PKN1 has a mutation status of T551T, The gene ILVBL has a mutation status of L126F, The gene CPAMD8 has a mutation status of D684N, The gene ZNF708 has a mutation status of P74S, The gene KIAA0355 has a mutation status of R623fs, The gene KIAA0355 has a mutation status of R623R, The gene LSR has a mutation status of T196T, The gene ZNF585A has a mutation status of R478Q, The gene WDR87 has a mutation status of G431G, The gene RYR1 has a mutation status of A2141V, The gene PRX has a mutation status of A35E, The gene NUMBL has a mutation status of E419Q, The gene CYP2A7 has a mutation status of V365M, The gene CCDC97 has a mutation status of C136S, The gene PSG11 has a mutation status of F262F, The gene CD177 has a mutation status of T156T, The gene CADM4 has a mutation status of R187H, The gene ZNF225 has a mutation status of Q279E, The gene ZSWIM9 has a mutation status of M51T, The gene KCNJ14 has a mutation status of G116S, The gene LMTK3 has a mutation status of G1272G, The gene NUCB1 has a mutation status of L12P, The gene FUZ has a mutation status of V121M, The gene IL4I1 has a mutation status of G189D, The gene POLD1 has a mutation status of A916V, The gene LRRC4B has a mutation status of R5H, The gene SIGLEC7 has a mutation status of R198C, The gene ZNF610 has a mutation status of G210C, The gene ZNF610 has a mutation status of L387L, The gene ZNF677 has a mutation status of R499C, The gene PRKCG has a mutation status of Q425*, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LAIR1 has a mutation status of A266fs, The gene LAIR1 has a mutation status of R265G, The gene KIR2DL1 has a mutation status of V111L, The gene EPN1 has a mutation status of E344V, The gene USP29 has a mutation status of T709T, The gene SIRPA has a mutation status of L44S, The gene FASTKD5 has a mutation status of I310M, The gene COX4I2 has a mutation status of A141V, The gene CDK5RAP1 has a mutation status of P63L, The gene MMP24 has a mutation status of R369R, The gene EYA2 has a mutation status of L58L, The gene DIDO1 has a mutation status of V1131V, The gene KCNQ2 has a mutation status of S751L, The gene MX2 has a mutation status of A686T, The gene WDR4 has a mutation status of Q323H, The gene TRPM2 has a mutation status of R634H, The gene BCL2L13 has a mutation status of S5fs, The gene KLHL22 has a mutation status of K260N, The gene KIAA1671 has a mutation status of G1359E, The gene SLC5A1 has a mutation status of I397T, The gene CSDC2 has a mutation status of D111N, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TTLL12 has a mutation status of G302S, The gene CELSR1 has a mutation status of R2677R, The gene TUBGCP6 has a mutation status of L1171L, The gene PPP6R2 has a mutation status of G760S, The gene SHROOM2 has a mutation status of A1523T, The gene FAM47A has a mutation status of W705*, The gene SPACA5B has a mutation status of G58G, The gene RBM3 has a mutation status of R145H, The gene TSPYL2 has a mutation status of I276I, The gene PHF8 has a mutation status of H31P, The gene ZXDA has a mutation status of G275G, The gene ZXDA has a mutation status of Q138L, The gene MAGEE1 has a mutation status of P154R, The gene NXF3 has a mutation status of R409W, The gene XIAP has a mutation status of F92F, The gene ABCD1 has a mutation status of M282T, The gene MT-ND2 has a mutation status of A109T, The gene MT-CO1 has a mutation status of H291H, The gene MT-CO3 has a mutation status of V254I, The gene MT-ND5 has a mutation status of S308S, The gene MT-ND6 has a mutation status of N119D, The gene MT-CYB has a mutation status of T212A
BRCA
The gene CAMTA1 has a mutation status of S856S, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene KDM1A has a mutation status of A828V, The gene PTPRU has a mutation status of R1319P, The gene GNL2 has a mutation status of S234C, The gene MPL has a mutation status of L524L, The gene ZNF326 has a mutation status of P127L, The gene DCLRE1B has a mutation status of T93T, The gene PHGDH has a mutation status of V508I, The gene HMGCS2 has a mutation status of A45A, The gene URB2 has a mutation status of K24K, The gene ACTN2 has a mutation status of I461I, The gene GREM2 has a mutation status of L60V, The gene SLC5A6 has a mutation status of S585S, The gene PPM1B has a mutation status of E263Q, The gene EMX1 has a mutation status of C6F, The gene LOXL3 has a mutation status of R598C, The gene FAHD2B has a mutation status of V222M, The gene ACVR2A has a mutation status of L310Q, The gene ABCB11 has a mutation status of D215V, The gene HOXD1 has a mutation status of H267Y, The gene NEUROD1 has a mutation status of Y5F, The gene ALS2 has a mutation status of H952N, The gene PARD3B has a mutation status of R773Q, The gene CFAP65 has a mutation status of E1804K, The gene SLC4A3 has a mutation status of A283V, The gene UGT1A3 has a mutation status of V154I, The gene ANKMY1 has a mutation status of R606Q, The gene HRH1 has a mutation status of S363P, The gene CCDC12 has a mutation status of G7G, The gene CDC25A has a mutation status of P419S, The gene GPR62 has a mutation status of L146L, The gene FLNB has a mutation status of H2355P, The gene ZBTB11 has a mutation status of R18R, The gene ADCY5 has a mutation status of V743I, The gene IL1RAP has a mutation status of C212F, The gene BOD1L1 has a mutation status of G2421G, The gene ATP10D has a mutation status of K166T, The gene UBA6 has a mutation status of Y576Y, The gene SHROOM3 has a mutation status of E645G, The gene AADAT has a mutation status of I256I, The gene TLR3 has a mutation status of A525E, The gene PDZD2 has a mutation status of T1186T, The gene NUDT12 has a mutation status of L232P, The gene PJA2 has a mutation status of Y422C, The gene EPB41L4A has a mutation status of N450S, The gene ANKHD1-EIF4EBP3 has a mutation status of P2545L, The gene TCERG1 has a mutation status of K785K, The gene RASGEF1C has a mutation status of D94E, The gene GCM2 has a mutation status of I457I, The gene HLA-DQA2 has a mutation status of F121F, The gene CUL7 has a mutation status of K855E, The gene NOX3 has a mutation status of W53L, The gene QKI has a mutation status of I209V, The gene GPNMB has a mutation status of K107fs, The gene POU6F2 has a mutation status of S575C, The gene VWC2 has a mutation status of P177R, The gene PSPH has a mutation status of L68P, The gene ZNF138 has a mutation status of D83E, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC17 has a mutation status of T993T, The gene RELN has a mutation status of R2684H, The gene FEZF1 has a mutation status of A156T, The gene RNF133 has a mutation status of H290R, The gene ZC3HAV1 has a mutation status of S724F, The gene PRSS1 has a mutation status of N77N, The gene ZNF425 has a mutation status of H408H, The gene TG has a mutation status of Q2405Q, The gene WDR97 has a mutation status of H1348H, The gene FOXD4L3 has a mutation status of A46G, The gene LCN9 has a mutation status of M42V, The gene CAMSAP1 has a mutation status of H969Q, The gene ANAPC2 has a mutation status of V303G, The gene AKR1C8P has a mutation status of N172K, The gene AKR1C8P has a mutation status of F171LLL*VCL**NQGD, The gene CUBN has a mutation status of C3113C, The gene OGDHL has a mutation status of R684C, The gene TACR2 has a mutation status of V54I, The gene PALD1 has a mutation status of A48V, The gene TCF7L2 has a mutation status of P489A, The gene ADAM12 has a mutation status of R834S, The gene MUC5AC has a mutation status of R3299Q, The gene OR5P2 has a mutation status of R27Q, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene CAPN1 has a mutation status of F610C, The gene MAP3K11 has a mutation status of R73Q, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene KMT2D has a mutation status of K5384fs, The gene KRT1 has a mutation status of T507K, The gene MDM1 has a mutation status of P250L, The gene E2F7 has a mutation status of R212Q, The gene PHETA1 has a mutation status of N20N, The gene CIT has a mutation status of A1120A, The gene RHOF has a mutation status of I129L, The gene NCOR2 has a mutation status of E676E, The gene EP400 has a mutation status of P2793P, The gene POLE has a mutation status of V1270F, The gene DOCK9 has a mutation status of D155D, The gene TGM1 has a mutation status of R34C, The gene BAZ1A has a mutation status of K1362K, The gene DNAAF2 has a mutation status of S732S, The gene BEGAIN has a mutation status of R240P, The gene MTA1 has a mutation status of N378N, The gene HERC2 has a mutation status of S895A, The gene TYRO3 has a mutation status of E509fs, The gene MGA has a mutation status of A2000T, The gene CDH11 has a mutation status of A281A, The gene ZCCHC14 has a mutation status of G374G, The gene PLD2 has a mutation status of Y47N, The gene CLDN7 has a mutation status of S172A, The gene KDM6B has a mutation status of R411W, The gene RAI1 has a mutation status of S1119S, The gene NOS2 has a mutation status of Q1026R, The gene NF1 has a mutation status of Q535*, The gene DBF4B has a mutation status of P25L, The gene CACNA1G has a mutation status of A447T, The gene ABCC3 has a mutation status of D940N, The gene FBF1 has a mutation status of A919G, The gene FBF1 has a mutation status of E918G, The gene SEH1L has a mutation status of R5P, The gene ANGPTL6 has a mutation status of R142H, The gene KRI1 has a mutation status of D403H, The gene CACNA1A has a mutation status of A2447D, The gene PSG6 has a mutation status of G325G, The gene XRCC1 has a mutation status of P483L, The gene IRGC has a mutation status of A358A, The gene CARD8 has a mutation status of V180G, The gene PRMT1 has a mutation status of N157N, The gene ADM5 has a mutation status of P69A, The gene SHANK1 has a mutation status of L2076L, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of T335T, The gene JAG1 has a mutation status of R1094Q, The gene ZSWIM3 has a mutation status of R216H, The gene PREX1 has a mutation status of K201K, The gene RBM38 has a mutation status of R116W, The gene TAF4 has a mutation status of A354S, The gene HELZ2 has a mutation status of A1957A, The gene MICAL3 has a mutation status of Y825Y, The gene ARVCF has a mutation status of A684T, The gene C1QTNF6 has a mutation status of A23A, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CELSR1 has a mutation status of E2757*, The gene DCAF8L1 has a mutation status of P117P, The gene NUDT10 has a mutation status of A156G, The gene IRAK1 has a mutation status of L263M, The gene IRAK1 has a mutation status of V260V
DLBC
The gene AGRN has a mutation status of C502*, The gene MFN2 has a mutation status of L146L, The gene PRAMEF12 has a mutation status of L342L, The gene PRAMEF12 has a mutation status of V361K, The gene PRAMEF1 has a mutation status of 275_276KL>NM, The gene HNRNPCL1 has a mutation status of L198L, The gene PRAMEF2 has a mutation status of T90T, The gene PRAMEF6 has a mutation status of Y163Y, The gene PRAMEF9 has a mutation status of A352V, The gene PRAMEF13 has a mutation status of N426D, The gene PRAMEF13 has a mutation status of R424G, The gene PRAMEF13 has a mutation status of V256G, The gene PRAMEF13 has a mutation status of R138C, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF17 has a mutation status of R169G, The gene CROCC has a mutation status of Q929H, The gene VWA5B1 has a mutation status of A1071P, The gene ZBTB40 has a mutation status of R1026G, The gene CEP85 has a mutation status of Q385*, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene FOXE3 has a mutation status of F105Y, The gene FGGY has a mutation status of L351L, The gene PDE4B has a mutation status of L282L, The gene ERICH3 has a mutation status of P410L, The gene ST6GALNAC3 has a mutation status of A287V, The gene RPAP2 has a mutation status of S235L, The gene ABCA4 has a mutation status of V1378M, The gene AMPD2 has a mutation status of L799L, The gene EPS8L3 has a mutation status of R465fs, The gene NBPF14 has a mutation status of E1268Q, The gene HRNR has a mutation status of G1127S, The gene OR6P1 has a mutation status of A237D, The gene FCER1A has a mutation status of W203R, The gene DCAF8 has a mutation status of K374Q, The gene SMG7 has a mutation status of E316K, The gene HMCN1 has a mutation status of L1504L, The gene PRG4 has a mutation status of A548T, The gene PRG4 has a mutation status of T718I, The gene IGFN1 has a mutation status of P11S, The gene CHIT1 has a mutation status of S275A, The gene UTP25 has a mutation status of L292L, The gene OR2T4 has a mutation status of C32*, The gene SNTG2 has a mutation status of P523P, The gene TPO has a mutation status of G771E, The gene KIDINS220 has a mutation status of S1488R, The gene CPSF3 has a mutation status of G171G, The gene NTSR2 has a mutation status of E90D, The gene NT5C1B-RDH14 has a mutation status of S191S, The gene C2orf16 has a mutation status of Q2975K, The gene CLIP4 has a mutation status of Y542H, The gene ALK has a mutation status of N369K, The gene PAIP2B has a mutation status of D78G, The gene INO80B has a mutation status of S63S, The gene REG1A has a mutation status of C154F, The gene POLR1A has a mutation status of I1583I, The gene CD8A has a mutation status of S158F, The gene MAL has a mutation status of 121_122HY>QH, The gene ANKRD36C has a mutation status of A601P, The gene KANSL3 has a mutation status of D496H, The gene TMEM131 has a mutation status of D1411E, The gene MAP4K4 has a mutation status of S845I, The gene MFSD9 has a mutation status of L324L, The gene ST6GAL2 has a mutation status of L24V, The gene RANBP2 has a mutation status of V1386F, The gene INSIG2 has a mutation status of M203V, The gene NCKAP5 has a mutation status of R411*, The gene MAP3K19 has a mutation status of S1226C, The gene ARHGAP15 has a mutation status of H349Y, The gene ITGB6 has a mutation status of T714M, The gene SCN2A has a mutation status of Q1394*, The gene SCN1A has a mutation status of D646Y, The gene TTN has a mutation status of L31486F, The gene TTN has a mutation status of G23404G, The gene TTN has a mutation status of V1099V, The gene NDUFB3 has a mutation status of W22R, The gene CD28 has a mutation status of S94*, The gene PARD3B has a mutation status of R984L, The gene PIKFYVE has a mutation status of V902F, The gene RPL37A has a mutation status of I83V, The gene IGFBP2 has a mutation status of P43fs, The gene DOCK10 has a mutation status of A1683S, The gene TEX44 has a mutation status of L383F, The gene USP40 has a mutation status of P94R, The gene UGT1A8 has a mutation status of A25T, The gene TRPM8 has a mutation status of K175N, The gene ERFE has a mutation status of R11L, The gene CCDC12 has a mutation status of E50G, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene UBA3 has a mutation status of M101T, The gene CRYBG3 has a mutation status of V2350E, The gene PHLDB2 has a mutation status of R206I, The gene CD80 has a mutation status of F229Y, The gene GOLGB1 has a mutation status of A3102V, The gene SEMA5B has a mutation status of V140A, The gene MYLK has a mutation status of V1213M, The gene DNAJC13 has a mutation status of K696E, The gene CLSTN2 has a mutation status of G703R, The gene ATR has a mutation status of I1900V, The gene ZIC1 has a mutation status of R315fs, The gene MME has a mutation status of E744G, The gene IQCJ-SCHIP1 has a mutation status of L204L, The gene EEF1AKMT4-ECE2 has a mutation status of A216G, The gene VPS8 has a mutation status of G1205R, The gene OPA1 has a mutation status of V865I, The gene MFSD10 has a mutation status of P227L, The gene C4orf50 has a mutation status of E782Q, The gene SORCS2 has a mutation status of C667Y, The gene NWD2 has a mutation status of A1352A, The gene CRACD has a mutation status of A283V, The gene ART3 has a mutation status of T164fs, The gene AFF1 has a mutation status of K582fs, The gene HSD17B13 has a mutation status of A277S, The gene SPP1 has a mutation status of D293E, The gene MMRN1 has a mutation status of E461K, The gene C4orf54 has a mutation status of P359P, The gene PPA2 has a mutation status of H272Y, The gene NDST4 has a mutation status of R473R, The gene SYNPO2 has a mutation status of T850A, The gene PABPC4L has a mutation status of R8L, The gene TMEM131L has a mutation status of F130L, The gene TDO2 has a mutation status of L52fs, The gene TRIM75P has a mutation status of Y427Y, The gene DDX60L has a mutation status of S508S, The gene GALNTL6 has a mutation status of R403R, The gene TENM3 has a mutation status of E379I, The gene MYO10 has a mutation status of S962S, The gene PRDM9 has a mutation status of K423E, The gene ADAMTS12 has a mutation status of V1560L, The gene ADAMTS12 has a mutation status of I350I, The gene SPEF2 has a mutation status of R1110G, The gene HCN1 has a mutation status of G809C, The gene MCIDAS has a mutation status of P158P, The gene DHX29 has a mutation status of W1270*, The gene MAP1B has a mutation status of L535L, The gene ARHGEF28 has a mutation status of L575F, The gene ZBED3 has a mutation status of L155A, The gene FAM151B has a mutation status of E111Q, The gene VCAN has a mutation status of E1783K, The gene SOWAHA has a mutation status of S37S, The gene PCDHB3 has a mutation status of A776S, The gene PCDHGA1 has a mutation status of V743A, The gene PCDH12 has a mutation status of S540R, The gene MARCOL has a mutation status of Q254Q, The gene CSF1R has a mutation status of G714S, The gene CSF1R has a mutation status of P517T, The gene RBM22 has a mutation status of G322R, The gene FAM114A2 has a mutation status of I92V, The gene SLIT3 has a mutation status of L180L, The gene DOCK2 has a mutation status of F280L, The gene BTNL9 has a mutation status of C401Y, The gene FAM217A has a mutation status of L224M, The gene HIVEP1 has a mutation status of V334A, The gene NUP153 has a mutation status of V963I, The gene HLA-F has a mutation status of P36T, The gene MUC22 has a mutation status of A1118A, The gene AL645922.1 has a mutation status of V1018A, The gene TNXB has a mutation status of S2784S, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DMB has a mutation status of L76L, The gene PACSIN1 has a mutation status of K51M, The gene MAPK14 has a mutation status of F348F, The gene FRS3 has a mutation status of C107Y, The gene BICRAL has a mutation status of Q877H, The gene TFAP2B has a mutation status of Q112K, The gene PAQR8 has a mutation status of L302L, The gene DDX43 has a mutation status of T205R, The gene TTK has a mutation status of Y810C, The gene SERINC1 has a mutation status of G260C, The gene TMEM200A has a mutation status of I76I, The gene BCLAF1 has a mutation status of R76R, The gene ECT2L has a mutation status of E330E, The gene UTRN has a mutation status of D384D, The gene GRM1 has a mutation status of P58L, The gene SYNE1 has a mutation status of A4961A, The gene TULP4 has a mutation status of L631V, The gene LPA has a mutation status of G1507V, The gene TBXT has a mutation status of M313V, The gene RADIL has a mutation status of E533E, The gene ZNF316 has a mutation status of G893C, The gene VWDE has a mutation status of A784D, The gene INHBA has a mutation status of N374Y, The gene PKD1L1 has a mutation status of R1690*, The gene PKD1L1 has a mutation status of G253V, The gene PSPH has a mutation status of L68P, The gene GSAP has a mutation status of G853G, The gene CACNA2D1 has a mutation status of E297Q, The gene ABCB4 has a mutation status of Q748Q, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of R931P, The gene MUC3A has a mutation status of G932A, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene PIK3CG has a mutation status of M1039T, The gene CTTNBP2 has a mutation status of A1401D, The gene TAS2R16 has a mutation status of P44S, The gene PRRT4 has a mutation status of G428V, The gene CPA5 has a mutation status of S98Y, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene CHCHD3 has a mutation status of D131N, The gene HIPK2 has a mutation status of H760R, The gene PRSS37 has a mutation status of Y222H, The gene PRSS2 has a mutation status of R68C, The gene EPHA1 has a mutation status of N187S, The gene GIMAP1 has a mutation status of V185A, The gene AGAP3 has a mutation status of G550G, The gene GBX1 has a mutation status of S187L, The gene ACTR3B has a mutation status of A103V, The gene CSMD1 has a mutation status of S2105R, The gene PRAG1 has a mutation status of A1237G, The gene XKR6 has a mutation status of D89Y, The gene TUSC3 has a mutation status of S267C, The gene MTMR7 has a mutation status of P20A, The gene SLC18A1 has a mutation status of A402A, The gene UNC5D has a mutation status of V237M, The gene ASPH has a mutation status of C648Y, The gene KCNB2 has a mutation status of G385V, The gene DPYS has a mutation status of L110L, The gene KCNV1 has a mutation status of R77S, The gene CSMD3 has a mutation status of T3016N, The gene COL22A1 has a mutation status of P1602P, The gene TRAPPC9 has a mutation status of R923S, The gene TRAPPC9 has a mutation status of C415C, The gene LYNX1-SLURP2 has a mutation status of T79N, The gene PYCR3 has a mutation status of R18L, The gene EPPK1 has a mutation status of A2633del, The gene MROH1 has a mutation status of N621N, The gene COMMD5 has a mutation status of A84S, The gene VLDLR has a mutation status of P647S, The gene NFIB has a mutation status of Q508*, The gene ZDHHC21 has a mutation status of S153F, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene PRSS3 has a mutation status of R122H, The gene PRSS3 has a mutation status of S215T, The gene RGP1 has a mutation status of W363*, The gene FOXD4L4 has a mutation status of D28D, The gene PRUNE2 has a mutation status of D99N, The gene CEP78 has a mutation status of T177A, The gene PHF2 has a mutation status of R354fs, The gene CCDC180 has a mutation status of R297H, The gene CAVIN4 has a mutation status of P228P, The gene OR13C8 has a mutation status of L36L, The gene FRRS1L has a mutation status of R51A, The gene ECPAS has a mutation status of I285L, The gene DENND1A has a mutation status of R23M, The gene ODF2 has a mutation status of Q794R, The gene HMCN2 has a mutation status of A22A, The gene COL5A1 has a mutation status of P705Q, The gene OLFM1 has a mutation status of L458L, The gene QSOX2 has a mutation status of G647W, The gene CCDC187 has a mutation status of T90M, The gene TRAF2 has a mutation status of P374S, The gene SFMBT2 has a mutation status of G132W, The gene DHTKD1 has a mutation status of P35L, The gene GAD2 has a mutation status of L526F, The gene ZNF438 has a mutation status of R707K, The gene IFIT3 has a mutation status of E323D, The gene CYP2C8 has a mutation status of L311L, The gene COX15 has a mutation status of V379V, The gene ADD3 has a mutation status of D587G, The gene RBM20 has a mutation status of P692P, The gene EIF3A has a mutation status of E852E, The gene HMX3 has a mutation status of R102T, The gene MKI67 has a mutation status of H2088H, The gene CFAP46 has a mutation status of V134V, The gene KNDC1 has a mutation status of S1517S, The gene LMNTD2 has a mutation status of R89Q, The gene MUC6 has a mutation status of A1593P, The gene MUC5AC has a mutation status of T2408P, The gene MUC5AC has a mutation status of L3022S, The gene MUC5AC has a mutation status of S4499S, The gene ASCL2 has a mutation status of P130P, The gene TRIM68 has a mutation status of S215G, The gene SLC17A6 has a mutation status of R88C, The gene KIAA1549L has a mutation status of G126R, The gene OR5T3 has a mutation status of M23I, The gene OR8H1 has a mutation status of T191T, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR5R1 has a mutation status of L185*, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TMX2 has a mutation status of K227M, The gene OR9Q2 has a mutation status of I214I, The gene CBLIF has a mutation status of P125T, The gene MS4A8 has a mutation status of V190L, The gene SLC22A8 has a mutation status of G284S, The gene GPR137 has a mutation status of G149R, The gene MRGPRF has a mutation status of L56L, The gene GRM5 has a mutation status of S440C, The gene DIXDC1 has a mutation status of R524C, The gene CADM1 has a mutation status of R25R, The gene OR8B4 has a mutation status of Y148H, The gene ST14 has a mutation status of D269D, The gene ERC1 has a mutation status of M107I, The gene CRACR2A has a mutation status of E108V, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R31 has a mutation status of F233S, The gene TAS2R31 has a mutation status of 150_151KE>NQ, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PRB4 has a mutation status of R122G, The gene DDX47 has a mutation status of M412I, The gene PLBD1 has a mutation status of L22fs, The gene PLBD1 has a mutation status of L21fs, The gene EPS8 has a mutation status of T223T, The gene GYS2 has a mutation status of V88F, The gene ITPR2 has a mutation status of K225Q, The gene SLC2A13 has a mutation status of A509P, The gene PDZRN4 has a mutation status of V307V, The gene DIP2B has a mutation status of E317*, The gene SHMT2 has a mutation status of W43C, The gene SYT1 has a mutation status of L300L, The gene ACACB has a mutation status of P1397P, The gene NOS1 has a mutation status of L460I, The gene COQ5 has a mutation status of I247T, The gene PITPNM2 has a mutation status of P821L, The gene EIF2B1 has a mutation status of P144P, The gene TMEM132C has a mutation status of A242A, The gene LRCOL1 has a mutation status of P4L, The gene ZNF26 has a mutation status of P285P, The gene GJB2 has a mutation status of L90P, The gene USPL1 has a mutation status of E96D, The gene COG6 has a mutation status of M484I, The gene CBY2 has a mutation status of L225M, The gene PCCA has a mutation status of A377A, The gene PABPN1 has a mutation status of R265C, The gene MYH7 has a mutation status of L1805L, The gene MIS18BP1 has a mutation status of R355R, The gene RTN1 has a mutation status of D486N, The gene PLEKHG3 has a mutation status of V102M, The gene GPHN has a mutation status of G606G, The gene PLEKHH1 has a mutation status of K77Q, The gene SLC8A3 has a mutation status of R5K, The gene ADAM20 has a mutation status of G20G, The gene ACOT2 has a mutation status of T185V, The gene SLC25A47 has a mutation status of Q28Q, The gene TECPR2 has a mutation status of Q116P, The gene EXOC3L4 has a mutation status of R198C, The gene INF2 has a mutation status of V557G, The gene MTA1 has a mutation status of Y397H, The gene GOLGA6L22 has a mutation status of V434M, The gene CYFIP1 has a mutation status of K297R, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene NPAP1 has a mutation status of H613Q, The gene SPTBN5 has a mutation status of A3347A, The gene STRC has a mutation status of V1467I, The gene LDHAL6B has a mutation status of H364P, The gene ANKDD1A has a mutation status of L516L, The gene CHRNA3 has a mutation status of A452A, The gene MESP2 has a mutation status of I17I, The gene SV2B has a mutation status of G22R, The gene ABCA3 has a mutation status of L1566fs, The gene ABCA3 has a mutation status of L1566M, The gene METTL22 has a mutation status of H31R, The gene AQP8 has a mutation status of G73W, The gene SEZ6L2 has a mutation status of P142S, The gene KCTD13 has a mutation status of L77L, The gene ZNF646 has a mutation status of P1184T, The gene FTO has a mutation status of F114L, The gene NDRG4 has a mutation status of I157M, The gene DYNC1LI2 has a mutation status of G450D, The gene CTCF has a mutation status of K606K, The gene SNTB2 has a mutation status of A56A, The gene WWP2 has a mutation status of W497F, The gene AARS1 has a mutation status of N340S, The gene VAC14 has a mutation status of V238F, The gene PELP1 has a mutation status of Q450Q, The gene KDM6B has a mutation status of R1016Q, The gene PER1 has a mutation status of M1231I, The gene MYH8 has a mutation status of R873Q, The gene MYH4 has a mutation status of A1636D, The gene MYH4 has a mutation status of I460I, The gene MAP2K3 has a mutation status of P229H, The gene SUZ12 has a mutation status of T438S, The gene TMEM132E has a mutation status of P280fs, The gene TMEM132E has a mutation status of P279P, The gene GAS2L2 has a mutation status of R586Q, The gene CCL23 has a mutation status of T57T, The gene SNF8 has a mutation status of E123*, The gene COL1A1 has a mutation status of A1075T, The gene COL1A1 has a mutation status of P129L, The gene STXBP4 has a mutation status of Q267Q, The gene DDX42 has a mutation status of Q634L, The gene PECAM1 has a mutation status of V513V, The gene ABCA5 has a mutation status of T14S, The gene KIF19 has a mutation status of A257T, The gene CD300C has a mutation status of R215I, The gene ATP5PD has a mutation status of V67M, The gene UNC13D has a mutation status of E653Q, The gene EXOC7 has a mutation status of V277L, The gene DNAH17 has a mutation status of P2076R, The gene RNF213 has a mutation status of R2846C, The gene FASN has a mutation status of P824S, The gene MTCL1 has a mutation status of E972K, The gene MTCL1 has a mutation status of E972D, The gene PIEZO2 has a mutation status of I17V, The gene FHOD3 has a mutation status of E1303Q, The gene SETBP1 has a mutation status of P1548R, The gene DYM has a mutation status of I399T, The gene SALL3 has a mutation status of A185L, The gene REXO1 has a mutation status of G1054R, The gene ADAT3 has a mutation status of A40V, The gene MKNK2 has a mutation status of K67K, The gene PEAK3 has a mutation status of L201L, The gene FBN3 has a mutation status of R893H, The gene MUC16 has a mutation status of L13880C, The gene MUC16 has a mutation status of G13530S, The gene ZNF121 has a mutation status of H354R, The gene COL5A3 has a mutation status of P1309H, The gene ICAM4 has a mutation status of I138T, The gene SMARCA4 has a mutation status of L1085fs, The gene ZNF653 has a mutation status of A225T, The gene ZNF442 has a mutation status of H395H, The gene TRIR has a mutation status of A129V, The gene FARSA has a mutation status of V30F, The gene RFX1 has a mutation status of G907G, The gene ADGRL1 has a mutation status of G107G, The gene AKAP8 has a mutation status of H506Q, The gene C19orf44 has a mutation status of N233fs, The gene ANKLE1 has a mutation status of R614W, The gene COLGALT1 has a mutation status of S247P, The gene AC008397.2 has a mutation status of E659Q, The gene TM6SF2 has a mutation status of F336C, The gene ZNF66 has a mutation status of R277I, The gene ZNF208 has a mutation status of P1056H, The gene ZNF607 has a mutation status of N256Y, The gene SAMD4B has a mutation status of P461A, The gene DEDD2 has a mutation status of R320Q, The gene IRGQ has a mutation status of P428L, The gene RELB has a mutation status of P30R, The gene CCDC61 has a mutation status of A488V, The gene IGFL2 has a mutation status of E73K, The gene IGFL2 has a mutation status of R75C, The gene SLC1A5 has a mutation status of E253M, The gene CCDC114 has a mutation status of E317A, The gene LILRB3 has a mutation status of Q270R, The gene LILRA2 has a mutation status of W163S, The gene LILRA2 has a mutation status of S395T, The gene LILRB1 has a mutation status of Q41Q, The gene LILRB1 has a mutation status of Y99I, The gene ZNF837 has a mutation status of V163V, The gene RNF225 has a mutation status of S215S, The gene SIRPA has a mutation status of E220E, The gene C20orf194 has a mutation status of R812C, The gene ASXL1 has a mutation status of L1413F, The gene BPI has a mutation status of I189I, The gene TOX2 has a mutation status of P59S, The gene ARFGAP1 has a mutation status of G388C, The gene COL20A1 has a mutation status of I355I, The gene HELZ2 has a mutation status of L2581L, The gene MYT1 has a mutation status of T178T, The gene GRIK1 has a mutation status of P805H, The gene OLIG1 has a mutation status of L155L, The gene BRWD1 has a mutation status of E398D, The gene C2CD2 has a mutation status of G367R, The gene UMODL1 has a mutation status of Q680H, The gene TRPM2 has a mutation status of A890E, The gene MYO18B has a mutation status of T1632I, The gene MN1 has a mutation status of G588fs, The gene XBP1 has a mutation status of M1V, The gene AP1B1 has a mutation status of A603T, The gene SEC14L4 has a mutation status of D313N, The gene CRLF2 has a mutation status of S323F, The gene BMX has a mutation status of L88L, The gene MAGEB1 has a mutation status of A132A, The gene SYN1 has a mutation status of A550P, The gene KDM5C has a mutation status of W93*, The gene AR has a mutation status of Y535fs, The gene OPHN1 has a mutation status of G525A, The gene ZDHHC15 has a mutation status of I270T, The gene ZDHHC15 has a mutation status of K268N, The gene PABPC5 has a mutation status of R330W, The gene TMSB15A has a mutation status of Q36H, The gene PLP1 has a mutation status of K151N, The gene NRK has a mutation status of R1294R, The gene COL4A6 has a mutation status of G588R, The gene SLC25A5 has a mutation status of T221R, The gene TEX13C has a mutation status of A175D, The gene ACTRT1 has a mutation status of C220F, The gene MAGEA3 has a mutation status of Y145Y, The gene MAGEA3 has a mutation status of S156D, The gene MAGEA3 has a mutation status of E311fs, The gene MAGEA12 has a mutation status of L304fs, The gene MAGEA6 has a mutation status of F239L, The gene AC236972.4 has a mutation status of S1611S, The gene AC236972.4 has a mutation status of A1638T, The gene PNMA6F has a mutation status of I49L, The gene ATP2B3 has a mutation status of R199W, The gene ABCD1 has a mutation status of D685N, The gene IRAK1 has a mutation status of P484P, The gene F8 has a mutation status of L1198V, The gene MT-ND1 has a mutation status of A249A, The gene MT-ND2 has a mutation status of M108M, The gene MT-ND2 has a mutation status of Y293Y, The gene MT-ND5 has a mutation status of I126T
LUAD
The gene RNF223 has a mutation status of C101*, The gene GPR153 has a mutation status of R455H, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene UBR4 has a mutation status of P3758P, The gene ECE1 has a mutation status of R2W, The gene COL16A1 has a mutation status of P452P, The gene AGO3 has a mutation status of T144T, The gene TAL1 has a mutation status of A264G, The gene CDCP2 has a mutation status of P408fs, The gene TRIM33 has a mutation status of D942H, The gene GDAP2 has a mutation status of N231N, The gene PPIAL4H has a mutation status of N102I, The gene NBPF12 has a mutation status of R1042R, The gene AC242842.3 has a mutation status of V503L, The gene KCNN3 has a mutation status of L268L, The gene GBA has a mutation status of K447K, The gene SPTA1 has a mutation status of L480L, The gene ATP1B1 has a mutation status of G231G, The gene FMO2 has a mutation status of R462G, The gene TPR has a mutation status of T647T, The gene CACNA1S has a mutation status of S177L, The gene TMEM9 has a mutation status of R163H, The gene IGFN1 has a mutation status of K1635E, The gene IGFN1 has a mutation status of G3682R, The gene PKP1 has a mutation status of Y642H, The gene RNPEP has a mutation status of V187I, The gene PPFIA4 has a mutation status of R472*, The gene SNRPE has a mutation status of I43I, The gene DSTYK has a mutation status of R551H, The gene PLXNA2 has a mutation status of P207R, The gene PRSS38 has a mutation status of I60fs, The gene KIF26B has a mutation status of S381L, The gene ZNF695 has a mutation status of A360T, The gene OR2M4 has a mutation status of P268S, The gene TPO has a mutation status of A506T, The gene ID2 has a mutation status of L106L, The gene EMILIN1 has a mutation status of A741A, The gene PLB1 has a mutation status of V414I, The gene PCARE has a mutation status of P781S, The gene CAPN13 has a mutation status of R472*, The gene GALNT14 has a mutation status of T237N, The gene LOXL3 has a mutation status of R236W, The gene ACTR1B has a mutation status of R257Q, The gene TTL has a mutation status of Q340R, The gene NEB has a mutation status of I7840T, The gene RAPGEF4 has a mutation status of T809I, The gene TTC30B has a mutation status of T231T, The gene TTN has a mutation status of I28064V, The gene GPR55 has a mutation status of S134Y, The gene DGKD has a mutation status of N178S, The gene UGT1A10 has a mutation status of W251R, The gene CROCC2 has a mutation status of E1400K, The gene TOPAZ1 has a mutation status of S746I, The gene IP6K2 has a mutation status of R139*, The gene STAB1 has a mutation status of R218W, The gene PTPRG has a mutation status of T536M, The gene ATXN7 has a mutation status of Q39P, The gene PDZRN3 has a mutation status of R729T, The gene PDZRN3 has a mutation status of R648C, The gene ROBO2 has a mutation status of S798S, The gene ROBO2 has a mutation status of Q1177P, The gene ARHGAP31 has a mutation status of A483V, The gene GOLGB1 has a mutation status of L326H, The gene SLC12A8 has a mutation status of I110V, The gene GRK7 has a mutation status of A207P, The gene TIPARP has a mutation status of D548N, The gene PTX3 has a mutation status of A137A, The gene MECOM has a mutation status of S945N, The gene XXYLT1 has a mutation status of P342R, The gene LRCH3 has a mutation status of L208L, The gene DGKQ has a mutation status of C149W, The gene HTT has a mutation status of S958S, The gene C4orf50 has a mutation status of V1075M, The gene USP17L18 has a mutation status of A396T, The gene USP17L18 has a mutation status of H412H, The gene APBB2 has a mutation status of L576L, The gene GABRA2 has a mutation status of N425N, The gene TENM3 has a mutation status of A1469V, The gene IRF2 has a mutation status of S348C, The gene PDCD6 has a mutation status of T86M, The gene TERT has a mutation status of S656W, The gene OTULIN has a mutation status of C129C, The gene CDH9 has a mutation status of K115fs, The gene IL7R has a mutation status of E72Q, The gene MOCS2 has a mutation status of A99V, The gene FAM151B has a mutation status of W89*, The gene DMXL1 has a mutation status of V1958V, The gene FTMT has a mutation status of A27T, The gene MYOT has a mutation status of W267C, The gene PCDHA10 has a mutation status of L519P, The gene PCDHA13 has a mutation status of A596T, The gene NR3C1 has a mutation status of D64H, The gene KIF4B has a mutation status of E26K, The gene ADAMTS2 has a mutation status of G206G, The gene PSMG4 has a mutation status of V6V, The gene EDN1 has a mutation status of I71V, The gene ZFP57 has a mutation status of R276H, The gene TRIM31 has a mutation status of N127K, The gene C6orf15 has a mutation status of R177Q, The gene EGFL8 has a mutation status of D146G, The gene MCM3 has a mutation status of D460N, The gene GSTA2 has a mutation status of E168A, The gene FAM135A has a mutation status of S221P, The gene RIMS1 has a mutation status of S40R, The gene HTR1E has a mutation status of L332L, The gene TAB2 has a mutation status of P494R, The gene SYNE1 has a mutation status of L6643L, The gene FOXK1 has a mutation status of P240P, The gene THSD7A has a mutation status of D1514D, The gene HOXA1 has a mutation status of A112A, The gene AMPH has a mutation status of S599Y, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene WDR91 has a mutation status of E368G, The gene PRSS1 has a mutation status of N77N, The gene EPHB6 has a mutation status of A710A, The gene GIMAP8 has a mutation status of I389M, The gene TMEM176B has a mutation status of E252K, The gene TDRP has a mutation status of A33A, The gene TNKS has a mutation status of K920R, The gene CHD7 has a mutation status of T2381S, The gene RUNX1T1 has a mutation status of A498A, The gene TMEM74 has a mutation status of S23S, The gene TRPS1 has a mutation status of S213Y, The gene COL22A1 has a mutation status of L1454R, The gene PYCR3 has a mutation status of P6L, The gene PLEC has a mutation status of R1709H, The gene MROH1 has a mutation status of D1010D, The gene UBAP2 has a mutation status of S597F, The gene KIF24 has a mutation status of T1077M, The gene KIF24 has a mutation status of I58V, The gene PIGO has a mutation status of R604fs, The gene RNF38 has a mutation status of V353A, The gene FRMPD1 has a mutation status of P925P, The gene AOPEP has a mutation status of Q527Q, The gene COL15A1 has a mutation status of S757P, The gene RNF20 has a mutation status of S544P, The gene FRRS1L has a mutation status of R51A, The gene OR1K1 has a mutation status of L95L, The gene RABEPK has a mutation status of E342E, The gene GARNL3 has a mutation status of R608R, The gene RAPGEF1 has a mutation status of G852G, The gene CCDC187 has a mutation status of Q1158R, The gene DIPK1B has a mutation status of K185E, The gene PNPLA7 has a mutation status of L698L, The gene BEND7 has a mutation status of S184N, The gene YME1L1 has a mutation status of C123S, The gene JCAD has a mutation status of R120W, The gene WASHC2C has a mutation status of K1199R, The gene SLC16A9 has a mutation status of G433V, The gene ABRAXAS2 has a mutation status of Y154C, The gene LMNTD2 has a mutation status of F477F, The gene MRGPRG has a mutation status of S13R, The gene OR51G1 has a mutation status of T17T, The gene ABTB2 has a mutation status of L969fs, The gene ABTB2 has a mutation status of 967_968insGVVFRGTSPNGT, The gene MYBPC3 has a mutation status of V1139I, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MYRF has a mutation status of I518I, The gene MRPL11 has a mutation status of S2L, The gene GAB2 has a mutation status of R354fs, The gene MRE11 has a mutation status of R576*, The gene ATM has a mutation status of R919M, The gene OR8D1 has a mutation status of A203V, The gene CHEK1 has a mutation status of I124fs, The gene NFRKB has a mutation status of L261F, The gene PLEKHG6 has a mutation status of D637P, The gene CD163 has a mutation status of H946Y, The gene CD69 has a mutation status of T52I, The gene KRAS has a mutation status of G12V, The gene PRICKLE1 has a mutation status of E710D, The gene KANSL2 has a mutation status of G386R, The gene MMP19 has a mutation status of S459L, The gene R3HDM2 has a mutation status of R295Q, The gene IL26 has a mutation status of N4N, The gene EEA1 has a mutation status of E136E, The gene HSP90B1 has a mutation status of K410N, The gene ALDH1L2 has a mutation status of P167T, The gene HECTD4 has a mutation status of E3730K, The gene RPH3A has a mutation status of R540H, The gene DTX1 has a mutation status of P331L, The gene MED13L has a mutation status of M1980T, The gene HPD has a mutation status of A97A, The gene FZD10 has a mutation status of R39H, The gene TRPC4 has a mutation status of H969H, The gene HNRNPA1L2 has a mutation status of G248C, The gene RNASE2 has a mutation status of R63*, The gene PCK2 has a mutation status of 18_19insRGF, The gene PCK2 has a mutation status of G20fs, The gene NIN has a mutation status of I993V, The gene NID2 has a mutation status of D233G, The gene SIX4 has a mutation status of S615C, The gene CCDC88C has a mutation status of L439L, The gene HSP90AA1 has a mutation status of C420C, The gene TDRD9 has a mutation status of R1311T, The gene AC135068.1 has a mutation status of V239M, The gene RPAP1 has a mutation status of L15L, The gene TYRO3 has a mutation status of D555fs, The gene TYRO3 has a mutation status of F674L, The gene FBN1 has a mutation status of V920V, The gene ZNF609 has a mutation status of D391E, The gene ANKDD1A has a mutation status of L516L, The gene NOX5 has a mutation status of P420T, The gene HIGD2B has a mutation status of Y65H, The gene RPP25 has a mutation status of P154P, The gene ROGDI has a mutation status of H24Q, The gene ATF7IP2 has a mutation status of A265E, The gene IL21R has a mutation status of R163W, The gene ZNF747 has a mutation status of D97G, The gene ZNF747 has a mutation status of K92E, The gene NOD2 has a mutation status of A707A, The gene CETP has a mutation status of R89R, The gene SETD6 has a mutation status of Q93R, The gene TERB1 has a mutation status of G458D, The gene HASPIN has a mutation status of M706V, The gene PLD2 has a mutation status of S192I, The gene TP53 has a mutation status of R282W, The gene ALOX12B has a mutation status of P422L, The gene TNS4 has a mutation status of E85*, The gene KRTAP9-6 has a mutation status of G106C, The gene EFTUD2 has a mutation status of I150M, The gene LRRC37A2 has a mutation status of N1079N, The gene HOXB8 has a mutation status of P136S, The gene AKAP1 has a mutation status of L548L, The gene RNF43 has a mutation status of F69C, The gene BRIP1 has a mutation status of I275F, The gene ACE has a mutation status of L1219P, The gene PRKAR1A has a mutation status of S238S, The gene GPR142 has a mutation status of V157A, The gene NUP85 has a mutation status of I582V, The gene CBX2 has a mutation status of K103E, The gene ANKRD30B has a mutation status of R13Q, The gene MIB1 has a mutation status of S810G, The gene EPG5 has a mutation status of N2384K, The gene RTTN has a mutation status of V964F, The gene SALL3 has a mutation status of A693T, The gene ARHGAP45 has a mutation status of T1140M, The gene AC006538.2 has a mutation status of A91V, The gene MATK has a mutation status of L247L, The gene FSD1 has a mutation status of R303H, The gene PTPRS has a mutation status of E780E, The gene KANK3 has a mutation status of E420V, The gene SYDE1 has a mutation status of E109D, The gene JAK3 has a mutation status of V1016V, The gene ELL has a mutation status of G11R, The gene SLC25A42 has a mutation status of P9L, The gene ZNF208 has a mutation status of G365V, The gene KIAA0355 has a mutation status of R941I, The gene CD22 has a mutation status of T262T, The gene ZNF226 has a mutation status of S376F, The gene PPP1R37 has a mutation status of S597fs, The gene STRN4 has a mutation status of V714M, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of H25P, The gene ZNF773 has a mutation status of C221*, The gene ZNF776 has a mutation status of R333H, The gene SOX12 has a mutation status of Q52fs, The gene SIRPA has a mutation status of L44S, The gene SIGLEC1 has a mutation status of C876R, The gene PANK2 has a mutation status of N355S, The gene MYH7B has a mutation status of Q1274Q, The gene ZNF334 has a mutation status of R249R, The gene CYP24A1 has a mutation status of T265A, The gene COL9A3 has a mutation status of R583H, The gene HELZ2 has a mutation status of T746T, The gene PPM1F has a mutation status of E105del, The gene PVALB has a mutation status of D95D, The gene MFNG has a mutation status of G217S, The gene EP300 has a mutation status of C1686S, The gene FANCB has a mutation status of T553M, The gene CXorf58 has a mutation status of R205H, The gene MAGEB5 has a mutation status of W204L, The gene HUWE1 has a mutation status of L3888L, The gene GNL3L has a mutation status of Q80L, The gene AMER1 has a mutation status of P456fs, The gene AR has a mutation status of L548F, The gene OTUD6A has a mutation status of A277A, The gene ACSL4 has a mutation status of Q168Q, The gene MAGEA6 has a mutation status of G141R, The gene FLNA has a mutation status of P1751S, The gene MT-ND1 has a mutation status of Y30H, The gene MT-ND5 has a mutation status of V92V, The gene MT-CYB has a mutation status of F18L, The gene PRKCZ has a mutation status of *410S, The gene CHD5 has a mutation status of Y1524*, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene UBR4 has a mutation status of P3758P, The gene COL16A1 has a mutation status of P452P, The gene CLSPN has a mutation status of M115I, The gene AGO3 has a mutation status of T144T, The gene CDCP2 has a mutation status of P408fs, The gene OMA1 has a mutation status of P473T, The gene LEPR has a mutation status of K359N, The gene LRIF1 has a mutation status of S430F, The gene TRIM33 has a mutation status of D942H, The gene GDAP2 has a mutation status of N231N, The gene NBPF10 has a mutation status of L891V, The gene PPIAL4H has a mutation status of N102I, The gene NBPF12 has a mutation status of R1042R, The gene NBPF14 has a mutation status of G628E, The gene HRNR has a mutation status of G1127S, The gene CHRNB2 has a mutation status of A375A, The gene KCNN3 has a mutation status of L268L, The gene GBA has a mutation status of K447K, The gene ATP1B1 has a mutation status of G231G, The gene SELL has a mutation status of G235W, The gene MROH9 has a mutation status of Y802Y, The gene FMO2 has a mutation status of R462G, The gene LAMC2 has a mutation status of V817L, The gene IGFN1 has a mutation status of G3682R, The gene PPP1R12B has a mutation status of L890L, The gene PPFIA4 has a mutation status of R472*, The gene DSTYK has a mutation status of S703P, The gene DSTYK has a mutation status of R551H, The gene PLXNA2 has a mutation status of P207R, The gene HEATR1 has a mutation status of A579A, The gene KIF26B has a mutation status of S381L, The gene ZNF695 has a mutation status of A360T, The gene NLRP3 has a mutation status of Q185*, The gene TPO has a mutation status of A506T, The gene PXDN has a mutation status of M1392T, The gene ID2 has a mutation status of L106L, The gene NCOA1 has a mutation status of S482C, The gene ADGRF3 has a mutation status of R609L, The gene EMILIN1 has a mutation status of A741A, The gene CAPN13 has a mutation status of R472*, The gene CFAP36 has a mutation status of N117fs, The gene ACTR1B has a mutation status of R257Q, The gene TTL has a mutation status of Q340R, The gene NEB has a mutation status of I7840T, The gene DPP4 has a mutation status of L180L, The gene LRP2 has a mutation status of S1212N, The gene RAPGEF4 has a mutation status of T809I, The gene TTN has a mutation status of I28064V, The gene SCYGR2 has a mutation status of H97S, The gene DGKD has a mutation status of N178S, The gene UGT1A10 has a mutation status of W251R, The gene NGLY1 has a mutation status of I12N, The gene SCN10A has a mutation status of R498W, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene PTPRG has a mutation status of T536M, The gene PDZRN3 has a mutation status of R648C, The gene ARHGAP31 has a mutation status of A483V, The gene GOLGB1 has a mutation status of C1050Y, The gene GOLGB1 has a mutation status of L326H, The gene SLC12A8 has a mutation status of I110V, The gene GRK7 has a mutation status of A207P, The gene PTX3 has a mutation status of A137A, The gene MECOM has a mutation status of S945N, The gene NDUFB5 has a mutation status of R150W, The gene TTC14 has a mutation status of T606T, The gene DGKQ has a mutation status of C149W, The gene HTT has a mutation status of S958S, The gene APBB2 has a mutation status of L576L, The gene IRF2 has a mutation status of S348C, The gene PDCD6 has a mutation status of T86M, The gene OTULIN has a mutation status of C129C, The gene ZNF622 has a mutation status of K192fs, The gene PELO has a mutation status of V213L, The gene PDE4D has a mutation status of T109T, The gene MAP1B has a mutation status of S1258P, The gene FAM151B has a mutation status of W89*, The gene XRCC4 has a mutation status of A168T, The gene PCDHA10 has a mutation status of L519P, The gene PCDHA13 has a mutation status of A596T, The gene KIF4B has a mutation status of E26K, The gene ADAMTS2 has a mutation status of G206G, The gene PSMG4 has a mutation status of V6V, The gene EDN1 has a mutation status of I71V, The gene ZFP57 has a mutation status of R276H, The gene TRIM31 has a mutation status of N127K, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Y42H, The gene HLA-DRB1 has a mutation status of I248L, The gene PKHD1 has a mutation status of G1651S, The gene MCM3 has a mutation status of D460N, The gene GSTA2 has a mutation status of E168A, The gene BEND6 has a mutation status of T147K, The gene FAM135A has a mutation status of S221P, The gene TAB2 has a mutation status of P494R, The gene SYNE1 has a mutation status of L6643L, The gene FOXK1 has a mutation status of P240P, The gene ZNF316 has a mutation status of V53M, The gene HOXA1 has a mutation status of A112A, The gene PKD1L1 has a mutation status of G2043A, The gene POM121L12 has a mutation status of S94S, The gene PSPH has a mutation status of L68P, The gene AUTS2 has a mutation status of P633S, The gene TRRAP has a mutation status of A516P, The gene TRRAP has a mutation status of A3829A, The gene STAG3 has a mutation status of S1147L, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S558T, The gene MUC3A has a mutation status of P1427P, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene WDR91 has a mutation status of E368G, The gene PRSS1 has a mutation status of G62A, The gene PRSS1 has a mutation status of N77N, The gene EPHB6 has a mutation status of A710A, The gene TMEM176B has a mutation status of E252K, The gene TNKS has a mutation status of K920R, The gene CHD7 has a mutation status of T2381S, The gene RUNX1T1 has a mutation status of A498A, The gene TRPS1 has a mutation status of S213Y, The gene FAM135B has a mutation status of N1151N, The gene PYCR3 has a mutation status of P6L, The gene MROH1 has a mutation status of D1010D, The gene SMARCA2 has a mutation status of L946S, The gene PRSS3 has a mutation status of G208R, The gene RNF38 has a mutation status of V353A, The gene AOPEP has a mutation status of Q527Q, The gene COL15A1 has a mutation status of S757P, The gene INVS has a mutation status of Q46R, The gene RNF20 has a mutation status of S544P, The gene FRRS1L has a mutation status of R51A, The gene CRB2 has a mutation status of C579F, The gene GARNL3 has a mutation status of R608R, The gene HMCN2 has a mutation status of R819H, The gene MED22 has a mutation status of L147R, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene CCDC187 has a mutation status of E1017E, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of H128H, The gene BEND7 has a mutation status of S184N, The gene YME1L1 has a mutation status of C123S, The gene WASHC2C has a mutation status of K1199R, The gene ABRAXAS2 has a mutation status of Y154C, The gene MRGPRG has a mutation status of S13R, The gene OR51G1 has a mutation status of T17T, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MS4A1 has a mutation status of S7S, The gene AP001273.2 has a mutation status of V140L, The gene MRE11 has a mutation status of R576*, The gene NXPE4 has a mutation status of L435M, The gene OR8D1 has a mutation status of A203V, The gene MSANTD2 has a mutation status of T109T, The gene CD69 has a mutation status of T52I, The gene TAS2R19 has a mutation status of L116F, The gene TAS2R31 has a mutation status of 150_151KE>NQ, The gene TAS2R46 has a mutation status of 296_297HV>QM, The gene TAS2R46 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PRB4 has a mutation status of R122G, The gene SLC15A5 has a mutation status of L507*, The gene KRAS has a mutation status of G12V, The gene GXYLT1 has a mutation status of V28K, The gene KANSL2 has a mutation status of G386R, The gene KRT5 has a mutation status of G552S, The gene KRT18 has a mutation status of T103N, The gene PCBP2 has a mutation status of Q303Q, The gene ESYT1 has a mutation status of I66M, The gene TRHDE has a mutation status of K938K, The gene KERA has a mutation status of K248N, The gene EEA1 has a mutation status of E136E, The gene HSP90B1 has a mutation status of K410N, The gene ALDH1L2 has a mutation status of P167T, The gene NUAK1 has a mutation status of S503F, The gene DTX1 has a mutation status of P331L, The gene RBM19 has a mutation status of F518F, The gene MED13L has a mutation status of M1980T, The gene GCN1 has a mutation status of R1435P, The gene FZD10 has a mutation status of R39H, The gene TUBA3C has a mutation status of D116E, The gene GJB2 has a mutation status of M1I, The gene TRPC4 has a mutation status of H969H, The gene TSC22D1 has a mutation status of P67P, The gene DACH1 has a mutation status of 81_82insGG, The gene RNASE2 has a mutation status of R63*, The gene PCK2 has a mutation status of 18_19insRGF, The gene PCK2 has a mutation status of G20fs, The gene NIN has a mutation status of I993V, The gene NID2 has a mutation status of D233G, The gene SIX4 has a mutation status of S615C, The gene CCDC88C has a mutation status of L439L, The gene HSP90AA1 has a mutation status of C420C, The gene MOK has a mutation status of P221A, The gene LINC02203 has a mutation status of I259M, The gene TYRO3 has a mutation status of F674L, The gene LDHAL6B has a mutation status of H364P, The gene C2CD4A has a mutation status of F238fs, The gene ANKDD1A has a mutation status of L516L, The gene MEGF11 has a mutation status of R561C, The gene MYO9A has a mutation status of T1956S, The gene ARID3B has a mutation status of H149R, The gene CSPG4 has a mutation status of A131T, The gene ST20 has a mutation status of M42I, The gene SAXO2 has a mutation status of Y70C, The gene SLC28A1 has a mutation status of A572A, The gene HMOX2 has a mutation status of A269T, The gene ROGDI has a mutation status of H24Q, The gene NOD2 has a mutation status of A707A, The gene CES5A has a mutation status of T478R, The gene CES5A has a mutation status of L25F, The gene CETP has a mutation status of R89R, The gene SETD6 has a mutation status of Q93R, The gene SGSM2 has a mutation status of V521V, The gene HASPIN has a mutation status of M706V, The gene PLD2 has a mutation status of S192I, The gene TP53 has a mutation status of R282W, The gene ALOX12B has a mutation status of P422L, The gene TNFAIP1 has a mutation status of D72fs, The gene HNF1B has a mutation status of 375_376VT>AP, The gene PTGES3L-AARSD1 has a mutation status of V201L, The gene HDAC5 has a mutation status of R23R, The gene EFTUD2 has a mutation status of I150M, The gene HOXB8 has a mutation status of P136S, The gene AKAP1 has a mutation status of L548L, The gene RNF43 has a mutation status of F69C, The gene BRIP1 has a mutation status of I275F, The gene ACE has a mutation status of L1219P, The gene PRKAR1A has a mutation status of S238S, The gene GPR142 has a mutation status of V157A, The gene FADS6 has a mutation status of P6P, The gene NUP85 has a mutation status of I582V, The gene MYO15B has a mutation status of G470D, The gene MYO15B has a mutation status of G474A, The gene MYO15B has a mutation status of S620H, The gene CBX2 has a mutation status of K103E, The gene EMILIN2 has a mutation status of T747T, The gene MIB1 has a mutation status of S810G, The gene EPG5 has a mutation status of N2384K, The gene SALL3 has a mutation status of A693T, The gene MED16 has a mutation status of R565C, The gene ARHGAP45 has a mutation status of T1140M, The gene AC006538.2 has a mutation status of A91V, The gene MATK has a mutation status of L247L, The gene FSD1 has a mutation status of R303H, The gene PTPRS has a mutation status of E780E, The gene KHSRP has a mutation status of G8G, The gene KANK3 has a mutation status of E420V, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of V13007G, The gene MUC16 has a mutation status of T12336L, The gene PODNL1 has a mutation status of Q78*, The gene SYDE1 has a mutation status of E109D, The gene JAK3 has a mutation status of V1016V, The gene ELL has a mutation status of G11R, The gene ZNF66 has a mutation status of L102fs, The gene CD22 has a mutation status of T262T, The gene ZNF226 has a mutation status of S376F, The gene STRN4 has a mutation status of V714M, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of S395T, The gene LILRA1 has a mutation status of T25P, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene LILRB1 has a mutation status of Y99I, The gene BRSK1 has a mutation status of E166D, The gene ZNF773 has a mutation status of C221*, The gene ZNF776 has a mutation status of R333H, The gene ZNF132 has a mutation status of W422fs, The gene SIRPA has a mutation status of L44S, The gene SIGLEC1 has a mutation status of C876R, The gene PANK2 has a mutation status of N355S, The gene MYH7B has a mutation status of Q1274Q, The gene DLGAP4 has a mutation status of S384I, The gene ZNF334 has a mutation status of R249R, The gene CYP24A1 has a mutation status of T265A, The gene TFIP11 has a mutation status of V484V, The gene PVALB has a mutation status of D95D, The gene MFNG has a mutation status of G217S, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene GLRA2 has a mutation status of L271F, The gene HUWE1 has a mutation status of L3888L, The gene GNL3L has a mutation status of Q80L, The gene AR has a mutation status of L548F, The gene OTUD6A has a mutation status of A277A, The gene SLC25A5 has a mutation status of T221R, The gene ELF4 has a mutation status of L579L, The gene CD40LG has a mutation status of S222Y, The gene SPANXN3 has a mutation status of P16S, The gene AC236972.4 has a mutation status of P1394A, The gene MT-ND1 has a mutation status of Y30H, The gene MT-CO2 has a mutation status of V64I, The gene MT-ND5 has a mutation status of V92V, The gene MT-CYB has a mutation status of F18L
PAAD
The gene AGRN has a mutation status of Q960K, The gene CPTP has a mutation status of R68K, The gene PLCH2 has a mutation status of R59R, The gene CCDC27 has a mutation status of S53Y, The gene CAMTA1 has a mutation status of A927S, The gene PRAMEF13 has a mutation status of V256G, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF17 has a mutation status of K346N, The gene TMEM82 has a mutation status of P56L, The gene TMCO4 has a mutation status of *635*, The gene FAM43B has a mutation status of A325A, The gene KIF17 has a mutation status of Q366*, The gene UBXN11 has a mutation status of P395L, The gene TXLNA has a mutation status of G229S, The gene ZMYM6 has a mutation status of N798K, The gene GRIK3 has a mutation status of D100G, The gene RSPO1 has a mutation status of N224S, The gene INPP5B has a mutation status of A876A, The gene CFAP57 has a mutation status of T1200I, The gene DPH2 has a mutation status of R282C, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene PTCH2 has a mutation status of A246A, The gene TSPAN1 has a mutation status of E226G, The gene TUT4 has a mutation status of K364E, The gene KANK4 has a mutation status of Q513H, The gene ERICH3 has a mutation status of S693P, The gene LHX8 has a mutation status of E23K, The gene ST6GALNAC3 has a mutation status of A147V, The gene PTGFR has a mutation status of L68R, The gene WDR63 has a mutation status of E605*, The gene GBP1 has a mutation status of D479E, The gene BARHL2 has a mutation status of S313L, The gene DDX20 has a mutation status of P700R, The gene DENND2C has a mutation status of F715L, The gene TENT5C has a mutation status of E178A, The gene SPAG17 has a mutation status of W18R, The gene NBPF20 has a mutation status of D202D, The gene HJV has a mutation status of V274M, The gene ACP6 has a mutation status of E309R, The gene FLG2 has a mutation status of Y2354Y, The gene SPRR5 has a mutation status of P99S, The gene RXFP4 has a mutation status of L267L, The gene MEF2D has a mutation status of Q109K, The gene BCAN has a mutation status of S704P, The gene FCRL6 has a mutation status of G364G, The gene IGSF8 has a mutation status of P536P, The gene ATP1A2 has a mutation status of R65L, The gene ARHGAP30 has a mutation status of S843P, The gene ARHGAP30 has a mutation status of Q213Q, The gene MPZL1 has a mutation status of T70T, The gene ADCY10 has a mutation status of H999R, The gene PRRC2C has a mutation status of P1914P, The gene TNN has a mutation status of H145fs, The gene KIAA1614 has a mutation status of H214Y, The gene LAMC1 has a mutation status of N1395D, The gene LAMC2 has a mutation status of N451D, The gene HMCN1 has a mutation status of G807D, The gene CFHR5 has a mutation status of R385K, The gene CFHR5 has a mutation status of G450G, The gene ASPM has a mutation status of F1920S, The gene IGFN1 has a mutation status of G1615G, The gene RNPEP has a mutation status of P8S, The gene TMEM183A has a mutation status of L73F, The gene PIK3C2B has a mutation status of P861P, The gene SRGAP2 has a mutation status of M1030V, The gene MIA3 has a mutation status of A313V, The gene CCDC185 has a mutation status of R266C, The gene DNAH14 has a mutation status of N1695N, The gene OBSCN has a mutation status of P3196P, The gene OBSCN has a mutation status of H5338C, The gene TRIM67 has a mutation status of A141V, The gene ACTN2 has a mutation status of S201S, The gene RYR2 has a mutation status of L4264L, The gene FMN2 has a mutation status of R1340K, The gene WDR64 has a mutation status of E101Q, The gene EFCAB2 has a mutation status of I159T, The gene PGBD2 has a mutation status of G299G, The gene FAM110C has a mutation status of P162H, The gene DCDC2C has a mutation status of R103*, The gene NBAS has a mutation status of R136*, The gene LDAH has a mutation status of I228fs, The gene APOB has a mutation status of F1480C, The gene APOB has a mutation status of P955S, The gene KLHL29 has a mutation status of P264S, The gene ITSN2 has a mutation status of R1670P, The gene DTNB has a mutation status of R247*, The gene ASXL2 has a mutation status of G1134S, The gene SLC35F6 has a mutation status of W145L, The gene PLB1 has a mutation status of P1150L, The gene LCLAT1 has a mutation status of R362Q, The gene NLRC4 has a mutation status of D1011Y, The gene LTBP1 has a mutation status of P190L, The gene MSH6 has a mutation status of H164R, The gene PPP4R3B has a mutation status of L209H, The gene APLF has a mutation status of N227fs, The gene SFTPB has a mutation status of G64R, The gene FER1L5 has a mutation status of R997Q, The gene GPR45 has a mutation status of N4K, The gene MARCO has a mutation status of L62M, The gene GLI2 has a mutation status of S839S, The gene RIF1 has a mutation status of S269G, The gene TANC1 has a mutation status of V822L, The gene BAZ2B has a mutation status of P137S, The gene MARCHF7 has a mutation status of E236G, The gene DLX2 has a mutation status of G252G, The gene TTN has a mutation status of Q30964Q, The gene ITGAV has a mutation status of Y251C, The gene FAM171B has a mutation status of I771S, The gene DNAH7 has a mutation status of I3169L, The gene CCDC150 has a mutation status of E957fs, The gene PLCL1 has a mutation status of G424G, The gene KIAA2012 has a mutation status of P628Q, The gene NBEAL1 has a mutation status of C15C, The gene RAPH1 has a mutation status of M286I, The gene STK36 has a mutation status of D405A, The gene CYP27A1 has a mutation status of R262C, The gene CHPF has a mutation status of E698Q, The gene STK11IP has a mutation status of Q671L, The gene SLC4A3 has a mutation status of S1004N, The gene CCDC195 has a mutation status of R86H, The gene SPHKAP has a mutation status of S781N, The gene INPP5D has a mutation status of GPP1178del, The gene COL6A3 has a mutation status of F1439L, The gene COL6A3 has a mutation status of I482N, The gene FARP2 has a mutation status of K768N, The gene SRGAP3 has a mutation status of Q598*, The gene IRAK2 has a mutation status of A290A, The gene TSEN2 has a mutation status of V260V, The gene BTD has a mutation status of T456I, The gene RFTN1 has a mutation status of Q164R, The gene RBMS3 has a mutation status of S50R, The gene ARPP21 has a mutation status of Q289H, The gene XIRP1 has a mutation status of P949P, The gene XIRP1 has a mutation status of P26P, The gene ZKSCAN7 has a mutation status of F728F, The gene CCR1 has a mutation status of L117F, The gene KLHL18 has a mutation status of F67L, The gene HYAL3 has a mutation status of S386N, The gene RAD54L2 has a mutation status of L1067L, The gene DNAH1 has a mutation status of V3906V, The gene ARHGEF3 has a mutation status of S18S, The gene ROBO2 has a mutation status of G1242G, The gene CHMP2B has a mutation status of A36S, The gene GPR156 has a mutation status of F70L, The gene HEG1 has a mutation status of R1217*, The gene ALDH1L1 has a mutation status of M430L, The gene KIAA1257 has a mutation status of S29G, The gene ISY1 has a mutation status of G51E, The gene COL6A5 has a mutation status of Q933Q, The gene IGSF10 has a mutation status of I458V, The gene ARHGEF26 has a mutation status of R426*, The gene GPR149 has a mutation status of V154A, The gene BCHE has a mutation status of K596E, The gene CLDN11 has a mutation status of T40P, The gene ZMAT3 has a mutation status of G256G, The gene ZNF639 has a mutation status of C291C, The gene FXR1 has a mutation status of H208Y, The gene TBCCD1 has a mutation status of L249L, The gene RUBCN has a mutation status of V652F, The gene FGFR3 has a mutation status of K651E, The gene ZFYVE28 has a mutation status of S631S, The gene SH3BP2 has a mutation status of S494S, The gene ADD1 has a mutation status of V183F, The gene PSAPL1 has a mutation status of C366C, The gene SORCS2 has a mutation status of A1039P, The gene HTRA3 has a mutation status of P393L, The gene WDR1 has a mutation status of T605P, The gene NWD2 has a mutation status of N1712S, The gene KLB has a mutation status of A672V, The gene ZAR1 has a mutation status of R174L, The gene ERVMER34-1 has a mutation status of P429Q, The gene SLC4A4 has a mutation status of V138L, The gene RCHY1 has a mutation status of E8K, The gene ODAPH has a mutation status of P117T, The gene CDKL2 has a mutation status of E294G, The gene CDS1 has a mutation status of N388T, The gene ARHGAP24 has a mutation status of R175*, The gene SPARCL1 has a mutation status of S296S, The gene SNCA has a mutation status of S150Y, The gene CCSER1 has a mutation status of S47S, The gene FAT4 has a mutation status of K4214E, The gene LARP1B has a mutation status of K560K, The gene LRBA has a mutation status of R167C, The gene SFRP2 has a mutation status of P101T, The gene AHRR has a mutation status of H473P, The gene SLC9A3 has a mutation status of I384V, The gene ZDHHC11B has a mutation status of P25P, The gene TERT has a mutation status of P246P, The gene MTRR has a mutation status of S217S, The gene TAS2R1 has a mutation status of T211A, The gene TRIO has a mutation status of F124L, The gene SKP2 has a mutation status of D301G, The gene CDC20B has a mutation status of A148E, The gene MTREX has a mutation status of S11G, The gene SLC38A9 has a mutation status of C14R, The gene PDE4D has a mutation status of I151T, The gene HOMER1 has a mutation status of A11A, The gene ADGRV1 has a mutation status of G310E, The gene MCTP1 has a mutation status of L88V, The gene FBN2 has a mutation status of E2423Q, The gene FBN2 has a mutation status of V407F, The gene SPOCK1 has a mutation status of N298T, The gene PCDHB3 has a mutation status of Y751C, The gene PCDHB6 has a mutation status of R788W, The gene SH3TC2 has a mutation status of T1033R, The gene HMGXB3 has a mutation status of N1232S, The gene CDX1 has a mutation status of G144G, The gene NMUR2 has a mutation status of V341G, The gene C5orf52 has a mutation status of I48I, The gene ADAMTS2 has a mutation status of R430W, The gene GFPT2 has a mutation status of E534D, The gene TXNDC5 has a mutation status of P348L, The gene TMEM170B has a mutation status of G101V, The gene MYLIP has a mutation status of V250M, The gene FAM8A1 has a mutation status of A308A, The gene KIF13A has a mutation status of L458F, The gene SLC17A3 has a mutation status of A432T, The gene H2BC7 has a mutation status of I74I, The gene OR2J1 has a mutation status of P59L, The gene OR2J3 has a mutation status of V225F, The gene TRIM39 has a mutation status of E366D, The gene ABHD16A has a mutation status of Q173E, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DQA2 has a mutation status of S75R, The gene UQCC2 has a mutation status of I103T, The gene MRPS18A has a mutation status of A55V, The gene TCTE1 has a mutation status of T6M, The gene TDRD6 has a mutation status of I937V, The gene RHAG has a mutation status of A123A, The gene CILK1 has a mutation status of N252D, The gene DST has a mutation status of K6310K, The gene ZNF451 has a mutation status of K322M, The gene COL9A1 has a mutation status of K126N, The gene GJB7 has a mutation status of A96V, The gene SMIM8 has a mutation status of R29R, The gene CDC40 has a mutation status of A53V, The gene DDO has a mutation status of L232F, The gene STXBP5 has a mutation status of K859E, The gene RSPH3 has a mutation status of T183I, The gene IGF2R has a mutation status of L1858L, The gene LPA has a mutation status of R1177R, The gene INTS1 has a mutation status of H1873P, The gene ELFN1 has a mutation status of H660Q, The gene SDK1 has a mutation status of R807fs, The gene ITGB8 has a mutation status of C481Y, The gene CDCA7L has a mutation status of R252R, The gene HOXA4 has a mutation status of H52P, The gene HOXA13 has a mutation status of Y290*, The gene DBNL has a mutation status of S153G, The gene AEBP1 has a mutation status of I817F, The gene NUDCD3 has a mutation status of T296T, The gene PSPH has a mutation status of L68P, The gene PHTF2 has a mutation status of F222F, The gene MAGI2 has a mutation status of R1222R, The gene CACNA2D1 has a mutation status of G903G, The gene RUNDC3B has a mutation status of R154I, The gene ERVW-1 has a mutation status of L333*, The gene ERVW-1 has a mutation status of Q260*, The gene PPP1R9A has a mutation status of Q1031Q, The gene FAM200A has a mutation status of K262N, The gene CYP3A43 has a mutation status of F203L, The gene COPS6 has a mutation status of C143C, The gene ZAN has a mutation status of I2055T, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T289M, The gene MUC3A has a mutation status of I491I, The gene MUC3A has a mutation status of T2198I, The gene MUC3A has a mutation status of V2475S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene KIAA1549 has a mutation status of S1801L, The gene KDM7A has a mutation status of I53I, The gene MGAM2 has a mutation status of L337P, The gene MGAM2 has a mutation status of T1941I, The gene OR6V1 has a mutation status of I69I, The gene WDR60 has a mutation status of K43K, The gene DLGAP2 has a mutation status of H234Y, The gene DLGAP2 has a mutation status of V856I, The gene KBTBD11 has a mutation status of A86G, The gene GATA4 has a mutation status of V431G, The gene DUSP4 has a mutation status of A72A, The gene NSD3 has a mutation status of G528G, The gene HTRA4 has a mutation status of L22F, The gene ANK1 has a mutation status of D920D, The gene SLC20A2 has a mutation status of T420T, The gene ST18 has a mutation status of L230P, The gene KCNB2 has a mutation status of M344T, The gene RUNX1T1 has a mutation status of D347E, The gene HAS2 has a mutation status of M444L, The gene WDYHV1 has a mutation status of N176H, The gene SLC45A4 has a mutation status of P247P, The gene ZNF623 has a mutation status of I396I, The gene PLEC has a mutation status of T4080N, The gene PLEC has a mutation status of S3479S, The gene PLEC has a mutation status of R890C, The gene SPATC1 has a mutation status of Q502K, The gene OPLAH has a mutation status of F1201L, The gene DGAT1 has a mutation status of R280Q, The gene CPSF1 has a mutation status of R140Q, The gene SLC39A4 has a mutation status of L635L, The gene FOCAD has a mutation status of E578G, The gene CDKN2A has a mutation status of H32Y, The gene UBAP2 has a mutation status of R11Q, The gene CNTNAP3B has a mutation status of L968L, The gene CNTNAP3B has a mutation status of L615fs, The gene SPATA31A6 has a mutation status of E258K, The gene SPATA31A6 has a mutation status of R282W, The gene SPATA31A6 has a mutation status of V327I, The gene SPATA31A6 has a mutation status of V338F, The gene VPS13A has a mutation status of Q2653Q, The gene TUT7 has a mutation status of R186Q, The gene GAS1 has a mutation status of R274R, The gene DAPK1 has a mutation status of R47del, The gene DAPK1 has a mutation status of H1293N, The gene DIRAS2 has a mutation status of K108R, The gene OR13F1 has a mutation status of L222F, The gene LPAR1 has a mutation status of L132L, The gene ECPAS has a mutation status of G203G, The gene ZFP37 has a mutation status of K159T, The gene PHF19 has a mutation status of A452S, The gene TTLL11 has a mutation status of S98N, The gene CRB2 has a mutation status of S364S, The gene SH2D3C has a mutation status of L572L, The gene TRUB2 has a mutation status of V194M, The gene IER5L has a mutation status of P325T, The gene HMCN2 has a mutation status of R819H, The gene HMCN2 has a mutation status of C1459S, The gene CACFD1 has a mutation status of L71L, The gene NACC2 has a mutation status of A153A, The gene QSOX2 has a mutation status of A585A, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of R294H, The gene CCDC187 has a mutation status of T90M, The gene AJM1 has a mutation status of N471Y, The gene DPP7 has a mutation status of I468T, The gene EXD3 has a mutation status of G294W, The gene ADARB2 has a mutation status of G95C, The gene AKR1C1 has a mutation status of V151V, The gene SLC39A12 has a mutation status of L425L, The gene MLLT10 has a mutation status of P537P, The gene MLLT10 has a mutation status of Q673R, The gene SPAG6 has a mutation status of A371S, The gene KIAA1217 has a mutation status of S161P, The gene ENKUR has a mutation status of C5F, The gene WAC has a mutation status of F460F, The gene JCAD has a mutation status of F736L, The gene C10orf71 has a mutation status of P1221P, The gene ANK3 has a mutation status of R961I, The gene STOX1 has a mutation status of T180T, The gene SUPV3L1 has a mutation status of G389V, The gene SLC29A3 has a mutation status of W68*, The gene ZSWIM8 has a mutation status of V1473V, The gene LRIT2 has a mutation status of P439L, The gene HHEX has a mutation status of S63S, The gene MYOF has a mutation status of R1072H, The gene FBXL15 has a mutation status of G84A, The gene MFSD13A has a mutation status of F192Y, The gene CALHM2 has a mutation status of V136G, The gene ADD3 has a mutation status of E623V, The gene NRAP has a mutation status of L1395L, The gene TACC2 has a mutation status of V673V, The gene MKI67 has a mutation status of Q2795K, The gene ADAM8 has a mutation status of N347N, The gene TUBGCP2 has a mutation status of H650H, The gene SYCE1 has a mutation status of Q256E, The gene LRRC56 has a mutation status of T429S, The gene DRD4 has a mutation status of A84T, The gene DRD4 has a mutation status of T368fs, The gene PIDD1 has a mutation status of P403L, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of T5121T, The gene MUC5B has a mutation status of T3033P, The gene OR52D1 has a mutation status of K315E, The gene APBB1 has a mutation status of 634_647MFWCEPNAASLSEA>I, The gene RBMXL2 has a mutation status of P154P, The gene PRR5L has a mutation status of R42R, The gene EXT2 has a mutation status of T89M, The gene TRIM49B has a mutation status of A354A, The gene OR5J2 has a mutation status of G112S, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene BTBD18 has a mutation status of S302T, The gene OR9Q2 has a mutation status of Q195H, The gene SLC22A10 has a mutation status of G207G, The gene SLC22A9 has a mutation status of G387G, The gene BAD has a mutation status of P88T, The gene GAL3ST3 has a mutation status of A256A, The gene PACS1 has a mutation status of E288*, The gene PELI3 has a mutation status of G221G, The gene CCDC87 has a mutation status of N241T, The gene ME3 has a mutation status of C34C, The gene CTSC has a mutation status of G4G, The gene GRM5 has a mutation status of R26R, The gene FAT3 has a mutation status of V1507L, The gene FAT3 has a mutation status of S1771I, The gene MED17 has a mutation status of A452E, The gene MMP13 has a mutation status of D317G, The gene SLC35F2 has a mutation status of S95L, The gene NXPE4 has a mutation status of D136G, The gene IL10RA has a mutation status of R63G, The gene TMPRSS4 has a mutation status of D163V, The gene OR8B12 has a mutation status of L172P, The gene DCPS has a mutation status of L297L, The gene KCNJ5 has a mutation status of R319R, The gene TMEM45B has a mutation status of E46*, The gene ANO2 has a mutation status of M86V, The gene ACRBP has a mutation status of Q293K, The gene MANSC1 has a mutation status of K32K, The gene SLCO1B3-SLCO1B7 has a mutation status of R675M, The gene BHLHE41 has a mutation status of P393R, The gene ERGIC2 has a mutation status of M1I, The gene BICD1 has a mutation status of K328K, The gene PDZRN4 has a mutation status of K769N, The gene GXYLT1 has a mutation status of E249R, The gene VDR has a mutation status of L440L, The gene KMT2D has a mutation status of Q3322*, The gene KMT2D has a mutation status of G1486D, The gene SPATS2 has a mutation status of T21N, The gene ITGA7 has a mutation status of P753P, The gene ARHGEF25 has a mutation status of A54P, The gene TSFM has a mutation status of D74G, The gene SRGAP1 has a mutation status of R937T, The gene TBC1D30 has a mutation status of R566Q, The gene MGAT4C has a mutation status of R99L, The gene PLXNC1 has a mutation status of V822A, The gene C12orf42 has a mutation status of A177E, The gene STAB2 has a mutation status of Y2519S, The gene FAM216A has a mutation status of P190H, The gene NOS1 has a mutation status of S379F, The gene VSIG10 has a mutation status of E472K, The gene RPLP0 has a mutation status of F14fs, The gene HPD has a mutation status of P44A, The gene B3GNT4 has a mutation status of G217E, The gene HIP1R has a mutation status of F337F, The gene HIP1R has a mutation status of M804T, The gene DNAH10 has a mutation status of Y1244N, The gene DHX37 has a mutation status of D506N, The gene GLT1D1 has a mutation status of P77T, The gene EP400 has a mutation status of P139L, The gene PABPC3 has a mutation status of F169L, The gene ATP8A2 has a mutation status of A1069T, The gene RFC3 has a mutation status of L322L, The gene FREM2 has a mutation status of E2915V, The gene DIAPH3 has a mutation status of E937V, The gene AL445238.1 has a mutation status of G23C, The gene DACH1 has a mutation status of 81_82insGG, The gene SLITRK5 has a mutation status of E609Q, The gene POGLUT2 has a mutation status of Y8H, The gene ATP11A has a mutation status of T672A, The gene ADPRHL1 has a mutation status of T65T, The gene ADPRHL1 has a mutation status of A7V, The gene OR11H2 has a mutation status of K240K, The gene OR4K1 has a mutation status of I223I, The gene KLHL33 has a mutation status of Y636Y, The gene KLHL33 has a mutation status of G275R, The gene DHRS1 has a mutation status of R80G, The gene TTC6 has a mutation status of S232T, The gene SPTB has a mutation status of R843W, The gene ARG2 has a mutation status of H130N, The gene CCDC177 has a mutation status of A114A, The gene PAPLN has a mutation status of L896L, The gene RIOX1 has a mutation status of R54S, The gene ACOT1 has a mutation status of V94G, The gene LTBP2 has a mutation status of S112S, The gene TTC7B has a mutation status of R539C, The gene UNC79 has a mutation status of C2309C, The gene DICER1 has a mutation status of E733E, The gene ATG2B has a mutation status of G1745E, The gene PLD4 has a mutation status of R317R, The gene ATP10A has a mutation status of I121I, The gene TJP1 has a mutation status of G1143C, The gene GOLGA8J has a mutation status of P444P, The gene TRPM1 has a mutation status of K1329*, The gene THBS1 has a mutation status of G126G, The gene KNL1 has a mutation status of M550T, The gene RMDN3 has a mutation status of R138P, The gene TTBK2 has a mutation status of T1163M, The gene TTBK2 has a mutation status of A644P, The gene UBR1 has a mutation status of P344S, The gene STRC has a mutation status of R1156R, The gene DUOX2 has a mutation status of A1060V, The gene SCG3 has a mutation status of D73G, The gene C15orf65 has a mutation status of V86L, The gene RFX7 has a mutation status of L738L, The gene FBXL22 has a mutation status of D41V, The gene ANKDD1A has a mutation status of L516L, The gene TBC1D21 has a mutation status of L71L, The gene CSPG4 has a mutation status of K1709K, The gene EFL1 has a mutation status of L996L, The gene GOLGA6L9 has a mutation status of R6H, The gene TM6SF1 has a mutation status of V155L, The gene TICRR has a mutation status of K1140N, The gene UNC45A has a mutation status of L887P, The gene LRRK1 has a mutation status of V1779D, The gene LRRK1 has a mutation status of T1883M, The gene WDR24 has a mutation status of A653S, The gene EME2 has a mutation status of G279G, The gene TEDC2 has a mutation status of E29E, The gene ZNF205 has a mutation status of L159M, The gene UBN1 has a mutation status of L368L, The gene PPL has a mutation status of L1219R, The gene C16orf72 has a mutation status of G16R, The gene GRIN2A has a mutation status of I422L, The gene PDILT has a mutation status of H437Y, The gene ARHGAP17 has a mutation status of K2K, The gene GTF3C1 has a mutation status of P1986P, The gene GTF3C1 has a mutation status of A156T, The gene HIRIP3 has a mutation status of S317S, The gene TBX6 has a mutation status of H175P, The gene KAT8 has a mutation status of L269I, The gene SLC5A2 has a mutation status of A7T, The gene LONP2 has a mutation status of R562H, The gene CYLD has a mutation status of V225V, The gene CHD9 has a mutation status of G1234E, The gene TRADD has a mutation status of T221K, The gene TRADD has a mutation status of V12L, The gene EDC4 has a mutation status of A95A, The gene EDC4 has a mutation status of S729F, The gene NFATC3 has a mutation status of P1043P, The gene TANGO6 has a mutation status of F147F, The gene NFAT5 has a mutation status of N353K, The gene ATXN1L has a mutation status of L563F, The gene ADAMTS18 has a mutation status of R281G, The gene BCO1 has a mutation status of Q150K, The gene DNAAF1 has a mutation status of K286N, The gene ZNF778 has a mutation status of C240C, The gene DPEP1 has a mutation status of V199M, The gene GAS8 has a mutation status of V182F, The gene PRDM7 has a mutation status of W46*, The gene SCGB1C2 has a mutation status of T64T, The gene ITGAE has a mutation status of D658D, The gene ATP2A3 has a mutation status of C417C, The gene ZZEF1 has a mutation status of N862S, The gene MINK1 has a mutation status of F1298V, The gene SLC52A1 has a mutation status of A322A, The gene KCTD11 has a mutation status of V229G, The gene TMEM95 has a mutation status of L184F, The gene TP53 has a mutation status of R175H, The gene DNAH2 has a mutation status of S312T, The gene DHRS7C has a mutation status of E271*, The gene MYH13 has a mutation status of L1084M, The gene SCO1 has a mutation status of I257L, The gene DNAH9 has a mutation status of R4317W, The gene NCOR1 has a mutation status of N947N, The gene NCOR1 has a mutation status of Q356E, The gene RNF112 has a mutation status of R481C, The gene SPAG5 has a mutation status of S183S, The gene TBC1D3B has a mutation status of S510G, The gene CCL4L2 has a mutation status of P67R, The gene AATF has a mutation status of R365C, The gene FBXO47 has a mutation status of V183I, The gene THRA has a mutation status of P87H, The gene P3H4 has a mutation status of D326D, The gene ACLY has a mutation status of T491P, The gene KCNH4 has a mutation status of C881W, The gene GJC1 has a mutation status of R366W, The gene NMT1 has a mutation status of N42S, The gene ACBD4 has a mutation status of S86C, The gene PLEKHM1 has a mutation status of A906A, The gene HOXB6 has a mutation status of F53F, The gene TOM1L1 has a mutation status of P376L, The gene PRR11 has a mutation status of V80I, The gene C17orf64 has a mutation status of G172W, The gene CACNG5 has a mutation status of Y35F, The gene MYO15B has a mutation status of G470D, The gene MYO15B has a mutation status of G474A, The gene MYO15B has a mutation status of S620H, The gene TMEM235 has a mutation status of L139L, The gene ZNF750 has a mutation status of E616K, The gene MEP1B has a mutation status of G540E, The gene KLHL14 has a mutation status of L610*, The gene CCDC178 has a mutation status of T821T, The gene ASXL3 has a mutation status of L266L, The gene ASXL3 has a mutation status of D555A, The gene PSTPIP2 has a mutation status of A212T, The gene SMAD2 has a mutation status of L87R, The gene MRO has a mutation status of Y234H, The gene ONECUT2 has a mutation status of P153T, The gene ZNF532 has a mutation status of T1183T, The gene CDC34 has a mutation status of F224F, The gene APC2 has a mutation status of R103R, The gene MKNK2 has a mutation status of I287I, The gene SF3A2 has a mutation status of V372G, The gene ZNF77 has a mutation status of F74F, The gene DAPK3 has a mutation status of F236F, The gene PLIN4 has a mutation status of H40Y, The gene KDM4B has a mutation status of S364L, The gene FUT6 has a mutation status of D219D, The gene MUC16 has a mutation status of T12336L, The gene MUC16 has a mutation status of P11299P, The gene MUC16 has a mutation status of R8882Q, The gene OR1M1 has a mutation status of T190M, The gene ICAM4 has a mutation status of V20A, The gene RAVER1 has a mutation status of G593G, The gene ZNF491 has a mutation status of T238I, The gene CYP4F3 has a mutation status of G417C, The gene GTPBP3 has a mutation status of C46G, The gene ZNF208 has a mutation status of V98L, The gene ZNF536 has a mutation status of D581Y, The gene CHST8 has a mutation status of R9W, The gene FFAR3 has a mutation status of R46H, The gene KMT2B has a mutation status of R843Q, The gene RYR1 has a mutation status of I448I, The gene FCGBP has a mutation status of P3531P, The gene FCGBP has a mutation status of G1859G, The gene SPTBN4 has a mutation status of R2149R, The gene LYPD5 has a mutation status of Y54H, The gene ZNF155 has a mutation status of I482L, The gene CEACAM16 has a mutation status of E85D, The gene APOC4-APOC2 has a mutation status of F95C, The gene PPP1R13L has a mutation status of A515V, The gene NPAS1 has a mutation status of S148S, The gene RASIP1 has a mutation status of W39L, The gene CGB1 has a mutation status of A18A, The gene PPFIA3 has a mutation status of L874L, The gene MYH14 has a mutation status of R244W, The gene HAS1 has a mutation status of P8L, The gene ZNF480 has a mutation status of F477F, The gene ZNF845 has a mutation status of S480L, The gene ZNF765 has a mutation status of G295*, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of T201M, The gene LILRB3 has a mutation status of M21V, The gene KIR2DL3 has a mutation status of L15W, The gene PEG3 has a mutation status of M473V, The gene ZNF749 has a mutation status of V759M, The gene ZNF416 has a mutation status of K216R, The gene VPS16 has a mutation status of A150V, The gene KAT14 has a mutation status of I293T, The gene KAT14 has a mutation status of D634D, The gene APMAP has a mutation status of H394Q, The gene NCOA6 has a mutation status of G156A, The gene SOGA1 has a mutation status of A195T, The gene MYBL2 has a mutation status of P274P, The gene UBE2C has a mutation status of S123S, The gene NCOA5 has a mutation status of R165G, The gene DDX27 has a mutation status of A20A, The gene APCDD1L has a mutation status of F373F, The gene ADRM1 has a mutation status of A348V, The gene NKAIN4 has a mutation status of V162L, The gene ADAMTS5 has a mutation status of N596Y, The gene TIAM1 has a mutation status of T158A, The gene LCA5L has a mutation status of N172S, The gene AIRE has a mutation status of K52E, The gene SLC25A1 has a mutation status of R118Q, The gene CLTCL1 has a mutation status of V652F, The gene GNAZ has a mutation status of A301T, The gene GSTT4 has a mutation status of P89L, The gene GSTT4 has a mutation status of L54L, The gene GGT5 has a mutation status of R182H, The gene MN1 has a mutation status of Q529Q, The gene NIPSNAP1 has a mutation status of N111N, The gene RFPL2 has a mutation status of T59S, The gene LARGE1 has a mutation status of R70H, The gene MCM5 has a mutation status of Y703S, The gene ELFN2 has a mutation status of H696P, The gene CARD10 has a mutation status of V875M, The gene GCAT has a mutation status of D209N, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TSPO has a mutation status of A90A, The gene NCAPH2 has a mutation status of L367L, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene AKAP17A has a mutation status of I376I, The gene CLTRN has a mutation status of A52A, The gene EIF1AX has a mutation status of R62G, The gene DDX53 has a mutation status of Y557Y, The gene IL1RAPL1 has a mutation status of P177S, The gene FAM47C has a mutation status of D56Y, The gene XAGE2 has a mutation status of T76I, The gene TRO has a mutation status of G1262V, The gene NLGN3 has a mutation status of P760S, The gene ERCC6L has a mutation status of E855Q, The gene ATP7A has a mutation status of S1417I, The gene RTL3 has a mutation status of N163K, The gene PCDH11X has a mutation status of L160I, The gene NXF3 has a mutation status of D310V, The gene ATG4A has a mutation status of A264A, The gene SLC25A5 has a mutation status of T221R, The gene SASH3 has a mutation status of S110S, The gene ATP11C has a mutation status of N995N, The gene MAGEC1 has a mutation status of R204P, The gene SLITRK4 has a mutation status of S550S, The gene ATP2B3 has a mutation status of V369V, The gene TKTL1 has a mutation status of P16P, The gene ATP6AP1 has a mutation status of A386V, The gene GDI1 has a mutation status of D196D, The gene LAGE3 has a mutation status of I121T, The gene MT-ND1 has a mutation status of A64V, The gene MT-ND2 has a mutation status of S52S, The gene MT-ND2 has a mutation status of M79L, The gene MT-ND5 has a mutation status of F103F, The gene MT-ND5 has a mutation status of L173L, The gene MT-ND5 has a mutation status of P367P, The gene MT-ND6 has a mutation status of T156I, The gene MT-CYB has a mutation status of L200L
DLBC
The gene VPS13D has a mutation status of P617L, The gene PRAMEF13 has a mutation status of E110G, The gene PRAMEF18 has a mutation status of L121P, The gene RAP1GAP has a mutation status of D552N, The gene ZBTB40 has a mutation status of E557D, The gene HTR1D has a mutation status of S267L, The gene ADGRB2 has a mutation status of P451S, The gene HMGB4 has a mutation status of R171G, The gene CSF3R has a mutation status of L65L, The gene C1orf109 has a mutation status of L63I, The gene YIPF1 has a mutation status of R227H, The gene VCAM1 has a mutation status of I39I, The gene LAMTOR5 has a mutation status of T165M, The gene NRAS has a mutation status of Q61K, The gene NBPF14 has a mutation status of I996F, The gene AC242842.3 has a mutation status of V503L, The gene HRNR has a mutation status of W1033*, The gene FCRL5 has a mutation status of L675L, The gene ATP1A4 has a mutation status of S596S, The gene SLAMF7 has a mutation status of C7Y, The gene MYOC has a mutation status of A445V, The gene HMCN1 has a mutation status of S2272S, The gene CFHR5 has a mutation status of P282Q, The gene RAB3GAP2 has a mutation status of T1232A, The gene OBSCN has a mutation status of M1582V, The gene ACTN2 has a mutation status of D893N, The gene CGREF1 has a mutation status of T5M, The gene ATP6V1B1 has a mutation status of R314C, The gene HK2 has a mutation status of G304S, The gene DUSP2 has a mutation status of R79C, The gene SEPTIN10 has a mutation status of P258P, The gene LRP1B has a mutation status of I4387M, The gene ACVR1 has a mutation status of S469C, The gene SCN1A has a mutation status of E1280D, The gene COL3A1 has a mutation status of R1109G, The gene MFF has a mutation status of R306H, The gene ITPR1 has a mutation status of G2099A, The gene ZDHHC3 has a mutation status of A140V, The gene DHX30 has a mutation status of K282R, The gene BSN has a mutation status of P85L, The gene CHCHD6 has a mutation status of R61K, The gene KNG1 has a mutation status of H403H, The gene JAKMIP1 has a mutation status of Y571C, The gene ATP8A1 has a mutation status of Y70*, The gene BMP2K has a mutation status of E762del, The gene C4orf54 has a mutation status of K1431T, The gene TBCK has a mutation status of P183S, The gene GATB has a mutation status of Q74H, The gene MFAP3L has a mutation status of P76S, The gene CYP4V2 has a mutation status of F488V, The gene SLC12A7 has a mutation status of N177N, The gene DNAH5 has a mutation status of E1623K, The gene SPEF2 has a mutation status of N882fs, The gene AC022414.1 has a mutation status of P315P, The gene FEM1C has a mutation status of L195L, The gene EIF4E1B has a mutation status of R134W, The gene SLC22A23 has a mutation status of L261L, The gene RIPOR2 has a mutation status of Q757*, The gene BTN3A3 has a mutation status of V384V, The gene TUBB has a mutation status of R282Q, The gene HLA-DRB1 has a mutation status of T106N, The gene HLA-DRB1 has a mutation status of W38E, The gene CLIC5 has a mutation status of I87K, The gene PRKAR1B has a mutation status of A67V, The gene C1GALT1 has a mutation status of F65L, The gene IGFBP3 has a mutation status of L15L, The gene ABCB1 has a mutation status of K915T, The gene PPP1R35 has a mutation status of A73V, The gene TFR2 has a mutation status of F280L, The gene SLC12A9 has a mutation status of A365V, The gene UFSP1 has a mutation status of K175E, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of I1108M, The gene MUC3A has a mutation status of L1112W, The gene MUC3A has a mutation status of P3166P, The gene GRM8 has a mutation status of R255H, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene MGAM has a mutation status of R369W, The gene MGAM has a mutation status of N438K, The gene PRSS1 has a mutation status of N77N, The gene KCNH2 has a mutation status of P347S, The gene KMT2C has a mutation status of T1904I, The gene C8orf48 has a mutation status of K140del, The gene TEX15 has a mutation status of I946V, The gene ST18 has a mutation status of K227T, The gene NCOA2 has a mutation status of S541S, The gene ATP6V0D2 has a mutation status of K128K, The gene CYP11B2 has a mutation status of L142L, The gene EPPK1 has a mutation status of A2633del, The gene HGH1 has a mutation status of G54V, The gene VLDLR has a mutation status of R634H, The gene FOCAD has a mutation status of I705I, The gene HRCT1 has a mutation status of 104_105insHP, The gene SUSD3 has a mutation status of A223A, The gene SLC44A1 has a mutation status of R16G, The gene FRRS1L has a mutation status of R51A, The gene PSMD5 has a mutation status of S51S, The gene PKN3 has a mutation status of R598W, The gene SETX has a mutation status of F2339Y, The gene FAM163B has a mutation status of N68N, The gene VAV2 has a mutation status of G812R, The gene FRMD4A has a mutation status of K717K, The gene DKK1 has a mutation status of H229H, The gene ARID5B has a mutation status of P965P, The gene PTEN has a mutation status of L57fs, The gene RRP12 has a mutation status of L1019L, The gene LRRC27 has a mutation status of R449L, The gene MUC6 has a mutation status of P2398S, The gene MUC5AC has a mutation status of P3013P, The gene MUC5B has a mutation status of T2655T, The gene USP47 has a mutation status of S478N, The gene RAG1 has a mutation status of P85P, The gene ACP2 has a mutation status of A161T, The gene NR1H3 has a mutation status of S419N, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene EHD1 has a mutation status of D436D, The gene NAALADL1 has a mutation status of R537W, The gene FAM181B has a mutation status of W414R, The gene DLG2 has a mutation status of T483I, The gene NPAT has a mutation status of T688M, The gene CEP164 has a mutation status of S407F, The gene GRIK4 has a mutation status of R872L, The gene BCL2L14 has a mutation status of P40A, The gene ANO6 has a mutation status of V875I, The gene FAIM2 has a mutation status of V226M, The gene CSAD has a mutation status of R75W, The gene STAT2 has a mutation status of G825C, The gene CPM has a mutation status of R289C, The gene LRRIQ1 has a mutation status of V427L, The gene HCAR3 has a mutation status of V329I, The gene NCOR2 has a mutation status of L724L, The gene LRCOL1 has a mutation status of S84L, The gene HSPH1 has a mutation status of R196Q, The gene WBP4 has a mutation status of S62P, The gene CCDC168 has a mutation status of T6725T, The gene RALGAPA1 has a mutation status of P1900S, The gene TMEM260 has a mutation status of A619T, The gene EXD2 has a mutation status of L224del, The gene PROX2 has a mutation status of P364T, The gene TMEM251 has a mutation status of L76M, The gene GOLGA6L6 has a mutation status of Q549fs, The gene GOLGA6L6 has a mutation status of KQEEKVWRQEEKIREQEEKIR481del, The gene GOLGA6L22 has a mutation status of E620G, The gene LPCAT4 has a mutation status of G17R, The gene FSIP1 has a mutation status of D324N, The gene LTK has a mutation status of F11L, The gene ANKDD1A has a mutation status of L516L, The gene IQCH has a mutation status of I175M, The gene ANP32A has a mutation status of K62R, The gene NR2F2 has a mutation status of C99R, The gene LRRK1 has a mutation status of V1816M, The gene DNAH3 has a mutation status of C948R, The gene HS3ST2 has a mutation status of R196*, The gene TNRC6A has a mutation status of QPQPQ114del, The gene PRRT2 has a mutation status of P152H, The gene FBRS has a mutation status of P361P, The gene CNGB1 has a mutation status of K342E, The gene EMC6 has a mutation status of V19L, The gene SPNS2 has a mutation status of Q144H, The gene SLC2A4 has a mutation status of E375G, The gene CTC1 has a mutation status of D893N, The gene CFAP52 has a mutation status of V491A, The gene FBXW10 has a mutation status of M563V, The gene ASIC2 has a mutation status of L456R, The gene CCL4L2 has a mutation status of P67R, The gene GRB7 has a mutation status of R255L, The gene KRTAP9-6 has a mutation status of G106C, The gene GHDC has a mutation status of T354T, The gene STAT5A has a mutation status of S434S, The gene TSPOAP1 has a mutation status of A1613A, The gene TBX2 has a mutation status of K432R, The gene BRIP1 has a mutation status of C350S, The gene UNC13D has a mutation status of R214R, The gene RHBDF2 has a mutation status of R715W, The gene TAF4B has a mutation status of S373A, The gene TRAPPC8 has a mutation status of A1168A, The gene C18orf54 has a mutation status of F85fs, The gene NCLN has a mutation status of I110I, The gene FSD1 has a mutation status of A41P, The gene KDM4B has a mutation status of L461V, The gene ACSBG2 has a mutation status of R104C, The gene RGL3 has a mutation status of G363R, The gene CASP14 has a mutation status of D193N, The gene NXNL1 has a mutation status of M94I, The gene NXNL1 has a mutation status of T22M, The gene PEPD has a mutation status of S251T, The gene GRAMD1A has a mutation status of L597L, The gene ZNF146 has a mutation status of E145D, The gene ZNF607 has a mutation status of R74S, The gene CYP2A13 has a mutation status of N375D, The gene PVR has a mutation status of M340I, The gene ZNF114 has a mutation status of P331P, The gene SIGLEC10 has a mutation status of A108V, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of T30T, The gene LILRB1 has a mutation status of E34E, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL3 has a mutation status of E295D, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of G283G, The gene KMT5C has a mutation status of P291P, The gene ZNF628 has a mutation status of P597L, The gene CHGB has a mutation status of E233A, The gene CHGB has a mutation status of E466G, The gene PLCB4 has a mutation status of N301D, The gene SUN5 has a mutation status of R54C, The gene CSE1L has a mutation status of L11L, The gene BCAS4 has a mutation status of Y173Y, The gene ATP9A has a mutation status of T304A, The gene SLCO4A1 has a mutation status of A347V, The gene NPBWR2 has a mutation status of P202P, The gene KRTAP23-1 has a mutation status of G63E, The gene KRTAP13-4 has a mutation status of C74C, The gene TBX1 has a mutation status of R280Q, The gene C22orf15 has a mutation status of T39T, The gene APOBEC3G has a mutation status of R326H, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene KIAA0930 has a mutation status of S206F, The gene SELENOO has a mutation status of G574W, The gene DCAF8L1 has a mutation status of P117P, The gene LONRF3 has a mutation status of L272M
GBMLGG
The gene KIF1B has a mutation status of T1508T, The gene PRAMEF12 has a mutation status of T199fs, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene DNAJC16 has a mutation status of V556I, The gene EPHA2 has a mutation status of G15G, The gene IL22RA1 has a mutation status of P258S, The gene ARID1A has a mutation status of G91C, The gene S100PBP has a mutation status of L326H, The gene ZNF684 has a mutation status of H201Y, The gene B4GALT2 has a mutation status of Q233H, The gene MAST2 has a mutation status of R1712S, The gene ZFYVE9 has a mutation status of V864V, The gene AGL has a mutation status of R864R, The gene CELSR2 has a mutation status of R2015K, The gene AP4B1 has a mutation status of V335A, The gene TARS2 has a mutation status of R684W, The gene BRINP3 has a mutation status of D249N, The gene F13B has a mutation status of L385V, The gene PLXNA2 has a mutation status of C826G, The gene FAM71A has a mutation status of T413T, The gene EPHX1 has a mutation status of G152G, The gene OBSCN has a mutation status of R1156C, The gene COX20 has a mutation status of F66Y, The gene ADCY3 has a mutation status of T1029N, The gene SUPT7L has a mutation status of A44D, The gene PCARE has a mutation status of S854F, The gene MTA3 has a mutation status of T133M, The gene CCDC85A has a mutation status of E76K, The gene MAL has a mutation status of I148I, The gene UNC50 has a mutation status of K33K, The gene CREG2 has a mutation status of Q237K, The gene ACVR1C has a mutation status of V434F, The gene ACVR1C has a mutation status of R432*, The gene FZD5 has a mutation status of R269C, The gene LRRFIP1 has a mutation status of M303V, The gene FGD5 has a mutation status of S458S, The gene ARIH2OS has a mutation status of A153G, The gene DNAH1 has a mutation status of F2489L, The gene RYBP has a mutation status of *17Q, The gene OR5K4 has a mutation status of L166*, The gene PHLDB2 has a mutation status of R385K, The gene COL6A6 has a mutation status of R1502H, The gene EPHB1 has a mutation status of P207S, The gene SERPINI1 has a mutation status of K318R, The gene ECT2 has a mutation status of V82A, The gene CLDN1 has a mutation status of P154S, The gene MFSD10 has a mutation status of T292K, The gene MRFAP1 has a mutation status of E22E, The gene ADAMTS3 has a mutation status of G682*, The gene CXCL1 has a mutation status of P54L, The gene SHROOM3 has a mutation status of P878R, The gene CENPE has a mutation status of E830G, The gene SEC24B has a mutation status of G87G, The gene MCUB has a mutation status of R184I, The gene AC126283.2 has a mutation status of N151S, The gene GYPE has a mutation status of R57H, The gene PLRG1 has a mutation status of L108F, The gene PALLD has a mutation status of E196Q, The gene BASP1 has a mutation status of D61D, The gene CDH12 has a mutation status of I330T, The gene PDZD2 has a mutation status of Q942K, The gene PTGER4 has a mutation status of P467P, The gene DHX29 has a mutation status of R1012C, The gene IQGAP2 has a mutation status of Q953R, The gene SLC12A2 has a mutation status of A642T, The gene NRG2 has a mutation status of P97S, The gene PCDHA8 has a mutation status of R98W, The gene SLC36A1 has a mutation status of G96S, The gene FAM71B has a mutation status of A314T, The gene LY86 has a mutation status of S92S, The gene BLOC1S5 has a mutation status of A175P, The gene SLC17A2 has a mutation status of I115K, The gene DAAM2 has a mutation status of P73P, The gene TTBK1 has a mutation status of G84G, The gene DLK2 has a mutation status of A138V, The gene DLK2 has a mutation status of A84G, The gene CAPN11 has a mutation status of R111W, The gene FILIP1 has a mutation status of S12F, The gene MRAP2 has a mutation status of R160S, The gene ASCC3 has a mutation status of G1401V, The gene MICAL1 has a mutation status of G853A, The gene MICAL1 has a mutation status of W852G, The gene SLC22A16 has a mutation status of W366*, The gene MARCKS has a mutation status of S6Y, The gene SLC18B1 has a mutation status of T393M, The gene ZNF12 has a mutation status of S338N, The gene GARS1 has a mutation status of D554N, The gene GLI3 has a mutation status of H1353N, The gene EGFR has a mutation status of D211G, The gene TBL2 has a mutation status of L155L, The gene PPP1R9A has a mutation status of E42V, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of P3166P, The gene LAMB4 has a mutation status of R528C, The gene EPHB6 has a mutation status of F792F, The gene KMT2C has a mutation status of P2051R, The gene PAXIP1 has a mutation status of A563A, The gene DCTN6 has a mutation status of P138S, The gene ST18 has a mutation status of T520T, The gene CNGB3 has a mutation status of F432S, The gene ERICH5 has a mutation status of V194I, The gene RGS22 has a mutation status of M1I, The gene NOL6 has a mutation status of S817S, The gene PIP5K1B has a mutation status of T242M, The gene TRPM6 has a mutation status of E799D, The gene AOPEP has a mutation status of D204H, The gene PGAP4 has a mutation status of R231C, The gene ZNF462 has a mutation status of Y123Y, The gene UGCG has a mutation status of Q270Q, The gene CDK5RAP2 has a mutation status of L1788M, The gene OLFML2A has a mutation status of A536A, The gene PKN3 has a mutation status of P90P, The gene OLFM1 has a mutation status of P371P, The gene NACC2 has a mutation status of AA155del, The gene NOTCH1 has a mutation status of C423W, The gene ABCA2 has a mutation status of S1552S, The gene PCBD1 has a mutation status of A83A, The gene CAMK2G has a mutation status of N513N, The gene WAPL has a mutation status of P389S, The gene PTEN has a mutation status of C124S, The gene ZNF511-PRAP1 has a mutation status of G226A, The gene SYCE1 has a mutation status of C14C, The gene MUC5B has a mutation status of W1905R, The gene OR51I1 has a mutation status of N5D, The gene OR56A5 has a mutation status of K303K, The gene FAM160A2 has a mutation status of V389I, The gene HPS5 has a mutation status of S129Y, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR6Q1 has a mutation status of F242L, The gene TUT1 has a mutation status of E171K, The gene OVOL1 has a mutation status of R166*, The gene SPTBN2 has a mutation status of A493T, The gene TMEM134 has a mutation status of H171Q, The gene BIRC2 has a mutation status of K17T, The gene ZNF202 has a mutation status of Q173H, The gene ZNF202 has a mutation status of T170I, The gene VWA5A has a mutation status of L116L, The gene ARHGAP32 has a mutation status of T721I, The gene CACNA1C has a mutation status of T568M, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene OR10AD1 has a mutation status of T49T, The gene GALNT6 has a mutation status of S458H, The gene ANKRD52 has a mutation status of R321C, The gene MARS1 has a mutation status of A837A, The gene OTOGL has a mutation status of L1261P, The gene EEA1 has a mutation status of M449R, The gene CFAP54 has a mutation status of L2508V, The gene TMPO has a mutation status of L375V, The gene BTBD11 has a mutation status of A784P, The gene MYO1H has a mutation status of D36D, The gene RIMBP2 has a mutation status of R949G, The gene POLE has a mutation status of V1270F, The gene REM2 has a mutation status of V339G, The gene DHRS4L2 has a mutation status of A103S, The gene GMPR2 has a mutation status of R120C, The gene HEATR5A has a mutation status of A1687fs, The gene HEATR5A has a mutation status of D902Y, The gene AKAP6 has a mutation status of D2151D, The gene TOGARAM1 has a mutation status of I1072F, The gene FANCM has a mutation status of K927N, The gene ADAM20 has a mutation status of N574S, The gene NUDT14 has a mutation status of E5*, The gene CYFIP1 has a mutation status of T420T, The gene HERC2 has a mutation status of S3789L, The gene DUT has a mutation status of S120S, The gene C2CD4A has a mutation status of P94Q, The gene GOLGA6L10 has a mutation status of I73V, The gene RGS11 has a mutation status of G359R, The gene GRIN2A has a mutation status of T1362T, The gene UMOD has a mutation status of S334N, The gene PRKCB has a mutation status of V444V, The gene SULT1A1 has a mutation status of R72*, The gene CDH16 has a mutation status of P797P, The gene LCAT has a mutation status of A235G, The gene CDH3 has a mutation status of K473N, The gene CLEC3A has a mutation status of A148T, The gene CDT1 has a mutation status of P403P, The gene SCGB1C2 has a mutation status of T22T, The gene MINK1 has a mutation status of V1171G, The gene ZNF232 has a mutation status of V24V, The gene NLGN2 has a mutation status of L33L, The gene DNAH2 has a mutation status of F2665S, The gene DNAH2 has a mutation status of Q2807*, The gene DNAH2 has a mutation status of H2946Q, The gene USP43 has a mutation status of G739R, The gene MYH8 has a mutation status of A1766A, The gene RHBDL3 has a mutation status of L186L, The gene CCL4L2 has a mutation status of P67R, The gene PSMD3 has a mutation status of P161P, The gene KRT17 has a mutation status of 332_333EN>DY, The gene EFCAB13 has a mutation status of A605V, The gene SNX11 has a mutation status of N45N, The gene CUEDC1 has a mutation status of L355L, The gene ENPP7 has a mutation status of K104N, The gene METRNL has a mutation status of G149S, The gene USP14 has a mutation status of V18I, The gene SEH1L has a mutation status of R5P, The gene MEP1B has a mutation status of R650R, The gene PHLPP1 has a mutation status of Y524H, The gene STX10 has a mutation status of L241L, The gene PRKACA has a mutation status of R135Q, The gene NOTCH3 has a mutation status of D866D, The gene ZNF729 has a mutation status of C908S, The gene GRIK5 has a mutation status of S723S, The gene PSG5 has a mutation status of T393A, The gene GEMIN7 has a mutation status of F129L, The gene NOP53 has a mutation status of L279M, The gene TRPM4 has a mutation status of Y859F, The gene ZNF611 has a mutation status of R605Q, The gene ZNF347 has a mutation status of Y41*, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of N187T, The gene LILRA1 has a mutation status of R296T, The gene SBK2 has a mutation status of P222P, The gene NLRP9 has a mutation status of P43L, The gene ZNF749 has a mutation status of C206S, The gene TRIB3 has a mutation status of K184M, The gene PAX1 has a mutation status of P233S, The gene ASXL1 has a mutation status of R411L, The gene ERG has a mutation status of F390F, The gene MICAL3 has a mutation status of S1700P, The gene MICAL3 has a mutation status of R745W, The gene GNB1L has a mutation status of D306V, The gene NF2 has a mutation status of P181fs, The gene APOBEC3H has a mutation status of R171G, The gene CACNA1I has a mutation status of G1231S, The gene PKDREJ has a mutation status of I1528M, The gene PPP6R2 has a mutation status of G664D, The gene CSF2RA has a mutation status of D256D, The gene IQSEC2 has a mutation status of I652I, The gene FAM104B has a mutation status of T19N, The gene ARHGAP36 has a mutation status of D83N, The gene FHL1 has a mutation status of A37G, The gene KIF1B has a mutation status of T1508T, The gene PRAMEF12 has a mutation status of T199fs, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRDM2 has a mutation status of R1580R, The gene DNAJC16 has a mutation status of V556I, The gene C1QB has a mutation status of D248H, The gene S100PBP has a mutation status of L326H, The gene TFAP2E has a mutation status of D362H, The gene PPT1 has a mutation status of D28G, The gene ZNF684 has a mutation status of H201Y, The gene SZT2 has a mutation status of D3219D, The gene MAST2 has a mutation status of R1712S, The gene DMRTA2 has a mutation status of P152P, The gene CELSR2 has a mutation status of R2015K, The gene ST7L has a mutation status of A15V, The gene AP4B1 has a mutation status of V335A, The gene TARS2 has a mutation status of R684W, The gene FLG has a mutation status of S3540S, The gene FLG has a mutation status of A892K, The gene PBXIP1 has a mutation status of R650L, The gene OR10Z1 has a mutation status of F12S, The gene CADM3 has a mutation status of S132T, The gene OR10J5 has a mutation status of V303L, The gene ATP1B1 has a mutation status of Y279Y, The gene IGFN1 has a mutation status of G2743C, The gene KDM5B has a mutation status of T518T, The gene PPFIA4 has a mutation status of A865V, The gene EPHX1 has a mutation status of G152G, The gene OBSCN has a mutation status of R1156C, The gene EXO1 has a mutation status of E50E, The gene COX20 has a mutation status of F66Y, The gene GREB1 has a mutation status of D1416N, The gene ADCY3 has a mutation status of T1029N, The gene SUPT7L has a mutation status of A44D, The gene PCARE has a mutation status of S854F, The gene CDC42EP3 has a mutation status of T98T, The gene MTA3 has a mutation status of T133M, The gene VAX2 has a mutation status of G4W, The gene DYSF has a mutation status of K674E, The gene UNC50 has a mutation status of K33K, The gene IL18RAP has a mutation status of F375F, The gene ST6GAL2 has a mutation status of P85H, The gene AMER3 has a mutation status of T626I, The gene ACVR1C has a mutation status of L31R, The gene CCDC148 has a mutation status of Q30*, The gene SCN3A has a mutation status of T235A, The gene MYO3B has a mutation status of V1137F, The gene TMEM198 has a mutation status of V238M, The gene SPHKAP has a mutation status of L139L, The gene COL6A3 has a mutation status of D3021H, The gene ESPNL has a mutation status of R932H, The gene FGD5 has a mutation status of A425S, The gene TBC1D5 has a mutation status of Q273R, The gene TRANK1 has a mutation status of A2789A, The gene TRANK1 has a mutation status of V1886G, The gene KLHL40 has a mutation status of D80H, The gene CCR5 has a mutation status of S63C, The gene LTF has a mutation status of P303Q, The gene NBEAL2 has a mutation status of S2404S, The gene CELSR3 has a mutation status of N2636N, The gene DAG1 has a mutation status of P728P, The gene DNAH1 has a mutation status of F2489L, The gene DNAH1 has a mutation status of I2790I, The gene RYBP has a mutation status of *17Q, The gene CRYBG3 has a mutation status of P95S, The gene OR5K4 has a mutation status of L166*, The gene PHLDB2 has a mutation status of R385K, The gene HCLS1 has a mutation status of Y360Y, The gene EEFSEC has a mutation status of E539K, The gene COL6A6 has a mutation status of R1502H, The gene SLCO2A1 has a mutation status of L40I, The gene EPHB1 has a mutation status of P207S, The gene RASA2 has a mutation status of S12F, The gene CCNL1 has a mutation status of P5S, The gene VEPH1 has a mutation status of P763S, The gene SERPINI1 has a mutation status of K318R, The gene ECT2 has a mutation status of V82A, The gene ABCC5 has a mutation status of E758E, The gene ADIPOQ has a mutation status of A88D, The gene CLDN1 has a mutation status of P154S, The gene TMEM175 has a mutation status of I150T, The gene EVC2 has a mutation status of R426G, The gene MRFAP1 has a mutation status of E22E, The gene ADAMTS3 has a mutation status of G682*, The gene SHROOM3 has a mutation status of P878R, The gene DSPP has a mutation status of S1133S, The gene SEC24B has a mutation status of G87G, The gene AC126283.2 has a mutation status of N151S, The gene ALPK1 has a mutation status of P1004P, The gene GYPE has a mutation status of R57H, The gene TKTL2 has a mutation status of H55Y, The gene PALLD has a mutation status of E196Q, The gene CCDC110 has a mutation status of S126F, The gene FAT1 has a mutation status of R3885R, The gene DUX4 has a mutation status of P6P, The gene DUX4 has a mutation status of I121L, The gene MYO10 has a mutation status of R1894R, The gene BASP1 has a mutation status of D61D, The gene CDH12 has a mutation status of I330T, The gene CDH9 has a mutation status of G242G, The gene CPLANE1 has a mutation status of R2952G, The gene DAB2 has a mutation status of G192G, The gene MROH2B has a mutation status of S1315Y, The gene DHX29 has a mutation status of R1012C, The gene MCCC2 has a mutation status of R180Q, The gene IQGAP2 has a mutation status of Q953R, The gene ZFYVE16 has a mutation status of E225G, The gene NRG2 has a mutation status of V182L, The gene PCDHA9 has a mutation status of T390R, The gene FAM71B has a mutation status of A314T, The gene GABRA6 has a mutation status of K122E, The gene RNF44 has a mutation status of H174Y, The gene GPRIN1 has a mutation status of E441Q, The gene TRIM7 has a mutation status of Q491R, The gene LY86 has a mutation status of S92S, The gene EDN1 has a mutation status of G145fs, The gene ACOT13 has a mutation status of N50S, The gene RIPOR2 has a mutation status of V746V, The gene SLC17A2 has a mutation status of I115K, The gene H2AC4 has a mutation status of A46S, The gene MDC1 has a mutation status of R1516M, The gene NEU1 has a mutation status of R357Q, The gene NOTCH4 has a mutation status of C359S, The gene SYNGAP1 has a mutation status of F792F, The gene DAAM2 has a mutation status of P73P, The gene DLK2 has a mutation status of A138V, The gene CAPN11 has a mutation status of R111W, The gene AARS2 has a mutation status of R554C, The gene DEFB112 has a mutation status of C42R, The gene IL17A has a mutation status of R43W, The gene MRAP2 has a mutation status of R160S, The gene GABRR1 has a mutation status of L286L, The gene ASCC3 has a mutation status of G1401V, The gene SLC22A16 has a mutation status of W366*, The gene SLC18B1 has a mutation status of T393M, The gene SYNE1 has a mutation status of F2809S, The gene TNRC18 has a mutation status of P423P, The gene ZNF12 has a mutation status of S338N, The gene ICA1 has a mutation status of I38V, The gene LRRC72 has a mutation status of S223S, The gene GARS1 has a mutation status of D554N, The gene NACAD has a mutation status of P117L, The gene ABCA13 has a mutation status of L4235P, The gene TRIM50 has a mutation status of A430A, The gene MLXIPL has a mutation status of E610*, The gene STEAP2 has a mutation status of H55Y, The gene PPP1R9A has a mutation status of E42V, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S568Y, The gene MUC3A has a mutation status of S1242N, The gene MUC3A has a mutation status of S3095S, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene LAMB4 has a mutation status of R528C, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene MGAM2 has a mutation status of A1224E, The gene PRSS1 has a mutation status of N77N, The gene CSMD1 has a mutation status of H2769Q, The gene RP1L1 has a mutation status of P861P, The gene GATA4 has a mutation status of G65G, The gene USP17L2 has a mutation status of P448P, The gene DPYSL2 has a mutation status of T285T, The gene DCTN6 has a mutation status of P138S, The gene ST18 has a mutation status of T520T, The gene CHD7 has a mutation status of W1994C, The gene KCNB2 has a mutation status of S625S, The gene ERICH5 has a mutation status of V194I, The gene EPPK1 has a mutation status of A2633del, The gene HGH1 has a mutation status of G54V, The gene BNC2 has a mutation status of S764G, The gene TRPM6 has a mutation status of W1397R, The gene BICD2 has a mutation status of Q494R, The gene PGAP4 has a mutation status of R231C, The gene FRRS1L has a mutation status of R51A, The gene OLFML2A has a mutation status of A536A, The gene SPTAN1 has a mutation status of L491F, The gene HMCN2 has a mutation status of P4992P, The gene OLFM1 has a mutation status of P371P, The gene NACC2 has a mutation status of AA155del, The gene CCDC183 has a mutation status of R97C, The gene ECHDC3 has a mutation status of R196R, The gene PTER has a mutation status of G6*, The gene FO681492.1 has a mutation status of S6L, The gene FAM170B has a mutation status of L255L, The gene PCBD1 has a mutation status of A83A, The gene FUT11 has a mutation status of F165F, The gene CAMK2G has a mutation status of N513N, The gene WAPL has a mutation status of P389S, The gene PTEN has a mutation status of C124S, The gene FFAR4 has a mutation status of A154S, The gene ERLIN1 has a mutation status of V17V, The gene PDZD7 has a mutation status of V169L, The gene PNLIP has a mutation status of A349T, The gene PNLIPRP1 has a mutation status of F10L, The gene KCNK18 has a mutation status of T322S, The gene FGFR2 has a mutation status of S24L, The gene MUC5AC has a mutation status of S2573I, The gene TSPAN32 has a mutation status of L208L, The gene OR51I1 has a mutation status of N5D, The gene UBQLN3 has a mutation status of Q526H, The gene OR56B1 has a mutation status of P27P, The gene OR56A5 has a mutation status of K303K, The gene FAM160A2 has a mutation status of V389I, The gene MICAL2 has a mutation status of S1945R, The gene SPON1 has a mutation status of G771R, The gene OR5R1 has a mutation status of T160T, The gene OR5AP2 has a mutation status of P64P, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MS4A6A has a mutation status of A43T, The gene TUT1 has a mutation status of E171K, The gene KCNK4 has a mutation status of S79S, The gene OVOL1 has a mutation status of R166*, The gene SPTBN2 has a mutation status of A493T, The gene GRK2 has a mutation status of G626S, The gene DNAJB13 has a mutation status of R311C, The gene USP28 has a mutation status of D1056G, The gene TMPRSS13 has a mutation status of S427F, The gene ARCN1 has a mutation status of D31G, The gene VWA5A has a mutation status of L116L, The gene PANX3 has a mutation status of L266P, The gene PRB4 has a mutation status of R122G, The gene ALG10B has a mutation status of P409S, The gene ADAMTS20 has a mutation status of S15S, The gene AMIGO2 has a mutation status of A460A, The gene VDR has a mutation status of V389A, The gene KRT85 has a mutation status of S316R, The gene KRT76 has a mutation status of G130C, The gene E2F7 has a mutation status of D244fs, The gene MYF6 has a mutation status of R101C, The gene CFAP54 has a mutation status of L2508V, The gene TMPO has a mutation status of L375V, The gene MYO1H has a mutation status of D36D, The gene C12orf76 has a mutation status of G90S, The gene RPH3A has a mutation status of R74C, The gene RASAL1 has a mutation status of R544W, The gene CIT has a mutation status of P1564Q, The gene PXN has a mutation status of E307K, The gene NUP58 has a mutation status of L373L, The gene DGKH has a mutation status of P838T, The gene LACC1 has a mutation status of R230C, The gene OLFM4 has a mutation status of P239H, The gene DACH1 has a mutation status of 81_82insGG, The gene MYCBP2 has a mutation status of Q1872K, The gene CCDC168 has a mutation status of Q851Q, The gene OR4K15 has a mutation status of R21R, The gene DHRS4L2 has a mutation status of A103S, The gene GMPR2 has a mutation status of R120C, The gene AKAP6 has a mutation status of D2151D, The gene TOGARAM1 has a mutation status of I1072F, The gene FANCM has a mutation status of K927N, The gene ARMH4 has a mutation status of D253N, The gene ADAM20 has a mutation status of N574S, The gene CEP170B has a mutation status of P976T, The gene GOLGA6L6 has a mutation status of E505E, The gene GOLGA6L22 has a mutation status of *811Q, The gene CYFIP1 has a mutation status of T420T, The gene TUBGCP5 has a mutation status of K988Q, The gene MAGEL2 has a mutation status of P567L, The gene HERC2 has a mutation status of T1472T, The gene OTUD7A has a mutation status of T10P, The gene FMN1 has a mutation status of T599A, The gene RYR3 has a mutation status of R1100Q, The gene HYPK has a mutation status of N111S, The gene DUT has a mutation status of S120S, The gene CGNL1 has a mutation status of S89R, The gene ANKDD1A has a mutation status of L516L, The gene AP3B2 has a mutation status of T524I, The gene AP3B2 has a mutation status of G409C, The gene UNC45A has a mutation status of V738I, The gene RGS11 has a mutation status of G359R, The gene PPL has a mutation status of Q1726*, The gene GRIN2A has a mutation status of T1362T, The gene UMOD has a mutation status of S334N, The gene APOBR has a mutation status of S1040P, The gene SULT1A1 has a mutation status of R72*, The gene TLCD3B has a mutation status of A219A, The gene CDH16 has a mutation status of P797P, The gene CDH16 has a mutation status of D659N, The gene CDH3 has a mutation status of K473N, The gene ATMIN has a mutation status of E499fs, The gene ZNF232 has a mutation status of V24V, The gene TEKT1 has a mutation status of N233S, The gene NLGN2 has a mutation status of L33L, The gene DNAH2 has a mutation status of F2665S, The gene DNAH2 has a mutation status of H2946Q, The gene MYH8 has a mutation status of A1766A, The gene MYH4 has a mutation status of L843L, The gene NCOR1 has a mutation status of Y1915Y, The gene LGALS9 has a mutation status of P224P, The gene EFCAB5 has a mutation status of A633D, The gene CRLF3 has a mutation status of E80E, The gene RHBDL3 has a mutation status of L186L, The gene TMEM132E has a mutation status of D447D, The gene TMEM132E has a mutation status of E777K, The gene SLFN5 has a mutation status of R290H, The gene CCL4L2 has a mutation status of P67R, The gene MED24 has a mutation status of S910S, The gene KRT39 has a mutation status of K156M, The gene HCRT has a mutation status of A124V, The gene FMNL1 has a mutation status of D959N, The gene EFCAB13 has a mutation status of A605V, The gene SNX11 has a mutation status of N45N, The gene STXBP4 has a mutation status of E277G, The gene ACE has a mutation status of V1004V, The gene SCN4A has a mutation status of R282C, The gene SLC39A11 has a mutation status of A151A, The gene RNF213 has a mutation status of K1550N, The gene GCGR has a mutation status of F319del, The gene ZNF750 has a mutation status of G405G, The gene USP14 has a mutation status of V18I, The gene LAMA1 has a mutation status of V1563V, The gene LAMA1 has a mutation status of D1057N, The gene PIEZO2 has a mutation status of S1718L, The gene CABLES1 has a mutation status of A18T, The gene SETBP1 has a mutation status of L1538P, The gene SETBP1 has a mutation status of P1543P, The gene CDH20 has a mutation status of I242fs, The gene PHLPP1 has a mutation status of Y524H, The gene MUC16 has a mutation status of T9907A, The gene S1PR5 has a mutation status of G380G, The gene KRI1 has a mutation status of AKKQEELK344del, The gene ZNF433 has a mutation status of K143T, The gene PRKACA has a mutation status of R135Q, The gene NOTCH3 has a mutation status of D866D, The gene BRD4 has a mutation status of P1012P, The gene WIZ has a mutation status of S792G, The gene NWD1 has a mutation status of R1455H, The gene ZNF626 has a mutation status of I495H, The gene ZNF676 has a mutation status of R501G, The gene ZNF729 has a mutation status of C908S, The gene ZNF536 has a mutation status of V652V, The gene FFAR1 has a mutation status of L140L, The gene KMT2B has a mutation status of Q348P, The gene PLEKHG2 has a mutation status of D987H, The gene HIPK4 has a mutation status of G409S, The gene GRIK5 has a mutation status of S723S, The gene ZNF222 has a mutation status of C399Y, The gene TRPM4 has a mutation status of Q854R, The gene SYT3 has a mutation status of E6D, The gene KLK7 has a mutation status of W43R, The gene CEACAM18 has a mutation status of D158D, The gene ZNF611 has a mutation status of R605Q, The gene ZNF347 has a mutation status of Y41*, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene LILRB1 has a mutation status of E34E, The gene SBK2 has a mutation status of P222P, The gene NLRP9 has a mutation status of P43L, The gene NLRP4 has a mutation status of R668C, The gene PEG3 has a mutation status of E1279D, The gene ZNF749 has a mutation status of C206S, The gene TRIB3 has a mutation status of K184M, The gene DTD1 has a mutation status of L75M, The gene RALGAPA2 has a mutation status of A341V, The gene PAX1 has a mutation status of A416A, The gene SYCP2 has a mutation status of H612Q, The gene TTC3 has a mutation status of S449S, The gene DYRK1A has a mutation status of G616S, The gene ERG has a mutation status of F390F, The gene ABCG1 has a mutation status of R627Q, The gene COL6A2 has a mutation status of E556E, The gene MICAL3 has a mutation status of R745W, The gene CSF2RB has a mutation status of R225H, The gene CACNA1I has a mutation status of G1231S, The gene SCUBE1 has a mutation status of N248H, The gene PKDREJ has a mutation status of I1528M, The gene PPP6R2 has a mutation status of G664D, The gene ARSA has a mutation status of G357S, The gene CSF2RA has a mutation status of D256D, The gene OFD1 has a mutation status of S5F, The gene UXT has a mutation status of D40V, The gene IQSEC2 has a mutation status of I652I, The gene ZXDA has a mutation status of Q138L, The gene PGAM4 has a mutation status of A245V, The gene SYTL4 has a mutation status of S155F, The gene TEX13C has a mutation status of Q803H, The gene ARHGAP36 has a mutation status of D83N, The gene MAGEC1 has a mutation status of P379H, The gene CLIC2 has a mutation status of N48I, The gene VAMP7 has a mutation status of K84N, The gene MT-CO3 has a mutation status of T2A
GBMLGG
The gene KLHL17 has a mutation status of T640P, The gene SDF4 has a mutation status of P249P, The gene CCNL2 has a mutation status of S25C, The gene PLCH2 has a mutation status of D962N, The gene MMEL1 has a mutation status of W206G, The gene CA6 has a mutation status of R96P, The gene C1orf127 has a mutation status of T31M, The gene EXOSC10 has a mutation status of R158H, The gene PRAMEF2 has a mutation status of V34G, The gene PRAMEF9 has a mutation status of L14L, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRDM2 has a mutation status of E1158E, The gene KAZN has a mutation status of N614N, The gene PADI1 has a mutation status of N188N, The gene IGSF21 has a mutation status of G65G, The gene HP1BP3 has a mutation status of R455K, The gene HSPG2 has a mutation status of R2730I, The gene ZSCAN20 has a mutation status of I470T, The gene TFAP2E has a mutation status of P56fs, The gene AGO1 has a mutation status of L678R, The gene TMEM269 has a mutation status of F168F, The gene CFAP57 has a mutation status of K973K, The gene CFAP57 has a mutation status of S1241C, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene EPS15 has a mutation status of I52V, The gene CC2D1B has a mutation status of R432Q, The gene MROH7 has a mutation status of S477C, The gene PATJ has a mutation status of R1717W, The gene CACHD1 has a mutation status of R446Q, The gene PDE4B has a mutation status of L486L, The gene LRRC7 has a mutation status of Q1201E, The gene SYDE2 has a mutation status of D173Y, The gene COL24A1 has a mutation status of F121I, The gene CLCA2 has a mutation status of T845M, The gene DNTTIP2 has a mutation status of R272K, The gene ABCA4 has a mutation status of N1296N, The gene PRMT6 has a mutation status of R274H, The gene CELSR2 has a mutation status of A158E, The gene NBPF26 has a mutation status of E798*, The gene NBPF14 has a mutation status of L1355V, The gene NBPF14 has a mutation status of C63C, The gene ANXA9 has a mutation status of L230F, The gene FLG has a mutation status of W1934C, The gene FLG has a mutation status of T1847M, The gene CRNN has a mutation status of L75Q, The gene ILF2 has a mutation status of E333E, The gene ARHGEF2 has a mutation status of R622C, The gene PEAR1 has a mutation status of R871C, The gene OR6P1 has a mutation status of D191D, The gene SPTA1 has a mutation status of G1882*, The gene ATP1A2 has a mutation status of Y113Y, The gene SLAMF6 has a mutation status of L124fs, The gene HSPA6 has a mutation status of D392V, The gene MAEL has a mutation status of D425Y, The gene MROH9 has a mutation status of T425M, The gene FMO3 has a mutation status of V110L, The gene SUCO has a mutation status of G450G, The gene RASAL2 has a mutation status of T1038T, The gene AXDND1 has a mutation status of Y790C, The gene CFHR1 has a mutation status of S204C, The gene CRB1 has a mutation status of R793Q, The gene NAV1 has a mutation status of R1040Q, The gene FMOD has a mutation status of T88T, The gene DSTYK has a mutation status of I728T, The gene USH2A has a mutation status of K3397T, The gene TP53BP2 has a mutation status of A766A, The gene FBXO28 has a mutation status of P35P, The gene OBSCN has a mutation status of P236S, The gene H3-4 has a mutation status of K37Q, The gene H2BU1 has a mutation status of S57S, The gene ACTA1 has a mutation status of A183A, The gene GNPAT has a mutation status of G460R, The gene SLC35F3 has a mutation status of A279A, The gene NID1 has a mutation status of T725I, The gene ZP4 has a mutation status of G80D, The gene OR2B11 has a mutation status of N179D, The gene OR2G3 has a mutation status of L276V, The gene MYT1L has a mutation status of A968V, The gene PUM2 has a mutation status of A484P, The gene APOB has a mutation status of C2933F, The gene ITSN2 has a mutation status of Q725L, The gene DPYSL5 has a mutation status of N380N, The gene THADA has a mutation status of I1383I, The gene PLEKHH2 has a mutation status of T832T, The gene EML6 has a mutation status of D1938D, The gene RTN4 has a mutation status of M380T, The gene PEX13 has a mutation status of P235S, The gene TMEM17 has a mutation status of N30S, The gene PCBP1 has a mutation status of Q227Q, The gene DYSF has a mutation status of L93L, The gene CCDC142 has a mutation status of F207fs, The gene M1AP has a mutation status of A44V, The gene TEX37 has a mutation status of P123P, The gene NCAPH has a mutation status of Q323R, The gene DPP10 has a mutation status of Y655C, The gene MYO7B has a mutation status of A2067E, The gene SFT2D3 has a mutation status of G15G, The gene WDR33 has a mutation status of P816P, The gene PDK1 has a mutation status of P56P, The gene MFSD6 has a mutation status of A247T, The gene NDUFS1 has a mutation status of V270V, The gene ABCA12 has a mutation status of T345P, The gene TTLL4 has a mutation status of S1143F, The gene WNT10A has a mutation status of A334T, The gene UGT1A5 has a mutation status of L132M, The gene MLPH has a mutation status of A177V, The gene ILKAP has a mutation status of D295D, The gene HDLBP has a mutation status of R534H, The gene IL17RE has a mutation status of M117I, The gene FANCD2OS has a mutation status of D122H, The gene SLC6A11 has a mutation status of F346F, The gene FBLN2 has a mutation status of G176S, The gene SLC6A6 has a mutation status of D133G, The gene KCNH8 has a mutation status of E839V, The gene ZNF385D has a mutation status of S352N, The gene ZNF385D has a mutation status of P300P, The gene GOLGA4 has a mutation status of S185L, The gene SCN11A has a mutation status of I201S, The gene CSRNP1 has a mutation status of Q260R, The gene CCR8 has a mutation status of V100V, The gene GASK1A has a mutation status of T123I, The gene CELSR3 has a mutation status of R1453C, The gene CELSR3 has a mutation status of V1030V, The gene PBRM1 has a mutation status of A1249T, The gene DNAH12 has a mutation status of E2938E, The gene OR5H1 has a mutation status of I158F, The gene OR5H15 has a mutation status of G161R, The gene ZBTB11 has a mutation status of E984E, The gene DPPA2 has a mutation status of C96Y, The gene ILDR1 has a mutation status of R418Q, The gene PARP14 has a mutation status of V160V, The gene PARP14 has a mutation status of D1063V, The gene ADCY5 has a mutation status of E516E, The gene ADCY5 has a mutation status of N191N, The gene MYLK has a mutation status of Y1353S, The gene MYLK has a mutation status of T331T, The gene PODXL2 has a mutation status of P325H, The gene EFCC1 has a mutation status of K539E, The gene RHO has a mutation status of P327T, The gene BFSP2 has a mutation status of R76Q, The gene PRR23C has a mutation status of E147*, The gene CLSTN2 has a mutation status of T376T, The gene IFT80 has a mutation status of M412T, The gene YEATS2 has a mutation status of E60D, The gene OPA1 has a mutation status of M592T, The gene TNK2 has a mutation status of A634T, The gene TNK2 has a mutation status of P628P, The gene LRCH3 has a mutation status of N365N, The gene DRD5 has a mutation status of L17L, The gene SEL1L3 has a mutation status of L519M, The gene DTHD1 has a mutation status of E595G, The gene ATP10D has a mutation status of K264K, The gene CRACD has a mutation status of E1083D, The gene EPHA5 has a mutation status of S673T, The gene SHROOM3 has a mutation status of R414Q, The gene SHROOM3 has a mutation status of S1599Y, The gene PAPSS1 has a mutation status of M496L, The gene SEC24B has a mutation status of V479V, The gene USP38 has a mutation status of EKTLI582del, The gene DCLK2 has a mutation status of A737G, The gene DCHS2 has a mutation status of A2562G, The gene FGA has a mutation status of S364R, The gene FGA has a mutation status of P255P, The gene NDUFS6 has a mutation status of R13R, The gene IRX2 has a mutation status of Y450Y, The gene CDH18 has a mutation status of L202L, The gene PDZD2 has a mutation status of P30R, The gene HMGCS1 has a mutation status of G122R, The gene PARP8 has a mutation status of R287H, The gene ITGA2 has a mutation status of G793R, The gene DDX4 has a mutation status of S113C, The gene ERBIN has a mutation status of D902D, The gene MAST4 has a mutation status of V1255M, The gene ANKRD31 has a mutation status of R606G, The gene CERT1 has a mutation status of V453I, The gene IQGAP2 has a mutation status of E474E, The gene VCAN has a mutation status of S1315G, The gene FBXL17 has a mutation status of P262P, The gene FBN2 has a mutation status of T1173S, The gene ACSL6 has a mutation status of P158P, The gene FSTL4 has a mutation status of P251H, The gene FSTL4 has a mutation status of A146T, The gene SLC4A9 has a mutation status of S614T, The gene ADRB2 has a mutation status of R259C, The gene FAT2 has a mutation status of R3649L, The gene SGCD has a mutation status of N211N, The gene SH3PXD2B has a mutation status of M428V, The gene CPEB4 has a mutation status of G221G, The gene GMCL2 has a mutation status of R447Q, The gene ADAMTS2 has a mutation status of V74M, The gene IRF4 has a mutation status of T92T, The gene FARS2 has a mutation status of Y113C, The gene E2F3 has a mutation status of L98F, The gene SLC17A1 has a mutation status of Q463Q, The gene ZNF391 has a mutation status of E294K, The gene OR11A1 has a mutation status of G18G, The gene HLA-B has a mutation status of Y140L, The gene CLIC1 has a mutation status of A98T, The gene AL645922.1 has a mutation status of R576H, The gene FANCE has a mutation status of N503N, The gene PNPLA1 has a mutation status of D233N, The gene BNIP5 has a mutation status of S487C, The gene BTBD9 has a mutation status of R40W, The gene DNAH8 has a mutation status of C688C, The gene C6orf132 has a mutation status of P989L, The gene RUNX2 has a mutation status of R426S, The gene TDRD6 has a mutation status of R519I, The gene IL17A has a mutation status of P31T, The gene DST has a mutation status of A1637V, The gene FILIP1 has a mutation status of V800V, The gene BCKDHB has a mutation status of P185P, The gene CEP162 has a mutation status of E85fs, The gene NT5E has a mutation status of V300V, The gene MDN1 has a mutation status of R5570L, The gene CASP8AP2 has a mutation status of R1836G, The gene GRIK2 has a mutation status of T317M, The gene CRYBG1 has a mutation status of R1191C, The gene AK9 has a mutation status of S1357G, The gene RSPH4A has a mutation status of E517D, The gene SMPDL3A has a mutation status of A102T, The gene LAMA2 has a mutation status of R1687Q, The gene L3MBTL3 has a mutation status of P92S, The gene AHI1 has a mutation status of T856S, The gene NHSL1 has a mutation status of V1081M, The gene NHSL1 has a mutation status of P734S, The gene ADGB has a mutation status of V841I, The gene SYNE1 has a mutation status of K3039N, The gene RGS17 has a mutation status of M61L, The gene SYNJ2 has a mutation status of R874W, The gene IGF2R has a mutation status of S347S, The gene GET4 has a mutation status of V111A, The gene ELFN1 has a mutation status of A796T, The gene MAD1L1 has a mutation status of E477K, The gene USP42 has a mutation status of K1200K, The gene GRID2IP has a mutation status of R184*, The gene VWDE has a mutation status of T243T, The gene DGKB has a mutation status of V795I, The gene DNAH11 has a mutation status of R265H, The gene DNAH11 has a mutation status of E3471K, The gene TNS3 has a mutation status of F713F, The gene ABCA13 has a mutation status of A4359A, The gene CDC14C has a mutation status of L165L, The gene EGFR has a mutation status of ELREA701del, The gene SPDYE17 has a mutation status of R158S, The gene GRM3 has a mutation status of I390I, The gene DMTF1 has a mutation status of N412K, The gene AKAP9 has a mutation status of G2529G, The gene PDK4 has a mutation status of S83P, The gene OCM2 has a mutation status of L36H, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene RELN has a mutation status of G1161G, The gene LAMB4 has a mutation status of V1506V, The gene BMT2 has a mutation status of L245L, The gene ZNF800 has a mutation status of H504fs, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene TMEM140 has a mutation status of L146L, The gene WDR91 has a mutation status of R40H, The gene NUP205 has a mutation status of E700Q, The gene SVOPL has a mutation status of R266del, The gene KIAA1549 has a mutation status of L493V, The gene SLC37A3 has a mutation status of L415P, The gene DENND11 has a mutation status of V270V, The gene MGAM has a mutation status of N1607N, The gene GIMAP4 has a mutation status of G124G, The gene GIMAP5 has a mutation status of E284K, The gene PTPRN2 has a mutation status of S208Y, The gene ARHGEF10 has a mutation status of T530T, The gene SH2D4A has a mutation status of R279Q, The gene INTS10 has a mutation status of L348H, The gene INTS10 has a mutation status of A505A, The gene NSD3 has a mutation status of V640V, The gene CHRNA6 has a mutation status of L338L, The gene HGSNAT has a mutation status of G424G, The gene SULF1 has a mutation status of G529E, The gene HNF4G has a mutation status of W300C, The gene PDP1 has a mutation status of H285H, The gene VPS13B has a mutation status of I3503I, The gene BAALC has a mutation status of A35S, The gene TNFRSF11B has a mutation status of G129fs, The gene COL14A1 has a mutation status of V930I, The gene ZFAT has a mutation status of G728R, The gene EPPK1 has a mutation status of G285S, The gene CPSF1 has a mutation status of A644D, The gene SLC39A4 has a mutation status of C57C, The gene ZNF16 has a mutation status of E87D, The gene RIC1 has a mutation status of H94N, The gene KIAA2026 has a mutation status of M188I, The gene RANBP6 has a mutation status of T513A, The gene CDKN2A has a mutation status of G16V, The gene PLAA has a mutation status of G327G, The gene TEK has a mutation status of G476G, The gene ACO1 has a mutation status of S428S, The gene CNTFR has a mutation status of S294C, The gene FAM205A has a mutation status of S414C, The gene TMEM8B has a mutation status of V96L, The gene OR13J1 has a mutation status of S264G, The gene CNTNAP3 has a mutation status of A1204T, The gene NMRK1 has a mutation status of E42D, The gene VPS13A has a mutation status of P974P, The gene SPATA31D1 has a mutation status of D183N, The gene IARS1 has a mutation status of P437L, The gene ZNF510 has a mutation status of E59D, The gene FRRS1L has a mutation status of G99E, The gene SVEP1 has a mutation status of T523T, The gene SLC2A8 has a mutation status of V261I, The gene DOLPP1 has a mutation status of L120*, The gene ABL1 has a mutation status of V130V, The gene NACC2 has a mutation status of A153A, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene CCDC187 has a mutation status of E1017E, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of S497L, The gene CCDC187 has a mutation status of T90M, The gene CCDC183 has a mutation status of L334R, The gene FBXW5 has a mutation status of S151L, The gene DIP2C has a mutation status of F780F, The gene ADARB2 has a mutation status of K70K, The gene DHTKD1 has a mutation status of G469G, The gene MALRD1 has a mutation status of D1753N, The gene DNAJC1 has a mutation status of P21R, The gene ZNF33B has a mutation status of H407Y, The gene AGAP4 has a mutation status of Q20Q, The gene RBP3 has a mutation status of G498G, The gene WDFY4 has a mutation status of V444V, The gene CSTF2T has a mutation status of P299H, The gene ZNF365 has a mutation status of N390fs, The gene PALD1 has a mutation status of V509M, The gene TBATA has a mutation status of I326T, The gene TBATA has a mutation status of L224F, The gene KAT6B has a mutation status of E1240K, The gene POLR3A has a mutation status of Y550C, The gene WAPL has a mutation status of G340R, The gene KIF20B has a mutation status of I1749V, The gene TNKS2 has a mutation status of D72D, The gene PLCE1 has a mutation status of E1354*, The gene PKD2L1 has a mutation status of V548I, The gene PPRC1 has a mutation status of T1148T, The gene C10orf95 has a mutation status of E51D, The gene SLK has a mutation status of Q670R, The gene NRAP has a mutation status of H1246Q, The gene FAM24A has a mutation status of I11V, The gene EDRF1 has a mutation status of S231S, The gene PHRF1 has a mutation status of S730S, The gene MUC6 has a mutation status of A1593P, The gene OR52R1 has a mutation status of L156M, The gene UBQLN3 has a mutation status of A268T, The gene TRIM6 has a mutation status of P299T, The gene CCKBR has a mutation status of R215H, The gene OTOG has a mutation status of Y977S, The gene PTPN5 has a mutation status of V210I, The gene CSRP3 has a mutation status of K152K, The gene MUC15 has a mutation status of K59T, The gene SLC5A12 has a mutation status of Q257*, The gene EXT2 has a mutation status of T89M, The gene PHF21A has a mutation status of E81E, The gene OR4C12 has a mutation status of N308N, The gene OR4A16 has a mutation status of N170N, The gene OR5I1 has a mutation status of N91K, The gene OR8K5 has a mutation status of R20L, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MS4A8 has a mutation status of N56T, The gene FADS3 has a mutation status of C55C, The gene RAB3IL1 has a mutation status of E44K, The gene TEX54 has a mutation status of K17*, The gene RPS6KA4 has a mutation status of G489G, The gene FRMD8 has a mutation status of H18P, The gene CTSF has a mutation status of L270L, The gene SPTBN2 has a mutation status of R2089K, The gene AIP has a mutation status of Q315P, The gene ACY3 has a mutation status of R75K, The gene TCIRG1 has a mutation status of A301A, The gene NADSYN1 has a mutation status of D670D, The gene TPBGL has a mutation status of A143T, The gene FAT3 has a mutation status of D2112Y, The gene MMP3 has a mutation status of G188G, The gene CWF19L2 has a mutation status of G748R, The gene ZBTB16 has a mutation status of R566H, The gene ZPR1 has a mutation status of P12fs, The gene ZPR1 has a mutation status of G10G, The gene TECTA has a mutation status of T1354I, The gene OR8B8 has a mutation status of I69I, The gene TBRG1 has a mutation status of L366F, The gene APLP2 has a mutation status of D234D, The gene VPS26B has a mutation status of G296G, The gene VWF has a mutation status of G142S, The gene GNB3 has a mutation status of R137W, The gene USP5 has a mutation status of E438E, The gene SLC2A14 has a mutation status of S27fs, The gene PRH2 has a mutation status of Q161K, The gene TAS2R46 has a mutation status of L98P, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene BCAT1 has a mutation status of W267*, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of E249R, The gene GXYLT1 has a mutation status of I220G, The gene KRT7 has a mutation status of V24V, The gene KRT85 has a mutation status of R16S, The gene KRT6B has a mutation status of N241N, The gene KRT2 has a mutation status of R45C, The gene MMP19 has a mutation status of H156Q, The gene STAT2 has a mutation status of R300C, The gene LRP1 has a mutation status of E153E, The gene INHBE has a mutation status of H214R, The gene KIF5A has a mutation status of Y936*, The gene B4GALNT1 has a mutation status of D397A, The gene MYRFL has a mutation status of N403D, The gene ZFC3H1 has a mutation status of V851V, The gene OTOGL has a mutation status of I1648T, The gene C12orf29 has a mutation status of D258N, The gene MYBPC1 has a mutation status of I769T, The gene NUAK1 has a mutation status of L181L, The gene ISCU has a mutation status of R8C, The gene SELPLG has a mutation status of E377*, The gene MAPKAPK5 has a mutation status of I273M, The gene OAS2 has a mutation status of L311P, The gene DDX54 has a mutation status of R86H, The gene RBM19 has a mutation status of P434L, The gene GCN1 has a mutation status of A1525V, The gene HIP1R has a mutation status of E308A, The gene DNAH10 has a mutation status of E179K, The gene RIMBP2 has a mutation status of A275V, The gene EP400 has a mutation status of A2577A, The gene RNF6 has a mutation status of V373L, The gene FRY has a mutation status of V341M, The gene RFC3 has a mutation status of V195M, The gene DACH1 has a mutation status of R650Q, The gene FBXL3 has a mutation status of V412V, The gene RBM26 has a mutation status of R555R, The gene DOCK9 has a mutation status of K1430K, The gene ZIC5 has a mutation status of P166P, The gene CCDC168 has a mutation status of A5113T, The gene CCDC168 has a mutation status of L4120L, The gene PROZ has a mutation status of T316M, The gene SALL2 has a mutation status of G407R, The gene PRMT5 has a mutation status of E177E, The gene ADCY4 has a mutation status of M244I, The gene TTC6 has a mutation status of S607S, The gene TOGARAM1 has a mutation status of D35G, The gene FANCM has a mutation status of L1759V, The gene STYX has a mutation status of R97C, The gene ACTN1 has a mutation status of R291H, The gene DNAL1 has a mutation status of V148L, The gene MIDEAS has a mutation status of P108P, The gene ABCD4 has a mutation status of A7T, The gene TTLL5 has a mutation status of Q1172K, The gene SERPINA11 has a mutation status of L276L, The gene ATG2B has a mutation status of N1089S, The gene AK7 has a mutation status of T81T, The gene POTEB3 has a mutation status of R450G, The gene GOLGA6L22 has a mutation status of K558R, The gene GOLGA6L22 has a mutation status of *811Q, The gene GOLGA8S has a mutation status of P300S, The gene GOLGA8S has a mutation status of I439V, The gene GOLGA6L7 has a mutation status of 323_324QE>HK, The gene GOLGA6L7 has a mutation status of E296K, The gene RYR3 has a mutation status of A3238A, The gene PHGR1 has a mutation status of P56L, The gene RPAP1 has a mutation status of T491T, The gene RPAP1 has a mutation status of L59L, The gene DUOX2 has a mutation status of W191*, The gene SEMA6D has a mutation status of N107K, The gene BCL2L10 has a mutation status of L27V, The gene VPS13C has a mutation status of F3218V, The gene ANKDD1A has a mutation status of L516L, The gene SPG21 has a mutation status of Y94Y, The gene THSD4 has a mutation status of I292I, The gene GOLGA6L10 has a mutation status of R300H, The gene GOLGA6L9 has a mutation status of Q151E, The gene AC245033.1 has a mutation status of S142S, The gene ADAMTSL3 has a mutation status of S1162W, The gene ZSCAN2 has a mutation status of E155D, The gene TTLL13P has a mutation status of R490R, The gene MAN2A2 has a mutation status of T79K, The gene GNPTG has a mutation status of G4A, The gene UNKL has a mutation status of A349A, The gene SLX4 has a mutation status of R1826Q, The gene ADCY9 has a mutation status of I473I, The gene DNAJA3 has a mutation status of V14V, The gene UBN1 has a mutation status of D207H, The gene ABAT has a mutation status of Q279R, The gene TVP23A has a mutation status of E209K, The gene ABCC6 has a mutation status of M848fs, The gene HIRIP3 has a mutation status of E486Q, The gene INO80E has a mutation status of L150L, The gene PRR14 has a mutation status of A540T, The gene CCDC189 has a mutation status of C145F, The gene ADCY7 has a mutation status of G934S, The gene CCDC102A has a mutation status of A275V, The gene CDH5 has a mutation status of S215S, The gene ELMO3 has a mutation status of L556L, The gene PRMT7 has a mutation status of A596A, The gene WWP2 has a mutation status of G344A, The gene SF3B3 has a mutation status of T1100T, The gene GLG1 has a mutation status of S527S, The gene ATMIN has a mutation status of V521I, The gene ANKRD11 has a mutation status of Q1176K, The gene ANKRD11 has a mutation status of C1130*, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene OR1G1 has a mutation status of V124M, The gene CYB5D2 has a mutation status of A90A, The gene ALOX15 has a mutation status of Y15H, The gene SLC52A1 has a mutation status of P42L, The gene ZNF232 has a mutation status of T251N, The gene TP53 has a mutation status of R248Q, The gene USP43 has a mutation status of L344R, The gene MYH13 has a mutation status of A1364A, The gene MYH13 has a mutation status of H1342H, The gene MYH13 has a mutation status of A1205A, The gene MYH8 has a mutation status of K1531E, The gene MYH1 has a mutation status of R1283H, The gene DNAH9 has a mutation status of Q1951*, The gene SREBF1 has a mutation status of R39G, The gene B9D1 has a mutation status of R160C, The gene MYO18A has a mutation status of N1746N, The gene TMEM132E has a mutation status of P136P, The gene SLFN14 has a mutation status of P526S, The gene CCL4L2 has a mutation status of P67R, The gene DUSP14 has a mutation status of V184I, The gene PCGF2 has a mutation status of A253A, The gene MSL1 has a mutation status of H410H, The gene RAPGEFL1 has a mutation status of L77P, The gene KRTAP9-8 has a mutation status of C76C, The gene KRT16 has a mutation status of A199V, The gene WNT9B has a mutation status of R258H, The gene BCAS3 has a mutation status of P519S, The gene CD300LF has a mutation status of G214R, The gene ITGB4 has a mutation status of K703R, The gene DNAH17 has a mutation status of N274S, The gene CBX2 has a mutation status of S459N, The gene CCDC40 has a mutation status of G48S, The gene RNF213 has a mutation status of D2603E, The gene CCDC57 has a mutation status of A236A, The gene GAREM1 has a mutation status of T656T, The gene SIGLEC15 has a mutation status of L11W, The gene ZBTB7C has a mutation status of DEEEE153del, The gene STARD6 has a mutation status of R86S, The gene ZNF516 has a mutation status of K1005K, The gene ZNF236 has a mutation status of A1381A, The gene MED16 has a mutation status of A83T, The gene CNN2 has a mutation status of M249T, The gene SPPL2B has a mutation status of S591L, The gene S1PR4 has a mutation status of A189S, The gene ZBTB7A has a mutation status of T94M, The gene STAP2 has a mutation status of T198A, The gene CHAF1A has a mutation status of R336T, The gene INSR has a mutation status of N1060N, The gene CAMSAP3 has a mutation status of D992D, The gene XAB2 has a mutation status of V615M, The gene XAB2 has a mutation status of R567R, The gene RETN has a mutation status of C74W, The gene FBN3 has a mutation status of V204M, The gene PRAM1 has a mutation status of C658Y, The gene ZNF414 has a mutation status of A312fs, The gene ZNF414 has a mutation status of A311G, The gene ZNF414 has a mutation status of P232P, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene S1PR2 has a mutation status of T320I, The gene TMEM205 has a mutation status of G8A, The gene HOOK2 has a mutation status of P22P, The gene MAST1 has a mutation status of A84A, The gene EPS15L1 has a mutation status of P240P, The gene ANKLE1 has a mutation status of S509S, The gene TSSK6 has a mutation status of A218V, The gene ZNF729 has a mutation status of M1036I, The gene ZNF729 has a mutation status of H1182R, The gene ZNF730 has a mutation status of I445M, The gene CLIP3 has a mutation status of N163N, The gene CATSPERG has a mutation status of Q610H, The gene SPRED3 has a mutation status of W215G, The gene ZNF546 has a mutation status of T265I, The gene CYP2B6 has a mutation status of A464T, The gene ARHGEF1 has a mutation status of S776S, The gene ATP1A3 has a mutation status of K81M, The gene CIC has a mutation status of A1923V, The gene ZNF404 has a mutation status of H433N, The gene ZNF284 has a mutation status of C205Y, The gene ZNF224 has a mutation status of H506D, The gene ZNF112 has a mutation status of L455fs, The gene MARK4 has a mutation status of R377R, The gene OPA3 has a mutation status of A81T, The gene EML2 has a mutation status of V30A, The gene RSPH6A has a mutation status of M271R, The gene PTGIR has a mutation status of F83C, The gene CABP5 has a mutation status of IEL70del, The gene PLEKHA4 has a mutation status of T659T, The gene LRRC4B has a mutation status of E616K, The gene SIGLEC9 has a mutation status of S437G, The gene SIGLEC8 has a mutation status of G288D, The gene HAS1 has a mutation status of H397Q, The gene ZNF665 has a mutation status of R330H, The gene ZNF331 has a mutation status of W32L, The gene VSTM1 has a mutation status of S195T, The gene LILRB3 has a mutation status of W205Q, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of H290H, The gene LILRA6 has a mutation status of H290N, The gene LILRA6 has a mutation status of Y121Y, The gene LILRA6 has a mutation status of I88M, The gene LENG9 has a mutation status of P423T, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of P224S, The gene KIR2DL1 has a mutation status of T91K, The gene KIR2DL1 has a mutation status of P175T, The gene KIR2DL1 has a mutation status of H192H, The gene KIR2DL1 has a mutation status of G283G, The gene NLRP2 has a mutation status of S179R, The gene SBK3 has a mutation status of D273Y, The gene ZNF865 has a mutation status of V757G, The gene ZSCAN5B has a mutation status of M412T, The gene PEG3 has a mutation status of R107*, The gene ZNF805 has a mutation status of F594F, The gene ZNF837 has a mutation status of L70L, The gene SLC27A5 has a mutation status of R164C, The gene TRIB3 has a mutation status of D343D, The gene BMP2 has a mutation status of T128T, The gene XRN2 has a mutation status of I208T, The gene THBD has a mutation status of T411I, The gene ACSS1 has a mutation status of T363N, The gene FOXS1 has a mutation status of P292A, The gene EYA2 has a mutation status of T393T, The gene NCOA3 has a mutation status of P261S, The gene PREX1 has a mutation status of E1135D, The gene APCDD1L has a mutation status of L221V, The gene PHACTR3 has a mutation status of K110N, The gene DIDO1 has a mutation status of P1918L, The gene COL20A1 has a mutation status of Q601fs, The gene RGS19 has a mutation status of L70L, The gene PCMTD2 has a mutation status of D37Y, The gene JAM2 has a mutation status of S112I, The gene ZNF280B has a mutation status of C449S, The gene IGLL1 has a mutation status of R81G, The gene MYO18B has a mutation status of H1045H, The gene RFPL3 has a mutation status of L122C, The gene TEX33 has a mutation status of G27G, The gene IL2RB has a mutation status of T476M, The gene MFNG has a mutation status of T38P, The gene GGA1 has a mutation status of D148N, The gene CACNA1I has a mutation status of I811I, The gene ZC3H7B has a mutation status of F585L, The gene POLR3H has a mutation status of H67H, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ARHGAP8 has a mutation status of G3G, The gene TAFA5 has a mutation status of G43V, The gene BRD1 has a mutation status of I948I, The gene CPT1B has a mutation status of Y202Y, The gene GTPBP6 has a mutation status of M181L, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene AKAP17A has a mutation status of S610N, The gene ARSH has a mutation status of A492V, The gene NLGN4X has a mutation status of V441V, The gene SHROOM2 has a mutation status of I56V, The gene CTPS2 has a mutation status of R103C, The gene CNKSR2 has a mutation status of L65L, The gene CFAP47 has a mutation status of K598I, The gene ITIH6 has a mutation status of Y1190H, The gene FOXR2 has a mutation status of S135C, The gene AMER1 has a mutation status of H879P, The gene GLRA4 has a mutation status of R370C, The gene IL13RA2 has a mutation status of P241S, The gene AGTR2 has a mutation status of L86L, The gene SLC25A5 has a mutation status of T221R, The gene NKAP has a mutation status of R281Q, The gene LAMP2 has a mutation status of C153Y, The gene DCAF12L2 has a mutation status of F382F, The gene CCDC160 has a mutation status of S27Y, The gene ZNF449 has a mutation status of G419E, The gene BRS3 has a mutation status of P372P, The gene CNGA2 has a mutation status of P433S, The gene F8 has a mutation status of E739E, The gene MT-ND1 has a mutation status of G29S, The gene MT-CO1 has a mutation status of L35P, The gene MT-CO3 has a mutation status of G20E, The gene MT-CO3 has a mutation status of E183E, The gene MT-ND5 has a mutation status of I576I, The gene MT-CYB has a mutation status of A354T, The gene SDF4 has a mutation status of P249P, The gene B3GALT6 has a mutation status of A70T, The gene CCNL2 has a mutation status of S25C, The gene PLCH2 has a mutation status of D962N, The gene TTC34 has a mutation status of R764H, The gene ACTRT2 has a mutation status of S277L, The gene KLHL21 has a mutation status of A285S, The gene CA6 has a mutation status of R96P, The gene C1orf127 has a mutation status of T31M, The gene EXOSC10 has a mutation status of R158H, The gene PRAMEF4 has a mutation status of Q81H, The gene PRAMEF9 has a mutation status of L14L, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRDM2 has a mutation status of E1158E, The gene KAZN has a mutation status of N614N, The gene CROCC has a mutation status of V142V, The gene PADI1 has a mutation status of N188N, The gene KLHDC7A has a mutation status of G589R, The gene HP1BP3 has a mutation status of R455K, The gene HSPG2 has a mutation status of R2730I, The gene SPOCD1 has a mutation status of S94S, The gene EIF3I has a mutation status of V244V, The gene RNF19B has a mutation status of S561fs, The gene NCDN has a mutation status of V422I, The gene TFAP2E has a mutation status of P56fs, The gene CSF3R has a mutation status of G366R, The gene CCDC30 has a mutation status of R290Q, The gene TMEM269 has a mutation status of F168F, The gene CFAP57 has a mutation status of K973K, The gene CFAP57 has a mutation status of S1241C, The gene SZT2 has a mutation status of Q1003Q, The gene SZT2 has a mutation status of Q3133fs, The gene RPS8 has a mutation status of G63G, The gene PTCH2 has a mutation status of L104P, The gene HECTD3 has a mutation status of A816T, The gene MAST2 has a mutation status of R1246L, The gene MAST2 has a mutation status of G1703G, The gene FAAH has a mutation status of A345A, The gene PDZK1IP1 has a mutation status of A36A, The gene SLC5A9 has a mutation status of I192L, The gene EPS15 has a mutation status of I52V, The gene CC2D1B has a mutation status of R432Q, The gene TCEANC2 has a mutation status of R89H, The gene MROH7 has a mutation status of S477C, The gene C8A has a mutation status of V114V, The gene PATJ has a mutation status of R1717W, The gene CACHD1 has a mutation status of R446Q, The gene PDE4B has a mutation status of L486L, The gene LRRC7 has a mutation status of P1152P, The gene LRRC7 has a mutation status of Q1201E, The gene SPATA1 has a mutation status of E95K, The gene SYDE2 has a mutation status of D173Y, The gene COL24A1 has a mutation status of F121I, The gene CLCA2 has a mutation status of R596C, The gene BTBD8 has a mutation status of R1650C, The gene DNTTIP2 has a mutation status of R272K, The gene ARHGAP29 has a mutation status of K12T, The gene CELSR2 has a mutation status of A158E, The gene CELSR2 has a mutation status of Q398L, The gene SLC6A17 has a mutation status of R270R, The gene PIFO has a mutation status of Y12Y, The gene SPAG17 has a mutation status of A2177E, The gene NBPF26 has a mutation status of E798*, The gene ANXA9 has a mutation status of L230F, The gene FLG has a mutation status of W1934C, The gene FLG has a mutation status of T1847M, The gene CRNN has a mutation status of L75Q, The gene PRR9 has a mutation status of E63*, The gene ILF2 has a mutation status of E333E, The gene DENND4B has a mutation status of L166L, The gene UBAP2L has a mutation status of R151L, The gene UBAP2L has a mutation status of T667T, The gene HAX1 has a mutation status of P198Q, The gene SHE has a mutation status of A39A, The gene ARHGEF2 has a mutation status of R622C, The gene PEAR1 has a mutation status of P651T, The gene PEAR1 has a mutation status of R871C, The gene OR6N1 has a mutation status of A237V, The gene AIM2 has a mutation status of A339E, The gene OR10J5 has a mutation status of V183V, The gene KCNJ9 has a mutation status of E277D, The gene ATP1A2 has a mutation status of Y113Y, The gene NHLH1 has a mutation status of R46Q, The gene SLAMF6 has a mutation status of L124fs, The gene HSPA6 has a mutation status of D392V, The gene RXRG has a mutation status of Q322K, The gene MROH9 has a mutation status of T425M, The gene FMO3 has a mutation status of V110L, The gene SUCO has a mutation status of G450G, The gene RASAL2 has a mutation status of T1038T, The gene AXDND1 has a mutation status of Y790C, The gene FAM163A has a mutation status of D52D, The gene CEP350 has a mutation status of E1121K, The gene CACNA1E has a mutation status of F1426L, The gene C1orf21 has a mutation status of K20N, The gene RGS2 has a mutation status of Q203K, The gene CFHR4 has a mutation status of S403S, The gene CRB1 has a mutation status of R793Q, The gene IGFN1 has a mutation status of K1635E, The gene FMOD has a mutation status of T88T, The gene ATP2B4 has a mutation status of R607W, The gene DSTYK has a mutation status of I728T, The gene USH2A has a mutation status of T3829I, The gene USH2A has a mutation status of K3397T, The gene USH2A has a mutation status of G2269A, The gene DNAH14 has a mutation status of A3518S, The gene IBA57 has a mutation status of L70L, The gene ACTA1 has a mutation status of A183A, The gene PGBD5 has a mutation status of R300W, The gene AGT has a mutation status of R237H, The gene GNPAT has a mutation status of G460R, The gene TBCE has a mutation status of L134L, The gene NID1 has a mutation status of T725I, The gene RYR2 has a mutation status of Q1123K, The gene ZP4 has a mutation status of G80D, The gene ZBTB18 has a mutation status of L274L, The gene OR2B11 has a mutation status of N179D, The gene MYT1L has a mutation status of A968V, The gene GEN1 has a mutation status of K721N, The gene APOB has a mutation status of C2933F, The gene APOB has a mutation status of L1073L, The gene APOB has a mutation status of Q436*, The gene KLHL29 has a mutation status of Q363fs, The gene ITSN2 has a mutation status of Q725L, The gene DPYSL5 has a mutation status of N380N, The gene IFT172 has a mutation status of A1200A, The gene PCARE has a mutation status of E1062Q, The gene ALK has a mutation status of E1299K, The gene THADA has a mutation status of I1383I, The gene PLEKHH2 has a mutation status of T832T, The gene KCNK12 has a mutation status of A203A, The gene STON1 has a mutation status of P575L, The gene EML6 has a mutation status of D1938D, The gene RTN4 has a mutation status of M380T, The gene PPP4R3B has a mutation status of E92E, The gene PEX13 has a mutation status of P235S, The gene BMP10 has a mutation status of S419S, The gene ANTXR1 has a mutation status of Q296Q, The gene PCBP1 has a mutation status of Q227Q, The gene DYSF has a mutation status of H746N, The gene TET3 has a mutation status of S1383fs, The gene TLX2 has a mutation status of E46E, The gene DOK1 has a mutation status of P373P, The gene M1AP has a mutation status of A44V, The gene GCFC2 has a mutation status of F451F, The gene SMYD1 has a mutation status of S358S, The gene TEX37 has a mutation status of P123P, The gene ZNF2 has a mutation status of E94*, The gene NCAPH has a mutation status of Q323R, The gene CNNM3 has a mutation status of Q660Q, The gene CNGA3 has a mutation status of D543N, The gene POU3F3 has a mutation status of A110A, The gene EN1 has a mutation status of R284L, The gene C1QL2 has a mutation status of A233V, The gene CFAP221 has a mutation status of A621V, The gene MYO7B has a mutation status of A2067E, The gene WDR33 has a mutation status of P816P, The gene TUBA3E has a mutation status of A330V, The gene MZT2A has a mutation status of S125S, The gene ARHGAP15 has a mutation status of K271I, The gene NEB has a mutation status of I7140T, The gene NEB has a mutation status of R3528C, The gene ACVR1 has a mutation status of G225D, The gene BAZ2B has a mutation status of Y2156fs, The gene MARCHF7 has a mutation status of S26Y, The gene SLC4A10 has a mutation status of P347P, The gene MYO3B has a mutation status of V1137V, The gene PDK1 has a mutation status of P56P, The gene GPR155 has a mutation status of S96F, The gene CHN1 has a mutation status of E455K, The gene HOXD11 has a mutation status of L174F, The gene HOXD11 has a mutation status of E246K, The gene TTC30B has a mutation status of G305R, The gene TTN has a mutation status of F25366L, The gene TTN has a mutation status of S14314S, The gene TTN has a mutation status of V13484L, The gene TTN has a mutation status of Q2087K, The gene FSIP2 has a mutation status of I2097fs, The gene MFSD6 has a mutation status of A247T, The gene C2CD6 has a mutation status of M1811fs, The gene C2CD6 has a mutation status of F1370C, The gene ALS2 has a mutation status of S100S, The gene NDUFS1 has a mutation status of V270V, The gene ABCA12 has a mutation status of T345P, The gene ATIC has a mutation status of Y435Y, The gene WNT10A has a mutation status of A334T, The gene ANKZF1 has a mutation status of K435N, The gene GLB1L has a mutation status of V358A, The gene DOCK10 has a mutation status of C232F, The gene SPHKAP has a mutation status of V568M, The gene TRIP12 has a mutation status of L191F, The gene ALPG has a mutation status of R154R, The gene ALPG has a mutation status of A206A, The gene CHRND has a mutation status of T175T, The gene UGT1A5 has a mutation status of L132M, The gene IQCA1 has a mutation status of I159I, The gene SNED1 has a mutation status of P870P, The gene HDLBP has a mutation status of R534H, The gene ITPR1 has a mutation status of D1822H, The gene TTLL3 has a mutation status of N206H, The gene FANCD2OS has a mutation status of D122H, The gene SLC6A11 has a mutation status of F346F, The gene FBLN2 has a mutation status of G176S, The gene C3orf20 has a mutation status of A282A, The gene C3orf20 has a mutation status of G449C, The gene ZNF385D has a mutation status of S352N, The gene ZNF385D has a mutation status of P300P, The gene NKIRAS1 has a mutation status of D109E, The gene TOP2B has a mutation status of D226N, The gene OXSM has a mutation status of G336G, The gene TRANK1 has a mutation status of S2299F, The gene TRANK1 has a mutation status of P1317L, The gene SCN11A has a mutation status of I201S, The gene CSRNP1 has a mutation status of Q260R, The gene CTNNB1 has a mutation status of T3I, The gene ZNF197 has a mutation status of K825K, The gene SLC6A20 has a mutation status of L179L, The gene KIF9 has a mutation status of H227H, The gene PTPN23 has a mutation status of E830D, The gene SCAP has a mutation status of I1020V, The gene MAP4 has a mutation status of E1044E, The gene SLC26A6 has a mutation status of P119P, The gene CELSR3 has a mutation status of V1030V, The gene QARS1 has a mutation status of L55L, The gene ITIH4 has a mutation status of S248F, The gene CACNA2D3 has a mutation status of E724D, The gene CADPS has a mutation status of L1141L, The gene CNTN3 has a mutation status of L323L, The gene CNTN3 has a mutation status of E177*, The gene CADM2 has a mutation status of T342S, The gene EPHA3 has a mutation status of H76N, The gene CRYBG3 has a mutation status of L137L, The gene CRYBG3 has a mutation status of L650fs, The gene OR5H1 has a mutation status of I158F, The gene ABI3BP has a mutation status of S357S, The gene ZBTB11 has a mutation status of E984E, The gene IFT57 has a mutation status of L53L, The gene DPPA2 has a mutation status of C96Y, The gene ILDR1 has a mutation status of R418Q, The gene PARP14 has a mutation status of V160V, The gene PARP14 has a mutation status of D1063V, The gene ADCY5 has a mutation status of E516E, The gene ADCY5 has a mutation status of N191N, The gene MYLK has a mutation status of V1008V, The gene MYLK has a mutation status of T331T, The gene PODXL2 has a mutation status of P325H, The gene EFCC1 has a mutation status of K539E, The gene RHO has a mutation status of P327T, The gene PLXND1 has a mutation status of T1579M, The gene COL6A5 has a mutation status of D2498D, The gene ACP3 has a mutation status of G45R, The gene BFSP2 has a mutation status of E273E, The gene TOPBP1 has a mutation status of S115fs, The gene ATR has a mutation status of L770K, The gene ATR has a mutation status of L769Q, The gene PLS1 has a mutation status of E262D, The gene P2RY12 has a mutation status of I257L, The gene IFT80 has a mutation status of M412T, The gene OTOL1 has a mutation status of R157P, The gene NLGN1 has a mutation status of P658L, The gene KLHL24 has a mutation status of R11I, The gene EIF4G1 has a mutation status of Y1401Y, The gene ST6GAL1 has a mutation status of L392L, The gene CCDC50 has a mutation status of Y144*, The gene OPA1 has a mutation status of M592T, The gene TNK2 has a mutation status of A634T, The gene TNK2 has a mutation status of P628P, The gene TFRC has a mutation status of T104T, The gene LRCH3 has a mutation status of N365N, The gene LRCH3 has a mutation status of L662L, The gene PDE6B has a mutation status of E747V, The gene SLC26A1 has a mutation status of L513L, The gene TMEM129 has a mutation status of F48F, The gene HAUS3 has a mutation status of Q433K, The gene HGFAC has a mutation status of A327A, The gene MAN2B2 has a mutation status of R572H, The gene SLC2A9 has a mutation status of P222P, The gene SEL1L3 has a mutation status of L519M, The gene DTHD1 has a mutation status of E595G, The gene ATP8A1 has a mutation status of T673T, The gene ATP10D has a mutation status of K264K, The gene TXK has a mutation status of L53W, The gene PDGFRA has a mutation status of V266V, The gene CRACD has a mutation status of E1083D, The gene EPHA5 has a mutation status of S673T, The gene CSN2 has a mutation status of V3V, The gene GC has a mutation status of A318S, The gene AFM has a mutation status of K37N, The gene SHROOM3 has a mutation status of R414Q, The gene SHROOM3 has a mutation status of S1599Y, The gene C4orf54 has a mutation status of K1074N, The gene TET2 has a mutation status of P1655R, The gene PAPSS1 has a mutation status of M496L, The gene SEC24B has a mutation status of V479V, The gene FAM241A has a mutation status of G11C, The gene NDST4 has a mutation status of N170D, The gene NDNF has a mutation status of L75F, The gene KIAA1109 has a mutation status of T1521I, The gene FAT4 has a mutation status of R1815C, The gene ELF2 has a mutation status of M159K, The gene ARHGAP10 has a mutation status of N222S, The gene DCLK2 has a mutation status of A737G, The gene TMEM131L has a mutation status of V211V, The gene DCHS2 has a mutation status of I3077I, The gene DCHS2 has a mutation status of A2562G, The gene FGA has a mutation status of S364R, The gene TLL1 has a mutation status of G694G, The gene SLC6A19 has a mutation status of L78M, The gene NDUFS6 has a mutation status of R13R, The gene ADCY2 has a mutation status of E898*, The gene FASTKD3 has a mutation status of E237*, The gene FBXL7 has a mutation status of H392H, The gene MYO10 has a mutation status of E1460E, The gene CDH18 has a mutation status of L202L, The gene CDH9 has a mutation status of V347V, The gene PDZD2 has a mutation status of P30R, The gene ADAMTS12 has a mutation status of A849S, The gene HMGCS1 has a mutation status of G122R, The gene PARP8 has a mutation status of R287H, The gene PARP8 has a mutation status of H723R, The gene DHX29 has a mutation status of G691R, The gene RGS7BP has a mutation status of H103Q, The gene ANKRD31 has a mutation status of R606G, The gene CERT1 has a mutation status of R211H, The gene IQGAP2 has a mutation status of E474E, The gene ZBED3 has a mutation status of L155A, The gene VCAN has a mutation status of S1315G, The gene FBN2 has a mutation status of T1173S, The gene SLC27A6 has a mutation status of V307V, The gene ACSL6 has a mutation status of P158P, The gene CCNI2 has a mutation status of R120H, The gene SHROOM1 has a mutation status of F36F, The gene FSTL4 has a mutation status of P251H, The gene FSTL4 has a mutation status of A146T, The gene C5orf24 has a mutation status of R92W, The gene TRPC7 has a mutation status of V624M, The gene SLC4A9 has a mutation status of S614T, The gene HARS2 has a mutation status of R215W, The gene PCDHA1 has a mutation status of A454E, The gene PCDHB13 has a mutation status of S505S, The gene FAT2 has a mutation status of R3649L, The gene GEMIN5 has a mutation status of S1267F, The gene SGCD has a mutation status of N211N, The gene FAM71B has a mutation status of T149T, The gene GABRA1 has a mutation status of C166Y, The gene SH3PXD2B has a mutation status of M428V, The gene RPL26L1 has a mutation status of R11C, The gene FAM153B has a mutation status of D140E, The gene GMCL2 has a mutation status of R447Q, The gene GRM6 has a mutation status of S306*, The gene ADAMTS2 has a mutation status of P98P, The gene ADAMTS2 has a mutation status of V74M, The gene MGAT4B has a mutation status of R4L, The gene FLT4 has a mutation status of E1106*, The gene IRF4 has a mutation status of T92T, The gene FARS2 has a mutation status of Y113C, The gene ATXN1 has a mutation status of HQHQQQ209del, The gene ATXN1 has a mutation status of E41D, The gene H4C1 has a mutation status of R20C, The gene H2AC11 has a mutation status of R18R, The gene ZNF391 has a mutation status of E294K, The gene OR11A1 has a mutation status of G18G, The gene MDC1 has a mutation status of R1932C, The gene PRRC2A has a mutation status of R853H, The gene DDAH2 has a mutation status of P73P, The gene CLIC1 has a mutation status of A98T, The gene VARS1 has a mutation status of Y174Y, The gene AL645922.1 has a mutation status of R576H, The gene DAXX has a mutation status of L330L, The gene ITPR3 has a mutation status of T2584T, The gene FANCE has a mutation status of N503N, The gene PNPLA1 has a mutation status of I139V, The gene PNPLA1 has a mutation status of D233N, The gene BNIP5 has a mutation status of S487C, The gene BTBD9 has a mutation status of R40W, The gene DNAH8 has a mutation status of C688C, The gene DNAH8 has a mutation status of R4629K, The gene C6orf132 has a mutation status of P989L, The gene ABCC10 has a mutation status of S1186S, The gene CAPN11 has a mutation status of E541*, The gene TDRD6 has a mutation status of R519I, The gene TDRD6 has a mutation status of P1871L, The gene ADGRF2 has a mutation status of E99E, The gene IL17A has a mutation status of P31T, The gene DST has a mutation status of A1637V, The gene EEF1A1 has a mutation status of E135E, The gene FILIP1 has a mutation status of V800V, The gene FILIP1 has a mutation status of L681Q, The gene HTR1B has a mutation status of K191K, The gene BCKDHB has a mutation status of P185P, The gene SYNCRIP has a mutation status of G155S, The gene POU3F2 has a mutation status of L419L, The gene CCNC has a mutation status of S33S, The gene CRYBG1 has a mutation status of R1191C, The gene AK9 has a mutation status of S1357G, The gene SLC22A16 has a mutation status of S169S, The gene LAMA4 has a mutation status of L485H, The gene RSPH4A has a mutation status of E517D, The gene SMPDL3A has a mutation status of A102T, The gene LAMA2 has a mutation status of R1687Q, The gene L3MBTL3 has a mutation status of P92S, The gene EPB41L2 has a mutation status of G892G, The gene OR2A4 has a mutation status of A56T, The gene AHI1 has a mutation status of T856S, The gene AHI1 has a mutation status of 232_233SE>KK, The gene NHSL1 has a mutation status of V1081M, The gene NHSL1 has a mutation status of P734S, The gene PLAGL1 has a mutation status of T227A, The gene ADGB has a mutation status of V841I, The gene ZC3H12D has a mutation status of K526N, The gene GINM1 has a mutation status of T66T, The gene SYNE1 has a mutation status of K3039N, The gene RGS17 has a mutation status of M61L, The gene CNKSR3 has a mutation status of L264I, The gene LPA has a mutation status of W895L, The gene PDE10A has a mutation status of G3G, The gene THBS2 has a mutation status of A882A, The gene THBS2 has a mutation status of D813E, The gene GET4 has a mutation status of V111A, The gene CYP2W1 has a mutation status of R187Q, The gene ELFN1 has a mutation status of P276S, The gene MAD1L1 has a mutation status of E477K, The gene MAD1L1 has a mutation status of E419K, The gene ACTB has a mutation status of S368T, The gene GRID2IP has a mutation status of L1085L, The gene GRID2IP has a mutation status of R184*, The gene THSD7A has a mutation status of E1014K, The gene VWDE has a mutation status of T243T, The gene DGKB has a mutation status of V795I, The gene HDAC9 has a mutation status of C680fs, The gene DNAH11 has a mutation status of R265H, The gene DNAH11 has a mutation status of E3471K, The gene HOXA2 has a mutation status of N266K, The gene ITPRID1 has a mutation status of E49E, The gene PDE1C has a mutation status of E595D, The gene EPDR1 has a mutation status of Y112C, The gene CDK13 has a mutation status of Q544H, The gene GCK has a mutation status of P145P, The gene IKZF1 has a mutation status of M311I, The gene EGFR has a mutation status of ELREA701del, The gene ZNF722P has a mutation status of V163I, The gene TYW1 has a mutation status of R406H, The gene AUTS2 has a mutation status of P747P, The gene BAZ1B has a mutation status of P1284P, The gene BAZ1B has a mutation status of H1033Y, The gene SRRM3 has a mutation status of S508C, The gene ZP3 has a mutation status of F114L, The gene ZP3 has a mutation status of A176S, The gene PCLO has a mutation status of A2867D, The gene DMTF1 has a mutation status of N412K, The gene ADAM22 has a mutation status of E665K, The gene ZNF804B has a mutation status of C846F, The gene PEG10 has a mutation status of S316L, The gene PDK4 has a mutation status of S83P, The gene OCM2 has a mutation status of L36H, The gene TAF6 has a mutation status of C268C, The gene PVRIG has a mutation status of S57Y, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of E725K, The gene MUC3A has a mutation status of T730I, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC17 has a mutation status of S1639N, The gene VGF has a mutation status of G76fs, The gene RELN has a mutation status of G1161G, The gene LAMB4 has a mutation status of V1506V, The gene BMT2 has a mutation status of L245L, The gene ASZ1 has a mutation status of S271I, The gene CFTR has a mutation status of L1254*, The gene ATP6V1FNB has a mutation status of T124M, The gene AC011005.1 has a mutation status of F56L, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PLXNA4 has a mutation status of L883P, The gene TMEM140 has a mutation status of L146L, The gene WDR91 has a mutation status of R40H, The gene NUP205 has a mutation status of E700Q, The gene SVOPL has a mutation status of R266del, The gene KIAA1549 has a mutation status of L493V, The gene TBXAS1 has a mutation status of A138A, The gene SLC37A3 has a mutation status of L415P, The gene DENND11 has a mutation status of V270V, The gene MGAM has a mutation status of N1607N, The gene TAS2R39 has a mutation status of I222I, The gene OR2A2 has a mutation status of V207V, The gene CNTNAP2 has a mutation status of T440T, The gene GIMAP4 has a mutation status of G124G, The gene GIMAP5 has a mutation status of V68V, The gene GIMAP5 has a mutation status of G139R, The gene GIMAP5 has a mutation status of E284K, The gene HTR5A has a mutation status of I118V, The gene RBM33 has a mutation status of M695I, The gene ARHGEF10 has a mutation status of T530T, The gene KBTBD11 has a mutation status of A325A, The gene CSMD1 has a mutation status of L1540V, The gene XKR6 has a mutation status of W333*, The gene SGCZ has a mutation status of L135F, The gene SH2D4A has a mutation status of R279Q, The gene INTS10 has a mutation status of L348H, The gene INTS10 has a mutation status of A505A, The gene LPL has a mutation status of L7F, The gene BNIP3L has a mutation status of L94F, The gene RAB11FIP1 has a mutation status of T1274fs, The gene NSD3 has a mutation status of V640V, The gene ANK1 has a mutation status of F1242F, The gene CHRNA6 has a mutation status of L338L, The gene HGSNAT has a mutation status of G424G, The gene OPRK1 has a mutation status of I44V, The gene CYP7B1 has a mutation status of D151H, The gene PREX2 has a mutation status of L1360L, The gene SULF1 has a mutation status of G529E, The gene RALYL has a mutation status of E208K, The gene PDP1 has a mutation status of H285H, The gene VPS13B has a mutation status of I3503I, The gene BAALC has a mutation status of A35S, The gene PKHD1L1 has a mutation status of I4021S, The gene COL14A1 has a mutation status of V930I, The gene MTBP has a mutation status of T571K, The gene MTBP has a mutation status of Q573K, The gene AC100868.1 has a mutation status of H258P, The gene ZFAT has a mutation status of G728R, The gene FAM135B has a mutation status of G527W, The gene ZNF623 has a mutation status of E47K, The gene EPPK1 has a mutation status of G285S, The gene PLEC has a mutation status of A1816A, The gene SPATC1 has a mutation status of E233K, The gene CPSF1 has a mutation status of A644D, The gene SLC39A4 has a mutation status of L130L, The gene SLC39A4 has a mutation status of C57C, The gene ARHGAP39 has a mutation status of G157fs, The gene ZNF16 has a mutation status of E87D, The gene RIC1 has a mutation status of H94N, The gene KIAA2026 has a mutation status of M188I, The gene RANBP6 has a mutation status of T513A, The gene PSIP1 has a mutation status of F43L, The gene CCDC171 has a mutation status of N157S, The gene CDKN2A has a mutation status of G16V, The gene PLAA has a mutation status of G327G, The gene TEK has a mutation status of G476G, The gene ACO1 has a mutation status of S428S, The gene CNTFR has a mutation status of S294C, The gene TMEM8B has a mutation status of V96L, The gene OR13J1 has a mutation status of S264G, The gene PAX5 has a mutation status of P320R, The gene AL358113.1 has a mutation status of A241T, The gene NMRK1 has a mutation status of E42D, The gene VPS13A has a mutation status of P974P, The gene SPATA31D1 has a mutation status of D183N, The gene SPATA31D1 has a mutation status of S258S, The gene IARS1 has a mutation status of P437L, The gene WNK2 has a mutation status of P972L, The gene WNK2 has a mutation status of P1892P, The gene NUTM2F has a mutation status of R242Q, The gene FBP2 has a mutation status of T106T, The gene HSD17B3 has a mutation status of D111D, The gene ZNF510 has a mutation status of E59D, The gene ZNF462 has a mutation status of E481K, The gene ABITRAM has a mutation status of A7S, The gene FRRS1L has a mutation status of G99E, The gene FRRS1L has a mutation status of R51A, The gene PTPN3 has a mutation status of S27S, The gene SVEP1 has a mutation status of T523T, The gene SHOC1 has a mutation status of E213K, The gene TLR4 has a mutation status of F768L, The gene OR1N2 has a mutation status of S275I, The gene SLC2A8 has a mutation status of V261I, The gene TOR1A has a mutation status of F306V, The gene FIBCD1 has a mutation status of Q94H, The gene GTF3C5 has a mutation status of Q409K, The gene FCN2 has a mutation status of G117S, The gene NACC2 has a mutation status of A153A, The gene CCDC187 has a mutation status of L747L, The gene GPSM1 has a mutation status of K605M, The gene SEC16A has a mutation status of P165S, The gene CCDC183 has a mutation status of L334R, The gene FBXW5 has a mutation status of S151L, The gene RNF224 has a mutation status of G80G, The gene CACNA1B has a mutation status of A624V, The gene DIP2C has a mutation status of F780F, The gene ADARB2 has a mutation status of K70K, The gene ADARB2 has a mutation status of R28W, The gene FBH1 has a mutation status of D282D, The gene DHTKD1 has a mutation status of G469G, The gene MALRD1 has a mutation status of D1753N, The gene DNAJC1 has a mutation status of P21R, The gene GAD2 has a mutation status of E158*, The gene MASTL has a mutation status of S597F, The gene MPP7 has a mutation status of K105N, The gene ITGB1 has a mutation status of I334F, The gene ZNF33B has a mutation status of H407Y, The gene RASGEF1A has a mutation status of V217M, The gene RBP3 has a mutation status of G498G, The gene WDFY4 has a mutation status of V444V, The gene CSTF2T has a mutation status of P299H, The gene BICC1 has a mutation status of D692N, The gene ZNF365 has a mutation status of N390fs, The gene HERC4 has a mutation status of I407F, The gene DNA2 has a mutation status of D898E, The gene DDX50 has a mutation status of D543Y, The gene PALD1 has a mutation status of V509M, The gene TBATA has a mutation status of I326T, The gene TBATA has a mutation status of L224F, The gene KAT6B has a mutation status of E1240K, The gene POLR3A has a mutation status of I1117fs, The gene POLR3A has a mutation status of Y550C, The gene WAPL has a mutation status of G340R, The gene KIF20B has a mutation status of I1749V, The gene TNKS2 has a mutation status of D72D, The gene CC2D2B has a mutation status of K254N, The gene LCOR has a mutation status of N402Y, The gene HPSE2 has a mutation status of R308R, The gene PKD2L1 has a mutation status of V548I, The gene PPRC1 has a mutation status of T1148T, The gene SLK has a mutation status of Q670R, The gene SORCS1 has a mutation status of R696M, The gene NRAP has a mutation status of H1246Q, The gene ADRB1 has a mutation status of F191F, The gene DMBT1 has a mutation status of C537W, The gene FAM24A has a mutation status of I11V, The gene EDRF1 has a mutation status of S231S, The gene TCERG1L has a mutation status of P19P, The gene ADGRA1 has a mutation status of A166A, The gene PHRF1 has a mutation status of S730S, The gene MUC5AC has a mutation status of C3226*, The gene TSPAN32 has a mutation status of D320D, The gene UBQLN3 has a mutation status of A268T, The gene OR52B6 has a mutation status of L295I, The gene TRIM6 has a mutation status of P299T, The gene CCKBR has a mutation status of R215H, The gene AKIP1 has a mutation status of A113E, The gene NCR3LG1 has a mutation status of L277I, The gene PTPN5 has a mutation status of V210I, The gene CSRP3 has a mutation status of K152K, The gene SLC5A12 has a mutation status of S49S, The gene FSHB has a mutation status of I26I, The gene EXT2 has a mutation status of T89M, The gene PHF21A has a mutation status of E81E, The gene LRP4 has a mutation status of A971S, The gene CELF1 has a mutation status of A229S, The gene MTCH2 has a mutation status of H119Y, The gene OR4A16 has a mutation status of N170N, The gene OR4C6 has a mutation status of C140G, The gene OR5L1 has a mutation status of S18L, The gene OR8K5 has a mutation status of R20L, The gene OR5R1 has a mutation status of D191Y, The gene OR9G1 has a mutation status of I196F, The gene ZDHHC5 has a mutation status of S673F, The gene OR9I1 has a mutation status of L312P, The gene OR5B2 has a mutation status of M134K, The gene OR4D10 has a mutation status of C240*, The gene OR4D11 has a mutation status of C189F, The gene MS4A8 has a mutation status of N56T, The gene MS4A18 has a mutation status of G72D, The gene FADS3 has a mutation status of C55C, The gene RAB3IL1 has a mutation status of E44K, The gene SLC22A25 has a mutation status of M21I, The gene SART1 has a mutation status of K414N, The gene RAB1B has a mutation status of I61I, The gene TBC1D10C has a mutation status of A99T, The gene AIP has a mutation status of Q315P, The gene LRP5 has a mutation status of P1434P, The gene TESMIN has a mutation status of K410N, The gene NADSYN1 has a mutation status of D670D, The gene ARHGEF17 has a mutation status of R93S, The gene C2CD3 has a mutation status of LRY1437del, The gene TPBGL has a mutation status of A143T, The gene RAB30 has a mutation status of S112R, The gene CCDC83 has a mutation status of Q201Q, The gene FAT3 has a mutation status of L39L, The gene FAT3 has a mutation status of L648L, The gene FAT3 has a mutation status of D2112Y, The gene JRKL has a mutation status of E85V, The gene BIRC3 has a mutation status of L174R, The gene MMP3 has a mutation status of G188G, The gene DYNC2H1 has a mutation status of Q630R, The gene NPAT has a mutation status of A1332G, The gene ATM has a mutation status of G509A, The gene C11orf87 has a mutation status of L115L, The gene DIXDC1 has a mutation status of Q72L, The gene ZBTB16 has a mutation status of R566H, The gene NNMT has a mutation status of V83L, The gene CEP164 has a mutation status of Q1135K, The gene GRIK4 has a mutation status of A48A, The gene TECTA has a mutation status of T1354I, The gene OR8B4 has a mutation status of S18L, The gene TBRG1 has a mutation status of L366F, The gene CDON has a mutation status of T1078T, The gene KIRREL3 has a mutation status of Q57K, The gene B4GALNT3 has a mutation status of K842Q, The gene CACNA1C has a mutation status of V203V, The gene CACNA1C has a mutation status of H322H, The gene DYRK4 has a mutation status of L193F, The gene NDUFA9 has a mutation status of W108L, The gene GALNT8 has a mutation status of L614L, The gene KCNA5 has a mutation status of I260I, The gene VWF has a mutation status of G142S, The gene TNFRSF1A has a mutation status of F374F, The gene CHD4 has a mutation status of A935S, The gene USP5 has a mutation status of E438E, The gene C1S has a mutation status of P28L, The gene C1S has a mutation status of V160L, The gene CD163L1 has a mutation status of S1284Y, The gene FOXJ2 has a mutation status of P310S, The gene PLEKHA5 has a mutation status of A488A, The gene SLCO1B1 has a mutation status of N151S, The gene SLCO1A2 has a mutation status of G447E, The gene ABCC9 has a mutation status of Q802K, The gene ETNK1 has a mutation status of V67M, The gene ALG10B has a mutation status of N189S, The gene CACNB3 has a mutation status of Q438fs, The gene FAM186A has a mutation status of N1292T, The gene KRT7 has a mutation status of V24V, The gene KRT85 has a mutation status of R16S, The gene KRT2 has a mutation status of R45C, The gene IGFBP6 has a mutation status of P106L, The gene HOXC11 has a mutation status of P130T, The gene NFE2 has a mutation status of ELER297del, The gene OR9K2 has a mutation status of R294R, The gene GDF11 has a mutation status of Y135D, The gene MMP19 has a mutation status of H156Q, The gene STAT2 has a mutation status of R300C, The gene LRP1 has a mutation status of E153E, The gene INHBE has a mutation status of H214R, The gene KIF5A has a mutation status of R26R, The gene KIF5A has a mutation status of Y936*, The gene SLC16A7 has a mutation status of F172Y, The gene TBC1D30 has a mutation status of Q149*, The gene MYRFL has a mutation status of N403D, The gene OTOGL has a mutation status of I1648T, The gene LRRIQ1 has a mutation status of Q260H, The gene C12orf29 has a mutation status of D258N, The gene ANKS1B has a mutation status of D837E, The gene ANKS1B has a mutation status of S35Y, The gene UHRF1BP1L has a mutation status of S342A, The gene UTP20 has a mutation status of F732L, The gene MYBPC1 has a mutation status of I769T, The gene PARPBP has a mutation status of Q131K, The gene PAH has a mutation status of F397C, The gene NUAK1 has a mutation status of L181L, The gene MAPKAPK5 has a mutation status of I273M, The gene HECTD4 has a mutation status of T3541T, The gene HECTD4 has a mutation status of S763F, The gene OAS2 has a mutation status of L311P, The gene DDX54 has a mutation status of R86H, The gene RBM19 has a mutation status of P434L, The gene TBX5 has a mutation status of P465L, The gene WSB2 has a mutation status of L406L, The gene GCN1 has a mutation status of A1525V, The gene MORN3 has a mutation status of R166S, The gene HIP1R has a mutation status of E308A, The gene ABCB9 has a mutation status of Y409S, The gene DNAH10 has a mutation status of E179K, The gene DNAH10 has a mutation status of G4306E, The gene TMEM132C has a mutation status of L788L, The gene RIMBP2 has a mutation status of A275V, The gene EP400 has a mutation status of A2577A, The gene NOC4L has a mutation status of L493V, The gene ANHX has a mutation status of P131P, The gene XPO4 has a mutation status of D271N, The gene MTMR6 has a mutation status of G350D, The gene RNF6 has a mutation status of V373L, The gene MTUS2 has a mutation status of Q51K, The gene FRY has a mutation status of V341M, The gene N4BP2L2 has a mutation status of D592D, The gene ZC3H13 has a mutation status of H647Q, The gene CPB2 has a mutation status of S5I, The gene RUBCNL has a mutation status of L496I, The gene CKAP2 has a mutation status of T578S, The gene KLHL1 has a mutation status of G94G, The gene DACH1 has a mutation status of R650Q, The gene FBXL3 has a mutation status of V412V, The gene EDNRB has a mutation status of E117E, The gene POU4F1 has a mutation status of R57R, The gene RBM26 has a mutation status of R555R, The gene DOCK9 has a mutation status of K1430K, The gene DOCK9 has a mutation status of L1200L, The gene CCDC168 has a mutation status of A5113T, The gene CCDC168 has a mutation status of L4120L, The gene LIG4 has a mutation status of *912S, The gene IRS2 has a mutation status of S491S, The gene COL4A1 has a mutation status of Q523H, The gene COL4A2 has a mutation status of C483F, The gene PROZ has a mutation status of T316M, The gene UPF3A has a mutation status of E234*, The gene TEP1 has a mutation status of L2252F, The gene PRMT5 has a mutation status of E177E, The gene SLC22A17 has a mutation status of H620H, The gene ADCY4 has a mutation status of M244I, The gene TTC6 has a mutation status of A69E, The gene TTC6 has a mutation status of S607S, The gene TOGARAM1 has a mutation status of D35G, The gene FANCM has a mutation status of L1759V, The gene MDGA2 has a mutation status of C630S, The gene KTN1 has a mutation status of S1171S, The gene RTN1 has a mutation status of P538H, The gene SNAPC1 has a mutation status of A13A, The gene HSPA2 has a mutation status of D369D, The gene ACTN1 has a mutation status of R291H, The gene PCNX1 has a mutation status of K520fs, The gene DNAL1 has a mutation status of V148L, The gene MIDEAS has a mutation status of P108P, The gene ABCD4 has a mutation status of A7T, The gene TTLL5 has a mutation status of Q1172K, The gene NRXN3 has a mutation status of Y1515Y, The gene SERPINA11 has a mutation status of L276L, The gene ATG2B has a mutation status of N1089S, The gene AK7 has a mutation status of T81T, The gene PPP2R5C has a mutation status of E124K, The gene CDC42BPB has a mutation status of S1683C, The gene INF2 has a mutation status of P1122H, The gene POTEB3 has a mutation status of R450G, The gene GOLGA6L22 has a mutation status of *811Q, The gene CYFIP1 has a mutation status of S619S, The gene CYFIP1 has a mutation status of Y234Y, The gene GOLGA8S has a mutation status of I439V, The gene PGBD4 has a mutation status of S511Y, The gene INO80 has a mutation status of L1518S, The gene RPAP1 has a mutation status of L59L, The gene SPTBN5 has a mutation status of P3286P, The gene CDAN1 has a mutation status of R544L, The gene SERF2 has a mutation status of P127S, The gene WDR76 has a mutation status of R509W, The gene CTDSPL2 has a mutation status of V315V, The gene DUOX2 has a mutation status of W191*, The gene TRPM7 has a mutation status of H1171Y, The gene UNC13C has a mutation status of R2147R, The gene VPS13C has a mutation status of F3218V, The gene TRIP4 has a mutation status of S140R, The gene ANKDD1A has a mutation status of L516L, The gene THSD4 has a mutation status of C428C, The gene HCN4 has a mutation status of W295S, The gene CYP1A1 has a mutation status of T54T, The gene GOLGA6L10 has a mutation status of M402L, The gene GOLGA6L9 has a mutation status of Q151E, The gene AC245033.1 has a mutation status of S142S, The gene FSD2 has a mutation status of R543Q, The gene ADAMTSL3 has a mutation status of S1162W, The gene MAN2A2 has a mutation status of T79K, The gene HBQ1 has a mutation status of E31K, The gene WDR24 has a mutation status of A93T, The gene UNKL has a mutation status of D346V, The gene HS3ST6 has a mutation status of D255N, The gene HS3ST6 has a mutation status of A36V, The gene E4F1 has a mutation status of E71K, The gene E4F1 has a mutation status of D130N, The gene RNPS1 has a mutation status of M189I, The gene MEFV has a mutation status of L348L, The gene SLX4 has a mutation status of R1826Q, The gene ADCY9 has a mutation status of R972W, The gene DNAJA3 has a mutation status of V14V, The gene ABAT has a mutation status of Q279R, The gene TVP23A has a mutation status of E209K, The gene ERCC4 has a mutation status of Q226H, The gene ABCC6 has a mutation status of A1128V, The gene ABCC6 has a mutation status of M848fs, The gene SMG1 has a mutation status of A3251P, The gene EEF2K has a mutation status of H411Y, The gene ERN2 has a mutation status of G58G, The gene AQP8 has a mutation status of A81S, The gene HS3ST4 has a mutation status of P115S, The gene SBK1 has a mutation status of G7E, The gene APOBR has a mutation status of A858V, The gene HIRIP3 has a mutation status of E486Q, The gene INO80E has a mutation status of L150L, The gene ZNF688 has a mutation status of L8L, The gene PRR14 has a mutation status of A540T, The gene RNF40 has a mutation status of P503L, The gene ZNF646 has a mutation status of R1095C, The gene ARMC5 has a mutation status of R68R, The gene ARMC5 has a mutation status of S639S, The gene LONP2 has a mutation status of D342E, The gene ZNF423 has a mutation status of T382K, The gene ADCY7 has a mutation status of G934S, The gene SALL1 has a mutation status of P317R, The gene TERB1 has a mutation status of Q352*, The gene ELMO3 has a mutation status of L556L, The gene SLC9A5 has a mutation status of Q445K, The gene PLA2G15 has a mutation status of M1L, The gene PRMT7 has a mutation status of A596A, The gene CDH1 has a mutation status of F39L, The gene CDH1 has a mutation status of T40K, The gene WWP2 has a mutation status of G344A, The gene SF3B3 has a mutation status of T1100T, The gene GLG1 has a mutation status of S527S, The gene ATMIN has a mutation status of V521I, The gene ANKRD11 has a mutation status of Q1176K, The gene ANKRD11 has a mutation status of C1130*, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene OR1G1 has a mutation status of V124M, The gene CYB5D2 has a mutation status of A90A, The gene ANKFY1 has a mutation status of S206R, The gene MYBBP1A has a mutation status of Q950Q, The gene ALOX15 has a mutation status of Y15H, The gene SLC52A1 has a mutation status of P42L, The gene ZNF232 has a mutation status of T251N, The gene ZNF594 has a mutation status of E116V, The gene TP53 has a mutation status of R248Q, The gene ARHGEF15 has a mutation status of P24P, The gene MFSD6L has a mutation status of G216G, The gene USP43 has a mutation status of L344R, The gene MYH13 has a mutation status of A1364A, The gene MYH13 has a mutation status of H1342H, The gene MYH13 has a mutation status of A1205A, The gene MYH8 has a mutation status of K1531E, The gene MYH1 has a mutation status of E1477E, The gene MYH1 has a mutation status of R1283H, The gene MYH1 has a mutation status of L891S, The gene HS3ST3A1 has a mutation status of F390F, The gene MPRIP has a mutation status of Q1020L, The gene SREBF1 has a mutation status of R39G, The gene MYO15A has a mutation status of V21V, The gene B9D1 has a mutation status of R160C, The gene SLC47A2 has a mutation status of L382L, The gene NOS2 has a mutation status of P706T, The gene SARM1 has a mutation status of L514L, The gene PIPOX has a mutation status of L259L, The gene MYO18A has a mutation status of N1746N, The gene TMEM132E has a mutation status of P136P, The gene UNC45B has a mutation status of A557A, The gene SLFN14 has a mutation status of P526S, The gene AP2B1 has a mutation status of M448I, The gene CCL4L2 has a mutation status of P67R, The gene DUSP14 has a mutation status of V184I, The gene PCGF2 has a mutation status of A253A, The gene MSL1 has a mutation status of H410H, The gene RAPGEFL1 has a mutation status of L77P, The gene KRT10 has a mutation status of 561_562insGYGGGSSSGG, The gene KRTAP3-1 has a mutation status of R27C, The gene KRTAP9-8 has a mutation status of C76C, The gene KRT16 has a mutation status of A199V, The gene PSMC3IP has a mutation status of E200K, The gene HROB has a mutation status of T533M, The gene UBTF has a mutation status of D740Y, The gene WNT9B has a mutation status of R258H, The gene LRRC46 has a mutation status of C278S, The gene EPN3 has a mutation status of P619P, The gene MPO has a mutation status of F222F, The gene PPM1E has a mutation status of C157C, The gene BCAS3 has a mutation status of P519S, The gene CEP95 has a mutation status of S116N, The gene PRKCA has a mutation status of T54T, The gene KCNJ16 has a mutation status of E354Q, The gene CDC42EP4 has a mutation status of S292I, The gene CD300LF has a mutation status of G214R, The gene ITGB4 has a mutation status of K703R, The gene MRPL38 has a mutation status of W6C, The gene DNAH17 has a mutation status of N274S, The gene CBX2 has a mutation status of S459N, The gene CCDC40 has a mutation status of G48S, The gene RNF213 has a mutation status of D2603E, The gene P4HB has a mutation status of A13S, The gene CCDC57 has a mutation status of A236A, The gene CETN1 has a mutation status of G119G, The gene TYMS has a mutation status of S195I, The gene LAMA1 has a mutation status of L533fs, The gene PIEZO2 has a mutation status of G1695R, The gene MPPE1 has a mutation status of M166I, The gene ROCK1 has a mutation status of A1109G, The gene CELF4 has a mutation status of H213L, The gene SIGLEC15 has a mutation status of L11W, The gene SKOR2 has a mutation status of L102L, The gene ZBTB7C has a mutation status of DEEEE153del, The gene CXXC1 has a mutation status of G565R, The gene STARD6 has a mutation status of R86S, The gene TNFRSF11A has a mutation status of C169R, The gene PHLPP1 has a mutation status of S279W, The gene NETO1 has a mutation status of E144Q, The gene ZNF407 has a mutation status of H611Q, The gene ZNF516 has a mutation status of K1005K, The gene ZNF516 has a mutation status of A554G, The gene ZNF236 has a mutation status of A1381A, The gene PLPPR3 has a mutation status of E487K, The gene MED16 has a mutation status of A83T, The gene GRIN3B has a mutation status of P138L, The gene GRIN3B has a mutation status of R932G, The gene MEX3D has a mutation status of A55A, The gene MEX3D has a mutation status of A55S, The gene KLF16 has a mutation status of P116P, The gene KLF16 has a mutation status of S2L, The gene SPPL2B has a mutation status of S591L, The gene S1PR4 has a mutation status of A189S, The gene ZBTB7A has a mutation status of R483*, The gene ZBTB7A has a mutation status of D452D, The gene STAP2 has a mutation status of T198A, The gene INSR has a mutation status of N1060N, The gene CAMSAP3 has a mutation status of D992D, The gene XAB2 has a mutation status of V615M, The gene RETN has a mutation status of C74W, The gene FBN3 has a mutation status of V204M, The gene PRAM1 has a mutation status of C658Y, The gene MYO1F has a mutation status of P995S, The gene MUC16 has a mutation status of T9716T, The gene S1PR2 has a mutation status of T320I, The gene S1PR2 has a mutation status of D294D, The gene RAVER1 has a mutation status of P620P, The gene S1PR5 has a mutation status of G172G, The gene TMEM205 has a mutation status of G8A, The gene ZNF440 has a mutation status of E169A, The gene WDR83 has a mutation status of R32Q, The gene HOOK2 has a mutation status of P22P, The gene MAST1 has a mutation status of A84A, The gene CACNA1A has a mutation status of H2255N, The gene ILVBL has a mutation status of Q165*, The gene NOTCH3 has a mutation status of R1893*, The gene NOTCH3 has a mutation status of T909T, The gene CYP4F22 has a mutation status of L197F, The gene EPS15L1 has a mutation status of P240P, The gene MYO9B has a mutation status of E1943K, The gene INSL3 has a mutation status of C123fs, The gene GDF1 has a mutation status of A255S, The gene NCAN has a mutation status of A52A, The gene NCAN has a mutation status of A936A, The gene ZNF729 has a mutation status of M1036I, The gene ZNF729 has a mutation status of H1182R, The gene ZNF99 has a mutation status of F213F, The gene ZNF91 has a mutation status of T485S, The gene IGFLR1 has a mutation status of P163L, The gene CLIP3 has a mutation status of N163N, The gene ZNF527 has a mutation status of Q11H, The gene CATSPERG has a mutation status of Q610H, The gene SPRED3 has a mutation status of V238V, The gene RYR1 has a mutation status of E1878V, The gene RYR1 has a mutation status of I2263I, The gene ZNF546 has a mutation status of T265I, The gene CYP2B6 has a mutation status of A464T, The gene CEACAM4 has a mutation status of R98*, The gene ARHGEF1 has a mutation status of S776S, The gene ATP1A3 has a mutation status of K81M, The gene CIC has a mutation status of A1923V, The gene MEGF8 has a mutation status of V1795V, The gene ZNF404 has a mutation status of H433N, The gene ZNF284 has a mutation status of C205Y, The gene ZNF224 has a mutation status of C206F, The gene ZNF224 has a mutation status of H506D, The gene PPP1R37 has a mutation status of S586A, The gene MARK4 has a mutation status of R377R, The gene OPA3 has a mutation status of A81T, The gene EML2 has a mutation status of V30A, The gene RSPH6A has a mutation status of M271R, The gene GRIN2D has a mutation status of A1076A, The gene GRIN2D has a mutation status of P1095P, The gene NTN5 has a mutation status of G284R, The gene PRR12 has a mutation status of P1003L, The gene LRRC4B has a mutation status of E616K, The gene SIGLEC9 has a mutation status of S437G, The gene SIGLEC7 has a mutation status of I372L, The gene SIGLEC8 has a mutation status of G288D, The gene HAS1 has a mutation status of H397Q, The gene ZNF610 has a mutation status of V92V, The gene ZNF665 has a mutation status of R330H, The gene ZNF665 has a mutation status of P289L, The gene ZNF761 has a mutation status of K613N, The gene VSTM1 has a mutation status of S195T, The gene OSCAR has a mutation status of A59E, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of Y121Y, The gene LILRA6 has a mutation status of I88M, The gene LENG9 has a mutation status of P423T, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene KIR3DL2 has a mutation status of L359L, The gene DNAAF3 has a mutation status of G491R, The gene UBE2S has a mutation status of E75Q, The gene SBK3 has a mutation status of D273Y, The gene U2AF2 has a mutation status of L278L, The gene NLRP13 has a mutation status of E669K, The gene ZSCAN5B has a mutation status of M412T, The gene ZNF835 has a mutation status of C115C, The gene ZNF805 has a mutation status of G497C, The gene ZNF837 has a mutation status of L70L, The gene SLC27A5 has a mutation status of R164C, The gene TRIB3 has a mutation status of D343D, The gene RSPO4 has a mutation status of L10L, The gene C20orf194 has a mutation status of R31Q, The gene BMP2 has a mutation status of T128T, The gene PLCB1 has a mutation status of T869I, The gene TASP1 has a mutation status of V406V, The gene FLRT3 has a mutation status of S600S, The gene KAT14 has a mutation status of D634D, The gene XRN2 has a mutation status of I208T, The gene ACSS1 has a mutation status of T363N, The gene VSX1 has a mutation status of V199L, The gene VSX1 has a mutation status of F31F, The gene REM1 has a mutation status of R82C, The gene FOXS1 has a mutation status of P292A, The gene EFCAB8 has a mutation status of E345K, The gene BPIFB1 has a mutation status of F388L, The gene KIAA1755 has a mutation status of E151D, The gene KCNK15 has a mutation status of F223F, The gene EYA2 has a mutation status of T393T, The gene ZMYND8 has a mutation status of Q844fs, The gene PREX1 has a mutation status of E1135D, The gene KCNB1 has a mutation status of I544F, The gene SPO11 has a mutation status of V163A, The gene APCDD1L has a mutation status of L221V, The gene PHACTR3 has a mutation status of E432K, The gene TAF4 has a mutation status of G177fs, The gene TAF4 has a mutation status of G175A, The gene LAMA5 has a mutation status of G275A, The gene DIDO1 has a mutation status of P1918L, The gene CHODL has a mutation status of T88S, The gene LTN1 has a mutation status of S532K, The gene LTN1 has a mutation status of S531K, The gene KRTAP19-5 has a mutation status of Y44*, The gene ITGB2 has a mutation status of D226D, The gene SPATC1L has a mutation status of P135S, The gene TBX1 has a mutation status of S32*, The gene ZNF280B has a mutation status of C449S, The gene GGTLC2 has a mutation status of A7T, The gene AC253536.7 has a mutation status of Q121K, The gene MYO18B has a mutation status of H1045H, The gene RFPL3 has a mutation status of L122C, The gene TEX33 has a mutation status of G27G, The gene GGA1 has a mutation status of D148N, The gene DDX17 has a mutation status of Q692Q, The gene MGAT3 has a mutation status of G114G, The gene CACNA1I has a mutation status of I811I, The gene ZC3H7B has a mutation status of F585L, The gene POLR3H has a mutation status of H67H, The gene SREBF2 has a mutation status of E658*, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TTLL12 has a mutation status of P261P, The gene PNPLA5 has a mutation status of C60fs, The gene PNPLA3 has a mutation status of L72L, The gene SAMM50 has a mutation status of Q107H, The gene PARVB has a mutation status of R199L, The gene TAFA5 has a mutation status of G43V, The gene BRD1 has a mutation status of I948I, The gene BRD1 has a mutation status of I60fs, The gene PANX2 has a mutation status of P414S, The gene KLHDC7B has a mutation status of T917fs, The gene KLHDC7B has a mutation status of GRG918del, The gene CPT1B has a mutation status of Y202Y, The gene ACR has a mutation status of T24M, The gene CRLF2 has a mutation status of P308P, The gene ARSH has a mutation status of I485I, The gene ARSH has a mutation status of A492V, The gene SHROOM2 has a mutation status of I56V, The gene TLR7 has a mutation status of F96F, The gene CTPS2 has a mutation status of R103C, The gene PPEF1 has a mutation status of V98E, The gene CNKSR2 has a mutation status of L65L, The gene POLA1 has a mutation status of Q719H, The gene CFAP47 has a mutation status of I74I, The gene MAOB has a mutation status of PFWR304del, The gene FOXP3 has a mutation status of 64_65MP>IT, The gene TEX11 has a mutation status of E887K, The gene SLC16A2 has a mutation status of D523H, The gene NEXMIF has a mutation status of P87P, The gene POU3F4 has a mutation status of I94M, The gene BTK has a mutation status of G302R, The gene GPRASP1 has a mutation status of L1325L, The gene ARMCX5-GPRASP2 has a mutation status of I289F, The gene GLRA4 has a mutation status of R370C, The gene NRK has a mutation status of P118T, The gene ALG13 has a mutation status of S772N, The gene IL13RA2 has a mutation status of P241S, The gene AGTR2 has a mutation status of L86L, The gene KLHL13 has a mutation status of V458V, The gene NKAP has a mutation status of R281Q, The gene TENM1 has a mutation status of E1861K, The gene CCDC160 has a mutation status of S27Y, The gene ZNF449 has a mutation status of G419E, The gene BRS3 has a mutation status of P372P, The gene ATP11C has a mutation status of H30Y, The gene SLITRK4 has a mutation status of H297Y, The gene SLITRK2 has a mutation status of N799I, The gene CNGA2 has a mutation status of P433S, The gene MAGEA4 has a mutation status of G189S, The gene PNMA3 has a mutation status of A365E, The gene FAM50A has a mutation status of A58fs, The gene GAB3 has a mutation status of R77R, The gene F8 has a mutation status of E739E, The gene MT-ND1 has a mutation status of G29S, The gene MT-CO3 has a mutation status of E183E, The gene MT-ND5 has a mutation status of I576I, The gene MT-ND6 has a mutation status of E108D, The gene MT-CYB has a mutation status of A354T
LUAD
The gene PRXL2B has a mutation status of L103V, The gene FBXO44 has a mutation status of E59K, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene KAZN has a mutation status of L26V, The gene SRRM1 has a mutation status of A353A, The gene THEMIS2 has a mutation status of A591A, The gene PPCS has a mutation status of R25P, The gene LRRC8B has a mutation status of A236D, The gene CELF3 has a mutation status of I197I, The gene ASH1L has a mutation status of R2533H, The gene NTRK1 has a mutation status of R119R, The gene ASTN1 has a mutation status of T505R, The gene CEP350 has a mutation status of A2527A, The gene NFASC has a mutation status of G362G, The gene CR1L has a mutation status of R128*, The gene URB2 has a mutation status of R1292H, The gene KIF26B has a mutation status of S160S, The gene PLEKHH2 has a mutation status of L1425V, The gene CNNM3 has a mutation status of R246G, The gene CNNM3 has a mutation status of L249M, The gene RANBP2 has a mutation status of 1054_1055QP>HS, The gene MZT2A has a mutation status of L25G, The gene PDE11A has a mutation status of P364P, The gene COL5A2 has a mutation status of P410S, The gene DNAH7 has a mutation status of P255R, The gene AOX1 has a mutation status of S502F, The gene ABCA12 has a mutation status of L855P, The gene NGEF has a mutation status of L102R, The gene AQP12A has a mutation status of P50P, The gene DLEC1 has a mutation status of T279T, The gene ARIH2OS has a mutation status of A153G, The gene USP19 has a mutation status of R737G, The gene NPHP3 has a mutation status of R1094Q, The gene CLSTN2 has a mutation status of A880A, The gene IQCJ-SCHIP1 has a mutation status of R149L, The gene PPP2R2C has a mutation status of R195C, The gene CCKAR has a mutation status of N304H, The gene RAP1GDS1 has a mutation status of V451L, The gene PRDM5 has a mutation status of G258V, The gene MAML3 has a mutation status of R747Q, The gene MAP9 has a mutation status of T343A, The gene CTSO has a mutation status of L241L, The gene IRX1 has a mutation status of G304G, The gene FBXL7 has a mutation status of R198L, The gene LIFR has a mutation status of R10*, The gene F2RL1 has a mutation status of S5T, The gene SLCO4C1 has a mutation status of A373S, The gene SEPTIN8 has a mutation status of V272M, The gene SHROOM1 has a mutation status of Q455K, The gene PCDHB3 has a mutation status of S442S, The gene STK10 has a mutation status of E550K, The gene ZNF354B has a mutation status of S479S, The gene TUBB2A has a mutation status of I4I, The gene SRPK1 has a mutation status of G50*, The gene SRPK1 has a mutation status of E47V, The gene AARS2 has a mutation status of V59G, The gene PKHD1 has a mutation status of R3914*, The gene EPB41L2 has a mutation status of Q393R, The gene AHI1 has a mutation status of A191A, The gene TNRC18 has a mutation status of R302R, The gene GARS1 has a mutation status of S227F, The gene GNAI1 has a mutation status of Q106P, The gene LMTK2 has a mutation status of R1101P, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of S455S, The gene MUC3A has a mutation status of V456V, The gene MUC3A has a mutation status of S2495L, The gene KLF14 has a mutation status of A39A, The gene ESYT2 has a mutation status of G198R, The gene REEP4 has a mutation status of I107V, The gene UNC5D has a mutation status of D205D, The gene PI15 has a mutation status of M67I, The gene GDF6 has a mutation status of I373I, The gene VPS13B has a mutation status of T1698I, The gene MROH1 has a mutation status of D521N, The gene CBWD6 has a mutation status of D159N, The gene TMOD1 has a mutation status of R144C, The gene C5 has a mutation status of F1574L, The gene GAPVD1 has a mutation status of G1062S, The gene SLC2A8 has a mutation status of S351S, The gene PBLD has a mutation status of G270R, The gene OIT3 has a mutation status of P71P, The gene LDB3 has a mutation status of P260P, The gene MTG1 has a mutation status of P334S, The gene MUC5AC has a mutation status of A497V, The gene MUC5AC has a mutation status of A5353K, The gene OR9G1 has a mutation status of T62V, The gene ARHGEF17 has a mutation status of A225A, The gene KDM4D has a mutation status of D499E, The gene DYNC2H1 has a mutation status of D921E, The gene DYNC2H1 has a mutation status of Q2699K, The gene RECQL has a mutation status of E71K, The gene KRAS has a mutation status of Q61R, The gene YARS2 has a mutation status of T270T, The gene KMT2D has a mutation status of G740G, The gene CALCOCO1 has a mutation status of Q201Q, The gene ARHGEF25 has a mutation status of S45L, The gene CCT2 has a mutation status of T103T, The gene TMTC2 has a mutation status of R139G, The gene NCOR2 has a mutation status of S647L, The gene TMEM132D has a mutation status of A161T, The gene RTRAF has a mutation status of D232Y, The gene FOXN3 has a mutation status of H209H, The gene ADSS1 has a mutation status of I291T, The gene JAG2 has a mutation status of D701H, The gene HERC2 has a mutation status of S895A, The gene FMN1 has a mutation status of G384E, The gene DNAJC17 has a mutation status of T170T, The gene TYRO3 has a mutation status of V233fs, The gene TGM7 has a mutation status of R439H, The gene TGM7 has a mutation status of A306K, The gene DENND4A has a mutation status of K1838Q, The gene BTBD1 has a mutation status of L45L, The gene BNC1 has a mutation status of D264E, The gene ZNF213 has a mutation status of A145A, The gene CLEC16A has a mutation status of P656P, The gene USP31 has a mutation status of G442R, The gene USB1 has a mutation status of M1V, The gene VAT1L has a mutation status of K217M, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene CTNS has a mutation status of D324N, The gene MYBBP1A has a mutation status of L601L, The gene TP53 has a mutation status of R273C, The gene MYH1 has a mutation status of S550F, The gene COX10 has a mutation status of H418P, The gene RAD51D has a mutation status of I105M, The gene CCL4L2 has a mutation status of P67R, The gene COL1A1 has a mutation status of A1075T, The gene MRPS23 has a mutation status of A56T, The gene BCAS3 has a mutation status of Q534Q, The gene ABCA8 has a mutation status of A479G, The gene SDK2 has a mutation status of R941H, The gene LLGL2 has a mutation status of R854C, The gene RNF213 has a mutation status of Q4846E, The gene SECTM1 has a mutation status of R69C, The gene TCF3 has a mutation status of E272K, The gene ZNF317 has a mutation status of L402L, The gene SMARCA4 has a mutation status of T910M, The gene DDX49 has a mutation status of D133N, The gene CILP2 has a mutation status of G959G, The gene ZNF536 has a mutation status of A1095T, The gene CD22 has a mutation status of D531D, The gene PLEKHG2 has a mutation status of H859L, The gene EID2 has a mutation status of S127S, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene NECTIN2 has a mutation status of F245F, The gene KLK6 has a mutation status of R165H, The gene ZNF160 has a mutation status of K703R, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene ZNF580 has a mutation status of S113S, The gene NLRP4 has a mutation status of A491T, The gene CPXM1 has a mutation status of L592L, The gene KAT14 has a mutation status of P740P, The gene HRH3 has a mutation status of P210L, The gene LAMA5 has a mutation status of H1084P, The gene TPTE has a mutation status of T163A, The gene TRPM2 has a mutation status of S146F, The gene PI4KA has a mutation status of S1511L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SCUBE1 has a mutation status of R535H, The gene SMC1B has a mutation status of Q601K, The gene PLXNB2 has a mutation status of T636P, The gene SPANXN5 has a mutation status of L67L, The gene RAB39B has a mutation status of E137K, The gene MT-CO1 has a mutation status of A32A, The gene MT-ATP6 has a mutation status of S182A, The gene MT-ND4 has a mutation status of F50L, The gene MT-ND4 has a mutation status of L84L, The gene MT-ND4 has a mutation status of A191A, The gene MT-CYB has a mutation status of C40C, The gene MT-CYB has a mutation status of M316T
PAAD
The gene PLCH2 has a mutation status of M55T, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene MACO1 has a mutation status of S573S, The gene COL9A2 has a mutation status of D52E, The gene PPCS has a mutation status of R25P, The gene SZT2 has a mutation status of D929G, The gene FOXD2 has a mutation status of L371P, The gene CPT2 has a mutation status of E81V, The gene PPIAL4H has a mutation status of N102I, The gene ZNF687 has a mutation status of L1142F, The gene F5 has a mutation status of R534Q, The gene KIF14 has a mutation status of R752I, The gene YOD1 has a mutation status of S226P, The gene PLXNA2 has a mutation status of C826G, The gene USH2A has a mutation status of V2794D, The gene ATP6V1B1 has a mutation status of I263I, The gene TEX37 has a mutation status of M76K, The gene PROM2 has a mutation status of R151C, The gene IL1RL1 has a mutation status of V89F, The gene THSD7B has a mutation status of S79C, The gene TTN has a mutation status of P17015P, The gene PTPRN has a mutation status of A585V, The gene DOCK10 has a mutation status of Q1396H, The gene TAMM41 has a mutation status of Y320D, The gene CELSR3 has a mutation status of S120G, The gene ARIH2OS has a mutation status of A153G, The gene RASSF1 has a mutation status of C82S, The gene DOCK3 has a mutation status of R1678H, The gene LRTM1 has a mutation status of H261P, The gene ZNF717 has a mutation status of R471I, The gene QTRT2 has a mutation status of C157Y, The gene PLXNA1 has a mutation status of V1753M, The gene PIK3CB has a mutation status of F508F, The gene SLITRK3 has a mutation status of A819A, The gene SLITRK3 has a mutation status of Q796R, The gene ZNF639 has a mutation status of A72G, The gene TMEM129 has a mutation status of A140A, The gene IRX4 has a mutation status of T144T, The gene ARL15 has a mutation status of R90W, The gene HTR1A has a mutation status of T13S, The gene SLC30A5 has a mutation status of H567H, The gene LMNB1 has a mutation status of S288R, The gene LARS1 has a mutation status of R836C, The gene H2BC5 has a mutation status of A98A, The gene H1-5 has a mutation status of T11I, The gene GTF2H4 has a mutation status of E419K, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Y42H, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene TRERF1 has a mutation status of G27G, The gene COL12A1 has a mutation status of T2618M, The gene CNR1 has a mutation status of H154H, The gene VPS41 has a mutation status of N715K, The gene POM121L12 has a mutation status of A3S, The gene PCLO has a mutation status of R3420Q, The gene AZGP1 has a mutation status of S264S, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S1242N, The gene MUC3A has a mutation status of S1250T, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene GPR37 has a mutation status of E74K, The gene KEL has a mutation status of A160A, The gene CNTNAP2 has a mutation status of S586R, The gene SHH has a mutation status of A162T, The gene MYOM2 has a mutation status of T274M, The gene ADAM28 has a mutation status of G321G, The gene EBF2 has a mutation status of S28T, The gene LRRC6 has a mutation status of E117E, The gene VLDLR has a mutation status of K548R, The gene ANKRD18B has a mutation status of C116F, The gene PRSS3 has a mutation status of R122H, The gene FRMPD1 has a mutation status of A1313P, The gene TUT7 has a mutation status of G59G, The gene OR1N2 has a mutation status of Y181C, The gene JMJD1C has a mutation status of Q2018Q, The gene SORCS1 has a mutation status of A842T, The gene LRRC27 has a mutation status of H146R, The gene SIRT3 has a mutation status of V28G, The gene SIGIRR has a mutation status of S392S, The gene CDHR5 has a mutation status of V363M, The gene PGAP2 has a mutation status of I38I, The gene EIF4G2 has a mutation status of A647A, The gene BBOX1 has a mutation status of C3F, The gene OR9G1 has a mutation status of I196F, The gene MS4A12 has a mutation status of Y131Y, The gene USP35 has a mutation status of G839G, The gene KDM4D has a mutation status of D499E, The gene GUCY1A2 has a mutation status of H241H, The gene PCSK7 has a mutation status of H219Q, The gene OR8D1 has a mutation status of F251F, The gene OR8D2 has a mutation status of Y177*, The gene KLHL42 has a mutation status of T425P, The gene ANP32D has a mutation status of R12W, The gene EIF4B has a mutation status of Y211C, The gene HOXC12 has a mutation status of P78P, The gene PPFIA2 has a mutation status of C1007W, The gene UTP20 has a mutation status of D2602D, The gene CHST11 has a mutation status of H267H, The gene OASL has a mutation status of K66Q, The gene KDM2B has a mutation status of E522E, The gene DNAH10 has a mutation status of T413M, The gene FREM2 has a mutation status of R1962W, The gene ATP11A has a mutation status of A1021T, The gene TOGARAM1 has a mutation status of A1541S, The gene SLC25A29 has a mutation status of L192L, The gene TDRD9 has a mutation status of R691L, The gene CYP11A1 has a mutation status of M193I, The gene EDC3 has a mutation status of H297R, The gene GTF3C1 has a mutation status of A1404E, The gene SLC5A2 has a mutation status of T308I, The gene CNOT1 has a mutation status of A715T, The gene THAP11 has a mutation status of QQQQQQQQ115del, The gene CDH3 has a mutation status of P154S, The gene ZCCHC14 has a mutation status of G374G, The gene ANKRD11 has a mutation status of A2075V, The gene SLC2A4 has a mutation status of L178V, The gene USP43 has a mutation status of G739R, The gene DNAH9 has a mutation status of Q2169H, The gene NCOR1 has a mutation status of Y2017C, The gene ZNF624 has a mutation status of N271D, The gene MYO15A has a mutation status of E2218K, The gene MYO15A has a mutation status of A244A, The gene CCDC144NL has a mutation status of E61D, The gene KCNJ12 has a mutation status of A382P, The gene CPD has a mutation status of T648T, The gene ATAD5 has a mutation status of I134V, The gene CCL4L2 has a mutation status of P67R, The gene KRT33A has a mutation status of Q76*, The gene CCDC103 has a mutation status of S190R, The gene PPP1R9B has a mutation status of G512S, The gene PECAM1 has a mutation status of A581T, The gene SEH1L has a mutation status of R5P, The gene CDH2 has a mutation status of M256I, The gene FUT6 has a mutation status of S175S, The gene MUC16 has a mutation status of M8698L, The gene RGL3 has a mutation status of E232fs, The gene C19orf44 has a mutation status of V345G, The gene SPACA4 has a mutation status of P15S, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB3 has a mutation status of A4A, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL3 has a mutation status of A304T, The gene KIR2DL1 has a mutation status of G283G, The gene SIRPA has a mutation status of L44S, The gene NANP has a mutation status of T119I, The gene ZNF341 has a mutation status of A623V, The gene KCNB1 has a mutation status of V841I, The gene SPATA2 has a mutation status of S485T, The gene FAM217B has a mutation status of I105L, The gene DSCAM has a mutation status of R1619R, The gene SEZ6L has a mutation status of T88A, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ASMTL has a mutation status of R564S, The gene MSL3 has a mutation status of D75G, The gene PORCN has a mutation status of L45L, The gene TCEAL6 has a mutation status of A50S, The gene BCORL1 has a mutation status of L1132P, The gene HTATSF1 has a mutation status of R340H, The gene RBMX has a mutation status of G121R, The gene NSDHL has a mutation status of E289*
DLBC
The gene TAS1R3 has a mutation status of E45K, The gene ATAD3C has a mutation status of I50N, The gene CDK11A has a mutation status of E107*, The gene PRAMEF13 has a mutation status of R138C, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF15 has a mutation status of C76W, The gene HSPG2 has a mutation status of C879S, The gene TENT5B has a mutation status of H416R, The gene SFPQ has a mutation status of A651A, The gene MAP7D1 has a mutation status of E717E, The gene MFSD2A has a mutation status of I69I, The gene SGIP1 has a mutation status of R8C, The gene NBPF11 has a mutation status of L86L, The gene NBPF14 has a mutation status of E1507D, The gene ASH1L has a mutation status of N744N, The gene KHDC4 has a mutation status of N331H, The gene OR6N2 has a mutation status of P79L, The gene KCNJ9 has a mutation status of E364E, The gene FCGR3A has a mutation status of G40I, The gene RYR2 has a mutation status of E535Q, The gene OR2T33 has a mutation status of S31A, The gene ABCG8 has a mutation status of G485R, The gene ANKRD36C has a mutation status of A501E, The gene EN1 has a mutation status of C171C, The gene ERCC3 has a mutation status of A694T, The gene TMEM163 has a mutation status of V52G, The gene FSIP2 has a mutation status of R740H, The gene RAPH1 has a mutation status of E261Q, The gene ANKZF1 has a mutation status of T469P, The gene OXSM has a mutation status of I345I, The gene NEK10 has a mutation status of V1140V, The gene DLEC1 has a mutation status of S412P, The gene BSN has a mutation status of D688D, The gene MAGI1 has a mutation status of E1385E, The gene POLQ has a mutation status of A2134T, The gene SEMA5B has a mutation status of L549L, The gene ALDH1L1 has a mutation status of D356N, The gene EFCAB12 has a mutation status of S169F, The gene COL6A6 has a mutation status of G1455E, The gene NCEH1 has a mutation status of A74A, The gene EIF4G1 has a mutation status of S1186S, The gene KNG1 has a mutation status of P382L, The gene LRCH3 has a mutation status of A8V, The gene UGT2B17 has a mutation status of E441K, The gene FRAS1 has a mutation status of N822N, The gene GK2 has a mutation status of D259N, The gene EDNRA has a mutation status of S289I, The gene FAT1 has a mutation status of A1880A, The gene ADAMTS12 has a mutation status of H97Y, The gene BRIX1 has a mutation status of G11D, The gene NIPBL has a mutation status of G2637G, The gene FSTL4 has a mutation status of *843C, The gene TMEM14B has a mutation status of 140_141CA>SP, The gene DEK has a mutation status of K221K, The gene H2BC7 has a mutation status of R34R, The gene HLA-DRB1 has a mutation status of S66N, The gene RNF8 has a mutation status of N83N, The gene TMEM63B has a mutation status of N462N, The gene LGSN has a mutation status of Y386Y, The gene DSE has a mutation status of T866A, The gene DSE has a mutation status of K869I, The gene IL22RA2 has a mutation status of Q213R, The gene ESR1 has a mutation status of N101N, The gene TIAM2 has a mutation status of G15G, The gene ARID1B has a mutation status of QQQQQQQ198del, The gene COL28A1 has a mutation status of I47T, The gene GSDME has a mutation status of S23L, The gene ANLN has a mutation status of V1107A, The gene EGFR has a mutation status of ELREA701del, The gene SBDS has a mutation status of I133V, The gene SEMA3A has a mutation status of V435I, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of S3095S, The gene MUC3A has a mutation status of P3166P, The gene LAMB4 has a mutation status of I624V, The gene IFRD1 has a mutation status of T313T, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PLXNA4 has a mutation status of Q1468Q, The gene ZNF746 has a mutation status of T584T, The gene INTS10 has a mutation status of N200K, The gene HGSNAT has a mutation status of L504L, The gene SULF1 has a mutation status of M216I, The gene NBN has a mutation status of L574I, The gene ERICH5 has a mutation status of D51H, The gene ERICH5 has a mutation status of D272H, The gene PKHD1L1 has a mutation status of C1543*, The gene SNTB1 has a mutation status of E336D, The gene KLHL38 has a mutation status of R31R, The gene TG has a mutation status of T332M, The gene KHDRBS3 has a mutation status of E320Q, The gene MROH1 has a mutation status of H375Q, The gene BOP1 has a mutation status of R183C, The gene IFNA17 has a mutation status of G128G, The gene CNTNAP3B has a mutation status of L110F, The gene PGM5 has a mutation status of A290V, The gene ZNF169 has a mutation status of P261L, The gene FRRS1L has a mutation status of R51A, The gene GARNL3 has a mutation status of L415M, The gene AK8 has a mutation status of I10I, The gene DBH has a mutation status of C269C, The gene CCDC187 has a mutation status of L747L, The gene DIPK1B has a mutation status of L123L, The gene NELFB has a mutation status of P169P, The gene TOR4A has a mutation status of A418A, The gene PFKFB3 has a mutation status of P455L, The gene ECHDC3 has a mutation status of A227V, The gene RASGEF1A has a mutation status of G210S, The gene FRMPD2 has a mutation status of S1314F, The gene PCDH15 has a mutation status of L381V, The gene GLUD1 has a mutation status of H278Y, The gene TCTN3 has a mutation status of T333N, The gene FGFR2 has a mutation status of N502N, The gene PKP3 has a mutation status of R261H, The gene MUC5AC has a mutation status of A497V, The gene MUC5AC has a mutation status of V1730I, The gene OR52E8 has a mutation status of A229A, The gene DENND2B has a mutation status of T534T, The gene PIK3C2A has a mutation status of C1524R, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene CD5 has a mutation status of H461C, The gene EML3 has a mutation status of G10C, The gene RSF1 has a mutation status of K1234T, The gene KCTD21 has a mutation status of V123V, The gene MMP20 has a mutation status of R273Q, The gene MMP12 has a mutation status of E201K, The gene CWF19L2 has a mutation status of D491N, The gene NCAM1 has a mutation status of P211P, The gene C1R has a mutation status of G259E, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of N76C, The gene PRB4 has a mutation status of R122G, The gene BICD1 has a mutation status of G567C, The gene GXYLT1 has a mutation status of C414H, The gene KMT2D has a mutation status of 888_889EP>A, The gene FMNL3 has a mutation status of R197C, The gene KRT86 has a mutation status of R267Q, The gene PTPRB has a mutation status of T218A, The gene HVCN1 has a mutation status of M71T, The gene SDSL has a mutation status of A209V, The gene NCOR2 has a mutation status of D1472N, The gene ZNF891 has a mutation status of K105K, The gene POSTN has a mutation status of D293E, The gene CBY2 has a mutation status of V309A, The gene IRF9 has a mutation status of K26fs, The gene FRMD6 has a mutation status of T398I, The gene PLEKHG3 has a mutation status of P1124P, The gene TTC7B has a mutation status of R271W, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L1 has a mutation status of W595R, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene ATP8B4 has a mutation status of V1023I, The gene LACTB has a mutation status of N277S, The gene ANKDD1A has a mutation status of L516L, The gene IGDCC3 has a mutation status of I647I, The gene DENND4A has a mutation status of T309A, The gene NEO1 has a mutation status of N1456N, The gene RASGRF1 has a mutation status of A985V, The gene MTHFS has a mutation status of V148I, The gene IL16 has a mutation status of L425L, The gene GOLGA6L10 has a mutation status of E217E, The gene GOLGA6L9 has a mutation status of R6H, The gene GOLGA6L9 has a mutation status of N187D, The gene HAPLN3 has a mutation status of R199W, The gene TICRR has a mutation status of T1848S, The gene KIF7 has a mutation status of P1320P, The gene ABCC1 has a mutation status of A953P, The gene UMOD has a mutation status of T249N, The gene ACSM2B has a mutation status of K327K, The gene DNAH3 has a mutation status of E2757Q, The gene ZP2 has a mutation status of S401fs, The gene PRSS36 has a mutation status of W81L, The gene ELMO3 has a mutation status of A628T, The gene CARMIL2 has a mutation status of K1326E, The gene GABARAPL2 has a mutation status of S39F, The gene PLCG2 has a mutation status of K557K, The gene CDH15 has a mutation status of L617L, The gene ZMYND15 has a mutation status of V556V, The gene MYH1 has a mutation status of I1609N, The gene HS3ST3A1 has a mutation status of G55G, The gene ZNF286A has a mutation status of T489S, The gene FBXW10 has a mutation status of P775P, The gene OMG has a mutation status of C11Y, The gene CCL4L2 has a mutation status of P67R, The gene MYCBPAP has a mutation status of R252Q, The gene MMD has a mutation status of L48L, The gene C17orf58 has a mutation status of R37R, The gene MYO15B has a mutation status of G470D, The gene MYO15B has a mutation status of G474A, The gene MYO15B has a mutation status of S620H, The gene JMJD6 has a mutation status of F35F, The gene USP36 has a mutation status of S756R, The gene EPB41L3 has a mutation status of P845L, The gene SERPINB3 has a mutation status of V134T, The gene DIPK1C has a mutation status of R233K, The gene CNN2 has a mutation status of S244S, The gene CNN2 has a mutation status of M249T, The gene SLC25A41 has a mutation status of R329Q, The gene CD209 has a mutation status of T165M, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of V13007G, The gene MUC16 has a mutation status of T12336L, The gene MUC16 has a mutation status of A4318D, The gene RAVER1 has a mutation status of L676L, The gene SMARCA4 has a mutation status of N1164Y, The gene MYO9B has a mutation status of R703C, The gene ZNF66 has a mutation status of T139A, The gene ZNF724 has a mutation status of K385R, The gene TDRD12 has a mutation status of P422L, The gene KMT2B has a mutation status of T2261K, The gene WDR87 has a mutation status of EEEEER2264del, The gene SPTBN4 has a mutation status of D211N, The gene BHMG1 has a mutation status of Q74Q, The gene LILRB3 has a mutation status of T201M, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Y99I, The gene SSC5D has a mutation status of I1336V, The gene ZNF543 has a mutation status of R570K, The gene ZNF543 has a mutation status of E589Q, The gene AL035461.4 has a mutation status of D855N, The gene ZFP64 has a mutation status of Q119L, The gene TAF4 has a mutation status of A767T, The gene OGFR has a mutation status of AGPAGDEPAESPSETPGPRP547del, The gene DIDO1 has a mutation status of E772K, The gene ADAMTS1 has a mutation status of F157S, The gene KRTAP21-1 has a mutation status of Y20S, The gene ERG has a mutation status of K89R, The gene COL18A1 has a mutation status of P991P, The gene PCNT has a mutation status of E3094Q, The gene CECR2 has a mutation status of R605Q, The gene GCAT has a mutation status of R249R, The gene ZC3H7B has a mutation status of T224M, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SULT4A1 has a mutation status of T227M, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene ARMCX5 has a mutation status of I552M, The gene AC236972.4 has a mutation status of S1611S, The gene MT-CO3 has a mutation status of E183E, The gene MT-ND4 has a mutation status of G211G, The gene MT-ND5 has a mutation status of V92V, The gene MT-ND5 has a mutation status of T533M, The gene MT-CYB has a mutation status of F18L
LUAD
The gene TNFRSF18 has a mutation status of E69K, The gene TAS1R3 has a mutation status of T153T, The gene FNDC10 has a mutation status of H225P, The gene CFAP74 has a mutation status of G1253G, The gene SKI has a mutation status of Y254S, The gene GPR157 has a mutation status of A199V, The gene PRAMEF2 has a mutation status of N293M, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene HSPG2 has a mutation status of A2967V, The gene HTR1D has a mutation status of G250R, The gene AUNIP has a mutation status of V13V, The gene CSMD2 has a mutation status of F1069V, The gene CSMD2 has a mutation status of G974G, The gene RIMS3 has a mutation status of G4G, The gene ATP6V0B has a mutation status of L172F, The gene MKNK1 has a mutation status of Y225Y, The gene HOOK1 has a mutation status of W54fs, The gene CSF1 has a mutation status of R53Q, The gene TAFA3 has a mutation status of P113P, The gene MAN1A2 has a mutation status of H93R, The gene PSMB4 has a mutation status of E239K, The gene S100A13 has a mutation status of A84G, The gene UBQLN4 has a mutation status of S129*, The gene LMNA has a mutation status of R624C, The gene ARHGEF11 has a mutation status of E653fs, The gene KCNJ9 has a mutation status of T98T, The gene KCNJ9 has a mutation status of A151A, The gene KCNJ9 has a mutation status of A168A, The gene KCNJ9 has a mutation status of T170T, The gene VANGL2 has a mutation status of P288P, The gene UHMK1 has a mutation status of V25V, The gene UHMK1 has a mutation status of R28R, The gene UHMK1 has a mutation status of H260H, The gene PBX1 has a mutation status of D295D, The gene PBX1 has a mutation status of D316D, The gene PBX1 has a mutation status of P320P, The gene ILDR2 has a mutation status of D267D, The gene ADCY10 has a mutation status of H402H, The gene TNR has a mutation status of T383M, The gene TNR has a mutation status of L367L, The gene ASTN1 has a mutation status of P470P, The gene RASAL2 has a mutation status of V484V, The gene ABL2 has a mutation status of N956N, The gene LHX4 has a mutation status of S289S, The gene STX6 has a mutation status of S187S, The gene IER5 has a mutation status of S14S, The gene LAMC1 has a mutation status of T122T, The gene LAMC1 has a mutation status of S131N, The gene SMG7 has a mutation status of Q735Q, The gene IVNS1ABP has a mutation status of L236P, The gene HMCN1 has a mutation status of V3122V, The gene BRINP3 has a mutation status of E59E, The gene RPS27AP5 has a mutation status of K6K, The gene CDC73 has a mutation status of D204D, The gene B3GALT2 has a mutation status of Q386Q, The gene KCNT2 has a mutation status of K441K, The gene ZNF281 has a mutation status of T777T, The gene ZNF281 has a mutation status of L749L, The gene ZNF281 has a mutation status of Y345Y, The gene ZNF281 has a mutation status of S69T, The gene CACNA1S has a mutation status of A877A, The gene IGFN1 has a mutation status of Y109Y, The gene PKP1 has a mutation status of V397V, The gene PHLDA3 has a mutation status of E35E, The gene PHLDA3 has a mutation status of V32V, The gene CYB5R1 has a mutation status of L199L, The gene PPFIA4 has a mutation status of L577L, The gene MYBPH has a mutation status of S383S, The gene MYBPH has a mutation status of A381A, The gene PLEKHA6 has a mutation status of C1016C, The gene TMCC2 has a mutation status of P218P, The gene MFSD4A has a mutation status of L39L, The gene CR2 has a mutation status of E889E, The gene KCNH1 has a mutation status of I334I, The gene RCOR3 has a mutation status of P465P, The gene PROX1 has a mutation status of M154V, The gene PROX1 has a mutation status of I172I, The gene PROX1 has a mutation status of N189N, The gene ESRRG has a mutation status of P48P, The gene SLC30A10 has a mutation status of A173A, The gene AIDA has a mutation status of F16L, The gene SUSD4 has a mutation status of H313H, The gene CAPN2 has a mutation status of F87F, The gene CDC42BPA has a mutation status of R585R, The gene CDC42BPA has a mutation status of D567D, The gene OBSCN has a mutation status of V2455L, The gene FMN2 has a mutation status of R456G, The gene WDR64 has a mutation status of I204L, The gene CEP170 has a mutation status of I453L, The gene ZBTB18 has a mutation status of V79V, The gene ZBTB18 has a mutation status of E104E, The gene ZBTB18 has a mutation status of A287A, The gene OR2W3 has a mutation status of I214I, The gene CMPK2 has a mutation status of S209G, The gene C2orf16 has a mutation status of S2788Y, The gene GALNT14 has a mutation status of G496A, The gene FAM98A has a mutation status of L17L, The gene STRN has a mutation status of E59E, The gene CYP1B1 has a mutation status of R101R, The gene CYP1B1 has a mutation status of R101S, The gene DHX57 has a mutation status of R765Q, The gene ARHGEF33 has a mutation status of P633P, The gene ARHGEF33 has a mutation status of A636A, The gene TMEM178A has a mutation status of D54D, The gene SIX3 has a mutation status of L82L, The gene SIX3 has a mutation status of C96C, The gene SIX3 has a mutation status of A136A, The gene SIX3 has a mutation status of V137V, The gene SIX3 has a mutation status of T318T, The gene SIX3 has a mutation status of S319S, The gene RHOQ has a mutation status of L10L, The gene RAB11FIP5 has a mutation status of G136R, The gene AL845331.2 has a mutation status of G155C, The gene STARD7 has a mutation status of R37R, The gene SNRNP200 has a mutation status of A1501A, The gene KANSL3 has a mutation status of G834S, The gene KANSL3 has a mutation status of L597F, The gene KANSL3 has a mutation status of N590N, The gene NPAS2 has a mutation status of Y185Y, The gene CNOT11 has a mutation status of I75I, The gene RNF149 has a mutation status of T305T, The gene FHL2 has a mutation status of R113C, The gene BCL2L11 has a mutation status of K52K, The gene PAX8 has a mutation status of P312P, The gene EN1 has a mutation status of V385V, The gene EN1 has a mutation status of S381S, The gene EN1 has a mutation status of R355R, The gene EN1 has a mutation status of T308T, The gene EN1 has a mutation status of A215G, The gene EN1 has a mutation status of P95P, The gene EN1 has a mutation status of H77H, The gene TFCP2L1 has a mutation status of I77I, The gene CLASP1 has a mutation status of P744P, The gene R3HDM1 has a mutation status of S86S, The gene UBXN4 has a mutation status of I8I, The gene UBXN4 has a mutation status of A10A, The gene DARS1 has a mutation status of M18V, The gene DARS1 has a mutation status of S10G, The gene ZEB2 has a mutation status of S138S, The gene ZEB2 has a mutation status of R131R, The gene ACVR2A has a mutation status of K75K, The gene MBD5 has a mutation status of R294R, The gene MBD5 has a mutation status of V374I, The gene MBD5 has a mutation status of M391V, The gene MBD5 has a mutation status of P408P, The gene MBD5 has a mutation status of N805N, The gene MBD5 has a mutation status of S806S, The gene EPC2 has a mutation status of K15K, The gene EPC2 has a mutation status of P18P, The gene PRPF40A has a mutation status of R8R, The gene PRPF40A has a mutation status of C2C, The gene KCNJ3 has a mutation status of A259A, The gene NR4A2 has a mutation status of I51I, The gene PKP4 has a mutation status of S75S, The gene BAZ2B has a mutation status of L1118L, The gene PSMD14 has a mutation status of G119G, The gene TBR1 has a mutation status of C274C, The gene TBR1 has a mutation status of P597A, The gene IFIH1 has a mutation status of S282R, The gene IFIH1 has a mutation status of L270F, The gene KCNH7 has a mutation status of P485P, The gene KCNH7 has a mutation status of R441R, The gene KCNH7 has a mutation status of E437E, The gene FIGN has a mutation status of K743K, The gene FIGN has a mutation status of Q664Q, The gene FIGN has a mutation status of R647R, The gene SCN3A has a mutation status of A640A, The gene CSRNP3 has a mutation status of L124R, The gene SCN1A has a mutation status of C1326C, The gene UBR3 has a mutation status of A146A, The gene TLK1 has a mutation status of Q18R, The gene DLX1 has a mutation status of A18A, The gene RAPGEF4 has a mutation status of S487A, The gene RAPGEF4 has a mutation status of P725S, The gene SP3 has a mutation status of N438N, The gene SP3 has a mutation status of G423G, The gene SP3 has a mutation status of E402D, The gene SP3 has a mutation status of A383A, The gene SP3 has a mutation status of T325A, The gene SP3 has a mutation status of I320V, The gene SP3 has a mutation status of G24G, The gene OLA1 has a mutation status of G319G, The gene OLA1 has a mutation status of A278A, The gene OLA1 has a mutation status of G277G, The gene SP9 has a mutation status of T435T, The gene CHN1 has a mutation status of G228G, The gene HOXD10 has a mutation status of S29S, The gene HOXD10 has a mutation status of L57L, The gene HOXD10 has a mutation status of D83D, The gene HOXD10 has a mutation status of N168N, The gene HOXD10 has a mutation status of T255T, The gene HOXD9 has a mutation status of L298L, The gene HOXD9 has a mutation status of K302K, The gene HOXD8 has a mutation status of P3P, The gene HOXD4 has a mutation status of T180T, The gene AGPS has a mutation status of N229N, The gene TTN has a mutation status of R23624R, The gene ZNF385B has a mutation status of D204E, The gene ZNF385B has a mutation status of A202A, The gene CWC22 has a mutation status of K728E, The gene CWC22 has a mutation status of K475K, The gene CWC22 has a mutation status of A473A, The gene CWC22 has a mutation status of K402K, The gene CWC22 has a mutation status of A261A, The gene ITPRID2 has a mutation status of K83K, The gene NCKAP1 has a mutation status of T29P, The gene ZC3H15 has a mutation status of V162V, The gene WDR75 has a mutation status of E675E, The gene SLC40A1 has a mutation status of T475T, The gene SLC40A1 has a mutation status of L474L, The gene MSTN has a mutation status of N197S, The gene GLS has a mutation status of T170T, The gene GLS has a mutation status of Q187Q, The gene DNAH7 has a mutation status of L1713L, The gene DNAH7 has a mutation status of S1372S, The gene COQ10B has a mutation status of Y124Y, The gene MOB4 has a mutation status of V68V, The gene SATB2 has a mutation status of I481V, The gene SATB2 has a mutation status of Y210Y, The gene NDUFS1 has a mutation status of R113fs, The gene KLF7 has a mutation status of A115T, The gene KLF7 has a mutation status of L25L, The gene CCNYL1 has a mutation status of L240L, The gene CCNYL1 has a mutation status of L244L, The gene FZD5 has a mutation status of R42R, The gene FZD5 has a mutation status of Q19E, The gene PIKFYVE has a mutation status of T401T, The gene PIKFYVE has a mutation status of G1118G, The gene MAP2 has a mutation status of T1452T, The gene CPS1 has a mutation status of L298I, The gene CPS1 has a mutation status of T308S, The gene CPS1 has a mutation status of G1077G, The gene CPS1 has a mutation status of P1080P, The gene IKZF2 has a mutation status of F480F, The gene IKZF2 has a mutation status of E98D, The gene IKZF2 has a mutation status of A91A, The gene ABCA12 has a mutation status of D505E, The gene TNS1 has a mutation status of H188H, The gene TNS1 has a mutation status of H187H, The gene CDK5R2 has a mutation status of P280P, The gene CDK5R2 has a mutation status of P283P, The gene CDK5R2 has a mutation status of R310R, The gene IHH has a mutation status of G98G, The gene IHH has a mutation status of T97T, The gene SPEG has a mutation status of S234S, The gene SPEG has a mutation status of R2076R, The gene SLC4A3 has a mutation status of P54T, The gene SLC4A3 has a mutation status of P62P, The gene EPHA4 has a mutation status of K240K, The gene CUL3 has a mutation status of T104T, The gene NYAP2 has a mutation status of P364P, The gene NYAP2 has a mutation status of L366L, The gene IRS1 has a mutation status of C69C, The gene IRS1 has a mutation status of L66L, The gene COL4A3 has a mutation status of P74P, The gene TRIP12 has a mutation status of T387T, The gene TRIP12 has a mutation status of A138P, The gene CAB39 has a mutation status of L141L, The gene CAB39 has a mutation status of G144G, The gene CHRNG has a mutation status of L236L, The gene EFHD1 has a mutation status of P125P, The gene EFHD1 has a mutation status of D143D, The gene EFHD1 has a mutation status of G144G, The gene GIGYF2 has a mutation status of G129G, The gene GIGYF2 has a mutation status of T1136T, The gene GIGYF2 has a mutation status of A1200V, The gene DGKD has a mutation status of D869D, The gene DGKD has a mutation status of A876A, The gene DGKD has a mutation status of T1167T, The gene ARL4C has a mutation status of D94D, The gene ARL4C has a mutation status of L75L, The gene AGAP1 has a mutation status of I46I, The gene KLHL30 has a mutation status of T542P, The gene HDAC4 has a mutation status of A909A, The gene LRRC3B has a mutation status of T257I, The gene DCLK3 has a mutation status of R33C, The gene TOPAZ1 has a mutation status of E187K, The gene CELSR3 has a mutation status of S2086S, The gene IL17RD has a mutation status of S667L, The gene ROBO2 has a mutation status of N844N, The gene TOMM70 has a mutation status of T512T, The gene TOMM70 has a mutation status of K501K, The gene SENP7 has a mutation status of R737Q, The gene TMPRSS7 has a mutation status of F83L, The gene DRD3 has a mutation status of N120N, The gene DRD3 has a mutation status of L119L, The gene STXBP5L has a mutation status of S16S, The gene PARP14 has a mutation status of C509R, The gene ADCY5 has a mutation status of R228R, The gene ADCY5 has a mutation status of S218S, The gene ZNF148 has a mutation status of P785P, The gene ZNF148 has a mutation status of N286N, The gene ZNF148 has a mutation status of H281H, The gene ZNF148 has a mutation status of I134V, The gene ZNF148 has a mutation status of S113S, The gene PPP2R3A has a mutation status of R167K, The gene PLD1 has a mutation status of I797V, The gene KLHL24 has a mutation status of L9L, The gene AC131160.1 has a mutation status of N161S, The gene ABCC5 has a mutation status of P483P, The gene DVL3 has a mutation status of L213L, The gene DVL3 has a mutation status of A704A, The gene CAMK2N2 has a mutation status of P75P, The gene EPHB3 has a mutation status of T993T, The gene IGF2BP2 has a mutation status of D72D, The gene DGKG has a mutation status of A338A, The gene DGKG has a mutation status of H337H, The gene RTP1 has a mutation status of E196E, The gene RTP1 has a mutation status of S204S, The gene RTP2 has a mutation status of A68P, The gene FGF12 has a mutation status of H88H, The gene FGF12 has a mutation status of L70L, The gene FGF12 has a mutation status of R23R, The gene FAM43A has a mutation status of P23P, The gene ACAP2 has a mutation status of E734E, The gene ACAP2 has a mutation status of E733E, The gene SLC49A3 has a mutation status of T368P, The gene SLC49A3 has a mutation status of T365T, The gene GAK has a mutation status of P480P, The gene OTOP1 has a mutation status of V69M, The gene ADGRA3 has a mutation status of G1303C, The gene ANKRD17 has a mutation status of I1789I, The gene ANKRD17 has a mutation status of Q1787Q, The gene ANKRD17 has a mutation status of G629G, The gene CCNI has a mutation status of L169W, The gene CXXC4 has a mutation status of S37L, The gene ENPEP has a mutation status of K923I, The gene ALPK1 has a mutation status of L1159F, The gene FAT4 has a mutation status of K2892E, The gene POU4F2 has a mutation status of D252D, The gene POU4F2 has a mutation status of A253A, The gene SPOCK3 has a mutation status of R112W, The gene TENM3 has a mutation status of V2504V, The gene TENM3 has a mutation status of Q2506Q, The gene WWC2 has a mutation status of K418K, The gene IRF2 has a mutation status of K31K, The gene TRIO has a mutation status of S2358S, The gene TRIO has a mutation status of S2506S, The gene TRIO has a mutation status of T2513T, The gene ANKH has a mutation status of L20L, The gene ANKH has a mutation status of L17L, The gene FBXL7 has a mutation status of A138A, The gene FBXL7 has a mutation status of R139R, The gene MARCHF11 has a mutation status of Q281Q, The gene MARCHF11 has a mutation status of A257A, The gene MARCHF11 has a mutation status of I246I, The gene RETREG1 has a mutation status of K137K, The gene GOLPH3 has a mutation status of E65E, The gene NIPBL has a mutation status of S68S, The gene NIPBL has a mutation status of A1787A, The gene GDNF has a mutation status of S18S, The gene PPIP5K2 has a mutation status of T1011T, The gene PCDHB2 has a mutation status of D448N, The gene TCERG1 has a mutation status of I636T, The gene SLC26A2 has a mutation status of H9R, The gene SLC36A2 has a mutation status of E286K, The gene FAT2 has a mutation status of L1892L, The gene LCP2 has a mutation status of P289L, The gene NEURL1B has a mutation status of V309V, The gene NEURL1B has a mutation status of I310I, The gene PPP1R3G has a mutation status of V35fs, The gene JARID2 has a mutation status of T527P, The gene GABBR1 has a mutation status of Q915Q, The gene SLC44A4 has a mutation status of R281Q, The gene PRRT1 has a mutation status of E267E, The gene RING1 has a mutation status of L16L, The gene RING1 has a mutation status of L18L, The gene ITPR3 has a mutation status of I13I, The gene ITPR3 has a mutation status of V14V, The gene KCNK5 has a mutation status of P372L, The gene ABCC10 has a mutation status of G605G, The gene ABCC10 has a mutation status of V607V, The gene TFAP2D has a mutation status of H143H, The gene DST has a mutation status of E5655K, The gene PTP4A1 has a mutation status of R18R, The gene PHF3 has a mutation status of A36T, The gene ADGRB3 has a mutation status of S31S, The gene ADGRB3 has a mutation status of L278L, The gene RIMS1 has a mutation status of V380V, The gene ZNF292 has a mutation status of T131I, The gene CASP8AP2 has a mutation status of S1298L, The gene MFSD4B has a mutation status of L182Y, The gene ADAP1 has a mutation status of Y364Y, The gene FOXK1 has a mutation status of T683P, The gene SLC29A4 has a mutation status of V435I, The gene HOXA13 has a mutation status of A296P, The gene SEPTIN7 has a mutation status of N271del, The gene EPDR1 has a mutation status of A35A, The gene PKD1L1 has a mutation status of P743P, The gene GRB10 has a mutation status of A349T, The gene PSPH has a mutation status of L68P, The gene SUMF2 has a mutation status of R3W, The gene VKORC1L1 has a mutation status of G26G, The gene STX1A has a mutation status of F269C, The gene TMEM120A has a mutation status of S71F, The gene GSAP has a mutation status of L622L, The gene SEMA3D has a mutation status of *295*, The gene AC004922.1 has a mutation status of H346H, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene MUC3A has a mutation status of G1212S, The gene MUC3A has a mutation status of L1361P, The gene MUC3A has a mutation status of D2269G, The gene MUC3A has a mutation status of K2298E, The gene MUC3A has a mutation status of P3166P, The gene EFCAB10 has a mutation status of G56G, The gene LMOD2 has a mutation status of E124V, The gene POT1 has a mutation status of Y271Y, The gene FLNC has a mutation status of R2462R, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene LUC7L2 has a mutation status of S18Y, The gene PRSS1 has a mutation status of N77N, The gene KRBA1 has a mutation status of E25G, The gene LRRC61 has a mutation status of G13G, The gene DLGAP2 has a mutation status of N389T, The gene CLDN23 has a mutation status of L172L, The gene CLU has a mutation status of R158H, The gene PURG has a mutation status of P303P, The gene ADGRA2 has a mutation status of T397P, The gene ADAM32 has a mutation status of R11R, The gene SFRP1 has a mutation status of A88A, The gene CEBPD has a mutation status of A204A, The gene UBE2V2 has a mutation status of N17N, The gene PCMTD1 has a mutation status of L82L, The gene SOX17 has a mutation status of G153G, The gene XKR4 has a mutation status of R106R, The gene XKR4 has a mutation status of S108S, The gene XKR4 has a mutation status of L264L, The gene XKR4 has a mutation status of L457L, The gene XKR4 has a mutation status of V463V, The gene MYBL1 has a mutation status of T183T, The gene VCPIP1 has a mutation status of E641E, The gene VCPIP1 has a mutation status of V435V, The gene ARFGEF1 has a mutation status of N514N, The gene ARFGEF1 has a mutation status of S506S, The gene SULF1 has a mutation status of D189D, The gene SLCO5A1 has a mutation status of A467A, The gene SLCO5A1 has a mutation status of F368F, The gene SLCO5A1 has a mutation status of L352L, The gene EYA1 has a mutation status of P93S, The gene SBSPON has a mutation status of P34P, The gene SBSPON has a mutation status of P30P, The gene JPH1 has a mutation status of G51V, The gene JPH1 has a mutation status of V49V, The gene PABPC1 has a mutation status of Y56Y, The gene TNFRSF11B has a mutation status of R111H, The gene ADGRB1 has a mutation status of R603R, The gene MAFA has a mutation status of P15P, The gene GRINA has a mutation status of E343E, The gene SCRT1 has a mutation status of S258S, The gene TAF1L has a mutation status of P1266L, The gene B4GALT1 has a mutation status of Y239C, The gene AL162231.1 has a mutation status of P71P, The gene UNC13B has a mutation status of R945C, The gene HRCT1 has a mutation status of HHH88del, The gene ZCCHC7 has a mutation status of D28Y, The gene ZCCHC7 has a mutation status of G147C, The gene PRKACG has a mutation status of E11*, The gene COL27A1 has a mutation status of A293A, The gene TLR4 has a mutation status of F342Y, The gene FBXW2 has a mutation status of L318L, The gene FBXW2 has a mutation status of K85K, The gene FBXW2 has a mutation status of L82L, The gene FBXW2 has a mutation status of L48L, The gene FBXW2 has a mutation status of D30D, The gene PHF19 has a mutation status of H381Q, The gene DAB2IP has a mutation status of C343C, The gene LHX6 has a mutation status of P31P, The gene LHX6 has a mutation status of Q28Q, The gene ZBTB26 has a mutation status of K366K, The gene ZBTB26 has a mutation status of D360D, The gene ZBTB26 has a mutation status of V319V, The gene ZBTB26 has a mutation status of A107A, The gene ZBTB26 has a mutation status of L86L, The gene RABGAP1 has a mutation status of L545L, The gene STRBP has a mutation status of D368D, The gene STRBP has a mutation status of L363L, The gene STRBP has a mutation status of E244E, The gene STRBP has a mutation status of V232V, The gene DENND1A has a mutation status of K443K, The gene DENND1A has a mutation status of A93A, The gene DENND1A has a mutation status of P38P, The gene LHX2 has a mutation status of S125S, The gene NR6A1 has a mutation status of K304K, The gene PPP6C has a mutation status of D147D, The gene MAPKAP1 has a mutation status of R94R, The gene MAPKAP1 has a mutation status of H18H, The gene PBX3 has a mutation status of E101E, The gene PBX3 has a mutation status of D105D, The gene PBX3 has a mutation status of A246A, The gene PBX3 has a mutation status of T247T, The gene PBX3 has a mutation status of Q372Q, The gene PBX3 has a mutation status of D390D, The gene LMX1B has a mutation status of L35L, The gene LMX1B has a mutation status of T41T, The gene LMX1B has a mutation status of P124P, The gene RALGPS1 has a mutation status of V105V, The gene RALGPS1 has a mutation status of L122L, The gene RALGPS1 has a mutation status of N513N, The gene GARNL3 has a mutation status of P478P, The gene GARNL3 has a mutation status of S486C, The gene NIBAN2 has a mutation status of L237L, The gene SH2D3C has a mutation status of R476R, The gene SH2D3C has a mutation status of E465E, The gene DNM1 has a mutation status of P852P, The gene ODF2 has a mutation status of G7G, The gene ODF2 has a mutation status of R23G, The gene SPTAN1 has a mutation status of K1067K, The gene ZER1 has a mutation status of G288G, The gene LRRC8A has a mutation status of I299I, The gene LRRC8A has a mutation status of T303T, The gene LRRC8A has a mutation status of I629I, The gene LRRC8A has a mutation status of I651I, The gene LRRC8A has a mutation status of P701P, The gene LRRC8A has a mutation status of I704I, The gene SH3GLB2 has a mutation status of Y264Y, The gene IER5L has a mutation status of S362S, The gene IER5L has a mutation status of R22R, The gene HMCN2 has a mutation status of A4193V, The gene PRDM12 has a mutation status of R263R, The gene PRDM12 has a mutation status of R297R, The gene ABL1 has a mutation status of T514T, The gene FAM78A has a mutation status of T39T, The gene FAM78A has a mutation status of I38I, The gene PLPP7 has a mutation status of P66P, The gene PLPP7 has a mutation status of S76S, The gene DDX31 has a mutation status of T695T, The gene TSC1 has a mutation status of H230H, The gene GFI1B has a mutation status of P303P, The gene AL162417.1 has a mutation status of S280S, The gene AL162417.1 has a mutation status of Q278Q, The gene SURF1 has a mutation status of V177V, The gene MYMK has a mutation status of V192V, The gene ADAMTSL2 has a mutation status of E615E, The gene OLFM1 has a mutation status of I138I, The gene LHX3 has a mutation status of A180A, The gene GPSM1 has a mutation status of T59T, The gene NOTCH1 has a mutation status of S1776S, The gene NOTCH1 has a mutation status of G1772G, The gene NOTCH1 has a mutation status of G881S, The gene ABCA2 has a mutation status of N1074N, The gene ABCA2 has a mutation status of P1071P, The gene GRIN1 has a mutation status of G369G, The gene GRIN1 has a mutation status of H371H, The gene GRIN1 has a mutation status of P872P, The gene GRIN1 has a mutation status of R893R, The gene TUBB4B has a mutation status of L151L, The gene NSMF has a mutation status of R245R, The gene EHMT1 has a mutation status of V211I, The gene EHMT1 has a mutation status of V212L, The gene CACNA1B has a mutation status of E2137D, The gene LARP4B has a mutation status of T629A, The gene GATA3 has a mutation status of P435P, The gene CELF2 has a mutation status of H7H, The gene CELF2 has a mutation status of E415E, The gene CELF2 has a mutation status of P427P, The gene USP6NL has a mutation status of R275R, The gene UPF2 has a mutation status of H630H, The gene UPF2 has a mutation status of T628T, The gene SEC61A2 has a mutation status of E189E, The gene HSPA14 has a mutation status of L473L, The gene MINDY3 has a mutation status of E44E, The gene C1QL3 has a mutation status of A203A, The gene C1QL3 has a mutation status of Y35Y, The gene C1QL3 has a mutation status of L3L, The gene PLXDC2 has a mutation status of G522G, The gene SKIDA1 has a mutation status of R465R, The gene SKIDA1 has a mutation status of G455G, The gene SKIDA1 has a mutation status of A28A, The gene SKIDA1 has a mutation status of F8F, The gene MLLT10 has a mutation status of E20E, The gene DNAJC1 has a mutation status of I128V, The gene DNAJC1 has a mutation status of Q105Q, The gene KIAA1217 has a mutation status of S1786A, The gene KIAA1217 has a mutation status of F1790C, The gene GPR158 has a mutation status of G110G, The gene MASTL has a mutation status of L790L, The gene ACBD5 has a mutation status of E78E, The gene ACBD5 has a mutation status of T76T, The gene ANKRD30A has a mutation status of R485V, The gene ZNF25 has a mutation status of E208G, The gene SORBS1 has a mutation status of D248N, The gene VWA2 has a mutation status of A372A, The gene KNDC1 has a mutation status of L134I, The gene CCKBR has a mutation status of R411P, The gene SMPD1 has a mutation status of P92S, The gene EIF4G2 has a mutation status of R505H, The gene NAV2 has a mutation status of S140S, The gene PAX6 has a mutation status of Q60E, The gene PAX6 has a mutation status of Q55Q, The gene PAX6 has a mutation status of L11L, The gene CSTF3 has a mutation status of Y54Y, The gene CSTF3 has a mutation status of E27E, The gene FJX1 has a mutation status of A231T, The gene FJX1 has a mutation status of A231A, The gene FJX1 has a mutation status of L417L, The gene PRR5L has a mutation status of G359D, The gene PRR5L has a mutation status of S360S, The gene TTC17 has a mutation status of V5I, The gene SLC35C1 has a mutation status of R115R, The gene PEX16 has a mutation status of E273G, The gene DGKZ has a mutation status of R902R, The gene ZNF408 has a mutation status of R522H, The gene MADD has a mutation status of E1595E, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene LRRC55 has a mutation status of R76C, The gene TMEM132A has a mutation status of E735G, The gene SLC15A3 has a mutation status of I468T, The gene NAA40 has a mutation status of R40Q, The gene TCIRG1 has a mutation status of A256S, The gene TCIRG1 has a mutation status of T731T, The gene RNF121 has a mutation status of I27I, The gene RNF121 has a mutation status of A28A, The gene NUMA1 has a mutation status of T2093P, The gene GPR83 has a mutation status of H133Y, The gene FAM76B has a mutation status of Q49Q, The gene YAP1 has a mutation status of S162A, The gene DYNC2H1 has a mutation status of G2828A, The gene SIK2 has a mutation status of F31F, The gene SIK2 has a mutation status of A32A, The gene ZBTB16 has a mutation status of G167G, The gene ZBTB16 has a mutation status of Y168Y, The gene CADM1 has a mutation status of H290H, The gene RNF214 has a mutation status of T633P, The gene RNF214 has a mutation status of Y644Y, The gene DSCAML1 has a mutation status of L1502L, The gene DSCAML1 has a mutation status of S1495S, The gene TMPRSS13 has a mutation status of Q83R, The gene KMT2A has a mutation status of S85S, The gene ARCN1 has a mutation status of L267L, The gene ARCN1 has a mutation status of A271A, The gene DDX6 has a mutation status of Q182Q, The gene BCL9L has a mutation status of P524P, The gene TRIM29 has a mutation status of A183A, The gene ARHGEF12 has a mutation status of Q1529Q, The gene GRIK4 has a mutation status of E78E, The gene GRAMD1B has a mutation status of Q247Q, The gene GRAMD1B has a mutation status of V317V, The gene TBRG1 has a mutation status of K27R, The gene TBRG1 has a mutation status of G165G, The gene PKNOX2 has a mutation status of T33T, The gene PKNOX2 has a mutation status of S97S, The gene FOXRED1 has a mutation status of Q333P, The gene DCPS has a mutation status of L180L, The gene FLI1 has a mutation status of L290L, The gene FLI1 has a mutation status of L291L, The gene NFRKB has a mutation status of E390E, The gene NFRKB has a mutation status of P220P, The gene APLP2 has a mutation status of G341G, The gene SLC6A12 has a mutation status of L137L, The gene CACNA1C has a mutation status of P1409P, The gene ITFG2 has a mutation status of V240L, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene GUCY2C has a mutation status of A48V, The gene PYROXD1 has a mutation status of P7P, The gene KLHL42 has a mutation status of A148P, The gene DNM1L has a mutation status of S563N, The gene SLC38A1 has a mutation status of K485N, The gene WNT1 has a mutation status of A18A, The gene WNT1 has a mutation status of A20T, The gene TUBA1A has a mutation status of D345D, The gene KCNH3 has a mutation status of S1040S, The gene KRT2 has a mutation status of R401H, The gene LRP1 has a mutation status of A2160T, The gene RXYLT1 has a mutation status of F221L, The gene PTPRB has a mutation status of A1948V, The gene TXNRD1 has a mutation status of K112K, The gene ISCU has a mutation status of A13G, The gene ACACB has a mutation status of K2148N, The gene PPP1CC has a mutation status of R191R, The gene GCN1 has a mutation status of V1899M, The gene ADGRD1 has a mutation status of S774S, The gene VWA8 has a mutation status of L25L, The gene PCDH8 has a mutation status of V739G, The gene IPO5 has a mutation status of S851G, The gene FARP1 has a mutation status of H703P, The gene TPP2 has a mutation status of E641E, The gene MYO16 has a mutation status of A1310A, The gene SOX1 has a mutation status of G64G, The gene MCF2L has a mutation status of F833F, The gene RALGAPA1 has a mutation status of P1018L, The gene TTC6 has a mutation status of E252D, The gene SOS2 has a mutation status of P1285S, The gene NIN has a mutation status of T1435T, The gene TTC7B has a mutation status of E244K, The gene TRIP11 has a mutation status of I1468R, The gene SLC25A29 has a mutation status of A116G, The gene NIPA1 has a mutation status of E18G, The gene GJD2 has a mutation status of V41V, The gene MEIS2 has a mutation status of M439V, The gene MEIS2 has a mutation status of Q418Q, The gene MEIS2 has a mutation status of A358A, The gene MEIS2 has a mutation status of L39L, The gene MEIS2 has a mutation status of V19G, The gene GPR176 has a mutation status of I53I, The gene ZFYVE19 has a mutation status of R223R, The gene INO80 has a mutation status of K1435K, The gene RPAP1 has a mutation status of V403V, The gene RPAP1 has a mutation status of R400R, The gene TYRO3 has a mutation status of 554_555insDIIAST, The gene MGA has a mutation status of E1427D, The gene EHD4 has a mutation status of E59E, The gene EHD4 has a mutation status of P51P, The gene CAPN3 has a mutation status of S606S, The gene CDAN1 has a mutation status of A230T, The gene CDAN1 has a mutation status of L208L, The gene CDAN1 has a mutation status of G190G, The gene TUBGCP4 has a mutation status of E338D, The gene TP53BP1 has a mutation status of H1922H, The gene SERF2 has a mutation status of D29D, The gene SERF2 has a mutation status of F69L, The gene SERF2 has a mutation status of V114V, The gene MFAP1 has a mutation status of R159R, The gene FRMD5 has a mutation status of Y259Y, The gene FRMD5 has a mutation status of S12S, The gene SEMA6D has a mutation status of N51N, The gene COPS2 has a mutation status of F131F, The gene GABPB1 has a mutation status of Q133Q, The gene FAM214A has a mutation status of T956T, The gene PRTG has a mutation status of L1150F, The gene RFX7 has a mutation status of T302S, The gene OAZ2 has a mutation status of Y5Y, The gene IGDCC3 has a mutation status of A353A, The gene SMAD6 has a mutation status of S377S, The gene SMAD6 has a mutation status of R382R, The gene NEO1 has a mutation status of A1274A, The gene NEO1 has a mutation status of G1282S, The gene HCN4 has a mutation status of V184A, The gene NPTN has a mutation status of P131P, The gene NPTN has a mutation status of S57S, The gene RPP25 has a mutation status of M50L, The gene RPP25 has a mutation status of R47R, The gene CSPG4 has a mutation status of R631R, The gene ADAMTS7 has a mutation status of S1251S, The gene KIF7 has a mutation status of P238H, The gene TM2D3 has a mutation status of E185G, The gene CLCN7 has a mutation status of N214N, The gene CLCN7 has a mutation status of P207P, The gene E4F1 has a mutation status of Q18G, The gene E4F1 has a mutation status of R23R, The gene CCNF has a mutation status of P83P, The gene CCNF has a mutation status of G86Q, The gene SRRM2 has a mutation status of R30R, The gene SRRM2 has a mutation status of R52R, The gene SRRM2 has a mutation status of A2658A, The gene SRRM2 has a mutation status of L2659L, The gene NLRC3 has a mutation status of Q669R, The gene CREBBP has a mutation status of Q2318Q, The gene UBALD1 has a mutation status of S106S, The gene MGRN1 has a mutation status of P363S, The gene GLYR1 has a mutation status of R298R, The gene RBFOX1 has a mutation status of A260G, The gene RBFOX1 has a mutation status of T379T, The gene USP7 has a mutation status of L1079L, The gene USP7 has a mutation status of V75V, The gene C16orf72 has a mutation status of K150K, The gene C16orf72 has a mutation status of S220P, The gene C16orf72 has a mutation status of S239T, The gene CIITA has a mutation status of R884S, The gene SOCS1 has a mutation status of L162L, The gene SOCS1 has a mutation status of L147L, The gene TXNDC11 has a mutation status of N378N, The gene TXNDC11 has a mutation status of E376E, The gene ZC3H7A has a mutation status of C506C, The gene SHISA9 has a mutation status of E184E, The gene COQ7 has a mutation status of P171S, The gene GPRC5B has a mutation status of D265Y, The gene TLCD3B has a mutation status of P83P, The gene ZNF319 has a mutation status of V507G, The gene CDH11 has a mutation status of V12V, The gene PARD6A has a mutation status of G84G, The gene ESRP2 has a mutation status of P19A, The gene RFWD3 has a mutation status of Y654Y, The gene CNTNAP4 has a mutation status of S1136R, The gene MAF has a mutation status of Q326Q, The gene MAF has a mutation status of P103P, The gene MAF has a mutation status of L101L, The gene CDYL2 has a mutation status of G361G, The gene CMIP has a mutation status of G637G, The gene CMIP has a mutation status of L691L, The gene KIAA0513 has a mutation status of E333Q, The gene ZCCHC14 has a mutation status of S970S, The gene ANKRD11 has a mutation status of S2051L, The gene ZNF276 has a mutation status of V152I, The gene ZNF276 has a mutation status of V155A, The gene GAS8 has a mutation status of R259R, The gene GAS8 has a mutation status of L265M, The gene CAMKK1 has a mutation status of A22T, The gene WSCD1 has a mutation status of P302T, The gene CLDN7 has a mutation status of S172A, The gene TP53 has a mutation status of E326*, The gene DNAH2 has a mutation status of N2075T, The gene DNAH2 has a mutation status of S2076P, The gene ATPAF2 has a mutation status of S24R, The gene SARM1 has a mutation status of G37C, The gene PIPOX has a mutation status of D291N, The gene MYO18A has a mutation status of V1382G, The gene NF1 has a mutation status of E1210*, The gene OMG has a mutation status of T408A, The gene CCL4L2 has a mutation status of L20L, The gene CCL4L2 has a mutation status of P67R, The gene CASC3 has a mutation status of P29P, The gene CASC3 has a mutation status of G32G, The gene HIGD1B has a mutation status of R23K, The gene SP2 has a mutation status of T168P, The gene CACNG4 has a mutation status of C41C, The gene CD300A has a mutation status of T13A, The gene SLC9A3R1 has a mutation status of V62G, The gene GRIN2C has a mutation status of A466G, The gene USP36 has a mutation status of T653T, The gene RAB12 has a mutation status of L139L, The gene CXXC1 has a mutation status of H155H, The gene FECH has a mutation status of *424C, The gene PIGN has a mutation status of T362T, The gene RELCH has a mutation status of A998A, The gene ZCCHC2 has a mutation status of Q473Q, The gene ZCCHC2 has a mutation status of V1085V, The gene ZCCHC2 has a mutation status of N1180fs, The gene BCL2 has a mutation status of H184H, The gene BCL2 has a mutation status of S167S, The gene BCL2 has a mutation status of R164R, The gene CDH7 has a mutation status of A505A, The gene CDH7 has a mutation status of V506V, The gene HCN2 has a mutation status of Y697Y, The gene KISS1R has a mutation status of R258W, The gene ARHGAP45 has a mutation status of S258C, The gene TLE2 has a mutation status of S357P, The gene TNFSF9 has a mutation status of P249H, The gene KANK3 has a mutation status of G621S, The gene ZNF699 has a mutation status of A34G, The gene ZNF433 has a mutation status of C153C, The gene HOOK2 has a mutation status of E260G, The gene ADGRL1 has a mutation status of G1322G, The gene GIPC1 has a mutation status of G6W, The gene BRD4 has a mutation status of L866L, The gene WIZ has a mutation status of R703G, The gene SIN3B has a mutation status of E583G, The gene SIN3B has a mutation status of A584G, The gene UNC13A has a mutation status of S274S, The gene MAST3 has a mutation status of P343S, The gene AC008397.1 has a mutation status of E216*, The gene SUGP1 has a mutation status of T352P, The gene CILP2 has a mutation status of V585G, The gene PRODH2 has a mutation status of V169G, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene B3GNT8 has a mutation status of S82A, The gene CD177 has a mutation status of S364T, The gene SYMPK has a mutation status of D879H, The gene NTF4 has a mutation status of R45L, The gene C19orf81 has a mutation status of T93A, The gene SIGLEC9 has a mutation status of P302S, The gene ZNF600 has a mutation status of R27R, The gene ZNF816 has a mutation status of D143D, The gene NLRP12 has a mutation status of S428S, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of H203R, The gene KIR2DL1 has a mutation status of K237E, The gene ZNF584 has a mutation status of R205*, The gene SIRPA has a mutation status of L44S, The gene EBF4 has a mutation status of P263P, The gene CENPB has a mutation status of L365L, The gene CENPB has a mutation status of A153A, The gene CENPB has a mutation status of T150P, The gene LRRN4 has a mutation status of A82G, The gene LRRN4 has a mutation status of L73L, The gene RRBP1 has a mutation status of H666P, The gene PAX1 has a mutation status of Y386S, The gene FOXA2 has a mutation status of Y186Y, The gene C20orf203 has a mutation status of G131W, The gene BPIFB6 has a mutation status of T96N, The gene CHMP4B has a mutation status of A15A, The gene EIF2S2 has a mutation status of Q266Q, The gene TRPC4AP has a mutation status of V694V, The gene TRPC4AP has a mutation status of L656L, The gene RBM39 has a mutation status of Q424*, The gene SGK2 has a mutation status of L228L, The gene ZSWIM1 has a mutation status of T272I, The gene SLC12A5 has a mutation status of G290G, The gene SLC12A5 has a mutation status of Q682Q, The gene SLC12A5 has a mutation status of D683D, The gene PREX1 has a mutation status of G735W, The gene KCNB1 has a mutation status of V465I, The gene CTCFL has a mutation status of L67L, The gene GNAS has a mutation status of H353P, The gene GNAS has a mutation status of R20R, The gene SLCO4A1 has a mutation status of R665H, The gene RBM11 has a mutation status of E267K, The gene NRIP1 has a mutation status of L132L, The gene USP25 has a mutation status of E192E, The gene BTG3 has a mutation status of R240R, The gene ATP5PF has a mutation status of R73M, The gene LTN1 has a mutation status of F1621F, The gene USP16 has a mutation status of L707L, The gene TIAM1 has a mutation status of F957F, The gene TIAM1 has a mutation status of S186S, The gene HUNK has a mutation status of G69G, The gene HUNK has a mutation status of F73F, The gene SYNJ1 has a mutation status of F396F, The gene SYNJ1 has a mutation status of L387L, The gene PAXBP1 has a mutation status of T384A, The gene PAXBP1 has a mutation status of R103R, The gene PAXBP1 has a mutation status of N87N, The gene OLIG2 has a mutation status of G179G, The gene SON has a mutation status of V2075V, The gene SON has a mutation status of N243S, The gene SLC5A3 has a mutation status of L171L, The gene SIM2 has a mutation status of P322P, The gene TTC3 has a mutation status of S310C, The gene DYRK1A has a mutation status of T653T, The gene DSCAM has a mutation status of L975I, The gene DSCAM has a mutation status of S969S, The gene DSCAM has a mutation status of Q933Q, The gene BACE2 has a mutation status of L308L, The gene BACE2 has a mutation status of A326T, The gene PFKL has a mutation status of C212C, The gene PRMT2 has a mutation status of S135F, The gene TBX1 has a mutation status of N124N, The gene TBX1 has a mutation status of P439P, The gene TBX1 has a mutation status of R442R, The gene PI4KA has a mutation status of L1011L, The gene HIC2 has a mutation status of T612T, The gene HIC2 has a mutation status of P614P, The gene UBE2L3 has a mutation status of P120P, The gene UBE2L3 has a mutation status of L121L, The gene VPREB1 has a mutation status of R120C, The gene HSCB has a mutation status of F15V, The gene NF2 has a mutation status of W74*, The gene TNRC6B has a mutation status of H101H, The gene RANGAP1 has a mutation status of G208W, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SAMM50 has a mutation status of D292G, The gene TAFA5 has a mutation status of A25A, The gene PANX2 has a mutation status of V61V, The gene SELENOO has a mutation status of G644V, The gene MXRA5 has a mutation status of S1147F, The gene ANOS1 has a mutation status of K161R, The gene TXLNG has a mutation status of I398I, The gene MAP3K15 has a mutation status of L1190F, The gene RPS6KA3 has a mutation status of L501L, The gene STARD8 has a mutation status of P653P, The gene STARD8 has a mutation status of G662A, The gene CHIC1 has a mutation status of R74P, The gene ARMCX2 has a mutation status of Q503Q, The gene SAGE1 has a mutation status of C82W, The gene MAGEC2 has a mutation status of R186C, The gene ABCD1 has a mutation status of V86G, The gene MT-ATP6 has a mutation status of L22L, The gene MT-CO3 has a mutation status of E64K, The gene MT-ND5 has a mutation status of S47S
SARC
The gene SAMD11 has a mutation status of R141R, The gene TNFRSF8 has a mutation status of T471P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene ACTL8 has a mutation status of L287L, The gene HSPG2 has a mutation status of P3441S, The gene PABPC4 has a mutation status of T48P, The gene BEND5 has a mutation status of Q191R, The gene YIPF1 has a mutation status of L147V, The gene MYSM1 has a mutation status of S432*, The gene GNG12 has a mutation status of I71V, The gene LRRC53 has a mutation status of Q567E, The gene PRPF38B has a mutation status of D517D, The gene PHTF1 has a mutation status of V82I, The gene NOTCH2 has a mutation status of R72C, The gene NBPF11 has a mutation status of Q55H, The gene LY9 has a mutation status of T277R, The gene TNN has a mutation status of A24P, The gene BRINP2 has a mutation status of N591T, The gene NMNAT2 has a mutation status of D217D, The gene ASPM has a mutation status of L3178P, The gene TMEM183A has a mutation status of 89_94EPCDII>V, The gene RASSF5 has a mutation status of P98P, The gene PLXNA2 has a mutation status of H683Y, The gene C1orf115 has a mutation status of R17S, The gene MIA3 has a mutation status of I387V, The gene PXDN has a mutation status of D379E, The gene TMEM178A has a mutation status of H64P, The gene GGCX has a mutation status of G279G, The gene SMYD1 has a mutation status of V114G, The gene CNOT11 has a mutation status of G43G, The gene IL18R1 has a mutation status of G252R, The gene TMEM182 has a mutation status of G17G, The gene TMEM185B has a mutation status of V54V, The gene LY75-CD302 has a mutation status of Y1525Y, The gene TTN has a mutation status of T20867T, The gene AC053503.6 has a mutation status of H101P, The gene ARMC9 has a mutation status of T671T, The gene HDLBP has a mutation status of N457N, The gene XIRP1 has a mutation status of P26P, The gene RFT1 has a mutation status of V44I, The gene CADPS has a mutation status of E860K, The gene BBX has a mutation status of K540E, The gene CASR has a mutation status of H1010P, The gene KALRN has a mutation status of Q388K, The gene ALDH1L1 has a mutation status of A626A, The gene RHO has a mutation status of V61I, The gene DBR1 has a mutation status of S351R, The gene IGSF10 has a mutation status of A1908A, The gene NMD3 has a mutation status of V96L, The gene HMX1 has a mutation status of S272P, The gene NWD2 has a mutation status of I131V, The gene SMIM14 has a mutation status of I51N, The gene GRSF1 has a mutation status of V171V, The gene MMRN1 has a mutation status of A720P, The gene DDIT4L has a mutation status of C64Y, The gene DDX60 has a mutation status of F39V, The gene IRF2 has a mutation status of K31K, The gene TRIO has a mutation status of N2724S, The gene ANKH has a mutation status of L197L, The gene AGXT2 has a mutation status of R422Q, The gene DEPDC1B has a mutation status of R406H, The gene MRPS27 has a mutation status of L240P, The gene ADGRV1 has a mutation status of L5037fs, The gene MCTP1 has a mutation status of G45G, The gene FER has a mutation status of I202V, The gene SLC22A4 has a mutation status of T394M, The gene CAMLG has a mutation status of V16G, The gene SLC35A4 has a mutation status of Y109Y, The gene PDGFRB has a mutation status of F889F, The gene NKX2-5 has a mutation status of Y253S, The gene FOXQ1 has a mutation status of G108G, The gene F13A1 has a mutation status of E203E, The gene F13A1 has a mutation status of R78H, The gene TMEM14B has a mutation status of A103T, The gene BTN2A1 has a mutation status of G411E, The gene HLA-A has a mutation status of T22T, The gene HLA-DRB5 has a mutation status of Q38W, The gene IP6K3 has a mutation status of H182P, The gene TCP11 has a mutation status of V208M, The gene DNAH8 has a mutation status of G2317G, The gene DEFB113 has a mutation status of P44P, The gene MCM3 has a mutation status of V6G, The gene MCM3 has a mutation status of G3G, The gene MYO6 has a mutation status of H227Y, The gene ESR1 has a mutation status of F97S, The gene PLG has a mutation status of C206C, The gene TTYH3 has a mutation status of Y509S, The gene WIPF3 has a mutation status of I145T, The gene IKZF1 has a mutation status of Y348S, The gene COL1A2 has a mutation status of M1257V, The gene GPC2 has a mutation status of R212C, The gene NYAP1 has a mutation status of H72P, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of R898W, The gene MUC3A has a mutation status of S909S, The gene MUC3A has a mutation status of T1234A, The gene MUC3A has a mutation status of P1241P, The gene PMPCB has a mutation status of V9G, The gene KLF14 has a mutation status of P58S, The gene NOBOX has a mutation status of G152A, The gene NOS3 has a mutation status of L832M, The gene XKR5 has a mutation status of I230V, The gene USP17L2 has a mutation status of T492M, The gene USP17L2 has a mutation status of S484S, The gene PURG has a mutation status of G53G, The gene NRG1 has a mutation status of T435N, The gene ANK1 has a mutation status of S1731S, The gene TRIM55 has a mutation status of A513V, The gene C8orf34 has a mutation status of K183I, The gene RDH10 has a mutation status of L105L, The gene VPS13B has a mutation status of N152K, The gene BOP1 has a mutation status of P188L, The gene CDKN2A has a mutation status of A36G, The gene S1PR3 has a mutation status of T139A, The gene TBC1D2 has a mutation status of V376G, The gene SLC44A1 has a mutation status of S8T, The gene FRRS1L has a mutation status of R51A, The gene DENND1A has a mutation status of R371R, The gene OLFML2A has a mutation status of Y534S, The gene SPTAN1 has a mutation status of S1724S, The gene DDX31 has a mutation status of R672*, The gene OLFM1 has a mutation status of A126V, The gene MRPS2 has a mutation status of T30P, The gene CCDC187 has a mutation status of G877A, The gene CCDC187 has a mutation status of A321T, The gene NOTCH1 has a mutation status of I1440T, The gene ANAPC2 has a mutation status of D445G, The gene ANAPC2 has a mutation status of V303G, The gene PROSER2 has a mutation status of S179P, The gene KIAA1217 has a mutation status of K44M, The gene GAD2 has a mutation status of S61G, The gene GJD4 has a mutation status of G107A, The gene RBP3 has a mutation status of V768G, The gene GLUD1 has a mutation status of P121S, The gene NOC3L has a mutation status of A342A, The gene WBP1L has a mutation status of H314P, The gene MCMBP has a mutation status of N327K, The gene WDR11 has a mutation status of D332E, The gene PNPLA2 has a mutation status of A463A, The gene MUC6 has a mutation status of A20T, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4116S, The gene MRGPRE has a mutation status of H155P, The gene DNHD1 has a mutation status of E918D, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of M269L, The gene ATG2A has a mutation status of P626L, The gene CFL1 has a mutation status of Q119Q, The gene LRP5 has a mutation status of Y1494S, The gene NEU3 has a mutation status of I49T, The gene FUT4 has a mutation status of D341A, The gene IL10RA has a mutation status of W523R, The gene ADAMTS8 has a mutation status of P464P, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene CCNT1 has a mutation status of T192T, The gene DHH has a mutation status of A391V, The gene KRT2 has a mutation status of F198V, The gene TNS2 has a mutation status of Y1044*, The gene CHST11 has a mutation status of T95K, The gene PRDM4 has a mutation status of Q413H, The gene SH2B3 has a mutation status of L6L, The gene RASAL1 has a mutation status of R731Q, The gene FBXW8 has a mutation status of A49D, The gene ORAI1 has a mutation status of A42T, The gene TMEM132B has a mutation status of S702R, The gene POLE has a mutation status of V1270F, The gene ZNF26 has a mutation status of P285P, The gene XPO4 has a mutation status of T154I, The gene CCNA1 has a mutation status of R59I, The gene KPNA3 has a mutation status of D316D, The gene COL4A2 has a mutation status of A725G, The gene NKX2-1 has a mutation status of F122S, The gene LRFN5 has a mutation status of P586S, The gene OTX2 has a mutation status of I73V, The gene FLRT2 has a mutation status of V90V, The gene BCL11B has a mutation status of S2P, The gene HERC2 has a mutation status of A4555A, The gene EPB42 has a mutation status of E629G, The gene ARRDC4 has a mutation status of E48*, The gene ARRDC4 has a mutation status of A54A, The gene BAIAP3 has a mutation status of T367A, The gene TBL3 has a mutation status of T101P, The gene NPIPB13 has a mutation status of P1074R, The gene NETO2 has a mutation status of P162T, The gene CNGB1 has a mutation status of N758T, The gene VPS9D1 has a mutation status of V399G, The gene SCGB1C2 has a mutation status of T22T, The gene SPNS3 has a mutation status of I457N, The gene KCTD11 has a mutation status of E228G, The gene KCTD11 has a mutation status of V229G, The gene ASIC2 has a mutation status of L128F, The gene CCL4L2 has a mutation status of P67R, The gene HSF5 has a mutation status of P102P, The gene TANC2 has a mutation status of P1448P, The gene GRIN2C has a mutation status of C1150F, The gene ENPP7 has a mutation status of T68P, The gene SLC38A10 has a mutation status of V186G, The gene CD7 has a mutation status of D213G, The gene MOCOS has a mutation status of E659K, The gene MUC16 has a mutation status of M4568V, The gene DNM2 has a mutation status of R846S, The gene TIMM29 has a mutation status of R47S, The gene ZNF443 has a mutation status of E216E, The gene CC2D1A has a mutation status of G9G, The gene ADGRL1 has a mutation status of G1322G, The gene BRD4 has a mutation status of R876G, The gene BRD4 has a mutation status of N875T, The gene ZNF493 has a mutation status of H763R, The gene SLC7A9 has a mutation status of R397I, The gene HAUS5 has a mutation status of T412P, The gene PSMD8 has a mutation status of V26G, The gene PSMD8 has a mutation status of I84T, The gene FBXO27 has a mutation status of G2G, The gene CEACAM6 has a mutation status of V205I, The gene ZNF574 has a mutation status of E890E, The gene CKM has a mutation status of T313P, The gene SIGLEC10 has a mutation status of P501L, The gene LILRB3 has a mutation status of L243F, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene ZBTB45 has a mutation status of V140V, The gene SIRPA has a mutation status of L44S, The gene PAX1 has a mutation status of G390A, The gene FOXA2 has a mutation status of G122G, The gene NCOA6 has a mutation status of K513*, The gene MYH7B has a mutation status of L1474L, The gene ACTR5 has a mutation status of V80G, The gene DHX35 has a mutation status of Y249Y, The gene SAMSN1 has a mutation status of T204T, The gene DOP1B has a mutation status of M2010T, The gene POTEH has a mutation status of W34*, The gene TRMT2A has a mutation status of L214I, The gene GSTT4 has a mutation status of Q197R, The gene CSF2RB has a mutation status of R517G, The gene KCTD17 has a mutation status of S206P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene RTL6 has a mutation status of M123I, The gene MXRA5 has a mutation status of F141V, The gene EIF2S3 has a mutation status of G3G, The gene CHST7 has a mutation status of A405A, The gene PPP1R3F has a mutation status of G221V, The gene FRMPD3 has a mutation status of M169T, The gene RBMXL3 has a mutation status of G927G, The gene ABCD1 has a mutation status of P53H, The gene RENBP has a mutation status of V58G, The gene PLXNA3 has a mutation status of R1361R, The gene MT-ND2 has a mutation status of A109A, The gene MT-ND4 has a mutation status of L238P, The gene MT-ND4 has a mutation status of S448S, The gene MT-ND5 has a mutation status of T556I, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of L49L, The gene MT-CYB has a mutation status of Y75Y, The gene MT-CYB has a mutation status of T158A
DLBC
The gene KLHL17 has a mutation status of T640P, The gene PRAMEF1 has a mutation status of F280L, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of M105L, The gene KIF17 has a mutation status of A994T, The gene MAP7D1 has a mutation status of S378T, The gene MAP7D1 has a mutation status of P379P, The gene MTF1 has a mutation status of P430P, The gene EBNA1BP2 has a mutation status of E41D, The gene KCND3 has a mutation status of I111L, The gene VANGL1 has a mutation status of S338*, The gene VTCN1 has a mutation status of F174C, The gene NBPF10 has a mutation status of E664E, The gene NBPF14 has a mutation status of S1376P, The gene OBSCN has a mutation status of Y6300F, The gene TAF1B has a mutation status of S323N, The gene CAD has a mutation status of A1971A, The gene MTIF2 has a mutation status of A50V, The gene RAB6C has a mutation status of T27T, The gene CHRNA1 has a mutation status of G94S, The gene TTN has a mutation status of V1518A, The gene HECW2 has a mutation status of P358P, The gene NOP58 has a mutation status of H144Y, The gene PIKFYVE has a mutation status of H439P, The gene SLC16A14 has a mutation status of F93F, The gene THUMPD3 has a mutation status of E100Q, The gene IL17RC has a mutation status of V25L, The gene ABHD14B has a mutation status of P81S, The gene POLQ has a mutation status of D1936Y, The gene SNX4 has a mutation status of P5P, The gene AMOTL2 has a mutation status of R497Q, The gene VWA5B2 has a mutation status of H669Q, The gene TNK2 has a mutation status of R957Q, The gene NCBP2AS2 has a mutation status of P87T, The gene BDH1 has a mutation status of K49T, The gene FYTTD1 has a mutation status of I162M, The gene PDE6B has a mutation status of R309Q, The gene MAN2B2 has a mutation status of R411H, The gene SORCS2 has a mutation status of V829M, The gene CLNK has a mutation status of R362C, The gene APBB2 has a mutation status of P214R, The gene SYNPO2 has a mutation status of V216V, The gene SYNPO2 has a mutation status of C307R, The gene MAML3 has a mutation status of P727P, The gene NR3C2 has a mutation status of F956L, The gene MSMO1 has a mutation status of H153R, The gene WDR17 has a mutation status of V833V, The gene GOLPH3 has a mutation status of D54D, The gene ERAP2 has a mutation status of T939T, The gene DMXL1 has a mutation status of E1675D, The gene ADAMTS19 has a mutation status of E404D, The gene CHSY3 has a mutation status of V499I, The gene PCDHGC3 has a mutation status of G44S, The gene PCDH12 has a mutation status of R308*, The gene SLC6A7 has a mutation status of R260H, The gene HMMR has a mutation status of L202L, The gene SLIT3 has a mutation status of T1295M, The gene FOXI1 has a mutation status of S236N, The gene SKIV2L has a mutation status of L839V, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene FANCE has a mutation status of E56D, The gene FAM83B has a mutation status of R480L, The gene ARFGEF3 has a mutation status of V1901G, The gene NOX3 has a mutation status of W53L, The gene UNC93A has a mutation status of F221L, The gene UNCX has a mutation status of S291R, The gene BRAT1 has a mutation status of A642G, The gene AP5Z1 has a mutation status of L73R, The gene HECW1 has a mutation status of V1150T, The gene AUTS2 has a mutation status of A970A, The gene AUTS2 has a mutation status of N973I, The gene AKAP9 has a mutation status of K703Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of T1234A, The gene PRSS1 has a mutation status of N77N, The gene DLGAP2 has a mutation status of D391E, The gene ERI1 has a mutation status of L18M, The gene FDFT1 has a mutation status of A80A, The gene FDFT1 has a mutation status of K254K, The gene UBR5 has a mutation status of 1886_1889LRTL>F, The gene TAF2 has a mutation status of R795H, The gene ADCY8 has a mutation status of S812L, The gene TRAPPC9 has a mutation status of S925N, The gene PLEC has a mutation status of A3447V, The gene HSF1 has a mutation status of R296H, The gene FOXD4 has a mutation status of Q185Q, The gene ADAMTSL2 has a mutation status of A840A, The gene AGPAT2 has a mutation status of A251A, The gene AJM1 has a mutation status of G487V, The gene PARD3 has a mutation status of H614H, The gene PRF1 has a mutation status of P22L, The gene SLC29A3 has a mutation status of N329N, The gene MYBPC3 has a mutation status of P4P, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene SPTBN2 has a mutation status of A784A, The gene SPTBN2 has a mutation status of E403G, The gene KDM4D has a mutation status of D499E, The gene BIRC2 has a mutation status of V303L, The gene DRD2 has a mutation status of R15K, The gene KMT2A has a mutation status of R130W, The gene CBL has a mutation status of P504P, The gene GPR162 has a mutation status of W288R, The gene ABCC9 has a mutation status of R939W, The gene LRRIQ1 has a mutation status of I583V, The gene LRCH1 has a mutation status of H21Y, The gene RB1 has a mutation status of R698I, The gene KLHL1 has a mutation status of Y708Y, The gene GPC6 has a mutation status of A36A, The gene SOX1 has a mutation status of Y2F, The gene ALDH6A1 has a mutation status of R107C, The gene SPATA7 has a mutation status of G574G, The gene ITPK1 has a mutation status of V293I, The gene SERPINA11 has a mutation status of G177V, The gene CRIP1 has a mutation status of N8N, The gene MYO5A has a mutation status of P16A, The gene UBL7 has a mutation status of M212V, The gene ZNF592 has a mutation status of R75C, The gene RCCD1 has a mutation status of R36R, The gene RCCD1 has a mutation status of G38S, The gene ASB7 has a mutation status of G214R, The gene CREBBP has a mutation status of G1757G, The gene ZFP3 has a mutation status of S98I, The gene CLDN7 has a mutation status of S172A, The gene SENP3 has a mutation status of S330S, The gene HS3ST3B1 has a mutation status of A70A, The gene MYO18A has a mutation status of E1896G, The gene CCL4L2 has a mutation status of P67R, The gene MRM1 has a mutation status of V149fs, The gene GFAP has a mutation status of R49W, The gene CSH2 has a mutation status of E114G, The gene KCNJ2 has a mutation status of N318S, The gene SLC25A10 has a mutation status of *288C, The gene ZNF750 has a mutation status of K37K, The gene ASXL3 has a mutation status of K406E, The gene ZNF532 has a mutation status of V580M, The gene DPP9 has a mutation status of G536G, The gene RFX1 has a mutation status of GGGGGGGGGGGGGSG387del, The gene CALR3 has a mutation status of M13V, The gene ZNF254 has a mutation status of N140S, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene NKPD1 has a mutation status of G152R, The gene PRKD2 has a mutation status of A678V, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene FERMT1 has a mutation status of Q223H, The gene LAMA5 has a mutation status of L1510Q, The gene KRTAP15-1 has a mutation status of N39D, The gene SUN2 has a mutation status of A195P, The gene L3MBTL2 has a mutation status of T168T, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TUBGCP6 has a mutation status of L1171L, The gene WWC3 has a mutation status of D176N, The gene HUWE1 has a mutation status of P2645H, The gene SLC7A3 has a mutation status of A85A, The gene CITED1 has a mutation status of N171S, The gene CLDN2 has a mutation status of P150Q, The gene GRIA3 has a mutation status of Q538H, The gene MAGEA10 has a mutation status of A292S, The gene CAMTA1 has a mutation status of A812T, The gene UTS2 has a mutation status of R131Q, The gene AADACL4 has a mutation status of R93C, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene EPHA2 has a mutation status of E914G, The gene KIF17 has a mutation status of A994T, The gene TENT5B has a mutation status of S65R, The gene GJA4 has a mutation status of A140V, The gene PPCS has a mutation status of V37G, The gene EBNA1BP2 has a mutation status of E41D, The gene TACSTD2 has a mutation status of T256T, The gene KCND3 has a mutation status of I111L, The gene VTCN1 has a mutation status of F174C, The gene SPAG17 has a mutation status of V1170V, The gene NBPF20 has a mutation status of L3033F, The gene NBPF10 has a mutation status of E664E, The gene NBPF14 has a mutation status of S1376P, The gene OTUD7B has a mutation status of A357A, The gene DENND1B has a mutation status of V426A, The gene NR5A2 has a mutation status of M428V, The gene IPO9 has a mutation status of V556M, The gene PIK3C2B has a mutation status of Q1596K, The gene PLXNA2 has a mutation status of C826G, The gene DNAH14 has a mutation status of R4418C, The gene OBSCN has a mutation status of Y6300F, The gene TAF1B has a mutation status of S323N, The gene LRATD1 has a mutation status of H71R, The gene CAD has a mutation status of A1971A, The gene XDH has a mutation status of T934A, The gene OXER1 has a mutation status of A326P, The gene OXER1 has a mutation status of S325P, The gene PPP1R21 has a mutation status of A238T, The gene MTIF2 has a mutation status of A50V, The gene CD8B has a mutation status of T14K, The gene SMYD1 has a mutation status of V114G, The gene SMYD1 has a mutation status of E115G, The gene PSD4 has a mutation status of F870S, The gene GAD1 has a mutation status of T576A, The gene CHRNA1 has a mutation status of G94S, The gene TTN has a mutation status of T4744A, The gene HECW2 has a mutation status of P358P, The gene NOP58 has a mutation status of H144Y, The gene INO80D has a mutation status of E619G, The gene NEK10 has a mutation status of T58R, The gene SCN11A has a mutation status of P77S, The gene GASK1A has a mutation status of W185L, The gene COL7A1 has a mutation status of G762G, The gene KLHDC8B has a mutation status of M17fs, The gene BSN has a mutation status of S746R, The gene GMPPB has a mutation status of G9S, The gene DOCK3 has a mutation status of P1852fs, The gene ABHD14B has a mutation status of P81S, The gene OR5AC2 has a mutation status of V27I, The gene GRAMD1C has a mutation status of N41K, The gene POLQ has a mutation status of D1936Y, The gene ATR has a mutation status of T415A, The gene ABCF3 has a mutation status of M534I, The gene BDH1 has a mutation status of K49T, The gene MAN2B2 has a mutation status of R411H, The gene CLNK has a mutation status of R362C, The gene FGFBP1 has a mutation status of V27fs, The gene CLRN2 has a mutation status of T226T, The gene APBB2 has a mutation status of P214R, The gene SYNPO2 has a mutation status of V216V, The gene SYNPO2 has a mutation status of C307R, The gene MAML3 has a mutation status of P727P, The gene MSMO1 has a mutation status of H153R, The gene WDR17 has a mutation status of V833V, The gene RAI14 has a mutation status of I145T, The gene PLPP1 has a mutation status of V134I, The gene RASA1 has a mutation status of G59G, The gene RASA1 has a mutation status of G62G, The gene ERAP2 has a mutation status of T939T, The gene TSLP has a mutation status of H74Y, The gene DMXL1 has a mutation status of E1675D, The gene FAM170A has a mutation status of E290D, The gene ADAMTS19 has a mutation status of E404D, The gene CHSY3 has a mutation status of V499I, The gene PCDHA2 has a mutation status of A703T, The gene PCDHB2 has a mutation status of G596G, The gene PCDHGC3 has a mutation status of G44S, The gene PCDH12 has a mutation status of R308*, The gene SLC6A7 has a mutation status of R260H, The gene HMMR has a mutation status of L202L, The gene SLIT3 has a mutation status of T1295M, The gene H1-2 has a mutation status of G103G, The gene HLA-A has a mutation status of I121R, The gene AGER has a mutation status of R77P, The gene HLA-DRB1 has a mutation status of S66N, The gene AARS2 has a mutation status of V59G, The gene TMEM14A has a mutation status of R45H, The gene EYS has a mutation status of G1108R, The gene RNF217 has a mutation status of E3D, The gene ARFGEF3 has a mutation status of A1076A, The gene ZC2HC1B has a mutation status of R146H, The gene EPM2A has a mutation status of V8V, The gene ESR1 has a mutation status of G20G, The gene SYNE1 has a mutation status of T4191T, The gene SYNE1 has a mutation status of M1683I, The gene UNC93A has a mutation status of F221L, The gene AP5Z1 has a mutation status of L73R, The gene USP42 has a mutation status of C1059C, The gene NFE2L3 has a mutation status of A175A, The gene STARD3NL has a mutation status of G206D, The gene HECW1 has a mutation status of V1150T, The gene ELN has a mutation status of G340C, The gene AKAP9 has a mutation status of K703Q, The gene ZAN has a mutation status of P594P, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene MUC3A has a mutation status of T1234A, The gene PLOD3 has a mutation status of A646V, The gene MKRN1 has a mutation status of I342V, The gene ZNF425 has a mutation status of C391R, The gene FDFT1 has a mutation status of A80A, The gene FDFT1 has a mutation status of K254K, The gene TAF2 has a mutation status of R795H, The gene ADCY8 has a mutation status of S812L, The gene PLEC has a mutation status of A3447V, The gene HSF1 has a mutation status of R296H, The gene DGAT1 has a mutation status of V301G, The gene FOXD4 has a mutation status of Q185Q, The gene SMARCA2 has a mutation status of R559K, The gene FREM1 has a mutation status of H185H, The gene ANKRD18A has a mutation status of R547H, The gene TMOD1 has a mutation status of V212L, The gene CRB2 has a mutation status of D978G, The gene HMCN2 has a mutation status of V4446V, The gene ADAMTSL2 has a mutation status of A840A, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of H128H, The gene SNAPC4 has a mutation status of V1292G, The gene AGPAT2 has a mutation status of A251A, The gene PARD3 has a mutation status of H614H, The gene CTNNA3 has a mutation status of V571A, The gene PRF1 has a mutation status of P22L, The gene SLC29A3 has a mutation status of N329N, The gene CDH23 has a mutation status of G3104G, The gene RAB11FIP2 has a mutation status of D368fs, The gene INPP5F has a mutation status of V640A, The gene MMP26 has a mutation status of I130I, The gene DNHD1 has a mutation status of R4615R, The gene BBOX1 has a mutation status of C3F, The gene PSMC3 has a mutation status of Q14K, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MYRF has a mutation status of S42C, The gene SPTBN2 has a mutation status of A784A, The gene FAT3 has a mutation status of G1978D, The gene ENDOD1 has a mutation status of L361M, The gene BIRC2 has a mutation status of V303L, The gene KMT2A has a mutation status of R130W, The gene BCL9L has a mutation status of P951P, The gene GLB1L3 has a mutation status of R506K, The gene DCP1B has a mutation status of I16T, The gene GPR162 has a mutation status of W288R, The gene SLC2A14 has a mutation status of T481T, The gene ABCC9 has a mutation status of R939W, The gene GDF11 has a mutation status of L9L, The gene CYP27B1 has a mutation status of R453C, The gene LRRIQ1 has a mutation status of I583V, The gene CHST11 has a mutation status of T95K, The gene SETD1B has a mutation status of T622N, The gene PIWIL1 has a mutation status of A681T, The gene ZAR1L has a mutation status of T42P, The gene RB1 has a mutation status of R698I, The gene RCBTB2 has a mutation status of L369I, The gene PCDH17 has a mutation status of *1160fs, The gene KLHL1 has a mutation status of Y708Y, The gene GPC6 has a mutation status of A36A, The gene COL4A2 has a mutation status of G1143C, The gene OR4M1 has a mutation status of S156Y, The gene MDGA2 has a mutation status of G104C, The gene SOS2 has a mutation status of R20L, The gene ALDH6A1 has a mutation status of R107C, The gene SPATA7 has a mutation status of G574G, The gene RIN3 has a mutation status of R949C, The gene ITPK1 has a mutation status of V293I, The gene DYNC1H1 has a mutation status of P2044P, The gene HERC2 has a mutation status of S895A, The gene SLC12A1 has a mutation status of M195V, The gene SLC12A1 has a mutation status of A337A, The gene MYO5A has a mutation status of P16A, The gene KBTBD13 has a mutation status of T206M, The gene UBL7 has a mutation status of M212V, The gene ZNF592 has a mutation status of R75C, The gene ASB7 has a mutation status of G214R, The gene CACNA1H has a mutation status of L1540I, The gene CACNA1H has a mutation status of M1757V, The gene PKD1 has a mutation status of T1589T, The gene CORO7 has a mutation status of R238R, The gene CARHSP1 has a mutation status of P42P, The gene NTAN1 has a mutation status of G84C, The gene NKD1 has a mutation status of I38I, The gene PSKH1 has a mutation status of R271R, The gene ZNF19 has a mutation status of R223K, The gene CTRB1 has a mutation status of Q175*, The gene KCNG4 has a mutation status of A311T, The gene WDR81 has a mutation status of L721I, The gene SENP3 has a mutation status of S330S, The gene KDM6B has a mutation status of T896fs, The gene HS3ST3B1 has a mutation status of A70A, The gene ABHD15 has a mutation status of T151T, The gene LIG3 has a mutation status of S294S, The gene CCL4L2 has a mutation status of P67R, The gene GFAP has a mutation status of R49W, The gene CLTC has a mutation status of A352D, The gene MED13 has a mutation status of R1319*, The gene KCNJ2 has a mutation status of N318S, The gene TEPSIN has a mutation status of G213G, The gene ZNF750 has a mutation status of K37K, The gene TXNDC2 has a mutation status of I135I, The gene ASXL3 has a mutation status of K406E, The gene LOXHD1 has a mutation status of Y1958*, The gene ZNF532 has a mutation status of V580M, The gene EEF2 has a mutation status of A528G, The gene ZNF560 has a mutation status of C689C, The gene SHFL has a mutation status of W191L, The gene SLC44A2 has a mutation status of R590I, The gene DOCK6 has a mutation status of S1484S, The gene ZNF69 has a mutation status of T269S, The gene CALR3 has a mutation status of M13V, The gene C19orf44 has a mutation status of D346E, The gene ZNF254 has a mutation status of N140S, The gene ZNF568 has a mutation status of S66S, The gene ZNF230 has a mutation status of V122A, The gene PRKD2 has a mutation status of A678V, The gene SPHK2 has a mutation status of L343P, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene ITPA has a mutation status of I140I, The gene AL035461.4 has a mutation status of M383T, The gene FERMT1 has a mutation status of Q223H, The gene GZF1 has a mutation status of Y505H, The gene VSX1 has a mutation status of S139S, The gene ASXL1 has a mutation status of S304C, The gene BPIFB4 has a mutation status of K417N, The gene BPIFA1 has a mutation status of L129L, The gene KIAA1755 has a mutation status of R1000C, The gene CTSA has a mutation status of R283H, The gene ZNF335 has a mutation status of G368G, The gene LAMA5 has a mutation status of L1510Q, The gene SRMS has a mutation status of E69G, The gene GMEB2 has a mutation status of V409I, The gene KRTAP15-1 has a mutation status of N39D, The gene SLC19A1 has a mutation status of A78V, The gene GSTT4 has a mutation status of Q197R, The gene ZNRF3 has a mutation status of E649G, The gene SUN2 has a mutation status of A195P, The gene L3MBTL2 has a mutation status of T168T, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TUBGCP6 has a mutation status of L1171L, The gene SHANK3 has a mutation status of T592T, The gene SHROOM2 has a mutation status of A1085T, The gene TMSB4X has a mutation status of A8V, The gene DDX3X has a mutation status of S662I, The gene PHF8 has a mutation status of D807Y, The gene STARD8 has a mutation status of G662A, The gene P2RY4 has a mutation status of Y197N, The gene SLC7A3 has a mutation status of A85A, The gene BX276092.9 has a mutation status of L256I, The gene CITED1 has a mutation status of N171S, The gene CLDN2 has a mutation status of P150Q, The gene KIAA1210 has a mutation status of M222T, The gene GRIA3 has a mutation status of Q538H, The gene OCRL has a mutation status of G534G, The gene BCORL1 has a mutation status of L1132P, The gene SOX3 has a mutation status of S288N, The gene CNGA2 has a mutation status of D662E, The gene MAGEA10 has a mutation status of A292S, The gene PLXNB3 has a mutation status of A1263T, The gene MT-CO1 has a mutation status of H291H, The gene MT-ND3 has a mutation status of L84L
SARC
The gene MTOR has a mutation status of L1129P, The gene HTR6 has a mutation status of V369V, The gene CRYBG2 has a mutation status of R1505C, The gene ADGRB2 has a mutation status of A231G, The gene CSMD2 has a mutation status of I921I, The gene GUCA2B has a mutation status of T109T, The gene KLF18 has a mutation status of P59L, The gene CCDC18 has a mutation status of L1437F, The gene PPM1J has a mutation status of A8A, The gene POGZ has a mutation status of S329F, The gene C1orf68 has a mutation status of P165L, The gene PRCC has a mutation status of G103G, The gene ARHGEF11 has a mutation status of E721V, The gene APCS has a mutation status of P196A, The gene TDRD5 has a mutation status of S96R, The gene B3GALT2 has a mutation status of I391T, The gene NAV1 has a mutation status of A11E, The gene RNPEP has a mutation status of K190T, The gene MAPKAPK2 has a mutation status of Q113P, The gene NVL has a mutation status of K226N, The gene OBSCN has a mutation status of F7436fs, The gene H3-4 has a mutation status of E74K, The gene ZNF496 has a mutation status of P292T, The gene OR2T33 has a mutation status of L205P, The gene MFSD2B has a mutation status of L67I, The gene DNMT3A has a mutation status of A462V, The gene CAPN14 has a mutation status of I565T, The gene XDH has a mutation status of G739C, The gene HEATR5B has a mutation status of A2044A, The gene MTA3 has a mutation status of G392E, The gene EML6 has a mutation status of D314E, The gene RTN4 has a mutation status of R91Q, The gene BCL11A has a mutation status of D798N, The gene KIAA1841 has a mutation status of E645E, The gene AFTPH has a mutation status of S216R, The gene CREG2 has a mutation status of Q237K, The gene ST6GAL2 has a mutation status of R77C, The gene ERCC3 has a mutation status of E707G, The gene ARHGEF4 has a mutation status of R468Q, The gene PLEKHB2 has a mutation status of Y157*, The gene PLEKHB2 has a mutation status of T154R, The gene MBD5 has a mutation status of P1118Q, The gene BARD1 has a mutation status of A721T, The gene GPR55 has a mutation status of F199C, The gene COPS9 has a mutation status of A8D, The gene KIF1A has a mutation status of R1344H, The gene GRM7 has a mutation status of G332R, The gene CAMK1 has a mutation status of T177T, The gene PRRT3 has a mutation status of G253R, The gene CCK has a mutation status of I92V, The gene TGM4 has a mutation status of T163T, The gene SACM1L has a mutation status of A52T, The gene C3orf62 has a mutation status of R19G, The gene ALDH1L1 has a mutation status of C27Y, The gene PLXNA1 has a mutation status of F41L, The gene SENP2 has a mutation status of T265A, The gene ST6GAL1 has a mutation status of K88Q, The gene SH3BP2 has a mutation status of R477Q, The gene ANAPC4 has a mutation status of C271S, The gene NOA1 has a mutation status of R193L, The gene RASGEF1B has a mutation status of E128Q, The gene EGF has a mutation status of R221T, The gene PRDM5 has a mutation status of K610E, The gene FHDC1 has a mutation status of R959R, The gene TRIML1 has a mutation status of Y298C, The gene PDZD2 has a mutation status of G1892V, The gene TARS1 has a mutation status of I509L, The gene ELOVL7 has a mutation status of M75I, The gene ARHGEF28 has a mutation status of P742Q, The gene ZBED3 has a mutation status of L155A, The gene CHSY3 has a mutation status of Q365K, The gene PCDHB13 has a mutation status of D684N, The gene PPP2R2B has a mutation status of L120L, The gene TCOF1 has a mutation status of K1380del, The gene FAT2 has a mutation status of G4306V, The gene CCNJL has a mutation status of T271T, The gene PRR7 has a mutation status of H89Q, The gene RASGEF1C has a mutation status of E433D, The gene IRF4 has a mutation status of P437P, The gene DSP has a mutation status of K906*, The gene BMP6 has a mutation status of V297A, The gene H2AC16 has a mutation status of R30P, The gene PPP1R10 has a mutation status of E339G, The gene HLA-DRB5 has a mutation status of I248L, The gene SLC26A8 has a mutation status of G110G, The gene KCNK16 has a mutation status of D275N, The gene TTBK1 has a mutation status of G84G, The gene MCM3 has a mutation status of G3G, The gene PHF3 has a mutation status of R866W, The gene CEP162 has a mutation status of A173A, The gene USP45 has a mutation status of Q516H, The gene TSPYL4 has a mutation status of R157S, The gene ECT2L has a mutation status of S91S, The gene NMBR has a mutation status of D297H, The gene RAB32 has a mutation status of G3G, The gene RAB32 has a mutation status of G4G, The gene LPA has a mutation status of T1257M, The gene PRKN has a mutation status of A92V, The gene BZW2 has a mutation status of E384E, The gene ABCB5 has a mutation status of L972L, The gene AKAP9 has a mutation status of Q3601Q, The gene SAMD9L has a mutation status of Q1381fs, The gene LMTK2 has a mutation status of Q661Q, The gene FBXO24 has a mutation status of M207V, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of T1370I, The gene MUC3A has a mutation status of F1372I, The gene MUC17 has a mutation status of T2355M, The gene RBM28 has a mutation status of P694L, The gene PRRT4 has a mutation status of L402V, The gene PARP12 has a mutation status of R128T, The gene PRSS1 has a mutation status of N77N, The gene FASTK has a mutation status of G51S, The gene LMBR1 has a mutation status of L206L, The gene CSMD1 has a mutation status of Y2080F, The gene MFHAS1 has a mutation status of D327G, The gene BMP1 has a mutation status of S692F, The gene NUGGC has a mutation status of A682A, The gene ADGRA2 has a mutation status of K1184R, The gene IKBKB has a mutation status of R118W, The gene CHD7 has a mutation status of S956S, The gene VCPIP1 has a mutation status of T23T, The gene ZFHX4 has a mutation status of G1086D, The gene ZBTB10 has a mutation status of K304I, The gene CHMP4C has a mutation status of S13C, The gene UQCRB has a mutation status of H122Q, The gene SPAG1 has a mutation status of I95fs, The gene TRMT12 has a mutation status of A22V, The gene LRATD2 has a mutation status of P21S, The gene SLA has a mutation status of D173S, The gene FAM135B has a mutation status of G983G, The gene CYP11B1 has a mutation status of P562L, The gene RHPN1 has a mutation status of E618D, The gene PLEC has a mutation status of R2004W, The gene DOCK8 has a mutation status of Y1969*, The gene GNE has a mutation status of T3A, The gene RORB has a mutation status of G154S, The gene VPS13A has a mutation status of M1245V, The gene ERCC6L2 has a mutation status of R242R, The gene SUSD1 has a mutation status of Q201E, The gene STRBP has a mutation status of Y647C, The gene COL5A1 has a mutation status of P1494L, The gene KCNT1 has a mutation status of S1178S, The gene CCDC187 has a mutation status of L747L, The gene SEC16A has a mutation status of P1887S, The gene TUBB4B has a mutation status of F20C, The gene TOR4A has a mutation status of S117N, The gene CDC123 has a mutation status of S137S, The gene DNAJC1 has a mutation status of L505L, The gene CCDC7 has a mutation status of D936fs, The gene FAM13C has a mutation status of P423P, The gene JMJD1C has a mutation status of S1460S, The gene CFAP70 has a mutation status of L1056V, The gene SFTPA1 has a mutation status of P20L, The gene PRXL2A has a mutation status of V107I, The gene TNKS2 has a mutation status of I347I, The gene SLIT1 has a mutation status of A346S, The gene BTRC has a mutation status of M160L, The gene NEURL1 has a mutation status of G438R, The gene CPXM2 has a mutation status of R406H, The gene MUC5AC has a mutation status of D3964D, The gene CARS1 has a mutation status of E189E, The gene DEPDC7 has a mutation status of T123T, The gene TTC17 has a mutation status of I603F, The gene MADD has a mutation status of K1584R, The gene PTPRJ has a mutation status of T781T, The gene OR4C5 has a mutation status of A42S, The gene TRIM51 has a mutation status of L41I, The gene OR8K1 has a mutation status of Y241Y, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene CD5 has a mutation status of Y13Y, The gene RAB3IL1 has a mutation status of A183S, The gene RAB3IL1 has a mutation status of T165T, The gene CCS has a mutation status of N142K, The gene PC has a mutation status of T391T, The gene GRK2 has a mutation status of N275N, The gene MAP6 has a mutation status of R203R, The gene TSKU has a mutation status of P326H, The gene FAT3 has a mutation status of V4431L, The gene IZUMO1R has a mutation status of E63E, The gene OR6M1 has a mutation status of T99R, The gene CCND2 has a mutation status of P281A, The gene SCNN1A has a mutation status of R204W, The gene TAS2R8 has a mutation status of A112A, The gene TAS2R9 has a mutation status of L108L, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene RPAP3 has a mutation status of E657K, The gene NCKAP5L has a mutation status of A858D, The gene ARHGEF25 has a mutation status of T360N, The gene TBC1D30 has a mutation status of N406N, The gene LEMD3 has a mutation status of L367F, The gene MYRFL has a mutation status of R454R, The gene UTP20 has a mutation status of I1873T, The gene STAB2 has a mutation status of D816D, The gene CHST11 has a mutation status of T95K, The gene BTBD11 has a mutation status of P278T, The gene ACACB has a mutation status of C1515C, The gene RBM19 has a mutation status of E264*, The gene SUCLA2 has a mutation status of R20G, The gene ATP7B has a mutation status of I582V, The gene RBM23 has a mutation status of G190G, The gene ADCY4 has a mutation status of V393F, The gene TOGARAM1 has a mutation status of C1283S, The gene TRIM9 has a mutation status of T230T, The gene FNTB has a mutation status of R313H, The gene POMT2 has a mutation status of W58G, The gene UNC79 has a mutation status of W1993*, The gene JAG2 has a mutation status of D888Y, The gene EMC4 has a mutation status of A18D, The gene LPCAT4 has a mutation status of D344D, The gene SPTBN5 has a mutation status of E913G, The gene LEO1 has a mutation status of G481G, The gene LCTL has a mutation status of R366C, The gene NEO1 has a mutation status of S161C, The gene CCDC33 has a mutation status of K33N, The gene SNUPN has a mutation status of P291L, The gene GOLGA6L10 has a mutation status of L399P, The gene GOLGA6L9 has a mutation status of D291N, The gene GRIN2A has a mutation status of V1018M, The gene ACSM5 has a mutation status of I166I, The gene ANKS4B has a mutation status of I363V, The gene INO80E has a mutation status of A104S, The gene PRR14 has a mutation status of P4P, The gene ARMC5 has a mutation status of C273S, The gene ADCY7 has a mutation status of V110V, The gene CDH8 has a mutation status of V604V, The gene ANKRD11 has a mutation status of P2018P, The gene ANKRD11 has a mutation status of A2017P, The gene GEMIN4 has a mutation status of K117R, The gene ZZEF1 has a mutation status of A2953P, The gene TP53 has a mutation status of R213Q, The gene MYH3 has a mutation status of G361R, The gene TRIM16L has a mutation status of Q136H, The gene SLFN14 has a mutation status of E792E, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP4-8 has a mutation status of CISSCCRPSCCVSSCCKPQCCQSVCCQPNCCRPSC95del, The gene MYCBPAP has a mutation status of R252Q, The gene CLTC has a mutation status of T1301I, The gene LRRC37A3 has a mutation status of P1140P, The gene BPTF has a mutation status of G1657S, The gene TTYH2 has a mutation status of R368Q, The gene RECQL5 has a mutation status of R182H, The gene TRIM65 has a mutation status of A390T, The gene BAHCC1 has a mutation status of H279P, The gene ANKRD12 has a mutation status of S717S, The gene CEP192 has a mutation status of M2378V, The gene DSG2 has a mutation status of P97R, The gene TMEM259 has a mutation status of P233P, The gene MIDN has a mutation status of S108C, The gene PTPRS has a mutation status of G1416C, The gene GPR108 has a mutation status of F403L, The gene PNPLA6 has a mutation status of E393E, The gene FBN3 has a mutation status of L978L, The gene ZNF317 has a mutation status of G480R, The gene ZNF561 has a mutation status of C133R, The gene DNMT1 has a mutation status of K335R, The gene MAP1S has a mutation status of A2V, The gene ARRDC2 has a mutation status of G245G, The gene ZNF850 has a mutation status of F290F, The gene FCGBP has a mutation status of A1165fs, The gene FCGBP has a mutation status of E1160fs, The gene PRX has a mutation status of R121W, The gene ZNF224 has a mutation status of K314T, The gene ZNF235 has a mutation status of S104P, The gene NOP53 has a mutation status of R36R, The gene SULT2B1 has a mutation status of G279G, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA4 has a mutation status of S302P, The gene LILRB1 has a mutation status of P3S, The gene FAM71E2 has a mutation status of V589M, The gene ZNF837 has a mutation status of R457Q, The gene SLC27A5 has a mutation status of A240T, The gene SLC4A11 has a mutation status of I674F, The gene SULF2 has a mutation status of N241N, The gene LAMA5 has a mutation status of L2185P, The gene LCA5L has a mutation status of H203R, The gene IGSF5 has a mutation status of T405N, The gene GSTT4 has a mutation status of Q197R, The gene GRK3 has a mutation status of I150V, The gene OSBP2 has a mutation status of L494P, The gene INPP5J has a mutation status of P52S, The gene CHADL has a mutation status of G110G, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TTLL8 has a mutation status of A802V, The gene PLXNB2 has a mutation status of E33E, The gene TBL1X has a mutation status of N215T, The gene SSX5 has a mutation status of S74S, The gene SHROOM4 has a mutation status of R409C, The gene ITIH6 has a mutation status of E551*, The gene ARHGEF9 has a mutation status of K288K, The gene STARD8 has a mutation status of G662A, The gene RTL5 has a mutation status of P141L, The gene TEX13B has a mutation status of A153A, The gene COL4A6 has a mutation status of T1655T, The gene CTAG2 has a mutation status of A60T, The gene RPS4Y2 has a mutation status of S32S, The gene MT-ND1 has a mutation status of W185W, The gene MT-ND3 has a mutation status of E68E, The gene MT-ND5 has a mutation status of L227L
GBMLGG
The gene AGRN has a mutation status of P565P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene ARHGEF19 has a mutation status of A686V, The gene OTUD3 has a mutation status of Q61P, The gene NIPAL3 has a mutation status of P175T, The gene MAN1C1 has a mutation status of A271A, The gene TENT5B has a mutation status of H416R, The gene RIMKLA has a mutation status of H53Y, The gene PPCS has a mutation status of R25P, The gene LINGO4 has a mutation status of G251R, The gene PRRC2C has a mutation status of R1350C, The gene TDRD5 has a mutation status of I735T, The gene ZNF281 has a mutation status of K594R, The gene KDM5B has a mutation status of V1014L, The gene KDM5B has a mutation status of S448S, The gene KCNK1 has a mutation status of S112I, The gene PXDN has a mutation status of E1041K, The gene SLC5A6 has a mutation status of G455G, The gene PLB1 has a mutation status of H1223N, The gene PCARE has a mutation status of Q1020R, The gene DHX57 has a mutation status of I1077I, The gene ZNF2 has a mutation status of D240D, The gene ARHGAP15 has a mutation status of P295L, The gene ZNF804A has a mutation status of A332P, The gene FAM171B has a mutation status of G490V, The gene FLACC1 has a mutation status of P5H, The gene METTL21A has a mutation status of A43A, The gene TMEM198 has a mutation status of S316N, The gene CHRND has a mutation status of P307S, The gene ASB18 has a mutation status of I379I, The gene SRGAP3 has a mutation status of R912W, The gene ACVR2B has a mutation status of L493F, The gene NKTR has a mutation status of H524N, The gene MST1R has a mutation status of *1401*, The gene TEX264 has a mutation status of I10T, The gene MUSTN1 has a mutation status of E71K, The gene PDE12 has a mutation status of 97_98insSRP, The gene MYH15 has a mutation status of L1718L, The gene GTPBP8 has a mutation status of V100G, The gene H1-8 has a mutation status of P79A, The gene A4GNT has a mutation status of P95L, The gene TNK2 has a mutation status of G565R, The gene ZNF721 has a mutation status of R596Q, The gene KLB has a mutation status of P652P, The gene RAP1GDS1 has a mutation status of E152K, The gene SGMS2 has a mutation status of H247H, The gene KIAA1109 has a mutation status of V2529M, The gene MGARP has a mutation status of A100E, The gene FGA has a mutation status of S660S, The gene AMACR has a mutation status of L235R, The gene EGFLAM has a mutation status of R919Q, The gene ACTBL2 has a mutation status of V65I, The gene ADGRV1 has a mutation status of Y2790C, The gene ADGRV1 has a mutation status of T5444K, The gene NR2F1 has a mutation status of A195T, The gene RAPGEF6 has a mutation status of S979T, The gene SH3TC2 has a mutation status of A461F, The gene CLINT1 has a mutation status of V404L, The gene SPDL1 has a mutation status of R453S, The gene DSP has a mutation status of N593S, The gene DHX16 has a mutation status of P573P, The gene HLA-B has a mutation status of G115R, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene GTPBP2 has a mutation status of A322A, The gene CAPN11 has a mutation status of K640E, The gene MYO6 has a mutation status of R980H, The gene PNISR has a mutation status of H97R, The gene PRDM13 has a mutation status of L707L, The gene TNFAIP3 has a mutation status of D169N, The gene LRP11 has a mutation status of F117L, The gene RADIL has a mutation status of L347L, The gene CREB5 has a mutation status of Q224H, The gene EGFR has a mutation status of M555V, The gene PSPH has a mutation status of L68P, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene SLC13A1 has a mutation status of A80T, The gene GPR37 has a mutation status of P253S, The gene FLNC has a mutation status of L2276L, The gene STRIP2 has a mutation status of F250L, The gene ZC3HAV1 has a mutation status of G59G, The gene KEL has a mutation status of A580D, The gene CNTNAP2 has a mutation status of E282*, The gene KCNH2 has a mutation status of A746S, The gene SLC7A2 has a mutation status of G476G, The gene LOXL2 has a mutation status of E210D, The gene PTK2B has a mutation status of C562G, The gene NAPRT has a mutation status of T416M, The gene UBAP2 has a mutation status of S597F, The gene CNTNAP3B has a mutation status of N798D, The gene OSTF1 has a mutation status of R199R, The gene FRMD3 has a mutation status of D135D, The gene SPATA31E1 has a mutation status of H239Q, The gene NUTM2G has a mutation status of P364P, The gene INVS has a mutation status of R899*, The gene GOLGA2 has a mutation status of D944H, The gene CRAT has a mutation status of M482T, The gene GPSM1 has a mutation status of E392*, The gene DIPK1B has a mutation status of L24L, The gene CCDC183 has a mutation status of V344G, The gene TPRN has a mutation status of E607Q, The gene OR13A1 has a mutation status of T28T, The gene PBLD has a mutation status of L123F, The gene CYP26C1 has a mutation status of G236G, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TAF6L has a mutation status of S512P, The gene SLC29A2 has a mutation status of A310T, The gene B3GNT6 has a mutation status of C111Y, The gene KDM4D has a mutation status of D499E, The gene SRSF8 has a mutation status of D19E, The gene CCDC82 has a mutation status of G72A, The gene PATE2 has a mutation status of Q70H, The gene CDCA3 has a mutation status of Q207R, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene CPNE8 has a mutation status of R542L, The gene KRT4 has a mutation status of G90W, The gene MYF5 has a mutation status of L255L, The gene MYO1H has a mutation status of A363E, The gene ZNF26 has a mutation status of P285P, The gene FRY has a mutation status of R1999L, The gene BRCA2 has a mutation status of K2950N, The gene RCBTB1 has a mutation status of L428L, The gene PCDH8 has a mutation status of Q101K, The gene GRK1 has a mutation status of R225W, The gene OR4N2 has a mutation status of I126N, The gene RBM25 has a mutation status of A16A, The gene LRRC74A has a mutation status of T485T, The gene TDP1 has a mutation status of A508A, The gene ASPG has a mutation status of C79G, The gene LINC02203 has a mutation status of I259M, The gene CAPN3 has a mutation status of Y89H, The gene DUOX1 has a mutation status of R491Q, The gene CSPG4 has a mutation status of A1331P, The gene WDR93 has a mutation status of L358F, The gene ABCC1 has a mutation status of T1337T, The gene EARS2 has a mutation status of I402I, The gene VKORC1 has a mutation status of G63G, The gene RPGRIP1L has a mutation status of R561H, The gene TEPP has a mutation status of H42Y, The gene NPIPB15 has a mutation status of A346A, The gene TLCD3A has a mutation status of Y89Y, The gene CLUH has a mutation status of S1158I, The gene ALOX15 has a mutation status of E612G, The gene TP53 has a mutation status of R273C, The gene DNAH2 has a mutation status of R2798*, The gene MYH8 has a mutation status of E1352D, The gene UNC119 has a mutation status of R168C, The gene CCL4L2 has a mutation status of P67R, The gene LHX1 has a mutation status of T206P, The gene MLLT6 has a mutation status of G716D, The gene CASC3 has a mutation status of Q672K, The gene KRT33B has a mutation status of T278T, The gene MTMR4 has a mutation status of K377R, The gene TEX14 has a mutation status of T1171T, The gene METTL2A has a mutation status of S147S, The gene AC127029.3 has a mutation status of R204H, The gene FBF1 has a mutation status of A919G, The gene FBF1 has a mutation status of E918G, The gene AATK has a mutation status of I532I, The gene FN3K has a mutation status of E2E, The gene SEH1L has a mutation status of R5P, The gene FAM210A has a mutation status of R201W, The gene ZBTB7C has a mutation status of P321T, The gene TMEM59L has a mutation status of H324H, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene GRIK5 has a mutation status of G897V, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of S388S, The gene LILRB1 has a mutation status of E34E, The gene SNRPB2 has a mutation status of A65S, The gene CLIC6 has a mutation status of D616E, The gene MN1 has a mutation status of P495P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CPT1B has a mutation status of T731M, The gene WWC3 has a mutation status of V676V, The gene STARD8 has a mutation status of G383D, The gene MT-ATP6 has a mutation status of L208L
SARC
The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene PDIK1L has a mutation status of T99T, The gene ARID1A has a mutation status of L2022P, The gene AKR1A1 has a mutation status of V178M, The gene MAST2 has a mutation status of H1139H, The gene POMGNT1 has a mutation status of I642F, The gene HOOK1 has a mutation status of M608I, The gene LRRC7 has a mutation status of R572*, The gene C1orf52 has a mutation status of L122L, The gene STXBP3 has a mutation status of S12S, The gene MAN1A2 has a mutation status of K297K, The gene WARS2 has a mutation status of P82A, The gene SLAMF7 has a mutation status of D266S, The gene PRG4 has a mutation status of T385A, The gene RHEX has a mutation status of N145I, The gene SRGAP2 has a mutation status of R840C, The gene PLXNA2 has a mutation status of C826G, The gene LBR has a mutation status of G298G, The gene OBSCN has a mutation status of R3219*, The gene OR2AK2 has a mutation status of L184L, The gene OR2L2 has a mutation status of R134C, The gene KIF3C has a mutation status of E470K, The gene OXER1 has a mutation status of M1T, The gene MRPL19 has a mutation status of A280A, The gene IL1RL1 has a mutation status of P114T, The gene UBXN4 has a mutation status of P438L, The gene ASNSD1 has a mutation status of L38S, The gene COL4A4 has a mutation status of E60Q, The gene COL4A3 has a mutation status of L1490F, The gene HDLBP has a mutation status of K1152N, The gene VILL has a mutation status of S348F, The gene SCN11A has a mutation status of R1679H, The gene BSN has a mutation status of H1723H, The gene ACY1 has a mutation status of S192fs, The gene SLC15A2 has a mutation status of L651L, The gene MELTF has a mutation status of C369R, The gene FAM53A has a mutation status of S149S, The gene HAUS3 has a mutation status of D236N, The gene EVC2 has a mutation status of V289I, The gene SLC10A4 has a mutation status of W89C, The gene SOWAHB has a mutation status of V72V, The gene ABRAXAS1 has a mutation status of S376G, The gene PTPN13 has a mutation status of L5L, The gene PTPN13 has a mutation status of L9M, The gene UNC5C has a mutation status of P604S, The gene DKK2 has a mutation status of R121H, The gene COL25A1 has a mutation status of A438A, The gene DCHS2 has a mutation status of D1129D, The gene KLKB1 has a mutation status of K613R, The gene PDZD2 has a mutation status of Q942K, The gene SUB1 has a mutation status of Q30fs, The gene VCAN has a mutation status of A2208F, The gene WDR36 has a mutation status of H156P, The gene WDR36 has a mutation status of T874T, The gene DDX46 has a mutation status of V597M, The gene GEMIN5 has a mutation status of D931V, The gene H4C3 has a mutation status of E53K, The gene H4C5 has a mutation status of A16V, The gene OR2H1 has a mutation status of Y192S, The gene HLA-A has a mutation status of F46F, The gene HLA-DRB5 has a mutation status of Q220W, The gene TTBK1 has a mutation status of P848S, The gene CDC5L has a mutation status of T510T, The gene MAN1A1 has a mutation status of G16D, The gene BCLAF1 has a mutation status of Q328K, The gene UTRN has a mutation status of I1689I, The gene IGF2R has a mutation status of I2110T, The gene TBX20 has a mutation status of V171G, The gene CCDC146 has a mutation status of T268M, The gene AGFG2 has a mutation status of F470F, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T1594T, The gene MUC3A has a mutation status of S2495L, The gene PLOD3 has a mutation status of G120V, The gene RNF133 has a mutation status of H290R, The gene KEL has a mutation status of M440R, The gene ZNF746 has a mutation status of E122K, The gene AGAP3 has a mutation status of T243T, The gene EPHX2 has a mutation status of F116Y, The gene ADHFE1 has a mutation status of R392H, The gene ZFHX4 has a mutation status of D2340H, The gene CCN4 has a mutation status of C136C, The gene TTC39B has a mutation status of L113L, The gene CDKN2A has a mutation status of Y44fs, The gene DMRTA1 has a mutation status of R93Q, The gene DCTN3 has a mutation status of L68V, The gene FAM120A has a mutation status of R116P, The gene CTSV has a mutation status of A143A, The gene PAPPA has a mutation status of D396D, The gene OBP2A has a mutation status of P160T, The gene PLXDC2 has a mutation status of A454T, The gene JCAD has a mutation status of R799W, The gene KIFBP has a mutation status of E240V, The gene SGPL1 has a mutation status of K228N, The gene STAMBPL1 has a mutation status of L110P, The gene PIK3AP1 has a mutation status of T793T, The gene COL17A1 has a mutation status of A489A, The gene HMX3 has a mutation status of P99P, The gene KNDC1 has a mutation status of N504N, The gene MUC5AC has a mutation status of A4396A, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene CBLIF has a mutation status of G227G, The gene PPP1R32 has a mutation status of Q80*, The gene FEN1 has a mutation status of I44L, The gene TSGA10IP has a mutation status of Q530P, The gene FAT3 has a mutation status of N3842Y, The gene TECTA has a mutation status of K1325N, The gene SLC6A12 has a mutation status of P522P, The gene TAS2R45 has a mutation status of N76C, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene KRAS has a mutation status of G12D, The gene ITGA7 has a mutation status of A785G, The gene CFAP54 has a mutation status of G2297G, The gene DNAH10 has a mutation status of F57C, The gene ZMYM2 has a mutation status of G1030G, The gene SACS has a mutation status of R53H, The gene MIPEP has a mutation status of M557T, The gene ERCC5 has a mutation status of T1317T, The gene BAZ1A has a mutation status of I640V, The gene PPP2R5C has a mutation status of G523S, The gene HERC2 has a mutation status of S895A, The gene GOLGA8H has a mutation status of K279*, The gene PRSS22 has a mutation status of A25A, The gene CENPT has a mutation status of F467C, The gene PKD1L3 has a mutation status of N426S, The gene TP53 has a mutation status of R248Q, The gene GLP2R has a mutation status of F52F, The gene DNAH9 has a mutation status of S3078S, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP4-8 has a mutation status of CISSCCRPSCCVSSCCKPQCCQSVCCQPNCCRPSC95del, The gene PSMC3IP has a mutation status of G34R, The gene BRCA1 has a mutation status of S1563C, The gene CD300LG has a mutation status of M218I, The gene SAMD14 has a mutation status of K392N, The gene MPO has a mutation status of P297P, The gene CARD14 has a mutation status of A990T, The gene NPTX1 has a mutation status of A263T, The gene POTEC has a mutation status of N79K, The gene SMAD4 has a mutation status of R135*, The gene PWWP3A has a mutation status of S564L, The gene PIAS4 has a mutation status of P163P, The gene PLIN4 has a mutation status of A808S, The gene PNPLA6 has a mutation status of Q707*, The gene MUC16 has a mutation status of M8698V, The gene CC2D1A has a mutation status of E90D, The gene ZNF493 has a mutation status of K564E, The gene ZNF728 has a mutation status of K387fs, The gene CATSPERG has a mutation status of Y835F, The gene NOVA2 has a mutation status of S69S, The gene NOVA2 has a mutation status of L68L, The gene FUZ has a mutation status of T216T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of W163S, The gene LILRA1 has a mutation status of T25P, The gene LILRA1 has a mutation status of T30T, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene IFT52 has a mutation status of A144S, The gene ZNFX1 has a mutation status of G80E, The gene HSPA13 has a mutation status of D258N, The gene IL17RA has a mutation status of E699G, The gene SGSM1 has a mutation status of S920S, The gene C22orf31 has a mutation status of L160V, The gene PES1 has a mutation status of E389K, The gene PES1 has a mutation status of E350*, The gene PES1 has a mutation status of E324K, The gene PES1 has a mutation status of E290E, The gene PES1 has a mutation status of D261N, The gene FBXO7 has a mutation status of E405*, The gene SYN3 has a mutation status of S473F, The gene MYH9 has a mutation status of K1585Q, The gene CACNA1I has a mutation status of S1996F, The gene CYP2D6 has a mutation status of S486T, The gene MAPK12 has a mutation status of A25A, The gene PLXNB2 has a mutation status of V804I, The gene PLXNB2 has a mutation status of T79K, The gene MAGED1 has a mutation status of A72T, The gene WNK3 has a mutation status of S344L, The gene DIAPH2 has a mutation status of A421A, The gene SRPX2 has a mutation status of G172G, The gene MCTS1 has a mutation status of Q32Q, The gene OR13H1 has a mutation status of D295E, The gene AFF2 has a mutation status of V1196F, The gene GAB3 has a mutation status of C409F, The gene MT-CYB has a mutation status of L363L
PAAD
The gene ATAD3B has a mutation status of L350P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene ARID1A has a mutation status of Q1212*, The gene PHACTR4 has a mutation status of S461S, The gene CSMD2 has a mutation status of M2984R, The gene EPHA10 has a mutation status of V507M, The gene COL24A1 has a mutation status of E718K, The gene ABCA4 has a mutation status of D596N, The gene SARS1 has a mutation status of A186V, The gene NBPF20 has a mutation status of A5619T, The gene NBPF12 has a mutation status of R1042R, The gene NBPF11 has a mutation status of L86L, The gene NBPF9 has a mutation status of A319S, The gene HRNR has a mutation status of H820N, The gene PIGC has a mutation status of G159S, The gene AXDND1 has a mutation status of P148Q, The gene RASSF5 has a mutation status of L128L, The gene OR2L2 has a mutation status of L221I, The gene OR2T4 has a mutation status of V109L, The gene LRPPRC has a mutation status of L238F, The gene FER1L5 has a mutation status of R142R, The gene RNF149 has a mutation status of L250F, The gene C2orf49 has a mutation status of D94E, The gene THSD7B has a mutation status of L1567V, The gene BAZ2B has a mutation status of S1432F, The gene STK39 has a mutation status of A50V, The gene MARS2 has a mutation status of S31S, The gene C2CD6 has a mutation status of N1583N, The gene STK36 has a mutation status of L133L, The gene SLC16A14 has a mutation status of I94F, The gene OXTR has a mutation status of E24K, The gene EMC3 has a mutation status of I22I, The gene ATP2B2 has a mutation status of D473D, The gene ATP2B2 has a mutation status of D324E, The gene PLCL2 has a mutation status of G8D, The gene TBC1D5 has a mutation status of I213V, The gene UBE2E2 has a mutation status of H129D, The gene CRTAP has a mutation status of A318V, The gene DLEC1 has a mutation status of R162W, The gene SCN10A has a mutation status of R302Q, The gene XCR1 has a mutation status of V187F, The gene PPM1M has a mutation status of L11L, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene DNAH12 has a mutation status of R2122Q, The gene PTPRG has a mutation status of C1362F, The gene CRYBG3 has a mutation status of Q1883P, The gene CPOX has a mutation status of S112L, The gene TXNRD3 has a mutation status of L496L, The gene U2SURP has a mutation status of D802H, The gene P3H2 has a mutation status of Y56C, The gene MFSD10 has a mutation status of A135D, The gene EVC2 has a mutation status of R796K, The gene BOD1L1 has a mutation status of G1795G, The gene ARAP2 has a mutation status of D641E, The gene NAP1L5 has a mutation status of A160A, The gene MMRN1 has a mutation status of D468N, The gene ADH6 has a mutation status of A72S, The gene ANK2 has a mutation status of D2399D, The gene GPM6A has a mutation status of G24D, The gene AGA has a mutation status of D80H, The gene IRF2 has a mutation status of E295D, The gene FRG2 has a mutation status of P243L, The gene AGXT2 has a mutation status of L179L, The gene ZSWIM6 has a mutation status of T623A, The gene ADGRV1 has a mutation status of V307V, The gene LVRN has a mutation status of E203V, The gene CXXC5 has a mutation status of K104K, The gene NRN1 has a mutation status of V77I, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Y42H, The gene TINAG has a mutation status of I368I, The gene COL12A1 has a mutation status of L1932L, The gene CYB5R4 has a mutation status of L125Q, The gene HTR1E has a mutation status of L78L, The gene CITED2 has a mutation status of A203T, The gene GHRHR has a mutation status of L332H, The gene IGFBP3 has a mutation status of S201S, The gene PHTF2 has a mutation status of T489I, The gene PCLO has a mutation status of L1392L, The gene KIAA1324L has a mutation status of G313A, The gene ERVW-1 has a mutation status of L333*, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T303V, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of M384T, The gene MUC3A has a mutation status of S395T, The gene MUC3A has a mutation status of S558T, The gene MUC3A has a mutation status of FTSSITTTENATHSTPN2127del, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene CTAGE6 has a mutation status of Q429G, The gene ARHGEF10 has a mutation status of E423K, The gene MYOM2 has a mutation status of A1460A, The gene MSR1 has a mutation status of T282A, The gene ADAM18 has a mutation status of P30S, The gene KAT6A has a mutation status of 1675_1676insP, The gene HNF4G has a mutation status of S382L, The gene LRP12 has a mutation status of A23S, The gene FAM83H has a mutation status of E992E, The gene EPPK1 has a mutation status of A2633del, The gene WDR97 has a mutation status of L935L, The gene HGH1 has a mutation status of G54V, The gene DENND4C has a mutation status of D488E, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene PRSS3 has a mutation status of R122H, The gene ZNF169 has a mutation status of E27Q, The gene TRMO has a mutation status of S367L, The gene TRIM14 has a mutation status of V66G, The gene GALNT12 has a mutation status of E273D, The gene FKBP15 has a mutation status of G372S, The gene HMCN2 has a mutation status of A506T, The gene HMCN2 has a mutation status of G833R, The gene CAMSAP1 has a mutation status of A367V, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of R294H, The gene ARMC3 has a mutation status of P13A, The gene OTUD1 has a mutation status of S326C, The gene FAM170B has a mutation status of S80S, The gene PARG has a mutation status of S95G, The gene WASHC2A has a mutation status of K948R, The gene OPN4 has a mutation status of A274V, The gene PPRC1 has a mutation status of V1283V, The gene SORCS3 has a mutation status of P122A, The gene ACSL5 has a mutation status of M157K, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P3013P, The gene DNHD1 has a mutation status of R2611Q, The gene SBF2 has a mutation status of A1297A, The gene MICAL2 has a mutation status of Q450*, The gene LARGE2 has a mutation status of N298N, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TMEM109 has a mutation status of Q105H, The gene CCDC88B has a mutation status of R907Q, The gene FGF4 has a mutation status of A98A, The gene DGAT2 has a mutation status of P345L, The gene THRSP has a mutation status of D100D, The gene GRM5 has a mutation status of K867N, The gene MRE11 has a mutation status of R380C, The gene DLAT has a mutation status of T68M, The gene CD3E has a mutation status of D23H, The gene CLSTN3 has a mutation status of R165W, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene ARNTL2 has a mutation status of G11G, The gene TROAP has a mutation status of R291Q, The gene GALNT6 has a mutation status of M376I, The gene EIF4B has a mutation status of N609fs, The gene TBC1D30 has a mutation status of R46W, The gene LEMD3 has a mutation status of L690S, The gene ABCB9 has a mutation status of A97T, The gene TMEM132C has a mutation status of K1052*, The gene ALG5 has a mutation status of L11V, The gene C13orf46 has a mutation status of S103N, The gene OR4M1 has a mutation status of A223A, The gene ZFYVE1 has a mutation status of H268D, The gene BBOF1 has a mutation status of T122I, The gene INF2 has a mutation status of P423P, The gene GOLGA6L22 has a mutation status of V434M, The gene GOLGA6L1 has a mutation status of Q428Q, The gene GOLGA6L2 has a mutation status of D196N, The gene GOLGA8M has a mutation status of Q136R, The gene WDR76 has a mutation status of D85N, The gene USP8 has a mutation status of N326S, The gene VPS13C has a mutation status of R728*, The gene ANKDD1A has a mutation status of L516L, The gene GOLGA6L9 has a mutation status of R6H, The gene CACNA1H has a mutation status of A2097A, The gene PERCC1 has a mutation status of S164S, The gene ZNF500 has a mutation status of Q51E, The gene AC099489.1 has a mutation status of G447S, The gene RPGRIP1L has a mutation status of I1197V, The gene MMP2 has a mutation status of N151N, The gene GLG1 has a mutation status of P98P, The gene BCAR1 has a mutation status of P357P, The gene GSE1 has a mutation status of R816K, The gene NCBP3 has a mutation status of D208H, The gene ACAP1 has a mutation status of R535H, The gene MAP2K4 has a mutation status of S184L, The gene COX10 has a mutation status of R355H, The gene CDK5R1 has a mutation status of S214S, The gene CCL4L2 has a mutation status of P67R, The gene TBC1D3F has a mutation status of C263C, The gene TTC25 has a mutation status of L394L, The gene DHX8 has a mutation status of S374fs, The gene ABCA5 has a mutation status of I1595V, The gene TSEN54 has a mutation status of S492C, The gene DNAH17 has a mutation status of E1961Q, The gene FHOD3 has a mutation status of F1029P, The gene MC4R has a mutation status of I173M, The gene SH2D3A has a mutation status of K208Q, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T12336L, The gene TYK2 has a mutation status of H396H, The gene RAB3D has a mutation status of T78A, The gene GET3 has a mutation status of E120K, The gene IER2 has a mutation status of S67Y, The gene RASAL3 has a mutation status of L306L, The gene KLHL26 has a mutation status of D584D, The gene CILP2 has a mutation status of P129R, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of W205Q, The gene LILRB3 has a mutation status of T201M, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of Q41Q, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene NLRP8 has a mutation status of K885Q, The gene ZNF671 has a mutation status of Q490E, The gene SLC24A3 has a mutation status of F29F, The gene XRN2 has a mutation status of S485C, The gene CABLES2 has a mutation status of P62S, The gene HLCS has a mutation status of F714F, The gene MCM3AP has a mutation status of V1358M, The gene CRYBB1 has a mutation status of L229L, The gene KCNJ4 has a mutation status of R427L, The gene MCAT has a mutation status of R246Q, The gene PRR5 has a mutation status of E140Q, The gene SMC1B has a mutation status of Q880H, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene ARSL has a mutation status of I348T, The gene MXRA5 has a mutation status of P30R, The gene CLCN4 has a mutation status of T532T, The gene USP11 has a mutation status of P698L, The gene CLCN5 has a mutation status of V192F, The gene HUWE1 has a mutation status of M495I, The gene GNL3L has a mutation status of E104D, The gene PCDH19 has a mutation status of V493M, The gene ARMCX4 has a mutation status of 1809_1810insEAGAGT, The gene ARMCX2 has a mutation status of Q503Q, The gene GPRASP1 has a mutation status of I1174T, The gene ELF4 has a mutation status of E86Q, The gene AC236972.4 has a mutation status of S1611S, The gene MT-ND2 has a mutation status of T226T, The gene MT-ND4 has a mutation status of L351L
BRCA
The gene ARHGEF16 has a mutation status of G143D, The gene VPS13D has a mutation status of V1819M, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene ATP13A2 has a mutation status of F1056F, The gene PADI3 has a mutation status of T581M, The gene IFFO2 has a mutation status of C305C, The gene EPHA10 has a mutation status of A403G, The gene KDM4A has a mutation status of R792R, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene NRDC has a mutation status of R608I, The gene PCSK9 has a mutation status of T664I, The gene EFCAB7 has a mutation status of A41T, The gene MTF2 has a mutation status of Y409C, The gene CELSR2 has a mutation status of S147A, The gene CELSR2 has a mutation status of R2015K, The gene AHCYL1 has a mutation status of C392Y, The gene AHCYL1 has a mutation status of I393L, The gene NBPF14 has a mutation status of V2614I, The gene F5 has a mutation status of R534Q, The gene RO60 has a mutation status of E3fs, The gene KCNH1 has a mutation status of V266M, The gene RAB3GAP2 has a mutation status of Q1214K, The gene OBSCN has a mutation status of T6604T, The gene LYST has a mutation status of A1284T, The gene RYR2 has a mutation status of P990L, The gene OR2T8 has a mutation status of F236fs, The gene OR2L2 has a mutation status of D270E, The gene APOB has a mutation status of S3494L, The gene RALB has a mutation status of A116P, The gene MYO3B has a mutation status of G377V, The gene PSMD1 has a mutation status of G517G, The gene SYN2 has a mutation status of P105A, The gene FBLN2 has a mutation status of R527T, The gene GRIP2 has a mutation status of R865Q, The gene SCN10A has a mutation status of I24L, The gene BSN has a mutation status of L2922L, The gene UBA7 has a mutation status of R988R, The gene NEK4 has a mutation status of G284V, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene P2RY1 has a mutation status of L157L, The gene DHX36 has a mutation status of 430_431QE>H*, The gene MECOM has a mutation status of G19G, The gene KCNMB2 has a mutation status of F152F, The gene TBCCD1 has a mutation status of E135E, The gene ARAP2 has a mutation status of K922fs, The gene COX18 has a mutation status of A15V, The gene FAM47E has a mutation status of D44Y, The gene C4orf54 has a mutation status of 366_367HY>QD, The gene ENPEP has a mutation status of A80G, The gene GLRB has a mutation status of A348V, The gene C7 has a mutation status of T158A, The gene ZBED3 has a mutation status of L155A, The gene CMYA5 has a mutation status of K2244E, The gene ISOC1 has a mutation status of A7L, The gene CDC23 has a mutation status of E566K, The gene HLA-B has a mutation status of Y140L, The gene HLA-DRB5 has a mutation status of T262R, The gene HLA-DRB1 has a mutation status of T106N, The gene HLA-DRB1 has a mutation status of W38E, The gene CUL9 has a mutation status of R1730H, The gene KHDC1 has a mutation status of H21L, The gene CFAP206 has a mutation status of R69Q, The gene PM20D2 has a mutation status of A202A, The gene CASP8AP2 has a mutation status of S1207P, The gene GRIK2 has a mutation status of F355F, The gene GPRC6A has a mutation status of A425S, The gene CCZ1 has a mutation status of H180N, The gene CPVL has a mutation status of K469Q, The gene PDE1C has a mutation status of S592A, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of M384T, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene LRWD1 has a mutation status of R416Q, The gene PTPRZ1 has a mutation status of A195E, The gene PTPRZ1 has a mutation status of R1102C, The gene POT1 has a mutation status of K39E, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene OR2A14 has a mutation status of V157V, The gene ADAM7 has a mutation status of E518D, The gene NSD3 has a mutation status of T556A, The gene NBN has a mutation status of K690Q, The gene VIRMA has a mutation status of T1346T, The gene LAPTM4B has a mutation status of M88K, The gene LAPTM4B has a mutation status of T90N, The gene CCDC166 has a mutation status of E96*, The gene EPPK1 has a mutation status of A2633del, The gene SCRT1 has a mutation status of A133S, The gene PPP1R16A has a mutation status of D385N, The gene BNC2 has a mutation status of S829S, The gene IZUMO3 has a mutation status of M218T, The gene FRRS1L has a mutation status of R51A, The gene OR1N2 has a mutation status of Y269S, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene CCDC187 has a mutation status of R294H, The gene NSMF has a mutation status of Q129Q, The gene EHMT1 has a mutation status of L1059V, The gene TAF3 has a mutation status of M154fs, The gene CELF2 has a mutation status of M1I, The gene PRPF18 has a mutation status of A205T, The gene TRDMT1 has a mutation status of G359R, The gene CSTF2T has a mutation status of GGMQGAGIQG526del, The gene JMJD1C has a mutation status of V1466I, The gene TSPAN14 has a mutation status of L140L, The gene NEURL1 has a mutation status of R227W, The gene CCDC186 has a mutation status of R457I, The gene B4GALNT4 has a mutation status of P568S, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of R2283S, The gene MUC5AC has a mutation status of L3616L, The gene MUC5AC has a mutation status of S3630P, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4396A, The gene TRPM5 has a mutation status of R699L, The gene DNHD1 has a mutation status of V2175V, The gene DNHD1 has a mutation status of T4106A, The gene FOLH1 has a mutation status of S613S, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TM7SF2 has a mutation status of L106P, The gene DYNC2H1 has a mutation status of L2157Q, The gene POU2F3 has a mutation status of G9G, The gene FKBP4 has a mutation status of R406W, The gene CD163 has a mutation status of E252E, The gene TAS2R46 has a mutation status of I245V, The gene GXYLT1 has a mutation status of V28K, The gene KRT18 has a mutation status of T103N, The gene TRHDE has a mutation status of I818T, The gene LIN7A has a mutation status of G117D, The gene FLT3 has a mutation status of 600_601insHVDFREYEYD, The gene RBM26 has a mutation status of V764L, The gene ARGLU1 has a mutation status of K16K, The gene IRS2 has a mutation status of PP1273del, The gene GRK1 has a mutation status of N330S, The gene TTC6 has a mutation status of E252D, The gene ATG2B has a mutation status of C1847R, The gene XRCC3 has a mutation status of V187A, The gene CEP170B has a mutation status of D322fs, The gene GOLGA6L22 has a mutation status of V434M, The gene RYR3 has a mutation status of R835S, The gene RMDN3 has a mutation status of L382L, The gene GALK2 has a mutation status of Q347*, The gene ANKDD1A has a mutation status of L516L, The gene PEAK1 has a mutation status of Q704R, The gene ADAMTS7 has a mutation status of G1428G, The gene GOLGA6L9 has a mutation status of M189I, The gene AC013489.1 has a mutation status of R423C, The gene SOX8 has a mutation status of T229T, The gene TSR3 has a mutation status of K77T, The gene SLX4 has a mutation status of L612P, The gene GTF3C1 has a mutation status of D881D, The gene NFATC2IP has a mutation status of P78S, The gene NOD2 has a mutation status of F739F, The gene KLHL36 has a mutation status of R291G, The gene NEURL4 has a mutation status of V161M, The gene CCL4L2 has a mutation status of P67R, The gene PCGF2 has a mutation status of T311del, The gene PCGF2 has a mutation status of PTPPSTASG300del, The gene SMARCE1 has a mutation status of S172N, The gene PIEZO2 has a mutation status of W1380C, The gene CABLES1 has a mutation status of P49L, The gene ZNF521 has a mutation status of E748Q, The gene MBD1 has a mutation status of D531H, The gene MC4R has a mutation status of S136P, The gene GRIN3B has a mutation status of P448R, The gene TIMM44 has a mutation status of E431*, The gene ECSIT has a mutation status of R35C, The gene GTPBP3 has a mutation status of P68S, The gene ZNF66 has a mutation status of F97F, The gene HNRNPUL1 has a mutation status of R550C, The gene CKM has a mutation status of R314C, The gene KPTN has a mutation status of E423G, The gene ZNF649 has a mutation status of I502V, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB2 has a mutation status of Y297S, The gene LILRB2 has a mutation status of R295T, The gene LILRA2 has a mutation status of W163S, The gene LILRA1 has a mutation status of T30T, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of P224S, The gene KIR2DL1 has a mutation status of N144S, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of T333A, The gene ZNF784 has a mutation status of R206C, The gene NRSN2 has a mutation status of S4T, The gene PTPRT has a mutation status of T1387T, The gene LAMA5 has a mutation status of A2614V, The gene COL20A1 has a mutation status of T256M, The gene ARFRP1 has a mutation status of D146E, The gene COL6A2 has a mutation status of D42D, The gene IL17RA has a mutation status of A676A, The gene GSTT4 has a mutation status of Q197R, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ARFGAP3 has a mutation status of S474N, The gene PHKA2 has a mutation status of H132fs, The gene USP11 has a mutation status of R160Q, The gene PPP1R3F has a mutation status of R127C, The gene FAM236C has a mutation status of T34T, The gene DACH2 has a mutation status of P36L, The gene KLHL4 has a mutation status of G669G, The gene ARMCX2 has a mutation status of Q503Q, The gene ARMCX2 has a mutation status of G210R, The gene SLC25A5 has a mutation status of T221R, The gene DCAF12L2 has a mutation status of G64V, The gene MAGEC1 has a mutation status of P232P, The gene MT-ATP6 has a mutation status of L208L
LAML
The gene MIB2 has a mutation status of V727L, The gene MMEL1 has a mutation status of F731F, The gene PRAMEF11 has a mutation status of R50R, The gene PRAMEF18 has a mutation status of L121P, The gene SPEN has a mutation status of A3248P, The gene EPHA2 has a mutation status of P460L, The gene NBPF1 has a mutation status of K283N, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene FAAH has a mutation status of R524G, The gene CYP4Z1 has a mutation status of W356*, The gene MIGA1 has a mutation status of V49A, The gene F3 has a mutation status of L187L, The gene NBPF10 has a mutation status of C1535W, The gene NBPF10 has a mutation status of L891V, The gene NBPF14 has a mutation status of S1390N, The gene TCHHL1 has a mutation status of F41S, The gene OR10J5 has a mutation status of T276M, The gene DPT has a mutation status of G85R, The gene PAPPA2 has a mutation status of R284W, The gene NCF2 has a mutation status of G369G, The gene IGFN1 has a mutation status of A2230E, The gene LAD1 has a mutation status of P76Q, The gene DISP1 has a mutation status of M532L, The gene LYPD8 has a mutation status of Q24P, The gene OTX1 has a mutation status of H276Y, The gene TTN has a mutation status of V29717V, The gene DNAJC10 has a mutation status of D269D, The gene COL6A3 has a mutation status of K2781R, The gene XIRP1 has a mutation status of I106I, The gene ULK4 has a mutation status of V30V, The gene POMGNT2 has a mutation status of Y534Y, The gene MAP4 has a mutation status of G1595*, The gene PRKAR2A has a mutation status of P63P, The gene PARP3 has a mutation status of R100H, The gene PPM1M has a mutation status of L366P, The gene FLNB has a mutation status of P631L, The gene FRMD4B has a mutation status of S685C, The gene CCDC14 has a mutation status of T392del, The gene KALRN has a mutation status of P165P, The gene PLXNA1 has a mutation status of L1683L, The gene VWA5B2 has a mutation status of R314Q, The gene PLAAT1 has a mutation status of T54K, The gene PIGG has a mutation status of E565G, The gene TMEM175 has a mutation status of G20G, The gene NSD2 has a mutation status of G1194G, The gene RGS12 has a mutation status of S379S, The gene HGFAC has a mutation status of N607N, The gene PCDH7 has a mutation status of P987P, The gene CWH43 has a mutation status of S481A, The gene SPATA18 has a mutation status of S427S, The gene EXOC1 has a mutation status of I514I, The gene CEP135 has a mutation status of E293D, The gene BBS7 has a mutation status of T386T, The gene PLK4 has a mutation status of E30E, The gene TLR2 has a mutation status of R723C, The gene DROSHA has a mutation status of E1198E, The gene LVRN has a mutation status of V318I, The gene SEC24A has a mutation status of T964T, The gene PCDHB5 has a mutation status of M616L, The gene ARHGEF37 has a mutation status of A258A, The gene WWC1 has a mutation status of Y466F, The gene KDM1B has a mutation status of A779A, The gene KDM1B has a mutation status of D781E, The gene BTN3A1 has a mutation status of K405E, The gene DDAH2 has a mutation status of T155M, The gene DAAM2 has a mutation status of R903W, The gene TDRD6 has a mutation status of G436A, The gene MYO6 has a mutation status of H786fs, The gene TPD52L1 has a mutation status of V65I, The gene SAMD3 has a mutation status of T520T, The gene SYNE1 has a mutation status of V1763G, The gene FSCN1 has a mutation status of T293T, The gene MPLKIP has a mutation status of R42L, The gene ANKIB1 has a mutation status of S1030R, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T303V, The gene MUC3A has a mutation status of S395T, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene CDHR3 has a mutation status of P883R, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene NUGGC has a mutation status of V324I, The gene SDR16C5 has a mutation status of D168G, The gene PREX2 has a mutation status of I636fs, The gene LRRC69 has a mutation status of P100T, The gene EPPK1 has a mutation status of A2633del, The gene MFSD3 has a mutation status of V138A, The gene RECQL4 has a mutation status of R623H, The gene PTPRD has a mutation status of E279A, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene PRSS3 has a mutation status of R122H, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene CCDC187 has a mutation status of E1017E, The gene CCDC187 has a mutation status of L747L, The gene SEC16A has a mutation status of P1238P, The gene DIPK1B has a mutation status of S400S, The gene MAMDC4 has a mutation status of E487K, The gene LARP4B has a mutation status of P116L, The gene ZNF438 has a mutation status of A103T, The gene CCDC7 has a mutation status of V347M, The gene RBP3 has a mutation status of I183T, The gene WDFY4 has a mutation status of V2992L, The gene ADD3 has a mutation status of E702del, The gene VWA2 has a mutation status of H204H, The gene PSTK has a mutation status of R16Q, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of R3590R, The gene MUC5AC has a mutation status of L3616L, The gene MUC5AC has a mutation status of S3630P, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of E4005K, The gene MUC5AC has a mutation status of A4396A, The gene MUC5AC has a mutation status of STTSASTA4496del, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene DPF2 has a mutation status of C161F, The gene SART1 has a mutation status of V468V, The gene CATSPER1 has a mutation status of R602Q, The gene CCDC82 has a mutation status of D276V, The gene ART4 has a mutation status of V49I, The gene MAP3K12 has a mutation status of V324V, The gene LRRIQ1 has a mutation status of L1591L, The gene TRPV4 has a mutation status of G13R, The gene NAA25 has a mutation status of S316R, The gene SLC8B1 has a mutation status of A186A, The gene SETD1B has a mutation status of P203L, The gene TMEM132C has a mutation status of D650H, The gene RNASE13 has a mutation status of Y124C, The gene SFTA3 has a mutation status of A3T, The gene VCPKMT has a mutation status of I47T, The gene SYNE2 has a mutation status of K3262N, The gene SERPINA1 has a mutation status of P393S, The gene PLCB2 has a mutation status of K179K, The gene LDHAL6B has a mutation status of S339N, The gene LDHAL6B has a mutation status of I343V, The gene ANKDD1A has a mutation status of L516L, The gene GOLGA6L9 has a mutation status of R6H, The gene UNKL has a mutation status of N85K, The gene ZNF598 has a mutation status of A326A, The gene SBK1 has a mutation status of A27A, The gene ASPHD1 has a mutation status of R186H, The gene LRRC29 has a mutation status of L25Q, The gene BHLHA9 has a mutation status of A183V, The gene ZZEF1 has a mutation status of H2633H, The gene MYO15A has a mutation status of L121L, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP4-3 has a mutation status of S23fs, The gene ATP6V0A1 has a mutation status of M752T, The gene SLC25A39 has a mutation status of P44L, The gene ADAM11 has a mutation status of V345V, The gene TEX14 has a mutation status of T979M, The gene ABCA10 has a mutation status of F477F, The gene LOXHD1 has a mutation status of K1745K, The gene MYO5B has a mutation status of P1615Q, The gene SALL3 has a mutation status of N1167N, The gene ADNP2 has a mutation status of V556M, The gene PTBP1 has a mutation status of D279D, The gene CNN2 has a mutation status of M249T, The gene POLR2E has a mutation status of P178S, The gene GIPC3 has a mutation status of P21R, The gene ANKRD24 has a mutation status of A579A, The gene TICAM1 has a mutation status of L549R, The gene MUC16 has a mutation status of L13880C, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene SSBP4 has a mutation status of M235T, The gene LTBP4 has a mutation status of P516P, The gene MEGF8 has a mutation status of G407D, The gene LIPE has a mutation status of A359V, The gene PSG3 has a mutation status of P3T, The gene PSG1 has a mutation status of D116G, The gene CCDC8 has a mutation status of L11L, The gene ELSPBP1 has a mutation status of N65S, The gene CCDC155 has a mutation status of E317K, The gene ZNF614 has a mutation status of N385S, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of V206L, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of Q401L, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL3 has a mutation status of R290S, The gene KIR2DL1 has a mutation status of G283G, The gene NLRP2 has a mutation status of E522G, The gene KMT5C has a mutation status of R9*, The gene ZNF584 has a mutation status of Q30L, The gene CST4 has a mutation status of G17E, The gene CEBPB has a mutation status of K260N, The gene HELZ2 has a mutation status of A527A, The gene ZBTB21 has a mutation status of S164N, The gene UMODL1 has a mutation status of V619V, The gene RRP1B has a mutation status of G268G, The gene TRAPPC10 has a mutation status of L671F, The gene SPATC1L has a mutation status of C325S, The gene MCM3AP has a mutation status of R1949*, The gene SPECC1L has a mutation status of D335E, The gene GUCD1 has a mutation status of S228S, The gene LRP5L has a mutation status of S185S, The gene NF2 has a mutation status of R57*, The gene TOM1 has a mutation status of E247K, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ATXN10 has a mutation status of V309I, The gene PLXNB2 has a mutation status of F1640del, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene TBL1X has a mutation status of T449M, The gene P2RY10 has a mutation status of T173S, The gene GUCY2F has a mutation status of S552G, The gene SLC25A5 has a mutation status of T221R, The gene MAGEC1 has a mutation status of L337P, The gene AC236972.4 has a mutation status of S1611S, The gene FLNA has a mutation status of V1731V, The gene MT-ND1 has a mutation status of K58K, The gene MT-CO1 has a mutation status of M417M, The gene MT-ATP6 has a mutation status of A177T, The gene MT-CO3 has a mutation status of L164L, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L
KIPAN
The gene TAS1R3 has a mutation status of W682*, The gene TP73 has a mutation status of T143M, The gene PRAMEF9 has a mutation status of L14L, The gene PRAMEF13 has a mutation status of T257I, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene USP48 has a mutation status of R284R, The gene HSPG2 has a mutation status of S936P, The gene SRSF4 has a mutation status of R266H, The gene DCDC2B has a mutation status of R31H, The gene ZC3H12A has a mutation status of E42G, The gene TRIT1 has a mutation status of G196G, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene PTCH2 has a mutation status of G201G, The gene ZFYVE9 has a mutation status of G253S, The gene YIPF1 has a mutation status of R227C, The gene LEPR has a mutation status of N567N, The gene HHLA3 has a mutation status of G59C, The gene USP33 has a mutation status of P741T, The gene CHI3L2 has a mutation status of K370K, The gene NBPF20 has a mutation status of C207Y, The gene NBPF10 has a mutation status of E3558K, The gene NBPF10 has a mutation status of L632F, The gene NBPF12 has a mutation status of R1042R, The gene NBPF11 has a mutation status of R385W, The gene AC242842.3 has a mutation status of V2458I, The gene SV2A has a mutation status of Q323H, The gene POGZ has a mutation status of Q164P, The gene CHTOP has a mutation status of G129G, The gene ARHGEF2 has a mutation status of G951W, The gene TMEM79 has a mutation status of R375H, The gene ADCY10 has a mutation status of V800I, The gene PRRC2C has a mutation status of M755I, The gene KLHL20 has a mutation status of A578A, The gene RGSL1 has a mutation status of F877C, The gene TPR has a mutation status of K1022Q, The gene RPS27AP5 has a mutation status of Q31fs, The gene PKP1 has a mutation status of P5P, The gene ATP2B4 has a mutation status of G133V, The gene ATP2B4 has a mutation status of E1152E, The gene PLXNA2 has a mutation status of F1757F, The gene FAM71A has a mutation status of V208M, The gene RAB3GAP2 has a mutation status of S915P, The gene TLR5 has a mutation status of V619I, The gene OBSCN has a mutation status of V2455L, The gene OBSCN has a mutation status of S2596N, The gene TRIM67 has a mutation status of G79R, The gene ACTN2 has a mutation status of G419S, The gene RYR2 has a mutation status of Q3844R, The gene PXDN has a mutation status of S38S, The gene TRAPPC12 has a mutation status of G255R, The gene NBAS has a mutation status of T1097M, The gene NT5C1B-RDH14 has a mutation status of R225C, The gene CCDC121 has a mutation status of R70*, The gene TMEM178A has a mutation status of I163V, The gene THADA has a mutation status of T525T, The gene FSHR has a mutation status of K146K, The gene USP34 has a mutation status of L2970L, The gene B3GNT2 has a mutation status of F218F, The gene WDPCP has a mutation status of N529K, The gene TGFA has a mutation status of R139W, The gene INPP4A has a mutation status of V785M, The gene LIPT1 has a mutation status of T187M, The gene NCK2 has a mutation status of D12N, The gene RGPD4 has a mutation status of L1067L, The gene NCKAP5 has a mutation status of N389D, The gene ZRANB3 has a mutation status of A495A, The gene LRP1B has a mutation status of I1263T, The gene NEB has a mutation status of C7119Y, The gene NEB has a mutation status of R3663H, The gene ARL5A has a mutation status of S174S, The gene SCN2A has a mutation status of Y1264Y, The gene TTN has a mutation status of L30861R, The gene TTN has a mutation status of V22999F, The gene TTN has a mutation status of V21672V, The gene TTN has a mutation status of N1534K, The gene TTN has a mutation status of A1532A, The gene CCDC150 has a mutation status of K1015R, The gene NBEAL1 has a mutation status of M2441I, The gene MAP2 has a mutation status of S186N, The gene SLC4A3 has a mutation status of V671V, The gene COL4A4 has a mutation status of G451G, The gene NEU4 has a mutation status of G430S, The gene RTP5 has a mutation status of S332L, The gene SRGAP3 has a mutation status of E933K, The gene THUMPD3 has a mutation status of Y480Y, The gene SLC6A11 has a mutation status of T108T, The gene NR2C2 has a mutation status of A40A, The gene HACL1 has a mutation status of Q462H, The gene SCN5A has a mutation status of A425T, The gene SETD2 has a mutation status of YR2023del, The gene SMARCC1 has a mutation status of P1075H, The gene WDR6 has a mutation status of V302G, The gene LAMB2 has a mutation status of R119Q, The gene SLC38A3 has a mutation status of R406W, The gene RBM15B has a mutation status of V182V, The gene TWF2 has a mutation status of I28L, The gene DNAH1 has a mutation status of S849R, The gene NT5DC2 has a mutation status of R32C, The gene CCDC66 has a mutation status of L793F, The gene DNAH12 has a mutation status of E2938E, The gene SYNPR has a mutation status of F22V, The gene ADAMTS9 has a mutation status of R1416W, The gene ALCAM has a mutation status of M321T, The gene PLA1A has a mutation status of L312L, The gene IQCB1 has a mutation status of Y465H, The gene PARP9 has a mutation status of M527I, The gene ADCY5 has a mutation status of Q508R, The gene EFCC1 has a mutation status of R298H, The gene SLC9A9 has a mutation status of A346T, The gene MECOM has a mutation status of T598R, The gene NLGN1 has a mutation status of V175V, The gene USP13 has a mutation status of L118I, The gene RTP4 has a mutation status of P104P, The gene POLN has a mutation status of H196R, The gene FAM193A has a mutation status of G385G, The gene NOP14 has a mutation status of R769Q, The gene ATP8A1 has a mutation status of T203A, The gene GABRB1 has a mutation status of T378M, The gene TXK has a mutation status of A300V, The gene SLAIN2 has a mutation status of S63F, The gene ARL9 has a mutation status of D216G, The gene CCNG2 has a mutation status of C328C, The gene ABCG2 has a mutation status of F489L, The gene ADH6 has a mutation status of V295V, The gene PPA2 has a mutation status of R301C, The gene TBCK has a mutation status of K489N, The gene KIAA1109 has a mutation status of G3230G, The gene INTU has a mutation status of D317D, The gene LRBA has a mutation status of F294L, The gene GLRB has a mutation status of A462G, The gene ANKH has a mutation status of L195H, The gene FBXL7 has a mutation status of M279I, The gene LMBRD2 has a mutation status of S302G, The gene DAB2 has a mutation status of K28R, The gene MAP1B has a mutation status of A481V, The gene SPZ1 has a mutation status of G347V, The gene FBXL17 has a mutation status of P262P, The gene PRDM6 has a mutation status of I548V, The gene MEGF10 has a mutation status of D180E, The gene BRD8 has a mutation status of K1110R, The gene NRG2 has a mutation status of P680T, The gene PCDHB4 has a mutation status of D555N, The gene PCDHB5 has a mutation status of V708M, The gene PCDHB16 has a mutation status of L30M, The gene AFAP1L1 has a mutation status of V534I, The gene TENM2 has a mutation status of N159N, The gene SLIT3 has a mutation status of R1495Q, The gene TLX3 has a mutation status of A92A, The gene SH3PXD2B has a mutation status of S142C, The gene UNC5A has a mutation status of A798V, The gene DOK3 has a mutation status of H300Y, The gene MAML1 has a mutation status of N358K, The gene ZNF311 has a mutation status of R343G, The gene OR12D3 has a mutation status of L53I, The gene HLA-F has a mutation status of S351C, The gene MICA has a mutation status of P18R, The gene SYNGAP1 has a mutation status of R771P, The gene DEF6 has a mutation status of R278R, The gene TRERF1 has a mutation status of V1192V, The gene PGM3 has a mutation status of T78K, The gene POU3F2 has a mutation status of G205V, The gene LAMA4 has a mutation status of N618D, The gene TMEM200A has a mutation status of A12A, The gene VNN2 has a mutation status of Y217F, The gene REPS1 has a mutation status of A444A, The gene ADGRG6 has a mutation status of T376P, The gene SHPRH has a mutation status of L400L, The gene ZDHHC14 has a mutation status of T405T, The gene DACT2 has a mutation status of AAP56del, The gene DLL1 has a mutation status of T303S, The gene INTS1 has a mutation status of P119L, The gene SDK1 has a mutation status of A1257A, The gene RADIL has a mutation status of L653L, The gene SCIN has a mutation status of V142V, The gene FERD3L has a mutation status of T154T, The gene DNAH11 has a mutation status of E3126D, The gene NFE2L3 has a mutation status of V441E, The gene ELMO1 has a mutation status of H601H, The gene TNS3 has a mutation status of P1116L, The gene LANCL2 has a mutation status of T218T, The gene PSPH has a mutation status of L68P, The gene CCT6A has a mutation status of A21A, The gene CASTOR2 has a mutation status of S260S, The gene PCLO has a mutation status of P2351S, The gene ERVW-1 has a mutation status of Q260*, The gene SGCE has a mutation status of S249R, The gene PON3 has a mutation status of F143L, The gene TRRAP has a mutation status of E2546E, The gene BUD31 has a mutation status of Q107P, The gene FAM200A has a mutation status of H35R, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene MUC17 has a mutation status of P1544H, The gene NAMPT has a mutation status of T44R, The gene IFRD1 has a mutation status of M282I, The gene PTPRZ1 has a mutation status of R764H, The gene RBM28 has a mutation status of Q136Q, The gene AHCYL2 has a mutation status of T455T, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PRSS1 has a mutation status of L210L, The gene KRBA1 has a mutation status of S403R, The gene KMT2C has a mutation status of P1838S, The gene DPP6 has a mutation status of S126T, The gene UBE3C has a mutation status of W317G, The gene CSMD1 has a mutation status of P1992S, The gene PRSS55 has a mutation status of S121R, The gene XKR6 has a mutation status of E29D, The gene SLC35G5 has a mutation status of R326Q, The gene FAM160B2 has a mutation status of G141R, The gene POLR3D has a mutation status of V363M, The gene PNOC has a mutation status of R97*, The gene SNAI2 has a mutation status of A173T, The gene RRS1 has a mutation status of P346P, The gene SLCO5A1 has a mutation status of V334A, The gene TERF1 has a mutation status of R19K, The gene DCAF4L2 has a mutation status of R172H, The gene NECAB1 has a mutation status of V173I, The gene RSPO2 has a mutation status of R69H, The gene ZNF572 has a mutation status of N94N, The gene TG has a mutation status of P777L, The gene TG has a mutation status of I2216I, The gene TG has a mutation status of D2595Y, The gene RECQL4 has a mutation status of Q821Q, The gene KANK1 has a mutation status of A664V, The gene VLDLR has a mutation status of D214N, The gene CDC37L1 has a mutation status of E228V, The gene ADAMTSL1 has a mutation status of V1265I, The gene FOCAD has a mutation status of T1635T, The gene IFNB1 has a mutation status of A77T, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene CREB3 has a mutation status of L74P, The gene CNTNAP3 has a mutation status of A1204T, The gene SPATA31A1 has a mutation status of A292T, The gene SPATA31A6 has a mutation status of V558F, The gene TMC1 has a mutation status of S253S, The gene PRUNE2 has a mutation status of E982K, The gene PRUNE2 has a mutation status of F402I, The gene ZNF169 has a mutation status of A100T, The gene OR13C3 has a mutation status of S151S, The gene FKBP15 has a mutation status of A4A, The gene PAPPA has a mutation status of R758H, The gene PAPPA has a mutation status of E1615del, The gene TLR4 has a mutation status of T175A, The gene HMCN2 has a mutation status of G833R, The gene HMCN2 has a mutation status of D2365E, The gene TTF1 has a mutation status of A454A, The gene REXO4 has a mutation status of S40R, The gene WDR5 has a mutation status of S50S, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of R294H, The gene CCDC187 has a mutation status of T90M, The gene SEC16A has a mutation status of L1677F, The gene LCN12 has a mutation status of G184G, The gene EHMT1 has a mutation status of Q990H, The gene DHTKD1 has a mutation status of K148R, The gene DHTKD1 has a mutation status of R715H, The gene MALRD1 has a mutation status of Q552Q, The gene MALRD1 has a mutation status of D685A, The gene ANKRD30A has a mutation status of E1004K, The gene RBP3 has a mutation status of D445H, The gene FRMPD2 has a mutation status of S935F, The gene C10orf53 has a mutation status of P97P, The gene PCDH15 has a mutation status of A234A, The gene BICC1 has a mutation status of H296Y, The gene ADAMTS14 has a mutation status of E787A, The gene ASCC1 has a mutation status of K89R, The gene LRIT1 has a mutation status of N222D, The gene CPEB3 has a mutation status of 232_233insAAA, The gene IDE has a mutation status of V956I, The gene NOC3L has a mutation status of R473Q, The gene TLL2 has a mutation status of V324I, The gene LCOR has a mutation status of TE883del, The gene DNMBP has a mutation status of R271Q, The gene WBP1L has a mutation status of H314P, The gene CALHM3 has a mutation status of A272A, The gene CALHM3 has a mutation status of R82H, The gene RBM20 has a mutation status of S75L, The gene FAM160B1 has a mutation status of L647L, The gene SEC23IP has a mutation status of S757S, The gene IKZF5 has a mutation status of P356L, The gene PKP3 has a mutation status of *798Q, The gene SSU72P3 has a mutation status of N79N, The gene ILK has a mutation status of D269N, The gene NRIP3 has a mutation status of C182S, The gene PRDM11 has a mutation status of R1131R, The gene TRIM64C has a mutation status of C166F, The gene OR5W2 has a mutation status of M118I, The gene OR5T3 has a mutation status of I107I, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of Q100Q, The gene OR8U1 has a mutation status of T106A, The gene OR8U1 has a mutation status of L131M, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene BTBD18 has a mutation status of S302T, The gene DAGLA has a mutation status of G883G, The gene TUT1 has a mutation status of P4L, The gene NRXN2 has a mutation status of L1463L, The gene RASGRP2 has a mutation status of G493A, The gene RASGRP2 has a mutation status of T242T, The gene TESMIN has a mutation status of I33F, The gene IGHMBP2 has a mutation status of H122H, The gene TPCN2 has a mutation status of A24V, The gene DGAT2 has a mutation status of F309F, The gene WNT11 has a mutation status of A125T, The gene B3GNT6 has a mutation status of A74P, The gene TRIM64B has a mutation status of Y170H, The gene SLC36A4 has a mutation status of N42N, The gene DEUP1 has a mutation status of S95S, The gene DDI1 has a mutation status of C7*, The gene KMT2A has a mutation status of S3582S, The gene OR10G8 has a mutation status of A20A, The gene KDM5A has a mutation status of Q1197P, The gene TULP3 has a mutation status of A175T, The gene VWF has a mutation status of D1529H, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R46 has a mutation status of L98P, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of N76C, The gene TAS2R45 has a mutation status of I33T, The gene EPS8 has a mutation status of A445V, The gene SOX5 has a mutation status of P440H, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of E249R, The gene GXYLT1 has a mutation status of I220G, The gene VDR has a mutation status of E155E, The gene OR8S1 has a mutation status of Y60C, The gene KMT2D has a mutation status of F5199fs, The gene SLC4A8 has a mutation status of G521R, The gene MYRFL has a mutation status of K262Q, The gene LIN7A has a mutation status of H146H, The gene LUM has a mutation status of R315C, The gene FGD6 has a mutation status of N932S, The gene ZCCHC8 has a mutation status of E280K, The gene DENR has a mutation status of I190I, The gene SERTM1 has a mutation status of F23V, The gene KBTBD6 has a mutation status of A7V, The gene PCDH17 has a mutation status of E1137D, The gene FARP1 has a mutation status of L480L, The gene FARP1 has a mutation status of G489R, The gene SLC15A1 has a mutation status of V450I, The gene CARS2 has a mutation status of G60R, The gene ATP11A has a mutation status of I807I, The gene TMEM255B has a mutation status of C162C, The gene OR4K2 has a mutation status of C97R, The gene ARHGEF40 has a mutation status of G1476G, The gene CARMIL3 has a mutation status of P1084fs, The gene RIPK3 has a mutation status of S482S, The gene TTC6 has a mutation status of I837V, The gene NEMF has a mutation status of G180D, The gene MAP4K5 has a mutation status of I446V, The gene PCNX4 has a mutation status of A563A, The gene PIGH has a mutation status of L55Q, The gene SMOC1 has a mutation status of R310K, The gene MAP3K9 has a mutation status of V492I, The gene SIPA1L1 has a mutation status of E717E, The gene ACOT4 has a mutation status of R57C, The gene SAMD15 has a mutation status of R622K, The gene NRDE2 has a mutation status of R316G, The gene TECPR2 has a mutation status of V947L, The gene KIF26A has a mutation status of G291V, The gene ADSS1 has a mutation status of I307fs, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene AQR has a mutation status of I313I, The gene MAPKBP1 has a mutation status of T790T, The gene MAPKBP1 has a mutation status of G833R, The gene SPTBN5 has a mutation status of P2175P, The gene EHD4 has a mutation status of A491A, The gene SPG11 has a mutation status of D146G, The gene DUOX2 has a mutation status of P1391A, The gene SEMA6D has a mutation status of S928S, The gene SLC24A5 has a mutation status of A342V, The gene LDHAL6B has a mutation status of H364P, The gene ANKDD1A has a mutation status of L516L, The gene INTS14 has a mutation status of L267L, The gene MEGF11 has a mutation status of G430E, The gene ITGA11 has a mutation status of K54K, The gene ADPGK has a mutation status of T376T, The gene ADAMTS7 has a mutation status of G196G, The gene GOLGA6L10 has a mutation status of C286R, The gene GOLGA6L9 has a mutation status of Q179Q, The gene KLHL25 has a mutation status of A324A, The gene TICRR has a mutation status of A1554T, The gene KIF7 has a mutation status of R788S, The gene MAN2A2 has a mutation status of T639T, The gene ADAMTS17 has a mutation status of G544R, The gene SLX4 has a mutation status of V1257G, The gene AC099489.1 has a mutation status of Y1520H, The gene METTL9 has a mutation status of A13V, The gene METTL9 has a mutation status of Y203Y, The gene COG7 has a mutation status of R313K, The gene SLC12A3 has a mutation status of N940N, The gene ADGRG3 has a mutation status of A430T, The gene CNGB1 has a mutation status of L479I, The gene EXOC3L1 has a mutation status of P327S, The gene SLC12A4 has a mutation status of T819M, The gene ZNF19 has a mutation status of C121Y, The gene DHODH has a mutation status of I267V, The gene PSMD7 has a mutation status of A216T, The gene GLG1 has a mutation status of A113V, The gene MBTPS1 has a mutation status of G309G, The gene GSE1 has a mutation status of E350fs, The gene GSE1 has a mutation status of E352fs, The gene CDK10 has a mutation status of Q227Q, The gene TRPV1 has a mutation status of Q39R, The gene P2RX5 has a mutation status of E397fs, The gene SLC16A11 has a mutation status of A124fs, The gene TP53 has a mutation status of H179Q, The gene TP53 has a mutation status of E11Q, The gene BORCS6 has a mutation status of E11Q, The gene SLC25A35 has a mutation status of R175Q, The gene LRRC75A has a mutation status of R210*, The gene MPRIP has a mutation status of G561V, The gene KCNJ18 has a mutation status of L15S, The gene VTN has a mutation status of T456I, The gene TBC1D3B has a mutation status of S510G, The gene CCL3L1 has a mutation status of P44L, The gene KRT31 has a mutation status of R240H, The gene PLEKHH3 has a mutation status of A50V, The gene NMT1 has a mutation status of K67K, The gene MAP3K14 has a mutation status of R138H, The gene CUEDC1 has a mutation status of D52D, The gene BRIP1 has a mutation status of M29I, The gene DDX5 has a mutation status of Y567Y, The gene UBE2O has a mutation status of G728G, The gene RHBDF2 has a mutation status of T288M, The gene SEC14L1 has a mutation status of I560V, The gene PGS1 has a mutation status of R16P, The gene SGSH has a mutation status of T421T, The gene PCYT2 has a mutation status of V23A, The gene MYADML2 has a mutation status of A100T, The gene PIK3C3 has a mutation status of S851S, The gene MC4R has a mutation status of L247M, The gene SLC66A2 has a mutation status of R109C, The gene POLRMT has a mutation status of R1013R, The gene ABCA7 has a mutation status of K288K, The gene ATP8B3 has a mutation status of A1108T, The gene ZNF57 has a mutation status of H151L, The gene MFSD12 has a mutation status of T254P, The gene GIPC3 has a mutation status of P20S, The gene PIP5K1C has a mutation status of A656V, The gene SEMA6B has a mutation status of A872V, The gene ZNRF4 has a mutation status of R380R, The gene CATSPERD has a mutation status of I247I, The gene GPR108 has a mutation status of R89Q, The gene SH2D3A has a mutation status of A209T, The gene LRRC8E has a mutation status of P715P, The gene ADAMTS10 has a mutation status of D446N, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of V13007G, The gene MUC16 has a mutation status of L12947L, The gene MUC16 has a mutation status of D6322F, The gene HOOK2 has a mutation status of R265C, The gene OR10H4 has a mutation status of N100H, The gene ZNF829 has a mutation status of L367P, The gene ZNF568 has a mutation status of A482fs, The gene RYR1 has a mutation status of V1830I, The gene FCGBP has a mutation status of V3624I, The gene NECTIN2 has a mutation status of R475W, The gene SIX5 has a mutation status of V448A, The gene LIG1 has a mutation status of L446L, The gene CA11 has a mutation status of N275N, The gene NTF4 has a mutation status of G122V, The gene GFY has a mutation status of P23S, The gene PRR12 has a mutation status of H1334R, The gene MED25 has a mutation status of F32F, The gene MYH14 has a mutation status of R1762H, The gene MYBPC2 has a mutation status of G382G, The gene KLK3 has a mutation status of R250Q, The gene HAS1 has a mutation status of R251Q, The gene ZNF347 has a mutation status of M542T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of Y121Y, The gene LILRA2 has a mutation status of D138D, The gene LILRB1 has a mutation status of R30S, The gene TNNT1 has a mutation status of R265R, The gene KMT5C has a mutation status of N14N, The gene ZNF581 has a mutation status of G141G, The gene ZNF543 has a mutation status of L585F, The gene ZNF550 has a mutation status of A310P, The gene ZSCAN1 has a mutation status of S360S, The gene SIRPA has a mutation status of L44S, The gene TMC2 has a mutation status of C440S, The gene CENPB has a mutation status of K101K, The gene CDC25B has a mutation status of R504R, The gene GZF1 has a mutation status of P701P, The gene CBFA2T2 has a mutation status of A450A, The gene CEP250 has a mutation status of R1401G, The gene CD40 has a mutation status of I208V, The gene ZMYND8 has a mutation status of S717A, The gene CSE1L has a mutation status of Q106K, The gene ATP9A has a mutation status of I293I, The gene ZNF217 has a mutation status of E233*, The gene OGFR has a mutation status of K492R, The gene KCNQ2 has a mutation status of A62V, The gene ZBTB46 has a mutation status of A96A, The gene BRWD1 has a mutation status of T1805K, The gene KRTAP10-9 has a mutation status of R257C, The gene FTCD has a mutation status of L468L, The gene TMEM121B has a mutation status of G66C, The gene MICAL3 has a mutation status of R745Q, The gene NF2 has a mutation status of K429K, The gene CACNA1I has a mutation status of D1844N, The gene SHISA8 has a mutation status of A266T, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TRMU has a mutation status of R93W, The gene MOV10L1 has a mutation status of A800A, The gene PLXNB2 has a mutation status of T931I, The gene PPP2R3B has a mutation status of A540E, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene FRMPD4 has a mutation status of V140I, The gene KLHL15 has a mutation status of R67R, The gene FUNDC1 has a mutation status of D15D, The gene ELK1 has a mutation status of A260A, The gene HDAC6 has a mutation status of A520A, The gene GPKOW has a mutation status of K299R, The gene AKAP4 has a mutation status of G588E, The gene DACH2 has a mutation status of R185H, The gene COL4A6 has a mutation status of P209R, The gene SPANXB1 has a mutation status of P35P, The gene SPANXC has a mutation status of V59V, The gene SPANXC has a mutation status of V59L, The gene PASD1 has a mutation status of EQLQQLR498del, The gene CSAG1 has a mutation status of V68I, The gene AC236972.4 has a mutation status of P1394A, The gene ABCD1 has a mutation status of T745P, The gene ARHGAP4 has a mutation status of R428Q, The gene IRAK1 has a mutation status of E437K, The gene DKC1 has a mutation status of K477K, The gene MT-ND2 has a mutation status of T122A, The gene MT-CO3 has a mutation status of W57W, The gene MT-ND4 has a mutation status of G146D, The gene MT-ND5 has a mutation status of L409L, The gene MT-ND6 has a mutation status of W158W, The gene MT-CYB has a mutation status of M303T
STES
The gene PERM1 has a mutation status of T274T, The gene UBE2J2 has a mutation status of G231G, The gene SCNN1D has a mutation status of H181Y, The gene MMEL1 has a mutation status of V668M, The gene WRAP73 has a mutation status of Y308C, The gene CHD5 has a mutation status of R240H, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene FHAD1 has a mutation status of E1115*, The gene GRIK3 has a mutation status of Y765Y, The gene CACHD1 has a mutation status of A1113V, The gene SEMA6C has a mutation status of S641G, The gene FLG has a mutation status of S316L, The gene TTC24 has a mutation status of A396G, The gene OR10R2 has a mutation status of F162F, The gene OR10X1 has a mutation status of I60M, The gene ASTN1 has a mutation status of L272L, The gene NPL has a mutation status of V200M, The gene TNNI1 has a mutation status of E74E, The gene PARP1 has a mutation status of L398L, The gene TAF5L has a mutation status of N106S, The gene GALNT2 has a mutation status of V133G, The gene CATSPERE has a mutation status of I380N, The gene ZNF496 has a mutation status of T393T, The gene TRAPPC12 has a mutation status of S242P, The gene TRAPPC12 has a mutation status of A244P, The gene ASXL2 has a mutation status of G912V, The gene BABAM2 has a mutation status of S329S, The gene QPCT has a mutation status of N68D, The gene EPAS1 has a mutation status of D753E, The gene CLEC4F has a mutation status of D78D, The gene ATP6V1B1 has a mutation status of A141A, The gene SLC4A5 has a mutation status of I610F, The gene HTRA2 has a mutation status of R104G, The gene LOXL3 has a mutation status of R172R, The gene SEMA4F has a mutation status of R403H, The gene EIF2AK3 has a mutation status of V70G, The gene IL18R1 has a mutation status of L163L, The gene PAX8 has a mutation status of Y245S, The gene LRP1B has a mutation status of R2219C, The gene COBLL1 has a mutation status of R1041H, The gene COBLL1 has a mutation status of G414R, The gene SCN3A has a mutation status of S540F, The gene OSBPL6 has a mutation status of K755R, The gene TTN has a mutation status of S28842S, The gene FSIP2 has a mutation status of Y1855H, The gene AOX1 has a mutation status of S195R, The gene UNC80 has a mutation status of G2941G, The gene AC053503.6 has a mutation status of H101P, The gene MRPL44 has a mutation status of T308T, The gene PASK has a mutation status of T1195T, The gene PASK has a mutation status of L315L, The gene CTNNB1 has a mutation status of S37A, The gene VWA5B2 has a mutation status of T157P, The gene UGT2B28 has a mutation status of A346T, The gene ANKRD17 has a mutation status of G629G, The gene SEPTIN11 has a mutation status of T291P, The gene WDFY3 has a mutation status of M2442T, The gene ATOH1 has a mutation status of P95S, The gene BMPR1B has a mutation status of D80D, The gene MAML3 has a mutation status of H363P, The gene WWC2 has a mutation status of A808A, The gene IRF2 has a mutation status of K31K, The gene CASP3 has a mutation status of I48V, The gene RICTOR has a mutation status of I1442S, The gene C7 has a mutation status of G14G, The gene SNCAIP has a mutation status of R668H, The gene TCF7 has a mutation status of P132P, The gene PCDHB11 has a mutation status of R790*, The gene FAM8A1 has a mutation status of G134I, The gene FAM8A1 has a mutation status of A140T, The gene HSPA1L has a mutation status of R51W, The gene HLA-DRB5 has a mutation status of Q38W, The gene ITPR3 has a mutation status of S865L, The gene IP6K3 has a mutation status of N172T, The gene SPDEF has a mutation status of P47P, The gene SPDEF has a mutation status of S46S, The gene LRFN2 has a mutation status of S577S, The gene ADGRF2 has a mutation status of R563*, The gene CRISP3 has a mutation status of V149I, The gene KHDRBS2 has a mutation status of E170*, The gene KCNQ5 has a mutation status of V111G, The gene COX7A2 has a mutation status of E37G, The gene SLC22A16 has a mutation status of H247L, The gene NT5DC1 has a mutation status of F61F, The gene AHI1 has a mutation status of S1067S, The gene RAB32 has a mutation status of G3G, The gene RAB32 has a mutation status of G4G, The gene SYNE1 has a mutation status of M7147T, The gene SYNE1 has a mutation status of Q3239E, The gene SYNJ2 has a mutation status of A1274G, The gene THBS2 has a mutation status of G225V, The gene SLC29A4 has a mutation status of G414G, The gene HOXA5 has a mutation status of D53N, The gene HIBADH has a mutation status of S324S, The gene NACAD has a mutation status of G633D, The gene GUSB has a mutation status of G184G, The gene TRRAP has a mutation status of T2720P, The gene AP4M1 has a mutation status of T395P, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of P3036L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene ORC5 has a mutation status of L80F, The gene KDM7A has a mutation status of G3A, The gene PRSS1 has a mutation status of N77N, The gene LRRC61 has a mutation status of G12G, The gene DLGAP2 has a mutation status of N389T, The gene NRG1 has a mutation status of E309K, The gene SYBU has a mutation status of P198Q, The gene EFR3A has a mutation status of S694S, The gene EPPK1 has a mutation status of D2607N, The gene MFSD3 has a mutation status of L104V, The gene MPDZ has a mutation status of E702M, The gene MPDZ has a mutation status of V135G, The gene BNC2 has a mutation status of K833N, The gene IFNA14 has a mutation status of M84I, The gene AQP7 has a mutation status of A291A, The gene TRPM6 has a mutation status of S2002L, The gene PRUNE2 has a mutation status of N1551D, The gene MFSD14B has a mutation status of T358T, The gene FRRS1L has a mutation status of R51fs, The gene ALAD has a mutation status of P253L, The gene WHRN has a mutation status of H675Y, The gene C5 has a mutation status of T268fs, The gene DPM2 has a mutation status of Q37fs, The gene GTF3C5 has a mutation status of G377V, The gene PAEP has a mutation status of Q126R, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene INPP5E has a mutation status of Q400E, The gene TOR4A has a mutation status of G163G, The gene CUBN has a mutation status of Q59E, The gene MRC1 has a mutation status of L756L, The gene TMEM72 has a mutation status of T135T, The gene SLC29A3 has a mutation status of P114A, The gene ZMIZ1 has a mutation status of D1059D, The gene DNTT has a mutation status of E506G, The gene SLIT1 has a mutation status of D1208N, The gene NRAP has a mutation status of T246T, The gene TACC2 has a mutation status of P397P, The gene C10orf90 has a mutation status of V100M, The gene MUC5B has a mutation status of V5710G, The gene FAM160A2 has a mutation status of T585T, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene SLC43A1 has a mutation status of I96F, The gene PC has a mutation status of C850C, The gene KMT5B has a mutation status of S116P, The gene C11orf24 has a mutation status of T51T, The gene SLCO2B1 has a mutation status of S166S, The gene FAT3 has a mutation status of L3609L, The gene CUL5 has a mutation status of Y373C, The gene DLAT has a mutation status of P189Q, The gene TTC12 has a mutation status of T590T, The gene TMPRSS13 has a mutation status of Q83R, The gene BCL9L has a mutation status of S956R, The gene CD163L1 has a mutation status of R470Q, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I91fs, The gene TAS2R45 has a mutation status of A28A, The gene CMAS has a mutation status of V321G, The gene ESYT1 has a mutation status of M295I, The gene RASSF3 has a mutation status of Q76K, The gene LEMD3 has a mutation status of R22A, The gene OSBPL8 has a mutation status of L16F, The gene RBM19 has a mutation status of H474Y, The gene PXN has a mutation status of D457G, The gene DDX51 has a mutation status of A403S, The gene ZNF26 has a mutation status of P285P, The gene COG3 has a mutation status of M456L, The gene TPP2 has a mutation status of E1020E, The gene HEATR5A has a mutation status of A1051T, The gene MDGA2 has a mutation status of P896R, The gene CHURC1 has a mutation status of G56S, The gene PCNX1 has a mutation status of D955D, The gene LTBP2 has a mutation status of R690R, The gene TTC7B has a mutation status of I839T, The gene HHIPL1 has a mutation status of A710A, The gene FAN1 has a mutation status of A261A, The gene CHAC1 has a mutation status of Y60H, The gene MGA has a mutation status of L2605L, The gene SNRPA1 has a mutation status of R75R, The gene IFT140 has a mutation status of T608T, The gene ZNF598 has a mutation status of Q616P, The gene CORO7 has a mutation status of R217W, The gene VPS35L has a mutation status of M73R, The gene DNAH3 has a mutation status of G2434G, The gene IL21R has a mutation status of G514G, The gene ATP2A1 has a mutation status of Y434H, The gene CKLF-CMTM1 has a mutation status of I32I, The gene CDH16 has a mutation status of P277fs, The gene SLC9A5 has a mutation status of A51A, The gene ZFHX3 has a mutation status of N1025N, The gene CDYL2 has a mutation status of P356P, The gene COTL1 has a mutation status of R57Q, The gene BANP has a mutation status of S384S, The gene TRAPPC2L has a mutation status of I5L, The gene PELP1 has a mutation status of S62P, The gene TP53 has a mutation status of R175H, The gene SLC13A2 has a mutation status of S222S, The gene CCL4L2 has a mutation status of P67R, The gene CCL4L2 has a mutation status of G65S, The gene GPR179 has a mutation status of K2045K, The gene MLLT6 has a mutation status of T585P, The gene KRT24 has a mutation status of S517R, The gene KRTAP4-12 has a mutation status of R142C, The gene DLX4 has a mutation status of E104D, The gene ACSF2 has a mutation status of S375S, The gene EPN3 has a mutation status of A408A, The gene DGKE has a mutation status of Q143E, The gene CCDC182 has a mutation status of L119F, The gene ABCA9 has a mutation status of L255F, The gene OTOP2 has a mutation status of E433K, The gene TBC1D16 has a mutation status of A206T, The gene SLC38A10 has a mutation status of V186G, The gene MYOM1 has a mutation status of G1635S, The gene GALNT1 has a mutation status of N379S, The gene ADNP2 has a mutation status of A932A, The gene KISS1R has a mutation status of H2H, The gene PCSK4 has a mutation status of V111G, The gene STAP2 has a mutation status of T150T, The gene PLIN4 has a mutation status of L1345V, The gene PLIN4 has a mutation status of G1337G, The gene SAFB has a mutation status of G15G, The gene RFX2 has a mutation status of R713H, The gene CCL25 has a mutation status of V83V, The gene MUC16 has a mutation status of A5705A, The gene ILF3 has a mutation status of T24T, The gene SMARCA4 has a mutation status of L639fs, The gene ADGRL1 has a mutation status of G1322G, The gene ADGRL1 has a mutation status of P1299P, The gene GIPC1 has a mutation status of A155T, The gene ERICH4 has a mutation status of R62H, The gene MEGF8 has a mutation status of I2245V, The gene PSG4 has a mutation status of K16K, The gene MEIS3 has a mutation status of R84H, The gene SPACA4 has a mutation status of V82I, The gene SPHK2 has a mutation status of Y342S, The gene SPHK2 has a mutation status of L343P, The gene ADM5 has a mutation status of P32P, The gene PNKP has a mutation status of G18G, The gene POLD1 has a mutation status of A805A, The gene SIGLEC8 has a mutation status of L41L, The gene LILRA2 has a mutation status of W163S, The gene CENPB has a mutation status of T150P, The gene XKR7 has a mutation status of G21C, The gene XKR7 has a mutation status of G46G, The gene GNAS has a mutation status of H353P, The gene PPP1R3D has a mutation status of V163V, The gene CCDC116 has a mutation status of R308C, The gene NCF4 has a mutation status of R60C, The gene ZC3H7B has a mutation status of V730G, The gene SAMM50 has a mutation status of D292G, The gene CERK has a mutation status of V384I, The gene MXRA5 has a mutation status of A2037V, The gene ACE2 has a mutation status of G211R, The gene DCAF8L1 has a mutation status of P117P, The gene CXorf38 has a mutation status of 318_319KA>NS, The gene SPANXN5 has a mutation status of L67L, The gene FGD1 has a mutation status of R132Q, The gene NEXMIF has a mutation status of P838S, The gene PASD1 has a mutation status of E385K, The gene MT-ND1 has a mutation status of K58K, The gene MT-CO1 has a mutation status of G205G, The gene MT-ATP6 has a mutation status of A177T, The gene MT-CO3 has a mutation status of T109T, The gene MT-CO3 has a mutation status of L164L, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4L has a mutation status of M43T, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND4 has a mutation status of G242G, The gene MT-ND4 has a mutation status of T372fs, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L
OV
The gene NPHP4 has a mutation status of Y1052S, The gene C1orf167 has a mutation status of R553Q, The gene PRAMEF9 has a mutation status of L14L, The gene PRAMEF9 has a mutation status of A24A, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene CPLANE2 has a mutation status of G174A, The gene SH2D5 has a mutation status of V167G, The gene HSPG2 has a mutation status of S2294F, The gene IL22RA1 has a mutation status of S134S, The gene ADGRB2 has a mutation status of S523S, The gene A3GALT2 has a mutation status of A273V, The gene CSMD2 has a mutation status of R2903R, The gene KCNQ4 has a mutation status of G64S, The gene FOXO6 has a mutation status of P334fs, The gene BEST4 has a mutation status of *474*, The gene ATG4C has a mutation status of S146fs, The gene PDE4B has a mutation status of S4N, The gene WLS has a mutation status of R405G, The gene SPATA1 has a mutation status of Y324N, The gene SPATA1 has a mutation status of Y324*, The gene DPYD has a mutation status of P393A, The gene NRAS has a mutation status of G13D, The gene IGSF3 has a mutation status of M950T, The gene TENT5C has a mutation status of I94fs, The gene NBPF10 has a mutation status of 2469_2470insED, The gene NBPF10 has a mutation status of K312R, The gene NBPF9 has a mutation status of V918L, The gene IFI16 has a mutation status of S480N, The gene FCGR3A has a mutation status of G40I, The gene ADCY10 has a mutation status of H320Y, The gene SUCO has a mutation status of M1I, The gene CEP350 has a mutation status of L1627L, The gene HMCN1 has a mutation status of L403H, The gene HMCN1 has a mutation status of R5413G, The gene IGFN1 has a mutation status of V3250V, The gene CHI3L1 has a mutation status of I55M, The gene CHIT1 has a mutation status of G353G, The gene CNTN2 has a mutation status of G130S, The gene RAB3GAP2 has a mutation status of W1024*, The gene RYR2 has a mutation status of E1127G, The gene OR2T27 has a mutation status of R234fs, The gene GDF7 has a mutation status of L234M, The gene FAM228B has a mutation status of Q303fs, The gene SULT6B1 has a mutation status of A9A, The gene MAP4K3 has a mutation status of D301D, The gene MTIF2 has a mutation status of A240G, The gene XPO1 has a mutation status of P2A, The gene GCC2 has a mutation status of G651G, The gene CHN1 has a mutation status of T174A, The gene TTN has a mutation status of E13379K, The gene DNAH7 has a mutation status of T1801T, The gene SPATS2L has a mutation status of E295K, The gene MOGAT1 has a mutation status of P297A, The gene IRS1 has a mutation status of G128A, The gene SCYGR2 has a mutation status of H97S, The gene SLC19A3 has a mutation status of D480N, The gene SP110 has a mutation status of D234D, The gene GIGYF2 has a mutation status of N91K, The gene OR6B2 has a mutation status of S10G, The gene CELSR3 has a mutation status of V810V, The gene NPRL2 has a mutation status of R311G, The gene DNAH1 has a mutation status of Y892H, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene DNAH12 has a mutation status of D2383E, The gene DZIP3 has a mutation status of D704N, The gene MASP1 has a mutation status of L264L, The gene LETM1 has a mutation status of L398L, The gene PDS5A has a mutation status of V250V, The gene EPHA5 has a mutation status of H401H, The gene DSPP has a mutation status of S1133S, The gene TLL1 has a mutation status of S447N, The gene ICE1 has a mutation status of S1599R, The gene ANXA2R has a mutation status of E106Q, The gene CCDC112 has a mutation status of R268T, The gene PCDHA12 has a mutation status of V255A, The gene PCDHB7 has a mutation status of S631G, The gene DIAPH1 has a mutation status of N1054K, The gene IRGM has a mutation status of LK26del, The gene SGCD has a mutation status of T197T, The gene ATP10B has a mutation status of Q1440fs, The gene RGS14 has a mutation status of T393S, The gene ZNF454 has a mutation status of A37A, The gene RIPK1 has a mutation status of A569V, The gene DSP has a mutation status of L143V, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB1 has a mutation status of W38E, The gene HLA-DQA2 has a mutation status of S75R, The gene PPP2R5D has a mutation status of F287F, The gene UBE3D has a mutation status of S113F, The gene PRDM13 has a mutation status of P600L, The gene DDO has a mutation status of F66fs, The gene ROS1 has a mutation status of R2205I, The gene MAP3K5 has a mutation status of G692W, The gene RSPH3 has a mutation status of I288T, The gene GPR146 has a mutation status of V35A, The gene OCM has a mutation status of K97K, The gene KIAA1324L has a mutation status of K652E, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene TRIM56 has a mutation status of L640L, The gene RELN has a mutation status of V1752V, The gene DOCK4 has a mutation status of G11G, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene TAS2R4 has a mutation status of L198L, The gene PRSS1 has a mutation status of N54R, The gene LRRC61 has a mutation status of S83Y, The gene AGAP3 has a mutation status of V279L, The gene CSMD1 has a mutation status of N1887S, The gene CCAR2 has a mutation status of R512R, The gene TEX15 has a mutation status of L1361L, The gene C8orf86 has a mutation status of V104F, The gene RNF170 has a mutation status of S134S, The gene PRKDC has a mutation status of H1175Y, The gene LRRCC1 has a mutation status of E38*, The gene CNGB3 has a mutation status of T83I, The gene ANGPT1 has a mutation status of A40A, The gene CSMD3 has a mutation status of I1366I, The gene CSMD3 has a mutation status of G3W, The gene AGO2 has a mutation status of P373P, The gene SCRIB has a mutation status of A701A, The gene EPPK1 has a mutation status of A2633del, The gene EPPK1 has a mutation status of R2547G, The gene EPPK1 has a mutation status of D2512E, The gene EPPK1 has a mutation status of G441S, The gene BOP1 has a mutation status of G51G, The gene FREM1 has a mutation status of L4L, The gene FOCAD has a mutation status of N507D, The gene GRHPR has a mutation status of R125W, The gene CNTNAP3B has a mutation status of A629V, The gene CEMIP2 has a mutation status of D1067D, The gene IARS1 has a mutation status of S35P, The gene NOL8 has a mutation status of L65L, The gene FRRS1L has a mutation status of R51A, The gene MIGA2 has a mutation status of T218S, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene CCDC187 has a mutation status of E1017E, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of H128H, The gene AKR1C8P has a mutation status of N172K, The gene VIM has a mutation status of S83S, The gene ZEB1 has a mutation status of N365S, The gene CCDC7 has a mutation status of R490*, The gene ANXA8L1 has a mutation status of Y92Y, The gene ANXA8L1 has a mutation status of K192N, The gene C10orf71 has a mutation status of S1130S, The gene LIPK has a mutation status of T153K, The gene TWNK has a mutation status of V449V, The gene NHLRC2 has a mutation status of S274L, The gene MCMBP has a mutation status of K431N, The gene DMBT1 has a mutation status of G1694G, The gene CALY has a mutation status of I123I, The gene LMNTD2 has a mutation status of E140E, The gene KCNQ1 has a mutation status of A287E, The gene NUP98 has a mutation status of L1120L, The gene NELL1 has a mutation status of Q220*, The gene FIBIN has a mutation status of S171F, The gene CHST1 has a mutation status of I230I, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MYRF has a mutation status of L294P, The gene SCYL1 has a mutation status of Q371*, The gene KDM2A has a mutation status of D486H, The gene ATM has a mutation status of E347K, The gene NLRX1 has a mutation status of R528H, The gene SORL1 has a mutation status of M335V, The gene ROBO3 has a mutation status of C121S, The gene IGSF9B has a mutation status of R1078R, The gene KDM5A has a mutation status of K430E, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R19 has a mutation status of L116F, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R31 has a mutation status of F233S, The gene TAS2R46 has a mutation status of I33T, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene TAS2R30 has a mutation status of I33T, The gene PLEKHA5 has a mutation status of M139V, The gene KRT18 has a mutation status of T103N, The gene DCN has a mutation status of L10L, The gene TMPO has a mutation status of L149L, The gene STAB2 has a mutation status of K469M, The gene SART3 has a mutation status of E167Q, The gene ATP12A has a mutation status of E67K, The gene BRCA2 has a mutation status of R2668G, The gene KBTBD6 has a mutation status of A518S, The gene VWA8 has a mutation status of A1693T, The gene DGKH has a mutation status of F211L, The gene PCDH17 has a mutation status of G352G, The gene METTL17 has a mutation status of R426H, The gene RIPK3 has a mutation status of W506*, The gene PRKD1 has a mutation status of L617S, The gene SEC23A has a mutation status of P44A, The gene FSCB has a mutation status of E609D, The gene TMEM260 has a mutation status of V637V, The gene LINC02203 has a mutation status of I259M, The gene TJP1 has a mutation status of T1212T, The gene OTUD7A has a mutation status of G551A, The gene MGA has a mutation status of S2932C, The gene UNC13C has a mutation status of D459D, The gene CSNK1G1 has a mutation status of R271fs, The gene ANKDD1A has a mutation status of L516L, The gene LCTL has a mutation status of V509L, The gene GOLGA6L10 has a mutation status of I73V, The gene KLHL25 has a mutation status of E72D, The gene ACAN has a mutation status of H2299R, The gene TPSB2 has a mutation status of M153fs, The gene ABCA3 has a mutation status of L506V, The gene SLX4 has a mutation status of E971*, The gene DNAH3 has a mutation status of Q55*, The gene PRSS53 has a mutation status of D412Y, The gene HEATR3 has a mutation status of H49Y, The gene NOB1 has a mutation status of Q344*, The gene HYDIN has a mutation status of L3335F, The gene SLC38A8 has a mutation status of G376G, The gene PIEZO1 has a mutation status of E2470E, The gene TCF25 has a mutation status of P227L, The gene INPP5K has a mutation status of P244S, The gene ZNF232 has a mutation status of S15G, The gene DNAH2 has a mutation status of L221L, The gene MYH13 has a mutation status of G233E, The gene KCNJ12 has a mutation status of T2T, The gene TP53I13 has a mutation status of P159A, The gene TBC1D3B has a mutation status of G466G, The gene TBC1D3B has a mutation status of R379G, The gene TBC1D3B has a mutation status of L201F, The gene CCL4L2 has a mutation status of P67R, The gene TMEM106A has a mutation status of L181I, The gene GPATCH8 has a mutation status of S510C, The gene OSBPL7 has a mutation status of R447H, The gene MFSD11 has a mutation status of L242F, The gene FHOD3 has a mutation status of S448S, The gene THEG has a mutation status of D3Y, The gene THOP1 has a mutation status of P327P, The gene UHRF1 has a mutation status of Y491Y, The gene VAV1 has a mutation status of R688R, The gene AC008878.3 has a mutation status of W301G, The gene UNC13A has a mutation status of E1679D, The gene ZNF66 has a mutation status of L102fs, The gene YIF1B has a mutation status of I198I, The gene PRX has a mutation status of S51*, The gene MEGF8 has a mutation status of R2153C, The gene PRKD2 has a mutation status of I425T, The gene SYT3 has a mutation status of E6D, The gene ZNF841 has a mutation status of T116A, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of Q29Q, The gene LILRA2 has a mutation status of G30G, The gene LILRA1 has a mutation status of L268R, The gene LILRA1 has a mutation status of P271R, The gene LILRB1 has a mutation status of Y99I, The gene FAM71E2 has a mutation status of H264Y, The gene ZNF550 has a mutation status of C220S, The gene AL035460.1 has a mutation status of R236*, The gene MMP24 has a mutation status of R542Q, The gene PPP1R16B has a mutation status of W445C, The gene ACOT8 has a mutation status of K169K, The gene SLC12A5 has a mutation status of G75del, The gene RIPOR3 has a mutation status of A557V, The gene FAM210B has a mutation status of P20T, The gene SLC2A4RG has a mutation status of F273I, The gene KCNE1B has a mutation status of N88D, The gene COL6A2 has a mutation status of E311*, The gene GSTT4 has a mutation status of P89L, The gene MEI1 has a mutation status of R1064W, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene MXRA5 has a mutation status of G1654E, The gene NLGN4X has a mutation status of L732L, The gene ZNF157 has a mutation status of E390Q, The gene ZNF157 has a mutation status of E411K, The gene SPANXN5 has a mutation status of L67L, The gene FAAH2 has a mutation status of R149C, The gene ATP7A has a mutation status of R703C, The gene RPS6KA6 has a mutation status of M737V, The gene ZNF280C has a mutation status of F528F, The gene MAGEC1 has a mutation status of D1105N, The gene AC236972.4 has a mutation status of S1611S, The gene AC236972.4 has a mutation status of A1638T, The gene AC236972.4 has a mutation status of G1663G, The gene HCFC1 has a mutation status of A1849T, The gene F8 has a mutation status of L1017L, The gene MT-ND1 has a mutation status of A147T, The gene MT-ND2 has a mutation status of T334T, The gene MT-CO3 has a mutation status of G114G, The gene MT-ND4 has a mutation status of K93fs, The gene MT-ND5 has a mutation status of Y35Y, The gene MT-CYB has a mutation status of H16R
DLBC
The gene KLHL17 has a mutation status of T640P, The gene PRKCZ has a mutation status of D44N, The gene ESPN has a mutation status of A457S, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene TRIM63 has a mutation status of E108K, The gene ZBTB8OS has a mutation status of N167N, The gene TRIM62 has a mutation status of A251E, The gene PPCS has a mutation status of R25P, The gene GPX7 has a mutation status of L182L, The gene C8B has a mutation status of R83M, The gene CRYZ has a mutation status of R257R, The gene CLCA4 has a mutation status of S735Y, The gene TAFA3 has a mutation status of E6Q, The gene SLC25A44 has a mutation status of S228L, The gene EEF1AKNMT has a mutation status of Q163*, The gene LYST has a mutation status of S2437C, The gene ZNF692 has a mutation status of Y61D, The gene PCARE has a mutation status of Q1020R, The gene EHD3 has a mutation status of I342I, The gene RTKN has a mutation status of A318V, The gene TMEM131 has a mutation status of S989P, The gene CREG2 has a mutation status of Q237K, The gene MAP4K4 has a mutation status of R459W, The gene UGGT1 has a mutation status of V1261I, The gene TTN has a mutation status of I27048M, The gene ABCB6 has a mutation status of V609L, The gene RBM44 has a mutation status of S710S, The gene TATDN2 has a mutation status of R67W, The gene GRIP2 has a mutation status of R919G, The gene CAPN7 has a mutation status of P806S, The gene EAF1 has a mutation status of S45C, The gene ARIH2OS has a mutation status of A153G, The gene IMPDH2 has a mutation status of A54A, The gene GTF2E1 has a mutation status of L139L, The gene KPNA4 has a mutation status of E5*, The gene ALG3 has a mutation status of R8R, The gene UGT2B28 has a mutation status of A346T, The gene UGT2A2 has a mutation status of V59M, The gene SMAD1 has a mutation status of P137A, The gene SPOCK3 has a mutation status of P181P, The gene SPATA4 has a mutation status of P46L, The gene FAT1 has a mutation status of C4151*, The gene C7 has a mutation status of T543I, The gene BDP1 has a mutation status of R721R, The gene THBS4 has a mutation status of V805L, The gene SEPTIN8 has a mutation status of N208N, The gene PURA has a mutation status of G38V, The gene TCOF1 has a mutation status of G515G, The gene ADRA1B has a mutation status of L151L, The gene SPDL1 has a mutation status of R453S, The gene DOCK2 has a mutation status of K835E, The gene OR2V1 has a mutation status of S88Y, The gene HLA-A has a mutation status of Y137N, The gene NUDT3 has a mutation status of E54E, The gene KCTD20 has a mutation status of P69S, The gene COL10A1 has a mutation status of Y632Y, The gene SYNE1 has a mutation status of I7873T, The gene TNRC18 has a mutation status of L56R, The gene FSCN1 has a mutation status of S350S, The gene SNX13 has a mutation status of T868T, The gene CCDC201 has a mutation status of P18T, The gene FGL2 has a mutation status of R329C, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of T987I, The gene ATXN7L1 has a mutation status of P716L, The gene LMOD2 has a mutation status of H251Q, The gene PRSS2 has a mutation status of R68C, The gene CUL1 has a mutation status of Q509H, The gene KMT2C has a mutation status of R2307G, The gene GDF6 has a mutation status of G89S, The gene VPS13B has a mutation status of R1143Q, The gene GSDMD has a mutation status of E66Q, The gene FAM83H has a mutation status of R770L, The gene PTPRD has a mutation status of K1171K, The gene MPDZ has a mutation status of E702M, The gene CNTNAP3B has a mutation status of A629V, The gene CRB2 has a mutation status of T122P, The gene MIGA2 has a mutation status of R230Q, The gene MAMDC4 has a mutation status of Q433*, The gene VIM has a mutation status of T48P, The gene CDH23 has a mutation status of S1880R, The gene EXOC6 has a mutation status of M244V, The gene MUC5AC has a mutation status of G2219G, The gene MUC5AC has a mutation status of R3992H, The gene MUC5AC has a mutation status of A4116S, The gene TRIM5 has a mutation status of R97C, The gene DNHD1 has a mutation status of R82H, The gene C11orf96 has a mutation status of S72S, The gene OR9G1 has a mutation status of I196F, The gene OR5B3 has a mutation status of V246V, The gene PRPF19 has a mutation status of D54V, The gene SLC25A45 has a mutation status of R228W, The gene PELI3 has a mutation status of G375C, The gene NUMA1 has a mutation status of E458K, The gene ARHGEF17 has a mutation status of P26L, The gene SCNN1A has a mutation status of R204W, The gene PZP has a mutation status of Q289Q, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene AEBP2 has a mutation status of I445I, The gene MCRS1 has a mutation status of R317Q, The gene AMHR2 has a mutation status of R270H, The gene MARCHF9 has a mutation status of K281K, The gene DCN has a mutation status of S121S, The gene GNPTAB has a mutation status of R1237W, The gene P2RX4 has a mutation status of L12L, The gene PCDH8 has a mutation status of V739G, The gene FARP1 has a mutation status of R27L, The gene ZNF219 has a mutation status of T146P, The gene YY1 has a mutation status of V324V, The gene ZNF839 has a mutation status of K577K, The gene LINC02203 has a mutation status of I259M, The gene PLCB2 has a mutation status of G948G, The gene WDR24 has a mutation status of S14S, The gene SRL has a mutation status of N78S, The gene SOCS1 has a mutation status of L73L, The gene ALDOA has a mutation status of A20V, The gene TBX6 has a mutation status of D177N, The gene MAPK3 has a mutation status of R15S, The gene EXOC3L1 has a mutation status of D675E, The gene SLC9A5 has a mutation status of Y609H, The gene KCTD19 has a mutation status of R276H, The gene DUS2 has a mutation status of M19V, The gene CFDP1 has a mutation status of E112Q, The gene ZZEF1 has a mutation status of K1954K, The gene EPN2 has a mutation status of S441S, The gene CCL4L2 has a mutation status of P67R, The gene MYO19 has a mutation status of V392G, The gene KRTAP4-1 has a mutation status of R85R, The gene MYO15B has a mutation status of L1913L, The gene DNAH17 has a mutation status of A3696S, The gene ENGASE has a mutation status of V583I, The gene HRH4 has a mutation status of S320S, The gene MC4R has a mutation status of K314E, The gene SALL3 has a mutation status of A185L, The gene SALL3 has a mutation status of P1039T, The gene PRSS57 has a mutation status of D246N, The gene PCSK4 has a mutation status of V111G, The gene JSRP1 has a mutation status of K303N, The gene LINGO3 has a mutation status of V93M, The gene MAP2K7 has a mutation status of A281A, The gene SMARCA4 has a mutation status of Q555*, The gene ZNF627 has a mutation status of P100P, The gene ZNF440 has a mutation status of L439L, The gene SLC5A5 has a mutation status of R374Q, The gene ZNF723 has a mutation status of R166K, The gene PMIS2 has a mutation status of A33A, The gene YIF1B has a mutation status of V72A, The gene AKT1S1 has a mutation status of A58V, The gene NUP62 has a mutation status of T278T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene KIR2DL4 has a mutation status of S282T, The gene EPS8L1 has a mutation status of A126G, The gene EPS8L1 has a mutation status of E127G, The gene MAVS has a mutation status of H453P, The gene CSF2RB has a mutation status of R64W, The gene ELFN2 has a mutation status of P651L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene KLHDC7B has a mutation status of G275C, The gene MAP3K15 has a mutation status of A830P, The gene CCDC120 has a mutation status of T355P, The gene ERCC6L has a mutation status of A298A, The gene ABCB7 has a mutation status of S262G, The gene ARMCX2 has a mutation status of Q503Q, The gene COL4A6 has a mutation status of 1640_1642RGT>P, The gene BCORL1 has a mutation status of L1132P, The gene FGF13 has a mutation status of I55I, The gene HCFC1 has a mutation status of T332P, The gene MT-CO3 has a mutation status of F235L, The gene MT-ND5 has a mutation status of T533M, The gene MT-CYB has a mutation status of A52A
SARC
The gene PRAMEF11 has a mutation status of L346L, The gene PRAMEF11 has a mutation status of V27I, The gene PRAMEF11 has a mutation status of A15V, The gene PRAMEF5 has a mutation status of P432A, The gene PRAMEF5 has a mutation status of K440G, The gene ATP13A2 has a mutation status of R397C, The gene KLHDC7A has a mutation status of E749M, The gene EXTL1 has a mutation status of S17F, The gene ZDHHC18 has a mutation status of I9I, The gene RIMS3 has a mutation status of T271T, The gene MAST2 has a mutation status of T274M, The gene MSH4 has a mutation status of R350*, The gene CELSR2 has a mutation status of R1331H, The gene NBPF12 has a mutation status of D607H, The gene HRNR has a mutation status of G300G, The gene SLC27A3 has a mutation status of S216S, The gene MUC1 has a mutation status of G42G, The gene F5 has a mutation status of R534Q, The gene CENPF has a mutation status of E1605*, The gene COQ8A has a mutation status of F93F, The gene CAPN9 has a mutation status of A661G, The gene ROCK2 has a mutation status of L623L, The gene CYP1B1 has a mutation status of D291D, The gene EPAS1 has a mutation status of D753E, The gene SLC9A2 has a mutation status of L208L, The gene MERTK has a mutation status of P7L, The gene SCN2A has a mutation status of V1408V, The gene TTN has a mutation status of E12549K, The gene ADAM23 has a mutation status of G5C, The gene UNC80 has a mutation status of S1800S, The gene SLC23A3 has a mutation status of V435V, The gene TRIP12 has a mutation status of G148E, The gene SLC16A14 has a mutation status of A73V, The gene FBLN2 has a mutation status of T1088P, The gene ZCWPW2 has a mutation status of Q83R, The gene MYD88 has a mutation status of S15S, The gene KLHL18 has a mutation status of E3A, The gene BSN has a mutation status of Q136fs, The gene DNAH1 has a mutation status of F2641F, The gene PROK2 has a mutation status of S54N, The gene ARMC8 has a mutation status of A584A, The gene MED12L has a mutation status of F471F, The gene SI has a mutation status of L652I, The gene PDCD10 has a mutation status of *213W, The gene SPON2 has a mutation status of A105E, The gene PARM1 has a mutation status of P32P, The gene FRAS1 has a mutation status of T3618I, The gene IRX2 has a mutation status of N113N, The gene CDH12 has a mutation status of Q60Q, The gene DROSHA has a mutation status of G379S, The gene NIPBL has a mutation status of L1978I, The gene AC022414.1 has a mutation status of A100A, The gene PGGT1B has a mutation status of S56S, The gene MATR3 has a mutation status of A778A, The gene PCDHB14 has a mutation status of A656T, The gene DELE1 has a mutation status of W21*, The gene SLIT3 has a mutation status of R775Q, The gene FGF18 has a mutation status of S3S, The gene UBTD2 has a mutation status of G6D, The gene CREBRF has a mutation status of K493I, The gene SFXN1 has a mutation status of A129A, The gene SIMC1 has a mutation status of R411C, The gene SIRT5 has a mutation status of E208E, The gene KDM1B has a mutation status of L211L, The gene BTN3A3 has a mutation status of I483I, The gene EHMT2 has a mutation status of T1210I, The gene RING1 has a mutation status of G217V, The gene TRERF1 has a mutation status of E999*, The gene CDC5L has a mutation status of N161N, The gene LGSN has a mutation status of R366*, The gene FAM135A has a mutation status of F240F, The gene L3MBTL3 has a mutation status of G223V, The gene UTRN has a mutation status of P3356T, The gene CCL26 has a mutation status of K67R, The gene PCLO has a mutation status of F2639L, The gene PCLO has a mutation status of T439S, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of E725K, The gene MUC3A has a mutation status of T730I, The gene MUC17 has a mutation status of T3138T, The gene GPR37 has a mutation status of R413Q, The gene FAM71F1 has a mutation status of R189H, The gene FLNC has a mutation status of R420Q, The gene KLF14 has a mutation status of A39A, The gene PLXNA4 has a mutation status of S1630I, The gene DGKI has a mutation status of Q111H, The gene BRAF has a mutation status of V600E, The gene PRSS1 has a mutation status of N77N, The gene PRKAG2 has a mutation status of S226C, The gene DLGAP2 has a mutation status of N389T, The gene DLGAP2 has a mutation status of D391E, The gene XKR6 has a mutation status of A230V, The gene USP17L2 has a mutation status of A525A, The gene SPIDR has a mutation status of S226P, The gene NSMAF has a mutation status of N328S, The gene CHD7 has a mutation status of N2216N, The gene ASPH has a mutation status of P331A, The gene C8orf34 has a mutation status of S518S, The gene SNX16 has a mutation status of R170C, The gene ABRA has a mutation status of E96E, The gene ZHX1-C8orf76 has a mutation status of H175R, The gene FBXL6 has a mutation status of D404G, The gene SLC39A4 has a mutation status of R251W, The gene CDKN2B has a mutation status of E16D, The gene CNTFR has a mutation status of H170H, The gene RECK has a mutation status of C709C, The gene KLF4 has a mutation status of T114I, The gene SLC27A4 has a mutation status of D99D, The gene SETX has a mutation status of N1409Y, The gene SNAPC4 has a mutation status of P914T, The gene JCAD has a mutation status of L1032L, The gene PARD3 has a mutation status of G904R, The gene SAMD8 has a mutation status of V290G, The gene CUTC has a mutation status of S34S, The gene BLOC1S2 has a mutation status of A22A, The gene MUC6 has a mutation status of G948R, The gene MUC5AC has a mutation status of T3044T, The gene ZNF195 has a mutation status of Q134K, The gene DNHD1 has a mutation status of R3978P, The gene OR5P2 has a mutation status of G249G, The gene E2F8 has a mutation status of P56P, The gene FNBP4 has a mutation status of Q48H, The gene FOLH1 has a mutation status of L35L, The gene OR4A5 has a mutation status of G39W, The gene OR9G1 has a mutation status of T62V, The gene RNF169 has a mutation status of E364D, The gene EED has a mutation status of P10S, The gene CASP5 has a mutation status of I114T, The gene C2CD2L has a mutation status of E178D, The gene RNF26 has a mutation status of V17M, The gene OR10G8 has a mutation status of S92A, The gene FAM118B has a mutation status of A76A, The gene LRRK2 has a mutation status of L425L, The gene COL2A1 has a mutation status of P1368A, The gene KRT2 has a mutation status of G107G, The gene LGR5 has a mutation status of H166H, The gene NAV3 has a mutation status of L1511V, The gene CHPT1 has a mutation status of E90K, The gene PAH has a mutation status of E39D, The gene SLC41A2 has a mutation status of Q34R, The gene WASHC4 has a mutation status of I664I, The gene NOS1 has a mutation status of M5I, The gene SIRT4 has a mutation status of R178R, The gene TSC22D1 has a mutation status of P120T, The gene RCBTB1 has a mutation status of S397S, The gene FBXL3 has a mutation status of Q85L, The gene FARP1 has a mutation status of P447P, The gene INSM2 has a mutation status of E50G, The gene FANCM has a mutation status of P90L, The gene NID2 has a mutation status of T567T, The gene RTN1 has a mutation status of E362Q, The gene SERPINA1 has a mutation status of I296I, The gene GOLGA6L6 has a mutation status of Q229E, The gene BUB1B has a mutation status of T620S, The gene CCNB2 has a mutation status of A134S, The gene ALPK3 has a mutation status of I548L, The gene PKD1 has a mutation status of V2267G, The gene NTAN1 has a mutation status of H115Y, The gene MVP has a mutation status of G269A, The gene MT1A has a mutation status of G52E, The gene TERF2 has a mutation status of Q475R, The gene CNTNAP4 has a mutation status of R841Q, The gene HSDL1 has a mutation status of Q233Q, The gene TP53 has a mutation status of A119fs, The gene CHD3 has a mutation status of Q445E, The gene CCL4L2 has a mutation status of P67R, The gene KRT31 has a mutation status of N255K, The gene KAT2A has a mutation status of P302L, The gene EFCAB13 has a mutation status of D218fs, The gene EFCAB13 has a mutation status of V217V, The gene LLGL2 has a mutation status of P955R, The gene LRRC45 has a mutation status of R148R, The gene ZBTB14 has a mutation status of F4L, The gene RAB12 has a mutation status of F11L, The gene SEH1L has a mutation status of R5P, The gene KLHL14 has a mutation status of Y453Y, The gene SETBP1 has a mutation status of P1536T, The gene RTTN has a mutation status of L1214L, The gene ZADH2 has a mutation status of V5G, The gene NFATC1 has a mutation status of P488P, The gene SLC25A23 has a mutation status of R243R, The gene ANGPTL4 has a mutation status of A92V, The gene MUC16 has a mutation status of T5257I, The gene S1PR2 has a mutation status of A230D, The gene ANKLE1 has a mutation status of R90R, The gene CEACAM5 has a mutation status of V588V, The gene PSG7 has a mutation status of N268H, The gene ERCC2 has a mutation status of R185Q, The gene POLD1 has a mutation status of A698A, The gene ZNF845 has a mutation status of C945S, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRB1 has a mutation status of Q401L, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL3 has a mutation status of E295D, The gene KIR2DL1 has a mutation status of P175T, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene NLRP7 has a mutation status of A826D, The gene OVOL2 has a mutation status of Q202*, The gene ABHD12 has a mutation status of A16A, The gene BPIFA2 has a mutation status of D34G, The gene TOMM34 has a mutation status of E96E, The gene TSHZ2 has a mutation status of I528I, The gene PPP1R3D has a mutation status of Q203Q, The gene DSCAM has a mutation status of T1701M, The gene COMT has a mutation status of N39D, The gene HORMAD2 has a mutation status of E18K, The gene TCN2 has a mutation status of S170S, The gene PISD has a mutation status of L161L, The gene PISD has a mutation status of H14H, The gene Z82190.2 has a mutation status of F77L, The gene TRIOBP has a mutation status of H1103H, The gene APOBEC3C has a mutation status of D99D, The gene IL13RA1 has a mutation status of F287S, The gene MECP2 has a mutation status of S149S, The gene MT-ATP6 has a mutation status of I24I, The gene MT-ND4 has a mutation status of S442S, The gene MT-ND5 has a mutation status of T13A, The gene MT-ND6 has a mutation status of V106A, The gene MT-ND6 has a mutation status of F19L, The gene MT-CYB has a mutation status of I14I
SARC
The gene MMP23B has a mutation status of R377H, The gene VPS13D has a mutation status of T770T, The gene VPS13D has a mutation status of S1513R, The gene PRAMEF9 has a mutation status of A352V, The gene PRAMEF13 has a mutation status of S245Y, The gene PRAMEF13 has a mutation status of Y166H, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene CPLANE2 has a mutation status of A225A, The gene PNRC2 has a mutation status of S51S, The gene EXTL1 has a mutation status of R544K, The gene EPB41 has a mutation status of A561A, The gene MTF1 has a mutation status of T703A, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene HFM1 has a mutation status of Q126*, The gene GPR88 has a mutation status of G249D, The gene TTF2 has a mutation status of N270Y, The gene FCGR1B has a mutation status of M172I, The gene NBPF15 has a mutation status of D237N, The gene NBPF12 has a mutation status of L965V, The gene NBPF14 has a mutation status of V1509V, The gene AC242842.3 has a mutation status of L2061L, The gene FLG has a mutation status of E3203D, The gene FLG2 has a mutation status of V11I, The gene LCE1F has a mutation status of G65C, The gene ARHGEF11 has a mutation status of M1320fs, The gene FCRLB has a mutation status of P91P, The gene TNR has a mutation status of L552L, The gene BRINP2 has a mutation status of G176G, The gene IL19 has a mutation status of C56*, The gene ESRRG has a mutation status of L84P, The gene AHCTF1 has a mutation status of I830V, The gene OR2T4 has a mutation status of V109L, The gene GCKR has a mutation status of L497L, The gene GPN1 has a mutation status of S364L, The gene PPP1R21 has a mutation status of D665D, The gene PSME4 has a mutation status of M1720T, The gene DNAH6 has a mutation status of S1266G, The gene EIF2AK3 has a mutation status of E1050K, The gene ADRA2B has a mutation status of A57A, The gene ERCC3 has a mutation status of T393T, The gene ITGB6 has a mutation status of P164R, The gene TTN has a mutation status of A32695F, The gene KCTD18 has a mutation status of R325H, The gene KANSL1L has a mutation status of H252H, The gene VIL1 has a mutation status of P694R, The gene AGAP1 has a mutation status of *805L, The gene USP4 has a mutation status of G73V, The gene SLC38A3 has a mutation status of E56K, The gene CACNA1D has a mutation status of K881K, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene ACOX2 has a mutation status of M81T, The gene IGSF11 has a mutation status of I73I, The gene GOLGB1 has a mutation status of L1896L, The gene HEG1 has a mutation status of G1345V, The gene C3orf56 has a mutation status of R236H, The gene AC131160.1 has a mutation status of S198S, The gene CHRNA9 has a mutation status of A45A, The gene CNOT6L has a mutation status of A301A, The gene TMEM150C has a mutation status of E236G, The gene FAT4 has a mutation status of S4458P, The gene TMEM131L has a mutation status of L497V, The gene GUCY1A1 has a mutation status of L299M, The gene CEP44 has a mutation status of N183N, The gene FAT1 has a mutation status of L2449I, The gene FAT1 has a mutation status of F2227F, The gene ARL15 has a mutation status of I77V, The gene ELL2 has a mutation status of N418N, The gene MEGF10 has a mutation status of H205H, The gene ZMAT2 has a mutation status of G109G, The gene PCDHB6 has a mutation status of G324G, The gene PCDHB10 has a mutation status of S68Y, The gene JAKMIP2 has a mutation status of Q797K, The gene ARSI has a mutation status of V175M, The gene KCNIP1 has a mutation status of E28*, The gene RIPK1 has a mutation status of A569V, The gene HIVEP1 has a mutation status of S1552C, The gene DDR1 has a mutation status of D776E, The gene PHF3 has a mutation status of K668R, The gene IL20RA has a mutation status of P443P, The gene SYNE1 has a mutation status of V4348M, The gene LPA has a mutation status of S1395G, The gene AGMO has a mutation status of A358G, The gene HDAC9 has a mutation status of G712R, The gene GLI3 has a mutation status of V608V, The gene ADCY1 has a mutation status of A797V, The gene ABCB1 has a mutation status of K624R, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2046L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene RELN has a mutation status of H1325Y, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PRSS1 has a mutation status of N29T, The gene PRSS1 has a mutation status of N54R, The gene CNTNAP2 has a mutation status of K710T, The gene ADGRA2 has a mutation status of E1245G, The gene ZFHX4 has a mutation status of L27R, The gene SLC7A13 has a mutation status of S126R, The gene TMEM64 has a mutation status of C315fs, The gene LYNX1 has a mutation status of L12F, The gene SCRIB has a mutation status of A796A, The gene EPPK1 has a mutation status of A2633del, The gene PLEC has a mutation status of F1283F, The gene CCL27 has a mutation status of D61E, The gene SECISBP2 has a mutation status of N187S, The gene PHF2 has a mutation status of R201P, The gene ERCC6L2 has a mutation status of R1068I, The gene FRRS1L has a mutation status of R51A, The gene PRPF4 has a mutation status of T268I, The gene NUP214 has a mutation status of M363V, The gene CCDC187 has a mutation status of L747L, The gene GATA3 has a mutation status of S166S, The gene DNAJC1 has a mutation status of R352R, The gene C10orf67 has a mutation status of A468A, The gene FRA10AC1 has a mutation status of Q75*, The gene FRA10AC1 has a mutation status of E59E, The gene RRP12 has a mutation status of E1058E, The gene PSD has a mutation status of N583N, The gene PCGF6 has a mutation status of T17S, The gene GPAM has a mutation status of C490F, The gene EMX2 has a mutation status of P91fs, The gene EMX2 has a mutation status of H92fs, The gene DMBT1 has a mutation status of L715L, The gene CPXM2 has a mutation status of S347G, The gene MKI67 has a mutation status of I2958T, The gene MUC5B has a mutation status of P2052L, The gene OR52J3 has a mutation status of L68I, The gene DCHS1 has a mutation status of A2963D, The gene IPO7 has a mutation status of N803S, The gene DCDC1 has a mutation status of E437D, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene RAB3IL1 has a mutation status of T163M, The gene AIP has a mutation status of R81*, The gene PGR has a mutation status of L691L, The gene NXPE4 has a mutation status of L39V, The gene SLC6A13 has a mutation status of V345V, The gene B4GALNT3 has a mutation status of K558R, The gene P3H3 has a mutation status of S502F, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R31 has a mutation status of I33T, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PLCZ1 has a mutation status of P263T, The gene DDX23 has a mutation status of S41P, The gene LRRIQ1 has a mutation status of H1090L, The gene CEP83 has a mutation status of E443V, The gene NOS1 has a mutation status of E1088Q, The gene HIP1R has a mutation status of F337F, The gene PARP4 has a mutation status of K1239N, The gene FREM2 has a mutation status of P1704T, The gene NALCN has a mutation status of P1191T, The gene FAM155A has a mutation status of S314S, The gene HECTD1 has a mutation status of G347R, The gene POLE2 has a mutation status of L11F, The gene TXNDC16 has a mutation status of E67K, The gene FERMT2 has a mutation status of T192N, The gene TMEM30B has a mutation status of A166T, The gene SYT16 has a mutation status of F106S, The gene PCNX1 has a mutation status of P280P, The gene CATSPERB has a mutation status of M901I, The gene GOLGA6L6 has a mutation status of MWREEEKMHEQEKIWEEEKRQEQEDKMWRQEEKIREQEE520del, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L1 has a mutation status of M518V, The gene ATP10A has a mutation status of G349V, The gene TRPM1 has a mutation status of G305E, The gene PLCB2 has a mutation status of A395V, The gene FBN1 has a mutation status of I849V, The gene LDHAL6B has a mutation status of S339N, The gene LDHAL6B has a mutation status of I343V, The gene ANKDD1A has a mutation status of L516L, The gene SCAPER has a mutation status of N1327K, The gene TMEM114 has a mutation status of L5L, The gene TP53 has a mutation status of R273C, The gene LLGL1 has a mutation status of E67E, The gene PECAM1 has a mutation status of V513V, The gene UBE2O has a mutation status of L460L, The gene L3MBTL4 has a mutation status of M409I, The gene GREB1L has a mutation status of L1112L, The gene IMPACT has a mutation status of L104R, The gene SLC39A6 has a mutation status of V750M, The gene SMIM21 has a mutation status of W78R, The gene MIDN has a mutation status of P325fs, The gene MRPL54 has a mutation status of R128H, The gene ZNF557 has a mutation status of Y348C, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T12336L, The gene MUC16 has a mutation status of D3437Y, The gene SLC1A6 has a mutation status of E450D, The gene ZNF493 has a mutation status of 597_598DK>EE, The gene ZNF227 has a mutation status of D142N, The gene KDELR1 has a mutation status of T160T, The gene NAPSA has a mutation status of P4Q, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of 350_351insGY, The gene LILRA1 has a mutation status of L268R, The gene LILRA1 has a mutation status of P271R, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene LILRB1 has a mutation status of Y99I, The gene LILRB1 has a mutation status of 171_172QP>HS, The gene LILRB1 has a mutation status of P189P, The gene LILRB1 has a mutation status of Q401L, The gene LZTS3 has a mutation status of P314Q, The gene KRTAP10-3 has a mutation status of S25N, The gene GSTT4 has a mutation status of Q197R, The gene LRRC75B has a mutation status of Y73C, The gene KIAA1671 has a mutation status of P818L, The gene FOXRED2 has a mutation status of P667P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SERHL2 has a mutation status of M309L, The gene PPP2R3B has a mutation status of W58*, The gene VCX3A has a mutation status of S108A, The gene PHKA2 has a mutation status of P498L, The gene FAM47C has a mutation status of P206L, The gene GAGE2A has a mutation status of R4*, The gene SPANXN5 has a mutation status of L67L, The gene KLHL13 has a mutation status of F545V, The gene SLC25A5 has a mutation status of T221R, The gene ACTRT1 has a mutation status of F363L, The gene OCRL has a mutation status of S683S, The gene MCF2 has a mutation status of R31R, The gene SOX3 has a mutation status of A117G, The gene AC236972.4 has a mutation status of S1611S, The gene PNMA6E has a mutation status of G636R, The gene PDZD4 has a mutation status of R243H, The gene MT-ND2 has a mutation status of T226T, The gene MT-CO3 has a mutation status of G234S, The gene MT-ND4 has a mutation status of L351L
DLBC
The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene TRIM63 has a mutation status of S110C, The gene ZDHHC18 has a mutation status of D371Y, The gene ZNF362 has a mutation status of A74A, The gene EPHA10 has a mutation status of V264G, The gene TSPAN1 has a mutation status of G224G, The gene LRP8 has a mutation status of T137P, The gene PARS2 has a mutation status of A271S, The gene CLCA1 has a mutation status of A819V, The gene CLCA4 has a mutation status of I612M, The gene STRIP1 has a mutation status of Q30H, The gene PROK1 has a mutation status of H61P, The gene DENND2D has a mutation status of R13G, The gene PPM1J has a mutation status of N30N, The gene NRAS has a mutation status of Q61K, The gene CELF3 has a mutation status of G324V, The gene SLC27A3 has a mutation status of K3N, The gene KCNN3 has a mutation status of P63Q, The gene TNFSF18 has a mutation status of V101M, The gene HMCN1 has a mutation status of Q760R, The gene ASPM has a mutation status of A22P, The gene IGFN1 has a mutation status of S2300S, The gene RASSF5 has a mutation status of Y13S, The gene OBSCN has a mutation status of A5522D, The gene OR2L13 has a mutation status of G218C, The gene OR2T4 has a mutation status of V109L, The gene TRMT61B has a mutation status of S69Y, The gene PKDCC has a mutation status of H194P, The gene UGP2 has a mutation status of I357T, The gene RAB11FIP5 has a mutation status of T276P, The gene CCDC142 has a mutation status of G287G, The gene ELMOD3 has a mutation status of D308H, The gene CNGA3 has a mutation status of L361L, The gene SOWAHC has a mutation status of G224D, The gene GLI2 has a mutation status of S1194N, The gene GALNT13 has a mutation status of L114I, The gene KCNJ3 has a mutation status of S69P, The gene SCN2A has a mutation status of V892I, The gene LRP2 has a mutation status of R948H, The gene NRP2 has a mutation status of R310R, The gene IDH1 has a mutation status of R132C, The gene PNKD has a mutation status of V193G, The gene AC053503.6 has a mutation status of C100S, The gene AC053503.6 has a mutation status of H101P, The gene GPC1 has a mutation status of G491G, The gene CRBN has a mutation status of H17P, The gene LMCD1 has a mutation status of A293A, The gene CCR5 has a mutation status of L39V, The gene LTF has a mutation status of T103T, The gene AC109583.1 has a mutation status of W124G, The gene COL7A1 has a mutation status of T1231I, The gene NCKIPSD has a mutation status of P544S, The gene BSN has a mutation status of G1633G, The gene BSN has a mutation status of S3450R, The gene DCP1A has a mutation status of S523S, The gene OR5H2 has a mutation status of Y218S, The gene CCDC54 has a mutation status of S148F, The gene PLXNA1 has a mutation status of G1254G, The gene GATA2 has a mutation status of H460P, The gene TFDP2 has a mutation status of V98L, The gene KPNA4 has a mutation status of N39K, The gene LRRIQ4 has a mutation status of H118H, The gene VWA5B2 has a mutation status of D1012A, The gene SH3BP2 has a mutation status of R292Q, The gene WFS1 has a mutation status of Q520*, The gene SOD3 has a mutation status of H139P, The gene SOD3 has a mutation status of H142P, The gene FREM3 has a mutation status of F723L, The gene FAT1 has a mutation status of P4347S, The gene TRIO has a mutation status of V2702I, The gene RXFP3 has a mutation status of T419P, The gene GFRA3 has a mutation status of M349I, The gene PURA has a mutation status of P51P, The gene CDX1 has a mutation status of Y14S, The gene MGAT4B has a mutation status of H111P, The gene H1-4 has a mutation status of K97R, The gene MICB has a mutation status of A17A, The gene HLA-DRB5 has a mutation status of Q220W, The gene TBCC has a mutation status of C237C, The gene AARS2 has a mutation status of R166W, The gene RNGTT has a mutation status of K239K, The gene HINT3 has a mutation status of N68S, The gene SOGA3 has a mutation status of A127P, The gene MICALL2 has a mutation status of L242P, The gene AMZ1 has a mutation status of T343P, The gene RAC1 has a mutation status of N111I, The gene FAM126A has a mutation status of Y272H, The gene CAMK2B has a mutation status of R509P, The gene MLXIPL has a mutation status of S607S, The gene DTX2 has a mutation status of G149R, The gene DTX2 has a mutation status of Y180S, The gene BET1 has a mutation status of K47R, The gene PPP1R35 has a mutation status of R191P, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene KLF14 has a mutation status of P58S, The gene KDM7A has a mutation status of V8G, The gene PRSS1 has a mutation status of N77N, The gene EPHA1 has a mutation status of T230A, The gene RBM33 has a mutation status of Q596H, The gene PRSS55 has a mutation status of P80L, The gene REEP4 has a mutation status of S78S, The gene CHRNA2 has a mutation status of G25G, The gene ADGRA2 has a mutation status of T397P, The gene PREX2 has a mutation status of A1523P, The gene ANGPT1 has a mutation status of I219T, The gene ADGRB1 has a mutation status of T1375P, The gene HGH1 has a mutation status of V159G, The gene DGAT1 has a mutation status of V301G, The gene NFX1 has a mutation status of H865P, The gene KIF24 has a mutation status of E401A, The gene FAM205A has a mutation status of Y1314S, The gene FRRS1L has a mutation status of R51A, The gene PTGES2 has a mutation status of V243G, The gene COL5A1 has a mutation status of A1320A, The gene CAMSAP1 has a mutation status of T1548T, The gene CCDC187 has a mutation status of L747L, The gene SNAPC4 has a mutation status of V1292G, The gene NOTCH1 has a mutation status of T701P, The gene ABCA2 has a mutation status of S1552S, The gene C1QL3 has a mutation status of T27P, The gene VIM has a mutation status of T48P, The gene GAD2 has a mutation status of M204T, The gene ZNF488 has a mutation status of V113G, The gene CDH23 has a mutation status of G2017G, The gene LMNTD2 has a mutation status of H301P, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of R4992R, The gene NLRP14 has a mutation status of D656N, The gene SLC17A6 has a mutation status of A224T, The gene OR9G1 has a mutation status of T62V, The gene DTX4 has a mutation status of T375K, The gene CD6 has a mutation status of P495P, The gene C11orf95 has a mutation status of A662A, The gene GPR137 has a mutation status of T364P, The gene CTSF has a mutation status of S76A, The gene TCIRG1 has a mutation status of V294V, The gene CLPB has a mutation status of D252N, The gene KLHL35 has a mutation status of T200P, The gene NAALAD2 has a mutation status of G201G, The gene FAT3 has a mutation status of A4136P, The gene DDI1 has a mutation status of R188M, The gene DDI1 has a mutation status of Q195L, The gene PPP2R1B has a mutation status of E31K, The gene PPP2R1B has a mutation status of G3G, The gene TMPRSS5 has a mutation status of V14G, The gene CACNA1C has a mutation status of P816P, The gene NRIP2 has a mutation status of L192R, The gene SLCO1A2 has a mutation status of Y89*, The gene DBX2 has a mutation status of G337W, The gene H1-7 has a mutation status of S19G, The gene KRT71 has a mutation status of E494G, The gene NT5DC3 has a mutation status of M224V, The gene GCN1 has a mutation status of G2102G, The gene PXN has a mutation status of T249P, The gene KNTC1 has a mutation status of I704V, The gene TMEM132B has a mutation status of P873H, The gene ADGRD1 has a mutation status of S894T, The gene KLF5 has a mutation status of P32P, The gene DZIP1 has a mutation status of Q166R, The gene F7 has a mutation status of H411P, The gene ADPRHL1 has a mutation status of G1442C, The gene C13orf46 has a mutation status of S103N, The gene CDC16 has a mutation status of E4K, The gene DHRS4L2 has a mutation status of E94G, The gene PTGER2 has a mutation status of D53G, The gene ACOT4 has a mutation status of D113A, The gene ENTPD5 has a mutation status of T130A, The gene CHGA has a mutation status of E211G, The gene ASB2 has a mutation status of H515P, The gene LINC02203 has a mutation status of I259M, The gene STARD9 has a mutation status of S2263I, The gene FOXB1 has a mutation status of T300P, The gene KBTBD13 has a mutation status of D290A, The gene C15orf39 has a mutation status of L385P, The gene C15orf39 has a mutation status of Y388C, The gene GOLGA6L9 has a mutation status of Q151E, The gene GOLGA6L9 has a mutation status of R228S, The gene WDR90 has a mutation status of P1013L, The gene MSLNL has a mutation status of G228R, The gene IGFALS has a mutation status of G535G, The gene XYLT1 has a mutation status of E664D, The gene POLR3E has a mutation status of R560P, The gene SETD1A has a mutation status of H749P, The gene PRSS36 has a mutation status of D488A, The gene PRSS36 has a mutation status of S147S, The gene CNGB1 has a mutation status of E163G, The gene CDH16 has a mutation status of G352G, The gene SMPD3 has a mutation status of S590S, The gene BCAR1 has a mutation status of V580G, The gene CNTNAP4 has a mutation status of E1305*, The gene MON1B has a mutation status of E211fs, The gene JPH3 has a mutation status of R503R, The gene CDT1 has a mutation status of T406P, The gene RPH3AL has a mutation status of H255P, The gene ITGAE has a mutation status of S918P, The gene KIF1C has a mutation status of V12G, The gene DHX33 has a mutation status of I76I, The gene NLGN2 has a mutation status of L729P, The gene SPEM3 has a mutation status of Q1149K, The gene CFAP52 has a mutation status of N66K, The gene FLII has a mutation status of E552G, The gene TRAF4 has a mutation status of K53K, The gene EVI2B has a mutation status of P407P, The gene LIG3 has a mutation status of T219S, The gene CCL4L2 has a mutation status of P67R, The gene FBXL20 has a mutation status of V280G, The gene KRTAP17-1 has a mutation status of G33R, The gene KRT32 has a mutation status of P427I, The gene BRCA1 has a mutation status of I1879T, The gene PLEKHM1 has a mutation status of A546G, The gene SGCA has a mutation status of V175V, The gene SGCA has a mutation status of A178A, The gene MYCBPAP has a mutation status of R73H, The gene SMIM36 has a mutation status of S79Y, The gene PECAM1 has a mutation status of V513V, The gene LLGL2 has a mutation status of P955R, The gene ENPP7 has a mutation status of T68P, The gene GAA has a mutation status of A820S, The gene ZNF521 has a mutation status of V284I, The gene KCTD1 has a mutation status of R844P, The gene ASXL3 has a mutation status of I1279K, The gene PLK5 has a mutation status of T235P, The gene LMNB2 has a mutation status of T556M, The gene DIRAS1 has a mutation status of V18G, The gene TLE2 has a mutation status of C461C, The gene TLE2 has a mutation status of P209R, The gene FZR1 has a mutation status of T300P, The gene MUC16 has a mutation status of E583K, The gene ZNF560 has a mutation status of L134M, The gene COL5A3 has a mutation status of F454L, The gene PDE4A has a mutation status of D517A, The gene FBXW9 has a mutation status of T55T, The gene CHERP has a mutation status of R823Q, The gene GDF1 has a mutation status of A158A, The gene WDR62 has a mutation status of I1263L, The gene CEACAM16 has a mutation status of T25P, The gene PNMA8B has a mutation status of V397G, The gene FAM83E has a mutation status of V231G, The gene FGF21 has a mutation status of A157A, The gene SHANK1 has a mutation status of L307L, The gene IGLON5 has a mutation status of S30P, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA4 has a mutation status of S387S, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene KIR3DL1 has a mutation status of G25D, The gene SHISA7 has a mutation status of P159P, The gene CPXM1 has a mutation status of L348R, The gene LZTS3 has a mutation status of G595G, The gene INSM1 has a mutation status of E299E, The gene NKX2-4 has a mutation status of Y137D, The gene ACSS1 has a mutation status of A70fs, The gene TM9SF4 has a mutation status of L14F, The gene SNTA1 has a mutation status of T499P, The gene SRC has a mutation status of L18R, The gene SYS1 has a mutation status of G3G, The gene COL18A1 has a mutation status of G671G, The gene CLDN5 has a mutation status of V32G, The gene GSTT4 has a mutation status of Q197R, The gene AP1B1 has a mutation status of D657Y, The gene SF3A1 has a mutation status of T416T, The gene MEI1 has a mutation status of T40P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SBF1 has a mutation status of A1299A, The gene ARHGAP6 has a mutation status of T963S, The gene FAM47B has a mutation status of R114P, The gene HDAC6 has a mutation status of T807P, The gene MSN has a mutation status of T235T, The gene PGK1 has a mutation status of Q300K, The gene SRPX2 has a mutation status of G172G, The gene ARMCX2 has a mutation status of Q503Q, The gene NKAP has a mutation status of S36P, The gene IGSF1 has a mutation status of L1056L, The gene F9 has a mutation status of V447V, The gene AVPR2 has a mutation status of W164L, The gene MT-ND1 has a mutation status of G203G, The gene MT-ATP6 has a mutation status of A177T, The gene MT-CO3 has a mutation status of W58W, The gene MT-ND3 has a mutation status of P43P, The gene MT-ND4 has a mutation status of I165T, The gene MT-CYB has a mutation status of L160L
SARC
The gene B3GALT6 has a mutation status of A34A, The gene PRAMEF13 has a mutation status of T257I, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF14 has a mutation status of R434W, The gene PRDM2 has a mutation status of V618I, The gene CELA2B has a mutation status of Y91Y, The gene DLGAP3 has a mutation status of D24D, The gene LRRIQ3 has a mutation status of M569K, The gene LRRIQ3 has a mutation status of E568K, The gene NBPF26 has a mutation status of P951R, The gene ANKRD35 has a mutation status of R3C, The gene NBPF12 has a mutation status of E80*, The gene NBPF14 has a mutation status of S1376P, The gene PLEKHO1 has a mutation status of R236Q, The gene SPRR3 has a mutation status of G73G, The gene DENND4B has a mutation status of S1329S, The gene FAM189B has a mutation status of T438P, The gene FCRL5 has a mutation status of S530C, The gene POGK has a mutation status of A352A, The gene METTL18 has a mutation status of V191fs, The gene SERPINC1 has a mutation status of T117M, The gene TNR has a mutation status of Q1357H, The gene IGFN1 has a mutation status of E1628G, The gene CAPN8 has a mutation status of G147R, The gene C1orf131 has a mutation status of G77D, The gene DISC1 has a mutation status of A835V, The gene LYST has a mutation status of A2360A, The gene RYR2 has a mutation status of I2721T, The gene WDR64 has a mutation status of T884I, The gene TET3 has a mutation status of A71T, The gene AFF3 has a mutation status of I330T, The gene ARHGEF4 has a mutation status of D139fs, The gene RAB3GAP1 has a mutation status of N382D, The gene DNAH7 has a mutation status of L1517L, The gene NYAP2 has a mutation status of S638T, The gene SCYGR1 has a mutation status of C12C, The gene NCL has a mutation status of G594S, The gene TMEM43 has a mutation status of E142Q, The gene PLCD1 has a mutation status of R527C, The gene SNRK has a mutation status of A436T, The gene CEP97 has a mutation status of R220R, The gene PLXND1 has a mutation status of A63T, The gene COL6A5 has a mutation status of A1864S, The gene IGSF10 has a mutation status of T1450A, The gene GNB4 has a mutation status of R46L, The gene CCDC39 has a mutation status of R51L, The gene GAK has a mutation status of H1000H, The gene CFAP99 has a mutation status of R689W, The gene ADGRA3 has a mutation status of D1241N, The gene KIT has a mutation status of D737H, The gene ADAMTS3 has a mutation status of P183P, The gene CTSO has a mutation status of P109P, The gene BASP1 has a mutation status of A137T, The gene CPLANE1 has a mutation status of P728A, The gene MRPS27 has a mutation status of V6V, The gene CMYA5 has a mutation status of T2899T, The gene EDIL3 has a mutation status of S375*, The gene CCNG1 has a mutation status of Y27C, The gene C5orf47 has a mutation status of E9K, The gene SLC17A4 has a mutation status of C223*, The gene HLA-DRB1 has a mutation status of S66N, The gene SLC22A7 has a mutation status of P52L, The gene COL19A1 has a mutation status of I178M, The gene FILIP1 has a mutation status of D797Y, The gene CRYBG1 has a mutation status of K845N, The gene MFSD4B has a mutation status of L182Y, The gene AHI1 has a mutation status of K237K, The gene AHI1 has a mutation status of R235K, The gene NHSL1 has a mutation status of E1218Q, The gene AIG1 has a mutation status of S154L, The gene MTHFD1L has a mutation status of A467S, The gene CCDC170 has a mutation status of A597S, The gene SNX9 has a mutation status of I506V, The gene SYTL3 has a mutation status of R524R, The gene RAC1 has a mutation status of A3A, The gene ABCB5 has a mutation status of L870H, The gene EEPD1 has a mutation status of D490N, The gene COBL has a mutation status of R333Q, The gene POM121 has a mutation status of V642M, The gene MLXIPL has a mutation status of L710L, The gene TRRAP has a mutation status of R1705H, The gene SMURF1 has a mutation status of G230S, The gene NYAP1 has a mutation status of A704V, The gene EPHB4 has a mutation status of T356S, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of S558T, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene AGBL3 has a mutation status of T642I, The gene PRSS1 has a mutation status of N77N, The gene ASAH1 has a mutation status of L257L, The gene PTK2B has a mutation status of P724S, The gene PRKDC has a mutation status of E1050del, The gene CYP7B1 has a mutation status of G44D, The gene PABPC1 has a mutation status of S4N, The gene DPYS has a mutation status of F101F, The gene PKHD1L1 has a mutation status of P4145P, The gene TAF2 has a mutation status of P1024A, The gene FER1L6 has a mutation status of N1290N, The gene AC100868.1 has a mutation status of H258P, The gene EPPK1 has a mutation status of A2633del, The gene PUM3 has a mutation status of L265V, The gene FOCAD has a mutation status of H602R, The gene FRRS1L has a mutation status of R51A, The gene DAB2IP has a mutation status of A950V, The gene ABL1 has a mutation status of A988T, The gene ANTXRL has a mutation status of G73G, The gene GPRIN2 has a mutation status of L428V, The gene C10orf71 has a mutation status of R467Q, The gene ERCC6 has a mutation status of P1095A, The gene ASAH2 has a mutation status of A346S, The gene HMX3 has a mutation status of A25A, The gene MUC5AC has a mutation status of D3964D, The gene RASSF10 has a mutation status of A207A, The gene INSC has a mutation status of R80W, The gene OR4C12 has a mutation status of R301K, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TNKS1BP1 has a mutation status of T575A, The gene INTS5 has a mutation status of T186T, The gene TRIM77 has a mutation status of V345M, The gene KBTBD3 has a mutation status of D403N, The gene PHLDB1 has a mutation status of S638R, The gene B4GALNT3 has a mutation status of L867L, The gene CRACR2A has a mutation status of R583H, The gene ENO2 has a mutation status of D178Y, The gene KRT2 has a mutation status of D494H, The gene IL26 has a mutation status of T71K, The gene SELPLG has a mutation status of Y373S, The gene TCHP has a mutation status of Q384E, The gene DNAH10 has a mutation status of R518W, The gene FOXO1 has a mutation status of S406S, The gene ZC3H13 has a mutation status of R66H, The gene EDNRB has a mutation status of V350F, The gene DZIP1 has a mutation status of V116V, The gene MCF2L has a mutation status of L840L, The gene GRTP1 has a mutation status of R76C, The gene PABPN1 has a mutation status of P84P, The gene PRPF39 has a mutation status of N217D, The gene GALNT16 has a mutation status of R413C, The gene ALDH6A1 has a mutation status of A132G, The gene DIO2 has a mutation status of A195S, The gene SLC25A47 has a mutation status of T29T, The gene FMN1 has a mutation status of P209S, The gene C2CD4A has a mutation status of A157V, The gene ANKDD1A has a mutation status of L516L, The gene ITGA11 has a mutation status of M803I, The gene ADAMTS7 has a mutation status of W1379G, The gene ADAMTS7 has a mutation status of M610I, The gene CAPN15 has a mutation status of M1L, The gene AC099489.1 has a mutation status of R1521W, The gene MAZ has a mutation status of A148T, The gene HYDIN has a mutation status of R4642C, The gene VAT1L has a mutation status of Y307D, The gene SGSM2 has a mutation status of V496M, The gene ZMYND15 has a mutation status of A640del, The gene GPS2 has a mutation status of Y164fs, The gene TP53 has a mutation status of C135F, The gene ALOXE3 has a mutation status of C9Y, The gene TEKT3 has a mutation status of D209E, The gene KSR1 has a mutation status of E764K, The gene SSH2 has a mutation status of D1411E, The gene PSMD11 has a mutation status of L111I, The gene CCL4L2 has a mutation status of P67R, The gene KRT14 has a mutation status of A179A, The gene AOC3 has a mutation status of N592S, The gene HROB has a mutation status of R92C, The gene MEIOC has a mutation status of A414V, The gene TACO1 has a mutation status of K73K, The gene CSHL1 has a mutation status of T169I, The gene NOL11 has a mutation status of A656V, The gene CEP295NL has a mutation status of P219fs, The gene RNF213 has a mutation status of E4942Q, The gene TBCD has a mutation status of P767P, The gene GRIN3B has a mutation status of L147M, The gene TMEM259 has a mutation status of G17G, The gene LONP1 has a mutation status of M569I, The gene PRR36 has a mutation status of S857P, The gene MUC16 has a mutation status of S13600I, The gene MUC16 has a mutation status of T7149A, The gene KEAP1 has a mutation status of P412S, The gene HOOK2 has a mutation status of A355G, The gene INSL3 has a mutation status of H36H, The gene PBX4 has a mutation status of R150C, The gene ZNF253 has a mutation status of E373D, The gene ZNF536 has a mutation status of P1261R, The gene RHPN2 has a mutation status of A29V, The gene FFAR3 has a mutation status of V50V, The gene CIC has a mutation status of G2506R, The gene MEGF8 has a mutation status of H1721H, The gene DMPK has a mutation status of Q92H, The gene PRKD2 has a mutation status of Q8E, The gene NOP53 has a mutation status of R36R, The gene ZSWIM9 has a mutation status of C810F, The gene LHB has a mutation status of Y57Y, The gene ZNF468 has a mutation status of D35D, The gene TARM1 has a mutation status of I156T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene LILRB1 has a mutation status of E34E, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of N144S, The gene KIR2DL1 has a mutation status of P175T, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene UBOX5 has a mutation status of H423R, The gene SEL1L2 has a mutation status of H640Y, The gene SMIM26 has a mutation status of T7T, The gene ZNF831 has a mutation status of P11L, The gene SYNJ1 has a mutation status of D1351Y, The gene SCARF2 has a mutation status of V61L, The gene KIAA1671 has a mutation status of P818L, The gene TRIOBP has a mutation status of A1291V, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene BIK has a mutation status of P125P, The gene PPP1R3F has a mutation status of L698del, The gene MTMR8 has a mutation status of E547E, The gene GPR174 has a mutation status of P289P, The gene SATL1 has a mutation status of S525N, The gene ARMCX2 has a mutation status of Q503Q, The gene NRK has a mutation status of G1267G, The gene SLC25A5 has a mutation status of T221R, The gene CCDC160 has a mutation status of L154L, The gene MAGEC1 has a mutation status of H795P, The gene BGN has a mutation status of T56I, The gene IL9R has a mutation status of V275I, The gene MT-ND1 has a mutation status of T229M, The gene MT-ND1 has a mutation status of T240A, The gene MT-ND2 has a mutation status of L179L, The gene MT-ATP6 has a mutation status of L199L, The gene MT-ND6 has a mutation status of V103V, The gene MT-ND6 has a mutation status of V31A
GBMLGG
The gene NOC2L has a mutation status of I479I, The gene CCNL2 has a mutation status of L92P, The gene MIB2 has a mutation status of N283T, The gene CHD5 has a mutation status of H1557P, The gene CHD5 has a mutation status of G1077S, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene EDN2 has a mutation status of D103A, The gene TOE1 has a mutation status of L100L, The gene TMEM69 has a mutation status of G194R, The gene FOXD3 has a mutation status of G128G, The gene ADGRL2 has a mutation status of L1056F, The gene LRIG2 has a mutation status of T545I, The gene CD101 has a mutation status of N648T, The gene H3C13 has a mutation status of R84C, The gene TTC24 has a mutation status of A396G, The gene IGSF9 has a mutation status of E150A, The gene RXRG has a mutation status of V72V, The gene DCAF6 has a mutation status of A45A, The gene NCF2 has a mutation status of D446Y, The gene ETNK2 has a mutation status of V222G, The gene KLHDC8A has a mutation status of L309F, The gene RASSF5 has a mutation status of Y13S, The gene SYT14 has a mutation status of S497P, The gene USH2A has a mutation status of N2334H, The gene ITPKB has a mutation status of S447A, The gene C1orf35 has a mutation status of P61R, The gene OBSCN has a mutation status of A5142A, The gene C1orf131 has a mutation status of K240T, The gene HNRNPU has a mutation status of Q176*, The gene SOX11 has a mutation status of T302P, The gene GREB1 has a mutation status of S530S, The gene ALK has a mutation status of S205S, The gene GALNT14 has a mutation status of R6P, The gene C2orf81 has a mutation status of Y240S, The gene SMYD1 has a mutation status of V114G, The gene SMYD1 has a mutation status of E115G, The gene VWA3B has a mutation status of L167L, The gene IL18R1 has a mutation status of R386Q, The gene INHBB has a mutation status of P44P, The gene IFIH1 has a mutation status of R77R, The gene SCN7A has a mutation status of K647K, The gene TTN has a mutation status of V2919L, The gene NABP1 has a mutation status of T144S, The gene ZDBF2 has a mutation status of S1112R, The gene GLB1L has a mutation status of K140E, The gene HJURP has a mutation status of G160D, The gene CSRNP1 has a mutation status of G49G, The gene TMEM158 has a mutation status of T269P, The gene STAB1 has a mutation status of D1491D, The gene CACNA1D has a mutation status of R85C, The gene ASB14 has a mutation status of L333F, The gene CRYBG3 has a mutation status of Q1953H, The gene CPOX has a mutation status of T286T, The gene BOC has a mutation status of V455V, The gene CCDC58 has a mutation status of M23I, The gene TPRA1 has a mutation status of E143G, The gene KPNA4 has a mutation status of N39K, The gene PHC3 has a mutation status of A453A, The gene MCCC1 has a mutation status of A446A, The gene VWA5B2 has a mutation status of D1012A, The gene CHRD has a mutation status of E822E, The gene SLC49A3 has a mutation status of P373R, The gene IDUA has a mutation status of T366P, The gene IDUA has a mutation status of T374P, The gene MSX1 has a mutation status of G268G, The gene NKX6-1 has a mutation status of P20S, The gene MYOZ2 has a mutation status of V223D, The gene PGRMC2 has a mutation status of S94S, The gene FSTL5 has a mutation status of A434A, The gene NEK1 has a mutation status of L822R, The gene FAM149A has a mutation status of D305G, The gene LPCAT1 has a mutation status of V175V, The gene TRIO has a mutation status of L1198L, The gene PRDM9 has a mutation status of T545A, The gene EGFLAM has a mutation status of H967R, The gene MROH2B has a mutation status of P346L, The gene ANKDD1B has a mutation status of L287V, The gene BHMT2 has a mutation status of Y211Y, The gene MCTP1 has a mutation status of L130P, The gene AC010255.3 has a mutation status of V54D, The gene ANKHD1 has a mutation status of G1747G, The gene NDUFA2 has a mutation status of V10V, The gene PCDH1 has a mutation status of Y98Y, The gene SH3PXD2B has a mutation status of Q52H, The gene MGAT1 has a mutation status of D46A, The gene PRRT1 has a mutation status of G91G, The gene RING1 has a mutation status of P159L, The gene TREML1 has a mutation status of Y40C, The gene CCND3 has a mutation status of I290T, The gene CALHM6 has a mutation status of Y51Y, The gene TNFAIP3 has a mutation status of G367G, The gene AFDN has a mutation status of S99S, The gene DLL1 has a mutation status of A488A, The gene FOXK1 has a mutation status of T683P, The gene GRID2IP has a mutation status of S726S, The gene DNAH11 has a mutation status of G2236V, The gene GPNMB has a mutation status of P326L, The gene YAE1 has a mutation status of K169N, The gene NPC1L1 has a mutation status of P282L, The gene PSPH has a mutation status of L68P, The gene AUTS2 has a mutation status of T957P, The gene TBL2 has a mutation status of A34G, The gene DTX2 has a mutation status of G424V, The gene PPP1R9A has a mutation status of V558V, The gene ZNF3 has a mutation status of D29N, The gene C7orf61 has a mutation status of S117C, The gene LRCH4 has a mutation status of A473P, The gene SLC12A9 has a mutation status of V432M, The gene TRIP6 has a mutation status of H265H, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of S1253N, The gene MUC12 has a mutation status of M5387K, The gene COL26A1 has a mutation status of Y37S, The gene SPDYE6 has a mutation status of H337R, The gene CDHR3 has a mutation status of D414G, The gene AASS has a mutation status of I491M, The gene CREB3L2 has a mutation status of P226P, The gene UBN2 has a mutation status of Q118L, The gene FMC1-LUC7L2 has a mutation status of Q81K, The gene TMEM178B has a mutation status of T48P, The gene AOC1 has a mutation status of Q368Q, The gene ASIC3 has a mutation status of R79*, The gene NEFM has a mutation status of S46P, The gene KAT6A has a mutation status of P1661P, The gene BHLHE22 has a mutation status of G106G, The gene BHLHE22 has a mutation status of V110G, The gene RDH10 has a mutation status of V38G, The gene ZFPM2 has a mutation status of E515E, The gene MYC has a mutation status of L149V, The gene PTP4A3 has a mutation status of D72N, The gene MROH6 has a mutation status of G4G, The gene PLEC has a mutation status of L4010M, The gene AL162231.3 has a mutation status of P66S, The gene ARHGEF39 has a mutation status of R244Q, The gene AOPEP has a mutation status of M1V, The gene FRRS1L has a mutation status of R51A, The gene HSDL2 has a mutation status of I332L, The gene SNX30 has a mutation status of A69V, The gene ZFP37 has a mutation status of T436T, The gene UCK1 has a mutation status of R275S, The gene COL5A1 has a mutation status of G16G, The gene MAN1B1 has a mutation status of R159K, The gene GJD4 has a mutation status of G107A, The gene FZD8 has a mutation status of T158P, The gene FZD8 has a mutation status of T157P, The gene ZNF33B has a mutation status of S622*, The gene LINC02881 has a mutation status of P86H, The gene OGDHL has a mutation status of F670L, The gene CCAR1 has a mutation status of Q71K, The gene ZNF503 has a mutation status of D382A, The gene PTEN has a mutation status of D268E, The gene PITX3 has a mutation status of A162P, The gene DMBT1 has a mutation status of D2340D, The gene CALY has a mutation status of A204E, The gene LMNTD2 has a mutation status of K103Q, The gene IRF7 has a mutation status of R480C, The gene MUC5AC has a mutation status of A497V, The gene MUC5AC has a mutation status of PTTSTTSA2360del, The gene MUC5AC has a mutation status of A5353K, The gene LSP1 has a mutation status of N100S, The gene PGAP2 has a mutation status of V10G, The gene RRAS2 has a mutation status of V18L, The gene ELP4 has a mutation status of I360V, The gene LRP4 has a mutation status of H1322P, The gene TRIM51GP has a mutation status of D207V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR5AN1 has a mutation status of P22S, The gene MRPL16 has a mutation status of S27I, The gene PRDX5 has a mutation status of R148W, The gene PPP2R5B has a mutation status of A70V, The gene FGF3 has a mutation status of T169P, The gene TYR has a mutation status of Y156C, The gene AP001781.2 has a mutation status of R833Q, The gene TMPRSS5 has a mutation status of V14G, The gene C3AR1 has a mutation status of F305F, The gene ARID2 has a mutation status of Y546C, The gene C1QL4 has a mutation status of Y236S, The gene KRT2 has a mutation status of F198V, The gene SLC39A5 has a mutation status of H370H, The gene PTPRB has a mutation status of S661N, The gene TRHDE has a mutation status of G112G, The gene CEP290 has a mutation status of K1326E, The gene HNF1A has a mutation status of T564P, The gene DNAH10 has a mutation status of L2546L, The gene FBRSL1 has a mutation status of R154I, The gene BRCA2 has a mutation status of V3079L, The gene PCDH8 has a mutation status of T289P, The gene IRS2 has a mutation status of S984I, The gene AKAP6 has a mutation status of K1909N, The gene NKX2-8 has a mutation status of Q95Q, The gene NKX2-8 has a mutation status of L90V, The gene PTGER2 has a mutation status of C56G, The gene HEATR4 has a mutation status of E863*, The gene ACOT4 has a mutation status of D113A, The gene GSC has a mutation status of A229V, The gene CEP170B has a mutation status of T1336P, The gene ATP10A has a mutation status of C55G, The gene KNSTRN has a mutation status of E5Q, The gene AP4E1 has a mutation status of L124L, The gene ARID3B has a mutation status of T408P, The gene TLNRD1 has a mutation status of S224S, The gene NR2F2 has a mutation status of P11P, The gene SOX8 has a mutation status of Y288S, The gene SRRM2 has a mutation status of G31G, The gene BICDL2 has a mutation status of G39G, The gene ADCY9 has a mutation status of P776H, The gene RBFOX1 has a mutation status of A127S, The gene MYLK3 has a mutation status of G183C, The gene MMP2 has a mutation status of R82R, The gene CDH16 has a mutation status of G352G, The gene HSF4 has a mutation status of A320P, The gene UTP4 has a mutation status of A90V, The gene NOB1 has a mutation status of E5G, The gene MARVELD3 has a mutation status of G102V, The gene TMEM170A has a mutation status of S12A, The gene ADAD2 has a mutation status of S26T, The gene CRISPLD2 has a mutation status of Y373N, The gene IRF8 has a mutation status of Q118K, The gene IRF8 has a mutation status of C120R, The gene FOXF1 has a mutation status of N298T, The gene ZFPM1 has a mutation status of S272P, The gene CDH15 has a mutation status of *815C, The gene NXN has a mutation status of V296G, The gene USP43 has a mutation status of G739R, The gene SHISA6 has a mutation status of R409R, The gene USP22 has a mutation status of K421*, The gene ASIC2 has a mutation status of L128F, The gene ASIC2 has a mutation status of V90G, The gene CCL4L2 has a mutation status of P67R, The gene IKZF3 has a mutation status of N160S, The gene IGFBP4 has a mutation status of T71P, The gene KRT10 has a mutation status of G540G, The gene HDAC5 has a mutation status of G411G, The gene MPO has a mutation status of V286F, The gene RAD51C has a mutation status of P127Q, The gene PPM1E has a mutation status of E94D, The gene GNA13 has a mutation status of Y89*, The gene FBF1 has a mutation status of R1035W, The gene QRICH2 has a mutation status of R390C, The gene CCDC40 has a mutation status of R1006H, The gene SGSH has a mutation status of T47P, The gene SLC26A11 has a mutation status of R237C, The gene ANKRD30B has a mutation status of T1152K, The gene CABLES1 has a mutation status of Q265P, The gene ARHGAP45 has a mutation status of Y12Y, The gene SBNO2 has a mutation status of E16D, The gene FZR1 has a mutation status of T300P, The gene TBXA2R has a mutation status of G56G, The gene PLIN4 has a mutation status of L1345V, The gene ADAMTS10 has a mutation status of V150V, The gene ZNF426 has a mutation status of R217G, The gene S1PR2 has a mutation status of V310G, The gene ZNF627 has a mutation status of R34Q, The gene TNPO2 has a mutation status of I639I, The gene GET3 has a mutation status of W8G, The gene ADGRL1 has a mutation status of T1366P, The gene ADGRL1 has a mutation status of G1322G, The gene ADGRL1 has a mutation status of G1318G, The gene BRD4 has a mutation status of V253V, The gene F2RL3 has a mutation status of G3W, The gene SLC5A5 has a mutation status of G492V, The gene MAST3 has a mutation status of T1156P, The gene UBA52 has a mutation status of R42C, The gene ZNF676 has a mutation status of GFSSVSTLNTHKAIHAEEKPYKCEECGKASNSSSKLMEHKRIHTGEKPYKCEECGK293del, The gene NUDT19 has a mutation status of G78G, The gene ATP4A has a mutation status of I148M, The gene WDR87 has a mutation status of G142V, The gene RYR1 has a mutation status of T1307P, The gene CNTD2 has a mutation status of V118G, The gene IRGC has a mutation status of S141P, The gene PPP1R37 has a mutation status of V73M, The gene CKM has a mutation status of T313P, The gene ZC3H4 has a mutation status of H853P, The gene VSIG10L has a mutation status of A430P, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of T333A, The gene ZBTB45 has a mutation status of T138P, The gene FERMT1 has a mutation status of L269L, The gene PLAGL2 has a mutation status of Y342H, The gene NECAB3 has a mutation status of V228G, The gene NCOA6 has a mutation status of Q704K, The gene RALGAPB has a mutation status of G1171A, The gene EEF1A2 has a mutation status of S416P, The gene HELZ2 has a mutation status of S1428S, The gene KRTAP26-1 has a mutation status of S8S, The gene KRTAP19-5 has a mutation status of S57G, The gene TRPM2 has a mutation status of A553A, The gene COL18A1 has a mutation status of T580P, The gene BCR has a mutation status of S69T, The gene GSTT4 has a mutation status of Q197R, The gene ZNRF3 has a mutation status of E649G, The gene SF3A1 has a mutation status of I420T, The gene HMOX1 has a mutation status of R262C, The gene TRIOBP has a mutation status of G2270V, The gene RANGAP1 has a mutation status of E267G, The gene FAM118A has a mutation status of D213D, The gene PPP2R3B has a mutation status of V273M, The gene WWC3 has a mutation status of G507V, The gene TLR8 has a mutation status of Q102Q, The gene CHST7 has a mutation status of G35G, The gene CHST7 has a mutation status of S114S, The gene GLOD5 has a mutation status of I158T, The gene CCDC120 has a mutation status of T355P, The gene EZHIP has a mutation status of S55L, The gene HEPH has a mutation status of K888K, The gene MED12 has a mutation status of V41E, The gene PHKA1 has a mutation status of Y104C, The gene KLHL4 has a mutation status of R360*, The gene TRPC5 has a mutation status of G962G, The gene PLXNB3 has a mutation status of A1151A, The gene HCFC1 has a mutation status of T332P, The gene MT-ND2 has a mutation status of F342F, The gene MT-CO1 has a mutation status of A313A, The gene MT-ATP6 has a mutation status of M60T, The gene MT-ND4 has a mutation status of A287A, The gene MT-ND6 has a mutation status of T159M, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A
DLBC
The gene SAMD11 has a mutation status of A202T, The gene DVL1 has a mutation status of A290A, The gene C1orf167 has a mutation status of G382W, The gene HNRNPCL2 has a mutation status of K230T, The gene PRAMEF13 has a mutation status of S245Y, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene HTR6 has a mutation status of C205W, The gene SH2D5 has a mutation status of V131V, The gene HSPG2 has a mutation status of T3909P, The gene CEP85 has a mutation status of Q580K, The gene MATN1 has a mutation status of Y206Y, The gene BSND has a mutation status of C231C, The gene GBP6 has a mutation status of E550Q, The gene CELSR2 has a mutation status of L1549L, The gene SIKE1 has a mutation status of L90L, The gene TSHB has a mutation status of R34T, The gene SLC22A15 has a mutation status of V3G, The gene AC242842.3 has a mutation status of V503L, The gene OTUD7B has a mutation status of P767T, The gene GOLPH3L has a mutation status of S206N, The gene FLG has a mutation status of R1360G, The gene C1orf61 has a mutation status of D122E, The gene TIPRL has a mutation status of V104F, The gene NIBAN1 has a mutation status of W167L, The gene PRELP has a mutation status of L368M, The gene PLXNA2 has a mutation status of C832G, The gene USH2A has a mutation status of N4292N, The gene OBSCN has a mutation status of G379R, The gene MTR has a mutation status of R29G, The gene CPSF3 has a mutation status of N645S, The gene TAF1B has a mutation status of S323N, The gene KCNS3 has a mutation status of A184T, The gene ALK has a mutation status of G1202G, The gene TMEM178A has a mutation status of H64P, The gene THUMPD2 has a mutation status of R415H, The gene EPAS1 has a mutation status of D753E, The gene CCT4 has a mutation status of N366S, The gene ETAA1 has a mutation status of E159K, The gene TRABD2A has a mutation status of S2N, The gene SMYD1 has a mutation status of V114G, The gene ANKRD23 has a mutation status of S11N, The gene ANKRD36 has a mutation status of P993S, The gene SEPTIN10 has a mutation status of R171H, The gene BUB1 has a mutation status of K660K, The gene GPR39 has a mutation status of V354G, The gene LCT has a mutation status of R1908R, The gene THSD7B has a mutation status of N774S, The gene TTN has a mutation status of G4085D, The gene ABI2 has a mutation status of I38V, The gene FZD5 has a mutation status of R532L, The gene CDK5R2 has a mutation status of V177G, The gene GPR55 has a mutation status of V279I, The gene ASB18 has a mutation status of A327G, The gene GPC1 has a mutation status of G491G, The gene CAPN10 has a mutation status of V432G, The gene PRRT3 has a mutation status of Q352*, The gene TRANK1 has a mutation status of A952A, The gene SCN11A has a mutation status of V698I, The gene P4HTM has a mutation status of T137P, The gene DOCK3 has a mutation status of D1966A, The gene PDZRN3 has a mutation status of A191S, The gene TOMM70 has a mutation status of G54G, The gene KALRN has a mutation status of Y972Y, The gene RPN1 has a mutation status of H238Y, The gene FOXL2 has a mutation status of A283A, The gene PLOD2 has a mutation status of Y676Y, The gene MME has a mutation status of H584H, The gene TP63 has a mutation status of R7Q, The gene DGKQ has a mutation status of T418I, The gene TACC3 has a mutation status of D192N, The gene TNIP2 has a mutation status of R229H, The gene GPR78 has a mutation status of G10G, The gene ANAPC4 has a mutation status of E377E, The gene LIMCH1 has a mutation status of L150P, The gene ARHGAP24 has a mutation status of K195T, The gene TERT has a mutation status of R277S, The gene TERT has a mutation status of S274S, The gene IRX4 has a mutation status of V289A, The gene ADCY2 has a mutation status of I92V, The gene ZSWIM6 has a mutation status of R108H, The gene BDP1 has a mutation status of S1528A, The gene MCTP1 has a mutation status of H128L, The gene ELL2 has a mutation status of T6A, The gene DMXL1 has a mutation status of A2404A, The gene NEUROG1 has a mutation status of H87H, The gene KLHL3 has a mutation status of F355V, The gene NRG2 has a mutation status of V4G, The gene HARS2 has a mutation status of E106E, The gene PCDHB9 has a mutation status of N274N, The gene CDX1 has a mutation status of Y14S, The gene NMUR2 has a mutation status of V206D, The gene BMP6 has a mutation status of G193S, The gene BMP6 has a mutation status of S487S, The gene DHX16 has a mutation status of G6G, The gene VWA7 has a mutation status of W179G, The gene MOCS1 has a mutation status of A54A, The gene WASF1 has a mutation status of P355P, The gene VGLL2 has a mutation status of S289I, The gene SAMD5 has a mutation status of H51P, The gene SASH1 has a mutation status of D663fs, The gene SASH1 has a mutation status of LLEE667del, The gene AKAP12 has a mutation status of G221E, The gene CYP2W1 has a mutation status of R73C, The gene MICALL2 has a mutation status of S110P, The gene TTYH3 has a mutation status of Y509S, The gene FOXK1 has a mutation status of T682P, The gene FOXK1 has a mutation status of T683P, The gene NPC1L1 has a mutation status of C78S, The gene METTL27 has a mutation status of A83A, The gene GNAT3 has a mutation status of D133H, The gene TRRAP has a mutation status of G1935G, The gene GIGYF1 has a mutation status of V409G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of S1373S, The gene MOGAT3 has a mutation status of R76C, The gene GPR22 has a mutation status of I174F, The gene ATP6V1F has a mutation status of R4G, The gene KLF14 has a mutation status of P58S, The gene DLGAP2 has a mutation status of D391E, The gene MATN2 has a mutation status of T276I, The gene OXR1 has a mutation status of F206L, The gene MROH6 has a mutation status of G4G, The gene PLEC has a mutation status of R4265W, The gene FBXL6 has a mutation status of A31G, The gene PSIP1 has a mutation status of G279fs, The gene CAAP1 has a mutation status of E267G, The gene PCSK5 has a mutation status of Q1382L, The gene TEX10 has a mutation status of H278R, The gene GPR21 has a mutation status of W154*, The gene UCK1 has a mutation status of *278W, The gene CCDC187 has a mutation status of A321T, The gene ABCA2 has a mutation status of A1451P, The gene LARP4B has a mutation status of S664F, The gene WDFY4 has a mutation status of M1778T, The gene CHAT has a mutation status of K114T, The gene KIFBP has a mutation status of Y128D, The gene CHST3 has a mutation status of N249T, The gene NEURL1 has a mutation status of A368D, The gene DOCK1 has a mutation status of I295M, The gene CFAP46 has a mutation status of V645G, The gene SIGIRR has a mutation status of S392S, The gene EPS8L2 has a mutation status of P410P, The gene OR10A3 has a mutation status of M228K, The gene LDHA has a mutation status of VI248del, The gene NAV2 has a mutation status of P1747P, The gene RAPSN has a mutation status of H186H, The gene FNBP4 has a mutation status of E397D, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene GLYATL1B has a mutation status of G212A, The gene AP5B1 has a mutation status of V526G, The gene CTTN has a mutation status of A546G, The gene ARAP1 has a mutation status of V292V, The gene C2CD3 has a mutation status of N1746K, The gene KDM4E has a mutation status of N29D, The gene ARHGEF12 has a mutation status of T1293K, The gene SORL1 has a mutation status of Q917R, The gene IQSEC3 has a mutation status of Y329C, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PIK3C2G has a mutation status of E602*, The gene SLCO1B3 has a mutation status of L329L, The gene RARG has a mutation status of G24G, The gene MAP3K12 has a mutation status of E421G, The gene HOXC11 has a mutation status of D164A, The gene ITGA5 has a mutation status of N593N, The gene ITGA5 has a mutation status of G279G, The gene ZC3H10 has a mutation status of A36G, The gene NACA has a mutation status of N208S, The gene ZBTB39 has a mutation status of T76T, The gene OSBPL8 has a mutation status of P802P, The gene WASHC4 has a mutation status of R596Q, The gene KCTD10 has a mutation status of E2K, The gene FAM222A has a mutation status of P169P, The gene IQCD has a mutation status of Q118E, The gene GCN1 has a mutation status of D2155Y, The gene TMEM120B has a mutation status of F123V, The gene PITPNM2 has a mutation status of R1270H, The gene STX2 has a mutation status of Q118Q, The gene EXOSC8 has a mutation status of K237N, The gene RBM26 has a mutation status of Y284Y, The gene OXGR1 has a mutation status of I55T, The gene OR4K13 has a mutation status of A230A, The gene AJUBA has a mutation status of P251A, The gene ACTR10 has a mutation status of E12G, The gene PPP4R4 has a mutation status of K375N, The gene CCDC85C has a mutation status of A157T, The gene INF2 has a mutation status of A1155V, The gene FMN1 has a mutation status of S272A, The gene PLA2G4D has a mutation status of R661R, The gene STARD9 has a mutation status of W4249C, The gene DPP8 has a mutation status of R493*, The gene RASGRF1 has a mutation status of K21R, The gene PLIN1 has a mutation status of S440P, The gene MESP1 has a mutation status of A213A, The gene IDH2 has a mutation status of T243P, The gene CHTF18 has a mutation status of V635V, The gene SOX8 has a mutation status of Y288S, The gene SLC9A3R2 has a mutation status of V199G, The gene PKD1 has a mutation status of I3367M, The gene NTN3 has a mutation status of T345P, The gene PAQR4 has a mutation status of H18Y, The gene C16orf90 has a mutation status of G91G, The gene CLUAP1 has a mutation status of P334P, The gene SULT1A3 has a mutation status of T7P, The gene CAPNS2 has a mutation status of F67F, The gene TMEM170A has a mutation status of S12A, The gene SPEM1 has a mutation status of N208T, The gene TP53 has a mutation status of P47fs, The gene CNTROB has a mutation status of T230I, The gene PFAS has a mutation status of G821G, The gene MYH8 has a mutation status of R1595T, The gene NT5M has a mutation status of G32G, The gene FAM83G has a mutation status of G749G, The gene NATD1 has a mutation status of N102T, The gene CCL4L2 has a mutation status of P67R, The gene GPR179 has a mutation status of D782A, The gene ACLY has a mutation status of A470P, The gene PLEKHH3 has a mutation status of S770P, The gene PLEKHH3 has a mutation status of T769P, The gene AOC2 has a mutation status of L160P, The gene EFCAB13 has a mutation status of A528A, The gene COIL has a mutation status of L66F, The gene COIL has a mutation status of E62G, The gene TSPOAP1 has a mutation status of V1770V, The gene PRKAR1A has a mutation status of I255fs, The gene OTOP3 has a mutation status of R384K, The gene FBF1 has a mutation status of A919G, The gene UBALD2 has a mutation status of T68P, The gene DNAH17 has a mutation status of V870A, The gene DNAH17 has a mutation status of P803P, The gene FAAP100 has a mutation status of G355G, The gene CCDC57 has a mutation status of R353H, The gene CTAGE1 has a mutation status of A160A, The gene ACAA2 has a mutation status of E365K, The gene SERPINB11 has a mutation status of G48E, The gene ZNF407 has a mutation status of T1697P, The gene SALL3 has a mutation status of D817A, The gene ARID3A has a mutation status of R40W, The gene WDR18 has a mutation status of L361L, The gene NDUFS7 has a mutation status of T125T, The gene APC2 has a mutation status of T1264I, The gene DOT1L has a mutation status of G1226G, The gene SEMA6B has a mutation status of A408V, The gene CD209 has a mutation status of A220T, The gene ZNF317 has a mutation status of R197C, The gene MAN2B1 has a mutation status of T451P, The gene ADGRL1 has a mutation status of G1322G, The gene BRD4 has a mutation status of A1034A, The gene CHERP has a mutation status of S834P, The gene NWD1 has a mutation status of A873T, The gene ZNF585B has a mutation status of F643I, The gene ZNF585B has a mutation status of G640G, The gene IFNL2 has a mutation status of H132Y, The gene FCGBP has a mutation status of P1883P, The gene FCGBP has a mutation status of TCRPSGGSL1234del, The gene COQ8B has a mutation status of V213G, The gene NOP53 has a mutation status of R36R, The gene FLT3LG has a mutation status of S53S, The gene PRR12 has a mutation status of V88F, The gene PNKP has a mutation status of G18G, The gene KCNC3 has a mutation status of P579P, The gene ZNF28 has a mutation status of K290R, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of H290H, The gene LILRA6 has a mutation status of H290N, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of H203R, The gene KIR2DL1 has a mutation status of S205A, The gene KIR2DL1 has a mutation status of G283G, The gene PPP6R1 has a mutation status of M57I, The gene ZNF835 has a mutation status of R279H, The gene ZBTB45 has a mutation status of T138P, The gene NOP56 has a mutation status of E107K, The gene LZTS3 has a mutation status of G595G, The gene CDC25B has a mutation status of S101S, The gene BFSP1 has a mutation status of R283Q, The gene ACTR5 has a mutation status of V575A, The gene KCNB1 has a mutation status of V33G, The gene TAF4 has a mutation status of V342G, The gene WDR4 has a mutation status of G221A, The gene COL18A1 has a mutation status of Q569E, The gene PCNT has a mutation status of E638D, The gene XBP1 has a mutation status of D145D, The gene SLC35E4 has a mutation status of G60G, The gene BPIFC has a mutation status of L95L, The gene C22orf23 has a mutation status of G15R, The gene ADSL has a mutation status of A49G, The gene EP300 has a mutation status of G69G, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CRELD2 has a mutation status of S295A, The gene BCLAF3 has a mutation status of C37Y, The gene DCAF8L1 has a mutation status of I340I, The gene CXorf38 has a mutation status of P105R, The gene PORCN has a mutation status of L45L, The gene WAS has a mutation status of H30H, The gene PCSK1N has a mutation status of S4A, The gene EZHIP has a mutation status of A267P, The gene IQSEC2 has a mutation status of L225V, The gene HUWE1 has a mutation status of Q928Q, The gene MAGEH1 has a mutation status of R124C, The gene ASB12 has a mutation status of L226P, The gene MTMR8 has a mutation status of E47E, The gene STARD8 has a mutation status of G662A, The gene MED12 has a mutation status of E881D, The gene GPRASP1 has a mutation status of F815C, The gene ADGRG4 has a mutation status of S277F, The gene CNGA2 has a mutation status of D662E, The gene PDZD4 has a mutation status of T513P, The gene DKC1 has a mutation status of I163T, The gene MT-CO1 has a mutation status of G205G, The gene MT-CO3 has a mutation status of G20G, The gene MT-ND4L has a mutation status of T13A, The gene MT-ND5 has a mutation status of T533M, The gene MT-ND5 has a mutation status of L601L, The gene MT-CYB has a mutation status of A29T, The gene MT-CYB has a mutation status of L236L
THCA
The gene CCNL2 has a mutation status of L92P, The gene CFAP74 has a mutation status of L1401L, The gene PRKCZ has a mutation status of D269N, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene FBLIM1 has a mutation status of P109P, The gene RAP1GAP has a mutation status of G548G, The gene HTR1D has a mutation status of A51V, The gene RHD has a mutation status of I60V, The gene BMP8B has a mutation status of G92S, The gene BMP8B has a mutation status of D87D, The gene PTPRF has a mutation status of P458A, The gene SPATA6 has a mutation status of P2L, The gene LEPR has a mutation status of A967V, The gene IL12RB2 has a mutation status of N66K, The gene RPL5 has a mutation status of Q122*, The gene PRMT6 has a mutation status of N326K, The gene CELSR2 has a mutation status of R2015K, The gene KCNA2 has a mutation status of G6R, The gene CTTNBP2NL has a mutation status of E171K, The gene H2BC18 has a mutation status of S37T, The gene LCE1A has a mutation status of S2S, The gene S100A13 has a mutation status of M60K, The gene GATAD2B has a mutation status of R249C, The gene FLAD1 has a mutation status of V167G, The gene TRIM46 has a mutation status of T86P, The gene HMCN1 has a mutation status of Y658C, The gene RPS27AP5 has a mutation status of D137V, The gene IGFN1 has a mutation status of G1209V, The gene NAV1 has a mutation status of P996T, The gene SLC26A9 has a mutation status of D844D, The gene LAMB3 has a mutation status of R300Q, The gene PACC1 has a mutation status of F83F, The gene USH2A has a mutation status of V3068A, The gene ESRRG has a mutation status of S149P, The gene WDR26 has a mutation status of A103A, The gene LBR has a mutation status of R372C, The gene OBSCN has a mutation status of I3936I, The gene OBSCN has a mutation status of V4877V, The gene URB2 has a mutation status of I884V, The gene EGLN1 has a mutation status of V138G, The gene SIPA1L2 has a mutation status of E879K, The gene KIF26B has a mutation status of P85P, The gene OR2G2 has a mutation status of V4A, The gene TAF1B has a mutation status of S323N, The gene RBKS has a mutation status of V20V, The gene USP34 has a mutation status of F928L, The gene DYSF has a mutation status of L2097L, The gene HTRA2 has a mutation status of G353R, The gene CTNNA2 has a mutation status of L458L, The gene DNAH6 has a mutation status of R1153G, The gene CFAP221 has a mutation status of Q247K, The gene TFCP2L1 has a mutation status of R383Q, The gene LRP1B has a mutation status of S4375G, The gene HOXD1 has a mutation status of D126D, The gene PTPRN has a mutation status of V347G, The gene AC053503.6 has a mutation status of H101P, The gene GPC1 has a mutation status of G491G, The gene PDCD6IP has a mutation status of P841L, The gene TTC21A has a mutation status of A1093D, The gene NKTR has a mutation status of R331W, The gene DOCK3 has a mutation status of V1962I, The gene GRM2 has a mutation status of V716G, The gene IL17RD has a mutation status of F534F, The gene FRG2C has a mutation status of V242V, The gene CHST13 has a mutation status of R207C, The gene TMCC1 has a mutation status of T159I, The gene TSC22D2 has a mutation status of P529A, The gene KPNA4 has a mutation status of N39K, The gene PRKCI has a mutation status of M10I, The gene FRYL has a mutation status of D1889G, The gene TECRL has a mutation status of T57M, The gene PPEF2 has a mutation status of K254*, The gene PTPN13 has a mutation status of S444G, The gene MANBA has a mutation status of Q269Q, The gene INPP4B has a mutation status of Q464L, The gene NIPBL has a mutation status of S2090G, The gene TNPO1 has a mutation status of P568L, The gene WDR36 has a mutation status of H156P, The gene APC has a mutation status of R24R, The gene MCC has a mutation status of S350*, The gene PCDHGC3 has a mutation status of M140del, The gene PCDHGC3 has a mutation status of K141del, The gene NDST1 has a mutation status of D58A, The gene SYNPO has a mutation status of C70G, The gene LARP1 has a mutation status of Y870F, The gene SLC34A1 has a mutation status of T637P, The gene DOK3 has a mutation status of T272K, The gene H2AC11 has a mutation status of R43Q, The gene TUBB has a mutation status of L117L, The gene HLA-DRB1 has a mutation status of S66N, The gene RXRB has a mutation status of P123P, The gene ADGRF5 has a mutation status of W633R, The gene PKHD1 has a mutation status of V881A, The gene SPACA1 has a mutation status of D286D, The gene CEP85L has a mutation status of R468R, The gene SYNE1 has a mutation status of G8543G, The gene IGF2R has a mutation status of L1152P, The gene PLG has a mutation status of R808T, The gene DACT2 has a mutation status of A617G, The gene MICALL2 has a mutation status of S110P, The gene FAM220A has a mutation status of L8F, The gene AMPH has a mutation status of T310N, The gene ADCY1 has a mutation status of V198V, The gene PSPH has a mutation status of L68P, The gene EIF4H has a mutation status of K245R, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T1218T, The gene MUC12 has a mutation status of A1802E, The gene SPDYE6 has a mutation status of H337R, The gene KLF14 has a mutation status of P58S, The gene AGBL3 has a mutation status of L895I, The gene KIAA1549 has a mutation status of V553M, The gene KLRG2 has a mutation status of K68I, The gene RP1L1 has a mutation status of D1220N, The gene MTUS1 has a mutation status of S544L, The gene NUDT18 has a mutation status of V204G, The gene NEFM has a mutation status of S46P, The gene PTK2B has a mutation status of N883S, The gene TTI2 has a mutation status of L67I, The gene NKX6-3 has a mutation status of R11S, The gene SULF1 has a mutation status of Q323Q, The gene CNBD1 has a mutation status of T414M, The gene DCAF4L2 has a mutation status of V122I, The gene TSPYL5 has a mutation status of A156A, The gene KLF10 has a mutation status of S296S, The gene SYBU has a mutation status of R307C, The gene SLC30A8 has a mutation status of S307S, The gene NRBP2 has a mutation status of S463N, The gene SCRT1 has a mutation status of A133S, The gene TMEM249 has a mutation status of V103L, The gene DNAJB5 has a mutation status of Q431*, The gene TRPM3 has a mutation status of T300T, The gene SPATA31D1 has a mutation status of N57Y, The gene FAM120A has a mutation status of R116P, The gene TMEM245 has a mutation status of I76I, The gene WDR31 has a mutation status of A145A, The gene HSPA5 has a mutation status of K553R, The gene FAM78A has a mutation status of R230Q, The gene COL5A1 has a mutation status of G892G, The gene COL5A1 has a mutation status of K1619N, The gene CCDC187 has a mutation status of A321T, The gene PLCE1 has a mutation status of R1964*, The gene ACSM6 has a mutation status of R155D, The gene KAZALD1 has a mutation status of C56R, The gene BAG3 has a mutation status of S279S, The gene MUC5AC has a mutation status of D852D, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4396A, The gene DCHS1 has a mutation status of A3102A, The gene CTR9 has a mutation status of A476V, The gene NR1H3 has a mutation status of A220G, The gene MTCH2 has a mutation status of G11D, The gene MTCH2 has a mutation status of V8M, The gene TRIM49B has a mutation status of E120G, The gene OR9G1 has a mutation status of T62V, The gene LRRC55 has a mutation status of T203T, The gene FADS1 has a mutation status of L207R, The gene OVOL1 has a mutation status of V165I, The gene TENM4 has a mutation status of S389I, The gene NAALAD2 has a mutation status of I431T, The gene DYNC2H1 has a mutation status of L1751M, The gene CEP164 has a mutation status of E641V, The gene SORL1 has a mutation status of T1044T, The gene LRTM2 has a mutation status of G319V, The gene ANO2 has a mutation status of M450V, The gene GPR162 has a mutation status of S38Y, The gene WBP11 has a mutation status of N150S, The gene PTPRO has a mutation status of G174R, The gene HDAC7 has a mutation status of R316R, The gene DDX23 has a mutation status of R58C, The gene WNT1 has a mutation status of L239L, The gene KMT2D has a mutation status of K3262*, The gene FAM186B has a mutation status of P375S, The gene OR6C76 has a mutation status of R303K, The gene GDF11 has a mutation status of V43G, The gene LRP1 has a mutation status of C2166G, The gene ZNF26 has a mutation status of P285P, The gene GJB6 has a mutation status of V207M, The gene PDS5B has a mutation status of E395Q, The gene PDS5B has a mutation status of D399H, The gene VPS36 has a mutation status of F217I, The gene FARP1 has a mutation status of H703P, The gene MCF2L has a mutation status of T872M, The gene GAS6 has a mutation status of E200D, The gene CHAMP1 has a mutation status of R420C, The gene LRFN5 has a mutation status of D258H, The gene KIAA0586 has a mutation status of D1112A, The gene VRTN has a mutation status of D490A, The gene SEL1L has a mutation status of I118T, The gene DIO3 has a mutation status of D104D, The gene TDRD9 has a mutation status of R385Q, The gene SPTBN5 has a mutation status of Q2566*, The gene TRIM69 has a mutation status of M284I, The gene MEGF11 has a mutation status of A724P, The gene NOX5 has a mutation status of K685E, The gene CCDC33 has a mutation status of G603A, The gene KIF7 has a mutation status of R234H, The gene NPRL3 has a mutation status of R92*, The gene RPL3L has a mutation status of T232K, The gene PKD1 has a mutation status of S3720A, The gene ACSM2B has a mutation status of N348K, The gene POLR3E has a mutation status of Q707Q, The gene ITGAM has a mutation status of T1124P, The gene ZFP90 has a mutation status of F459F, The gene HYDIN has a mutation status of E3339D, The gene FAM92B has a mutation status of V282G, The gene OVCA2 has a mutation status of D50G, The gene NLRP1 has a mutation status of V1398D, The gene SPEM3 has a mutation status of V417F, The gene MFSD6L has a mutation status of M52V, The gene MYH8 has a mutation status of V1597L, The gene CENPV has a mutation status of E240E, The gene SPAG5 has a mutation status of E1018A, The gene LRRC37B has a mutation status of N276T, The gene CCL7 has a mutation status of Y51Y, The gene CCL4L2 has a mutation status of P67R, The gene KRT31 has a mutation status of E227E, The gene SP2 has a mutation status of T168P, The gene TSPOAP1 has a mutation status of H1243H, The gene RNF43 has a mutation status of K568K, The gene CACNG4 has a mutation status of G51G, The gene ABCA6 has a mutation status of T289S, The gene OTOP3 has a mutation status of D62G, The gene TMC6 has a mutation status of H302P, The gene CABYR has a mutation status of A215S, The gene OSBPL1A has a mutation status of N208N, The gene DAZAP1 has a mutation status of D365A, The gene MEX3D has a mutation status of D364A, The gene VMAC has a mutation status of L16P, The gene RETN has a mutation status of W81R, The gene RETN has a mutation status of D82G, The gene MYO1F has a mutation status of R878L, The gene MUC16 has a mutation status of T4130T, The gene UBL5 has a mutation status of C18C, The gene GIPC1 has a mutation status of D310Y, The gene CPAMD8 has a mutation status of G430W, The gene ZNF429 has a mutation status of E457Q, The gene ZNF536 has a mutation status of T1191T, The gene CEP89 has a mutation status of E127Q, The gene GRAMD1A has a mutation status of M1I, The gene LRFN3 has a mutation status of R318Q, The gene ZNF345 has a mutation status of H388Q, The gene ZNF585B has a mutation status of C356F, The gene FCGBP has a mutation status of S1228fs, The gene FCGBP has a mutation status of T1203fs, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene GEMIN7 has a mutation status of F129L, The gene AP2S1 has a mutation status of D41D, The gene CABP5 has a mutation status of E71D, The gene ZNF614 has a mutation status of G407A, The gene VN1R2 has a mutation status of V133E, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA4 has a mutation status of S387S, The gene LENG8 has a mutation status of G377G, The gene LILRA2 has a mutation status of W163S, The gene EPN1 has a mutation status of D402G, The gene SIRPA has a mutation status of L44S, The gene LZTS3 has a mutation status of S268A, The gene SLC24A3 has a mutation status of A10T, The gene DEFB116 has a mutation status of I75I, The gene TGM2 has a mutation status of S212P, The gene GNAS has a mutation status of P457Q, The gene UCKL1 has a mutation status of A445S, The gene TRAPPC10 has a mutation status of H336Y, The gene PI4KA has a mutation status of Y1628S, The gene SNAP29 has a mutation status of G118V, The gene GSTT4 has a mutation status of Q197R, The gene KIAA1671 has a mutation status of E122G, The gene KIAA1671 has a mutation status of P818L, The gene RNF215 has a mutation status of R283W, The gene FBXO7 has a mutation status of P327S, The gene SMC1B has a mutation status of K1165K, The gene OFD1 has a mutation status of R568H, The gene MAP3K15 has a mutation status of A830P, The gene POLA1 has a mutation status of Y1061Y, The gene NDP has a mutation status of S80S, The gene PRICKLE3 has a mutation status of G467S, The gene KDM5C has a mutation status of R888C, The gene ZMYM3 has a mutation status of A722A, The gene TAF1 has a mutation status of G68D, The gene BX276092.9 has a mutation status of D93H, The gene RPA4 has a mutation status of H197D, The gene NXF3 has a mutation status of C279Y, The gene RADX has a mutation status of H760R, The gene BCORL1 has a mutation status of L1132P, The gene AFF2 has a mutation status of L1034I, The gene CNGA2 has a mutation status of D662E, The gene LAGE3 has a mutation status of G19G
DLBC
The gene TPRG1L has a mutation status of R172C, The gene PRAMEF13 has a mutation status of Y166H, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of S225I, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of L121P, The gene PRAMEF18 has a mutation status of W98R, The gene PADI2 has a mutation status of M514V, The gene PADI1 has a mutation status of M183V, The gene ALDH4A1 has a mutation status of A407T, The gene HTR6 has a mutation status of D424N, The gene ELOA has a mutation status of E425V, The gene UBXN11 has a mutation status of G224E, The gene ERI3 has a mutation status of L171L, The gene CYP4A11 has a mutation status of S331F, The gene MROH7 has a mutation status of E1125K, The gene PALMD has a mutation status of E137fs, The gene AMPD2 has a mutation status of V664V, The gene SLC22A15 has a mutation status of A66S, The gene GDAP2 has a mutation status of A335P, The gene ASPM has a mutation status of R866G, The gene KIF14 has a mutation status of M536V, The gene LMOD1 has a mutation status of A242S, The gene PPP1R12B has a mutation status of G851V, The gene RPS6KC1 has a mutation status of L121L, The gene OR2T1 has a mutation status of L129R, The gene TRMT61B has a mutation status of A35S, The gene SPTBN1 has a mutation status of G1876G, The gene ANKRD36 has a mutation status of D317A, The gene RFX8 has a mutation status of D146E, The gene TTC21B has a mutation status of R908R, The gene SP5 has a mutation status of P164L, The gene TTN has a mutation status of A26265F, The gene PRKAG3 has a mutation status of R186C, The gene SCYGR2 has a mutation status of H97S, The gene TRPM8 has a mutation status of A102V, The gene AGAP1 has a mutation status of R356Q, The gene TGFBR2 has a mutation status of S156fs, The gene HHATL has a mutation status of A280T, The gene AC006059.2 has a mutation status of I131V, The gene ARIH2OS has a mutation status of S166P, The gene PBRM1 has a mutation status of R549*, The gene CD86 has a mutation status of K188E, The gene PPP2R3A has a mutation status of R110K, The gene BCHE has a mutation status of N209Y, The gene MAP3K13 has a mutation status of T389M, The gene RCHY1 has a mutation status of A168V, The gene OSMR has a mutation status of C853G, The gene ITGA2 has a mutation status of N475S, The gene MAP1B has a mutation status of P1709P, The gene ZBED3 has a mutation status of L155A, The gene VCAN has a mutation status of S2639C, The gene ADGRV1 has a mutation status of D1938D, The gene CDC23 has a mutation status of L179F, The gene PCDHA9 has a mutation status of E40K, The gene GPR151 has a mutation status of G68R, The gene CDX1 has a mutation status of Y14S, The gene RACK1 has a mutation status of I40V, The gene MYLIP has a mutation status of P225P, The gene MUC22 has a mutation status of S480S, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DRB1 has a mutation status of I248L, The gene HLA-DQA2 has a mutation status of H30H, The gene PTCHD4 has a mutation status of F56F, The gene PGM3 has a mutation status of A117V, The gene SYNJ2 has a mutation status of F78F, The gene TMEM181 has a mutation status of P594L, The gene PLG has a mutation status of T200A, The gene GLI3 has a mutation status of S1028I, The gene PCLO has a mutation status of T2362S, The gene ERVW-1 has a mutation status of L333*, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of V43A, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene SH2B2 has a mutation status of A368P, The gene RELN has a mutation status of V1999V, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene CSMD1 has a mutation status of P1922P, The gene DEFB136 has a mutation status of V39V, The gene STMN4 has a mutation status of P116S, The gene JPH1 has a mutation status of E85fs, The gene JPH1 has a mutation status of G84G, The gene KLF10 has a mutation status of P304H, The gene PKHD1L1 has a mutation status of G3990E, The gene EPPK1 has a mutation status of A2633del, The gene EPPK1 has a mutation status of R1621W, The gene RANBP6 has a mutation status of P769R, The gene FRRS1L has a mutation status of R51A, The gene OR1L4 has a mutation status of F105F, The gene TTF1 has a mutation status of D519Y, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene SEC16A has a mutation status of N299S, The gene DIP2C has a mutation status of A813A, The gene DIP2C has a mutation status of S442G, The gene PTF1A has a mutation status of R241C, The gene ANKRD30A has a mutation status of R485V, The gene ANXA8 has a mutation status of T207M, The gene ANXA8 has a mutation status of K112K, The gene ARID5B has a mutation status of V176L, The gene KNDC1 has a mutation status of E1615E, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene OR52N4 has a mutation status of Y130S, The gene OR52L1 has a mutation status of V102L, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene PPP1CA has a mutation status of G316G, The gene GSTP1 has a mutation status of A152S, The gene CCDC90B has a mutation status of A164V, The gene KDM4D has a mutation status of R368K, The gene FOXJ2 has a mutation status of P191L, The gene TAS2R46 has a mutation status of 296_297HV>QM, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene TNS2 has a mutation status of A255V, The gene HOXC10 has a mutation status of A151V, The gene ACACB has a mutation status of R193L, The gene ATXN2 has a mutation status of I599T, The gene LATS2 has a mutation status of G385S, The gene NUP58 has a mutation status of T521A, The gene CBY2 has a mutation status of P314P, The gene MED4 has a mutation status of L187L, The gene RBM26 has a mutation status of R828R, The gene MYO16 has a mutation status of A1220T, The gene OXA1L has a mutation status of F30L, The gene EFS has a mutation status of P178P, The gene TTC6 has a mutation status of E252D, The gene SOS2 has a mutation status of S379R, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L22 has a mutation status of E575K, The gene GOLGA8S has a mutation status of I439V, The gene ATP10A has a mutation status of R793W, The gene MEIS2 has a mutation status of P56S, The gene ANKDD1A has a mutation status of L516L, The gene REC114 has a mutation status of V7G, The gene AKAP13 has a mutation status of D1355V, The gene UNC45A has a mutation status of G466S, The gene LRRK1 has a mutation status of T715M, The gene JPH3 has a mutation status of A671T, The gene TP53 has a mutation status of I255N, The gene PER1 has a mutation status of L1045I, The gene MPRIP has a mutation status of D374Y, The gene SREBF1 has a mutation status of S979G, The gene CDRT15L2 has a mutation status of A118V, The gene NF1 has a mutation status of G1417S, The gene CCL4L2 has a mutation status of P67R, The gene BRCA1 has a mutation status of I571T, The gene RNF43 has a mutation status of M18fs, The gene TEX14 has a mutation status of S1249fs, The gene ST8SIA5 has a mutation status of G179R, The gene CNDP1 has a mutation status of L272I, The gene PTPRS has a mutation status of R646*, The gene AC119396.1 has a mutation status of L33M, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T12336L, The gene ZNF66 has a mutation status of F97F, The gene FCGBP has a mutation status of A2939P, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA2 has a mutation status of W163S, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene KIR2DL3 has a mutation status of G12A, The gene KIR2DL3 has a mutation status of P224S, The gene KIR2DL1 has a mutation status of N144S, The gene KIR2DL1 has a mutation status of P175T, The gene KIR2DL1 has a mutation status of H192H, The gene NLRP4 has a mutation status of G442R, The gene SIRPA has a mutation status of L44S, The gene CEP250 has a mutation status of D943D, The gene ADAMTS1 has a mutation status of S384R, The gene RANBP1 has a mutation status of Q201H, The gene EP300 has a mutation status of K1488fs, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CRLF2 has a mutation status of S323F, The gene ZFX has a mutation status of D320D, The gene ARMCX2 has a mutation status of Q503Q, The gene SLC25A5 has a mutation status of T221R, The gene SMARCA1 has a mutation status of R706C, The gene MAGEC1 has a mutation status of P232L, The gene SLITRK2 has a mutation status of A710S, The gene AC236972.4 has a mutation status of S1611S, The gene BGN has a mutation status of Y344H, The gene PLXNA3 has a mutation status of F26F, The gene IL9R has a mutation status of T103A, The gene MT-CO1 has a mutation status of W494W, The gene MT-ND4 has a mutation status of F56F, The gene MT-ND5 has a mutation status of L94L, The gene MT-ND5 has a mutation status of G281S, The gene MT-ND6 has a mutation status of T156I
PAAD
The gene RNF223 has a mutation status of G139G, The gene CDK11B has a mutation status of A198A, The gene NOL9 has a mutation status of R76R, The gene VPS13D has a mutation status of S1800P, The gene PRAMEF13 has a mutation status of N426S, The gene PRAMEF13 has a mutation status of T233N, The gene PRAMEF18 has a mutation status of S225I, The gene PRAMEF18 has a mutation status of L121P, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF5 has a mutation status of P432A, The gene PRAMEF33 has a mutation status of H144R, The gene ELOVL1 has a mutation status of P17P, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene NBPF15 has a mutation status of R75Q, The gene NBPF10 has a mutation status of F1298L, The gene NBPF14 has a mutation status of G116W, The gene FCRL5 has a mutation status of G430E, The gene LAD1 has a mutation status of H34R, The gene OR2T8 has a mutation status of C146S, The gene FAM110C has a mutation status of L15F, The gene NRXN1 has a mutation status of H879Y, The gene SULT1C3 has a mutation status of P95S, The gene GPR148 has a mutation status of T13R, The gene KYNU has a mutation status of K276K, The gene SATB2 has a mutation status of R399H, The gene FANCD2 has a mutation status of D645Y, The gene CHCHD4 has a mutation status of E127*, The gene ZNF860 has a mutation status of R492C, The gene SCN10A has a mutation status of T337N, The gene FAM240A has a mutation status of R52H, The gene CACNA2D2 has a mutation status of Q605Q, The gene DNAH12 has a mutation status of E2938E, The gene ZNF717 has a mutation status of S56fs, The gene CSNKA2IP has a mutation status of S386L, The gene DIPK2A has a mutation status of E117Q, The gene ZBBX has a mutation status of V286L, The gene HS3ST1 has a mutation status of G182D, The gene TLR1 has a mutation status of H111R, The gene SDAD1 has a mutation status of P337S, The gene SYNPO2 has a mutation status of E423K, The gene SETD7 has a mutation status of R68C, The gene MAML3 has a mutation status of F758F, The gene GALNTL6 has a mutation status of R321R, The gene VCAN has a mutation status of A3035A, The gene TUBB2B has a mutation status of D443G, The gene SLC35B3 has a mutation status of A7V, The gene MYLIP has a mutation status of Y185C, The gene SYNGAP1 has a mutation status of G1049D, The gene OPN5 has a mutation status of G180R, The gene DST has a mutation status of D65N, The gene RFX6 has a mutation status of V822I, The gene AKAP9 has a mutation status of R3237W, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of S3095S, The gene MUC12 has a mutation status of S53T, The gene SLC13A1 has a mutation status of T384T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene LZTS1 has a mutation status of R343R, The gene ADAM28 has a mutation status of Q491*, The gene SFRP1 has a mutation status of Y127*, The gene PXDNL has a mutation status of I268V, The gene GEM has a mutation status of R264R, The gene RIMS2 has a mutation status of Q61H, The gene ZFPM2 has a mutation status of D789N, The gene CSMD3 has a mutation status of V2624V, The gene EPPK1 has a mutation status of A2633del, The gene EPPK1 has a mutation status of R2547G, The gene EPPK1 has a mutation status of D2512E, The gene CPSF1 has a mutation status of A1287T, The gene C8orf33 has a mutation status of S161F, The gene FRRS1L has a mutation status of R51A, The gene PRRC2B has a mutation status of N70K, The gene CCDC187 has a mutation status of L747L, The gene ZNF33B has a mutation status of T602I, The gene NPY4R has a mutation status of L231L, The gene WASHC2A has a mutation status of G698R, The gene MUC5AC has a mutation status of C843C, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1569L, The gene MUC5AC has a mutation status of T1570T, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S2302fs, The gene MUC5AC has a mutation status of T2425R, The gene MUC5AC has a mutation status of R3590R, The gene MUC5AC has a mutation status of A4396A, The gene NUP98 has a mutation status of A1596A, The gene OR8U1 has a mutation status of N42N, The gene OR9G1 has a mutation status of T62V, The gene MYRF has a mutation status of M365K, The gene B3GAT3 has a mutation status of R169Q, The gene FAT3 has a mutation status of G4267E, The gene DRD2 has a mutation status of A273S, The gene OR10G7 has a mutation status of T8K, The gene CHD4 has a mutation status of S556S, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PLCZ1 has a mutation status of S96F, The gene ABCC9 has a mutation status of I253I, The gene PKP2 has a mutation status of G330G, The gene GXYLT1 has a mutation status of I220G, The gene KRT18 has a mutation status of T103N, The gene TPCN1 has a mutation status of A621D, The gene HSPB8 has a mutation status of S66L, The gene BICDL1 has a mutation status of F4F, The gene PIWIL1 has a mutation status of E260K, The gene GOLGA3 has a mutation status of Y343C, The gene ATP7B has a mutation status of S177L, The gene CCDC168 has a mutation status of P1001S, The gene ADPRHL1 has a mutation status of E1710E, The gene REM2 has a mutation status of A193V, The gene ACIN1 has a mutation status of R935R, The gene CARMIL3 has a mutation status of S840Y, The gene NRXN3 has a mutation status of N58N, The gene LINC02203 has a mutation status of I259M, The gene GOLGA8S has a mutation status of I439V, The gene MAGEL2 has a mutation status of G9G, The gene PHGR1 has a mutation status of G48H, The gene ZNF106 has a mutation status of R547W, The gene PPIP5K1 has a mutation status of L1032P, The gene DMXL2 has a mutation status of T1450T, The gene UNC13C has a mutation status of H536R, The gene ANKDD1A has a mutation status of L516L, The gene DENND4A has a mutation status of Y547C, The gene LARP6 has a mutation status of R168R, The gene GRAMD2A has a mutation status of R336R, The gene CSPG4 has a mutation status of Q1750K, The gene CSPG4 has a mutation status of R740P, The gene GOLGA6L10 has a mutation status of L399P, The gene GOLGA6L10 has a mutation status of R385R, The gene GOLGA6L10 has a mutation status of I73V, The gene GOLGA6L9 has a mutation status of A373P, The gene AC245033.1 has a mutation status of M554I, The gene ST8SIA2 has a mutation status of G170S, The gene TPSB2 has a mutation status of T141M, The gene SLC12A3 has a mutation status of E121D, The gene TRPV2 has a mutation status of S597S, The gene SLFN11 has a mutation status of R48L, The gene TBC1D3B has a mutation status of L201F, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP2-2 has a mutation status of 80_81CP>WT, The gene JUP has a mutation status of L376L, The gene RNF213 has a mutation status of L1541L, The gene DTNA has a mutation status of D26E, The gene WDR7 has a mutation status of L230I, The gene SERPINB10 has a mutation status of P216S, The gene CNN2 has a mutation status of M249T, The gene C3 has a mutation status of E689K, The gene MBD3L1 has a mutation status of T92T, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene ZNF66 has a mutation status of F97F, The gene ZNF100 has a mutation status of C235G, The gene WDR87 has a mutation status of E2752K, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of W163S, The gene LILRA2 has a mutation status of S395T, The gene LILRB1 has a mutation status of P3S, The gene KIR2DL1 has a mutation status of T91K, The gene KIR2DL1 has a mutation status of P175T, The gene KIR2DL1 has a mutation status of H192H, The gene PEG3 has a mutation status of S1578P, The gene CDH4 has a mutation status of R246Q, The gene KCNE1B has a mutation status of N88D, The gene TMPRSS15 has a mutation status of G907E, The gene GGTLC2 has a mutation status of T143T, The gene CABIN1 has a mutation status of R1888L, The gene SREBF2 has a mutation status of D582N, The gene SREBF2 has a mutation status of P870R, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TCF20 has a mutation status of P1942A, The gene TTLL1 has a mutation status of I316I, The gene TUBGCP6 has a mutation status of R793C, The gene GTPBP6 has a mutation status of M181L, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene SSX5 has a mutation status of T153T, The gene SHROOM4 has a mutation status of H401Y, The gene TNMD has a mutation status of N211N, The gene ARMCX6 has a mutation status of N120S, The gene RBMXL3 has a mutation status of H162Q, The gene SLC25A5 has a mutation status of G121C, The gene SMIM10L2B has a mutation status of F47L, The gene GABRE has a mutation status of L364L, The gene MT-ND1 has a mutation status of Q138Q, The gene MT-ND2 has a mutation status of M307M, The gene MT-ND2 has a mutation status of H319H, The gene MT-CO1 has a mutation status of L48L, The gene MT-CO1 has a mutation status of V83V, The gene MT-ND4 has a mutation status of L39L, The gene MT-ND4 has a mutation status of L158L, The gene MT-ND5 has a mutation status of G228G, The gene MT-ND5 has a mutation status of F466F
DLBC
The gene OR4F5 has a mutation status of L195F, The gene INTS11 has a mutation status of H226H, The gene DVL1 has a mutation status of R594H, The gene PLCH2 has a mutation status of V577V, The gene NPHP4 has a mutation status of D656N, The gene ICMT has a mutation status of G233S, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene NIPAL3 has a mutation status of T379A, The gene DCDC2B has a mutation status of R112G, The gene DLGAP3 has a mutation status of Q462E, The gene ZMYM4 has a mutation status of S110S, The gene ZMYM4 has a mutation status of Q859*, The gene EPHA10 has a mutation status of A642V, The gene KCNQ4 has a mutation status of R420W, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene UROD has a mutation status of Q53R, The gene PIK3R3 has a mutation status of P41S, The gene BEND5 has a mutation status of A73E, The gene PODN has a mutation status of R13C, The gene SLC1A7 has a mutation status of N462N, The gene GLIS1 has a mutation status of A17D, The gene FAM151A has a mutation status of L142L, The gene DAB1 has a mutation status of V129I, The gene GIPC2 has a mutation status of G29C, The gene SYDE2 has a mutation status of V758V, The gene ZNHIT6 has a mutation status of V466I, The gene LRRC8C has a mutation status of Q558Q, The gene ZNF326 has a mutation status of N189N, The gene BTBD8 has a mutation status of N1558fs, The gene NTNG1 has a mutation status of L378L, The gene SLC6A17 has a mutation status of I107F, The gene NOTCH2 has a mutation status of R1260H, The gene NBPF20 has a mutation status of S245P, The gene NBPF10 has a mutation status of L891V, The gene SLC39A1 has a mutation status of P14P, The gene DCST1 has a mutation status of Y75C, The gene DCST1 has a mutation status of M537I, The gene LRRC71 has a mutation status of I534V, The gene FCRL4 has a mutation status of T393T, The gene FCRL2 has a mutation status of Y332Y, The gene CD1C has a mutation status of S108S, The gene IFI16 has a mutation status of T287T, The gene VSIG8 has a mutation status of G155R, The gene IGSF9 has a mutation status of T205P, The gene NCSTN has a mutation status of A570A, The gene SLAMF1 has a mutation status of L185R, The gene UHMK1 has a mutation status of D346D, The gene DUSP27 has a mutation status of A809V, The gene CREG1 has a mutation status of M1V, The gene TBX19 has a mutation status of F186F, The gene SEC16B has a mutation status of S920L, The gene CLEC20A has a mutation status of T382I, The gene CEP350 has a mutation status of K1433K, The gene RNASEL has a mutation status of A140S, The gene HMCN1 has a mutation status of A2652V, The gene HMCN1 has a mutation status of R4604C, The gene CACNA1S has a mutation status of V646I, The gene CACNA1S has a mutation status of I99I, The gene IGFN1 has a mutation status of R344W, The gene NUAK2 has a mutation status of G522G, The gene LAMB3 has a mutation status of D384G, The gene FAM71A has a mutation status of A300T, The gene USH2A has a mutation status of T4347I, The gene CDC42BPA has a mutation status of Y790C, The gene ZNF678 has a mutation status of S334S, The gene OBSCN has a mutation status of L3010L, The gene TRIM11 has a mutation status of T338P, The gene SPRTN has a mutation status of E237D, The gene NID1 has a mutation status of K1161Q, The gene TMEM18 has a mutation status of T27S, The gene MSGN1 has a mutation status of G81A, The gene DRC1 has a mutation status of D541G, The gene CAPN14 has a mutation status of K668T, The gene SRBD1 has a mutation status of T694T, The gene MSH2 has a mutation status of A733T, The gene XPO1 has a mutation status of C585F, The gene CCT4 has a mutation status of D273D, The gene CNRIP1 has a mutation status of P18H, The gene ANTXR1 has a mutation status of A408A, The gene MYO7B has a mutation status of N340N, The gene TMEM163 has a mutation status of V52G, The gene MAP3K19 has a mutation status of R473K, The gene NEB has a mutation status of S8192G, The gene CCDC148 has a mutation status of L248V, The gene GCG has a mutation status of V136V, The gene COBLL1 has a mutation status of N572S, The gene HOXD9 has a mutation status of S80P, The gene PRKRA has a mutation status of T204fs, The gene TTN has a mutation status of A21043A, The gene FAM171B has a mutation status of L133L, The gene COL5A2 has a mutation status of P808P, The gene C2CD6 has a mutation status of N1605K, The gene KIAA2012 has a mutation status of Q1040K, The gene UNC80 has a mutation status of R817C, The gene SPAG16 has a mutation status of L367fs, The gene SLC11A1 has a mutation status of N465N, The gene NYAP2 has a mutation status of V344L, The gene COL6A3 has a mutation status of D1293E, The gene SNED1 has a mutation status of P647S, The gene ANO7 has a mutation status of A124A, The gene SETD5 has a mutation status of P169A, The gene CIDEC has a mutation status of N160N, The gene TSEN2 has a mutation status of V260V, The gene IQSEC1 has a mutation status of D554N, The gene NR2C2 has a mutation status of G121G, The gene TRANK1 has a mutation status of L2570L, The gene GOLGA4 has a mutation status of L1097P, The gene SCN10A has a mutation status of T1181M, The gene ULK4 has a mutation status of P124S, The gene CYP8B1 has a mutation status of S342S, The gene KIF15 has a mutation status of R34C, The gene CELSR3 has a mutation status of T1580T, The gene CELSR3 has a mutation status of G1477G, The gene BSN has a mutation status of Q240Q, The gene HYAL3 has a mutation status of A313G, The gene MAPKAPK3 has a mutation status of R360W, The gene RBM15B has a mutation status of S9C, The gene GLYCTK has a mutation status of P48P, The gene STAB1 has a mutation status of N1403K, The gene IL17RD has a mutation status of R535L, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of C2598C, The gene BOC has a mutation status of E619K, The gene GPR156 has a mutation status of S207S, The gene POLQ has a mutation status of I1926I, The gene COL6A5 has a mutation status of R850Q, The gene MRPL3 has a mutation status of P28L, The gene ARL14 has a mutation status of P155S, The gene LRRC31 has a mutation status of L82L, The gene TMEM41A has a mutation status of L20L, The gene ZNF732 has a mutation status of G107*, The gene DOK7 has a mutation status of I48T, The gene ZBTB49 has a mutation status of H553H, The gene ARAP2 has a mutation status of D1099Y, The gene FRYL has a mutation status of W1356G, The gene CRACD has a mutation status of K160R, The gene PRR27 has a mutation status of P55T, The gene ANKRD17 has a mutation status of L1169L, The gene BMP2K has a mutation status of R656I, The gene THAP9 has a mutation status of W53L, The gene DSPP has a mutation status of S1142S, The gene FAM13A has a mutation status of D483D, The gene SEC24D has a mutation status of Q302*, The gene IQCM has a mutation status of F278L, The gene SPOCK3 has a mutation status of T188N, The gene CCDC110 has a mutation status of K590E, The gene TLR3 has a mutation status of G12R, The gene ADAMTS16 has a mutation status of T783A, The gene TRIO has a mutation status of P2408P, The gene ADAMTS12 has a mutation status of S1341I, The gene SPEF2 has a mutation status of K1227N, The gene MROH2B has a mutation status of G149E, The gene ITGA2 has a mutation status of N927S, The gene MAST4 has a mutation status of S1133S, The gene VCAN has a mutation status of D2895H, The gene HSD17B4 has a mutation status of F72L, The gene SNCAIP has a mutation status of P382L, The gene SLC12A2 has a mutation status of 95_96insAAAAA, The gene CSF2 has a mutation status of R21C, The gene AFF4 has a mutation status of A1094T, The gene GFRA3 has a mutation status of Y61Y, The gene MZB1 has a mutation status of R80G, The gene PCDHA2 has a mutation status of P737P, The gene LSM11 has a mutation status of P46L, The gene NKX2-5 has a mutation status of A103A, The gene NKX2-5 has a mutation status of P100P, The gene ELOVL2 has a mutation status of S194C, The gene HLA-C has a mutation status of D220A, The gene HLA-B has a mutation status of Y140L, The gene TNXB has a mutation status of V3468V, The gene TNXB has a mutation status of A2812V, The gene NOTCH4 has a mutation status of R1410H, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB1 has a mutation status of I248L, The gene HSD17B8 has a mutation status of G105fs, The gene ZFAND3 has a mutation status of A49V, The gene ADGRF1 has a mutation status of L793L, The gene PKHD1 has a mutation status of F2779V, The gene MLIP has a mutation status of P448R, The gene HTR1E has a mutation status of A208T, The gene ZNF292 has a mutation status of V2681A, The gene MDN1 has a mutation status of A664A, The gene FIG4 has a mutation status of V328L, The gene DDO has a mutation status of R145Q, The gene SMPDL3A has a mutation status of H293Y, The gene LAMA2 has a mutation status of A763V, The gene NHSL1 has a mutation status of V1081M, The gene NHSL1 has a mutation status of P734S, The gene ECT2L has a mutation status of I741T, The gene TXLNB has a mutation status of A668P, The gene EPM2A has a mutation status of P10P, The gene EPM2A has a mutation status of F5L, The gene CCR6 has a mutation status of K340T, The gene FOXK1 has a mutation status of A552V, The gene RNF216 has a mutation status of P277L, The gene NXPH1 has a mutation status of E221E, The gene HOXA3 has a mutation status of S354S, The gene TRIL has a mutation status of A347T, The gene PSPH has a mutation status of L68P, The gene AUTS2 has a mutation status of P63Q, The gene SPDYE5 has a mutation status of P24L, The gene PCLO has a mutation status of S4837P, The gene ANKIB1 has a mutation status of S805G, The gene ERVW-1 has a mutation status of L38L, The gene BAIAP2L1 has a mutation status of T368T, The gene TMEM130 has a mutation status of T71T, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene LAMB4 has a mutation status of V1506V, The gene PAX4 has a mutation status of R129W, The gene COPG2 has a mutation status of I103M, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene NUP205 has a mutation status of L1186L, The gene PARP12 has a mutation status of E270K, The gene EPHB6 has a mutation status of A330D, The gene KEL has a mutation status of G4E, The gene CLCN1 has a mutation status of I241V, The gene REPIN1 has a mutation status of A81A, The gene AOC1 has a mutation status of H81H, The gene PTPRN2 has a mutation status of K454*, The gene WDR60 has a mutation status of P586T, The gene PRSS55 has a mutation status of P44C, The gene RP1L1 has a mutation status of D2021fs, The gene LONRF1 has a mutation status of E755K, The gene LONRF1 has a mutation status of R596*, The gene DLC1 has a mutation status of R338H, The gene PDGFRL has a mutation status of L7L, The gene CDCA2 has a mutation status of A95T, The gene NSD3 has a mutation status of D639D, The gene KAT6A has a mutation status of S1054S, The gene HGSNAT has a mutation status of A20A, The gene SNTG1 has a mutation status of C403Y, The gene PRDM14 has a mutation status of D180H, The gene SBSPON has a mutation status of P113P, The gene GDF6 has a mutation status of T126M, The gene GSDMC has a mutation status of P491L, The gene TG has a mutation status of A686T, The gene ZC3H3 has a mutation status of L631F, The gene SCRIB has a mutation status of A1277T, The gene SCRIB has a mutation status of L1242V, The gene EPPK1 has a mutation status of A2633del, The gene SCRT1 has a mutation status of P338S, The gene DOCK8 has a mutation status of Y1969*, The gene KANK1 has a mutation status of A664V, The gene MPDZ has a mutation status of L351F, The gene TEK has a mutation status of G476G, The gene UNC13B has a mutation status of R1049W, The gene PAX5 has a mutation status of T251N, The gene AL358113.1 has a mutation status of R1315R, The gene KIF27 has a mutation status of L998L, The gene BICD2 has a mutation status of L348L, The gene WNK2 has a mutation status of A2177A, The gene FRRS1L has a mutation status of R51A, The gene SVEP1 has a mutation status of I2698I, The gene CDK5RAP2 has a mutation status of R144W, The gene LHX2 has a mutation status of V217M, The gene CIZ1 has a mutation status of A451V, The gene CERCAM has a mutation status of L367L, The gene HMCN2 has a mutation status of R819H, The gene RAPGEF1 has a mutation status of D648N, The gene SETX has a mutation status of A2591T, The gene FAM163B has a mutation status of N68N, The gene CCDC187 has a mutation status of R294H, The gene LRRC26 has a mutation status of G200D, The gene PNPLA7 has a mutation status of I451I, The gene MRC1 has a mutation status of S1454S, The gene MAP3K8 has a mutation status of R59C, The gene ANKRD30A has a mutation status of R485V, The gene ALOX5 has a mutation status of G31D, The gene RBP3 has a mutation status of A309A, The gene WASHC2A has a mutation status of D370H, The gene ZNF365 has a mutation status of V329A, The gene CDHR1 has a mutation status of R15L, The gene KLLN has a mutation status of R62G, The gene LIPA has a mutation status of T337A, The gene CYP26C1 has a mutation status of L476P, The gene PLCE1 has a mutation status of D2124E, The gene ALDH18A1 has a mutation status of A152S, The gene CHUK has a mutation status of L7fs, The gene PPRC1 has a mutation status of D208D, The gene NEURL1 has a mutation status of D184D, The gene CFAP58 has a mutation status of R207H, The gene HABP2 has a mutation status of G316E, The gene BAG3 has a mutation status of R258W, The gene WDR11 has a mutation status of E648E, The gene TACC2 has a mutation status of A788P, The gene KNDC1 has a mutation status of P401P, The gene TALDO1 has a mutation status of G182G, The gene AC132217.2 has a mutation status of R56Q, The gene NUP98 has a mutation status of P1164H, The gene NRIP3 has a mutation status of C182S, The gene MICAL2 has a mutation status of R1330G, The gene COPB1 has a mutation status of R612R, The gene OTOG has a mutation status of V295M, The gene RAG2 has a mutation status of L21L, The gene API5 has a mutation status of V286V, The gene OR5L1 has a mutation status of I282T, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR10V1 has a mutation status of R187C, The gene SLC22A12 has a mutation status of R239C, The gene ATG2A has a mutation status of P1043S, The gene KAT5 has a mutation status of D164A, The gene GPR152 has a mutation status of P98P, The gene SHANK2 has a mutation status of M182L, The gene RELT has a mutation status of L307R, The gene GAB2 has a mutation status of P317L, The gene TENM4 has a mutation status of G2266S, The gene DYNC2H1 has a mutation status of V1771V, The gene DYNC2H1 has a mutation status of L4113V, The gene BCL9L has a mutation status of A401S, The gene CCDC153 has a mutation status of D97G, The gene TECTA has a mutation status of T1354I, The gene OR8B4 has a mutation status of G254G, The gene VSIG2 has a mutation status of M325V, The gene SLC6A13 has a mutation status of Y486H, The gene CACNA1C has a mutation status of V1454M, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R31 has a mutation status of 150_151KE>NQ, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene LRMP has a mutation status of H273H, The gene CASC1 has a mutation status of K660K, The gene ITPR2 has a mutation status of V2074G, The gene PKP2 has a mutation status of K724T, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of E249R, The gene NELL2 has a mutation status of T295S, The gene AMIGO2 has a mutation status of R245G, The gene ACVR1B has a mutation status of Q30R, The gene OR6C70 has a mutation status of S247S, The gene PTGES3 has a mutation status of T90T, The gene NAV3 has a mutation status of A613A, The gene OTOGL has a mutation status of A1322V, The gene C12orf29 has a mutation status of E242G, The gene CCDC38 has a mutation status of Q58K, The gene SLC17A8 has a mutation status of G205W, The gene SLC5A8 has a mutation status of S415S, The gene NT5DC3 has a mutation status of 374_375LK>F*, The gene TRPV4 has a mutation status of P498P, The gene PPTC7 has a mutation status of R67R, The gene ACAD10 has a mutation status of R11H, The gene ACAD10 has a mutation status of Y578C, The gene OAS2 has a mutation status of K681Q, The gene MPHOSPH9 has a mutation status of N676S, The gene DNAH10 has a mutation status of A4290A, The gene STX2 has a mutation status of D161D, The gene EP400 has a mutation status of T2839T, The gene GOLGA3 has a mutation status of G1203E, The gene PAN3 has a mutation status of T633T, The gene KBTBD7 has a mutation status of L50V, The gene CCDC122 has a mutation status of A38T, The gene PCDH17 has a mutation status of D667V, The gene PCCA has a mutation status of V12V, The gene LRRC9 has a mutation status of S1491L, The gene LRRC9 has a mutation status of N1492K, The gene SYNE2 has a mutation status of S4912L, The gene MAP3K9 has a mutation status of V231V, The gene ACOT6 has a mutation status of L45L, The gene CCDC88C has a mutation status of S1985C, The gene DYNC1H1 has a mutation status of V3212V, The gene AMN has a mutation status of M346L, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L22 has a mutation status of K792del, The gene GOLGA6L22 has a mutation status of *811Q, The gene CYFIP1 has a mutation status of K503K, The gene RYR3 has a mutation status of G1716G, The gene PLA2G4D has a mutation status of A279A, The gene MINDY2 has a mutation status of T434T, The gene LDHAL6B has a mutation status of I267T, The gene GCNT3 has a mutation status of C70Y, The gene ANKDD1A has a mutation status of L516L, The gene GOLGA6L10 has a mutation status of N426del, The gene GOLGA6L10 has a mutation status of C251H, The gene GOLGA6L9 has a mutation status of R6H, The gene ZNF592 has a mutation status of P44A, The gene AKAP13 has a mutation status of K2639N, The gene MESP1 has a mutation status of T22S, The gene TTLL13P has a mutation status of R490R, The gene LMF1 has a mutation status of I79I, The gene TELO2 has a mutation status of E811K, The gene PKD1 has a mutation status of E2111K, The gene PKD1 has a mutation status of R1546W, The gene UBN1 has a mutation status of A144A, The gene CLEC16A has a mutation status of C566C, The gene AC099489.1 has a mutation status of L2311L, The gene RSL1D1 has a mutation status of L241F, The gene DNAH3 has a mutation status of P56Q, The gene VWA3A has a mutation status of N69N, The gene NSMCE1 has a mutation status of V50I, The gene PHKG2 has a mutation status of T58T, The gene HEATR3 has a mutation status of T251I, The gene BBS2 has a mutation status of Q693Q, The gene ARL2BP has a mutation status of V104V, The gene DOK4 has a mutation status of R115H, The gene ADGRG1 has a mutation status of G555G, The gene CIAO2B has a mutation status of T81I, The gene HSD11B2 has a mutation status of T88T, The gene THAP11 has a mutation status of 123_124insQQQQQ, The gene ZFHX3 has a mutation status of E3535K, The gene PLCG2 has a mutation status of R653R, The gene ACSF3 has a mutation status of A221T, The gene TRPV1 has a mutation status of N192D, The gene HASPIN has a mutation status of I189T, The gene ALOX15 has a mutation status of Y15H, The gene ZMYND15 has a mutation status of M645V, The gene TMEM95 has a mutation status of L184F, The gene TP53 has a mutation status of F134fs, The gene DNAH2 has a mutation status of P72P, The gene ALOX12B has a mutation status of L187L, The gene AC129492.3 has a mutation status of 0_1insAPA, The gene MYH10 has a mutation status of L1096L, The gene MYH4 has a mutation status of I199I, The gene HS3ST3A1 has a mutation status of K162N, The gene TRPV2 has a mutation status of G35R, The gene MYO15A has a mutation status of E1406K, The gene MAPK7 has a mutation status of A296T, The gene DHRS13 has a mutation status of R191Q, The gene MYO18A has a mutation status of A647V, The gene RHOT1 has a mutation status of H654H, The gene SLFN13 has a mutation status of Q634E, The gene CCL4L2 has a mutation status of P67R, The gene TADA2A has a mutation status of *444*, The gene SOCS7 has a mutation status of P227A, The gene STARD3 has a mutation status of S405W, The gene MSL1 has a mutation status of P485P, The gene KRT13 has a mutation status of R378H, The gene STAT5B has a mutation status of A130V, The gene AKAP1 has a mutation status of V209M, The gene MARCHF10 has a mutation status of Q53K, The gene AC127029.3 has a mutation status of F123L, The gene LRRC37A3 has a mutation status of L29L, The gene AXIN2 has a mutation status of L499P, The gene ARSG has a mutation status of P21P, The gene WIPI1 has a mutation status of S175S, The gene CDR2L has a mutation status of L45L, The gene CYBC1 has a mutation status of P176L, The gene CEP76 has a mutation status of V443F, The gene FAM210A has a mutation status of L38S, The gene ANKRD30B has a mutation status of Y1319C, The gene TTC39C has a mutation status of P251L, The gene TAF4B has a mutation status of R34R, The gene DSG1 has a mutation status of T930I, The gene ZBTB7C has a mutation status of Y331Y, The gene STARD6 has a mutation status of R86S, The gene CCDC68 has a mutation status of M16T, The gene SERPINB11 has a mutation status of Q258H, The gene CDH19 has a mutation status of K30N, The gene ATP9B has a mutation status of G61S, The gene MEX3D has a mutation status of S592S, The gene REXO1 has a mutation status of D551A, The gene DENND1C has a mutation status of D607N, The gene FBN3 has a mutation status of Q2138Q, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T10751I, The gene PPAN-P2RY11 has a mutation status of T280A, The gene KEAP1 has a mutation status of 119_120GM>V, The gene CACNA1A has a mutation status of G2331D, The gene IL12RB1 has a mutation status of Y308C, The gene UPF1 has a mutation status of L813L, The gene TMEM161A has a mutation status of I420I, The gene NCAN has a mutation status of S766R, The gene ZNF66 has a mutation status of F97F, The gene ZNF430 has a mutation status of G547G, The gene ZNF729 has a mutation status of H1182R, The gene MAG has a mutation status of D314E, The gene ZNF585A has a mutation status of N338D, The gene RYR1 has a mutation status of P4386T, The gene ZNF780B has a mutation status of R202Q, The gene CEACAM1 has a mutation status of S151T, The gene PPP1R37 has a mutation status of P534L, The gene NOVA2 has a mutation status of V457G, The gene PPP5C has a mutation status of R44Q, The gene NTN5 has a mutation status of G233D, The gene TRPM4 has a mutation status of I897V, The gene SHANK1 has a mutation status of P1185Q, The gene SIGLEC6 has a mutation status of L57V, The gene ZNF616 has a mutation status of Q91Q, The gene ZNF761 has a mutation status of R449Q, The gene NLRP12 has a mutation status of A929T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA2 has a mutation status of N189H, The gene LILRA2 has a mutation status of S190A, The gene LILRB1 has a mutation status of L114fs, The gene HSPBP1 has a mutation status of G160A, The gene RNF225 has a mutation status of P276R, The gene SIRPA has a mutation status of L44S, The gene CHGB has a mutation status of N19I, The gene SYNDIG1 has a mutation status of P76S, The gene BPIFA3 has a mutation status of N134S, The gene RALGAPB has a mutation status of I176M, The gene PIGT has a mutation status of V11V, The gene SLC12A5 has a mutation status of GG75del, The gene BCAS4 has a mutation status of T181M, The gene NFATC2 has a mutation status of P237S, The gene CYP24A1 has a mutation status of R120H, The gene PPP1R3D has a mutation status of R22G, The gene FAM217B has a mutation status of N163N, The gene CDH4 has a mutation status of T65T, The gene CDH4 has a mutation status of A394E, The gene LAMA5 has a mutation status of H3497H, The gene ZBTB46 has a mutation status of A96A, The gene ADAMTS1 has a mutation status of P470L, The gene KRTAP13-1 has a mutation status of R115S, The gene RCAN1 has a mutation status of G4G, The gene DOP1B has a mutation status of T1099T, The gene KRTAP10-2 has a mutation status of S176F, The gene MICAL3 has a mutation status of R745Q, The gene ZDHHC8 has a mutation status of P415P, The gene SERPIND1 has a mutation status of N6N, The gene KIAA1671 has a mutation status of T681T, The gene ASPHD2 has a mutation status of V33G, The gene TTC28 has a mutation status of V1078L, The gene EMID1 has a mutation status of G229D, The gene SLC5A1 has a mutation status of V33I, The gene ISX has a mutation status of H95H, The gene ANKRD54 has a mutation status of A26T, The gene EP300 has a mutation status of M2161V, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TSPO has a mutation status of E70D, The gene EFCAB6 has a mutation status of G1095R, The gene FBLN1 has a mutation status of R287C, The gene BRD1 has a mutation status of I143I, The gene TTLL8 has a mutation status of V554M, The gene GTPBP6 has a mutation status of A212T, The gene GTPBP6 has a mutation status of M181L, The gene GTPBP6 has a mutation status of G61R, The gene ARSF has a mutation status of L217F, The gene TAB3 has a mutation status of Q522Q, The gene FAM47A has a mutation status of L387L, The gene FAM47A has a mutation status of L387I, The gene KRBOX4 has a mutation status of R135W, The gene ELK1 has a mutation status of A301A, The gene ZNF182 has a mutation status of P85P, The gene KCND1 has a mutation status of T512P, The gene OPHN1 has a mutation status of P735P, The gene KIF4A has a mutation status of V921L, The gene MAGEE1 has a mutation status of R14G, The gene DRP2 has a mutation status of V441M, The gene RAB40A has a mutation status of V189G, The gene SLC25A5 has a mutation status of T221R, The gene TENM1 has a mutation status of T2245S, The gene MAGEC1 has a mutation status of P232P, The gene AFF2 has a mutation status of G547D, The gene AFF2 has a mutation status of R708L, The gene AFF2 has a mutation status of R1238S, The gene IDH3G has a mutation status of L330M, The gene IDH3G has a mutation status of T328I, The gene L1CAM has a mutation status of G758G, The gene TMEM187 has a mutation status of G16G, The gene RPS4Y2 has a mutation status of T57A, The gene MT-ND1 has a mutation status of I314I, The gene MT-ND2 has a mutation status of T119A, The gene MT-ATP6 has a mutation status of T13A, The gene MT-ATP6 has a mutation status of H90Y, The gene MT-ATP6 has a mutation status of I192T, The gene MT-CO3 has a mutation status of G113G, The gene MT-ND4L has a mutation status of A56A, The gene MT-ND4 has a mutation status of Y259Y, The gene MT-CYB has a mutation status of I79I, The gene MT-CYB has a mutation status of F274L
LUAD
The gene PRDM16 has a mutation status of S890Y, The gene H6PD has a mutation status of D417N, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene DNAJC16 has a mutation status of E394*, The gene TMCO4 has a mutation status of R293C, The gene TMCO4 has a mutation status of E75G, The gene ZC3H12A has a mutation status of S62S, The gene PPCS has a mutation status of R25P, The gene CLCA2 has a mutation status of S485P, The gene ABCA4 has a mutation status of E1087K, The gene DENND2C has a mutation status of P672T, The gene POGZ has a mutation status of N136S, The gene CELF3 has a mutation status of G136G, The gene FLG has a mutation status of G3250G, The gene ATP8B2 has a mutation status of T732I, The gene PMVK has a mutation status of E155A, The gene FCRL4 has a mutation status of E204D, The gene BLZF1 has a mutation status of V12I, The gene TNR has a mutation status of R565Q, The gene PAPPA2 has a mutation status of I868V, The gene AXDND1 has a mutation status of K111K, The gene C4BPA has a mutation status of R206H, The gene PTPN14 has a mutation status of P528L, The gene PTPN14 has a mutation status of G504G, The gene MTR has a mutation status of R1146R, The gene OR14I1 has a mutation status of C150*, The gene SOS1 has a mutation status of N233Y, The gene EPAS1 has a mutation status of D753E, The gene MOB1A has a mutation status of A44fs, The gene CREG2 has a mutation status of Q237K, The gene GCC2 has a mutation status of F33F, The gene POLR1B has a mutation status of Y551F, The gene ZRANB3 has a mutation status of H513R, The gene PPIG has a mutation status of S695S, The gene TTN has a mutation status of I29172I, The gene SRGAP3 has a mutation status of T983K, The gene HRH1 has a mutation status of N5N, The gene FGD5 has a mutation status of S458S, The gene IMPDH2 has a mutation status of P123R, The gene NICN1 has a mutation status of T70A, The gene PHLDB2 has a mutation status of D127D, The gene FBXO40 has a mutation status of R614K, The gene MYLK has a mutation status of T74T, The gene H1-8 has a mutation status of P79A, The gene BFSP2 has a mutation status of L341L, The gene IL1RAP has a mutation status of E453A, The gene CCKAR has a mutation status of V311A, The gene ADGRL3 has a mutation status of T1236I, The gene UGT2A1 has a mutation status of Y221H, The gene UNC5C has a mutation status of R543R, The gene TRMT10A has a mutation status of R76Q, The gene TET2 has a mutation status of S825*, The gene PLEKHG4B has a mutation status of L470L, The gene IRX4 has a mutation status of R165P, The gene PCDHA13 has a mutation status of P240P, The gene PCDHB6 has a mutation status of P104L, The gene ARL10 has a mutation status of P8P, The gene RIPK1 has a mutation status of A569V, The gene KIF13A has a mutation status of G1598G, The gene ZKSCAN3 has a mutation status of W463*, The gene DDR1 has a mutation status of S378R, The gene CCHCR1 has a mutation status of L305F, The gene MSH5 has a mutation status of A364A, The gene HLA-DRB5 has a mutation status of L246L, The gene HLA-DRB5 has a mutation status of Q220W, The gene SYNGAP1 has a mutation status of G935S, The gene TNFRSF21 has a mutation status of K391K, The gene PEX7 has a mutation status of L238F, The gene NOX3 has a mutation status of W53L, The gene PDE10A has a mutation status of P764P, The gene PLEKHA8 has a mutation status of V435I, The gene TBRG4 has a mutation status of T223I, The gene IKZF1 has a mutation status of D186Y, The gene PSPH has a mutation status of L68P, The gene AUTS2 has a mutation status of S612Y, The gene DYNC1I1 has a mutation status of F279L, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T289M, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene MUC3A has a mutation status of T1510I, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene MUC3A has a mutation status of T3202A, The gene LRRC17 has a mutation status of T173M, The gene KMT2E has a mutation status of T525T, The gene EXOC4 has a mutation status of L612L, The gene TBXAS1 has a mutation status of N245S, The gene EZH2 has a mutation status of R690H, The gene AGAP3 has a mutation status of T243T, The gene EN2 has a mutation status of R65G, The gene CLN8 has a mutation status of R70H, The gene MYOM2 has a mutation status of T182T, The gene INTS10 has a mutation status of C564G, The gene CDCA2 has a mutation status of N411D, The gene PMP2 has a mutation status of L6Q, The gene ESRP1 has a mutation status of Y176D, The gene MTDH has a mutation status of E254A, The gene LURAP1L has a mutation status of S85R, The gene FOCAD has a mutation status of K37N, The gene FRMPD1 has a mutation status of H1386Y, The gene SEMA4D has a mutation status of A686A, The gene NFIL3 has a mutation status of R91C, The gene KIAA1958 has a mutation status of R425W, The gene FIBCD1 has a mutation status of A67A, The gene CAMSAP1 has a mutation status of H969Q, The gene C10orf71 has a mutation status of S673P, The gene ZNF503 has a mutation status of S315S, The gene HPSE2 has a mutation status of T351I, The gene KNDC1 has a mutation status of P6Q, The gene MUC5AC has a mutation status of A2623A, The gene OR51E1 has a mutation status of V42L, The gene PPFIBP2 has a mutation status of V729V, The gene SOX6 has a mutation status of A283S, The gene PIK3C2A has a mutation status of K356K, The gene E2F8 has a mutation status of S533N, The gene SLC5A12 has a mutation status of L250L, The gene OR9G1 has a mutation status of T62V, The gene OR10Q1 has a mutation status of C184C, The gene PLCB3 has a mutation status of R1137H, The gene GPR152 has a mutation status of A404P, The gene KDM4D has a mutation status of D499E, The gene GRIA4 has a mutation status of S866R, The gene CDON has a mutation status of H1081Q, The gene IGSF9B has a mutation status of S973R, The gene ATN1 has a mutation status of A453A, The gene POU6F1 has a mutation status of G363V, The gene NAP1L1 has a mutation status of D382N, The gene PTPN11 has a mutation status of R265Q, The gene C1QTNF9B has a mutation status of V264E, The gene SIAH3 has a mutation status of R50Q, The gene OLFM4 has a mutation status of R51M, The gene CARS2 has a mutation status of A481V, The gene VRTN has a mutation status of A251S, The gene CHRM5 has a mutation status of W525*, The gene EIF2AK4 has a mutation status of T791K, The gene GNB5 has a mutation status of K189Q, The gene SCAMP2 has a mutation status of G246V, The gene KLHL25 has a mutation status of V209M, The gene MMP25 has a mutation status of R438L, The gene MEFV has a mutation status of R528C, The gene NLRC3 has a mutation status of S582S, The gene CREBBP has a mutation status of G221V, The gene EARS2 has a mutation status of D281G, The gene N4BP1 has a mutation status of L684L, The gene SETD6 has a mutation status of E63D, The gene MARVELD3 has a mutation status of A342G, The gene ZCCHC14 has a mutation status of G374G, The gene CLDN7 has a mutation status of S172A, The gene USP43 has a mutation status of G739R, The gene HS3ST3A1 has a mutation status of G51E, The gene SLFN12L has a mutation status of K60N, The gene GAS2L2 has a mutation status of Q199H, The gene CCL4L2 has a mutation status of P67R, The gene MRM1 has a mutation status of L150P, The gene SRCIN1 has a mutation status of P836S, The gene CWC25 has a mutation status of S299R, The gene KRT28 has a mutation status of G126R, The gene KRT10 has a mutation status of S42F, The gene KRTAP4-1 has a mutation status of R85R, The gene NXPH3 has a mutation status of V132I, The gene FADS6 has a mutation status of P6P, The gene FBF1 has a mutation status of A919G, The gene CYGB has a mutation status of S123L, The gene SGSH has a mutation status of R441Q, The gene AATK has a mutation status of C547*, The gene CEP131 has a mutation status of L927L, The gene TBCD has a mutation status of V988M, The gene MYOM1 has a mutation status of V413M, The gene CNDP1 has a mutation status of V418I, The gene PCSK4 has a mutation status of V111G, The gene FUT3 has a mutation status of L335L, The gene WDR83 has a mutation status of L82F, The gene C19orf57 has a mutation status of A375V, The gene CEACAM20 has a mutation status of S444S, The gene MAMSTR has a mutation status of E212D, The gene MAMSTR has a mutation status of R10M, The gene KCNA7 has a mutation status of A275V, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of Y99I, The gene KIR2DL3 has a mutation status of G12A, The gene KIR2DL4 has a mutation status of P17L, The gene ISOC2 has a mutation status of V146G, The gene NLRP5 has a mutation status of K1090N, The gene DUXA has a mutation status of P177L, The gene SIRPA has a mutation status of L44S, The gene HSPA12B has a mutation status of L410L, The gene ASXL1 has a mutation status of Y591*, The gene ADAMTS1 has a mutation status of V825F, The gene PDXK has a mutation status of Q288P, The gene INPP5J has a mutation status of N171K, The gene APOL5 has a mutation status of A146A, The gene PACSIN2 has a mutation status of E227D, The gene SLC25A6 has a mutation status of P28S, The gene SMC1A has a mutation status of G707E, The gene APEX2 has a mutation status of R125W, The gene TRMT2B has a mutation status of T128M, The gene MT-CO1 has a mutation status of L283L, The gene MT-ATP6 has a mutation status of I197I, The gene MT-ND4 has a mutation status of L351L
LAML
The gene PEX10 has a mutation status of G132V, The gene HES3 has a mutation status of G55V, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF15 has a mutation status of L407L, The gene SLC25A34 has a mutation status of T252T, The gene PADI4 has a mutation status of K244R, The gene ARHGEF10L has a mutation status of M347L, The gene CEP85 has a mutation status of T98T, The gene CSMD2 has a mutation status of I3420V, The gene BEND5 has a mutation status of L262L, The gene SGIP1 has a mutation status of G14A, The gene LRRC7 has a mutation status of R10W, The gene ERICH3 has a mutation status of S1009L, The gene PRMT6 has a mutation status of Y324S, The gene H2AC20 has a mutation status of L24R, The gene TARS2 has a mutation status of F416F, The gene LCE2C has a mutation status of S72F, The gene C1orf68 has a mutation status of G220R, The gene FCRL5 has a mutation status of T484T, The gene CASQ1 has a mutation status of E233V, The gene NECTIN4 has a mutation status of V368V, The gene TNFSF18 has a mutation status of S105T, The gene BRINP3 has a mutation status of F576F, The gene PIK3C2B has a mutation status of T1344M, The gene LAMB3 has a mutation status of V753G, The gene PTPN14 has a mutation status of M775I, The gene OR2T2 has a mutation status of I321T, The gene OR2T27 has a mutation status of V260M, The gene UCN has a mutation status of L15L, The gene PCGF1 has a mutation status of E167K, The gene SCN1A has a mutation status of T1913T, The gene OSBPL6 has a mutation status of N593K, The gene TTN has a mutation status of L32097V, The gene CHPF has a mutation status of E700M, The gene ERFE has a mutation status of A300A, The gene SCN5A has a mutation status of L56M, The gene KLHL40 has a mutation status of D175V, The gene TMEM45A has a mutation status of Y155C, The gene NXPE3 has a mutation status of L23P, The gene MYH15 has a mutation status of C1352Y, The gene PLCXD2 has a mutation status of L106P, The gene GTF2E1 has a mutation status of D385D, The gene SEC22A has a mutation status of N162S, The gene NEK11 has a mutation status of S469P, The gene TM4SF4 has a mutation status of F160F, The gene KCNMB3 has a mutation status of I259M, The gene IGF2BP2 has a mutation status of P163L, The gene MASP1 has a mutation status of Y131C, The gene RTP2 has a mutation status of V163I, The gene ACAP2 has a mutation status of T579M, The gene SLC49A3 has a mutation status of P373R, The gene DGKQ has a mutation status of S634P, The gene CTBP1 has a mutation status of R173G, The gene SLBP has a mutation status of S20C, The gene TMEM129 has a mutation status of S143S, The gene ARAP2 has a mutation status of R305C, The gene PAICS has a mutation status of D221N, The gene LEF1 has a mutation status of S112S, The gene ENPEP has a mutation status of W408C, The gene KIAA1109 has a mutation status of L3722F, The gene FHDC1 has a mutation status of F682F, The gene GLRB has a mutation status of S93P, The gene CTNND2 has a mutation status of L307V, The gene PDZD2 has a mutation status of I637V, The gene MOCS2 has a mutation status of A70V, The gene IL31RA has a mutation status of A715T, The gene GPBP1 has a mutation status of D136V, The gene GPBP1 has a mutation status of V278V, The gene SLF1 has a mutation status of T999N, The gene MCC has a mutation status of N283S, The gene MCC has a mutation status of L179L, The gene SLC22A5 has a mutation status of I89V, The gene LECT2 has a mutation status of E78D, The gene SPOCK1 has a mutation status of T352M, The gene PCDHB12 has a mutation status of DR477del, The gene ATP10B has a mutation status of R1029C, The gene FGF18 has a mutation status of H205R, The gene RASGEF1C has a mutation status of D94E, The gene GFOD1 has a mutation status of D281D, The gene JARID2 has a mutation status of A695G, The gene ATXN1 has a mutation status of R359R, The gene OR2B6 has a mutation status of R20G, The gene HLA-A has a mutation status of G314V, The gene TRIM39 has a mutation status of E283G, The gene VARS2 has a mutation status of R795Q, The gene HLA-DRB5 has a mutation status of G8E, The gene HLA-DMB has a mutation status of L133L, The gene KIFC1 has a mutation status of T598T, The gene NCR2 has a mutation status of S59L, The gene AARS2 has a mutation status of V59G, The gene PKHD1 has a mutation status of G1261G, The gene CASP8AP2 has a mutation status of K1536Q, The gene NDUFAF4 has a mutation status of D98N, The gene RSPH4A has a mutation status of I471T, The gene ARFGEF3 has a mutation status of V1901G, The gene SAMD5 has a mutation status of P16P, The gene SYNE1 has a mutation status of G7350R, The gene SYNE1 has a mutation status of R677H, The gene BRAT1 has a mutation status of A642G, The gene DNAH11 has a mutation status of P2006L, The gene PKD1L1 has a mutation status of S993S, The gene EGFR has a mutation status of ELR701del, The gene EGFR has a mutation status of A705P, The gene AC004922.1 has a mutation status of T412T, The gene GAL3ST4 has a mutation status of R102H, The gene ZAN has a mutation status of P2252P, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T303V, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of T987I, The gene CPA5 has a mutation status of M428R, The gene KLF14 has a mutation status of A39A, The gene MKRN1 has a mutation status of A26S, The gene RP1L1 has a mutation status of S1214I, The gene DDHD2 has a mutation status of Y112C, The gene FABP4 has a mutation status of D48Y, The gene ABRA has a mutation status of P83P, The gene TG has a mutation status of A519A, The gene TG has a mutation status of G1868G, The gene MROH1 has a mutation status of D521N, The gene MROH1 has a mutation status of S1298L, The gene RUSC2 has a mutation status of R711W, The gene GLIPR2 has a mutation status of A120V, The gene CORO2A has a mutation status of R33H, The gene ZNF483 has a mutation status of A587A, The gene KIAA1958 has a mutation status of A377A, The gene FCN1 has a mutation status of A218T, The gene LHX3 has a mutation status of S348R, The gene TASOR2 has a mutation status of F2412L, The gene PROSER2 has a mutation status of E219K, The gene CUBN has a mutation status of T2007M, The gene CUL2 has a mutation status of S481N, The gene CEP55 has a mutation status of D247E, The gene RNH1 has a mutation status of Q448R, The gene CEND1 has a mutation status of K62T, The gene CARS1 has a mutation status of P246S, The gene DNHD1 has a mutation status of R3978P, The gene DENND5A has a mutation status of I952V, The gene TRIM51 has a mutation status of R152R, The gene TRIM51 has a mutation status of A153D, The gene OR5M8 has a mutation status of R19H, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene PLCB3 has a mutation status of S292A, The gene CDC42BPG has a mutation status of A1224A, The gene PPP6R3 has a mutation status of R350Q, The gene HEPHL1 has a mutation status of Y416D, The gene DSCAML1 has a mutation status of S2060S, The gene MFRP has a mutation status of E20E, The gene ARHGAP32 has a mutation status of A264V, The gene VWF has a mutation status of A2414T, The gene ACRBP has a mutation status of R273G, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene ITPR2 has a mutation status of K1697N, The gene LRRK2 has a mutation status of K258K, The gene LRRK2 has a mutation status of Y636H, The gene SPATS2 has a mutation status of E162E, The gene POU6F1 has a mutation status of G53G, The gene SLC4A8 has a mutation status of V286A, The gene OS9 has a mutation status of V322L, The gene IRF9 has a mutation status of T51I, The gene NPAS3 has a mutation status of T805T, The gene PAX9 has a mutation status of Q257H, The gene PLEKHG3 has a mutation status of P1019P, The gene PAPLN has a mutation status of I1249F, The gene FCF1 has a mutation status of Q22R, The gene DIO2 has a mutation status of V75G, The gene SERINC4 has a mutation status of L499L, The gene CLK3 has a mutation status of S95L, The gene RASGRF1 has a mutation status of A895A, The gene JMJD8 has a mutation status of R78Q, The gene IFT140 has a mutation status of V569A, The gene ZNF598 has a mutation status of S352S, The gene TRAF7 has a mutation status of E73E, The gene CCNF has a mutation status of H69Y, The gene AC093525.2 has a mutation status of V67L, The gene CLN3 has a mutation status of Y124C, The gene TAOK2 has a mutation status of P355L, The gene ZNF668 has a mutation status of H358N, The gene ITGAM has a mutation status of K1134R, The gene NLRC5 has a mutation status of L607F, The gene WWP2 has a mutation status of E719E, The gene GSE1 has a mutation status of E1105K, The gene ZCCHC14 has a mutation status of G374G, The gene TRPV1 has a mutation status of D615G, The gene TP53 has a mutation status of Y205H, The gene MYH1 has a mutation status of R1438S, The gene DNAH9 has a mutation status of L2070L, The gene CCDC144A has a mutation status of K1223I, The gene EFCAB5 has a mutation status of Q38H, The gene CCL4L2 has a mutation status of P67R, The gene MED24 has a mutation status of A114T, The gene TMEM94 has a mutation status of L553V, The gene HGS has a mutation status of F589F, The gene MYOM1 has a mutation status of G1635S, The gene LAMA1 has a mutation status of G2292G, The gene LIPG has a mutation status of P217L, The gene CDH7 has a mutation status of L242R, The gene MBP has a mutation status of C142W, The gene MUC16 has a mutation status of P5040S, The gene ICAM5 has a mutation status of L21V, The gene DOCK6 has a mutation status of L1488F, The gene ZNF433 has a mutation status of V12M, The gene ADGRE5 has a mutation status of G634V, The gene ADGRE2 has a mutation status of L765L, The gene CRLF1 has a mutation status of P420L, The gene GMIP has a mutation status of P779L, The gene CEP89 has a mutation status of G349V, The gene FCGBP has a mutation status of GP1230del, The gene FCGBP has a mutation status of T1203fs, The gene FCGBP has a mutation status of A1165fs, The gene FCGBP has a mutation status of E1160fs, The gene SHKBP1 has a mutation status of P698L, The gene ITPKC has a mutation status of F568V, The gene CEACAM6 has a mutation status of I38T, The gene ZNF428 has a mutation status of P40P, The gene KPTN has a mutation status of D289Y, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of Q401L, The gene ZNF444 has a mutation status of R289S, The gene PTPRA has a mutation status of L459L, The gene DDRGK1 has a mutation status of E155E, The gene CFAP61 has a mutation status of E209K, The gene TPTE has a mutation status of R261G, The gene TRIOBP has a mutation status of L106V, The gene PLA2G6 has a mutation status of T575T, The gene CACNA1I has a mutation status of S569R, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SHOX has a mutation status of A214D, The gene ARSD has a mutation status of T310M, The gene SHROOM2 has a mutation status of D613A, The gene RAI2 has a mutation status of N60N, The gene SLC38A5 has a mutation status of T156T, The gene CACNA1F has a mutation status of N380N, The gene IQSEC2 has a mutation status of E222*, The gene RTL3 has a mutation status of L268Q, The gene SYTL4 has a mutation status of P144R, The gene GUCY2F has a mutation status of P1069L, The gene AMOT has a mutation status of G398G, The gene TENM1 has a mutation status of E1117E, The gene BCORL1 has a mutation status of L1132P, The gene DNASE1L1 has a mutation status of T202N, The gene MT-ATP6 has a mutation status of I50V
LUAD
The gene ATAD3B has a mutation status of R638W, The gene CHD5 has a mutation status of S1895S, The gene PEX14 has a mutation status of R350H, The gene MTOR has a mutation status of E1799K, The gene C1orf167 has a mutation status of Q358Q, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene UBR4 has a mutation status of A230A, The gene FAM43B has a mutation status of N7S, The gene TCEA3 has a mutation status of G25G, The gene SESN2 has a mutation status of Q465K, The gene HDAC1 has a mutation status of F241L, The gene ADPRS has a mutation status of A2S, The gene EPHA10 has a mutation status of V264G, The gene MAST2 has a mutation status of T666S, The gene ROR1 has a mutation status of S435S, The gene ASB17 has a mutation status of D252E, The gene RPAP2 has a mutation status of I329L, The gene PPIAL4H has a mutation status of N102I, The gene NBPF11 has a mutation status of Q55H, The gene AC242842.3 has a mutation status of V503L, The gene IQGAP3 has a mutation status of E590*, The gene TNN has a mutation status of A24P, The gene FMOD has a mutation status of YLQG319del, The gene PACC1 has a mutation status of F83F, The gene RAB3GAP2 has a mutation status of E1029E, The gene CAPN9 has a mutation status of A661G, The gene WDR43 has a mutation status of T467T, The gene CAPN13 has a mutation status of E639*, The gene HAAO has a mutation status of V103L, The gene CFAP36 has a mutation status of V263A, The gene USP34 has a mutation status of A598E, The gene MEIS1 has a mutation status of I19T, The gene CNRIP1 has a mutation status of L137L, The gene DNAH6 has a mutation status of R1153G, The gene CREG2 has a mutation status of Q237K, The gene CCDC74B has a mutation status of V29V, The gene SLC4A10 has a mutation status of A1062T, The gene SF3B1 has a mutation status of I1084I, The gene SATB2 has a mutation status of R11R, The gene CFAP65 has a mutation status of R1156R, The gene MTERF4 has a mutation status of P210Q, The gene TRANK1 has a mutation status of T1312M, The gene DLEC1 has a mutation status of L71M, The gene CCDC12 has a mutation status of E101D, The gene UBA7 has a mutation status of V488A, The gene MON1A has a mutation status of G87G, The gene RASSF1 has a mutation status of C102F, The gene ERC2 has a mutation status of S448L, The gene RIOX2 has a mutation status of D270N, The gene OR5K4 has a mutation status of E52K, The gene BBX has a mutation status of W28*, The gene ZBTB20 has a mutation status of G184D, The gene WDR5B has a mutation status of W282*, The gene KALRN has a mutation status of P221P, The gene AMOTL2 has a mutation status of R183R, The gene ETV5 has a mutation status of A192V, The gene DGKG has a mutation status of E672*, The gene TPRG1 has a mutation status of Y61fs, The gene BOD1L1 has a mutation status of S2209G, The gene LAP3 has a mutation status of P5H, The gene PGM2 has a mutation status of E597D, The gene UGT2B15 has a mutation status of G100D, The gene RCHY1 has a mutation status of K36E, The gene HELQ has a mutation status of H139L, The gene PGRMC2 has a mutation status of T157R, The gene POU4F2 has a mutation status of L286fs, The gene LRBA has a mutation status of F294L, The gene LRRC14B has a mutation status of A110D, The gene ADAMTS12 has a mutation status of V593I, The gene NIPBL has a mutation status of S140S, The gene HCN1 has a mutation status of I693V, The gene MCC has a mutation status of A376A, The gene SLC12A2 has a mutation status of D1066N, The gene SLC23A1 has a mutation status of V160V, The gene PCDHB8 has a mutation status of S490S, The gene GABRA1 has a mutation status of T333R, The gene SPDL1 has a mutation status of R453S, The gene NPM1 has a mutation status of N38D, The gene LMAN2 has a mutation status of R223H, The gene TBC1D9B has a mutation status of H63Q, The gene SLC22A23 has a mutation status of S116*, The gene SOX4 has a mutation status of G183A, The gene OR5V1 has a mutation status of V157V, The gene HLA-DQA2 has a mutation status of A16T, The gene RUNX2 has a mutation status of A525S, The gene PHF3 has a mutation status of R673C, The gene RIMS1 has a mutation status of A417A, The gene IFNGR1 has a mutation status of P26P, The gene REPS1 has a mutation status of P45P, The gene AKAP12 has a mutation status of R961W, The gene INTS1 has a mutation status of A302A, The gene AP5Z1 has a mutation status of F509F, The gene ABCA13 has a mutation status of H1648R, The gene EGFR has a mutation status of A244D, The gene PSPH has a mutation status of L68P, The gene HSPB1 has a mutation status of Y23Y, The gene PCLO has a mutation status of Q941Q, The gene KIAA1324L has a mutation status of D417D, The gene VPS50 has a mutation status of D46fs, The gene EPHB4 has a mutation status of L504L, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene LSMEM1 has a mutation status of N114N, The gene CFTR has a mutation status of T690A, The gene GCC1 has a mutation status of L45L, The gene PAX4 has a mutation status of A298T, The gene SMKR1 has a mutation status of L46L, The gene CPA4 has a mutation status of L331L, The gene C8orf74 has a mutation status of A202D, The gene NPBWR1 has a mutation status of A114D, The gene PKHD1L1 has a mutation status of T2782I, The gene EPPK1 has a mutation status of A2155P, The gene TMEM8B has a mutation status of A173E, The gene FOXB2 has a mutation status of A414D, The gene SLC28A3 has a mutation status of P409S, The gene COL15A1 has a mutation status of K693K, The gene AKNA has a mutation status of S316G, The gene PTGES2 has a mutation status of V243G, The gene FCN2 has a mutation status of K304*, The gene CCDC187 has a mutation status of G891G, The gene ANAPC2 has a mutation status of L442V, The gene USP6NL has a mutation status of Q17K, The gene MRC1 has a mutation status of S288R, The gene ARHGAP22 has a mutation status of A139T, The gene SEC24C has a mutation status of R222Q, The gene HECTD2 has a mutation status of A18V, The gene SLIT1 has a mutation status of N1103S, The gene SLIT1 has a mutation status of P708S, The gene HPSE2 has a mutation status of R466Q, The gene DNMBP has a mutation status of L1107L, The gene OGA has a mutation status of R610R, The gene CALHM1 has a mutation status of S142N, The gene CRACR2B has a mutation status of A125V, The gene MUC5AC has a mutation status of R2283S, The gene MUC5AC has a mutation status of T3668P, The gene SLC22A18 has a mutation status of I202T, The gene STIM1 has a mutation status of V280F, The gene OR56A3 has a mutation status of G297R, The gene CYB5R2 has a mutation status of *277K, The gene TMEM86A has a mutation status of R166W, The gene PTPN5 has a mutation status of P13P, The gene OR9G1 has a mutation status of T62V, The gene PRPF19 has a mutation status of T268N, The gene CD6 has a mutation status of L27I, The gene CD6 has a mutation status of D191H, The gene DAGLA has a mutation status of E342K, The gene MEN1 has a mutation status of A412A, The gene PAAF1 has a mutation status of S328F, The gene FAT3 has a mutation status of K1798R, The gene ST14 has a mutation status of A240S, The gene IQSEC3 has a mutation status of R328C, The gene ITFG2 has a mutation status of M178L, The gene FGD4 has a mutation status of I20I, The gene C12orf54 has a mutation status of R30K, The gene TESPA1 has a mutation status of R508R, The gene CHST11 has a mutation status of T95K, The gene CUX2 has a mutation status of R701S, The gene VSIG10 has a mutation status of P311L, The gene FLT1 has a mutation status of E689K, The gene KL has a mutation status of P100P, The gene FREM2 has a mutation status of F127L, The gene KLF12 has a mutation status of R314R, The gene AL136295.3 has a mutation status of I4I, The gene PRORP has a mutation status of S476L, The gene FSCB has a mutation status of R438P, The gene KLHDC1 has a mutation status of D115N, The gene ERO1A has a mutation status of L17M, The gene DACT1 has a mutation status of P17L, The gene PLEKHD1 has a mutation status of S327P, The gene SLC8A3 has a mutation status of R355L, The gene LTBP2 has a mutation status of G729V, The gene FCF1 has a mutation status of R188Q, The gene CEP170B has a mutation status of E355K, The gene JAG2 has a mutation status of V244V, The gene ATP10A has a mutation status of M650I, The gene TTBK2 has a mutation status of L695H, The gene TGM7 has a mutation status of E10*, The gene GCNT3 has a mutation status of R388Q, The gene MINAR1 has a mutation status of S717G, The gene GOLGA6L10 has a mutation status of 387_388insDRLREL, The gene GOLGA6L9 has a mutation status of Q151E, The gene MESP1 has a mutation status of S237I, The gene CACNA1H has a mutation status of R762W, The gene CCNF has a mutation status of T327K, The gene CLUAP1 has a mutation status of P334P, The gene AC099489.1 has a mutation status of R1529M, The gene ARHGAP17 has a mutation status of N828T, The gene TBX6 has a mutation status of G12R, The gene SRCAP has a mutation status of P2364L, The gene NKD1 has a mutation status of D314D, The gene SLC38A7 has a mutation status of N62N, The gene DUS2 has a mutation status of T390T, The gene RFWD3 has a mutation status of S735S, The gene CTU2 has a mutation status of G265G, The gene PIEZO1 has a mutation status of V1162I, The gene TNK1 has a mutation status of E168E, The gene ZBTB4 has a mutation status of A254A, The gene TP53 has a mutation status of R248Q, The gene TMEM88 has a mutation status of P82P, The gene MYO18A has a mutation status of A1897G, The gene CCL4L2 has a mutation status of P67R, The gene TOP2A has a mutation status of T930I, The gene RUNDC1 has a mutation status of Q293R, The gene PRAC2 has a mutation status of P77P, The gene WFIKKN2 has a mutation status of R541L, The gene MPO has a mutation status of L54L, The gene CYB561 has a mutation status of G139G, The gene AC113554.1 has a mutation status of T663T, The gene SCN4A has a mutation status of D356N, The gene CACNG1 has a mutation status of T12I, The gene MRPL58 has a mutation status of R185Q, The gene FASN has a mutation status of R1724R, The gene LRRC30 has a mutation status of D65N, The gene CEP76 has a mutation status of A409T, The gene TAF4B has a mutation status of S373*, The gene ZNF236 has a mutation status of E452A, The gene BSG has a mutation status of G94D, The gene FSD1 has a mutation status of P364P, The gene CLEC4G has a mutation status of R29S, The gene MYO1F has a mutation status of D648D, The gene ZNF562 has a mutation status of M28I, The gene EPS15L1 has a mutation status of I393F, The gene ELL has a mutation status of D46V, The gene ZNF792 has a mutation status of R358R, The gene ARHGAP33 has a mutation status of Q553K, The gene ALKBH6 has a mutation status of A214A, The gene ZNF382 has a mutation status of I127V, The gene IFNL3 has a mutation status of P32P, The gene LRFN1 has a mutation status of A126E, The gene SUPT5H has a mutation status of T768T, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene NUMBL has a mutation status of A25S, The gene FKRP has a mutation status of E285*, The gene FKRP has a mutation status of R404R, The gene TRPM4 has a mutation status of R770C, The gene PRR12 has a mutation status of L30F, The gene ASPDH has a mutation status of G279G, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA4 has a mutation status of C195C, The gene KIR2DL4 has a mutation status of R137H, The gene AURKC has a mutation status of I45I, The gene PABPC1L has a mutation status of T121I, The gene CTSA has a mutation status of N422S, The gene CDH22 has a mutation status of E741D, The gene MC3R has a mutation status of V63M, The gene FAM217B has a mutation status of S93S, The gene RBBP8NL has a mutation status of P243P, The gene HELZ2 has a mutation status of L194I, The gene LTN1 has a mutation status of D790N, The gene DSCAM has a mutation status of E1274K, The gene IL17RA has a mutation status of N67D, The gene TRMT2A has a mutation status of L214I, The gene GSTT4 has a mutation status of Q197R, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CELSR1 has a mutation status of T2407T, The gene SHANK3 has a mutation status of A1204D, The gene ARAF has a mutation status of I232M, The gene IQSEC2 has a mutation status of V581L, The gene ITIH6 has a mutation status of G1202G, The gene BX276092.9 has a mutation status of V284V, The gene CDX4 has a mutation status of F44F, The gene DACH2 has a mutation status of A11E, The gene BTK has a mutation status of C464F, The gene ENOX2 has a mutation status of G53A, The gene MPP1 has a mutation status of R32R, The gene MT-CYB has a mutation status of L357L
GBMLGG
The gene PRDM16 has a mutation status of D630G, The gene TAS1R1 has a mutation status of T198I, The gene PRAMEF4 has a mutation status of C76H, The gene PRAMEF9 has a mutation status of L14L, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene KAZN has a mutation status of D485E, The gene SYTL1 has a mutation status of A202T, The gene TMEM200B has a mutation status of R153R, The gene SRSF4 has a mutation status of R139C, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene ERI3 has a mutation status of Q259Q, The gene ORC1 has a mutation status of D513D, The gene WDR78 has a mutation status of K794R, The gene C1orf141 has a mutation status of D10N, The gene PRKACB has a mutation status of V199V, The gene DNASE2B has a mutation status of G138V, The gene SNX7 has a mutation status of P32P, The gene CELSR2 has a mutation status of R2015K, The gene STRIP1 has a mutation status of E811G, The gene TBX15 has a mutation status of R189Q, The gene NBPF10 has a mutation status of L891V, The gene NBPF11 has a mutation status of Q55H, The gene SELL has a mutation status of I2M, The gene NAV1 has a mutation status of A75H, The gene SPATA45 has a mutation status of P52P, The gene PTPN14 has a mutation status of G1014G, The gene TAF5L has a mutation status of R535H, The gene RYR2 has a mutation status of H1710N, The gene FMN2 has a mutation status of A160V, The gene SDCCAG8 has a mutation status of L638L, The gene OR2T4 has a mutation status of V109L, The gene ZNF672 has a mutation status of R128G, The gene NBAS has a mutation status of V1220I, The gene SLC8A1 has a mutation status of V777L, The gene MTIF2 has a mutation status of G76G, The gene CNGA3 has a mutation status of T153T, The gene BIN1 has a mutation status of G289D, The gene GPR148 has a mutation status of S108P, The gene CXCR4 has a mutation status of T55T, The gene SCN1A has a mutation status of R1900G, The gene FSIP2 has a mutation status of I3880M, The gene MARS2 has a mutation status of A15T, The gene INO80D has a mutation status of S481S, The gene CPO has a mutation status of R169H, The gene TMBIM1 has a mutation status of P8R, The gene SYN2 has a mutation status of P105A, The gene KCNH8 has a mutation status of I472V, The gene ARPP21 has a mutation status of P612S, The gene SCN5A has a mutation status of R121Q, The gene KLHL40 has a mutation status of F117L, The gene FYCO1 has a mutation status of L574L, The gene SLC25A20 has a mutation status of T40T, The gene PARP3 has a mutation status of R100H, The gene DNAH1 has a mutation status of K1844N, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene CADPS has a mutation status of R1280Q, The gene BBX has a mutation status of T506T, The gene PHLDB2 has a mutation status of I183V, The gene CFAP44 has a mutation status of G768S, The gene TEX55 has a mutation status of V463A, The gene KIAA1257 has a mutation status of M906L, The gene PLSCR4 has a mutation status of P6H, The gene C3orf33 has a mutation status of L83*, The gene MFSD1 has a mutation status of L362L, The gene HRG has a mutation status of G296E, The gene DLG1 has a mutation status of S693I, The gene POLN has a mutation status of N382S, The gene KIAA0232 has a mutation status of V574A, The gene C1QTNF7 has a mutation status of Q240H, The gene DNAJB14 has a mutation status of N365S, The gene ZNF827 has a mutation status of K176K, The gene NPY2R has a mutation status of T13R, The gene HPF1 has a mutation status of S135Y, The gene MARCHF6 has a mutation status of R113C, The gene OTULIN has a mutation status of R30L, The gene CDH10 has a mutation status of G244S, The gene OXCT1 has a mutation status of S33T, The gene ZBED3 has a mutation status of L155A, The gene RHOBTB3 has a mutation status of A237A, The gene GRXCR2 has a mutation status of C235F, The gene ANXA6 has a mutation status of K620N, The gene SPARC has a mutation status of D120N, The gene NMUR2 has a mutation status of F215L, The gene SLIT3 has a mutation status of K1472K, The gene FAM8A1 has a mutation status of L338I, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB1 has a mutation status of I248L, The gene MDFI has a mutation status of A230T, The gene TDRD6 has a mutation status of T512I, The gene TDRD6 has a mutation status of A1619P, The gene ADGRF2 has a mutation status of V271D, The gene DST has a mutation status of R7276H, The gene CD24 has a mutation status of A17A, The gene MFSD4B has a mutation status of L182Y, The gene UTRN has a mutation status of Q2900Q, The gene TCP10 has a mutation status of H85C, The gene SMOC2 has a mutation status of V157I, The gene STK31 has a mutation status of Y359Y, The gene TRIM50 has a mutation status of V281M, The gene PCLO has a mutation status of T3186K, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene FSCN3 has a mutation status of V129I, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PLXNA4 has a mutation status of M1017I, The gene ZYX has a mutation status of A400V, The gene GIMAP5 has a mutation status of Y184Y, The gene CDCA2 has a mutation status of S968S, The gene SPIDR has a mutation status of S4L, The gene PRKDC has a mutation status of K3873R, The gene COL14A1 has a mutation status of R846H, The gene EPPK1 has a mutation status of V5016V, The gene EPPK1 has a mutation status of R2547G, The gene HGH1 has a mutation status of G54V, The gene PTPRD has a mutation status of Y891Y, The gene ZNF658 has a mutation status of G822R, The gene C9orf57 has a mutation status of T6T, The gene FRRS1L has a mutation status of R51A, The gene STKLD1 has a mutation status of R191H, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of T90M, The gene NOTCH1 has a mutation status of H2428fs, The gene PLXDC2 has a mutation status of I120T, The gene WASHC2A has a mutation status of S90fs, The gene KIF20B has a mutation status of E590D, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of D915D, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of L3616L, The gene MUC5AC has a mutation status of S3630P, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4396A, The gene NUP98 has a mutation status of T459fs, The gene DEPDC7 has a mutation status of K255*, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene PATL1 has a mutation status of V500F, The gene DAGLA has a mutation status of Q696Q, The gene ATG2A has a mutation status of A1835A, The gene NAALADL1 has a mutation status of D485D, The gene UNC93B1 has a mutation status of P575Q, The gene NUMA1 has a mutation status of A1342V, The gene PGM2L1 has a mutation status of I415I, The gene DYNC2H1 has a mutation status of R2309W, The gene ANKK1 has a mutation status of G715G, The gene TECTA has a mutation status of D250Y, The gene KIRREL3 has a mutation status of P650L, The gene SLC6A13 has a mutation status of T596K, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R46 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene AMIGO2 has a mutation status of L273R, The gene KMT2D has a mutation status of P2938L, The gene TMDD1 has a mutation status of 249_250insG, The gene CCDC62 has a mutation status of T394T, The gene PITPNM2 has a mutation status of C611C, The gene DNAH10 has a mutation status of R1835Q, The gene SFSWAP has a mutation status of S835S, The gene MMP17 has a mutation status of G430S, The gene MEDAG has a mutation status of S157F, The gene RFXAP has a mutation status of E228*, The gene SUPT20H has a mutation status of P421P, The gene SSTR1 has a mutation status of R197H, The gene OTX2 has a mutation status of Q295*, The gene ADAM20 has a mutation status of V547V, The gene SLIRP has a mutation status of R7R, The gene TMEM121 has a mutation status of K142E, The gene LINC02203 has a mutation status of I259M, The gene ANKDD1A has a mutation status of L516L, The gene STRA6 has a mutation status of A300fs, The gene GOLGA6L10 has a mutation status of C286R, The gene CRTC3 has a mutation status of S99S, The gene PRR35 has a mutation status of P260P, The gene PKD1 has a mutation status of L3901V, The gene GPRC5B has a mutation status of I57F, The gene RRAD has a mutation status of P28T, The gene MTSS2 has a mutation status of L168M, The gene ZNF23 has a mutation status of E324E, The gene CTRB2 has a mutation status of C219C, The gene PABPN1L has a mutation status of D233fs, The gene ABR has a mutation status of N755S, The gene CTNS has a mutation status of G110S, The gene PLSCR3 has a mutation status of E107*, The gene TP53 has a mutation status of Q317*, The gene TP53 has a mutation status of G245D, The gene CTC1 has a mutation status of C82F, The gene WSB1 has a mutation status of E90E, The gene CCL4L2 has a mutation status of P67R, The gene PLXDC1 has a mutation status of R149R, The gene IKZF3 has a mutation status of L162R, The gene NFE2L1 has a mutation status of L402V, The gene EVPL has a mutation status of L156V, The gene ST6GALNAC2 has a mutation status of H119L, The gene CBX4 has a mutation status of V505V, The gene NOTUM has a mutation status of G61A, The gene TUBB8B has a mutation status of H41P, The gene PPP4R1 has a mutation status of P255P, The gene TXNDC2 has a mutation status of P353S, The gene WDR7 has a mutation status of T650A, The gene ZNF516 has a mutation status of P680T, The gene ARID3A has a mutation status of D30fs, The gene WDR18 has a mutation status of V216M, The gene CBARP has a mutation status of I181M, The gene TCF3 has a mutation status of E501D, The gene INSR has a mutation status of R902C, The gene AC008878.3 has a mutation status of Q230R, The gene MUC16 has a mutation status of S8972P, The gene MEF2B has a mutation status of N49S, The gene ZNF208 has a mutation status of G1203V, The gene ZNF729 has a mutation status of C908S, The gene NFKBID has a mutation status of D10D, The gene RYR1 has a mutation status of A4739V, The gene POU2F2 has a mutation status of V113V, The gene MEGF8 has a mutation status of V2511M, The gene PGLYRP1 has a mutation status of T24T, The gene HIF3A has a mutation status of D546E, The gene NOP53 has a mutation status of R38R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRB2 has a mutation status of R295T, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Y99I, The gene KIR3DL3 has a mutation status of G295S, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of D184N, The gene KIR2DL1 has a mutation status of G283G, The gene KIR3DL1 has a mutation status of A371S, The gene NLRP4 has a mutation status of P834L, The gene SLC17A9 has a mutation status of L205L, The gene NCAM2 has a mutation status of I489T, The gene HDHD5 has a mutation status of N123S, The gene SF3A1 has a mutation status of N63N, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TRABD has a mutation status of R111C, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene NHS has a mutation status of E511E, The gene CDKL5 has a mutation status of N325N, The gene ACOT9 has a mutation status of R420R, The gene DCAF8L1 has a mutation status of A31V, The gene ZMAT1 has a mutation status of E622*, The gene SERPINA7 has a mutation status of H176H, The gene ATG4A has a mutation status of N234K, The gene RTL9 has a mutation status of V870A, The gene SLC25A5 has a mutation status of T221R, The gene IGSF1 has a mutation status of S921S, The gene AC236972.4 has a mutation status of A34T, The gene AC236972.4 has a mutation status of S1611S, The gene MT-ATP8 has a mutation status of I23T, The gene MT-ND4 has a mutation status of L262L, The gene MT-ND5 has a mutation status of V92V, The gene MT-ND5 has a mutation status of T533M
DLBC
The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene CELA3A has a mutation status of S26S, The gene SLC30A2 has a mutation status of A302V, The gene PRRC2C has a mutation status of P2083H, The gene CACNA1E has a mutation status of T655T, The gene PTPRC has a mutation status of A113S, The gene CAMSAP2 has a mutation status of G426G, The gene PLXNA2 has a mutation status of C826G, The gene FAM71A has a mutation status of L116S, The gene OBSCN has a mutation status of P236A, The gene OR14A2 has a mutation status of Y121C, The gene ADCY3 has a mutation status of R314R, The gene TMEM131 has a mutation status of S396S, The gene COL3A1 has a mutation status of P656P, The gene WDFY1 has a mutation status of G323R, The gene D2HGDH has a mutation status of R107R, The gene ARIH2OS has a mutation status of A153G, The gene PRKCD has a mutation status of N193Y, The gene KDR has a mutation status of H381Y, The gene POU4F2 has a mutation status of A238A, The gene TMEM184C has a mutation status of V141I, The gene ADAMTS12 has a mutation status of S1044G, The gene TRIM36 has a mutation status of E405D, The gene HSD17B4 has a mutation status of S265R, The gene DDX41 has a mutation status of T236R, The gene ADAMTS2 has a mutation status of A35T, The gene HLA-DRB5 has a mutation status of T262R, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q38W, The gene LRFN2 has a mutation status of D181D, The gene KLHL31 has a mutation status of D24V, The gene LPA has a mutation status of V44V, The gene TBP has a mutation status of K337N, The gene BRAT1 has a mutation status of A642G, The gene HOXA3 has a mutation status of S80G, The gene SRRM3 has a mutation status of S506S, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene MUC3A has a mutation status of T987I, The gene AHCYL2 has a mutation status of G48V, The gene TMEM209 has a mutation status of G366V, The gene PARP12 has a mutation status of M1I, The gene DENND2A has a mutation status of A276A, The gene RP1L1 has a mutation status of P552P, The gene DLC1 has a mutation status of H1105Y, The gene GPAT4 has a mutation status of L14L, The gene PXDNL has a mutation status of Y486Y, The gene ZFPM2 has a mutation status of D345D, The gene CSMD3 has a mutation status of G187S, The gene TRIB1 has a mutation status of Q69E, The gene SLC39A4 has a mutation status of R251W, The gene TONSL has a mutation status of R1076C, The gene MFSD3 has a mutation status of A43V, The gene PUM3 has a mutation status of P552A, The gene PLAA has a mutation status of R354R, The gene UNC13B has a mutation status of A439P, The gene CAMSAP1 has a mutation status of H969Q, The gene NACC2 has a mutation status of L187P, The gene FUT7 has a mutation status of L23L, The gene SKIDA1 has a mutation status of E422E, The gene ZNF248 has a mutation status of Y520C, The gene LDB3 has a mutation status of YTPSPAPAYTPSPAPA319del, The gene WBP1L has a mutation status of H314P, The gene MKI67 has a mutation status of Q2202H, The gene MKI67 has a mutation status of E998K, The gene PWWP2B has a mutation status of T97P, The gene MUC5AC has a mutation status of T3668P, The gene OR51M1 has a mutation status of T89T, The gene SLC35C1 has a mutation status of R229S, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene DAGLA has a mutation status of D256D, The gene VEGFB has a mutation status of T156P, The gene GPR137 has a mutation status of T364P, The gene KDM2A has a mutation status of S104G, The gene NEU3 has a mutation status of L234L, The gene UBASH3B has a mutation status of D409N, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene MYF5 has a mutation status of S216F, The gene CHST11 has a mutation status of D233D, The gene CCDC63 has a mutation status of Y216H, The gene P2RX7 has a mutation status of I568N, The gene TNFRSF19 has a mutation status of S24L, The gene CKAP2 has a mutation status of N277D, The gene DACH1 has a mutation status of SGGGGGSSGNGGGGGGGGGGSNCNPNLAAASNGSGGGGGG82del, The gene DNAJC3 has a mutation status of T237A, The gene AJUBA has a mutation status of R218W, The gene SAV1 has a mutation status of H40R, The gene DICER1 has a mutation status of N1138N, The gene PAPOLA has a mutation status of L184L, The gene PLCB2 has a mutation status of V855I, The gene SNX22 has a mutation status of W119*, The gene LOXL1 has a mutation status of Y52C, The gene TBL3 has a mutation status of Q710H, The gene AMDHD2 has a mutation status of G300S, The gene PPL has a mutation status of T1600T, The gene ATF7IP2 has a mutation status of S105S, The gene GP2 has a mutation status of H125Y, The gene SEZ6L2 has a mutation status of I353T, The gene KIFC3 has a mutation status of A12D, The gene ZC3H18 has a mutation status of I376M, The gene P2RX1 has a mutation status of D320D, The gene GP1BA has a mutation status of L105L, The gene CLDN7 has a mutation status of G179G, The gene MYH2 has a mutation status of P83P, The gene TBC1D28 has a mutation status of I117N, The gene RUNDC1 has a mutation status of A3V, The gene ADAM11 has a mutation status of E682E, The gene KIF2B has a mutation status of V446I, The gene LLGL2 has a mutation status of P955R, The gene C19orf25 has a mutation status of A30V, The gene C19orf25 has a mutation status of E25*, The gene KRI1 has a mutation status of A456A, The gene RFX1 has a mutation status of A21P, The gene IQCN has a mutation status of G234G, The gene ARHGAP33 has a mutation status of P966P, The gene PRODH2 has a mutation status of C44*, The gene NPHS1 has a mutation status of N436S, The gene ACP7 has a mutation status of A74T, The gene FCGBP has a mutation status of P1883P, The gene GEMIN7 has a mutation status of F129L, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of Y121Y, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene ZNF579 has a mutation status of V291G, The gene SLC4A11 has a mutation status of R352H, The gene CDC25B has a mutation status of T556T, The gene MMP24 has a mutation status of R428H, The gene DLGAP4 has a mutation status of S609S, The gene RBL1 has a mutation status of R481Q, The gene KIAA1755 has a mutation status of L450V, The gene SLC9A8 has a mutation status of V454I, The gene SLC19A1 has a mutation status of R333L, The gene GGT5 has a mutation status of H523H, The gene APOL5 has a mutation status of E224G, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene DHRSX has a mutation status of L261L, The gene GK has a mutation status of R155H, The gene PHF8 has a mutation status of F455S, The gene STARD8 has a mutation status of G662A, The gene CLIC2 has a mutation status of I192V, The gene MT-ND1 has a mutation status of K58K, The gene MT-ATP6 has a mutation status of A177T, The gene MT-CO3 has a mutation status of L164L, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L
DLBC
The gene CASZ1 has a mutation status of R690H, The gene MIIP has a mutation status of R226C, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene TCEA3 has a mutation status of R237R, The gene PDIK1L has a mutation status of E281K, The gene FCN3 has a mutation status of R115R, The gene TSSK3 has a mutation status of M76T, The gene PHC2 has a mutation status of R697L, The gene CLSPN has a mutation status of R323W, The gene HSPB11 has a mutation status of F148F, The gene LEPR has a mutation status of T685T, The gene CLCA1 has a mutation status of T574N, The gene AGL has a mutation status of R1460H, The gene NRAS has a mutation status of G12D, The gene NBPF20 has a mutation status of Q384K, The gene NBPF14 has a mutation status of I1394V, The gene ZNF687 has a mutation status of L1142F, The gene SPRR2B has a mutation status of P65R, The gene PAPPA2 has a mutation status of S1103S, The gene RALGPS2 has a mutation status of A150A, The gene SOAT1 has a mutation status of R219C, The gene CACNA1E has a mutation status of N665D, The gene ASPM has a mutation status of Q1613*, The gene PM20D1 has a mutation status of V399I, The gene PLXNA2 has a mutation status of R1705L, The gene TATDN3 has a mutation status of Q179*, The gene CNIH3 has a mutation status of E58Q, The gene H3-3A has a mutation status of K28M, The gene SIPA1L2 has a mutation status of P589P, The gene GREM2 has a mutation status of M158K, The gene ATAD2B has a mutation status of Q896E, The gene FAM228B has a mutation status of Q303fs, The gene RMDN2 has a mutation status of A342G, The gene PRKCE has a mutation status of V160A, The gene EPAS1 has a mutation status of D753E, The gene DCTN1 has a mutation status of V60M, The gene DNAH6 has a mutation status of R1153G, The gene SMYD1 has a mutation status of V114G, The gene UNC50 has a mutation status of S137S, The gene RANBP2 has a mutation status of 1054_1055QP>HS, The gene CSRNP3 has a mutation status of F349L, The gene ITGA4 has a mutation status of I400S, The gene FSIP2 has a mutation status of L1991F, The gene DNAH7 has a mutation status of T2224K, The gene STK36 has a mutation status of L344L, The gene PTMA has a mutation status of D23D, The gene TRPM8 has a mutation status of L1096L, The gene SETD5 has a mutation status of C109S, The gene NEK10 has a mutation status of D769V, The gene CLASP2 has a mutation status of G1110R, The gene XIRP1 has a mutation status of L30R, The gene SNRK has a mutation status of S675F, The gene KIF15 has a mutation status of S1083S, The gene TMEM115 has a mutation status of A39T, The gene AC097637.1 has a mutation status of Q761K, The gene FLNB has a mutation status of M1I, The gene ADGRG7 has a mutation status of G113G, The gene CFAP44 has a mutation status of E989E, The gene GRAMD1C has a mutation status of D90N, The gene TRIM42 has a mutation status of A136T, The gene NMD3 has a mutation status of V96L, The gene HTT has a mutation status of N2626D, The gene KIAA0232 has a mutation status of G1360*, The gene CCKAR has a mutation status of S424L, The gene REST has a mutation status of R1067S, The gene TMPRSS11B has a mutation status of P373T, The gene FRAS1 has a mutation status of E2212V, The gene PTPN13 has a mutation status of R2343R, The gene RAP1GDS1 has a mutation status of V447V, The gene ADH1A has a mutation status of S118T, The gene SLC39A8 has a mutation status of I317I, The gene NOCT has a mutation status of L13L, The gene FAT1 has a mutation status of G2925E, The gene CCT5 has a mutation status of H495L, The gene DNAH5 has a mutation status of A2298T, The gene DNAH5 has a mutation status of A1205T, The gene OSMR has a mutation status of V230A, The gene HCN1 has a mutation status of S721T, The gene PDE4D has a mutation status of D139E, The gene MAN2A1 has a mutation status of D355H, The gene PCDHA10 has a mutation status of N264N, The gene DOCK2 has a mutation status of R214Q, The gene HLA-A has a mutation status of I121R, The gene HLA-A has a mutation status of K292E, The gene PRRC2A has a mutation status of P696P, The gene AGER has a mutation status of R77P, The gene SAYSD1 has a mutation status of P56S, The gene TTBK1 has a mutation status of E351D, The gene PTPRK has a mutation status of L637L, The gene MAP3K5 has a mutation status of A369V, The gene TAB2 has a mutation status of L46L, The gene MAP3K4 has a mutation status of V622V, The gene RPS6KA2 has a mutation status of A543S, The gene SNX13 has a mutation status of S713N, The gene GLI3 has a mutation status of S1028I, The gene ZNF735 has a mutation status of S227S, The gene MTERF1 has a mutation status of F44L, The gene SEM1 has a mutation status of L110L, The gene MUC3A has a mutation status of S123L, The gene SH2B2 has a mutation status of G351S, The gene SPDYE6 has a mutation status of H337R, The gene RELN has a mutation status of N2624I, The gene PRSS1 has a mutation status of N77N, The gene ZNF783 has a mutation status of G522S, The gene TNKS has a mutation status of D59E, The gene FAM160B2 has a mutation status of F307F, The gene OPRK1 has a mutation status of P278T, The gene ZFHX4 has a mutation status of S1166fs, The gene STK3 has a mutation status of N470N, The gene ANXA13 has a mutation status of R37Q, The gene EPPK1 has a mutation status of T1986R, The gene PLEC has a mutation status of V1402V, The gene MROH1 has a mutation status of D521N, The gene DGAT1 has a mutation status of V301G, The gene IARS1 has a mutation status of T1193I, The gene GRIN3A has a mutation status of R337R, The gene FRRS1L has a mutation status of R51A, The gene COL5A1 has a mutation status of L1415F, The gene NACC2 has a mutation status of AA155del, The gene ABCA2 has a mutation status of E120V, The gene ITIH5 has a mutation status of A154T, The gene PARD3 has a mutation status of F844F, The gene OGDHL has a mutation status of D859D, The gene CYP26C1 has a mutation status of L9L, The gene ZFYVE27 has a mutation status of P306L, The gene CYP17A1 has a mutation status of D281N, The gene NT5C2 has a mutation status of R238W, The gene KCNK18 has a mutation status of A156E, The gene FANK1 has a mutation status of D138V, The gene MUC5AC has a mutation status of T3113I, The gene RASSF10 has a mutation status of Q351*, The gene ANO5 has a mutation status of V742V, The gene APIP has a mutation status of I241T, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TBX10 has a mutation status of R30Q, The gene NUMA1 has a mutation status of T2084P, The gene PDZD3 has a mutation status of A334A, The gene C1R has a mutation status of P37L, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene ETV6 has a mutation status of T31T, The gene NELL2 has a mutation status of G290S, The gene KMT2D has a mutation status of S543*, The gene CBX5 has a mutation status of T188K, The gene ZNF385A has a mutation status of A333T, The gene ZFC3H1 has a mutation status of C1778C, The gene TCHP has a mutation status of L304L, The gene MEDAG has a mutation status of A4G, The gene MEDAG has a mutation status of A5G, The gene TNFSF11 has a mutation status of Y241Y, The gene PCDH17 has a mutation status of R611R, The gene FGF14 has a mutation status of P37L, The gene MYO16 has a mutation status of N1219N, The gene ADPRHL1 has a mutation status of A1912D, The gene ZNF219 has a mutation status of G401V, The gene PRKD1 has a mutation status of R8W, The gene HEATR5A has a mutation status of A701A, The gene PCNX1 has a mutation status of R1660R, The gene GOLGA8S has a mutation status of I439V, The gene LACTB has a mutation status of A107D, The gene HCN4 has a mutation status of L1025L, The gene STRA6 has a mutation status of T565T, The gene FAH has a mutation status of N87N, The gene CHD2 has a mutation status of E412T, The gene PGP has a mutation status of S95I, The gene AC099489.1 has a mutation status of E2074K, The gene TGFB1I1 has a mutation status of E233K, The gene ADCY7 has a mutation status of K1059K, The gene ZNF469 has a mutation status of H2569N, The gene CBFA2T3 has a mutation status of S189S, The gene ANKRD11 has a mutation status of G2273A, The gene ANKRD11 has a mutation status of D815D, The gene OR1D2 has a mutation status of A109A, The gene KDM6B has a mutation status of P1056L, The gene ELAC2 has a mutation status of L536L, The gene EVPLL has a mutation status of R140C, The gene FBXW10 has a mutation status of R295I, The gene GOSR1 has a mutation status of G96D, The gene CCL4L2 has a mutation status of S29R, The gene CCL4L2 has a mutation status of P67R, The gene PLXDC1 has a mutation status of G408S, The gene KRT10 has a mutation status of S275R, The gene NAGLU has a mutation status of F236F, The gene GPATCH8 has a mutation status of G1075G, The gene CACNA1G has a mutation status of D2286E, The gene TSPAN10 has a mutation status of G383G, The gene KCTD1 has a mutation status of K393*, The gene GAREM1 has a mutation status of A522V, The gene MYO5B has a mutation status of E1755K, The gene RTTN has a mutation status of L1641L, The gene SF3A2 has a mutation status of L247M, The gene NDUFA13 has a mutation status of V101L, The gene ZNF208 has a mutation status of K964R, The gene SIPA1L3 has a mutation status of P1525P, The gene TGFB1 has a mutation status of S209R, The gene PRKD2 has a mutation status of T270T, The gene ZC3H4 has a mutation status of P666R, The gene POLD1 has a mutation status of I337N, The gene LILRB3 has a mutation status of H300Y, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene FAM71E2 has a mutation status of G351W, The gene RFPL4A has a mutation status of Q95K, The gene PIGT has a mutation status of F496I, The gene HSPA13 has a mutation status of V85A, The gene SLC19A1 has a mutation status of R23Q, The gene GSTT4 has a mutation status of Q197R, The gene PISD has a mutation status of P42H, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene KLHDC7B has a mutation status of L62L, The gene AC231657.3 has a mutation status of T167P, The gene EFNB1 has a mutation status of R154H, The gene TEX13C has a mutation status of P299T, The gene HS6ST2 has a mutation status of I223I, The gene CT45A10 has a mutation status of G83R, The gene FLNA has a mutation status of H1292H, The gene MT-ND1 has a mutation status of K58K, The gene MT-ATP6 has a mutation status of A177T, The gene MT-ATP6 has a mutation status of T189T, The gene MT-CO3 has a mutation status of L164L, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND4 has a mutation status of K206K, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L
DLBC
The gene TTLL10 has a mutation status of G234*, The gene SCNN1D has a mutation status of P573P, The gene FNDC10 has a mutation status of W93C, The gene MIB2 has a mutation status of A127T, The gene MIB2 has a mutation status of G765G, The gene SLC35E2B has a mutation status of G208C, The gene TMEM52 has a mutation status of L201I, The gene PRDM16 has a mutation status of P865P, The gene MEGF6 has a mutation status of V733V, The gene PLEKHG5 has a mutation status of G820R, The gene PER3 has a mutation status of A627A, The gene PEX14 has a mutation status of E26E, The gene SPEN has a mutation status of P3245T, The gene KLHDC7A has a mutation status of A442fs, The gene TAS1R2 has a mutation status of R317A, The gene SYF2 has a mutation status of A14S, The gene SELENON has a mutation status of A436A, The gene TENT5B has a mutation status of L368L, The gene PTPRU has a mutation status of S1185S, The gene TMEM54 has a mutation status of V46M, The gene CSMD2 has a mutation status of N1056D, The gene ZMYM1 has a mutation status of A51T, The gene NCDN has a mutation status of T155T, The gene NCDN has a mutation status of L340I, The gene MACF1 has a mutation status of V1980L, The gene SLFNL1 has a mutation status of P355L, The gene HIVEP3 has a mutation status of P2134Q, The gene FOXJ3 has a mutation status of Q272Q, The gene HECTD3 has a mutation status of N113T, The gene CYP4Z1 has a mutation status of M155V, The gene CDCP2 has a mutation status of H216H, The gene MROH7 has a mutation status of T239T, The gene PCSK9 has a mutation status of I424V, The gene DAB1 has a mutation status of M66I, The gene L1TD1 has a mutation status of D34A, The gene ADGRL4 has a mutation status of S81S, The gene LRRC8C has a mutation status of L525L, The gene CCDC18 has a mutation status of R365*, The gene RTCA has a mutation status of Q177fs, The gene CELSR2 has a mutation status of R2191H, The gene ATXN7L2 has a mutation status of P114Q, The gene AMPD1 has a mutation status of D256D, The gene PTGFRN has a mutation status of H201N, The gene ADAM30 has a mutation status of G319E, The gene RNF115 has a mutation status of T214T, The gene NBPF9 has a mutation status of V918M, The gene AC242842.3 has a mutation status of V3767M, The gene C1orf54 has a mutation status of S120L, The gene PRUNE1 has a mutation status of V246I, The gene TCHH has a mutation status of R1417C, The gene FLAD1 has a mutation status of F351L, The gene TRIM46 has a mutation status of T86P, The gene SCAMP3 has a mutation status of R47Q, The gene PKLR has a mutation status of V238F, The gene SMG5 has a mutation status of P723P, The gene CADM3 has a mutation status of L382L, The gene NCSTN has a mutation status of G133G, The gene ARHGAP30 has a mutation status of K8K, The gene FCRLA has a mutation status of V216M, The gene PRRC2C has a mutation status of N174K, The gene PRRC2C has a mutation status of V1323V, The gene TOR3A has a mutation status of N274K, The gene AXDND1 has a mutation status of G506G, The gene QSOX1 has a mutation status of D376D, The gene PLA2G4A has a mutation status of G654G, The gene RO60 has a mutation status of Y136Y, The gene GPR25 has a mutation status of R317L, The gene IGFN1 has a mutation status of G442G, The gene LGR6 has a mutation status of E103*, The gene RABIF has a mutation status of R29P, The gene PLEKHA6 has a mutation status of R193R, The gene SLC45A3 has a mutation status of G449E, The gene FCMR has a mutation status of K361N, The gene CR1 has a mutation status of C266S, The gene CENPF has a mutation status of E2553K, The gene WDR26 has a mutation status of P87H, The gene DNAH14 has a mutation status of R1842del, The gene OBSCN has a mutation status of R225L, The gene OBSCN has a mutation status of P2906R, The gene OBSCN has a mutation status of R3385Q, The gene TBCE has a mutation status of R223W, The gene KIF26B has a mutation status of P284Q, The gene TRIM58 has a mutation status of W116G, The gene TRIM58 has a mutation status of V117G, The gene SOX11 has a mutation status of P128P, The gene RAD51AP2 has a mutation status of P119S, The gene OTOF has a mutation status of L1995L, The gene PRR30 has a mutation status of H188H, The gene SUPT7L has a mutation status of K274T, The gene SUPT7L has a mutation status of K121K, The gene SPAST has a mutation status of S276S, The gene SLC30A6 has a mutation status of P188L, The gene ARHGEF33 has a mutation status of F825L, The gene CCT4 has a mutation status of V390F, The gene DYSF has a mutation status of S680*, The gene PRADC1 has a mutation status of A20A, The gene VAMP8 has a mutation status of Q29K, The gene FER1L5 has a mutation status of A1305V, The gene LIPT1 has a mutation status of T187M, The gene CHST10 has a mutation status of T265T, The gene POLR1B has a mutation status of V353V, The gene CCDC74B has a mutation status of A254V, The gene TUBA3E has a mutation status of A273T, The gene ARHGEF4 has a mutation status of R355C, The gene LRP1B has a mutation status of Y2231Y, The gene RBM43 has a mutation status of V24A, The gene UPP2 has a mutation status of D227G, The gene LY75-CD302 has a mutation status of R676Q, The gene KCNH7 has a mutation status of S296S, The gene FASTKD1 has a mutation status of L342L, The gene HOXD9 has a mutation status of S80P, The gene PDE11A has a mutation status of P495L, The gene OSBPL6 has a mutation status of A832A, The gene TTN has a mutation status of V17998I, The gene TTN has a mutation status of A15902V, The gene TTN has a mutation status of V13766M, The gene TTN has a mutation status of R13564C, The gene TTN has a mutation status of M9240V, The gene GLS has a mutation status of A537E, The gene BMPR2 has a mutation status of Q92H, The gene UNC80 has a mutation status of L2959M, The gene LANCL1 has a mutation status of L333L, The gene ABCA12 has a mutation status of K2017T, The gene ABCA12 has a mutation status of T345P, The gene SLC11A1 has a mutation status of L393L, The gene USP37 has a mutation status of R348K, The gene ZNF142 has a mutation status of P1012S, The gene RNF25 has a mutation status of G429S, The gene CFAP65 has a mutation status of E400V, The gene CNPPD1 has a mutation status of H337P, The gene AC053503.6 has a mutation status of H101P, The gene OBSL1 has a mutation status of P860S, The gene INHA has a mutation status of L151L, The gene COL4A3 has a mutation status of G49W, The gene DGKD has a mutation status of F644F, The gene UGT1A4 has a mutation status of N119N, The gene ESPNL has a mutation status of H125N, The gene PER2 has a mutation status of P932L, The gene LMCD1 has a mutation status of A293A, The gene TTLL3 has a mutation status of E317K, The gene CRELD1 has a mutation status of L111L, The gene SEC13 has a mutation status of T119I, The gene CLASP2 has a mutation status of S1158S, The gene CLASP2 has a mutation status of N344S, The gene PDCD6IP has a mutation status of P342L, The gene ITGA9 has a mutation status of P764Q, The gene PLCD1 has a mutation status of R530*, The gene XYLB has a mutation status of G370G, The gene XYLB has a mutation status of L516F, The gene ULK4 has a mutation status of K216E, The gene PTH1R has a mutation status of A369A, The gene DNAH1 has a mutation status of A1047T, The gene ACOX2 has a mutation status of S417S, The gene PDZRN3 has a mutation status of G88C, The gene GSK3B has a mutation status of V126I, The gene PARP15 has a mutation status of N251I, The gene SEMA5B has a mutation status of P1095P, The gene HACD2 has a mutation status of P34P, The gene AC024558.2 has a mutation status of R7R, The gene COPG1 has a mutation status of A124A, The gene UBA5 has a mutation status of R37W, The gene PLCH1 has a mutation status of L305L, The gene GOLIM4 has a mutation status of H360H, The gene TNIK has a mutation status of Q747Q, The gene KCNMB3 has a mutation status of R249K, The gene ABCC5 has a mutation status of Q1071Q, The gene VPS8 has a mutation status of R1268C, The gene TFRC has a mutation status of A102A, The gene SENP5 has a mutation status of T384del, The gene MELTF has a mutation status of P4P, The gene TACC3 has a mutation status of E506K, The gene MFSD10 has a mutation status of G334W, The gene HTT has a mutation status of F785S, The gene MSX1 has a mutation status of G268G, The gene TRMT44 has a mutation status of R70R, The gene CEP135 has a mutation status of Q207P, The gene UGT2A1 has a mutation status of I256I, The gene BDH2 has a mutation status of V138I, The gene PITX2 has a mutation status of D48Y, The gene ZNF827 has a mutation status of S928S, The gene DCHS2 has a mutation status of P3297P, The gene VEGFC has a mutation status of H92Y, The gene TENM3 has a mutation status of S2582S, The gene TENM3 has a mutation status of F2690L, The gene TRAPPC11 has a mutation status of V895A, The gene SNX25 has a mutation status of T548M, The gene SORBS2 has a mutation status of S526N, The gene FRG1 has a mutation status of T39T, The gene PLEKHG4B has a mutation status of R1335H, The gene ICE1 has a mutation status of E5*, The gene ITGA1 has a mutation status of V11V, The gene SNX18 has a mutation status of G186G, The gene KIF2A has a mutation status of R665R, The gene ZBED3 has a mutation status of L155A, The gene ARSK has a mutation status of H236R, The gene GPR150 has a mutation status of A268E, The gene PAM has a mutation status of H724H, The gene MEGF10 has a mutation status of C587Y, The gene SLC12A2 has a mutation status of D176G, The gene CHSY3 has a mutation status of Q501Q, The gene RAPGEF6 has a mutation status of S570A, The gene RAD50 has a mutation status of L642V, The gene FSTL4 has a mutation status of P251H, The gene DDX46 has a mutation status of E763E, The gene PITX1 has a mutation status of P67T, The gene STING1 has a mutation status of L170L, The gene PCDHB6 has a mutation status of I480T, The gene PCDHGA1 has a mutation status of R747W, The gene PCDH12 has a mutation status of S540S, The gene SLC6A7 has a mutation status of G659C, The gene LARP1 has a mutation status of I566I, The gene GEMIN5 has a mutation status of P53T, The gene ZNF354B has a mutation status of V19M, The gene ZNF879 has a mutation status of P371P, The gene RREB1 has a mutation status of G946A, The gene RIOK1 has a mutation status of T259I, The gene HIVEP1 has a mutation status of M1378V, The gene TBC1D7 has a mutation status of A198V, The gene SCGN has a mutation status of K257K, The gene ZNF391 has a mutation status of K222N, The gene ZNF391 has a mutation status of I242T, The gene GABBR1 has a mutation status of F645L, The gene ZFP57 has a mutation status of R38Q, The gene PPP1R10 has a mutation status of A294A, The gene HLA-C has a mutation status of S140L, The gene AL645922.1 has a mutation status of R357H, The gene CYP21A2 has a mutation status of E137L, The gene TNXB has a mutation status of V3468V, The gene HLA-DRA has a mutation status of W168R, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q220W, The gene BRD2 has a mutation status of N429S, The gene CPNE5 has a mutation status of E66K, The gene UBR2 has a mutation status of D353D, The gene TTBK1 has a mutation status of G84G, The gene ABCC10 has a mutation status of L263L, The gene CYP39A1 has a mutation status of R389H, The gene ADGRF2 has a mutation status of S607P, The gene MCM3 has a mutation status of V84V, The gene KLHL31 has a mutation status of A541E, The gene FAM83B has a mutation status of V397A, The gene ZNF451 has a mutation status of C813S, The gene COX7A2 has a mutation status of E37G, The gene IRAK1BP1 has a mutation status of Q101Q, The gene CYB5R4 has a mutation status of K446E, The gene MARCKS has a mutation status of A274V, The gene TRDN has a mutation status of L32L, The gene RSPO3 has a mutation status of G226G, The gene LAMA2 has a mutation status of R2001K, The gene IL20RA has a mutation status of A439A, The gene GJE1 has a mutation status of A48V, The gene PHACTR2 has a mutation status of R63H, The gene ZC2HC1B has a mutation status of R147Q, The gene SAMD5 has a mutation status of H51P, The gene SYNE1 has a mutation status of T7356T, The gene SYNE1 has a mutation status of A6121A, The gene SYNJ2 has a mutation status of R874W, The gene MAP3K4 has a mutation status of S1219N, The gene PDE10A has a mutation status of A600A, The gene PRR18 has a mutation status of G284W, The gene AFDN has a mutation status of S1046S, The gene DLL1 has a mutation status of R484M, The gene UNCX has a mutation status of K375N, The gene GSDME has a mutation status of F260F, The gene VPS41 has a mutation status of L153L, The gene AEBP1 has a mutation status of P387P, The gene ABCA13 has a mutation status of E1274G, The gene EGFR has a mutation status of A1003V, The gene PSPH has a mutation status of L68P, The gene ZNF727 has a mutation status of T244fs, The gene AUTS2 has a mutation status of P1054T, The gene NSUN5 has a mutation status of P291P, The gene HIP1 has a mutation status of T722T, The gene TEX47 has a mutation status of K78Q, The gene SAMD9L has a mutation status of N783K, The gene NYAP1 has a mutation status of V44G, The gene GIGYF1 has a mutation status of P749T, The gene ZAN has a mutation status of I1611fs, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of I3082I, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene TRIM56 has a mutation status of S323S, The gene SPDYE6 has a mutation status of H337R, The gene HILPDA has a mutation status of L9L, The gene CALU has a mutation status of A82A, The gene SMKR1 has a mutation status of M32I, The gene HIPK2 has a mutation status of T894T, The gene OR2F2 has a mutation status of V71V, The gene OR2A12 has a mutation status of C96S, The gene ATG9B has a mutation status of G8W, The gene ASIC3 has a mutation status of P96P, The gene DPP6 has a mutation status of S482S, The gene UBE3C has a mutation status of K868N, The gene PTPRN2 has a mutation status of A469A, The gene CSMD1 has a mutation status of G473W, The gene XKR5 has a mutation status of P600H, The gene PRSS55 has a mutation status of N203fs, The gene PCM1 has a mutation status of H1438H, The gene INTS10 has a mutation status of A505A, The gene NSD3 has a mutation status of S409G, The gene FGFR1 has a mutation status of G103C, The gene CYP7A1 has a mutation status of M227I, The gene ASPH has a mutation status of E200K, The gene VPS13B has a mutation status of N3954N, The gene UBR5 has a mutation status of R1901H, The gene ZFPM2 has a mutation status of A1026A, The gene TRHR has a mutation status of Y103C, The gene PKHD1L1 has a mutation status of R2846H, The gene FAM83A has a mutation status of V53G, The gene TRAPPC9 has a mutation status of R902L, The gene PTP4A3 has a mutation status of E127D, The gene TSNARE1 has a mutation status of A114A, The gene LYNX1 has a mutation status of Y88Y, The gene CYHR1 has a mutation status of G6V, The gene FOXH1 has a mutation status of V112M, The gene ARHGAP39 has a mutation status of E470G, The gene ZNF16 has a mutation status of E87D, The gene VLDLR has a mutation status of P156P, The gene PLIN2 has a mutation status of R315G, The gene IFNA10 has a mutation status of P49H, The gene FAM205C has a mutation status of R48W, The gene RUSC2 has a mutation status of H626N, The gene CNTNAP3 has a mutation status of A1182A, The gene NXNL2 has a mutation status of L5M, The gene NXNL2 has a mutation status of D50Y, The gene GABBR2 has a mutation status of Y531D, The gene RAD23B has a mutation status of P19P, The gene ECPAS has a mutation status of S192S, The gene ZNF618 has a mutation status of P306L, The gene TTLL11 has a mutation status of P795P, The gene OR1J2 has a mutation status of L238L, The gene RPL12 has a mutation status of F5F, The gene PIP5KL1 has a mutation status of G126V, The gene LCN2 has a mutation status of M71I, The gene SPTAN1 has a mutation status of S1061S, The gene IER5L has a mutation status of A228A, The gene USP20 has a mutation status of R330H, The gene HMCN2 has a mutation status of E3469D, The gene PRRC2B has a mutation status of P1474A, The gene UCK1 has a mutation status of R275S, The gene SARDH has a mutation status of G89V, The gene C9orf116 has a mutation status of V30V, The gene LHX3 has a mutation status of A158A, The gene SNAPC4 has a mutation status of H860N, The gene SNAPC4 has a mutation status of V711M, The gene PMPCA has a mutation status of G273V, The gene ABCA2 has a mutation status of A1451P, The gene NPDC1 has a mutation status of R136L, The gene ANAPC2 has a mutation status of L650L, The gene STPG3 has a mutation status of P47T, The gene DIP2C has a mutation status of P12S, The gene ADARB2 has a mutation status of P208T, The gene AKR1C8P has a mutation status of N172K, The gene AKR1C8P has a mutation status of F171fs, The gene PFKFB3 has a mutation status of F87L, The gene DHTKD1 has a mutation status of G469G, The gene PLXDC2 has a mutation status of L329I, The gene DNAJC1 has a mutation status of L360L, The gene EBLN1 has a mutation status of K267N, The gene BMI1 has a mutation status of A246V, The gene FZD8 has a mutation status of E112E, The gene ARHGAP22 has a mutation status of D223D, The gene WDFY4 has a mutation status of C582W, The gene ANK3 has a mutation status of L1488P, The gene KIFBP has a mutation status of I506K, The gene SRGN has a mutation status of S46F, The gene SPOCK2 has a mutation status of D88A, The gene SPOCK2 has a mutation status of T85P, The gene DLG5 has a mutation status of V196M, The gene LDB3 has a mutation status of A312T, The gene LDB3 has a mutation status of T317I, The gene CYP26C1 has a mutation status of P490P, The gene EXOSC1 has a mutation status of T28P, The gene HPS1 has a mutation status of A167A, The gene DNMBP has a mutation status of E1188E, The gene PAX2 has a mutation status of P151L, The gene LZTS2 has a mutation status of P315Q, The gene PSD has a mutation status of E59G, The gene CNNM2 has a mutation status of A740A, The gene NT5C2 has a mutation status of L347F, The gene SH3PXD2A has a mutation status of R267Q, The gene NRAP has a mutation status of V46L, The gene AFAP1L2 has a mutation status of E595K, The gene PRDX3 has a mutation status of R31G, The gene HTRA1 has a mutation status of A281A, The gene CPXM2 has a mutation status of P741P, The gene MMP21 has a mutation status of K487E, The gene NKX6-2 has a mutation status of S184S, The gene KNDC1 has a mutation status of D493Y, The gene KNDC1 has a mutation status of V1369V, The gene SCART1 has a mutation status of G177C, The gene CDHR5 has a mutation status of G22V, The gene DRD4 has a mutation status of R150R, The gene TSPAN4 has a mutation status of G127S, The gene AP2A2 has a mutation status of L326L, The gene MUC6 has a mutation status of T1071P, The gene MUC5B has a mutation status of T3738T, The gene AC132217.2 has a mutation status of E129D, The gene AC132217.2 has a mutation status of R56Q, The gene TIMM10B has a mutation status of R3L, The gene ZNF143 has a mutation status of A539G, The gene DKK3 has a mutation status of T119T, The gene ABCC8 has a mutation status of P551P, The gene MRGPRX1 has a mutation status of L51V, The gene LDLRAD3 has a mutation status of A300V, The gene CHST1 has a mutation status of C34fs, The gene DGKZ has a mutation status of P80Q, The gene CELF1 has a mutation status of P252Q, The gene OR5D13 has a mutation status of S190S, The gene OR5D18 has a mutation status of T280T, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene LRRC55 has a mutation status of G35D, The gene SMTNL1 has a mutation status of V484V, The gene OR4D6 has a mutation status of R233W, The gene OR4D9 has a mutation status of D70D, The gene MS4A18 has a mutation status of G157G, The gene SYT7 has a mutation status of S147S, The gene RAB3IL1 has a mutation status of Q58K, The gene SCGB2A1 has a mutation status of L7L, The gene STX5 has a mutation status of P51L, The gene LGALS12 has a mutation status of G110V, The gene PYGM has a mutation status of R270R, The gene ATG2A has a mutation status of V191I, The gene TM7SF2 has a mutation status of G102C, The gene LTBP3 has a mutation status of G738R, The gene EHBP1L1 has a mutation status of G1177G, The gene MAP3K11 has a mutation status of D339D, The gene ZDHHC24 has a mutation status of R114R, The gene CCS has a mutation status of G117R, The gene CARNS1 has a mutation status of P815P, The gene AIP has a mutation status of Q315P, The gene LRP5 has a mutation status of P8Q, The gene LRP5 has a mutation status of T662I, The gene CAPN5 has a mutation status of D29A, The gene MYO7A has a mutation status of P1687Q, The gene TENM4 has a mutation status of A1322A, The gene FAT3 has a mutation status of G1366G, The gene FAT3 has a mutation status of T3075T, The gene IZUMO1R has a mutation status of S176S, The gene MAML2 has a mutation status of G19W, The gene PGR has a mutation status of A442A, The gene CEP126 has a mutation status of S367L, The gene DYNC2H1 has a mutation status of K2127E, The gene DDX6 has a mutation status of N289S, The gene TBRG1 has a mutation status of P288P, The gene VSIG10L2 has a mutation status of E451K, The gene RPUSD4 has a mutation status of T39M, The gene ADAMTS15 has a mutation status of D169D, The gene GLB1L2 has a mutation status of H628N, The gene WNT5B has a mutation status of P273P, The gene CACNA2D4 has a mutation status of D885V, The gene GALNT8 has a mutation status of R431*, The gene P3H3 has a mutation status of T399T, The gene PHC1 has a mutation status of G289C, The gene GUCY2C has a mutation status of R1021H, The gene PIK3C2G has a mutation status of L660P, The gene AEBP2 has a mutation status of R203R, The gene SLCO1B3 has a mutation status of I196V, The gene SLCO1A2 has a mutation status of G122E, The gene SOX5 has a mutation status of I269I, The gene BHLHE41 has a mutation status of P421P, The gene FGD4 has a mutation status of S180F, The gene RAPGEF3 has a mutation status of E746*, The gene RAPGEF3 has a mutation status of F386L, The gene KMT2D has a mutation status of G2501W, The gene FIGNL2 has a mutation status of G94W, The gene KRT83 has a mutation status of C476*, The gene MON2 has a mutation status of K976Q, The gene RASSF9 has a mutation status of T196S, The gene ALDH1L2 has a mutation status of G894G, The gene GCN1 has a mutation status of K1137E, The gene ABCB9 has a mutation status of V121M, The gene TMEM132C has a mutation status of D1042G, The gene CRYL1 has a mutation status of R19*, The gene IPO5 has a mutation status of Y902Y, The gene FARP1 has a mutation status of H703P, The gene COL4A1 has a mutation status of L1447P, The gene CARS2 has a mutation status of C296C, The gene CARS2 has a mutation status of R40R, The gene ZFHX2 has a mutation status of T946I, The gene JPH4 has a mutation status of Q132*, The gene LTB4R2 has a mutation status of A80D, The gene NOVA1 has a mutation status of T382A, The gene SCFD1 has a mutation status of I399I, The gene BRMS1L has a mutation status of D77A, The gene TTC6 has a mutation status of R996S, The gene KLHDC1 has a mutation status of G29V, The gene ARMH4 has a mutation status of P4L, The gene RTN1 has a mutation status of P538T, The gene HIF1A has a mutation status of G727D, The gene SYT16 has a mutation status of S291T, The gene PLEKHG3 has a mutation status of T363T, The gene SLC8A3 has a mutation status of F150F, The gene PAPLN has a mutation status of S78R, The gene IFT43 has a mutation status of G155W, The gene VASH1 has a mutation status of P25H, The gene NRXN3 has a mutation status of T1401A, The gene GPR65 has a mutation status of C283Y, The gene EML5 has a mutation status of G967R, The gene TTC8 has a mutation status of G123A, The gene PPP4R3A has a mutation status of P686L, The gene LGMN has a mutation status of A344A, The gene BTBD7 has a mutation status of A983P, The gene ATG2B has a mutation status of N1185S, The gene DYNC1H1 has a mutation status of D4257G, The gene TNFAIP2 has a mutation status of P240T, The gene TRMT61A has a mutation status of A188A, The gene TMEM179 has a mutation status of V145V, The gene MTA1 has a mutation status of P629H, The gene FMN1 has a mutation status of H200Y, The gene EIF2AK4 has a mutation status of P940S, The gene SPTBN5 has a mutation status of A2517A, The gene SPTBN5 has a mutation status of R342R, The gene PLA2G4E has a mutation status of V632M, The gene PLA2G4F has a mutation status of S578L, The gene TGM5 has a mutation status of R274H, The gene CTDSPL2 has a mutation status of N223S, The gene SPG11 has a mutation status of L2316W, The gene TRPM7 has a mutation status of R194T, The gene MYO5C has a mutation status of L1588L, The gene MYO5A has a mutation status of K1286K, The gene CCPG1 has a mutation status of Q638*, The gene SNX22 has a mutation status of P11H, The gene IGDCC4 has a mutation status of P209L, The gene MEGF11 has a mutation status of G430E, The gene DIS3L has a mutation status of R307R, The gene RPL4 has a mutation status of G288R, The gene NOX5 has a mutation status of R419Q, The gene ISLR2 has a mutation status of V580G, The gene ULK3 has a mutation status of P4P, The gene CHRNA5 has a mutation status of I262N, The gene RASGRF1 has a mutation status of M1239I, The gene MEX3B has a mutation status of G413W, The gene ADAMTSL3 has a mutation status of D368Y, The gene PLIN1 has a mutation status of T233T, The gene IDH2 has a mutation status of D116N, The gene FAM174B has a mutation status of A34E, The gene CERS3 has a mutation status of I270L, The gene ARHGDIG has a mutation status of G33W, The gene AXIN1 has a mutation status of L506L, The gene METTL26 has a mutation status of R170Q, The gene WDR90 has a mutation status of D743D, The gene RHOT2 has a mutation status of V15V, The gene CCDC78 has a mutation status of E82D, The gene TELO2 has a mutation status of Q634K, The gene PKD1 has a mutation status of N890N, The gene PKD1 has a mutation status of S629F, The gene ZSCAN10 has a mutation status of P343L, The gene CREBBP has a mutation status of G2019V, The gene C16orf96 has a mutation status of P998H, The gene UBN1 has a mutation status of A144A, The gene XYLT1 has a mutation status of S16S, The gene CCP110 has a mutation status of E423K, The gene DNAH3 has a mutation status of N3193S, The gene SRCAP has a mutation status of S3215Y, The gene ZNF668 has a mutation status of S526A, The gene ZNF646 has a mutation status of G1112E, The gene ITGAD has a mutation status of G415R, The gene NOL3 has a mutation status of R117L, The gene TSNAXIP1 has a mutation status of Y143*, The gene DPEP3 has a mutation status of P67Q, The gene SLC7A6 has a mutation status of A172V, The gene SMPD3 has a mutation status of D638A, The gene TMEM170A has a mutation status of S12A, The gene CPHXL has a mutation status of L108F, The gene COTL1 has a mutation status of *143Y, The gene FOXC2 has a mutation status of A312S, The gene ZCCHC14 has a mutation status of G971C, The gene SLC7A5 has a mutation status of G5G, The gene ZFPM1 has a mutation status of P117Q, The gene ANKRD11 has a mutation status of Y2015S, The gene RAP1GAP2 has a mutation status of P662Q, The gene NCBP3 has a mutation status of G35C, The gene SPNS2 has a mutation status of P337Q, The gene PITPNM3 has a mutation status of P939P, The gene GPS2 has a mutation status of T306A, The gene NEURL4 has a mutation status of R1041H, The gene NEURL4 has a mutation status of E644G, The gene TP53 has a mutation status of H233del, The gene KDM6B has a mutation status of P342P, The gene KDM6B has a mutation status of P610P, The gene GAS7 has a mutation status of V416G, The gene PIGL has a mutation status of L64S, The gene MYO15A has a mutation status of Y2401Y, The gene LLGL1 has a mutation status of S227*, The gene SLC47A1 has a mutation status of S23*, The gene CCDC144NL has a mutation status of R89L, The gene SLC13A2 has a mutation status of L44F, The gene RAB11FIP4 has a mutation status of Q50H, The gene CCL4L2 has a mutation status of P67R, The gene TADA2A has a mutation status of R412K, The gene SYNRG has a mutation status of H1290H, The gene ZPBP2 has a mutation status of R3R, The gene CSF3 has a mutation status of G183V, The gene KRTAP4-11 has a mutation status of H136R, The gene KRT35 has a mutation status of V356I, The gene KCNH4 has a mutation status of P411P, The gene PLCD3 has a mutation status of R70L, The gene ABI3 has a mutation status of P191Q, The gene NGFR has a mutation status of Y111Y, The gene ACSF2 has a mutation status of T358M, The gene SEPTIN4 has a mutation status of D66D, The gene MRC2 has a mutation status of P1336P, The gene MARCHF10 has a mutation status of E742K, The gene TANC2 has a mutation status of Q1062K, The gene CEP112 has a mutation status of E288D, The gene ABCA8 has a mutation status of E603E, The gene ITGB4 has a mutation status of N1229D, The gene FBF1 has a mutation status of A465A, The gene EXOC7 has a mutation status of E21*, The gene RHBDF2 has a mutation status of P599P, The gene DNAH17 has a mutation status of D284N, The gene CCDC40 has a mutation status of E382K, The gene RPTOR has a mutation status of F263S, The gene CEP131 has a mutation status of A494T, The gene FASN has a mutation status of G396G, The gene SLC16A3 has a mutation status of A37A, The gene COLEC12 has a mutation status of T615T, The gene EMILIN2 has a mutation status of C688S, The gene L3MBTL4 has a mutation status of R311K, The gene ZNF521 has a mutation status of N1206N, The gene SS18 has a mutation status of Q81*, The gene DSC2 has a mutation status of K121N, The gene DSC1 has a mutation status of Q42H, The gene EPG5 has a mutation status of S16R, The gene SERPINB13 has a mutation status of S30S, The gene RTTN has a mutation status of E1309E, The gene CTDP1 has a mutation status of G421G, The gene SBNO2 has a mutation status of C686C, The gene RPS15 has a mutation status of V112V, The gene APC2 has a mutation status of R1789R, The gene DOT1L has a mutation status of K1228N, The gene HMG20B has a mutation status of K58N, The gene MAP2K2 has a mutation status of V8V, The gene TNFAIP8L1 has a mutation status of G178G, The gene DPP9 has a mutation status of Y835S, The gene LONP1 has a mutation status of T638T, The gene KHSRP has a mutation status of G246G, The gene MBD3L2B has a mutation status of D196D, The gene MCOLN1 has a mutation status of A416V, The gene LRRC8E has a mutation status of R756H, The gene KANK3 has a mutation status of R323R, The gene PRAM1 has a mutation status of S484L, The gene MUC16 has a mutation status of S2595R, The gene MUC16 has a mutation status of E388D, The gene ZNF560 has a mutation status of Q246L, The gene MAN2B1 has a mutation status of P30P, The gene HOOK2 has a mutation status of E260G, The gene CACNA1A has a mutation status of G2331G, The gene ADGRL1 has a mutation status of G1322G, The gene OR10H4 has a mutation status of I8M, The gene CALR3 has a mutation status of L276V, The gene MAP1S has a mutation status of S655S, The gene ELL has a mutation status of Q552H, The gene FFAR1 has a mutation status of H86N, The gene RBM42 has a mutation status of P16P, The gene THAP8 has a mutation status of P123Q, The gene LRFN1 has a mutation status of T46T, The gene SUPT5H has a mutation status of P172T, The gene HIPK4 has a mutation status of E400A, The gene CYP2A13 has a mutation status of G313S, The gene CCDC97 has a mutation status of E249D, The gene DMRTC2 has a mutation status of C344R, The gene ARHGEF1 has a mutation status of G412S, The gene MEGF8 has a mutation status of R26L, The gene MEGF8 has a mutation status of V1288I, The gene LIPE has a mutation status of G1070G, The gene LIPE has a mutation status of H290H, The gene PSG3 has a mutation status of C9Y, The gene PSG5 has a mutation status of L237P, The gene PSG9 has a mutation status of P416L, The gene PSG9 has a mutation status of L204I, The gene ZNF225 has a mutation status of L219L, The gene BCAM has a mutation status of T606T, The gene MARK4 has a mutation status of N638N, The gene FOSB has a mutation status of S191S, The gene CYTH2 has a mutation status of H255D, The gene NUCB1 has a mutation status of Y342Y, The gene DHDH has a mutation status of I72V, The gene PNKP has a mutation status of N425T, The gene SHANK1 has a mutation status of R1895R, The gene SIGLEC7 has a mutation status of N399K, The gene ZNF845 has a mutation status of R79H, The gene ZNF765 has a mutation status of S189Y, The gene CNOT3 has a mutation status of D558D, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of D252N, The gene LILRA6 has a mutation status of N187T, The gene PPP6R1 has a mutation status of V314V, The gene ZNF71 has a mutation status of A198V, The gene SMIM17 has a mutation status of W29L, The gene ZNF547 has a mutation status of L102L, The gene SOX12 has a mutation status of P126P, The gene SIRPA has a mutation status of L44S, The gene EBF4 has a mutation status of R243H, The gene LZTS3 has a mutation status of T522P, The gene HSPA12B has a mutation status of R295S, The gene SHLD1 has a mutation status of S40R, The gene CST8 has a mutation status of K26N, The gene XKR7 has a mutation status of T558M, The gene MYH7B has a mutation status of D724D, The gene SOGA1 has a mutation status of S1126S, The gene TGM2 has a mutation status of A71A, The gene FAM83D has a mutation status of P21P, The gene CDH22 has a mutation status of A778A, The gene CDH22 has a mutation status of P766P, The gene RIPOR3 has a mutation status of K213R, The gene GNAS has a mutation status of K223N, The gene TAF4 has a mutation status of L383L, The gene LSM14B has a mutation status of A57A, The gene LAMA5 has a mutation status of G3129V, The gene LAMA5 has a mutation status of G704W, The gene SLCO4A1 has a mutation status of P170P, The gene KCNQ2 has a mutation status of T847P, The gene HELZ2 has a mutation status of L2371V, The gene RTEL1 has a mutation status of E990E, The gene USP16 has a mutation status of H758N, The gene IL10RB has a mutation status of I103I, The gene DSCAM has a mutation status of Q1623H, The gene TRPM2 has a mutation status of R1454Q, The gene TSPEAR has a mutation status of R662M, The gene KRTAP10-8 has a mutation status of R214H, The gene ADARB1 has a mutation status of A186V, The gene TRMT2A has a mutation status of A432A, The gene ASPHD2 has a mutation status of V307V, The gene TTC28 has a mutation status of S1963Y, The gene TTC28 has a mutation status of F603F, The gene CCDC157 has a mutation status of Q457K, The gene SEC14L3 has a mutation status of V215G, The gene RAC2 has a mutation status of T160T, The gene CBX6 has a mutation status of G403V, The gene APOBEC3H has a mutation status of D167E, The gene NAGA has a mutation status of P197P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CELSR1 has a mutation status of P624H, The gene CELSR1 has a mutation status of A186D, The gene TTLL8 has a mutation status of G561G, The gene PPP6R2 has a mutation status of G346G, The gene SBF1 has a mutation status of L274L, The gene ARSL has a mutation status of G502W, The gene TBL1X has a mutation status of R493Q, The gene SHROOM2 has a mutation status of P1178H, The gene RBBP7 has a mutation status of A337A, The gene CDKL5 has a mutation status of T431A, The gene ACOT9 has a mutation status of S375S, The gene KLHL15 has a mutation status of T461S, The gene MAOA has a mutation status of Q418K, The gene MAOB has a mutation status of M1K, The gene SLC9A7 has a mutation status of R117M, The gene PIM2 has a mutation status of T45T, The gene CCDC22 has a mutation status of R321R, The gene CLCN5 has a mutation status of Q124K, The gene CCNB3 has a mutation status of R1266H, The gene EZHIP has a mutation status of S55L, The gene IQSEC2 has a mutation status of P347Q, The gene SMC1A has a mutation status of S882S, The gene HUWE1 has a mutation status of G1196R, The gene AMER1 has a mutation status of R621M, The gene NLGN3 has a mutation status of P87T, The gene TCEAL3 has a mutation status of G193D, The gene NRK has a mutation status of P426A, The gene RADX has a mutation status of G653G, The gene RNF128 has a mutation status of G91V, The gene COL4A5 has a mutation status of P196H, The gene TENM1 has a mutation status of S1503L, The gene BCORL1 has a mutation status of R1149R, The gene SLITRK2 has a mutation status of K252*, The gene IL9R has a mutation status of S100T, The gene AMELY has a mutation status of R166Q, The gene USP9Y has a mutation status of R211C, The gene USP9Y has a mutation status of P2109P, The gene MT-ND1 has a mutation status of T73A, The gene MT-ND1 has a mutation status of D248N, The gene MT-ND1 has a mutation status of Y255Y, The gene MT-ND2 has a mutation status of L294L, The gene MT-CO1 has a mutation status of F184F, The gene MT-CO1 has a mutation status of T259T, The gene MT-CO2 has a mutation status of L33L, The gene MT-CO2 has a mutation status of V90I, The gene MT-CO3 has a mutation status of L206L, The gene MT-ND3 has a mutation status of I96T, The gene MT-ND5 has a mutation status of L23L, The gene MT-ND5 has a mutation status of Y159H, The gene MT-ND5 has a mutation status of T556A
LAML
The gene KLHL17 has a mutation status of T640P, The gene EXOSC10 has a mutation status of I191fs, The gene PRAMEF13 has a mutation status of S245Y, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PTPRU has a mutation status of R635W, The gene PTPRU has a mutation status of R1343H, The gene MACF1 has a mutation status of D3223Y, The gene PPCS has a mutation status of R25P, The gene PTPRF has a mutation status of P606P, The gene IPO13 has a mutation status of N41K, The gene DPH2 has a mutation status of A137V, The gene SLC5A9 has a mutation status of L474V, The gene TUT4 has a mutation status of V1369I, The gene FUBP1 has a mutation status of G492G, The gene IFI44 has a mutation status of L405V, The gene AMPD1 has a mutation status of L627F, The gene SPAG17 has a mutation status of S1242C, The gene LAMC1 has a mutation status of G45W, The gene LAMC1 has a mutation status of V1066V, The gene PTGS2 has a mutation status of S601S, The gene CFHR5 has a mutation status of R435*, The gene MDM4 has a mutation status of D375C, The gene OR2T4 has a mutation status of V109L, The gene OR2G6 has a mutation status of G146S, The gene MTA3 has a mutation status of D69Y, The gene KDM3A has a mutation status of G186G, The gene IL18R1 has a mutation status of P272S, The gene SLC9A4 has a mutation status of Q728*, The gene PTPN18 has a mutation status of R61H, The gene BAZ2B has a mutation status of R1876T, The gene COL5A2 has a mutation status of P133L, The gene MYO1B has a mutation status of A610A, The gene KCTD18 has a mutation status of L107F, The gene RETREG2 has a mutation status of E34*, The gene RETREG2 has a mutation status of S37I, The gene EPHA4 has a mutation status of N423K, The gene SLC16A14 has a mutation status of F93F, The gene SLC6A11 has a mutation status of R292Q, The gene CAND2 has a mutation status of A551A, The gene MYRIP has a mutation status of H62N, The gene COL7A1 has a mutation status of G905V, The gene ARIH2OS has a mutation status of A153G, The gene MST1R has a mutation status of V323fs, The gene PRKCD has a mutation status of D202N, The gene GRK7 has a mutation status of N13S, The gene XRN1 has a mutation status of I317V, The gene LAP3 has a mutation status of R11fs, The gene PHOX2B has a mutation status of M21L, The gene ZGRF1 has a mutation status of P1688P, The gene ANXA5 has a mutation status of R18Q, The gene EXOSC9 has a mutation status of N79N, The gene PCDH10 has a mutation status of V363L, The gene MGARP has a mutation status of E178K, The gene USP38 has a mutation status of L745L, The gene SLC6A18 has a mutation status of E151E, The gene CDH12 has a mutation status of R774H, The gene CDH6 has a mutation status of N723S, The gene AGXT2 has a mutation status of E456V, The gene BDP1 has a mutation status of K1003N, The gene CANX has a mutation status of D577G, The gene FOXC1 has a mutation status of L518F, The gene H1-2 has a mutation status of G98G, The gene HLA-A has a mutation status of I121R, The gene PKHD1 has a mutation status of T1592A, The gene ADGRG6 has a mutation status of N143S, The gene NOX3 has a mutation status of W53L, The gene FAM120B has a mutation status of T754T, The gene MAFK has a mutation status of T2T, The gene FBXL18 has a mutation status of G626S, The gene FERD3L has a mutation status of P28P, The gene HOXA2 has a mutation status of A116V, The gene NUDCD3 has a mutation status of G318G, The gene COBL has a mutation status of C439C, The gene ZNF655 has a mutation status of F138L, The gene AGFG2 has a mutation status of G336R, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of S2495L, The gene TRIM56 has a mutation status of A440V, The gene DOCK5 has a mutation status of C1223C, The gene ASH2L has a mutation status of I394L, The gene MOS has a mutation status of R246C, The gene MPDZ has a mutation status of A1577A, The gene SPATA31D1 has a mutation status of S635S, The gene NUTM2G has a mutation status of A27G, The gene KLF4 has a mutation status of L48L, The gene HMCN2 has a mutation status of A1887E, The gene KLF6 has a mutation status of S177G, The gene CUBN has a mutation status of G596C, The gene ADAMTS14 has a mutation status of 139_141DFR>G, The gene CFAP58 has a mutation status of K312R, The gene WDR11 has a mutation status of R1099H, The gene MUC5AC has a mutation status of T2793K, The gene MUC5AC has a mutation status of T3668P, The gene ALX4 has a mutation status of P199S, The gene CKAP5 has a mutation status of Q14Q, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MPEG1 has a mutation status of G500S, The gene MS4A14 has a mutation status of S215G, The gene CD5 has a mutation status of H461C, The gene SYVN1 has a mutation status of P398A, The gene TPCN2 has a mutation status of V604F, The gene FAT3 has a mutation status of F3902S, The gene MED17 has a mutation status of A452E, The gene ATM has a mutation status of R2832C, The gene UPK2 has a mutation status of K184K, The gene KDM5A has a mutation status of R519K, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene KIF21A has a mutation status of D313E, The gene KMT2D has a mutation status of A1598V, The gene KRT82 has a mutation status of V275A, The gene R3HDM2 has a mutation status of S960S, The gene LRRIQ1 has a mutation status of K244I, The gene CEP290 has a mutation status of Q853H, The gene NR1H4 has a mutation status of D400G, The gene CHST11 has a mutation status of T95K, The gene ANAPC5 has a mutation status of W29R, The gene TTC6 has a mutation status of V1784I, The gene TTLL5 has a mutation status of R78C, The gene SERPINA9 has a mutation status of V272D, The gene CCNK has a mutation status of K137Q, The gene KIF26A has a mutation status of A1484T, The gene AHNAK2 has a mutation status of P52P, The gene TYRO3 has a mutation status of K235fs, The gene SPPL2A has a mutation status of T157I, The gene SGF29 has a mutation status of R115H, The gene ZNF747 has a mutation status of G261R, The gene COQ9 has a mutation status of A36A, The gene KIFC3 has a mutation status of K216N, The gene BCAR1 has a mutation status of V580G, The gene NEURL4 has a mutation status of R1382H, The gene RPL26 has a mutation status of R84L, The gene PIK3R5 has a mutation status of G566R, The gene TEKT3 has a mutation status of S76S, The gene EFCAB5 has a mutation status of R869Q, The gene CCL4L2 has a mutation status of P67R, The gene CCDC178 has a mutation status of E716K, The gene CDH7 has a mutation status of V622G, The gene MISP has a mutation status of D46E, The gene ABCA7 has a mutation status of N58K, The gene ZNF57 has a mutation status of Q116Q, The gene EEF2 has a mutation status of A528G, The gene EEF2 has a mutation status of C136C, The gene ZNRF4 has a mutation status of R177H, The gene FUT3 has a mutation status of N116S, The gene PPAN-P2RY11 has a mutation status of R223H, The gene NFIX has a mutation status of G7G, The gene DCAF15 has a mutation status of V564G, The gene TSHZ3 has a mutation status of P63P, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene SHKBP1 has a mutation status of P685P, The gene PSG3 has a mutation status of P3T, The gene SYMPK has a mutation status of G538G, The gene CA11 has a mutation status of D322Y, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of N187T, The gene LILRA6 has a mutation status of I88M, The gene SIGLEC1 has a mutation status of L445L, The gene TRPC4AP has a mutation status of L366L, The gene MMP24 has a mutation status of G424S, The gene MMP24 has a mutation status of A427T, The gene DOK5 has a mutation status of D87G, The gene RTEL1 has a mutation status of P891L, The gene SAMSN1 has a mutation status of Y130H, The gene ADAMTS5 has a mutation status of R97R, The gene COL6A2 has a mutation status of K966K, The gene APOBEC3H has a mutation status of R171G, The gene TNRC6B has a mutation status of P76L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene RAI2 has a mutation status of Q521R, The gene ZNF157 has a mutation status of K78*, The gene GNL3L has a mutation status of V131V, The gene ARMCX6 has a mutation status of T76N, The gene TEX13A has a mutation status of H100R, The gene GLUD2 has a mutation status of A40A, The gene NLGN4Y has a mutation status of V343A, The gene MT-ATP6 has a mutation status of A177T, The gene MT-CO3 has a mutation status of L164L, The gene MT-CO3 has a mutation status of G170G, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND6 has a mutation status of E169E
DLBC
The gene KIF1B has a mutation status of R1027Q, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF15 has a mutation status of Y276S, The gene HMGCL has a mutation status of I180I, The gene HOOK1 has a mutation status of A455V, The gene DOCK7 has a mutation status of L844R, The gene SLC44A3 has a mutation status of T369S, The gene SLC6A17 has a mutation status of D56N, The gene PPIAL4A has a mutation status of G146W, The gene NBPF9 has a mutation status of A319S, The gene AC242842.3 has a mutation status of V503L, The gene TCHH has a mutation status of E1625Q, The gene FCRL4 has a mutation status of E204D, The gene PEA15 has a mutation status of R83R, The gene PRRC2C has a mutation status of P1918P, The gene TNN has a mutation status of R1021W, The gene PAPPA2 has a mutation status of G328V, The gene CACNA1E has a mutation status of V105V, The gene RPS6KC1 has a mutation status of Q740*, The gene OBSCN has a mutation status of V1396M, The gene ABCB10 has a mutation status of L160L, The gene OR2L2 has a mutation status of S8L, The gene OTOF has a mutation status of A1801V, The gene FSHR has a mutation status of Q437*, The gene ATP6V1B1 has a mutation status of A437A, The gene ANKRD36 has a mutation status of R405S, The gene AFF3 has a mutation status of T830T, The gene RAB6D has a mutation status of K144Q, The gene HOXD3 has a mutation status of R221R, The gene DNAH7 has a mutation status of S3460S, The gene PNKD has a mutation status of V193G, The gene SLC4A3 has a mutation status of D894P, The gene DOCK10 has a mutation status of Y799C, The gene SYN2 has a mutation status of P105A, The gene XPC has a mutation status of L856L, The gene XIRP1 has a mutation status of L30R, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene DNAH12 has a mutation status of A2517T, The gene DNAH12 has a mutation status of D2383E, The gene EPHA3 has a mutation status of K500N, The gene MYLK has a mutation status of A2V, The gene ZXDC has a mutation status of S753T, The gene MASP1 has a mutation status of I485L, The gene TNK2 has a mutation status of A903T, The gene UCHL1 has a mutation status of L3L, The gene RASL11B has a mutation status of V183A, The gene EXOC1L has a mutation status of S18L, The gene UGT2B15 has a mutation status of K231K, The gene UGT2B11 has a mutation status of E301*, The gene UGT2A1 has a mutation status of Y337*, The gene MMRN1 has a mutation status of A489V, The gene PPP3CA has a mutation status of R217*, The gene SH3RF1 has a mutation status of R302Q, The gene SLC9A3 has a mutation status of L556L, The gene C5orf38 has a mutation status of K72*, The gene TAF11L11 has a mutation status of A9P, The gene PTGER4 has a mutation status of F348L, The gene ZBED3 has a mutation status of R78R, The gene AP3B1 has a mutation status of S261T, The gene MACROH2A1 has a mutation status of L268L, The gene SLC35A4 has a mutation status of N290N, The gene PCDHB13 has a mutation status of A719V, The gene SAP30L has a mutation status of V143M, The gene C1QTNF2 has a mutation status of G185V, The gene FAM193B has a mutation status of R694W, The gene AC113348.1 has a mutation status of P150L, The gene ZNF354C has a mutation status of R404G, The gene TMEM14B has a mutation status of 140_141CA>SP, The gene CDKAL1 has a mutation status of A115G, The gene SCUBE3 has a mutation status of A241S, The gene DEF6 has a mutation status of G177R, The gene PI16 has a mutation status of N170N, The gene KCNK16 has a mutation status of Q48H, The gene LRFN2 has a mutation status of R556R, The gene C6orf132 has a mutation status of A924V, The gene SLC25A27 has a mutation status of T247T, The gene CRISP1 has a mutation status of T97N, The gene VGLL2 has a mutation status of V10V, The gene L3MBTL3 has a mutation status of I388F, The gene DACT2 has a mutation status of L518M, The gene PHF14 has a mutation status of T152T, The gene TAX1BP1 has a mutation status of E321V, The gene POM121L12 has a mutation status of F229L, The gene SEMA3A has a mutation status of V435I, The gene RBM48 has a mutation status of H356Y, The gene HEPACAM2 has a mutation status of N320S, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of M384T, The gene MUC3A has a mutation status of S395T, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene RNF133 has a mutation status of G156A, The gene COPG2 has a mutation status of T552T, The gene ZNF398 has a mutation status of H35H, The gene SLC18A1 has a mutation status of M1T, The gene DOK2 has a mutation status of A249A, The gene EPHX2 has a mutation status of S478Y, The gene TEX15 has a mutation status of Y2163Y, The gene PMP2 has a mutation status of M21V, The gene CYC1 has a mutation status of G52R, The gene WDR97 has a mutation status of T143T, The gene DOCK8 has a mutation status of Q318*, The gene MOB3B has a mutation status of M210T, The gene CNTNAP3 has a mutation status of A1182A, The gene SPATA31A6 has a mutation status of Q1152H, The gene SPATA31D1 has a mutation status of G997W, The gene TDRD7 has a mutation status of W932*, The gene NANS has a mutation status of S294P, The gene SVEP1 has a mutation status of N2760N, The gene TLR4 has a mutation status of I633I, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene ERCC6 has a mutation status of S846S, The gene SLC29A3 has a mutation status of L353L, The gene LRIT1 has a mutation status of F243F, The gene BMPR1A has a mutation status of W271R, The gene ATAD1 has a mutation status of R304Q, The gene IFIT3 has a mutation status of P272fs, The gene CC2D2B has a mutation status of V693G, The gene LCOR has a mutation status of T1416T, The gene PGAM1 has a mutation status of N209T, The gene GOLGA7B has a mutation status of S16L, The gene ADRB1 has a mutation status of S186P, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5B has a mutation status of I4642V, The gene OR52K2 has a mutation status of H133N, The gene OR2D2 has a mutation status of I77V, The gene DGKZ has a mutation status of A725V, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OSBP has a mutation status of I600T, The gene C2CD3 has a mutation status of V1103M, The gene EMSY has a mutation status of S993P, The gene USP35 has a mutation status of G839G, The gene CCDC81 has a mutation status of D437D, The gene CHORDC1 has a mutation status of T60T, The gene USP28 has a mutation status of V940fs, The gene IQSEC3 has a mutation status of Q125fs, The gene SLC6A12 has a mutation status of P88L, The gene FOXM1 has a mutation status of F796L, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene GXYLT1 has a mutation status of K440R, The gene GXYLT1 has a mutation status of C414H, The gene KRT75 has a mutation status of Q143*, The gene PPP1R12A has a mutation status of R523Q, The gene MYBPC1 has a mutation status of G508R, The gene SSH1 has a mutation status of S581S, The gene ULK1 has a mutation status of D700G, The gene AL592490.1 has a mutation status of R268S, The gene MYO16 has a mutation status of Y1196Y, The gene MCF2L has a mutation status of I665M, The gene OR4N5 has a mutation status of C240Y, The gene CCNB1IP1 has a mutation status of T64T, The gene MYH6 has a mutation status of V39M, The gene SYNE2 has a mutation status of L1898P, The gene SPATA7 has a mutation status of L122I, The gene TDRD9 has a mutation status of V743L, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene ATP10A has a mutation status of R1005R, The gene ANKDD1A has a mutation status of L516L, The gene GOLGA6L10 has a mutation status of C286R, The gene NPRL3 has a mutation status of S341R, The gene TRAF7 has a mutation status of I505I, The gene ITPRIPL2 has a mutation status of T288P, The gene SRCAP has a mutation status of P87P, The gene ZNF423 has a mutation status of T109P, The gene RFWD3 has a mutation status of S758N, The gene CFDP1 has a mutation status of V39M, The gene ZNF469 has a mutation status of D1418D, The gene TRARG1 has a mutation status of K36R, The gene SMG6 has a mutation status of A785V, The gene TMEM95 has a mutation status of L184F, The gene DNAH2 has a mutation status of S950N, The gene MYH10 has a mutation status of D520N, The gene MYH4 has a mutation status of D957N, The gene DNAH9 has a mutation status of S835Y, The gene NF1 has a mutation status of K1423M, The gene UNC45B has a mutation status of L452L, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP4-1 has a mutation status of R85R, The gene EFTUD2 has a mutation status of D273Y, The gene TRIM37 has a mutation status of N144S, The gene MYO15B has a mutation status of G1101F, The gene MTCL1 has a mutation status of A276E, The gene CABLES1 has a mutation status of S432C, The gene RIOK3 has a mutation status of S231C, The gene TTC39C has a mutation status of I263M, The gene SALL3 has a mutation status of S662S, The gene PARD6G has a mutation status of G226A, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of T12336L, The gene ZNF317 has a mutation status of M437I, The gene ZNF66 has a mutation status of F97F, The gene RBM42 has a mutation status of P217P, The gene ZNF229 has a mutation status of Q16K, The gene CEACAM20 has a mutation status of I453I, The gene TOMM40 has a mutation status of L265W, The gene SIGLEC11 has a mutation status of V161I, The gene SIGLEC8 has a mutation status of R208Q, The gene LILRB3 has a mutation status of T201M, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of W163S, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Y99I, The gene LILRB1 has a mutation status of L619L, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of P224S, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of G283G, The gene NLRP13 has a mutation status of L356Q, The gene MZF1 has a mutation status of Q140R, The gene PCED1A has a mutation status of D49D, The gene SLC12A5 has a mutation status of GG75del, The gene ZNF831 has a mutation status of D1530E, The gene RTEL1 has a mutation status of L748L, The gene CLTCL1 has a mutation status of D1051D, The gene MN1 has a mutation status of T916P, The gene Z82206.1 has a mutation status of Q33*, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CELSR1 has a mutation status of A716T, The gene GTPBP6 has a mutation status of G61R, The gene ATRX has a mutation status of N564S, The gene SLC25A5 has a mutation status of T221R, The gene MAGEC1 has a mutation status of P232L, The gene AC236972.4 has a mutation status of S1611S, The gene MT-CO1 has a mutation status of D4N, The gene MT-ATP6 has a mutation status of A177T, The gene MT-CO3 has a mutation status of L164L, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND4 has a mutation status of T420T, The gene MT-ND5 has a mutation status of A134A, The gene MT-ND5 has a mutation status of E145E, The gene MT-ND5 has a mutation status of A475T, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L
GBMLGG
The gene ATAD3A has a mutation status of A158A, The gene CDK11B has a mutation status of A198A, The gene PRAMEF4 has a mutation status of C76H, The gene PRAMEF9 has a mutation status of L14L, The gene PRAMEF9 has a mutation status of A24A, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF5 has a mutation status of P432A, The gene CTRC has a mutation status of W164fs, The gene CROCC has a mutation status of R1275Q, The gene MACF1 has a mutation status of K2667R, The gene FOXO6 has a mutation status of P334fs, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene MRPL37 has a mutation status of A325T, The gene FUBP1 has a mutation status of A557V, The gene LRRC8B has a mutation status of Y104C, The gene SLC6A17 has a mutation status of K603Q, The gene ATP1A1 has a mutation status of L367L, The gene NBPF26 has a mutation status of K1078K, The gene GJA5 has a mutation status of S357*, The gene NBPF11 has a mutation status of V159F, The gene NBPF9 has a mutation status of V918L, The gene NPR1 has a mutation status of Q298fs, The gene CEP350 has a mutation status of R1378G, The gene LAD1 has a mutation status of S453G, The gene PLEKHA6 has a mutation status of E897Q, The gene NUCKS1 has a mutation status of P180R, The gene OR2T2 has a mutation status of A318M, The gene IAH1 has a mutation status of Q31R, The gene BIRC6 has a mutation status of I1006I, The gene SULT6B1 has a mutation status of G125S, The gene AL845331.2 has a mutation status of A335D, The gene LRP2 has a mutation status of R3775R, The gene SPEG has a mutation status of G1267S, The gene GLB1 has a mutation status of D599N, The gene DNAH1 has a mutation status of L2013L, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene SH3TC1 has a mutation status of A1049A, The gene CC2D2A has a mutation status of R92K, The gene PHOX2B has a mutation status of T49T, The gene LRRC66 has a mutation status of I97L, The gene RASGEF1B has a mutation status of W61*, The gene DSPP has a mutation status of D1116N, The gene DDIT4L has a mutation status of Q70P, The gene FGG has a mutation status of A383P, The gene WDR17 has a mutation status of R640S, The gene DNAJC21 has a mutation status of R339W, The gene NIPBL has a mutation status of M1156V, The gene ZBED3 has a mutation status of L155A, The gene MCC has a mutation status of L707L, The gene COMMD10 has a mutation status of R36Q, The gene SEC24A has a mutation status of L470W, The gene NEUROG1 has a mutation status of S23F, The gene SH3TC2 has a mutation status of Q86K, The gene PDGFRB has a mutation status of Q519H, The gene LARP1 has a mutation status of S247I, The gene HAVCR2 has a mutation status of A251E, The gene RARS1 has a mutation status of R79R, The gene RIPK1 has a mutation status of A569V, The gene CAP2 has a mutation status of K380N, The gene HLA-B has a mutation status of Y140L, The gene HLA-DRB1 has a mutation status of I248L, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene RING1 has a mutation status of R204H, The gene PKHD1 has a mutation status of Q960K, The gene DST has a mutation status of M1401I, The gene PHIP has a mutation status of S1207fs, The gene HOXA3 has a mutation status of Q302P, The gene HOXA3 has a mutation status of D8Y, The gene CDK13 has a mutation status of R336R, The gene IGFBP1 has a mutation status of Y211*, The gene ZNF107 has a mutation status of P691A, The gene POM121C has a mutation status of S486T, The gene POM121C has a mutation status of L478P, The gene ANKIB1 has a mutation status of P181L, The gene ERVW-1 has a mutation status of Q260*, The gene NPTX2 has a mutation status of C253C, The gene OR2AE1 has a mutation status of S214Y, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of Y1992C, The gene MUC3A has a mutation status of S3095S, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene PTPRZ1 has a mutation status of T341N, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene BPGM has a mutation status of L87fs, The gene ZNF777 has a mutation status of Y318F, The gene TMEM176B has a mutation status of T91P, The gene PREX2 has a mutation status of Q765H, The gene KLHL38 has a mutation status of G339D, The gene AC100868.1 has a mutation status of W261*, The gene EPPK1 has a mutation status of A2633del, The gene EPPK1 has a mutation status of R2547G, The gene RANBP6 has a mutation status of C274R, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene EXOSC3 has a mutation status of K209N, The gene FRRS1L has a mutation status of R51A, The gene PALM2AKAP2 has a mutation status of L706L, The gene PTBP3 has a mutation status of I253V, The gene CRB2 has a mutation status of E67D, The gene HMCN2 has a mutation status of G833R, The gene POMT1 has a mutation status of P509S, The gene SURF6 has a mutation status of A6V, The gene CCDC187 has a mutation status of V854M, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene CCDC187 has a mutation status of H128H, The gene INPP5E has a mutation status of R512W, The gene OTUD1 has a mutation status of S326C, The gene AGAP4 has a mutation status of Q20Q, The gene ASAH2B has a mutation status of T69N, The gene SFTPD has a mutation status of Q126R, The gene TCERG1L has a mutation status of E507D, The gene DPYSL4 has a mutation status of A60T, The gene PGGHG has a mutation status of S434S, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of L1683P, The gene MUC5AC has a mutation status of I1961I, The gene MRGPRG has a mutation status of A203A, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene FERMT3 has a mutation status of R129H, The gene TCIRG1 has a mutation status of N462N, The gene TENM4 has a mutation status of Y48Y, The gene PIH1D2 has a mutation status of I221V, The gene GLB1L3 has a mutation status of L547L, The gene C12orf57 has a mutation status of M36L, The gene A2M has a mutation status of L818F, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene GXYLT1 has a mutation status of E249R, The gene SLC38A1 has a mutation status of P290L, The gene DAZAP2 has a mutation status of L130A, The gene KRT18 has a mutation status of V48M, The gene STAT6 has a mutation status of P169P, The gene DNAH10 has a mutation status of F57C, The gene IFT88 has a mutation status of L534P, The gene LRRC63 has a mutation status of R520S, The gene DACH1 has a mutation status of 81_82insGG, The gene LMO7 has a mutation status of E1172D, The gene RAP2A has a mutation status of A168T, The gene LIG4 has a mutation status of T817T, The gene COL4A2 has a mutation status of R1410R, The gene CDH24 has a mutation status of I556T, The gene GOLGA6L6 has a mutation status of E315E, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene GOLGA6L1 has a mutation status of Q428Q, The gene UNC13C has a mutation status of A595A, The gene ANKDD1A has a mutation status of L516L, The gene SCAMP2 has a mutation status of A97A, The gene GOLGA6L10 has a mutation status of N514S, The gene GOLGA6L10 has a mutation status of I73V, The gene GOLGA6L9 has a mutation status of A373P, The gene ALPK3 has a mutation status of P1326S, The gene AGBL1 has a mutation status of R265K, The gene TPSB2 has a mutation status of M153fs, The gene RIPOR1 has a mutation status of P950L, The gene NFAT5 has a mutation status of V326V, The gene ADAMTS18 has a mutation status of A374S, The gene TAF1C has a mutation status of P836S, The gene LLGL1 has a mutation status of A645A, The gene SPACA3 has a mutation status of T116I, The gene MMP28 has a mutation status of P453S, The gene TBC1D3B has a mutation status of G466G, The gene TBC1D3B has a mutation status of L201F, The gene CCL4L2 has a mutation status of L20L, The gene CCL4L2 has a mutation status of P67R, The gene CNTNAP1 has a mutation status of E293K, The gene PECAM1 has a mutation status of V513V, The gene SLC26A11 has a mutation status of L342M, The gene GCGR has a mutation status of W83fs, The gene GAREM1 has a mutation status of P417S, The gene INO80C has a mutation status of A25D, The gene FHOD3 has a mutation status of E809*, The gene GRIN3B has a mutation status of I770T, The gene MKNK2 has a mutation status of R404R, The gene RPL36 has a mutation status of M7V, The gene FBN3 has a mutation status of A2258D, The gene MUC16 has a mutation status of T13896S, The gene MUC16 has a mutation status of V13007G, The gene ICAM5 has a mutation status of G892G, The gene HOOK2 has a mutation status of R656R, The gene C19orf67 has a mutation status of G286S, The gene SLC5A5 has a mutation status of E640D, The gene ZNF66 has a mutation status of L102fs, The gene ZNF99 has a mutation status of R436L, The gene SUPT5H has a mutation status of I706I, The gene DMAC2 has a mutation status of W5S, The gene ATP1A3 has a mutation status of L715L, The gene PVR has a mutation status of M340I, The gene NKPD1 has a mutation status of L452L, The gene IRF2BP1 has a mutation status of S371C, The gene FUT1 has a mutation status of V257I, The gene ZNF577 has a mutation status of P423L, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene ANKEF1 has a mutation status of L659I, The gene MYH7B has a mutation status of A1013T, The gene RBL1 has a mutation status of V302M, The gene NCOA3 has a mutation status of P444P, The gene CDH4 has a mutation status of N302H, The gene PTK6 has a mutation status of R132H, The gene NRIP1 has a mutation status of D174H, The gene TMEM121B has a mutation status of W318C, The gene KIAA1671 has a mutation status of S1265Y, The gene PLA2G3 has a mutation status of F426F, The gene MPPED1 has a mutation status of T270T, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene PNPLA4 has a mutation status of A169T, The gene CFAP47 has a mutation status of I313V, The gene ZNF630 has a mutation status of Y431C, The gene HUWE1 has a mutation status of Q3378L, The gene ZXDA has a mutation status of K318Q, The gene PSMD10 has a mutation status of D86E, The gene COL4A6 has a mutation status of L123M, The gene SLC25A5 has a mutation status of G121C, The gene SLC25A5 has a mutation status of Y165C, The gene SLC25A5 has a mutation status of T221R, The gene NKRF has a mutation status of P17P, The gene PRRG3 has a mutation status of E54A, The gene MAGEA6 has a mutation status of I279V, The gene MT-CO1 has a mutation status of P106P, The gene MT-CO1 has a mutation status of Y129Y, The gene MT-CO1 has a mutation status of S156S, The gene MT-CO2 has a mutation status of V191V, The gene MT-ATP8 has a mutation status of P10S, The gene MT-ND5 has a mutation status of T544A, The gene MT-ND6 has a mutation status of N117N
DLBC
The gene CHD5 has a mutation status of I736V, The gene DISP3 has a mutation status of L1360L, The gene C1orf167 has a mutation status of V953G, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene VWA5B1 has a mutation status of A891S, The gene WNT4 has a mutation status of S286R, The gene COL16A1 has a mutation status of IPG1562del, The gene IQCC has a mutation status of P284P, The gene MACF1 has a mutation status of D4905N, The gene CDKN2C has a mutation status of V130A, The gene TUT4 has a mutation status of A77T, The gene HSPB11 has a mutation status of A205S, The gene PGM1 has a mutation status of A403T, The gene DNAJC6 has a mutation status of S436S, The gene NBPF26 has a mutation status of M724I, The gene PPIAL4H has a mutation status of N102I, The gene OR6K2 has a mutation status of L277L, The gene DCAF8 has a mutation status of R527W, The gene UFC1 has a mutation status of D152E, The gene UHMK1 has a mutation status of S264N, The gene CACNA1E has a mutation status of A841A, The gene HMCN1 has a mutation status of C814S, The gene ZNF281 has a mutation status of A133A, The gene RPS6KC1 has a mutation status of S144*, The gene TP53BP2 has a mutation status of R60C, The gene YIPF4 has a mutation status of D73E, The gene HAAO has a mutation status of P20S, The gene OTX1 has a mutation status of E41G, The gene SPR has a mutation status of L26H, The gene GNLY has a mutation status of R129Q, The gene AL845331.2 has a mutation status of L290R, The gene CREG2 has a mutation status of Q237K, The gene MYO7B has a mutation status of A1380G, The gene SMPD4 has a mutation status of T179T, The gene ARHGEF4 has a mutation status of A199T, The gene FMNL2 has a mutation status of V328V, The gene LRP2 has a mutation status of A2044T, The gene SCRN3 has a mutation status of T8T, The gene TTN has a mutation status of S3213C, The gene DNAH7 has a mutation status of Q3131Q, The gene CATIP has a mutation status of F87F, The gene CFAP65 has a mutation status of Y1074H, The gene LARS2 has a mutation status of Q858K, The gene SMARCC1 has a mutation status of D215D, The gene PLXNB1 has a mutation status of A825T, The gene NPRL2 has a mutation status of N374D, The gene MANF has a mutation status of L144V, The gene MITF has a mutation status of L442L, The gene ZNF148 has a mutation status of T543T, The gene SLC41A3 has a mutation status of K113K, The gene ACP3 has a mutation status of S62S, The gene STAG1 has a mutation status of K293N, The gene VWA5B2 has a mutation status of A369V, The gene HMX1 has a mutation status of S272P, The gene MED28 has a mutation status of N120N, The gene LRRC66 has a mutation status of I234V, The gene DDX60L has a mutation status of A746A, The gene FAT1 has a mutation status of I3243V, The gene TERT has a mutation status of V763G, The gene CPLANE1 has a mutation status of E3146E, The gene CPLANE1 has a mutation status of W1541*, The gene GDNF has a mutation status of R168G, The gene TCF7 has a mutation status of K98R, The gene SIL1 has a mutation status of L404L, The gene NDST1 has a mutation status of D58A, The gene SYNPO has a mutation status of E6G, The gene FLT4 has a mutation status of R3R, The gene TRIM7 has a mutation status of V418M, The gene TAP1 has a mutation status of W797*, The gene COL12A1 has a mutation status of A2612S, The gene IMPG1 has a mutation status of M54I, The gene MAP3K5 has a mutation status of L1317L, The gene RSPH3 has a mutation status of T19P, The gene TCP1 has a mutation status of I112V, The gene SLC22A1 has a mutation status of G389G, The gene DACT2 has a mutation status of R457*, The gene SLC29A4 has a mutation status of G414G, The gene FBXL18 has a mutation status of G156S, The gene ZNF107 has a mutation status of G47S, The gene TRRAP has a mutation status of V2273I, The gene ZAN has a mutation status of G2627R, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of G1349G, The gene MUC3A has a mutation status of T1687T, The gene OR9A4 has a mutation status of R53C, The gene EPHB6 has a mutation status of M16G, The gene EPHB6 has a mutation status of V17G, The gene EPHA1 has a mutation status of C969R, The gene EZH2 has a mutation status of P219P, The gene XKR6 has a mutation status of T62P, The gene SLC7A2 has a mutation status of V380V, The gene ZNF703 has a mutation status of S174*, The gene NKX6-3 has a mutation status of I58S, The gene PSKH2 has a mutation status of S241G, The gene TIGD5 has a mutation status of V616G, The gene MFSD3 has a mutation status of L104V, The gene ANKRD20A1 has a mutation status of C115F, The gene ZNF367 has a mutation status of D141V, The gene TLR4 has a mutation status of R745C, The gene SETX has a mutation status of D1197N, The gene CAMSAP1 has a mutation status of V78L, The gene CCDC187 has a mutation status of A1090E, The gene CCDC187 has a mutation status of E1017E, The gene RNF224 has a mutation status of T46N, The gene SFMBT2 has a mutation status of E791D, The gene CUBN has a mutation status of G2691R, The gene NSUN6 has a mutation status of F39I, The gene RAB18 has a mutation status of D132Y, The gene TMEM273 has a mutation status of L22L, The gene BICC1 has a mutation status of G30D, The gene ANK3 has a mutation status of L897L, The gene MYPN has a mutation status of R919H, The gene TBATA has a mutation status of R178Q, The gene TBATA has a mutation status of Q86L, The gene DNAJC9 has a mutation status of K121R, The gene KIF20B has a mutation status of R386Q, The gene CC2D2B has a mutation status of F534L, The gene ZNF518A has a mutation status of Q818Q, The gene FBXW4 has a mutation status of T152K, The gene CNNM2 has a mutation status of L842L, The gene CALHM1 has a mutation status of L198fs, The gene TACC2 has a mutation status of P1921L, The gene DMBT1 has a mutation status of T719T, The gene MUC6 has a mutation status of T1071P, The gene MUC5AC has a mutation status of D3964D, The gene UBQLNL has a mutation status of D68N, The gene OR52B2 has a mutation status of V70L, The gene TRIM3 has a mutation status of A129G, The gene OR9G1 has a mutation status of T62V, The gene MPEG1 has a mutation status of V45D, The gene GPR137 has a mutation status of T364P, The gene CDC42BPG has a mutation status of D23H, The gene SPDYC has a mutation status of R196W, The gene SSH3 has a mutation status of R328*, The gene MYO7A has a mutation status of G780G, The gene BUD13 has a mutation status of Q306Q, The gene ETS1 has a mutation status of L246F, The gene NRIP2 has a mutation status of E195G, The gene TBC1D30 has a mutation status of A151S, The gene SLC41A2 has a mutation status of L549L, The gene WSB2 has a mutation status of L161L, The gene CIT has a mutation status of A1875D, The gene NCOR2 has a mutation status of A1647S, The gene CENPJ has a mutation status of S220L, The gene RNASEH2B has a mutation status of N152S, The gene ERCC5 has a mutation status of S71S, The gene ZNF219 has a mutation status of H206Y, The gene TOX4 has a mutation status of Q458K, The gene DCAF5 has a mutation status of E899E, The gene PGF has a mutation status of D165N, The gene GPR68 has a mutation status of V230G, The gene HSP90AA1 has a mutation status of S16F, The gene SCG3 has a mutation status of G426*, The gene DAPK2 has a mutation status of A51A, The gene ZNF609 has a mutation status of G477V, The gene GOLGA6B has a mutation status of G501R, The gene MAN2C1 has a mutation status of S174S, The gene PDE8A has a mutation status of Q348H, The gene ANPEP has a mutation status of R98R, The gene OR4F15 has a mutation status of N202S, The gene NPRL3 has a mutation status of S415P, The gene JMJD8 has a mutation status of Q59*, The gene SYNGR3 has a mutation status of P227P, The gene NTN3 has a mutation status of P24Q, The gene C16orf71 has a mutation status of L443L, The gene DNAH3 has a mutation status of M2051V, The gene USP31 has a mutation status of A58V, The gene SLC38A7 has a mutation status of R237K, The gene MTSS2 has a mutation status of A726P, The gene CDH15 has a mutation status of T310T, The gene ABR has a mutation status of D269N, The gene SHPK has a mutation status of P370P, The gene KDM6B has a mutation status of P342P, The gene GSG1L2 has a mutation status of E97K, The gene RAD51D has a mutation status of L45F, The gene CCL4L2 has a mutation status of P67R, The gene TCAP has a mutation status of V10L, The gene CACNA1G has a mutation status of L982F, The gene PGS1 has a mutation status of R315M, The gene MYL12A has a mutation status of R16C, The gene DLGAP1 has a mutation status of V285M, The gene ANKRD12 has a mutation status of R1302*, The gene HCN2 has a mutation status of E412*, The gene ZFR2 has a mutation status of R523K, The gene ALKBH7 has a mutation status of R197H, The gene FBN3 has a mutation status of P2029L, The gene C19orf44 has a mutation status of V345G, The gene SMIM7 has a mutation status of E33E, The gene CPAMD8 has a mutation status of *1886Q, The gene NIBAN3 has a mutation status of G372G, The gene ZNF529 has a mutation status of G540E, The gene ZNF461 has a mutation status of D10Y, The gene FCGBP has a mutation status of GP1230del, The gene FCGBP has a mutation status of S1228fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene ZNF221 has a mutation status of Q517Q, The gene PVR has a mutation status of M340I, The gene RSPH6A has a mutation status of L604V, The gene KLK13 has a mutation status of R259C, The gene NLRP12 has a mutation status of G536D, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of Y121Y, The gene LILRB1 has a mutation status of Q401L, The gene ISOC2 has a mutation status of V146G, The gene FAM110A has a mutation status of R82H, The gene RSPO4 has a mutation status of L223L, The gene SIRPB2 has a mutation status of V117V, The gene SIRPA has a mutation status of L44S, The gene PLCB1 has a mutation status of K825R, The gene BFSP1 has a mutation status of P586S, The gene RRBP1 has a mutation status of D870D, The gene NCOA6 has a mutation status of T932P, The gene SOGA1 has a mutation status of H1644Y, The gene PTPRT has a mutation status of L490E, The gene GATA5 has a mutation status of A65A, The gene NRIP1 has a mutation status of R281Q, The gene TTC3 has a mutation status of S455G, The gene MX2 has a mutation status of Q31P, The gene MX2 has a mutation status of Q32L, The gene MX1 has a mutation status of R522R, The gene C2CD2 has a mutation status of D546V, The gene GSTT4 has a mutation status of Q197R, The gene CABIN1 has a mutation status of G1421G, The gene ASPHD2 has a mutation status of N352N, The gene ZNRF3 has a mutation status of G647G, The gene ZNRF3 has a mutation status of E649G, The gene TRIOBP has a mutation status of S651F, The gene APOBEC3H has a mutation status of R171G, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SCUBE1 has a mutation status of S447N, The gene ZBED4 has a mutation status of M981V, The gene SYN1 has a mutation status of S96R, The gene AMER1 has a mutation status of G149G, The gene SRPX2 has a mutation status of G172G, The gene SPANXB1 has a mutation status of Q42P, The gene CNGA2 has a mutation status of D662E, The gene MT-CO2 has a mutation status of Q59Q, The gene MT-CO3 has a mutation status of M44T, The gene MT-CYB has a mutation status of S56S, The gene MT-CYB has a mutation status of T203T
SARC
The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of M105L, The gene SPEN has a mutation status of A3248P, The gene ARHGEF10L has a mutation status of Q914L, The gene IFFO2 has a mutation status of N61I, The gene AKR7A2 has a mutation status of A39A, The gene ARID1A has a mutation status of S614A, The gene PPCS has a mutation status of R25P, The gene PLK3 has a mutation status of N507S, The gene POMGNT1 has a mutation status of T118T, The gene STRIP1 has a mutation status of A40E, The gene SPTA1 has a mutation status of S1066Y, The gene LRRC52 has a mutation status of L240P, The gene SCYL3 has a mutation status of V90V, The gene MYOC has a mutation status of D478Y, The gene TPR has a mutation status of Q2239Q, The gene UTP25 has a mutation status of S112I, The gene RYR2 has a mutation status of S3959S, The gene ASXL2 has a mutation status of D1148N, The gene DPYSL5 has a mutation status of L11L, The gene ABCG5 has a mutation status of K212E, The gene CREG2 has a mutation status of Q237K, The gene RALB has a mutation status of E106K, The gene SLC16A14 has a mutation status of F93F, The gene SNED1 has a mutation status of G612G, The gene SNED1 has a mutation status of H614Q, The gene ACVR2B has a mutation status of Y410*, The gene LIMD1 has a mutation status of S304T, The gene RBM15B has a mutation status of D743E, The gene ITIH3 has a mutation status of F3L, The gene MAGI1 has a mutation status of L1059M, The gene DCBLD2 has a mutation status of A29S, The gene PARP14 has a mutation status of S50N, The gene KALRN has a mutation status of H294N, The gene C3orf56 has a mutation status of R238C, The gene EEFSEC has a mutation status of P465P, The gene XRN1 has a mutation status of N1133K, The gene AGTR1 has a mutation status of R126*, The gene PLCH1 has a mutation status of N800N, The gene ATP13A5 has a mutation status of S535T, The gene GAK has a mutation status of A479G, The gene FRAS1 has a mutation status of R2362Q, The gene RWDD4 has a mutation status of I17V, The gene MSH3 has a mutation status of C833W, The gene BMP6 has a mutation status of P120L, The gene GCNT2 has a mutation status of H82R, The gene DDX39B has a mutation status of D252H, The gene HLA-DRB5 has a mutation status of L246L, The gene HLA-DRB5 has a mutation status of Q220W, The gene KCNK16 has a mutation status of A39G, The gene C6orf132 has a mutation status of A690V, The gene C6orf132 has a mutation status of P672T, The gene TTBK1 has a mutation status of G84G, The gene COL21A1 has a mutation status of D920D, The gene COL12A1 has a mutation status of R1522H, The gene GABRR2 has a mutation status of R69*, The gene VTA1 has a mutation status of P9L, The gene EPM2A has a mutation status of E19*, The gene MTHFD1L has a mutation status of Q11K, The gene IL6 has a mutation status of Q103R, The gene RAMP3 has a mutation status of T146M, The gene CFAP69 has a mutation status of N523K, The gene GIGYF1 has a mutation status of G19D, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of E725K, The gene MUC3A has a mutation status of T730I, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of I1108M, The gene PRRT4 has a mutation status of E88*, The gene KEL has a mutation status of R86W, The gene ERICH1 has a mutation status of I425I, The gene SGCZ has a mutation status of Q278E, The gene MROH1 has a mutation status of C804R, The gene SCRT1 has a mutation status of A133S, The gene DOCK8 has a mutation status of Y1969*, The gene FOXD4L3 has a mutation status of A46G, The gene ABCA1 has a mutation status of S368Y, The gene ECPAS has a mutation status of I1653I, The gene DENND1A has a mutation status of A341G, The gene CAMSAP1 has a mutation status of H969Q, The gene SEC16A has a mutation status of G2075V, The gene AKR1C8P has a mutation status of F171LLL*VCL**NQGD, The gene MYOF has a mutation status of R1644L, The gene FRAT2 has a mutation status of C113C, The gene SORCS1 has a mutation status of Y273C, The gene ATRNL1 has a mutation status of N681Y, The gene EMX2 has a mutation status of A5S, The gene SIGIRR has a mutation status of S392S, The gene LMNTD2 has a mutation status of P625R, The gene OR51B2 has a mutation status of S202P, The gene OR52W1 has a mutation status of L289L, The gene PDE3B has a mutation status of L92M, The gene DGKZ has a mutation status of R829C, The gene OR9G1 has a mutation status of T62V, The gene NRXN2 has a mutation status of P1622P, The gene PITPNM1 has a mutation status of S781S, The gene MAP6 has a mutation status of P149L, The gene TENM4 has a mutation status of V740V, The gene MAML2 has a mutation status of Q596Q, The gene IL18 has a mutation status of E192*, The gene CBL has a mutation status of L209V, The gene OR10G7 has a mutation status of D265H, The gene PRDM10 has a mutation status of S954S, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene GRIN2B has a mutation status of H1364H, The gene CERS5 has a mutation status of P52T, The gene LGR5 has a mutation status of L448I, The gene DENR has a mutation status of A51T, The gene ZNF26 has a mutation status of P285P, The gene CCDC122 has a mutation status of H135Y, The gene NEK3 has a mutation status of P201T, The gene DOCK9 has a mutation status of G1039V, The gene ARGLU1 has a mutation status of H14H, The gene RASA3 has a mutation status of V316M, The gene POTEG has a mutation status of H86D, The gene VASH1 has a mutation status of R203C, The gene CIPC has a mutation status of S42S, The gene DUOX2 has a mutation status of I550T, The gene AP4E1 has a mutation status of L299L, The gene VPS13C has a mutation status of V1013I, The gene SMAD6 has a mutation status of F266F, The gene ZNF592 has a mutation status of E261E, The gene UNC45A has a mutation status of R633W, The gene NDUFB10 has a mutation status of I34I, The gene ZSCAN32 has a mutation status of F415F, The gene NPIPB2 has a mutation status of R135R, The gene RBL2 has a mutation status of I634L, The gene KATNB1 has a mutation status of V237I, The gene TLE7 has a mutation status of G14E, The gene DNAAF1 has a mutation status of L227F, The gene MYBBP1A has a mutation status of V248L, The gene CLDN7 has a mutation status of S172A, The gene CHD3 has a mutation status of P90P, The gene GUCY2D has a mutation status of L697I, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP4-1 has a mutation status of R85R, The gene HSD17B1 has a mutation status of R132K, The gene AOC2 has a mutation status of F333S, The gene TMEM101 has a mutation status of A62V, The gene KIF18B has a mutation status of S633N, The gene EPX has a mutation status of H233D, The gene EPX has a mutation status of D234D, The gene SLC38A10 has a mutation status of A206P, The gene ANKRD30B has a mutation status of V221D, The gene RBBP8 has a mutation status of R536G, The gene ZNF532 has a mutation status of L164S, The gene ZNF532 has a mutation status of S721S, The gene ZNF358 has a mutation status of S174S, The gene MUC16 has a mutation status of P14438P, The gene MUC16 has a mutation status of P14438T, The gene OR1M1 has a mutation status of T190M, The gene F2RL3 has a mutation status of G18G, The gene GDF15 has a mutation status of T290S, The gene CHST8 has a mutation status of S396S, The gene FCGBP has a mutation status of P1883P, The gene FCGBP has a mutation status of A1165fs, The gene FCGBP has a mutation status of E1160fs, The gene HNRNPUL1 has a mutation status of S212S, The gene CIC has a mutation status of G1950G, The gene CADM4 has a mutation status of E371E, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene ZNF256 has a mutation status of A4A, The gene ANGPT4 has a mutation status of W453L, The gene SIRPA has a mutation status of L44S, The gene SMOX has a mutation status of V328M, The gene ADRA1D has a mutation status of E12K, The gene C2CD2 has a mutation status of A79G, The gene SPECC1L has a mutation status of K704K, The gene FOXRED2 has a mutation status of S4F, The gene C1QTNF6 has a mutation status of A23V, The gene CACNA1I has a mutation status of E1024D, The gene CACNA1I has a mutation status of R1028R, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TRMU has a mutation status of L4V, The gene IQSEC2 has a mutation status of E222*, The gene WDR44 has a mutation status of P277S, The gene L1CAM has a mutation status of N369N, The gene MT-CO1 has a mutation status of P131P, The gene MT-ND5 has a mutation status of A162T
LAML
The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene IGSF21 has a mutation status of R272H, The gene PPCS has a mutation status of R25P, The gene FCGR1B has a mutation status of M172I, The gene NBPF11 has a mutation status of Q55H, The gene ARNT has a mutation status of Q162H, The gene TUFT1 has a mutation status of V222A, The gene TDRD10 has a mutation status of V326A, The gene AL691442.2 has a mutation status of C105Y, The gene NAXE has a mutation status of A266T, The gene FCER1A has a mutation status of P254L, The gene SLAMF7 has a mutation status of D266S, The gene DDR2 has a mutation status of R680C, The gene LMX1A has a mutation status of R313L, The gene CHI3L1 has a mutation status of R369G, The gene TTC27 has a mutation status of R444C, The gene FSHR has a mutation status of S26S, The gene EPB41L5 has a mutation status of D275Y, The gene AMER3 has a mutation status of A693A, The gene LRP1B has a mutation status of L555L, The gene GPR155 has a mutation status of W730R, The gene ZDBF2 has a mutation status of V1427A, The gene SLC19A3 has a mutation status of R78P, The gene NUP210 has a mutation status of L880L, The gene XIRP1 has a mutation status of K697K, The gene ARIH2OS has a mutation status of A153G, The gene PLXND1 has a mutation status of A370V, The gene ACTRT3 has a mutation status of C371Y, The gene NFKB1 has a mutation status of T585M, The gene ALPK1 has a mutation status of A331T, The gene FAT1 has a mutation status of D3258Y, The gene DNAH5 has a mutation status of A1606S, The gene IL6ST has a mutation status of H855N, The gene PCDH1 has a mutation status of P959P, The gene CSF1R has a mutation status of Y571D, The gene ZNF300 has a mutation status of Q336H, The gene CCNJL has a mutation status of N252N, The gene ERVFRD-1 has a mutation status of S50F, The gene HLA-DRB5 has a mutation status of T262R, The gene HLA-DRB5 has a mutation status of Q220W, The gene PEX6 has a mutation status of T648T, The gene SDHAF4 has a mutation status of Q46W, The gene NOX3 has a mutation status of W53L, The gene AP5Z1 has a mutation status of E621E, The gene INHBA has a mutation status of A297S, The gene KIAA1324L has a mutation status of T655I, The gene GIGYF1 has a mutation status of E139K, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of T3202A, The gene RBM28 has a mutation status of N94Y, The gene CNTNAP2 has a mutation status of H883H, The gene CSMD1 has a mutation status of V1878I, The gene PTK2B has a mutation status of T978M, The gene RGS22 has a mutation status of K606N, The gene TG has a mutation status of Q85H, The gene GPIHBP1 has a mutation status of G123E, The gene PLEC has a mutation status of Y4668Y, The gene BOP1 has a mutation status of R523C, The gene GPT has a mutation status of Y189Y, The gene TYRP1 has a mutation status of D234Y, The gene CDKN2A has a mutation status of D23P, The gene SPATA31A1 has a mutation status of N17N, The gene FAM120A has a mutation status of R116P, The gene COL5A1 has a mutation status of G1414S, The gene DIP2C has a mutation status of T1133A, The gene GPRIN2 has a mutation status of G166G, The gene ASAH2 has a mutation status of A558A, The gene JMJD1C has a mutation status of P702L, The gene GPR26 has a mutation status of D219N, The gene ZNF511-PRAP1 has a mutation status of L29L, The gene MUC6 has a mutation status of T1071P, The gene MUC5AC has a mutation status of A5353K, The gene MUC5B has a mutation status of R3288G, The gene OR51B2 has a mutation status of S312G, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene GPR137 has a mutation status of T364P, The gene CARNS1 has a mutation status of A320V, The gene EED has a mutation status of D237E, The gene FAT3 has a mutation status of E353K, The gene FAT3 has a mutation status of R3536H, The gene CNTN5 has a mutation status of T309M, The gene CEP126 has a mutation status of R68Q, The gene USP28 has a mutation status of A739V, The gene CBL has a mutation status of R420Q, The gene ARHGAP32 has a mutation status of E269G, The gene NECAP1 has a mutation status of S122T, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene LRIG3 has a mutation status of A19A, The gene ZNF26 has a mutation status of P285P, The gene ZMYM5 has a mutation status of D30N, The gene FREM2 has a mutation status of Y1345C, The gene SLITRK6 has a mutation status of C31Y, The gene SPACA7 has a mutation status of P48L, The gene OR4N2 has a mutation status of D191N, The gene VSX2 has a mutation status of M1I, The gene VSX2 has a mutation status of G6V, The gene JAG2 has a mutation status of N547N, The gene LINC02203 has a mutation status of I259M, The gene FSIP1 has a mutation status of M360V, The gene IREB2 has a mutation status of V944V, The gene ADAMTS7 has a mutation status of S695P, The gene FANCI has a mutation status of L619Q, The gene LINS1 has a mutation status of S42S, The gene ARHGDIG has a mutation status of L13M, The gene CRAMP1 has a mutation status of H903R, The gene NAGPA has a mutation status of S105S, The gene ZNF768 has a mutation status of V190L, The gene HEATR3 has a mutation status of E632Q, The gene CHD9 has a mutation status of Q170Q, The gene FCSK has a mutation status of S479S, The gene CRISPLD2 has a mutation status of R364K, The gene PRPF8 has a mutation status of D1598V, The gene CLDN7 has a mutation status of S172A, The gene CCL4L2 has a mutation status of P67R, The gene CDC27 has a mutation status of G159G, The gene NFE2L1 has a mutation status of P724P, The gene COG1 has a mutation status of M918V, The gene RPTOR has a mutation status of T1035M, The gene PLIN3 has a mutation status of N342N, The gene RFX2 has a mutation status of R280R, The gene MBD3L1 has a mutation status of K162N, The gene RAVER1 has a mutation status of G195G, The gene ICAM3 has a mutation status of G482R, The gene TYK2 has a mutation status of I995I, The gene JAK3 has a mutation status of L898L, The gene ZNF253 has a mutation status of T330P, The gene TIMM50 has a mutation status of Q53Q, The gene BAX has a mutation status of T167M, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL1 has a mutation status of P175T, The gene KIR2DL1 has a mutation status of G283G, The gene ISOC2 has a mutation status of V146G, The gene ERG has a mutation status of D345N, The gene RIMBP3 has a mutation status of S447I, The gene GGA1 has a mutation status of R299W, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ANOS1 has a mutation status of S396L, The gene RPS6KA6 has a mutation status of A241P, The gene MT-ND1 has a mutation status of G101D, The gene MT-CO2 has a mutation status of V143V, The gene MT-ND5 has a mutation status of V254V, The gene MT-CYB has a mutation status of T158A
LAML
The gene CDK11B has a mutation status of R604R, The gene CDK11B has a mutation status of A198A, The gene PIK3CD has a mutation status of L283L, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF5 has a mutation status of P432A, The gene PRAMEF33 has a mutation status of Q338E, The gene VWA5B1 has a mutation status of R321W, The gene LYPLA2 has a mutation status of S128S, The gene ZNF593 has a mutation status of E50A, The gene MFSD2A has a mutation status of T198T, The gene FOXO6 has a mutation status of P334fs, The gene PTPRF has a mutation status of T1148T, The gene NRDC has a mutation status of A787T, The gene C8B has a mutation status of R132K, The gene USP1 has a mutation status of S704G, The gene NOTCH2 has a mutation status of V1666V, The gene NBPF26 has a mutation status of K1078K, The gene NBPF12 has a mutation status of R1120G, The gene NBPF14 has a mutation status of I996F, The gene NBPF9 has a mutation status of V918L, The gene AC242842.3 has a mutation status of V503L, The gene RPRD2 has a mutation status of R202C, The gene UBQLN4 has a mutation status of G146E, The gene SPTA1 has a mutation status of S1009S, The gene COPA has a mutation status of Q1051E, The gene KLHL20 has a mutation status of L367*, The gene KIF21B has a mutation status of A1396G, The gene CACNA1S has a mutation status of S813S, The gene RBBP5 has a mutation status of N170N, The gene OR2B11 has a mutation status of G243G, The gene OR2T11 has a mutation status of E19G, The gene TRAPPC12 has a mutation status of Q133R, The gene TAF1B has a mutation status of R111C, The gene GDF7 has a mutation status of L234M, The gene ZNF514 has a mutation status of V44I, The gene CIAO1 has a mutation status of R65W, The gene FER1L5 has a mutation status of S576A, The gene SCN1A has a mutation status of A935S, The gene FZD7 has a mutation status of S358C, The gene RAPH1 has a mutation status of P1006P, The gene UNC80 has a mutation status of L2735L, The gene SPEG has a mutation status of S1231S, The gene C2orf72 has a mutation status of P66R, The gene PTPN23 has a mutation status of P1547R, The gene MON1A has a mutation status of A134T, The gene STAB1 has a mutation status of P197P, The gene ZBED2 has a mutation status of E190E, The gene ZBED2 has a mutation status of G116S, The gene ZBED2 has a mutation status of G32E, The gene UROC1 has a mutation status of R493C, The gene ZBTB49 has a mutation status of P195L, The gene AFAP1 has a mutation status of L229L, The gene FAM90A26 has a mutation status of R160H, The gene ZNF518B has a mutation status of V353A, The gene FAM184B has a mutation status of E420del, The gene SOD3 has a mutation status of G175G, The gene EPHA5 has a mutation status of R2R, The gene CABS1 has a mutation status of D279D, The gene HERC6 has a mutation status of R678*, The gene ANKRD50 has a mutation status of R434T, The gene FREM3 has a mutation status of N1503N, The gene TTC29 has a mutation status of E444E, The gene SH3RF1 has a mutation status of K717T, The gene WWC2 has a mutation status of R378R, The gene EXOC3 has a mutation status of E36D, The gene ZBED3 has a mutation status of L155A, The gene HSPA4 has a mutation status of S155*, The gene SRA1 has a mutation status of Q166*, The gene BTNL8 has a mutation status of S136P, The gene GMPR has a mutation status of A206A, The gene ATF6B has a mutation status of P433S, The gene PNPLA1 has a mutation status of I185I, The gene BYSL has a mutation status of P222P, The gene RRP36 has a mutation status of R245*, The gene TRAM2 has a mutation status of V121V, The gene CFAP206 has a mutation status of R550C, The gene TMEM200A has a mutation status of P30L, The gene MAP3K5 has a mutation status of V685V, The gene SYNE1 has a mutation status of Q2486Q, The gene ARID1B has a mutation status of G1532S, The gene SYNJ2 has a mutation status of D652N, The gene TBXT has a mutation status of K114fs, The gene SDK1 has a mutation status of T1392I, The gene ANKRD61 has a mutation status of T234M, The gene GHRHR has a mutation status of G363R, The gene TBRG4 has a mutation status of L153L, The gene PKD1L1 has a mutation status of A2662A, The gene GNAT3 has a mutation status of M232I, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene PLOD3 has a mutation status of L403L, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene CALD1 has a mutation status of R117W, The gene CLCN1 has a mutation status of Q675*, The gene NOS3 has a mutation status of E677*, The gene FAM90A9P has a mutation status of A383T, The gene COL14A1 has a mutation status of E1691K, The gene WASHC5 has a mutation status of P809R, The gene EPPK1 has a mutation status of H4804R, The gene EPPK1 has a mutation status of A2633del, The gene EPPK1 has a mutation status of R2547G, The gene EPPK1 has a mutation status of D2512E, The gene PLEC has a mutation status of A1608P, The gene PLEC has a mutation status of R1496H, The gene ADCK5 has a mutation status of E390del, The gene VLDLR has a mutation status of C318C, The gene GLIS3 has a mutation status of G749R, The gene FREM1 has a mutation status of N1729S, The gene MOB3B has a mutation status of R27S, The gene SPAG8 has a mutation status of V225G, The gene HRCT1 has a mutation status of 97_98insHHLHHHHHPHRHHPRHTL, The gene HRCT1 has a mutation status of 104_105insHP, The gene FRMPD1 has a mutation status of I1226L, The gene IGFBPL1 has a mutation status of G173R, The gene SPATA31A1 has a mutation status of R1129R, The gene ANKRD20A3P has a mutation status of G123G, The gene TUT7 has a mutation status of E901K, The gene ELP1 has a mutation status of E1071D, The gene CTNNAL1 has a mutation status of T139T, The gene FRRS1L has a mutation status of R51A, The gene SVEP1 has a mutation status of A3208L, The gene RNF183 has a mutation status of C40G, The gene ASTN2 has a mutation status of E525E, The gene SH3GLB2 has a mutation status of I201S, The gene RAPGEF1 has a mutation status of P431P, The gene WDR5 has a mutation status of V93I, The gene CARD9 has a mutation status of R202W, The gene CACNA1B has a mutation status of P1055R, The gene PHYH has a mutation status of L130L, The gene DNAJC1 has a mutation status of R321Q, The gene ANKRD30A has a mutation status of R485V, The gene ANXA8 has a mutation status of G177A, The gene ANXA8 has a mutation status of P176P, The gene FO681492.1 has a mutation status of L391L, The gene WDFY4 has a mutation status of G965E, The gene AGAP5 has a mutation status of L630L, The gene AGAP5 has a mutation status of S350S, The gene CNNM1 has a mutation status of S940S, The gene SEMA4G has a mutation status of G621R, The gene KNDC1 has a mutation status of P422L, The gene MUC6 has a mutation status of A1266A, The gene BRSK2 has a mutation status of P277P, The gene OSBPL5 has a mutation status of R26R, The gene AC104389.6 has a mutation status of V61I, The gene CCDC34 has a mutation status of R159W, The gene OR5D14 has a mutation status of F207S, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR1S1 has a mutation status of G274G, The gene OR5B17 has a mutation status of LITILKRHTGKGYQKPLSTCGSHLI220del, The gene GLYATL1 has a mutation status of W128C, The gene PPP1R32 has a mutation status of K315fs, The gene EML3 has a mutation status of V33L, The gene SPTBN2 has a mutation status of H777H, The gene TBX10 has a mutation status of S188S, The gene CHKA has a mutation status of I228I, The gene ARAP1 has a mutation status of V575L, The gene GRM5 has a mutation status of I432T, The gene DDI1 has a mutation status of L366F, The gene BCO2 has a mutation status of T186I, The gene PHLDB1 has a mutation status of G1016S, The gene SORL1 has a mutation status of K214N, The gene OR8B12 has a mutation status of F11F, The gene CD163 has a mutation status of N1104Y, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene GUCY2C has a mutation status of L764L, The gene GXYLT1 has a mutation status of E249R, The gene KRT86 has a mutation status of Q139T, The gene KRT18 has a mutation status of V48M, The gene IGFBP6 has a mutation status of N187S, The gene MYRFL has a mutation status of R454W, The gene ZFC3H1 has a mutation status of F1673F, The gene LIN7A has a mutation status of V186A, The gene ACACB has a mutation status of G1982G, The gene MPHOSPH9 has a mutation status of T535M, The gene ZNF26 has a mutation status of P285P, The gene TPT1 has a mutation status of L114L, The gene PCDH9 has a mutation status of L524fs, The gene ADPRHL1 has a mutation status of E1710E, The gene TMEM255B has a mutation status of T47T, The gene NIN has a mutation status of T2092I, The gene ARID4A has a mutation status of D620Y, The gene AK7 has a mutation status of P367L, The gene HHIPL1 has a mutation status of G550G, The gene EIF5 has a mutation status of L46V, The gene PPP1R13B has a mutation status of A376G, The gene GOLGA6L6 has a mutation status of R589R, The gene GOLGA6L6 has a mutation status of K425E, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene FAN1 has a mutation status of N861N, The gene TRPM1 has a mutation status of V998M, The gene ANKDD1A has a mutation status of L516L, The gene NOX5 has a mutation status of R419W, The gene GOLGA6L10 has a mutation status of I73V, The gene GOLGA6L9 has a mutation status of A373P, The gene WDR73 has a mutation status of H78N, The gene RHCG has a mutation status of S474L, The gene RHCG has a mutation status of P148P, The gene TBL3 has a mutation status of R705P, The gene PRSS36 has a mutation status of C772Y, The gene HNRNPA1P48 has a mutation status of V114M, The gene IRX5 has a mutation status of Q118L, The gene CES1 has a mutation status of F6L, The gene FA2H has a mutation status of P112R, The gene SPEM1 has a mutation status of V60A, The gene SREBF1 has a mutation status of A35T, The gene FBXW10 has a mutation status of SLPL204del, The gene FBXW10 has a mutation status of S221F, The gene FBXW10 has a mutation status of F277F, The gene FBXW10 has a mutation status of P367S, The gene TAOK1 has a mutation status of G957D, The gene EFCAB5 has a mutation status of N1146N, The gene CCT6B has a mutation status of V235I, The gene RDM1 has a mutation status of T97T, The gene TBC1D3B has a mutation status of L201F, The gene CCL4L2 has a mutation status of P67R, The gene STAC2 has a mutation status of E274E, The gene KRTAP9-6 has a mutation status of G106C, The gene KRT34 has a mutation status of R250C, The gene HOXB7 has a mutation status of L58F, The gene DGKE has a mutation status of E567A, The gene TMEM94 has a mutation status of R1201C, The gene SPHK1 has a mutation status of E393K, The gene GAA has a mutation status of F858F, The gene BAHCC1 has a mutation status of Y156C, The gene CLUL1 has a mutation status of V476I, The gene LAMA1 has a mutation status of I124T, The gene ANKRD30B has a mutation status of V434I, The gene CDH7 has a mutation status of P375P, The gene RBFA has a mutation status of N149S, The gene APC2 has a mutation status of E1266E, The gene ABHD17A has a mutation status of I258V, The gene DOHH has a mutation status of I116L, The gene ANGPTL4 has a mutation status of G361R, The gene ZNF121 has a mutation status of K235K, The gene HAUS8 has a mutation status of V249M, The gene PLVAP has a mutation status of I294I, The gene ZNF66 has a mutation status of F97F, The gene C19orf12 has a mutation status of E2Q, The gene ACTN4 has a mutation status of F901F, The gene FCGBP has a mutation status of P2760Q, The gene FCGBP has a mutation status of L2757P, The gene ZNF180 has a mutation status of S208S, The gene CD33 has a mutation status of R119W, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of H290H, The gene LILRA6 has a mutation status of H290N, The gene LILRA6 has a mutation status of D252N, The gene LILRB2 has a mutation status of Y297S, The gene LILRB2 has a mutation status of R295T, The gene LILRA2 has a mutation status of S395T, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene LILRB1 has a mutation status of Y99I, The gene BFSP1 has a mutation status of A36F, The gene ID1 has a mutation status of A13A, The gene BPIFB4 has a mutation status of G186D, The gene SOGA1 has a mutation status of T1392T, The gene CHD6 has a mutation status of L1859L, The gene SEZ6L has a mutation status of I961I, The gene MN1 has a mutation status of L721R, The gene LARGE1 has a mutation status of R626K, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ATP5MGL has a mutation status of G77R, The gene ARHGAP6 has a mutation status of I367V, The gene PPP1R2C has a mutation status of Y63Y, The gene DIPK2B has a mutation status of R205C, The gene SLC25A5 has a mutation status of Y165C, The gene SLC25A5 has a mutation status of T221R, The gene AC236972.4 has a mutation status of S1611S, The gene AC236972.4 has a mutation status of A1638T, The gene AC236972.4 has a mutation status of G1663G, The gene MT-CO1 has a mutation status of H291H, The gene MT-CYB has a mutation status of H308H
SARC
The gene PLEKHN1 has a mutation status of E237*, The gene PLEKHN1 has a mutation status of W239L, The gene AGRN has a mutation status of R233H, The gene INTS11 has a mutation status of D59D, The gene TAS1R3 has a mutation status of M110T, The gene TAS1R3 has a mutation status of A733V, The gene ARHGEF16 has a mutation status of S602L, The gene MEGF6 has a mutation status of P1515L, The gene NPHP4 has a mutation status of S496*, The gene H6PD has a mutation status of A399T, The gene SLC25A33 has a mutation status of V152L, The gene UBE4B has a mutation status of S196S, The gene VPS13D has a mutation status of I2332V, The gene MRTO4 has a mutation status of E114E, The gene TMCO4 has a mutation status of A174T, The gene MYOM3 has a mutation status of E144L, The gene EXTL1 has a mutation status of V98L, The gene TRNP1 has a mutation status of V155L, The gene AHDC1 has a mutation status of L857L, The gene AZIN2 has a mutation status of P265P, The gene AGO4 has a mutation status of T347T, The gene MACF1 has a mutation status of R5877C, The gene PPCS has a mutation status of R25P, The gene MPL has a mutation status of *636W, The gene FAAH has a mutation status of W462C, The gene TAL1 has a mutation status of G148G, The gene DMRTA2 has a mutation status of P443P, The gene TTC4 has a mutation status of H166Y, The gene RAVER2 has a mutation status of P77T, The gene SGIP1 has a mutation status of S482C, The gene MIER1 has a mutation status of E21K, The gene RABGGTB has a mutation status of T17T, The gene ST6GALNAC5 has a mutation status of P36S, The gene GNG5 has a mutation status of L48M, The gene CLCA2 has a mutation status of T845M, The gene GBP1 has a mutation status of L187P, The gene ZNF644 has a mutation status of T242T, The gene TGFBR3 has a mutation status of N503S, The gene DPYD has a mutation status of D213D, The gene VCAM1 has a mutation status of E179K, The gene FNDC7 has a mutation status of T606T, The gene KIAA1324 has a mutation status of S273S, The gene HIPK1 has a mutation status of V1014V, The gene TRIM33 has a mutation status of V892V, The gene CGN has a mutation status of R811L, The gene HRNR has a mutation status of S1515I, The gene FLG has a mutation status of S680A, The gene FLG has a mutation status of A361T, The gene NUP210L has a mutation status of E831K, The gene MTX1 has a mutation status of S55S, The gene HCN3 has a mutation status of S407R, The gene LRRC71 has a mutation status of F525F, The gene FCGR2B has a mutation status of R72R, The gene UCK2 has a mutation status of S70A, The gene DUSP27 has a mutation status of G326G, The gene DUSP27 has a mutation status of S328S, The gene DUSP27 has a mutation status of A809V, The gene DPT has a mutation status of T88T, The gene CCDC181 has a mutation status of R125I, The gene TOR1AIP1 has a mutation status of A2E, The gene RGL1 has a mutation status of S779I, The gene HMCN1 has a mutation status of A2652V, The gene TNNT2 has a mutation status of V21V, The gene CHIT1 has a mutation status of A149S, The gene PLEKHA6 has a mutation status of S982S, The gene PLEKHA6 has a mutation status of R322H, The gene PPP1R15B has a mutation status of P314S, The gene PPP1R15B has a mutation status of P276S, The gene PLXNA2 has a mutation status of P1546L, The gene PLXNA2 has a mutation status of C826G, The gene FAM71A has a mutation status of V208M, The gene ANGEL2 has a mutation status of N77H, The gene PROX1 has a mutation status of P304P, The gene MARK1 has a mutation status of G384G, The gene HHIPL2 has a mutation status of A466V, The gene CAPN9 has a mutation status of S608S, The gene WDR64 has a mutation status of F905S, The gene OR2L2 has a mutation status of V108A, The gene OR2T33 has a mutation status of R318G, The gene MYT1L has a mutation status of L1116L, The gene NBAS has a mutation status of K1801R, The gene WDCP has a mutation status of L77L, The gene GPN1 has a mutation status of G6V, The gene B3GNT2 has a mutation status of L345L, The gene CEP68 has a mutation status of N87S, The gene APLF has a mutation status of G4G, The gene GGCX has a mutation status of R108C, The gene PTCD3 has a mutation status of E311K, The gene SCTR has a mutation status of A160T, The gene INHBB has a mutation status of S285N, The gene LRP1B has a mutation status of E1080fs, The gene CCDC148 has a mutation status of E90*, The gene SCN2A has a mutation status of F328V, The gene TTC21B has a mutation status of T292T, The gene XIRP2 has a mutation status of P285S, The gene TTC30A has a mutation status of P633T, The gene TTC30A has a mutation status of G3G, The gene OSBPL6 has a mutation status of L592Q, The gene TTN has a mutation status of T29802N, The gene HECW2 has a mutation status of D1460D, The gene INO80D has a mutation status of G32G, The gene WNT10A has a mutation status of A334T, The gene SP100 has a mutation status of N257I, The gene GIGYF2 has a mutation status of G148A, The gene CNTN4 has a mutation status of C1008C, The gene IL5RA has a mutation status of R99Q, The gene SRGAP3 has a mutation status of V1081M, The gene TTLL3 has a mutation status of M144I, The gene IRAK2 has a mutation status of R504*, The gene SEC13 has a mutation status of D20D, The gene BTD has a mutation status of H283Y, The gene RFTN1 has a mutation status of R460M, The gene TOP2B has a mutation status of V13V, The gene VILL has a mutation status of F610L, The gene SCN5A has a mutation status of L1215I, The gene SCN5A has a mutation status of T423I, The gene CYP8B1 has a mutation status of S342S, The gene KIF15 has a mutation status of R34C, The gene NBEAL2 has a mutation status of A1778V, The gene NBEAL2 has a mutation status of Q2726K, The gene PTPN23 has a mutation status of P1562P, The gene MAP4 has a mutation status of K1555E, The gene CELSR3 has a mutation status of P2990R, The gene BSN has a mutation status of G1633G, The gene PARP3 has a mutation status of W8L, The gene TASOR has a mutation status of L846L, The gene GRAMD1C has a mutation status of V268M, The gene PLA1A has a mutation status of L312L, The gene IQCB1 has a mutation status of K437K, The gene HACD2 has a mutation status of S150S, The gene IFT122 has a mutation status of R1229C, The gene TRH has a mutation status of E169K, The gene TRH has a mutation status of E171E, The gene STAG1 has a mutation status of T768T, The gene GRK7 has a mutation status of P122P, The gene P2RY12 has a mutation status of E181E, The gene LRRC31 has a mutation status of G352G, The gene ACTL6A has a mutation status of V15V, The gene LIPH has a mutation status of C212S, The gene ZDHHC19 has a mutation status of P9L, The gene ZNF732 has a mutation status of T82T, The gene FAM53A has a mutation status of T146S, The gene SORCS2 has a mutation status of S1150S, The gene PTTG2 has a mutation status of R45L, The gene UGT2B28 has a mutation status of A346T, The gene ADAMTS3 has a mutation status of R1143K, The gene ADH1B has a mutation status of G205S, The gene BDH2 has a mutation status of A14T, The gene CYP2U1 has a mutation status of S126T, The gene ZGRF1 has a mutation status of P526P, The gene METTL14 has a mutation status of A176T, The gene USP53 has a mutation status of L895L, The gene LARP1B has a mutation status of R716C, The gene GYPE has a mutation status of T22A, The gene DCHS2 has a mutation status of R716W, The gene GLRB has a mutation status of A294T, The gene HAND2 has a mutation status of L47I, The gene HAND2 has a mutation status of G45G, The gene TENM3 has a mutation status of K4K, The gene TRIML2 has a mutation status of R215G, The gene NSUN2 has a mutation status of S461C, The gene ZNF622 has a mutation status of T67A, The gene PDZD2 has a mutation status of Q942K, The gene UGT3A1 has a mutation status of M500T, The gene UGT3A1 has a mutation status of T387A, The gene RICTOR has a mutation status of R855Q, The gene PDE4D has a mutation status of K293N, The gene BDP1 has a mutation status of N26S, The gene FOXD1 has a mutation status of G43V, The gene S100Z has a mutation status of Q60Q, The gene ADGRV1 has a mutation status of R1488W, The gene MAN2A1 has a mutation status of R981R, The gene FEM1C has a mutation status of L488L, The gene SNCAIP has a mutation status of S127S, The gene PFDN1 has a mutation status of Q24Q, The gene PCDHB5 has a mutation status of V56V, The gene PCDHGA2 has a mutation status of F472S, The gene PPARGC1B has a mutation status of Y943Y, The gene SH3PXD2B has a mutation status of M1I, The gene DBN1 has a mutation status of P563L, The gene ADAMTS2 has a mutation status of R691R, The gene NQO2 has a mutation status of Y76C, The gene HIVEP1 has a mutation status of P829L, The gene ATXN1 has a mutation status of V268I, The gene H2BC13 has a mutation status of I95fs, The gene H2BC15 has a mutation status of D52D, The gene HLA-A has a mutation status of A18D, The gene AL645922.1 has a mutation status of N833D, The gene PBX2 has a mutation status of S159S, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DPA1 has a mutation status of L225L, The gene ITPR3 has a mutation status of N2564T, The gene UHRF1BP1 has a mutation status of L579F, The gene UHRF1BP1 has a mutation status of R847G, The gene DNAH8 has a mutation status of R4490C, The gene KCNK17 has a mutation status of A129S, The gene UNC5CL has a mutation status of G89G, The gene TRERF1 has a mutation status of T365T, The gene LRRC73 has a mutation status of S293R, The gene VEGFA has a mutation status of P92P, The gene C6orf223 has a mutation status of K31N, The gene CAPN11 has a mutation status of G171S, The gene AARS2 has a mutation status of V59G, The gene TDRD6 has a mutation status of G387G, The gene TDRD6 has a mutation status of A1009E, The gene PKHD1 has a mutation status of S3210C, The gene PKHD1 has a mutation status of N3062D, The gene PKHD1 has a mutation status of I2364N, The gene ZNF292 has a mutation status of Q172K, The gene KLHL32 has a mutation status of H170Y, The gene TUBE1 has a mutation status of E198K, The gene MARCKS has a mutation status of A274V, The gene DSE has a mutation status of R350H, The gene TRMT11 has a mutation status of S448S, The gene SYNE1 has a mutation status of N5523S, The gene LPA has a mutation status of Q1085Q, The gene SNX8 has a mutation status of P438T, The gene BRAT1 has a mutation status of A642G, The gene TNRC18 has a mutation status of R1465Q, The gene EVX1 has a mutation status of G155R, The gene NOD1 has a mutation status of G772R, The gene TBX20 has a mutation status of T331A, The gene AMPH has a mutation status of Q188Q, The gene PURB has a mutation status of S8I, The gene PKD1L1 has a mutation status of S1598S, The gene GRB10 has a mutation status of P448L, The gene SPDYE21 has a mutation status of RSRIPLLRKRWFQLGRSMNPRARKN278del, The gene AUTS2 has a mutation status of S201S, The gene CYP51A1 has a mutation status of K297R, The gene PILRB has a mutation status of L147V, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of G307H, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of L2752F, The gene MUC3A has a mutation status of P3166P, The gene SLC26A4 has a mutation status of E765del, The gene LAMB1 has a mutation status of A524A, The gene FLNC has a mutation status of A1831A, The gene CREB3L2 has a mutation status of L75H, The gene HIPK2 has a mutation status of I519I, The gene MGAM2 has a mutation status of T967T, The gene ZNF746 has a mutation status of S631Y, The gene ATP6V0E2 has a mutation status of L63L, The gene NUB1 has a mutation status of E570*, The gene KMT2C has a mutation status of S3547P, The gene KMT2C has a mutation status of Q2997*, The gene USP17L2 has a mutation status of V58fs, The gene NUDT18 has a mutation status of S280N, The gene BIN3 has a mutation status of D224A, The gene HMBOX1 has a mutation status of P357P, The gene PPP2CB has a mutation status of R49H, The gene KCNU1 has a mutation status of P728L, The gene ZNF703 has a mutation status of G365V, The gene IDO2 has a mutation status of D144D, The gene FNTA has a mutation status of S49S, The gene TTPA has a mutation status of R5L, The gene MCMDC2 has a mutation status of L90L, The gene LACTB2 has a mutation status of T249T, The gene EYA1 has a mutation status of D388fs, The gene PI15 has a mutation status of P228P, The gene ZFHX4 has a mutation status of P2053H, The gene CYP11B2 has a mutation status of P37P, The gene BOP1 has a mutation status of T197T, The gene PLGRKT has a mutation status of A72A, The gene SNAPC3 has a mutation status of T125I, The gene NOL6 has a mutation status of P295H, The gene GNE has a mutation status of D117V, The gene FAM189A2 has a mutation status of E521del, The gene FAM120A has a mutation status of I791V, The gene CCDC180 has a mutation status of R107Q, The gene CCDC180 has a mutation status of A1618T, The gene FOXE1 has a mutation status of A170A, The gene TGFBR1 has a mutation status of N45Y, The gene ZNF462 has a mutation status of P548P, The gene SVEP1 has a mutation status of T577S, The gene ZNF883 has a mutation status of Q294K, The gene OR1L1 has a mutation status of R235C, The gene LHX2 has a mutation status of A339A, The gene SCAI has a mutation status of A5T, The gene SETX has a mutation status of R20C, The gene SLC2A6 has a mutation status of L375V, The gene SARDH has a mutation status of R785R, The gene CAMSAP1 has a mutation status of H969Q, The gene NACC2 has a mutation status of A153A, The gene NOTCH1 has a mutation status of Q1134R, The gene NOXA1 has a mutation status of P369P, The gene AKR1C4 has a mutation status of L63Q, The gene IL2RA has a mutation status of E137G, The gene SFMBT2 has a mutation status of T807M, The gene DHTKD1 has a mutation status of D565D, The gene GPR158 has a mutation status of E1148S, The gene OR13A1 has a mutation status of L168L, The gene PHYHIPL has a mutation status of I61V, The gene TMEM26 has a mutation status of A68A, The gene RTKN2 has a mutation status of Y68C, The gene ADO has a mutation status of P182P, The gene DNA2 has a mutation status of V67L, The gene NRG3 has a mutation status of E126D, The gene SLIT1 has a mutation status of G938A, The gene GBF1 has a mutation status of S1620S, The gene MXI1 has a mutation status of E25*, The gene INPP5F has a mutation status of Q14H, The gene PWWP2B has a mutation status of P251T, The gene RIC8A has a mutation status of T485I, The gene SIGIRR has a mutation status of W237C, The gene SIGIRR has a mutation status of R235L, The gene CD151 has a mutation status of G227S, The gene MUC5AC has a mutation status of R2064W, The gene MUC5AC has a mutation status of V2103I, The gene UBQLNL has a mutation status of M191L, The gene TTC17 has a mutation status of R892C, The gene TRIM51 has a mutation status of S286S, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene SMTNL1 has a mutation status of K493N, The gene OR5B12 has a mutation status of P180A, The gene OR10V1 has a mutation status of R187C, The gene ZP1 has a mutation status of L243L, The gene CD6 has a mutation status of G111G, The gene CD5 has a mutation status of N203S, The gene CCDC88B has a mutation status of A988A, The gene SLC22A11 has a mutation status of S104S, The gene MEN1 has a mutation status of R461fs, The gene DNAJB13 has a mutation status of V91G, The gene FAT3 has a mutation status of R2780G, The gene FAT3 has a mutation status of T3075T, The gene IL10RA has a mutation status of L565L, The gene TMEM25 has a mutation status of P7Q, The gene HYOU1 has a mutation status of V559I, The gene VPS11 has a mutation status of E225E, The gene HSPA8 has a mutation status of K423K, The gene FLI1 has a mutation status of A419T, The gene C12orf4 has a mutation status of C487C, The gene VWF has a mutation status of S1930R, The gene VWF has a mutation status of E1389E, The gene SCNN1A has a mutation status of S518S, The gene NOP2 has a mutation status of T136T, The gene KRAS has a mutation status of Q61H, The gene LRRK2 has a mutation status of L794V, The gene ASIC1 has a mutation status of P15P, The gene SLC11A2 has a mutation status of I158I, The gene BIN2 has a mutation status of R366C, The gene NR4A1 has a mutation status of T567T, The gene KRT6A has a mutation status of A339A, The gene EIF4B has a mutation status of D568E, The gene IRAK3 has a mutation status of G247R, The gene NAV3 has a mutation status of E1629E, The gene OTOGL has a mutation status of P1807Q, The gene OTOGL has a mutation status of Y1812C, The gene GNPTAB has a mutation status of V872I, The gene RPLP0 has a mutation status of A117A, The gene TUBA3C has a mutation status of R123C, The gene ZMYM5 has a mutation status of S492del, The gene GJB2 has a mutation status of L79fs, The gene AMER2 has a mutation status of A40V, The gene STARD13 has a mutation status of M862I, The gene KCTD4 has a mutation status of A111A, The gene ZC3H13 has a mutation status of L1410I, The gene CYSLTR2 has a mutation status of F36L, The gene THSD1 has a mutation status of Q351Q, The gene DIS3 has a mutation status of G927G, The gene TBC1D4 has a mutation status of S681S, The gene RNF113B has a mutation status of S89R, The gene MYO16 has a mutation status of N219N, The gene TMEM255B has a mutation status of P257P, The gene MDGA2 has a mutation status of S692G, The gene SMOC1 has a mutation status of R362Q, The gene MIDEAS has a mutation status of P657P, The gene NEK9 has a mutation status of E508K, The gene ESRRB has a mutation status of R209W, The gene GPR68 has a mutation status of W254L, The gene ITPK1 has a mutation status of L407L, The gene SYNE3 has a mutation status of H650Q, The gene ASPG has a mutation status of Q518*, The gene KIF26A has a mutation status of E247*, The gene TEDC1 has a mutation status of L291R, The gene LINC02203 has a mutation status of I259M, The gene HERC2 has a mutation status of S2422P, The gene ARHGAP11A has a mutation status of A423T, The gene C15orf41 has a mutation status of A38P, The gene KNL1 has a mutation status of S782L, The gene CAPN3 has a mutation status of V331V, The gene PPIP5K1 has a mutation status of T1272R, The gene OAZ2 has a mutation status of P70S, The gene PIF1 has a mutation status of A383T, The gene PDCD7 has a mutation status of P16H, The gene CORO2B has a mutation status of R13H, The gene CORO2B has a mutation status of E171E, The gene NOX5 has a mutation status of K477N, The gene WHAMM has a mutation status of I295T, The gene ALPK3 has a mutation status of P1121P, The gene PDE8A has a mutation status of R46C, The gene POLG has a mutation status of A703A, The gene MEF2A has a mutation status of P465A, The gene PGAP6 has a mutation status of L278R, The gene DECR2 has a mutation status of G270R, The gene CAPN15 has a mutation status of G19C, The gene PRR35 has a mutation status of A228A, The gene PRR35 has a mutation status of R257S, The gene CACNA1H has a mutation status of A2181A, The gene TRAF7 has a mutation status of R283C, The gene NLRC3 has a mutation status of S582S, The gene NLRC3 has a mutation status of P244T, The gene RBFOX1 has a mutation status of Q119P, The gene METTL22 has a mutation status of V230I, The gene ACSM1 has a mutation status of R8W, The gene GTF3C1 has a mutation status of N1665N, The gene GTF3C1 has a mutation status of P1664P, The gene PRRT2 has a mutation status of S174R, The gene MVP has a mutation status of D525D, The gene STX4 has a mutation status of E39del, The gene ZNF267 has a mutation status of K357*, The gene CPNE2 has a mutation status of Y408Y, The gene PLLP has a mutation status of L37L, The gene CDH16 has a mutation status of V437V, The gene CDH16 has a mutation status of T432M, The gene SLC9A5 has a mutation status of V63L, The gene ZFHX3 has a mutation status of A2433V, The gene TAF1C has a mutation status of R138C, The gene ZCCHC14 has a mutation status of G374G, The gene CLUH has a mutation status of A955V, The gene DVL2 has a mutation status of L278L, The gene TP53 has a mutation status of Y220C, The gene MYH1 has a mutation status of H1594R, The gene DNAH9 has a mutation status of I4188T, The gene ELAC2 has a mutation status of L451L, The gene LLGL1 has a mutation status of W409*, The gene KSR1 has a mutation status of P239P, The gene PIGS has a mutation status of D246H, The gene PROCA1 has a mutation status of E292K, The gene TBC1D3B has a mutation status of M251V, The gene CCL4L2 has a mutation status of P67R, The gene SRCIN1 has a mutation status of T689T, The gene ZPBP2 has a mutation status of R3R, The gene TOP2A has a mutation status of T530A, The gene CCR7 has a mutation status of W183*, The gene KRTAP17-1 has a mutation status of E15G, The gene CNP has a mutation status of L174L, The gene COASY has a mutation status of A375V, The gene RETREG3 has a mutation status of A290T, The gene CNTNAP1 has a mutation status of R834C, The gene WNK4 has a mutation status of P916P, The gene MEOX1 has a mutation status of P109P, The gene XYLT2 has a mutation status of E449K, The gene LUC7L3 has a mutation status of P57P, The gene MTMR4 has a mutation status of K935K, The gene SCN4A has a mutation status of R18C, The gene DDX5 has a mutation status of M584I, The gene CEP112 has a mutation status of R692W, The gene KPNA2 has a mutation status of A397G, The gene GRIN2C has a mutation status of H1148Q, The gene FDXR has a mutation status of P300S, The gene FBF1 has a mutation status of A919G, The gene UBE2O has a mutation status of D650E, The gene ST6GALNAC1 has a mutation status of H184del, The gene DNAH17 has a mutation status of R4395W, The gene SLC26A11 has a mutation status of V369M, The gene SLC38A10 has a mutation status of N8D, The gene SLC25A10 has a mutation status of L250L, The gene MTCL1 has a mutation status of R750W, The gene ANKRD12 has a mutation status of K948E, The gene APCDD1 has a mutation status of L21L, The gene MC5R has a mutation status of A81V, The gene SIGLEC15 has a mutation status of V281fs, The gene MYO5B has a mutation status of A209A, The gene CCDC102B has a mutation status of K105E, The gene TSHZ1 has a mutation status of H430N, The gene NFATC1 has a mutation status of D297N, The gene ARID3A has a mutation status of R13R, The gene WDR18 has a mutation status of S205S, The gene PCSK4 has a mutation status of V111G, The gene ATP8B3 has a mutation status of E791K, The gene ZNF77 has a mutation status of K238K, The gene MFSD12 has a mutation status of Q212fs, The gene MATK has a mutation status of W374*, The gene ANKRD24 has a mutation status of R1013Q, The gene SHD has a mutation status of Q324R, The gene SHD has a mutation status of L329L, The gene ARRDC5 has a mutation status of C124F, The gene STXBP2 has a mutation status of L212F, The gene FBN3 has a mutation status of E1972K, The gene ANGPTL4 has a mutation status of R230L, The gene PPAN-P2RY11 has a mutation status of N168S, The gene EIF3G has a mutation status of N311N, The gene ICAM4 has a mutation status of F48L, The gene KANK2 has a mutation status of S498I, The gene PALM3 has a mutation status of G442V, The gene OR7C1 has a mutation status of Y60Y, The gene RASAL3 has a mutation status of K766N, The gene RASAL3 has a mutation status of G764G, The gene CYP4F8 has a mutation status of V81L, The gene EPS15L1 has a mutation status of S503L, The gene ANO8 has a mutation status of E557D, The gene SSBP4 has a mutation status of L176I, The gene LPAR2 has a mutation status of E224E, The gene DPF1 has a mutation status of G11R, The gene SNRPA has a mutation status of D24D, The gene CYP2F1 has a mutation status of R482W, The gene AXL has a mutation status of V150A, The gene DEDD2 has a mutation status of A212A, The gene ZNF224 has a mutation status of T177T, The gene SIX5 has a mutation status of T552T, The gene AP2S1 has a mutation status of K29K, The gene KPTN has a mutation status of A428V, The gene BICRA has a mutation status of V1330M, The gene PRR12 has a mutation status of P650P, The gene SCAF1 has a mutation status of P617Q, The gene MED25 has a mutation status of F32F, The gene IL4I1 has a mutation status of A523S, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of G175R, The gene LILRA6 has a mutation status of Y121Y, The gene USP29 has a mutation status of V678V, The gene TRIB3 has a mutation status of P115R, The gene ANGPT4 has a mutation status of R259L, The gene SIRPA has a mutation status of L44S, The gene SIRPA has a mutation status of S314R, The gene PTPRA has a mutation status of K239R, The gene ADAM33 has a mutation status of G436G, The gene THBD has a mutation status of S149R, The gene APMAP has a mutation status of G6W, The gene RBM12 has a mutation status of P197P, The gene WFDC3 has a mutation status of C5C, The gene ACOT8 has a mutation status of P4P, The gene ADNP has a mutation status of T64T, The gene MTG2 has a mutation status of V18M, The gene DIDO1 has a mutation status of P2016A, The gene SLC17A9 has a mutation status of L127L, The gene DOP1B has a mutation status of R1217S, The gene COL18A1 has a mutation status of P21H, The gene PCNT has a mutation status of K2944del, The gene TBX1 has a mutation status of P452T, The gene HIC2 has a mutation status of D47D, The gene PPM1F has a mutation status of Q269*, The gene GRK3 has a mutation status of L407L, The gene GRK3 has a mutation status of V409M, The gene AC004997.1 has a mutation status of I235I, The gene C1QTNF6 has a mutation status of N196K, The gene TOMM22 has a mutation status of P16L, The gene SELENOO has a mutation status of R424G, The gene GYG2 has a mutation status of L115L, The gene VEGFD has a mutation status of R108K, The gene ZRSR2 has a mutation status of T207T, The gene DMD has a mutation status of Q1163Q, The gene DMD has a mutation status of L1162I, The gene ZNF182 has a mutation status of R217Q, The gene MAGIX has a mutation status of V46I, The gene XAGE5 has a mutation status of E50D, The gene AMER1 has a mutation status of G149G, The gene IGBP1 has a mutation status of R188H, The gene OGT has a mutation status of G940V, The gene NHSL2 has a mutation status of R497Q, The gene RPS4X has a mutation status of T196T, The gene COL4A6 has a mutation status of G1434G, The gene TEX13D has a mutation status of P325T, The gene ADGRG4 has a mutation status of L101Q, The gene MT-CO2 has a mutation status of P145P, The gene MT-CO2 has a mutation status of G222G, The gene MT-ATP6 has a mutation status of T146T, The gene MT-CO3 has a mutation status of L206L, The gene MT-ND3 has a mutation status of L16L, The gene MT-ND5 has a mutation status of L450P, The gene MT-CYB has a mutation status of N260D
PAAD
The gene TMEM52 has a mutation status of P151L, The gene CFAP74 has a mutation status of D621G, The gene PRDM16 has a mutation status of E1154A, The gene NPHP4 has a mutation status of G1113G, The gene KCNAB2 has a mutation status of P341P, The gene PRAMEF1 has a mutation status of R213F, The gene PRAMEF2 has a mutation status of M28V, The gene PRAMEF2 has a mutation status of G208Q, The gene PRAMEF2 has a mutation status of N293M, The gene PRAMEF2 has a mutation status of N426D, The gene PRAMEF10 has a mutation status of R402G, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene TMCO4 has a mutation status of E75G, The gene PLA2G2A has a mutation status of KTTY122del, The gene IFNLR1 has a mutation status of N226S, The gene GPATCH3 has a mutation status of L134L, The gene COL16A1 has a mutation status of G1601G, The gene RBBP4 has a mutation status of A359A, The gene AGBL4 has a mutation status of Y398Y, The gene DMRTA2 has a mutation status of G134D, The gene YIPF1 has a mutation status of R96R, The gene C8A has a mutation status of W430*, The gene AGL has a mutation status of R675R, The gene KCNA10 has a mutation status of N156S, The gene VTCN1 has a mutation status of P175S, The gene SETDB1 has a mutation status of V132fs, The gene FLG has a mutation status of R3277L, The gene FLG2 has a mutation status of G2198G, The gene ATP8B2 has a mutation status of E610E, The gene KCNN3 has a mutation status of S300S, The gene PMVK has a mutation status of G34R, The gene NTRK1 has a mutation status of G519G, The gene DUSP27 has a mutation status of A809V, The gene SELP has a mutation status of T597T, The gene TNR has a mutation status of T1306S, The gene SMG7 has a mutation status of V297L, The gene COLGALT2 has a mutation status of A27A, The gene USH2A has a mutation status of G4106R, The gene OBSCN has a mutation status of P4171L, The gene OR11L1 has a mutation status of G152R, The gene PXDN has a mutation status of P1131P, The gene CAD has a mutation status of I1330I, The gene SLC4A1AP has a mutation status of R451Q, The gene LTBP1 has a mutation status of A340A, The gene FAM98A has a mutation status of G407V, The gene ABCG8 has a mutation status of M429V, The gene LRPPRC has a mutation status of A1360T, The gene CFAP36 has a mutation status of R272*, The gene FBXO41 has a mutation status of R567L, The gene ALMS1 has a mutation status of V806L, The gene ANKRD36 has a mutation status of N769K, The gene NMS has a mutation status of R69S, The gene PDCL3 has a mutation status of E93D, The gene TUBA3E has a mutation status of R156Q, The gene PTPN18 has a mutation status of S76S, The gene NEB has a mutation status of A1804E, The gene GALNT13 has a mutation status of V336A, The gene SLC38A11 has a mutation status of T133A, The gene XIRP2 has a mutation status of P285S, The gene TTC30A has a mutation status of N152N, The gene TTN has a mutation status of N4127N, The gene NBEAL1 has a mutation status of S899N, The gene RNF25 has a mutation status of G429S, The gene CFAP65 has a mutation status of L1864M, The gene CFAP65 has a mutation status of F647S, The gene ANKZF1 has a mutation status of A667T, The gene SCG2 has a mutation status of K341K, The gene SP110 has a mutation status of F442L, The gene SP100 has a mutation status of G6S, The gene HDLBP has a mutation status of V79V, The gene FGD5 has a mutation status of S458S, The gene LTF has a mutation status of A393V, The gene AC109583.1 has a mutation status of T230M, The gene SMARCC1 has a mutation status of G116G, The gene ARIH2OS has a mutation status of A153G, The gene CRYBG3 has a mutation status of H2514Q, The gene CCDC191 has a mutation status of F330F, The gene TF has a mutation status of A76V, The gene LRRIQ4 has a mutation status of K499M, The gene PHC3 has a mutation status of S695G, The gene TNIK has a mutation status of R632C, The gene TP63 has a mutation status of D78V, The gene FAM43A has a mutation status of K59R, The gene UVSSA has a mutation status of V502M, The gene TACC3 has a mutation status of P395R, The gene FGFR3 has a mutation status of G65R, The gene CCKAR has a mutation status of L305L, The gene YTHDC1 has a mutation status of P407P, The gene UGT2B7 has a mutation status of V147I, The gene FRAS1 has a mutation status of H492H, The gene AC126283.2 has a mutation status of R201S, The gene PCDH18 has a mutation status of F409F, The gene TIGD4 has a mutation status of S301S, The gene TENM3 has a mutation status of K4K, The gene SNX25 has a mutation status of Q287*, The gene FAT1 has a mutation status of R1257Q, The gene FAT1 has a mutation status of G1067del, The gene CLPTM1L has a mutation status of L407L, The gene ADAMTS16 has a mutation status of H247R, The gene HTR1A has a mutation status of W161*, The gene SREK1 has a mutation status of T194M, The gene ZFYVE16 has a mutation status of Q741R, The gene VCAN has a mutation status of P828S, The gene ADGRV1 has a mutation status of R4802Q, The gene SLCO6A1 has a mutation status of G496fs, The gene SLCO6A1 has a mutation status of A322T, The gene TSLP has a mutation status of R153R, The gene WDR36 has a mutation status of I657V, The gene WDR36 has a mutation status of L700F, The gene LVRN has a mutation status of A693D, The gene FAM170A has a mutation status of Q155R, The gene RAD50 has a mutation status of L642V, The gene FSTL4 has a mutation status of P251H, The gene SPOCK1 has a mutation status of R418Q, The gene WNT8A has a mutation status of T193K, The gene ARHGEF37 has a mutation status of Q155K, The gene TCOF1 has a mutation status of A325A, The gene FAT2 has a mutation status of S1713F, The gene MFAP3 has a mutation status of Y357C, The gene GPRIN1 has a mutation status of S294L, The gene TBC1D9B has a mutation status of Q1108E, The gene RASGEF1C has a mutation status of D94E, The gene EXOC2 has a mutation status of T594M, The gene FOXC1 has a mutation status of L518F, The gene F13A1 has a mutation status of P384S, The gene RREB1 has a mutation status of P817R, The gene MAK has a mutation status of S354S, The gene AL031777.2 has a mutation status of D91D, The gene H1-3 has a mutation status of A8T, The gene C6orf15 has a mutation status of N274N, The gene HLA-B has a mutation status of Y140L, The gene HLA-B has a mutation status of N104K, The gene HLA-B has a mutation status of A93R, The gene BRD2 has a mutation status of E505E, The gene MAPK13 has a mutation status of S350S, The gene MCM3 has a mutation status of G437V, The gene TINAG has a mutation status of N399K, The gene KHDC1L has a mutation status of I47T, The gene DOP1A has a mutation status of H944H, The gene DOP1A has a mutation status of R1355Q, The gene ME1 has a mutation status of K330N, The gene PNISR has a mutation status of H558Q, The gene RFX6 has a mutation status of T124K, The gene ENPP3 has a mutation status of S730S, The gene TAAR2 has a mutation status of S124L, The gene ARFGEF3 has a mutation status of T1833T, The gene UTRN has a mutation status of R885H, The gene UTRN has a mutation status of S2448S, The gene SYNJ2 has a mutation status of E403D, The gene LPA has a mutation status of T1255T, The gene HOXA1 has a mutation status of I131M, The gene BMPER has a mutation status of R444fs, The gene CDK13 has a mutation status of G714S, The gene CDK13 has a mutation status of R1366H, The gene ADCY1 has a mutation status of G931G, The gene ABCA13 has a mutation status of A3744S, The gene COBL has a mutation status of P23P, The gene PSPH has a mutation status of L68P, The gene TBL2 has a mutation status of R360W, The gene ABHD11 has a mutation status of E185Q, The gene ABHD11 has a mutation status of V34L, The gene COL1A2 has a mutation status of H512Q, The gene PON2 has a mutation status of K91K, The gene DYNC1I1 has a mutation status of R258L, The gene ZNF655 has a mutation status of M429I, The gene ACTL6B has a mutation status of F138F, The gene MUC3A has a mutation status of S123L, The gene MUC17 has a mutation status of P2117L, The gene LRWD1 has a mutation status of P593T, The gene RELN has a mutation status of S566T, The gene HBP1 has a mutation status of S209S, The gene GPR22 has a mutation status of Y357Y, The gene COG5 has a mutation status of T136M, The gene DLD has a mutation status of T319A, The gene MKLN1 has a mutation status of G689C, The gene CALD1 has a mutation status of E5E, The gene TAS2R5 has a mutation status of Y80C, The gene PIP has a mutation status of L23L, The gene KCNH2 has a mutation status of S951I, The gene GALNT11 has a mutation status of D197Y, The gene PTPRN2 has a mutation status of V771M, The gene MYOM2 has a mutation status of R617Q, The gene XKR6 has a mutation status of V390M, The gene PNMA2 has a mutation status of K202fs, The gene DCTN6 has a mutation status of E57E, The gene PXDNL has a mutation status of L821R, The gene PKHD1L1 has a mutation status of A2086T, The gene ST3GAL1 has a mutation status of Y287Y, The gene CYP11B2 has a mutation status of P37P, The gene MAFA has a mutation status of L11P, The gene SCRIB has a mutation status of A1539T, The gene SCRIB has a mutation status of A1537V, The gene RLN2 has a mutation status of V73L, The gene MPDZ has a mutation status of T1008A, The gene MPDZ has a mutation status of N128Y, The gene PIGO has a mutation status of H357Y, The gene CNTNAP3B has a mutation status of S794L, The gene PHF2 has a mutation status of 986_987insTPAS, The gene TRMO has a mutation status of P15P, The gene DAB2IP has a mutation status of R1103C, The gene ASB6 has a mutation status of R32R, The gene VAV2 has a mutation status of Y159Y, The gene COL5A1 has a mutation status of A1755T, The gene OLFM1 has a mutation status of N280N, The gene LCN9 has a mutation status of T22T, The gene CLIC3 has a mutation status of I225I, The gene DPH7 has a mutation status of L298F, The gene DPH7 has a mutation status of R251Q, The gene CACNA1B has a mutation status of M1756L, The gene FBH1 has a mutation status of D676D, The gene SFMBT2 has a mutation status of K577K, The gene BAMBI has a mutation status of G108A, The gene VSTM4 has a mutation status of S56C, The gene BICC1 has a mutation status of P601P, The gene ANK3 has a mutation status of F1348S, The gene HKDC1 has a mutation status of H338H, The gene ZSWIM8 has a mutation status of G1084G, The gene BMPR1A has a mutation status of R120Q, The gene PIK3AP1 has a mutation status of E551K, The gene ENTPD7 has a mutation status of Q405Q, The gene DCLRE1A has a mutation status of R1002C, The gene ADGRA1 has a mutation status of D444D, The gene ADGRA1 has a mutation status of L290V, The gene EPS8L2 has a mutation status of V677L, The gene OR51Q1 has a mutation status of R167*, The gene FAM160A2 has a mutation status of L784L, The gene PPFIBP2 has a mutation status of C556S, The gene CTR9 has a mutation status of N922S, The gene CD82 has a mutation status of R167C, The gene ARHGAP1 has a mutation status of P52Q, The gene TRIM51 has a mutation status of D175N, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene SMTNL1 has a mutation status of G227R, The gene PELI3 has a mutation status of N240K, The gene IGHMBP2 has a mutation status of G801G, The gene ARHGEF17 has a mutation status of F1114F, The gene SYTL2 has a mutation status of G184G, The gene GRM5 has a mutation status of V709I, The gene FAT3 has a mutation status of S963S, The gene DYNC2H1 has a mutation status of L2599L, The gene SIDT2 has a mutation status of T650T, The gene TECTA has a mutation status of A1970T, The gene TBRG1 has a mutation status of P288P, The gene ROBO4 has a mutation status of T404A, The gene ADAMTS15 has a mutation status of S417S, The gene ERC1 has a mutation status of R335Q, The gene FGF23 has a mutation status of V83V, The gene USP5 has a mutation status of G215F, The gene MANSC1 has a mutation status of K32K, The gene CASC1 has a mutation status of E442E, The gene TSPAN11 has a mutation status of T74T, The gene SENP1 has a mutation status of H218Y, The gene DHH has a mutation status of P19P, The gene KRT7 has a mutation status of D139N, The gene KRT6B has a mutation status of G538G, The gene TNS2 has a mutation status of G603E, The gene GPR84 has a mutation status of P163T, The gene ITGA7 has a mutation status of R1014Q, The gene CCDC38 has a mutation status of D316G, The gene FOXN4 has a mutation status of A399T, The gene MYO1H has a mutation status of E73K, The gene RNFT2 has a mutation status of L174L, The gene ABCB9 has a mutation status of V121M, The gene ATP6V0A2 has a mutation status of D318D, The gene RNF17 has a mutation status of S633G, The gene DIS3 has a mutation status of S557F, The gene PIBF1 has a mutation status of S521S, The gene IRS2 has a mutation status of P1265P, The gene COL4A1 has a mutation status of P1096P, The gene OR4K15 has a mutation status of V270D, The gene OR11H4 has a mutation status of R234R, The gene OR5AU1 has a mutation status of N294I, The gene SCFD1 has a mutation status of V341D, The gene KLHDC1 has a mutation status of L263L, The gene MAP4K5 has a mutation status of V701V, The gene PCNX1 has a mutation status of G2338G, The gene AHSA1 has a mutation status of W27R, The gene CCDC88C has a mutation status of A1943V, The gene RIN3 has a mutation status of S614S, The gene SERPINA9 has a mutation status of N167fs, The gene DYNC1H1 has a mutation status of V3212V, The gene CEP170B has a mutation status of P1525H, The gene HERC2 has a mutation status of S895A, The gene FMN1 has a mutation status of T325T, The gene CDAN1 has a mutation status of C1175Y, The gene EPB42 has a mutation status of D33E, The gene AQP9 has a mutation status of L134L, The gene MYO1E has a mutation status of T560I, The gene HERC1 has a mutation status of P1366P, The gene MAP2K5 has a mutation status of P214A, The gene NEO1 has a mutation status of R486R, The gene CYP11A1 has a mutation status of Y80N, The gene ADAMTS7 has a mutation status of A423A, The gene TM6SF1 has a mutation status of V155L, The gene MFGE8 has a mutation status of Q334fs, The gene TARS3 has a mutation status of L652V, The gene RGS11 has a mutation status of I348I, The gene AXIN1 has a mutation status of G74G, The gene PGAP6 has a mutation status of P150P, The gene RHBDL1 has a mutation status of N54N, The gene SSTR5 has a mutation status of P173P, The gene CACNA1H has a mutation status of A2108A, The gene PKD1 has a mutation status of I4105L, The gene DNASE1L2 has a mutation status of I191F, The gene ZNF205 has a mutation status of N217Y, The gene DNAH3 has a mutation status of A1613S, The gene USP31 has a mutation status of Y371C, The gene PRKCB has a mutation status of R238R, The gene SLC38A7 has a mutation status of L70L, The gene CDH8 has a mutation status of E675E, The gene HAS3 has a mutation status of V241V, The gene SF3B3 has a mutation status of T1100T, The gene CMIP has a mutation status of S517S, The gene CDH15 has a mutation status of T208T, The gene TSR1 has a mutation status of I450T, The gene ALOX15 has a mutation status of Y56Y, The gene CXCL16 has a mutation status of M1T, The gene MINK1 has a mutation status of Y881Y, The gene DERL2 has a mutation status of F49F, The gene TNK1 has a mutation status of R456Q, The gene MPDU1 has a mutation status of A52S, The gene DHRS7C has a mutation status of L66Q, The gene LLGL1 has a mutation status of Q20E, The gene KSR1 has a mutation status of T347M, The gene RSKR has a mutation status of D126H, The gene MRM1 has a mutation status of V149P, The gene CDC6 has a mutation status of R94*, The gene KRTAP4-11 has a mutation status of H136R, The gene KRT33B has a mutation status of C26Y, The gene KRT15 has a mutation status of E377G, The gene FKBP10 has a mutation status of P458P, The gene COASY has a mutation status of G295G, The gene FMNL1 has a mutation status of R1048Q, The gene MRPL10 has a mutation status of P226P, The gene MYCBPAP has a mutation status of GSQKA669del, The gene WFIKKN2 has a mutation status of H42H, The gene DGKE has a mutation status of W452*, The gene TLK2 has a mutation status of T515T, The gene MARCHF10 has a mutation status of L754V, The gene TANC2 has a mutation status of S1147P, The gene KCNJ16 has a mutation status of K239K, The gene GPR142 has a mutation status of P454fs, The gene CASKIN2 has a mutation status of K21K, The gene DNAH17 has a mutation status of S2286L, The gene NPTX1 has a mutation status of E52*, The gene NPTX1 has a mutation status of G50V, The gene RPTOR has a mutation status of T1257T, The gene L3MBTL4 has a mutation status of M163I, The gene LAMA1 has a mutation status of N1498N, The gene PSMA8 has a mutation status of A202T, The gene TRAPPC8 has a mutation status of P1194P, The gene ZNF24 has a mutation status of L143F, The gene ZNF532 has a mutation status of S284S, The gene SERPINB13 has a mutation status of N157N, The gene REXO1 has a mutation status of E962del, The gene ANKRD24 has a mutation status of G639G, The gene TICAM1 has a mutation status of R532R, The gene DENND1C has a mutation status of R759R, The gene ADGRE1 has a mutation status of T325A, The gene MUC16 has a mutation status of V13518L, The gene ZNF846 has a mutation status of H199H, The gene ANGPTL6 has a mutation status of G435S, The gene SMARCA4 has a mutation status of R1192H, The gene TRIR has a mutation status of M73I, The gene NOTCH3 has a mutation status of R75P, The gene OR10H1 has a mutation status of R139W, The gene TPM4 has a mutation status of E69del, The gene TSSK6 has a mutation status of K225K, The gene ZNF43 has a mutation status of I160I, The gene ZNF99 has a mutation status of I200M, The gene ZNF91 has a mutation status of M79I, The gene TSHZ3 has a mutation status of S325C, The gene SIPA1L3 has a mutation status of E1564Q, The gene FCGBP has a mutation status of K3883K, The gene NECTIN2 has a mutation status of V315I, The gene APOE has a mutation status of A304A, The gene KLC3 has a mutation status of E319K, The gene IRF2BP1 has a mutation status of S558S, The gene STRN4 has a mutation status of D416E, The gene SAE1 has a mutation status of V292A, The gene DHX34 has a mutation status of V394V, The gene NOP53 has a mutation status of Y193Y, The gene LIG1 has a mutation status of L454L, The gene PLEKHA4 has a mutation status of R91R, The gene NAPSA has a mutation status of T86M, The gene SYT3 has a mutation status of L475L, The gene ZNF816 has a mutation status of R529K, The gene ZNF415 has a mutation status of R291W, The gene ZNF677 has a mutation status of Y183Y, The gene CACNG6 has a mutation status of A17fs, The gene TNNT1 has a mutation status of R265R, The gene PTPRH has a mutation status of H987H, The gene MZF1 has a mutation status of E642K, The gene DDRGK1 has a mutation status of R147Q, The gene NECAB3 has a mutation status of P258L, The gene NCOA6 has a mutation status of P1758H, The gene CHD6 has a mutation status of Q1624P, The gene PREX1 has a mutation status of L1080L, The gene BMP7 has a mutation status of Q49Q, The gene SOX18 has a mutation status of A129A, The gene RBM11 has a mutation status of E6Q, The gene DNMT3L has a mutation status of E12K, The gene COL6A2 has a mutation status of R843Q, The gene ARVCF has a mutation status of R397W, The gene PPIL2 has a mutation status of S371S, The gene NF2 has a mutation status of Q389*, The gene MICALL1 has a mutation status of L344R, The gene CACNA1I has a mutation status of I811I, The gene EP300 has a mutation status of M556V, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PHF21B has a mutation status of P83P, The gene ALG12 has a mutation status of A213A, The gene WWC3 has a mutation status of L844V, The gene FANCB has a mutation status of T663A, The gene TAB3 has a mutation status of Q522Q, The gene FAM47A has a mutation status of L721F, The gene CFAP47 has a mutation status of P478S, The gene FAM47C has a mutation status of P572P, The gene WNK3 has a mutation status of L98W, The gene MAGED2 has a mutation status of G8L, The gene STARD8 has a mutation status of S694P, The gene PDZD11 has a mutation status of P27P, The gene RPL36A has a mutation status of R24W, The gene KCNE5 has a mutation status of 92_93DE>E*, The gene BCORL1 has a mutation status of P384T, The gene CCDC160 has a mutation status of Y201C, The gene ADGRG4 has a mutation status of Y490H, The gene MAGEC2 has a mutation status of P77S, The gene MAGEA4 has a mutation status of R306H, The gene MAGEA6 has a mutation status of K115E, The gene IRAK1 has a mutation status of T304I, The gene SPRY3 has a mutation status of Q116Q, The gene MT-CO3 has a mutation status of W57W, The gene MT-ND6 has a mutation status of W158W, The gene MT-CYB has a mutation status of I153T
KIPAN
The gene CHD5 has a mutation status of L47H, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene DDI2 has a mutation status of V15V, The gene CSMD2 has a mutation status of A3234A, The gene INSL5 has a mutation status of L28F, The gene LRRC53 has a mutation status of Q360H, The gene NBPF26 has a mutation status of A267A, The gene NBPF20 has a mutation status of L3357L, The gene NBPF10 has a mutation status of V1509V, The gene MINDY1 has a mutation status of S163S, The gene PEAR1 has a mutation status of Q957H, The gene SPTA1 has a mutation status of A871V, The gene ZBTB41 has a mutation status of Q884Q, The gene IGFN1 has a mutation status of K1635E, The gene SYT14 has a mutation status of S133L, The gene PACC1 has a mutation status of F83F, The gene ACTN2 has a mutation status of I461I, The gene FMN2 has a mutation status of P1121P, The gene ASAP2 has a mutation status of H666H, The gene ITSN2 has a mutation status of A397S, The gene CYP1B1 has a mutation status of Y249S, The gene EML4 has a mutation status of Y702C, The gene EPAS1 has a mutation status of G686R, The gene EPCAM has a mutation status of A135T, The gene FAM161A has a mutation status of V126I, The gene PROKR1 has a mutation status of R144C, The gene DQX1 has a mutation status of D341N, The gene WIPF1 has a mutation status of G148G, The gene TTN has a mutation status of Y26704C, The gene TTN has a mutation status of H22376H, The gene ANKAR has a mutation status of F1154fs, The gene PARD3B has a mutation status of G1179G, The gene NYAP2 has a mutation status of S624L, The gene CHL1 has a mutation status of A46A, The gene PRRT3 has a mutation status of R421*, The gene SYN2 has a mutation status of P105A, The gene NBEAL2 has a mutation status of V1515G, The gene CELSR3 has a mutation status of I893T, The gene LRIG1 has a mutation status of I610I, The gene CRYBG3 has a mutation status of G1680D, The gene TMEM39A has a mutation status of L245Q, The gene NMNAT3 has a mutation status of R128P, The gene GPR149 has a mutation status of V127fs, The gene PLCH1 has a mutation status of T263M, The gene LRRC34 has a mutation status of R391H, The gene USP13 has a mutation status of M499I, The gene SOX2 has a mutation status of M217I, The gene ATP11B has a mutation status of F96F, The gene TMEM44 has a mutation status of A4A, The gene FAM193A has a mutation status of P68P, The gene STX18 has a mutation status of K46fs, The gene STX18 has a mutation status of 37_44ELFRRSPR>G, The gene USP17L5 has a mutation status of P243T, The gene STIM2 has a mutation status of S523L, The gene NIPAL1 has a mutation status of S158C, The gene GSX2 has a mutation status of L163F, The gene UGT2A3 has a mutation status of I370I, The gene DSPP has a mutation status of S1133S, The gene PKD2 has a mutation status of D120E, The gene TACR3 has a mutation status of C311fs, The gene PRMT9 has a mutation status of K243E, The gene FAM149A has a mutation status of P265P, The gene DNAH5 has a mutation status of L4191P, The gene PDZD2 has a mutation status of T649I, The gene PRLR has a mutation status of V253A, The gene CPLANE1 has a mutation status of Y2674S, The gene CPLANE1 has a mutation status of L2654L, The gene RICTOR has a mutation status of V1003L, The gene RIOK2 has a mutation status of P34P, The gene APC has a mutation status of 2117_2118insA, The gene RNF14 has a mutation status of R6*, The gene CLK4 has a mutation status of G171G, The gene TRIM40 has a mutation status of S112S, The gene GTF2H4 has a mutation status of H366Q, The gene TCF19 has a mutation status of V247F, The gene KCNK5 has a mutation status of Q41H, The gene RRP36 has a mutation status of P34T, The gene METTL24 has a mutation status of R66R, The gene NOX3 has a mutation status of W481fs, The gene SLC22A2 has a mutation status of I398I, The gene NUDT1 has a mutation status of E73E, The gene EIF2AK1 has a mutation status of I604T, The gene HECW1 has a mutation status of H49H, The gene FKBP6 has a mutation status of R204L, The gene TMEM270 has a mutation status of L145L, The gene FAM237B has a mutation status of M75I, The gene SLC12A9 has a mutation status of S438G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of V1672D, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene MUC17 has a mutation status of P1319L, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene ATP6V0A4 has a mutation status of S500R, The gene MGAM has a mutation status of S2267S, The gene PRSS1 has a mutation status of N77N, The gene NOBOX has a mutation status of L410P, The gene ZNF596 has a mutation status of N207I, The gene MYOM2 has a mutation status of V245A, The gene MTMR9 has a mutation status of K181Q, The gene USP17L7 has a mutation status of H334L, The gene GFRA2 has a mutation status of A193G, The gene DMTN has a mutation status of N142K, The gene DOCK5 has a mutation status of D745N, The gene CHRNA6 has a mutation status of P58R, The gene BHLHE22 has a mutation status of G225fs, The gene TERF1 has a mutation status of I108V, The gene PSKH2 has a mutation status of S241R, The gene COLEC10 has a mutation status of A36T, The gene EPPK1 has a mutation status of A2633del, The gene PLEC has a mutation status of A4684A, The gene HGH1 has a mutation status of G54V, The gene MROH1 has a mutation status of I874I, The gene HSF1 has a mutation status of P364P, The gene SCRT1 has a mutation status of A133S, The gene RECQL4 has a mutation status of P103L, The gene TOPORS has a mutation status of V297V, The gene NOL6 has a mutation status of D789G, The gene PRUNE2 has a mutation status of T1618T, The gene FGD3 has a mutation status of G410C, The gene FRRS1L has a mutation status of R51A, The gene FKBP15 has a mutation status of E201K, The gene ADGRD2 has a mutation status of A495V, The gene SPTAN1 has a mutation status of E2433K, The gene HMCN2 has a mutation status of G833R, The gene CCDC187 has a mutation status of L747L, The gene RNF224 has a mutation status of T74T, The gene CAMK1D has a mutation status of G139G, The gene EBLN1 has a mutation status of N7T, The gene MTPAP has a mutation status of A219T, The gene AL117339.4 has a mutation status of G115G, The gene FO681492.1 has a mutation status of S6L, The gene WASHC2A has a mutation status of G698R, The gene CDH23 has a mutation status of V1299I, The gene NFKB2 has a mutation status of T642T, The gene ACSL5 has a mutation status of 75_76insTM, The gene TACC2 has a mutation status of E2053K, The gene CLRN3 has a mutation status of T173M, The gene PPP2R2D has a mutation status of G25G, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of L3616L, The gene MUC5AC has a mutation status of S3630P, The gene MUC5AC has a mutation status of T3668P, The gene OR52J3 has a mutation status of V151V, The gene OR52E8 has a mutation status of T143K, The gene PLEKHA7 has a mutation status of V165M, The gene PRDM11 has a mutation status of C22Y, The gene OR9G1 has a mutation status of I196F, The gene SLC22A24 has a mutation status of H456Y, The gene PLCB3 has a mutation status of E277V, The gene RPS6KA4 has a mutation status of G346V, The gene CHKA has a mutation status of G193G, The gene SMIM38 has a mutation status of D37N, The gene INPPL1 has a mutation status of A902S, The gene KLHL35 has a mutation status of R17C, The gene OR6X1 has a mutation status of V198I, The gene OR4D5 has a mutation status of I277V, The gene OR8B8 has a mutation status of P79R, The gene KCNA5 has a mutation status of I359V, The gene PEX5 has a mutation status of M369fs, The gene STRAP has a mutation status of N181T, The gene C2CD5 has a mutation status of T505A, The gene PTHLH has a mutation status of H41Y, The gene LRRK2 has a mutation status of R493C, The gene FKBP11 has a mutation status of R4R, The gene PRPF40B has a mutation status of F38L, The gene KRT82 has a mutation status of E351K, The gene MAP3K12 has a mutation status of K525R, The gene ESYT1 has a mutation status of S101R, The gene MON2 has a mutation status of I1029F, The gene TRHDE has a mutation status of T671S, The gene KCNC2 has a mutation status of H19Q, The gene NR2C1 has a mutation status of T258T, The gene VEZT has a mutation status of I722N, The gene STAB2 has a mutation status of S909L, The gene TDG has a mutation status of 260_261insLCY, The gene PTPN11 has a mutation status of D180D, The gene DTX1 has a mutation status of A309P, The gene CFAP73 has a mutation status of L188P, The gene RNF34 has a mutation status of E339*, The gene WDR66 has a mutation status of R311K, The gene DNAH10 has a mutation status of I4533V, The gene ZNF140 has a mutation status of H93Y, The gene ZNF268 has a mutation status of P695S, The gene SGCG has a mutation status of I218T, The gene KATNAL1 has a mutation status of R395H, The gene IPO5 has a mutation status of P877L, The gene LIG4 has a mutation status of K782N, The gene CCDC177 has a mutation status of G615C, The gene ADSS1 has a mutation status of D58D, The gene OTUD7A has a mutation status of G286G, The gene LTK has a mutation status of R59R, The gene ANKDD1A has a mutation status of L516L, The gene ARID3B has a mutation status of R455fs, The gene GOLGA6L9 has a mutation status of K124Q, The gene GOLGA6L9 has a mutation status of Q151E, The gene UBE2Q2L has a mutation status of P26P, The gene PRC1 has a mutation status of G558C, The gene PKD1 has a mutation status of R3169Q, The gene NUDT16L1 has a mutation status of E185D, The gene GRIN2A has a mutation status of T333T, The gene TUFM has a mutation status of E335D, The gene ITGAM has a mutation status of V1020fs, The gene ABCC11 has a mutation status of V584I, The gene CLEC18B has a mutation status of S245G, The gene ZZEF1 has a mutation status of R2440W, The gene TP53 has a mutation status of C176F, The gene ELAC2 has a mutation status of R781H, The gene COX10 has a mutation status of N327N, The gene CCL4L2 has a mutation status of P67R, The gene KRT10 has a mutation status of 561_562insGYGGGSSSGG, The gene KRTAP9-6 has a mutation status of G106C, The gene TTC25 has a mutation status of Q538H, The gene GRN has a mutation status of G93R, The gene CDK5RAP3 has a mutation status of G24G, The gene MRPL58 has a mutation status of R141H, The gene RBFOX3 has a mutation status of A8fs, The gene RMC1 has a mutation status of I147V, The gene TNFRSF11A has a mutation status of G429G, The gene NFATC1 has a mutation status of R571I, The gene AC008770.2 has a mutation status of S44P, The gene ZNF763 has a mutation status of V212F, The gene KIAA0355 has a mutation status of Y850fs, The gene ZNF568 has a mutation status of M4I, The gene LRFN1 has a mutation status of E764D, The gene SUPT5H has a mutation status of D456E, The gene SUPT5H has a mutation status of E556D, The gene LYPD4 has a mutation status of R108H, The gene SRRM5 has a mutation status of P176R, The gene CEACAM20 has a mutation status of A189A, The gene QPCTL has a mutation status of A227A, The gene LMTK3 has a mutation status of A1298T, The gene POLD1 has a mutation status of E52E, The gene ASPDH has a mutation status of R4S, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRB2 has a mutation status of N80N, The gene LILRA1 has a mutation status of R296T, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene KIR2DL4 has a mutation status of C97F, The gene SIRPA has a mutation status of L44S, The gene FASTKD5 has a mutation status of L278F, The gene PAK5 has a mutation status of PTM280del, The gene TASP1 has a mutation status of F332I, The gene MATN4 has a mutation status of Q621E, The gene PTGIS has a mutation status of V203I, The gene SYCP2 has a mutation status of Q785K, The gene ABHD16B has a mutation status of L377V, The gene FAM207A has a mutation status of G212G, The gene GGT1 has a mutation status of L24L, The gene SEC14L3 has a mutation status of K194R, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CRLF2 has a mutation status of V313V, The gene ARSF has a mutation status of T343T, The gene ZNF157 has a mutation status of K300N, The gene GPRASP2 has a mutation status of S793fs, The gene STAG2 has a mutation status of Q735*, The gene MAGEC1 has a mutation status of SFSSTLLSIFQSSPERTQSTFEGFAQSPLQIPVSPSSSSTLLSLFQSFSERTQSTFEGFAQSSLQIPVSP205del, The gene MT-ND2 has a mutation status of T303T, The gene MT-CO1 has a mutation status of V83V, The gene MT-ND5 has a mutation status of V24I, The gene MT-ND5 has a mutation status of S99S
SARC
The gene KLHL17 has a mutation status of T640P, The gene NPHP4 has a mutation status of P1035P, The gene NPHP4 has a mutation status of V107M, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene MYOM3 has a mutation status of Q413Q, The gene OPRD1 has a mutation status of A359A, The gene COL8A2 has a mutation status of G560G, The gene COL8A2 has a mutation status of K558R, The gene KLF18 has a mutation status of T606N, The gene JUN has a mutation status of C320Y, The gene LRRIQ3 has a mutation status of K242R, The gene ASB17 has a mutation status of R234I, The gene GFI1 has a mutation status of A166V, The gene FNBP1L has a mutation status of R238H, The gene CELSR2 has a mutation status of R2015K, The gene AP4B1 has a mutation status of R206R, The gene PTGFRN has a mutation status of A182V, The gene ZNF697 has a mutation status of S475S, The gene NBPF12 has a mutation status of L1378V, The gene NBPF11 has a mutation status of Q55H, The gene ARNT has a mutation status of T534T, The gene VPS72 has a mutation status of R147Q, The gene SPRR1B has a mutation status of K60N, The gene GATAD2B has a mutation status of V285A, The gene DENND4B has a mutation status of S1112L, The gene RUSC1 has a mutation status of A335T, The gene SMG5 has a mutation status of D319Y, The gene ETV3L has a mutation status of T183S, The gene GPR161 has a mutation status of D40D, The gene SERPINC1 has a mutation status of D206D, The gene ASPM has a mutation status of P3311L, The gene PTPN7 has a mutation status of H224H, The gene PACC1 has a mutation status of F83F, The gene CENPF has a mutation status of L2756R, The gene RAB3GAP2 has a mutation status of C155C, The gene ITPKB has a mutation status of V914I, The gene GJC2 has a mutation status of G160G, The gene OBSCN has a mutation status of V23M, The gene MAP1LC3C has a mutation status of S137S, The gene HNRNPU has a mutation status of P705S, The gene NT5C1B-RDH14 has a mutation status of R354C, The gene RASGRP3 has a mutation status of P392S, The gene HEATR5B has a mutation status of A435T, The gene MSH6 has a mutation status of R243C, The gene CCDC88A has a mutation status of Q1591H, The gene EGR4 has a mutation status of L304M, The gene RETSAT has a mutation status of A476A, The gene KDM3A has a mutation status of D187E, The gene NEURL3 has a mutation status of A117A, The gene SEPTIN10 has a mutation status of V270V, The gene NCKAP5 has a mutation status of P1211L, The gene SCN9A has a mutation status of Q794*, The gene TTN has a mutation status of I2929R, The gene TTN has a mutation status of N2593N, The gene ITGA4 has a mutation status of S411S, The gene CAVIN2 has a mutation status of E9*, The gene ADAM23 has a mutation status of S242S, The gene SPEG has a mutation status of K3100K, The gene TRPM8 has a mutation status of A156S, The gene COL6A3 has a mutation status of T2880T, The gene SLC6A6 has a mutation status of H72Q, The gene UBP1 has a mutation status of Y433Y, The gene SCN5A has a mutation status of R620H, The gene ZKSCAN7 has a mutation status of Q149K, The gene LIMD1 has a mutation status of A299T, The gene PFKFB4 has a mutation status of R344W, The gene ARIH2OS has a mutation status of A153G, The gene SLC38A3 has a mutation status of V259M, The gene NEK4 has a mutation status of R742C, The gene ITIH1 has a mutation status of A133A, The gene C3orf67 has a mutation status of R746Q, The gene ADAMTS9 has a mutation status of K633T, The gene NEPRO has a mutation status of K240E, The gene CCDC191 has a mutation status of M125fs, The gene STAG1 has a mutation status of D842D, The gene SPSB4 has a mutation status of R88R, The gene MED12L has a mutation status of R468C, The gene CCDC39 has a mutation status of V97V, The gene TNK2 has a mutation status of D735N, The gene KCTD8 has a mutation status of A192G, The gene ADGRL3 has a mutation status of Q64K, The gene WDFY3 has a mutation status of R3149*, The gene ADH4 has a mutation status of Q25Q, The gene LARP1B has a mutation status of L726F, The gene FBXW7 has a mutation status of E409*, The gene DDX60L has a mutation status of N1055S, The gene MFAP3L has a mutation status of P384P, The gene WWC2 has a mutation status of R35W, The gene ADCY2 has a mutation status of G21G, The gene PDZD2 has a mutation status of E1941K, The gene ADAMTS12 has a mutation status of R587C, The gene LIFR has a mutation status of R932H, The gene MTREX has a mutation status of V696L, The gene HTR1A has a mutation status of R333C, The gene NLN has a mutation status of V388M, The gene ARSB has a mutation status of T107A, The gene BHMT2 has a mutation status of A212T, The gene SSBP2 has a mutation status of M213T, The gene CAST has a mutation status of T60T, The gene APC has a mutation status of E1317*, The gene FBN2 has a mutation status of R1021C, The gene TMCO6 has a mutation status of R130Q, The gene PCDHA13 has a mutation status of A592A, The gene RNF44 has a mutation status of V329M, The gene RREB1 has a mutation status of A1469A, The gene CARMIL1 has a mutation status of T375I, The gene BTN2A1 has a mutation status of T289R, The gene TNF has a mutation status of S80P, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene GLO1 has a mutation status of S120*, The gene BMP5 has a mutation status of D169Y, The gene TRDN has a mutation status of D627Y, The gene MYB has a mutation status of C528G, The gene NOX3 has a mutation status of W53L, The gene ARID1B has a mutation status of P533S, The gene RADIL has a mutation status of M1053T, The gene TNRC18 has a mutation status of L1666L, The gene ZNF853 has a mutation status of L329M, The gene C1GALT1 has a mutation status of L176V, The gene SNX13 has a mutation status of K76*, The gene VPS41 has a mutation status of R246R, The gene CCDC201 has a mutation status of A130A, The gene CCDC201 has a mutation status of S127Y, The gene TNS3 has a mutation status of P1124P, The gene ABCA13 has a mutation status of L1545L, The gene LIMK1 has a mutation status of H644P, The gene POM121C has a mutation status of F955F, The gene PDK4 has a mutation status of S337F, The gene CASTOR3 has a mutation status of I115I, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of L570T, The gene MUC3A has a mutation status of P572H, The gene MUC3A has a mutation status of L1361P, The gene MUC3A has a mutation status of S2042S, The gene MUC3A has a mutation status of K2298E, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene MUC17 has a mutation status of R2042Q, The gene LAMB1 has a mutation status of RISELE1647del, The gene STRIP2 has a mutation status of I606I, The gene MGAM has a mutation status of W2427*, The gene MGAM2 has a mutation status of L254M, The gene PRSS1 has a mutation status of N77N, The gene OR6B1 has a mutation status of A258V, The gene CNTNAP2 has a mutation status of S693L, The gene CUL1 has a mutation status of E124K, The gene AOC1 has a mutation status of R719Q, The gene KCNH2 has a mutation status of A40A, The gene PREX2 has a mutation status of H446N, The gene TRPA1 has a mutation status of D547D, The gene STAU2 has a mutation status of G176G, The gene ZFHX4 has a mutation status of K3407M, The gene HEY1 has a mutation status of P163P, The gene FER1L6 has a mutation status of L1284L, The gene AGO2 has a mutation status of P295L, The gene HGH1 has a mutation status of P53T, The gene MROH1 has a mutation status of D521N, The gene MFSD3 has a mutation status of L283S, The gene GLDC has a mutation status of P166P, The gene MPDZ has a mutation status of T1989I, The gene ABCA1 has a mutation status of I1103V, The gene PAPPA has a mutation status of T648M, The gene ADGRD2 has a mutation status of L729I, The gene WDR34 has a mutation status of P32L, The gene NACC2 has a mutation status of Q143H, The gene PFKP has a mutation status of E62K, The gene CCDC3 has a mutation status of H135H, The gene TMEM236 has a mutation status of W66C, The gene MRC1 has a mutation status of L88L, The gene LINC02881 has a mutation status of K97E, The gene OR13A1 has a mutation status of T28T, The gene RBP3 has a mutation status of T361T, The gene ZNF488 has a mutation status of S100R, The gene WDFY4 has a mutation status of G1235G, The gene PARG has a mutation status of D555Y, The gene PRF1 has a mutation status of S331S, The gene TBATA has a mutation status of V47M, The gene MYOZ1 has a mutation status of G95E, The gene CPEB3 has a mutation status of A199E, The gene CPEB3 has a mutation status of P196H, The gene CYP2C9 has a mutation status of D143D, The gene ALDH18A1 has a mutation status of L455fs, The gene NRAP has a mutation status of V545V, The gene TIAL1 has a mutation status of Q230H, The gene DPYSL4 has a mutation status of G441A, The gene LRRC27 has a mutation status of E359D, The gene SIGIRR has a mutation status of S392S, The gene LSP1 has a mutation status of Q95H, The gene OR56B1 has a mutation status of I183T, The gene APBB1 has a mutation status of R451C, The gene LRRC4C has a mutation status of R175C, The gene MADD has a mutation status of R1077Q, The gene OR9G1 has a mutation status of I196F, The gene FADS3 has a mutation status of A162V, The gene PCNX3 has a mutation status of N1852N, The gene TMEM151A has a mutation status of T308T, The gene SPTBN2 has a mutation status of E403G, The gene C11orf80 has a mutation status of P507A, The gene CARNS1 has a mutation status of G734S, The gene SHANK2 has a mutation status of P1580P, The gene ZNF705E has a mutation status of Q18K, The gene AP000812.5 has a mutation status of T100A, The gene LRRC32 has a mutation status of R251Q, The gene DDIAS has a mutation status of A427E, The gene FAT3 has a mutation status of R1914C, The gene MMP1 has a mutation status of F464L, The gene MPZL3 has a mutation status of W90*, The gene OR10S1 has a mutation status of P321H, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene KRAS has a mutation status of G12D, The gene FGD4 has a mutation status of L279I, The gene RAPGEF3 has a mutation status of R8R, The gene RAPGEF3 has a mutation status of R5M, The gene XPOT has a mutation status of R102*, The gene DEPDC4 has a mutation status of P3L, The gene BTBD11 has a mutation status of D625G, The gene INTS6 has a mutation status of K256R, The gene CCDC168 has a mutation status of P1956P, The gene OR11H6 has a mutation status of R311L, The gene ARHGEF40 has a mutation status of P897P, The gene NIN has a mutation status of G60G, The gene KTN1 has a mutation status of Q202Q, The gene SYNE2 has a mutation status of L5126L, The gene PCNX1 has a mutation status of T2099I, The gene INF2 has a mutation status of A945V, The gene HERC2 has a mutation status of V1740I, The gene HERC2 has a mutation status of S895A, The gene JMJD7-PLA2G4B has a mutation status of I636I, The gene MINDY2 has a mutation status of A17A, The gene VPS13C has a mutation status of N599K, The gene HMG20A has a mutation status of E306G, The gene HYKK has a mutation status of H202R, The gene ADAMTS7 has a mutation status of D857E, The gene ADAMTS7 has a mutation status of P635P, The gene TELO2 has a mutation status of L196L, The gene FAHD1 has a mutation status of P54P, The gene NTHL1 has a mutation status of R92C, The gene CLDN9 has a mutation status of D215N, The gene SLX4 has a mutation status of R278Q, The gene RBFOX1 has a mutation status of T124T, The gene ABCC1 has a mutation status of R98W, The gene ZNF747 has a mutation status of F190F, The gene DRC7 has a mutation status of C776Y, The gene EXOC3L1 has a mutation status of R67C, The gene ZFP90 has a mutation status of P177S, The gene CHST4 has a mutation status of D110Y, The gene ATMIN has a mutation status of E67G, The gene GSE1 has a mutation status of P96P, The gene SERPINF2 has a mutation status of S432S, The gene AC087498.1 has a mutation status of P10P, The gene ZZEF1 has a mutation status of P2950S, The gene RABEP1 has a mutation status of R834R, The gene YBX2 has a mutation status of G67G, The gene SPEM2 has a mutation status of V470G, The gene TP53 has a mutation status of G245S, The gene SPACA3 has a mutation status of T108N, The gene MRM1 has a mutation status of V149P, The gene GJD3 has a mutation status of P244T, The gene ITGA2B has a mutation status of L1014L, The gene EPN3 has a mutation status of S38S, The gene KIF2B has a mutation status of R36L, The gene TSPOAP1 has a mutation status of V1786M, The gene HEATR6 has a mutation status of A1163D, The gene LLGL2 has a mutation status of P955R, The gene TMEM200C has a mutation status of S546C, The gene GAREM1 has a mutation status of G796G, The gene RAX has a mutation status of A124A, The gene IZUMO4 has a mutation status of W41*, The gene MYO1F has a mutation status of Q1013H, The gene MUC16 has a mutation status of S10457P, The gene PPAN-P2RY11 has a mutation status of A206T, The gene KRI1 has a mutation status of R592Q, The gene ARRDC2 has a mutation status of G245G, The gene GDF15 has a mutation status of G96G, The gene REX1BD has a mutation status of P12T, The gene LSM14A has a mutation status of E32D, The gene ZNF781 has a mutation status of N311N, The gene SIPA1L3 has a mutation status of L352V, The gene TTC9B has a mutation status of R128R, The gene TTC9B has a mutation status of Q126K, The gene CEACAM16 has a mutation status of A55A, The gene PRR12 has a mutation status of S865G, The gene ATF5 has a mutation status of A221A, The gene SHANK1 has a mutation status of H1590H, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene NCR1 has a mutation status of A21A, The gene BRSK1 has a mutation status of R445L, The gene PEG3 has a mutation status of R221P, The gene ANGPT4 has a mutation status of R344W, The gene DDRGK1 has a mutation status of E199E, The gene BTBD3 has a mutation status of G353G, The gene KIF16B has a mutation status of E871V, The gene ACSS1 has a mutation status of R411Q, The gene OSER1 has a mutation status of F260F, The gene CDH26 has a mutation status of Q426L, The gene MTG2 has a mutation status of 55_56QE>HK, The gene MTG2 has a mutation status of G108E, The gene RTEL1 has a mutation status of S236C, The gene HSPA13 has a mutation status of A161S, The gene DOP1B has a mutation status of H1375L, The gene BACE2 has a mutation status of D144D, The gene IL17RA has a mutation status of L26M, The gene CECR2 has a mutation status of P754L, The gene SUSD2 has a mutation status of R442W, The gene MYO18B has a mutation status of L1942I, The gene KCNJ4 has a mutation status of V93M, The gene PKDREJ has a mutation status of L2150L, The gene DMD has a mutation status of E767K, The gene FAM47B has a mutation status of P285P, The gene IQSEC2 has a mutation status of E222*, The gene BX276092.9 has a mutation status of L453S, The gene ARMCX2 has a mutation status of Q503Q, The gene SOX3 has a mutation status of V254M, The gene BGN has a mutation status of N37N, The gene L1CAM has a mutation status of R322Q, The gene PLXNA3 has a mutation status of V276M, The gene NLGN4Y has a mutation status of N515N, The gene MT-CO2 has a mutation status of P145P, The gene MT-ND4 has a mutation status of T134T
COAD
The gene MEGF6 has a mutation status of Q814*, The gene PRAMEF9 has a mutation status of A352V, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene ZNF436 has a mutation status of S347L, The gene TMEM54 has a mutation status of F133S, The gene MACF1 has a mutation status of R2501L, The gene TMCO2 has a mutation status of S28C, The gene ARTN has a mutation status of G118A, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene KLF18 has a mutation status of A428T, The gene TRABD2B has a mutation status of P459P, The gene ZFYVE9 has a mutation status of R254K, The gene LRRC39 has a mutation status of R21fs, The gene DENND2C has a mutation status of E55fs, The gene NBPF10 has a mutation status of L891V, The gene NBPF9 has a mutation status of V776A, The gene CRNN has a mutation status of T338S, The gene QSOX1 has a mutation status of G140G, The gene CRB1 has a mutation status of C836Y, The gene MIA3 has a mutation status of L1085V, The gene LYPD8 has a mutation status of Q24P, The gene SPTBN1 has a mutation status of M133T, The gene SPTBN1 has a mutation status of R1432W, The gene FAM136A has a mutation status of H227Y, The gene REG3G has a mutation status of P91P, The gene DNAH6 has a mutation status of E1112*, The gene DNAH6 has a mutation status of G1275V, The gene FOXI3 has a mutation status of S337N, The gene NCK2 has a mutation status of T139T, The gene IMP4 has a mutation status of S180L, The gene PLEKHB2 has a mutation status of A117V, The gene LCT has a mutation status of Q511Q, The gene NEB has a mutation status of D7430V, The gene RBMS1 has a mutation status of T393T, The gene TTN has a mutation status of G7623R, The gene DNAH7 has a mutation status of A1406A, The gene ADAM23 has a mutation status of V306A, The gene SMARCAL1 has a mutation status of S200S, The gene CXCR2 has a mutation status of V82I, The gene PTPRN has a mutation status of A636T, The gene SLC4A3 has a mutation status of D894P, The gene SNED1 has a mutation status of Q1242P, The gene HDLBP has a mutation status of V801A, The gene SYN2 has a mutation status of P105A, The gene KLHL18 has a mutation status of Y386C, The gene DNAH12 has a mutation status of E2938E, The gene ROBO2 has a mutation status of A54V, The gene TOMM70 has a mutation status of Y548C, The gene OSBPL11 has a mutation status of G442E, The gene NSD2 has a mutation status of G1172G, The gene ACOX3 has a mutation status of V643M, The gene RBM47 has a mutation status of R137H, The gene ALPK1 has a mutation status of R1084Q, The gene FREM3 has a mutation status of L1284P, The gene DCHS2 has a mutation status of V2759V, The gene FSTL5 has a mutation status of V421M, The gene CFAP97 has a mutation status of E78Q, The gene SLC6A19 has a mutation status of L461V, The gene EGFLAM has a mutation status of R444Q, The gene VCAN has a mutation status of F3308L, The gene LNPEP has a mutation status of Y288Y, The gene SYNPO has a mutation status of Q431H, The gene RANBP9 has a mutation status of T443S, The gene ALDH5A1 has a mutation status of A193A, The gene SLC17A3 has a mutation status of N332Y, The gene H1-2 has a mutation status of A180A, The gene PRRC2A has a mutation status of G909R, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DRB1 has a mutation status of W38E, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene ADGRF1 has a mutation status of V45F, The gene COL19A1 has a mutation status of D852N, The gene ADGRG6 has a mutation status of V35V, The gene TULP4 has a mutation status of P772P, The gene FOXL3 has a mutation status of R175C, The gene NUDT1 has a mutation status of L146M, The gene FOXK1 has a mutation status of R259R, The gene SLC29A4 has a mutation status of G145G, The gene MACC1 has a mutation status of D687fs, The gene NFE2L3 has a mutation status of G138E, The gene AC004080.3 has a mutation status of R108*, The gene HIBADH has a mutation status of A116V, The gene AEBP1 has a mutation status of T452S, The gene PSPH has a mutation status of L68P, The gene ZNF736 has a mutation status of S326L, The gene POR has a mutation status of C569Y, The gene VPS50 has a mutation status of L891L, The gene TRRAP has a mutation status of R695H, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S395T, The gene MUC3A has a mutation status of T2263S, The gene VGF has a mutation status of N401K, The gene TES has a mutation status of H14H, The gene CADPS2 has a mutation status of T589A, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene ZNF786 has a mutation status of R619G, The gene PEBP4 has a mutation status of Q221P, The gene LETM2 has a mutation status of L310F, The gene NSMAF has a mutation status of S110T, The gene VCPIP1 has a mutation status of S350S, The gene COL14A1 has a mutation status of L1496L, The gene KCNQ3 has a mutation status of P693P, The gene KCNK9 has a mutation status of D289D, The gene EPPK1 has a mutation status of A2633del, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene FAM214B has a mutation status of L310P, The gene GNE has a mutation status of R13S, The gene S1PR3 has a mutation status of G159W, The gene FGD3 has a mutation status of P660P, The gene CAVIN4 has a mutation status of P327H, The gene ZNF462 has a mutation status of P103L, The gene CEL has a mutation status of R185Q, The gene SURF1 has a mutation status of D108N, The gene ADAMTSL2 has a mutation status of A840A, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene TPRN has a mutation status of N499N, The gene ITGA8 has a mutation status of A1063A, The gene AGAP4 has a mutation status of Q20Q, The gene DNTT has a mutation status of P11P, The gene MMS19 has a mutation status of R983C, The gene FAM53B has a mutation status of D75D, The gene CTBP2 has a mutation status of P418P, The gene JAKMIP3 has a mutation status of R166R, The gene SPRN has a mutation status of A80A, The gene MUC5AC has a mutation status of R477K, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of G1443R, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P2233R, The gene OR52N2 has a mutation status of Y125N, The gene HARBI1 has a mutation status of P241fs, The gene OR4A16 has a mutation status of K22Q, The gene OR4A16 has a mutation status of I319A, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR9G1 has a mutation status of I196F, The gene OR10Q1 has a mutation status of P133L, The gene CCDC87 has a mutation status of G512E, The gene PITPNM1 has a mutation status of G53R, The gene KLHL35 has a mutation status of H5R, The gene MYO7A has a mutation status of R1818R, The gene FAT3 has a mutation status of Y463*, The gene CARD16 has a mutation status of I62T, The gene RPUSD4 has a mutation status of K230G, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene GXYLT1 has a mutation status of C414H, The gene KRT82 has a mutation status of A504D, The gene KRT6B has a mutation status of G133R, The gene ANKRD52 has a mutation status of H759H, The gene OSBPL8 has a mutation status of D307E, The gene DEPDC4 has a mutation status of K171R, The gene VPS29 has a mutation status of S18S, The gene OAS3 has a mutation status of R195C, The gene B3GNT4 has a mutation status of S35S, The gene PITPNM2 has a mutation status of R991C, The gene GTF2H3 has a mutation status of V110I, The gene FREM2 has a mutation status of S705S, The gene AL445989.1 has a mutation status of G7S, The gene DACH1 has a mutation status of 81_82insGG, The gene ADPRHL1 has a mutation status of E1726G, The gene POTEG has a mutation status of S126S, The gene TTC6 has a mutation status of E252D, The gene GPR137C has a mutation status of L127L, The gene HIF1A has a mutation status of Y660N, The gene ZFYVE26 has a mutation status of H1584Q, The gene ZFYVE26 has a mutation status of R255W, The gene GOLGA6L6 has a mutation status of TMWRQEEKIREQEKKIREQEEKIREQEEMMQEQEEKMWEQEEKMCEQEEKMQEQEE643del, The gene GOLGA6L1 has a mutation status of W595R, The gene GOLGA6L1 has a mutation status of E592K, The gene PHGR1 has a mutation status of G48H, The gene DUOX2 has a mutation status of A126S, The gene HERC1 has a mutation status of A399T, The gene ANKDD1A has a mutation status of L516L, The gene ITGA11 has a mutation status of D115N, The gene GOLGA6C has a mutation status of L624P, The gene GOLGA6L10 has a mutation status of C286R, The gene TICRR has a mutation status of S1074P, The gene CHD2 has a mutation status of K173Q, The gene MVP has a mutation status of P491L, The gene KATNB1 has a mutation status of N545N, The gene AC025287.4 has a mutation status of R17R, The gene PABPN1L has a mutation status of G157R, The gene MYO1C has a mutation status of Y613Y, The gene AC004706.3 has a mutation status of R725Q, The gene TP53 has a mutation status of K139fs, The gene KCNAB3 has a mutation status of L291P, The gene TVP23C has a mutation status of I158I, The gene ZNF830 has a mutation status of D109D, The gene CCL4L2 has a mutation status of P67R, The gene NFE2L1 has a mutation status of L286L, The gene MPO has a mutation status of T478T, The gene SMIM5 has a mutation status of V45G, The gene DNAH17 has a mutation status of E2880D, The gene MTCL1 has a mutation status of A276E, The gene TRAPPC8 has a mutation status of D373N, The gene MYO5B has a mutation status of T1546T, The gene CDH19 has a mutation status of F50C, The gene C18orf63 has a mutation status of V550M, The gene SALL3 has a mutation status of A185L, The gene SALL3 has a mutation status of P532S, The gene PIAS4 has a mutation status of A409T, The gene PTPRS has a mutation status of A952S, The gene MUC16 has a mutation status of T12336L, The gene CACNA1A has a mutation status of N1115N, The gene KCNN1 has a mutation status of P37P, The gene LRRC25 has a mutation status of P303S, The gene KLHL26 has a mutation status of H45H, The gene ZNF90 has a mutation status of M598I, The gene ZNF729 has a mutation status of I424I, The gene ZNF536 has a mutation status of N1177N, The gene RYR1 has a mutation status of N2213H, The gene RYR1 has a mutation status of G4975C, The gene CIC has a mutation status of Q420fs, The gene CIC has a mutation status of L421fs, The gene NKPD1 has a mutation status of H147H, The gene FOXA3 has a mutation status of A179V, The gene SLC8A2 has a mutation status of L334L, The gene GFY has a mutation status of P510A, The gene LILRB3 has a mutation status of V574A, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of G12A, The gene KIR2DL3 has a mutation status of P224S, The gene KIR2DL1 has a mutation status of T91K, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of T286S, The gene KIR3DL1 has a mutation status of D163N, The gene PEG3 has a mutation status of F1291F, The gene SIRPA has a mutation status of L44S, The gene TMC2 has a mutation status of G331V, The gene CFAP61 has a mutation status of K707I, The gene CEBPB has a mutation status of G155G, The gene CASS4 has a mutation status of V500A, The gene BIRC7 has a mutation status of P105P, The gene ESS2 has a mutation status of A307A, The gene CLTCL1 has a mutation status of Y1368Y, The gene ZNF280B has a mutation status of D337N, The gene MMP11 has a mutation status of R451R, The gene TPST2 has a mutation status of P332L, The gene AP1B1 has a mutation status of P796T, The gene LARGE1 has a mutation status of V40A, The gene TOM1 has a mutation status of E433K, The gene GTPBP6 has a mutation status of G61R, The gene VCX has a mutation status of A108S, The gene ZNF674 has a mutation status of L25R, The gene EBP has a mutation status of T217M, The gene DGKK has a mutation status of 113_114insATEP, The gene ZXDA has a mutation status of A680A, The gene RLIM has a mutation status of C610C, The gene ARMCX2 has a mutation status of R312H, The gene RBMXL3 has a mutation status of R379Q, The gene SLC25A5 has a mutation status of T221R, The gene IGSF1 has a mutation status of H407Y, The gene AC236972.4 has a mutation status of S1611S, The gene RENBP has a mutation status of T420P, The gene G6PD has a mutation status of D282H, The gene MT-CO2 has a mutation status of L170L, The gene MT-ND4 has a mutation status of F121L, The gene MT-ND5 has a mutation status of T489M, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A
PRAD
The gene SKI has a mutation status of Y254S, The gene CASZ1 has a mutation status of R1246C, The gene VPS13D has a mutation status of I3125I, The gene PRAMEF11 has a mutation status of Q419*, The gene PRAMEF18 has a mutation status of P294P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF19 has a mutation status of P458T, The gene UBR4 has a mutation status of G1507G, The gene ID3 has a mutation status of P91L, The gene ARID1A has a mutation status of D1961fs, The gene CSMD2 has a mutation status of F842F, The gene YRDC has a mutation status of G247R, The gene CITED4 has a mutation status of P17S, The gene CFAP57 has a mutation status of R414H, The gene PTPRF has a mutation status of R579C, The gene PPM1J has a mutation status of R133G, The gene AC253572.1 has a mutation status of T273S, The gene SETDB1 has a mutation status of I1283I, The gene FLG has a mutation status of H3888Q, The gene OR10Z1 has a mutation status of A133T, The gene CCDC190 has a mutation status of R110H, The gene TP53BP2 has a mutation status of Y356C, The gene SCCPDH has a mutation status of Q31E, The gene OR2T4 has a mutation status of V109L, The gene OR2T11 has a mutation status of S170N, The gene LYPD8 has a mutation status of Q24P, The gene ALK has a mutation status of S439R, The gene BIRC6 has a mutation status of L3202L, The gene ALMS1 has a mutation status of R2263W, The gene MGAT5 has a mutation status of E606K, The gene SPOPL has a mutation status of R240Q, The gene SYN2 has a mutation status of P105A, The gene TRIM71 has a mutation status of C220C, The gene ZNF501 has a mutation status of G196V, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of R2520*, The gene MCM2 has a mutation status of L877F, The gene GRXCR1 has a mutation status of E187K, The gene REST has a mutation status of T205A, The gene FRAS1 has a mutation status of S2055C, The gene ANK2 has a mutation status of G2288V, The gene CLGN has a mutation status of V105L, The gene GAB1 has a mutation status of G231V, The gene LINC02218 has a mutation status of V148F, The gene PLCXD3 has a mutation status of D164E, The gene PARP8 has a mutation status of P366S, The gene TMEM174 has a mutation status of E148E, The gene GLRX has a mutation status of A67T, The gene GRXCR2 has a mutation status of N104S, The gene GALNT10 has a mutation status of L485P, The gene FAM8A1 has a mutation status of L338I, The gene KDM1B has a mutation status of P304S, The gene HLA-A has a mutation status of K292E, The gene HLA-C has a mutation status of P44T, The gene MSH5 has a mutation status of Q292H, The gene SLC44A4 has a mutation status of M1I, The gene HLA-DRA has a mutation status of R101R, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Y42H, The gene HLA-DRB1 has a mutation status of I248L, The gene HLA-DRB1 has a mutation status of D57I, The gene HLA-DRB1 has a mutation status of F55N, The gene HLA-DQA2 has a mutation status of S75R, The gene ZNF76 has a mutation status of S269Y, The gene ETV7 has a mutation status of P321P, The gene DAAM2 has a mutation status of R885R, The gene GUCA1A has a mutation status of L112L, The gene RARS2 has a mutation status of T296T, The gene DSE has a mutation status of S585R, The gene GRM1 has a mutation status of H54Y, The gene POM121 has a mutation status of N37N, The gene ADAM22 has a mutation status of K844E, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of V1672D, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene PRKAR2B has a mutation status of N107S, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene FAM167A has a mutation status of E170D, The gene GATA4 has a mutation status of R283H, The gene ZFHX4 has a mutation status of M1764I, The gene RSPO2 has a mutation status of C93C, The gene MTBP has a mutation status of I291M, The gene EPPK1 has a mutation status of A2633del, The gene KCNV2 has a mutation status of P92H, The gene CDKN2A has a mutation status of S8fs, The gene IZUMO3 has a mutation status of G46C, The gene ACO1 has a mutation status of I643I, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene RUSC2 has a mutation status of S1441Y, The gene FRMPD1 has a mutation status of G765V, The gene RMI1 has a mutation status of G272D, The gene SLC44A1 has a mutation status of S8T, The gene FRRS1L has a mutation status of R51A, The gene SETX has a mutation status of L2463V, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of R294H, The gene CACNA1B has a mutation status of R2132C, The gene FAM25C has a mutation status of K53T, The gene DLG5 has a mutation status of G1782S, The gene DLG5 has a mutation status of Q14Q, The gene PTEN has a mutation status of R130G, The gene HTR7 has a mutation status of R408W, The gene CRTAC1 has a mutation status of L92L, The gene VWA2 has a mutation status of S225S, The gene TACC2 has a mutation status of P385P, The gene TACC2 has a mutation status of A1838C, The gene INSYN2A has a mutation status of R73R, The gene FOXI2 has a mutation status of R151C, The gene PWWP2B has a mutation status of P110P, The gene PWWP2B has a mutation status of G264R, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of K745K, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of Y1116Y, The gene MUC5AC has a mutation status of I1311I, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of P1569L, The gene MUC5AC has a mutation status of T1570T, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of T3668P, The gene SLC22A18AS has a mutation status of L89L, The gene DCHS1 has a mutation status of L598P, The gene OLFML1 has a mutation status of E98*, The gene ACCS has a mutation status of C20R, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of A116A, The gene OR9G1 has a mutation status of I196F, The gene TCN1 has a mutation status of Q289*, The gene CD5 has a mutation status of H461C, The gene VWCE has a mutation status of C404L, The gene SLC25A45 has a mutation status of V275V, The gene GRK2 has a mutation status of L243V, The gene TBC1D10C has a mutation status of S29I, The gene CARNS1 has a mutation status of R64G, The gene TESMIN has a mutation status of A148fs, The gene DEUP1 has a mutation status of Q80Q, The gene FDX1 has a mutation status of A3A, The gene IFT46 has a mutation status of H214Q, The gene VSIG10L2 has a mutation status of H138Y, The gene SCNN1A has a mutation status of R204W, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R31 has a mutation status of 150_151KE>NQ, The gene TAS2R46 has a mutation status of 296_297HV>QM, The gene TAS2R46 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene KRAS has a mutation status of G12C, The gene GXYLT1 has a mutation status of V28K, The gene OR8S1 has a mutation status of R220C, The gene LARP4 has a mutation status of D567Y, The gene HOXC12 has a mutation status of Q164P, The gene NXPH4 has a mutation status of L16V, The gene CFAP73 has a mutation status of A186P, The gene FGF9 has a mutation status of F77I, The gene ATP8A2 has a mutation status of 624_625LR>FW, The gene UBE2L5 has a mutation status of H119R, The gene VWA8 has a mutation status of I733T, The gene IRS2 has a mutation status of S210C, The gene COL4A2 has a mutation status of P766P, The gene PNP has a mutation status of T177T, The gene TGM1 has a mutation status of D406H, The gene GZMB has a mutation status of D57N, The gene PSMA6 has a mutation status of T231A, The gene ABHD12B has a mutation status of K236fs, The gene FBXO34 has a mutation status of V192L, The gene TTLL5 has a mutation status of D73G, The gene CCDC9B has a mutation status of G510*, The gene TRPM7 has a mutation status of S1396Y, The gene ANKDD1A has a mutation status of L516L, The gene EDC3 has a mutation status of P496P, The gene NEIL1 has a mutation status of H275Q, The gene PEAK1 has a mutation status of S255R, The gene GOLGA6L10 has a mutation status of N514S, The gene GOLGA6L10 has a mutation status of I73V, The gene CAPN15 has a mutation status of E186A, The gene ABCA3 has a mutation status of A1054G, The gene NLRC3 has a mutation status of E304K, The gene NXN has a mutation status of E79G, The gene OR1E2 has a mutation status of P271S, The gene ZZEF1 has a mutation status of R1212Q, The gene ASGR1 has a mutation status of Q6E, The gene TP53 has a mutation status of K101fs, The gene CNTROB has a mutation status of R462R, The gene CCL4L2 has a mutation status of P67R, The gene KANSL1 has a mutation status of R720H, The gene CDC27 has a mutation status of S553S, The gene TSPOAP1 has a mutation status of A1584P, The gene ENGASE has a mutation status of E109E, The gene TSPAN10 has a mutation status of G247R, The gene ZNF407 has a mutation status of G1952S, The gene SALL3 has a mutation status of P485R, The gene CIRBP has a mutation status of G157G, The gene NFIC has a mutation status of A393V, The gene ACSBG2 has a mutation status of T255fs, The gene MUC16 has a mutation status of T13896S, The gene MUC16 has a mutation status of L13880C, The gene ZNF317 has a mutation status of A269G, The gene ZNF878 has a mutation status of K178K, The gene NOP53 has a mutation status of R36R, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB3 has a mutation status of A4A, The gene LILRA6 has a mutation status of H290N, The gene LILRA6 has a mutation status of Y121Y, The gene LILRA6 has a mutation status of I88M, The gene LILRA2 has a mutation status of W163S, The gene LILRB1 has a mutation status of P86L, The gene LILRB1 has a mutation status of S177S, The gene LILRB1 has a mutation status of T335T, The gene LILRB1 has a mutation status of Q401L, The gene ZNF335 has a mutation status of T578M, The gene KRTAP19-5 has a mutation status of S57G, The gene UMODL1 has a mutation status of I1123F, The gene COL6A1 has a mutation status of A660T, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TUBGCP6 has a mutation status of E788G, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene RAI2 has a mutation status of P202T, The gene TFE3 has a mutation status of A21fs, The gene SLC25A5 has a mutation status of T221R, The gene ZIC3 has a mutation status of R116R, The gene ATP11C has a mutation status of T54K, The gene GDI1 has a mutation status of Q346R, The gene MT-ND4 has a mutation status of G311S, The gene MT-ND4 has a mutation status of L369L
OV
The gene HES4 has a mutation status of D103P, The gene SLC25A33 has a mutation status of Y187C, The gene C1orf167 has a mutation status of R137S, The gene C1orf167 has a mutation status of R647Q, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene SPEN has a mutation status of A3248P, The gene PADI2 has a mutation status of P144P, The gene USP48 has a mutation status of K424M, The gene MYOM3 has a mutation status of P433S, The gene PAFAH2 has a mutation status of A63D, The gene CSMD2 has a mutation status of R3157C, The gene KCNQ4 has a mutation status of L373L, The gene PPCS has a mutation status of R25P, The gene MPL has a mutation status of A490G, The gene C8A has a mutation status of S379S, The gene CELSR2 has a mutation status of R2015K, The gene CHIA has a mutation status of T405T, The gene SPAG17 has a mutation status of S1103fs, The gene SSR2 has a mutation status of E63D, The gene RGS4 has a mutation status of K187N, The gene KLHL20 has a mutation status of E229E, The gene CAMK1G has a mutation status of S326G, The gene CENPF has a mutation status of R209W, The gene CENPF has a mutation status of D2313N, The gene CDC42BPA has a mutation status of D1674N, The gene GNPAT has a mutation status of D361G, The gene C2orf16 has a mutation status of E1474D, The gene QPCT has a mutation status of A171P, The gene PLEKHH2 has a mutation status of D100D, The gene EPAS1 has a mutation status of D753E, The gene SLC1A4 has a mutation status of K66K, The gene ADRA2B has a mutation status of S180F, The gene KANSL3 has a mutation status of R899L, The gene ANKRD39 has a mutation status of S62L, The gene SLC9A4 has a mutation status of W647*, The gene XIRP2 has a mutation status of T537I, The gene CCDC173 has a mutation status of Y97C, The gene TTN has a mutation status of G18227G, The gene TTN has a mutation status of D16390N, The gene MYO1B has a mutation status of N408N, The gene SGPP2 has a mutation status of T317T, The gene SCYGR7 has a mutation status of C94*, The gene DNER has a mutation status of T145T, The gene HHATL has a mutation status of R28W, The gene PPM1M has a mutation status of G72G, The gene BAP1 has a mutation status of A95D, The gene RHO has a mutation status of E232E, The gene SLC25A36 has a mutation status of V89G, The gene ZMAT3 has a mutation status of A62A, The gene SLC4A4 has a mutation status of R554R, The gene HSD17B11 has a mutation status of R283Q, The gene TIGD2 has a mutation status of A408D, The gene ADH7 has a mutation status of A103S, The gene SEC24B has a mutation status of A471V, The gene PDE5A has a mutation status of I414I, The gene CCDC152 has a mutation status of *255*, The gene SLF1 has a mutation status of R99C, The gene HARS2 has a mutation status of Q182H, The gene PCDHB6 has a mutation status of E203D, The gene SLC36A2 has a mutation status of A137V, The gene PHYKPL has a mutation status of P404A, The gene F13A1 has a mutation status of P28H, The gene FAM8A1 has a mutation status of A2D, The gene MRS2 has a mutation status of M383V, The gene H3C3 has a mutation status of A32A, The gene ZFP57 has a mutation status of K498K, The gene TRIM15 has a mutation status of A368D, The gene HLA-C has a mutation status of Q204K, The gene TREM1 has a mutation status of T158S, The gene VEGFA has a mutation status of M120V, The gene OPN5 has a mutation status of W188R, The gene UTRN has a mutation status of L974P, The gene RAB32 has a mutation status of G3G, The gene RAB32 has a mutation status of G4G, The gene TMEM181 has a mutation status of L367F, The gene PDE10A has a mutation status of R247S, The gene EIF3B has a mutation status of P151R, The gene AP5Z1 has a mutation status of R179Q, The gene PMS2 has a mutation status of Q237Q, The gene TYW1 has a mutation status of H502Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2046L, The gene POT1 has a mutation status of M159V, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene TMEM178B has a mutation status of G205W, The gene CTAGE6 has a mutation status of Q429G, The gene ESYT2 has a mutation status of R150W, The gene CSMD1 has a mutation status of N2133K, The gene BLK has a mutation status of R131W, The gene PRKDC has a mutation status of V1479L, The gene MATN2 has a mutation status of R645Q, The gene SYBU has a mutation status of A65A, The gene PHF20L1 has a mutation status of S492F, The gene AC138647.1 has a mutation status of P22P, The gene PLEC has a mutation status of E710K, The gene MFSD3 has a mutation status of L104V, The gene ADAMTSL1 has a mutation status of S1663P, The gene NDUFB6 has a mutation status of V34V, The gene MYORG has a mutation status of T659T, The gene C9orf135 has a mutation status of R53H, The gene FOXE1 has a mutation status of A179S, The gene CYLC2 has a mutation status of M1V, The gene AKNA has a mutation status of H484Y, The gene RC3H2 has a mutation status of P344L, The gene MAPKAP1 has a mutation status of D178N, The gene SURF4 has a mutation status of I225V, The gene NACC2 has a mutation status of S65N, The gene CCDC187 has a mutation status of P1104P, The gene CCDC187 has a mutation status of L747L, The gene TRAF2 has a mutation status of L501L, The gene NOXA1 has a mutation status of Q112K, The gene AKR1C8P has a mutation status of N172K, The gene AKR1C8P has a mutation status of F171fs, The gene MPP7 has a mutation status of H402Y, The gene JCAD has a mutation status of S680P, The gene USP54 has a mutation status of L675L, The gene ZNF503 has a mutation status of C427Y, The gene LIPJ has a mutation status of N86S, The gene EXOC6 has a mutation status of T352T, The gene CYP2C8 has a mutation status of M345T, The gene SORCS3 has a mutation status of Q1079K, The gene ADRA2A has a mutation status of R263L, The gene MCMBP has a mutation status of D27E, The gene MUC6 has a mutation status of T1071P, The gene MUC5AC has a mutation status of P1480A, The gene DNHD1 has a mutation status of P4422S, The gene C1QTNF4 has a mutation status of G22S, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR1S1 has a mutation status of F140F, The gene CABP4 has a mutation status of M205R, The gene FAM86C1 has a mutation status of A85V, The gene TECTA has a mutation status of T83M, The gene ROBO4 has a mutation status of E449K, The gene GNB3 has a mutation status of T165R, The gene ENO2 has a mutation status of P148S, The gene FAM186A has a mutation status of T1088N, The gene ESPL1 has a mutation status of W1776*, The gene GDF11 has a mutation status of V43G, The gene GPR182 has a mutation status of L100L, The gene NUAK1 has a mutation status of I417V, The gene POLR3B has a mutation status of V969V, The gene HIP1R has a mutation status of H647Y, The gene ZNF605 has a mutation status of E621*, The gene FARP1 has a mutation status of H703P, The gene LIG4 has a mutation status of D300N, The gene GAS6 has a mutation status of Y258A, The gene OR4K13 has a mutation status of H105H, The gene EMC9 has a mutation status of R52C, The gene TCL1A has a mutation status of D55D, The gene HSP90AA1 has a mutation status of L579L, The gene C14orf180 has a mutation status of G95S, The gene TYRO3 has a mutation status of E509fs, The gene SHF has a mutation status of T86A, The gene ALDH1A2 has a mutation status of C320C, The gene CILP has a mutation status of R1176T, The gene RCCD1 has a mutation status of P109Q, The gene PIGQ has a mutation status of R425Q, The gene RNPS1 has a mutation status of S35S, The gene DCTN5 has a mutation status of S48S, The gene KIAA0556 has a mutation status of N623N, The gene PIEZO1 has a mutation status of R1461W, The gene VPS9D1 has a mutation status of G90G, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene RTN4RL1 has a mutation status of A263V, The gene ANKFY1 has a mutation status of V559V, The gene RABEP1 has a mutation status of G5V, The gene ALDOC has a mutation status of Y186Y, The gene SDF2 has a mutation status of L6L, The gene CCL4L2 has a mutation status of P67R, The gene KRT32 has a mutation status of F56L, The gene KRT17 has a mutation status of L190L, The gene DCAKD has a mutation status of R108C, The gene SLC35B1 has a mutation status of F74fs, The gene EPX has a mutation status of S34S, The gene EPX has a mutation status of I518V, The gene SEH1L has a mutation status of R5P, The gene ANKRD30B has a mutation status of E888K, The gene B4GALT6 has a mutation status of A39V, The gene NARS1 has a mutation status of R263R, The gene CDH20 has a mutation status of S759A, The gene ZNF407 has a mutation status of T1697P, The gene ATP9B has a mutation status of L1133L, The gene TIMM44 has a mutation status of C11G, The gene MUC16 has a mutation status of S3959I, The gene ICAM1 has a mutation status of T108T, The gene TYK2 has a mutation status of A567P, The gene DOCK6 has a mutation status of R1338*, The gene ZNF763 has a mutation status of V212F, The gene TM6SF2 has a mutation status of A263S, The gene ZNF792 has a mutation status of M590V, The gene MAG has a mutation status of T612T, The gene KMT2B has a mutation status of E2182D, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene SNRPA has a mutation status of I277F, The gene SRRM5 has a mutation status of A103D, The gene ZNF541 has a mutation status of A607D, The gene PNKP has a mutation status of E13Q, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of P175T, The gene KIR2DL1 has a mutation status of T333A, The gene SSC5D has a mutation status of D798D, The gene SSTR4 has a mutation status of A245E, The gene NCOA3 has a mutation status of T184T, The gene BCAS1 has a mutation status of F96L, The gene HIC2 has a mutation status of K138R, The gene PPM1F has a mutation status of G105E, The gene MYO18B has a mutation status of S2240L, The gene OSBP2 has a mutation status of S42P, The gene FOXRED2 has a mutation status of M45L, The gene CYTH4 has a mutation status of V214M, The gene TTC38 has a mutation status of L337L, The gene FAM120C has a mutation status of E997fs, The gene AMER1 has a mutation status of G306G, The gene AMER1 has a mutation status of G149G, The gene LAS1L has a mutation status of L697L, The gene ZMAT1 has a mutation status of F72G, The gene BCORL1 has a mutation status of L1132P, The gene SPANXB1 has a mutation status of Q42P, The gene RBMY1F has a mutation status of N16N, The gene RBMY1J has a mutation status of N16N, The gene MT-CO3 has a mutation status of L31L, The gene MT-CYB has a mutation status of G351*
KIPAN
The gene TMEM201 has a mutation status of C70C, The gene DISP3 has a mutation status of D646D, The gene TNFRSF8 has a mutation status of T471P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene ALDH4A1 has a mutation status of W295*, The gene PINK1 has a mutation status of R422H, The gene EPHB2 has a mutation status of S212S, The gene RHD has a mutation status of G314V, The gene PUM1 has a mutation status of A688T, The gene AK4 has a mutation status of E76K, The gene GLMN has a mutation status of R574*, The gene AGL has a mutation status of T1195R, The gene DENND2C has a mutation status of C42W, The gene IGSF3 has a mutation status of R290Q, The gene TARS2 has a mutation status of G175V, The gene ZNF687 has a mutation status of L1142F, The gene TDRKH has a mutation status of A404F, The gene SLC27A3 has a mutation status of R100*, The gene DENND4B has a mutation status of R597C, The gene SEMA4A has a mutation status of G484A, The gene ARHGEF11 has a mutation status of I1096L, The gene ATP1A4 has a mutation status of G737A, The gene ITLN1 has a mutation status of T171T, The gene CHI3L1 has a mutation status of W71C, The gene SOX13 has a mutation status of S592L, The gene PGBD2 has a mutation status of G427A, The gene EIF2B4 has a mutation status of R88P, The gene C2orf16 has a mutation status of E3942A, The gene PLEKHH2 has a mutation status of S329C, The gene EPAS1 has a mutation status of D753E, The gene NRXN1 has a mutation status of M730V, The gene EGR4 has a mutation status of F7S, The gene CREG2 has a mutation status of Q237K, The gene MERTK has a mutation status of G787D, The gene ZRANB3 has a mutation status of A509A, The gene OSBPL6 has a mutation status of L116L, The gene SLC39A10 has a mutation status of N150K, The gene SF3B1 has a mutation status of 699_700QK>HE, The gene CNPPD1 has a mutation status of T348P, The gene HACL1 has a mutation status of M1T, The gene XIRP1 has a mutation status of R1275C, The gene CSPG5 has a mutation status of H366H, The gene CDC25A has a mutation status of R506W, The gene MITF has a mutation status of K198T, The gene DCBLD2 has a mutation status of E646K, The gene TEX55 has a mutation status of R196H, The gene CD86 has a mutation status of S87fs, The gene PLXNA1 has a mutation status of N466Y, The gene SLC35G2 has a mutation status of S277S, The gene PRR23B has a mutation status of S118S, The gene USP13 has a mutation status of R39R, The gene NSD2 has a mutation status of P1291P, The gene TADA2B has a mutation status of A419A, The gene CPZ has a mutation status of Y258C, The gene COL25A1 has a mutation status of V47V, The gene KIAA1109 has a mutation status of G646G, The gene ADAD1 has a mutation status of T39T, The gene TRIML1 has a mutation status of T275T, The gene SV2C has a mutation status of G166S, The gene CMYA5 has a mutation status of T695T, The gene POLR3G has a mutation status of K5fs, The gene CHSY3 has a mutation status of L410L, The gene PCDHA13 has a mutation status of D429D, The gene FAM71B has a mutation status of T381M, The gene MAT2B has a mutation status of G3G, The gene ZFP2 has a mutation status of R122S, The gene FOXC1 has a mutation status of L518F, The gene H1-3 has a mutation status of A29T, The gene ZSCAN9 has a mutation status of P16P, The gene OR10C1 has a mutation status of R233C, The gene HLA-DRB5 has a mutation status of Y42H, The gene MDFI has a mutation status of P101P, The gene ADGRF2 has a mutation status of C45F, The gene DST has a mutation status of D6547V, The gene COL12A1 has a mutation status of D1829N, The gene SLC35A1 has a mutation status of P126P, The gene MFSD4B has a mutation status of L182Y, The gene FRK has a mutation status of P453P, The gene ALDH8A1 has a mutation status of R69H, The gene MAP7 has a mutation status of R573C, The gene TNFAIP3 has a mutation status of G156V, The gene STXBP5 has a mutation status of A519T, The gene KIF25 has a mutation status of 245_246LA>FS, The gene TNRC18 has a mutation status of Q2894Q, The gene TBX20 has a mutation status of V171G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S326A, The gene MUC3A has a mutation status of M384T, The gene PPP1R3A has a mutation status of T286S, The gene PODXL has a mutation status of R495W, The gene PRSS1 has a mutation status of C139S, The gene REPIN1 has a mutation status of A239V, The gene AGAP3 has a mutation status of T243T, The gene KMT2C has a mutation status of D2201H, The gene KMT2C has a mutation status of D2024H, The gene KMT2C has a mutation status of G2002E, The gene KMT2C has a mutation status of V1973V, The gene KMT2C has a mutation status of M1938I, The gene DEFB1 has a mutation status of C44R, The gene KAT6A has a mutation status of R26C, The gene PPDPFL has a mutation status of S24P, The gene TCEA1 has a mutation status of I215L, The gene HSF1 has a mutation status of V172G, The gene FRMPD1 has a mutation status of S690N, The gene PCSK5 has a mutation status of Q1799Q, The gene VPS13A has a mutation status of D575D, The gene GABBR2 has a mutation status of V317M, The gene SMC2 has a mutation status of S342*, The gene OR5C1 has a mutation status of R8Q, The gene RAPGEF1 has a mutation status of E77D, The gene MAMDC4 has a mutation status of D917I, The gene ARHGAP21 has a mutation status of P1252fs, The gene GPR158 has a mutation status of T759M, The gene DDIT4 has a mutation status of L227L, The gene CYP26C1 has a mutation status of G13G, The gene INPP5F has a mutation status of P1057T, The gene ADAM12 has a mutation status of R834S, The gene MUC5AC has a mutation status of R3992H, The gene RAG2 has a mutation status of V272F, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TKFC has a mutation status of H253H, The gene FEN1 has a mutation status of E215E, The gene EML3 has a mutation status of V685V, The gene LRP5 has a mutation status of T1578T, The gene CAPN5 has a mutation status of D29A, The gene ALG8 has a mutation status of H200R, The gene TENM4 has a mutation status of Q2708*, The gene SLC36A4 has a mutation status of I312V, The gene KDM4D has a mutation status of D499E, The gene GUCY1A2 has a mutation status of K717N, The gene SCN2B has a mutation status of Q70Q, The gene CHD4 has a mutation status of K53K, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of A28A, The gene KRAS has a mutation status of G12D, The gene SENP1 has a mutation status of G604G, The gene KRT6C has a mutation status of D459D, The gene KRT77 has a mutation status of E432fs, The gene IRAK3 has a mutation status of L86V, The gene TMPO has a mutation status of *695*, The gene UBE3B has a mutation status of D721D, The gene RIMBP2 has a mutation status of R851W, The gene GOLGA3 has a mutation status of E790K, The gene BRCA2 has a mutation status of V484V, The gene KLF5 has a mutation status of H389N, The gene IRS2 has a mutation status of P1265P, The gene FRMD6 has a mutation status of T398I, The gene PCNX4 has a mutation status of P613R, The gene BTBD7 has a mutation status of S979R, The gene UNC13C has a mutation status of A1885T, The gene ADAMTS7 has a mutation status of T1662S, The gene NTRK3 has a mutation status of E224K, The gene PDZD9 has a mutation status of S146P, The gene AQP8 has a mutation status of V79V, The gene SLC5A2 has a mutation status of E632E, The gene ABCC12 has a mutation status of D1113N, The gene MMP15 has a mutation status of T313P, The gene NOB1 has a mutation status of I267I, The gene CFAP52 has a mutation status of I487V, The gene USP43 has a mutation status of G739R, The gene PIGS has a mutation status of H333Y, The gene RSKR has a mutation status of S196L, The gene CCT6B has a mutation status of V477L, The gene CCL4L2 has a mutation status of P67R, The gene MRM1 has a mutation status of V149P, The gene TMEM106A has a mutation status of S6N, The gene HOXB2 has a mutation status of E292E, The gene TSPOAP1 has a mutation status of L1102F, The gene RNFT1 has a mutation status of G316C, The gene CSH2 has a mutation status of E114G, The gene FDXR has a mutation status of R219H, The gene CHMP6 has a mutation status of I140V, The gene CD7 has a mutation status of A84A, The gene LRRC30 has a mutation status of S227S, The gene ASXL3 has a mutation status of S667S, The gene APC2 has a mutation status of A797T, The gene APC2 has a mutation status of A800V, The gene CATSPERD has a mutation status of T354I, The gene MUC16 has a mutation status of S10457P, The gene ZNF440 has a mutation status of E525V, The gene C19orf44 has a mutation status of V345G, The gene ZNF91 has a mutation status of H960Y, The gene FAM187B has a mutation status of T271T, The gene ETV2 has a mutation status of G52D, The gene PROSER3 has a mutation status of E340K, The gene QPCTL has a mutation status of L228L, The gene LILRB3 has a mutation status of L243F, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of Y99I, The gene LILRB1 has a mutation status of T335T, The gene NLRP13 has a mutation status of E917K, The gene AL049634.2 has a mutation status of L95S, The gene AL049634.2 has a mutation status of P87P, The gene SIRPA has a mutation status of L44S, The gene SIGLEC1 has a mutation status of V764M, The gene PLCB4 has a mutation status of R254Q, The gene ASXL1 has a mutation status of H556H, The gene ARFGEF2 has a mutation status of L40H, The gene KCNB1 has a mutation status of R294R, The gene MOCS3 has a mutation status of E13D, The gene TSHZ2 has a mutation status of T1016T, The gene SRMS has a mutation status of G237G, The gene PCNT has a mutation status of E2293K, The gene COMT has a mutation status of N39D, The gene TRIOBP has a mutation status of E384G, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PKDREJ has a mutation status of S1932L, The gene COL4A6 has a mutation status of 1640_1642RGT>P, The gene MAGEA3 has a mutation status of V308A, The gene MAGEA3 has a mutation status of L309F, The gene SRPK3 has a mutation status of H147H, The gene SRPK3 has a mutation status of I555I, The gene LAGE3 has a mutation status of R114H, The gene CTAG2 has a mutation status of R86H, The gene MT-ND1 has a mutation status of T67A, The gene MT-CO1 has a mutation status of L209L, The gene MT-ND4 has a mutation status of T396T, The gene MT-CYB has a mutation status of V343V, The gene VWA1 has a mutation status of D280G, The gene NPHP4 has a mutation status of P527L, The gene ESPN has a mutation status of E57K, The gene PEX14 has a mutation status of H259H, The gene PEX14 has a mutation status of D332N, The gene C1orf127 has a mutation status of T31M, The gene FBXO6 has a mutation status of P201T, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF15 has a mutation status of L149V, The gene SPEN has a mutation status of V2856V, The gene FAM43B has a mutation status of L2L, The gene HSPG2 has a mutation status of P1129Q, The gene EPHA8 has a mutation status of A866T, The gene HNRNPR has a mutation status of T137T, The gene NIPAL3 has a mutation status of V103M, The gene AHDC1 has a mutation status of P738P, The gene PTPRU has a mutation status of G891D, The gene KHDRBS1 has a mutation status of Y440Y, The gene YARS1 has a mutation status of E20E, The gene ZSCAN20 has a mutation status of L338L, The gene CLSPN has a mutation status of A126V, The gene MACF1 has a mutation status of M1931R, The gene ZSWIM5 has a mutation status of S921G, The gene DMBX1 has a mutation status of Q30K, The gene NRDC has a mutation status of E395Q, The gene RAB3B has a mutation status of L39L, The gene LMO4 has a mutation status of C47C, The gene PTBP2 has a mutation status of V524V, The gene PPM1J has a mutation status of A39A, The gene DENND2C has a mutation status of E222A, The gene NBPF20 has a mutation status of K59N, The gene NBPF9 has a mutation status of C803C, The gene AC242842.3 has a mutation status of E91D, The gene HRNR has a mutation status of G637G, The gene FLG has a mutation status of E777E, The gene FLG2 has a mutation status of L45M, The gene RUSC1 has a mutation status of L24F, The gene COPA has a mutation status of Q1199R, The gene GPA33 has a mutation status of P144A, The gene KIFAP3 has a mutation status of L96V, The gene PRRC2C has a mutation status of R911Q, The gene SLC9C2 has a mutation status of Y310F, The gene RC3H1 has a mutation status of L970L, The gene TNR has a mutation status of Y1022Y, The gene SEC16B has a mutation status of S840T, The gene AXDND1 has a mutation status of F266L, The gene NPHS2 has a mutation status of A27G, The gene ZBTB41 has a mutation status of L16L, The gene IGFN1 has a mutation status of K1635E, The gene IPO9 has a mutation status of I80V, The gene UBE2T has a mutation status of E148E, The gene FMOD has a mutation status of Y39Y, The gene PLEKHA6 has a mutation status of N19K, The gene DSTYK has a mutation status of R40R, The gene LAMB3 has a mutation status of R1143C, The gene C1orf74 has a mutation status of L55L, The gene IRF6 has a mutation status of L3L, The gene DNAH14 has a mutation status of K226K, The gene EPHX1 has a mutation status of T26S, The gene OBSCN has a mutation status of A5327T, The gene NTPCR has a mutation status of G116G, The gene PCNX2 has a mutation status of G1339G, The gene CEP170 has a mutation status of G433G, The gene KIF26B has a mutation status of G118C, The gene TRAPPC12 has a mutation status of E113*, The gene TRAPPC12 has a mutation status of M300V, The gene APOB has a mutation status of N3051S, The gene MFSD2B has a mutation status of V380G, The gene FAM228B has a mutation status of Q303fs, The gene ITSN2 has a mutation status of Y980C, The gene CENPO has a mutation status of S31Y, The gene WDR43 has a mutation status of H412R, The gene SLC30A6 has a mutation status of T257T, The gene SOCS5 has a mutation status of A393A, The gene FSHR has a mutation status of L8F, The gene CCDC88A has a mutation status of T1304T, The gene MXD1 has a mutation status of T94T, The gene ACTG2 has a mutation status of L174L, The gene LRRTM4 has a mutation status of L383L, The gene GGCX has a mutation status of L270P, The gene POLR1A has a mutation status of T957T, The gene PDCL3 has a mutation status of A33A, The gene CNOT11 has a mutation status of P288P, The gene EDAR has a mutation status of S380R, The gene CCDC93 has a mutation status of F612L, The gene SCTR has a mutation status of A417A, The gene EPB41L5 has a mutation status of T194T, The gene MAP3K2 has a mutation status of I110V, The gene HS6ST1 has a mutation status of S207S, The gene ARHGEF4 has a mutation status of L717L, The gene MCM6 has a mutation status of T245T, The gene RBM43 has a mutation status of V24A, The gene COBLL1 has a mutation status of S623S, The gene SCN7A has a mutation status of N538S, The gene SCRN3 has a mutation status of D202D, The gene TTC30B has a mutation status of R605H, The gene FKBP7 has a mutation status of P131L, The gene FSIP2 has a mutation status of T1337I, The gene ITGAV has a mutation status of R241Q, The gene ORC2 has a mutation status of N505D, The gene PLEKHM3 has a mutation status of H182R, The gene MAP2 has a mutation status of L326S, The gene FN1 has a mutation status of I594T, The gene PECR has a mutation status of S271L, The gene TMBIM1 has a mutation status of A38A, The gene SLC11A1 has a mutation status of N465N, The gene TTLL4 has a mutation status of S156S, The gene CYP27A1 has a mutation status of V238M, The gene OBSL1 has a mutation status of S903S, The gene DOCK10 has a mutation status of R1654C, The gene COL4A4 has a mutation status of P1426A, The gene COL4A3 has a mutation status of T477I, The gene SP110 has a mutation status of R645H, The gene ECEL1 has a mutation status of G666R, The gene PRSS56 has a mutation status of S340F, The gene MROH2A has a mutation status of K714K, The gene COL6A3 has a mutation status of D1293E, The gene SNED1 has a mutation status of K1217N, The gene HDLBP has a mutation status of I1068I, The gene CHL1 has a mutation status of V180L, The gene SSUH2 has a mutation status of C372S, The gene IL17RC has a mutation status of S56N, The gene CAND2 has a mutation status of I483M, The gene OSBPL10 has a mutation status of D133N, The gene DLEC1 has a mutation status of T611T, The gene MYRIP has a mutation status of D739D, The gene TOPAZ1 has a mutation status of C937W, The gene KIF15 has a mutation status of D748E, The gene PTPN23 has a mutation status of R1237C, The gene APEH has a mutation status of Q572H, The gene DOCK3 has a mutation status of N483K, The gene RRP9 has a mutation status of R140R, The gene STAB1 has a mutation status of F2542fs, The gene EOGT has a mutation status of H56R, The gene IFT57 has a mutation status of S120S, The gene NAA50 has a mutation status of R21T, The gene DRD3 has a mutation status of H359H, The gene GTF2E1 has a mutation status of A18A, The gene SLC12A8 has a mutation status of N390N, The gene PLXNA1 has a mutation status of R942Q, The gene MGLL has a mutation status of V165V, The gene KIAA1257 has a mutation status of P621R, The gene H1-8 has a mutation status of S44I, The gene A4GNT has a mutation status of F36F, The gene ATR has a mutation status of D1915G, The gene IGSF10 has a mutation status of P1773S, The gene GPR149 has a mutation status of N423K, The gene PLCH1 has a mutation status of G436A, The gene SHOX2 has a mutation status of A296A, The gene IL12A has a mutation status of P60P, The gene SLITRK3 has a mutation status of S173S, The gene KCNMB3 has a mutation status of R249K, The gene YEATS2 has a mutation status of I339V, The gene YEATS2 has a mutation status of P1118L, The gene EIF4G1 has a mutation status of Y1401Y, The gene SENP2 has a mutation status of H537H, The gene ST6GAL1 has a mutation status of L326L, The gene MB21D2 has a mutation status of T135T, The gene NKX1-1 has a mutation status of P210A, The gene DOK7 has a mutation status of I48T, The gene EVC has a mutation status of H607Q, The gene LDB2 has a mutation status of D47V, The gene ADGRA3 has a mutation status of L1004H, The gene KLF3 has a mutation status of P120P, The gene TLR1 has a mutation status of G417V, The gene YIPF7 has a mutation status of T127S, The gene REST has a mutation status of T696A, The gene SHROOM3 has a mutation status of A1002A, The gene SHROOM3 has a mutation status of H1237R, The gene GPRIN3 has a mutation status of S111*, The gene ADH7 has a mutation status of E239D, The gene CENPE has a mutation status of N391Y, The gene ZGRF1 has a mutation status of M2023T, The gene LARP7 has a mutation status of Q317H, The gene ADAD1 has a mutation status of T36M, The gene FAT4 has a mutation status of G4887V, The gene LRBA has a mutation status of A2546G, The gene RPS3A has a mutation status of T11T, The gene FSTL5 has a mutation status of T607A, The gene FSTL5 has a mutation status of T606I, The gene C4orf47 has a mutation status of I226T, The gene SORBS2 has a mutation status of N338K, The gene FAM149A has a mutation status of E187*, The gene ATPSCKMT has a mutation status of R132Q, The gene ANKH has a mutation status of V87I, The gene FBXL7 has a mutation status of H98Y, The gene MYO10 has a mutation status of E1146K, The gene RXFP3 has a mutation status of P313L, The gene NIPBL has a mutation status of S1517*, The gene ITGA2 has a mutation status of G793R, The gene SHLD3 has a mutation status of I217M, The gene ERBIN has a mutation status of N1083S, The gene MAST4 has a mutation status of S1870del, The gene OTP has a mutation status of A71V, The gene ADGRV1 has a mutation status of E2446K, The gene ADGRV1 has a mutation status of R4802Q, The gene AP3S1 has a mutation status of I182V, The gene LVRN has a mutation status of I766V, The gene ZNF474 has a mutation status of S78L, The gene TGFBI has a mutation status of P501T, The gene SLC4A9 has a mutation status of S614T, The gene PCDHB2 has a mutation status of V266D, The gene PCDHGA1 has a mutation status of A761A, The gene PCDHGA2 has a mutation status of D536Y, The gene SPINK14 has a mutation status of T53M, The gene HK3 has a mutation status of T895T, The gene IRF4 has a mutation status of T92T, The gene DSP has a mutation status of K1581E, The gene GCNT2 has a mutation status of E130G, The gene MYLIP has a mutation status of S354L, The gene H2BC7 has a mutation status of T91T, The gene H3C8 has a mutation status of L104L, The gene OR2B2 has a mutation status of R270G, The gene LTA has a mutation status of M1I, The gene PBX2 has a mutation status of E180K, The gene TBCC has a mutation status of I335V, The gene TBCC has a mutation status of T276I, The gene PTK7 has a mutation status of P698R, The gene ZNF318 has a mutation status of A1580T, The gene POLH has a mutation status of T478M, The gene GTPBP2 has a mutation status of V21A, The gene IMPG1 has a mutation status of K621K, The gene TTK has a mutation status of P468L, The gene TBX18 has a mutation status of E29K, The gene CDK19 has a mutation status of A38A, The gene GPRC6A has a mutation status of T253T, The gene STX7 has a mutation status of L76L, The gene HBS1L has a mutation status of M174V, The gene TXLNB has a mutation status of R243G, The gene RAET1E has a mutation status of L60L, The gene SYNE1 has a mutation status of T7356T, The gene SYNE1 has a mutation status of L6024L, The gene CNKSR3 has a mutation status of S306C, The gene SNX9 has a mutation status of I28L, The gene SYNJ2 has a mutation status of R744R, The gene ERMARD has a mutation status of A68A, The gene INTS1 has a mutation status of V1094A, The gene CHST12 has a mutation status of R222L, The gene TTYH3 has a mutation status of L174L, The gene RADIL has a mutation status of S56S, The gene RNF216 has a mutation status of E707Q, The gene PMS2 has a mutation status of Y313C, The gene THSD7A has a mutation status of P488T, The gene TMEM196 has a mutation status of E154D, The gene DNAH11 has a mutation status of W1733C, The gene DNAH11 has a mutation status of R2044Q, The gene STEAP1B has a mutation status of H32R, The gene TAX1BP1 has a mutation status of E618G, The gene PLEKHA8 has a mutation status of E269V, The gene ITPRID1 has a mutation status of T780M, The gene UBE2D4 has a mutation status of C111S, The gene RAMP3 has a mutation status of N58K, The gene ASL has a mutation status of E50E, The gene SSC4D has a mutation status of G318R, The gene ABCB4 has a mutation status of A791S, The gene FZD1 has a mutation status of E3Q, The gene AKAP9 has a mutation status of L603L, The gene AKAP9 has a mutation status of K3276K, The gene COL1A2 has a mutation status of A765A, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of P2041L, The gene PTPRZ1 has a mutation status of E1306Q, The gene FEZF1 has a mutation status of K203K, The gene GCC1 has a mutation status of A279A, The gene PAX4 has a mutation status of R191C, The gene FLNC has a mutation status of T1880N, The gene ATP6V1FNB has a mutation status of A9A, The gene IRF5 has a mutation status of K73K, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene TCAF1 has a mutation status of V62M, The gene CNTNAP2 has a mutation status of G965G, The gene ZNF783 has a mutation status of Y168Y, The gene ZNF746 has a mutation status of I426I, The gene REPIN1 has a mutation status of R513R, The gene NOS3 has a mutation status of G116S, The gene NUB1 has a mutation status of Q13R, The gene DPP6 has a mutation status of V650V, The gene CSMD1 has a mutation status of T295T, The gene BLK has a mutation status of Q392Q, The gene MTMR7 has a mutation status of I175T, The gene GFRA2 has a mutation status of A182V, The gene LOXL2 has a mutation status of G465G, The gene DOCK5 has a mutation status of Q1614H, The gene STMN4 has a mutation status of A188A, The gene NSD3 has a mutation status of R1309T, The gene ADAM18 has a mutation status of T628I, The gene RP1 has a mutation status of R761R, The gene RP1 has a mutation status of E964K, The gene PDE7A has a mutation status of R65P, The gene CRH has a mutation status of 51_52insP, The gene TRPA1 has a mutation status of Q1070R, The gene RGS22 has a mutation status of K429E, The gene COL14A1 has a mutation status of A1620A, The gene AC100868.1 has a mutation status of H258P, The gene JRK has a mutation status of Q434R, The gene EPPK1 has a mutation status of A2633del, The gene PLEC has a mutation status of A2194A, The gene PLEC has a mutation status of G1814S, The gene PLEC has a mutation status of V1538V, The gene PARP10 has a mutation status of R747Q, The gene MROH1 has a mutation status of D613A, The gene MROH1 has a mutation status of I874I, The gene MROH1 has a mutation status of P1321S, The gene MROH1 has a mutation status of A1497V, The gene SLC39A4 has a mutation status of G180G, The gene KANK1 has a mutation status of A1203V, The gene KIAA2026 has a mutation status of T1259I, The gene RANBP6 has a mutation status of K547R, The gene MPDZ has a mutation status of I1011T, The gene CER1 has a mutation status of K53T, The gene CCDC171 has a mutation status of E363K, The gene ADAMTSL1 has a mutation status of V1265I, The gene CDKN2A has a mutation status of G84G, The gene CDKN2A has a mutation status of H15R, The gene AQP7 has a mutation status of L181L, The gene HRCT1 has a mutation status of 101_102insHHHHHPRHTPHHL, The gene SPAAR has a mutation status of R49H, The gene NTRK2 has a mutation status of H300H, The gene ZNF484 has a mutation status of A812G, The gene WNK2 has a mutation status of V1035V, The gene PTCH1 has a mutation status of R893H, The gene TBC1D2 has a mutation status of A348T, The gene TBC1D2 has a mutation status of A257S, The gene FRRS1L has a mutation status of R51A, The gene PTPN3 has a mutation status of L384L, The gene ASTN2 has a mutation status of Y1060Y, The gene TTLL11 has a mutation status of S98N, The gene RABGAP1 has a mutation status of N1005Y, The gene FAM102A has a mutation status of L146L, The gene SPTAN1 has a mutation status of A2140T, The gene RAPGEF1 has a mutation status of A487V, The gene SPACA9 has a mutation status of V104I, The gene STKLD1 has a mutation status of L631P, The gene DBH has a mutation status of T467M, The gene TMEM250 has a mutation status of A30T, The gene NOTCH1 has a mutation status of H1176H, The gene TRAF2 has a mutation status of T401T, The gene ITIH2 has a mutation status of R464S, The gene ATP5F1C has a mutation status of R277C, The gene FRMD4A has a mutation status of S798S, The gene RSU1 has a mutation status of P217R, The gene CUBN has a mutation status of K1954K, The gene MALRD1 has a mutation status of I1837L, The gene SVIL has a mutation status of P659S, The gene HNRNPF has a mutation status of V204M, The gene ZNF239 has a mutation status of K435R, The gene OR13A1 has a mutation status of L205V, The gene WDFY4 has a mutation status of N648N, The gene ERCC6 has a mutation status of S1062S, The gene OGDHL has a mutation status of A533A, The gene PCDH15 has a mutation status of G1152G, The gene CCAR1 has a mutation status of R327H, The gene PLAU has a mutation status of P160S, The gene DUPD1 has a mutation status of P36S, The gene SHLD2 has a mutation status of C159Y, The gene EXOC6 has a mutation status of T765A, The gene CPN1 has a mutation status of R24H, The gene ARMH3 has a mutation status of R494W, The gene GBF1 has a mutation status of S1357S, The gene PSD has a mutation status of P466P, The gene SLK has a mutation status of Q670R, The gene ADRB1 has a mutation status of 296_297insAT, The gene PNLIP has a mutation status of Y58H, The gene FGFR2 has a mutation status of F417V, The gene EBF3 has a mutation status of A397V, The gene SCART1 has a mutation status of E200K, The gene LRRC56 has a mutation status of L143F, The gene DEAF1 has a mutation status of A436A, The gene MUC6 has a mutation status of V105I, The gene PGAP2 has a mutation status of F93F, The gene TRIM68 has a mutation status of E111D, The gene SCUBE2 has a mutation status of N405S, The gene USP47 has a mutation status of L223L, The gene PIK3C2A has a mutation status of D1364D, The gene ABCC8 has a mutation status of R1221Q, The gene KCNC1 has a mutation status of S537S, The gene HPS5 has a mutation status of R184W, The gene ANO3 has a mutation status of F183F, The gene KCNA4 has a mutation status of F228V, The gene FBXO3 has a mutation status of M423V, The gene RAG2 has a mutation status of R300H, The gene MYBPC3 has a mutation status of K89Q, The gene NUP160 has a mutation status of P635P, The gene OR4C16 has a mutation status of W21fs, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR5AK2 has a mutation status of R138R, The gene RPS6KA4 has a mutation status of Y408Y, The gene ATG2A has a mutation status of S1251G, The gene CD248 has a mutation status of D152D, The gene RIN1 has a mutation status of L360L, The gene RIN1 has a mutation status of E315*, The gene PC has a mutation status of S603N, The gene GAL has a mutation status of R107C, The gene PPFIA1 has a mutation status of L371L, The gene DHCR7 has a mutation status of A452T, The gene PAAF1 has a mutation status of G213A, The gene RPS3 has a mutation status of Y183Y, The gene MYO7A has a mutation status of T1992M, The gene DLG2 has a mutation status of F55L, The gene FAT3 has a mutation status of Y2104Y, The gene FAT3 has a mutation status of K2936Q, The gene VPS11 has a mutation status of A451V, The gene TECTA has a mutation status of V1171M, The gene HSPA8 has a mutation status of K561N, The gene PRDM10 has a mutation status of N740N, The gene APLP2 has a mutation status of G295S, The gene CACNA1C has a mutation status of Q1964R, The gene GPR162 has a mutation status of F39F, The gene C1S has a mutation status of P338A, The gene TAS2R7 has a mutation status of L29L, The gene SLCO1B3 has a mutation status of C142F, The gene ETNK1 has a mutation status of V67M, The gene PKP2 has a mutation status of L471L, The gene ADAMTS20 has a mutation status of E786fs, The gene SCAF11 has a mutation status of L1389L, The gene SLC38A1 has a mutation status of I399T, The gene RAPGEF3 has a mutation status of H832H, The gene CCNT1 has a mutation status of S475S, The gene KMT2D has a mutation status of P1097R, The gene SPATS2 has a mutation status of S507P, The gene KRT6C has a mutation status of G508G, The gene OR6C74 has a mutation status of D87V, The gene OR6C70 has a mutation status of S247S, The gene OR10P1 has a mutation status of T159I, The gene RDH5 has a mutation status of V14V, The gene ESYT1 has a mutation status of L302L, The gene LRP1 has a mutation status of I3965I, The gene MSRB3 has a mutation status of L11F, The gene BEST3 has a mutation status of S624T, The gene OTOGL has a mutation status of R1915P, The gene NTN4 has a mutation status of T572M, The gene NTN4 has a mutation status of E59K, The gene HAL has a mutation status of E115E, The gene TMPO has a mutation status of G80R, The gene PMCH has a mutation status of S87S, The gene NT5DC3 has a mutation status of S531S, The gene PRDM4 has a mutation status of L303F, The gene ISCU has a mutation status of A13V, The gene ATP2A2 has a mutation status of D886Y, The gene BRAP has a mutation status of V506I, The gene BRAP has a mutation status of V311V, The gene OAS2 has a mutation status of D508H, The gene DDX54 has a mutation status of R86H, The gene IQCD has a mutation status of K231E, The gene BICDL1 has a mutation status of S82C, The gene ABCB9 has a mutation status of V121M, The gene DNAH10 has a mutation status of V3620fs, The gene GLT1D1 has a mutation status of D185E, The gene RIMBP2 has a mutation status of N159S, The gene SFSWAP has a mutation status of F188I, The gene ATP8A2 has a mutation status of L256V, The gene FRY has a mutation status of S2432R, The gene SMAD9 has a mutation status of P145Q, The gene RB1 has a mutation status of GVRLYYRVME449del, The gene RB1 has a mutation status of H483R, The gene INTS6 has a mutation status of S295S, The gene DACH1 has a mutation status of 81_82insGG, The gene DCT has a mutation status of V475V, The gene ABCC4 has a mutation status of G430G, The gene CLDN10 has a mutation status of L49L, The gene CLDN10 has a mutation status of S68T, The gene RNF113B has a mutation status of S89R, The gene SLC15A1 has a mutation status of V450I, The gene NALCN has a mutation status of H1189N, The gene CCDC168 has a mutation status of T4719A, The gene ERCC5 has a mutation status of E1181K, The gene ERCC5 has a mutation status of E1341K, The gene SLC10A2 has a mutation status of S35R, The gene ATP11A has a mutation status of K500T, The gene UPF3A has a mutation status of A66S, The gene POTEG has a mutation status of L278R, The gene OR4K15 has a mutation status of V270D, The gene ARHGEF40 has a mutation status of P1395A, The gene OR4E2 has a mutation status of R226*, The gene ADCY4 has a mutation status of K220K, The gene PRKD1 has a mutation status of G32G, The gene TTC6 has a mutation status of I837V, The gene MIA2 has a mutation status of M1180T, The gene FANCM has a mutation status of H721R, The gene VCPKMT has a mutation status of S59P, The gene RTN1 has a mutation status of P13L, The gene SYT16 has a mutation status of S291T, The gene SYNE2 has a mutation status of F1979F, The gene SMOC1 has a mutation status of D309D, The gene ACOT4 has a mutation status of R57C, The gene TMEM63C has a mutation status of H242H, The gene CATSPERB has a mutation status of T323N, The gene TC2N has a mutation status of Q362fs, The gene COX8C has a mutation status of R5L, The gene WARS1 has a mutation status of Y100Y, The gene RTL1 has a mutation status of P51L, The gene PPP2R5C has a mutation status of N306N, The gene ZBTB42 has a mutation status of V28V, The gene AHNAK2 has a mutation status of S245F, The gene LPCAT4 has a mutation status of G17R, The gene VPS18 has a mutation status of A918A, The gene VPS39 has a mutation status of A248A, The gene GANC has a mutation status of R652Q, The gene CAPN3 has a mutation status of R315Q, The gene NEDD4 has a mutation status of Q60R, The gene HERC1 has a mutation status of R2997I, The gene ANKDD1A has a mutation status of L516L, The gene DENND4A has a mutation status of N1109H, The gene SEMA7A has a mutation status of L308L, The gene GOLGA6L10 has a mutation status of M402L, The gene GOLGA6L9 has a mutation status of Q151E, The gene PEX11A has a mutation status of E33K, The gene SYNM has a mutation status of R187Q, The gene SELENOS has a mutation status of S140G, The gene WDR90 has a mutation status of D743D, The gene RHBDL1 has a mutation status of S137S, The gene LMF1 has a mutation status of G410R, The gene TPSB2 has a mutation status of H269Q, The gene NME3 has a mutation status of K51R, The gene NTHL1 has a mutation status of R25K, The gene PKD1 has a mutation status of A639V, The gene SRRM2 has a mutation status of P1278R, The gene SRRM2 has a mutation status of P2324S, The gene PRSS41 has a mutation status of P195P, The gene LINC00514 has a mutation status of G230*, The gene UBN1 has a mutation status of R117C, The gene RBFOX1 has a mutation status of G177S, The gene NPIPB2 has a mutation status of R94C, The gene CPPED1 has a mutation status of V72I, The gene XYLT1 has a mutation status of P721P, The gene COQ7 has a mutation status of R23W, The gene PDILT has a mutation status of E519G, The gene VWA3A has a mutation status of N69N, The gene ALDOA has a mutation status of D68N, The gene ZNF689 has a mutation status of E323E, The gene ITGAM has a mutation status of F457F, The gene ADCY7 has a mutation status of G934S, The gene TSNAXIP1 has a mutation status of F306del, The gene PDPR has a mutation status of Q205H, The gene PMFBP1 has a mutation status of M582I, The gene PMFBP1 has a mutation status of D567H, The gene WDR59 has a mutation status of H70L, The gene KLHL36 has a mutation status of A213A, The gene ANKRD11 has a mutation status of Y214Y, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene PRPF8 has a mutation status of S2205Y, The gene PRPF8 has a mutation status of I2199I, The gene OR1D2 has a mutation status of R292S, The gene ANKFY1 has a mutation status of V592A, The gene GGT6 has a mutation status of T423S, The gene CAMTA2 has a mutation status of D58D, The gene FBXO39 has a mutation status of I437I, The gene CD68 has a mutation status of A10T, The gene TP53 has a mutation status of R267W, The gene TP53 has a mutation status of E171del, The gene ARHGAP44 has a mutation status of T51T, The gene COX10 has a mutation status of E335K, The gene RAI1 has a mutation status of S788S, The gene SLC13A2 has a mutation status of V533M, The gene EFCAB5 has a mutation status of G1073E, The gene ZNF207 has a mutation status of A294T, The gene SLC35G3 has a mutation status of A223A, The gene HEATR9 has a mutation status of M403I, The gene HEATR9 has a mutation status of E396K, The gene CCL4L2 has a mutation status of P67R, The gene GGNBP2 has a mutation status of E184K, The gene PCGF2 has a mutation status of A253A, The gene KRT40 has a mutation status of L292P, The gene KRTAP9-2 has a mutation status of G106D, The gene KRTAP9-6 has a mutation status of G106C, The gene CAVIN1 has a mutation status of D18D, The gene WNK4 has a mutation status of L619L, The gene NAGS has a mutation status of M169L, The gene GNGT2 has a mutation status of E7K, The gene SEPTIN4 has a mutation status of Y421Y, The gene ACE has a mutation status of M828T, The gene CSH1 has a mutation status of F36fs, The gene SDK2 has a mutation status of R1172C, The gene RECQL5 has a mutation status of V879V, The gene TRIM65 has a mutation status of R360Q, The gene TMC6 has a mutation status of R783S, The gene DNAH17 has a mutation status of Y3712F, The gene DNAH17 has a mutation status of D3181D, The gene GAA has a mutation status of S940S, The gene AATK has a mutation status of T196T, The gene NPC1 has a mutation status of S167S, The gene TPGS2 has a mutation status of G154G, The gene EPG5 has a mutation status of K257R, The gene ST8SIA3 has a mutation status of R188H, The gene RELCH has a mutation status of Q883H, The gene CNDP1 has a mutation status of S135R, The gene GZMM has a mutation status of G254S, The gene BSG has a mutation status of D149E, The gene ARID3A has a mutation status of G103G, The gene SBNO2 has a mutation status of C686C, The gene SPPL2B has a mutation status of P517A, The gene SLC25A23 has a mutation status of R11R, The gene LRRC8E has a mutation status of V169V, The gene FBN3 has a mutation status of G2133S, The gene MUC16 has a mutation status of T4266P, The gene ANGPTL6 has a mutation status of G140W, The gene ANGPTL6 has a mutation status of A85A, The gene TYK2 has a mutation status of R701T, The gene DOCK6 has a mutation status of A1267V, The gene EPOR has a mutation status of E84Q, The gene ZNF20 has a mutation status of Y434Y, The gene MAN2B1 has a mutation status of A957G, The gene PGLYRP2 has a mutation status of D529N, The gene C19orf44 has a mutation status of S265S, The gene MYO9B has a mutation status of L1728R, The gene OCEL1 has a mutation status of R214R, The gene JAK3 has a mutation status of I213F, The gene SLC5A5 has a mutation status of L408L, The gene UPF1 has a mutation status of L1035L, The gene DDX49 has a mutation status of R119Q, The gene ZNF254 has a mutation status of I286T, The gene PLEKHF1 has a mutation status of K106R, The gene NUDT19 has a mutation status of P27P, The gene PEPD has a mutation status of R314H, The gene ZNF30 has a mutation status of C543*, The gene UPK1A has a mutation status of A85T, The gene NPHS1 has a mutation status of T5M, The gene GGN has a mutation status of P509P, The gene FAM98C has a mutation status of E76del, The gene RINL has a mutation status of L368F, The gene PLEKHG2 has a mutation status of D75D, The gene FCGBP has a mutation status of D126H, The gene HIPK4 has a mutation status of S372L, The gene TMEM91 has a mutation status of A114V, The gene ARHGEF1 has a mutation status of V417I, The gene GRIK5 has a mutation status of A944V, The gene PSG7 has a mutation status of K371T, The gene KLC3 has a mutation status of A226A, The gene VASP has a mutation status of P77S, The gene GPR4 has a mutation status of S348S, The gene PGLYRP1 has a mutation status of L98L, The gene PRKD2 has a mutation status of L631L, The gene CCDC9 has a mutation status of G495S, The gene CCDC114 has a mutation status of T523T, The gene PLEKHA4 has a mutation status of R91R, The gene SCAF1 has a mutation status of S621S, The gene CLEC11A has a mutation status of P104R, The gene CLEC11A has a mutation status of V127L, The gene KLK11 has a mutation status of G97S, The gene ZNF175 has a mutation status of D31D, The gene TMC4 has a mutation status of L379L, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene PPP6R1 has a mutation status of G738E, The gene NLRP11 has a mutation status of R534C, The gene ZIM2 has a mutation status of S320L, The gene PEG3 has a mutation status of L1134L, The gene TRAPPC2B has a mutation status of H87fs, The gene MZF1 has a mutation status of E642K, The gene C20orf96 has a mutation status of K184K, The gene SNPH has a mutation status of L264L, The gene OXT has a mutation status of L101S, The gene PANK2 has a mutation status of L129L, The gene SEC23B has a mutation status of S127F, The gene CFAP61 has a mutation status of R1115C, The gene TM9SF4 has a mutation status of G576R, The gene DNMT3B has a mutation status of A513V, The gene CNBD2 has a mutation status of T71T, The gene AAR2 has a mutation status of L298L, The gene MROH8 has a mutation status of N711H, The gene MROH8 has a mutation status of T290T, The gene KIAA1755 has a mutation status of A546A, The gene ARHGAP40 has a mutation status of S136S, The gene LPIN3 has a mutation status of D477Y, The gene PLTP has a mutation status of V123V, The gene PREX1 has a mutation status of A1562A, The gene ZNF831 has a mutation status of A1037D, The gene FAM217B has a mutation status of N163N, The gene CDH26 has a mutation status of L74L, The gene EEF1A2 has a mutation status of A125A, The gene HELZ2 has a mutation status of T2566A, The gene HELZ2 has a mutation status of R1988S, The gene ABHD16B has a mutation status of P313L, The gene KRTAP13-4 has a mutation status of S46P, The gene KRTAP11-1 has a mutation status of S6C, The gene URB1 has a mutation status of T1967T, The gene RCAN1 has a mutation status of P143P, The gene CBR1 has a mutation status of P213P, The gene DOP1B has a mutation status of S2264S, The gene RIPK4 has a mutation status of P584P, The gene C2CD2 has a mutation status of L599Q, The gene TRPM2 has a mutation status of R1454Q, The gene KRTAP10-8 has a mutation status of R214H, The gene ADARB1 has a mutation status of D503D, The gene PCBP3 has a mutation status of Q340Q, The gene FTCD has a mutation status of G336V, The gene PCNT has a mutation status of E2471E, The gene PRMT2 has a mutation status of I223I, The gene DGCR6L has a mutation status of Q139Q, The gene LZTR1 has a mutation status of D315D, The gene ZNF280B has a mutation status of S225L, The gene CABIN1 has a mutation status of P1741P, The gene MYO18B has a mutation status of Q1607Q, The gene MTFP1 has a mutation status of R76K, The gene SLC35E4 has a mutation status of A174T, The gene Z82190.2 has a mutation status of V288A, The gene HMGXB4 has a mutation status of K33R, The gene TRIOBP has a mutation status of P1230L, The gene TRIOBP has a mutation status of P390L, The gene RPL3 has a mutation status of S304S, The gene ENTHD1 has a mutation status of L312L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene FAM118A has a mutation status of G289R, The gene SMC1B has a mutation status of Q227Q, The gene TYMP has a mutation status of A14A, The gene CPT1B has a mutation status of F734F, The gene IL3RA has a mutation status of R84Q, The gene WWC3 has a mutation status of C954R, The gene RS1 has a mutation status of P192P, The gene FAM47A has a mutation status of T764T, The gene CXorf38 has a mutation status of R69G, The gene PPP1R2C has a mutation status of D108Y, The gene ZNF630 has a mutation status of K401T, The gene HDAC6 has a mutation status of P1033S, The gene PPP1R3F has a mutation status of C98C, The gene GNL3L has a mutation status of Y351Y, The gene ALAS2 has a mutation status of G364A, The gene KLF8 has a mutation status of K171T, The gene AR has a mutation status of D354E, The gene AR has a mutation status of K633T, The gene MED12 has a mutation status of L36P, The gene RLIM has a mutation status of R515T, The gene NEXMIF has a mutation status of G1093E, The gene DACH2 has a mutation status of S206S, The gene DIAPH2 has a mutation status of D882N, The gene GPRASP1 has a mutation status of R1167W, The gene IRS4 has a mutation status of H910D, The gene DOCK11 has a mutation status of L1522L, The gene TENM1 has a mutation status of L850H, The gene TENM1 has a mutation status of M516V, The gene OR13H1 has a mutation status of L153R, The gene OPN1LW has a mutation status of F287F, The gene AMELY has a mutation status of R166Q, The gene USP9Y has a mutation status of R211C, The gene USP9Y has a mutation status of P2109P, The gene MT-ND2 has a mutation status of T122A, The gene MT-ND2 has a mutation status of T213T, The gene MT-CO2 has a mutation status of S94S, The gene MT-CO2 has a mutation status of S205S, The gene MT-CYB has a mutation status of G251S, The gene MT-CYB has a mutation status of V284V, The gene MT-CYB has a mutation status of I372V, The gene VWA1 has a mutation status of D280G, The gene ATAD3B has a mutation status of R290S, The gene NPHP4 has a mutation status of P527L, The gene PEX14 has a mutation status of H259H, The gene PEX14 has a mutation status of D332N, The gene AGTRAP has a mutation status of L98L, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF15 has a mutation status of L149V, The gene SPEN has a mutation status of V2856V, The gene FAM43B has a mutation status of L2L, The gene HSPG2 has a mutation status of P1129Q, The gene EPHA8 has a mutation status of A866T, The gene HNRNPR has a mutation status of T137T, The gene ZNF436 has a mutation status of D18G, The gene NIPAL3 has a mutation status of V103M, The gene AHDC1 has a mutation status of P738P, The gene PTPRU has a mutation status of G891D, The gene KHDRBS1 has a mutation status of Y440Y, The gene TMEM39B has a mutation status of P111T, The gene YARS1 has a mutation status of E20E, The gene ZSCAN20 has a mutation status of L338L, The gene CLSPN has a mutation status of A126V, The gene PPCS has a mutation status of V37G, The gene B4GALT2 has a mutation status of Q233H, The gene ZSWIM5 has a mutation status of S921G, The gene DMBX1 has a mutation status of Q30K, The gene RAB3B has a mutation status of F47F, The gene RAB3B has a mutation status of L39L, The gene CDCP2 has a mutation status of P401P, The gene LMO4 has a mutation status of C47C, The gene PTBP2 has a mutation status of V524V, The gene PPM1J has a mutation status of A39A, The gene DENND2C has a mutation status of E222A, The gene NBPF20 has a mutation status of K59N, The gene NBPF9 has a mutation status of N855D, The gene NBPF9 has a mutation status of C803C, The gene AC242842.3 has a mutation status of E91D, The gene HRNR has a mutation status of G637G, The gene RUSC1 has a mutation status of L24F, The gene COPA has a mutation status of Q1199R, The gene SLC9C2 has a mutation status of Y310F, The gene RC3H1 has a mutation status of L970L, The gene TNR has a mutation status of Y1022Y, The gene SEC16B has a mutation status of S840T, The gene AXDND1 has a mutation status of F266L, The gene NPHS2 has a mutation status of A27G, The gene ZBTB41 has a mutation status of L16L, The gene NAV1 has a mutation status of K1107K, The gene IPO9 has a mutation status of I80V, The gene UBE2T has a mutation status of E148E, The gene FMOD has a mutation status of Y39Y, The gene PLEKHA6 has a mutation status of N19K, The gene C1orf74 has a mutation status of L55L, The gene DNAH14 has a mutation status of K226K, The gene EPHX1 has a mutation status of T26S, The gene OBSCN has a mutation status of A5327T, The gene NTPCR has a mutation status of G116G, The gene PCNX2 has a mutation status of G1339G, The gene CEP170 has a mutation status of G433G, The gene OR2T4 has a mutation status of V109L, The gene TRAPPC12 has a mutation status of E113*, The gene TRAPPC12 has a mutation status of M300V, The gene APOB has a mutation status of N3051S, The gene MFSD2B has a mutation status of V380G, The gene FAM228B has a mutation status of Q303fs, The gene CENPO has a mutation status of S31Y, The gene WDR43 has a mutation status of H412R, The gene SLC30A6 has a mutation status of T257T, The gene SOCS5 has a mutation status of A393A, The gene CCDC88A has a mutation status of T1304T, The gene CCDC88A has a mutation status of T1304A, The gene AAK1 has a mutation status of K419N, The gene MXD1 has a mutation status of T94T, The gene RAB11FIP5 has a mutation status of P881R, The gene RAB11FIP5 has a mutation status of L726L, The gene ACTG2 has a mutation status of L174L, The gene LRRTM4 has a mutation status of L383L, The gene GGCX has a mutation status of L270P, The gene POLR1A has a mutation status of T957T, The gene FAHD2A has a mutation status of V52I, The gene PDCL3 has a mutation status of A33A, The gene CNOT11 has a mutation status of P288P, The gene EDAR has a mutation status of S380R, The gene CCDC93 has a mutation status of F612L, The gene SCTR has a mutation status of A417A, The gene EPB41L5 has a mutation status of T194T, The gene MAP3K2 has a mutation status of I110V, The gene HS6ST1 has a mutation status of S207S, The gene ARHGEF4 has a mutation status of L717L, The gene MCM6 has a mutation status of T245T, The gene RBM43 has a mutation status of V24A, The gene COBLL1 has a mutation status of S623S, The gene SCN7A has a mutation status of N538S, The gene SCRN3 has a mutation status of D202D, The gene TTC30B has a mutation status of R605H, The gene FKBP7 has a mutation status of P131L, The gene FSIP2 has a mutation status of T1337I, The gene ITGAV has a mutation status of R241Q, The gene KCTD18 has a mutation status of V227G, The gene ORC2 has a mutation status of N505D, The gene MAP2 has a mutation status of L326S, The gene FN1 has a mutation status of I594T, The gene PECR has a mutation status of S271L, The gene TTLL4 has a mutation status of S156S, The gene CYP27A1 has a mutation status of V238M, The gene DNAJB2 has a mutation status of G297W, The gene AC053503.6 has a mutation status of A157A, The gene OBSL1 has a mutation status of S903S, The gene DOCK10 has a mutation status of R1654C, The gene COL4A4 has a mutation status of P1426A, The gene COL4A3 has a mutation status of T477I, The gene ARMC9 has a mutation status of P737T, The gene ECEL1 has a mutation status of G666R, The gene MROH2A has a mutation status of K714K, The gene HJURP has a mutation status of K39R, The gene SNED1 has a mutation status of K1217N, The gene HDLBP has a mutation status of I1068I, The gene CHL1 has a mutation status of V180L, The gene CRBN has a mutation status of H17P, The gene SSUH2 has a mutation status of L305I, The gene FGD5 has a mutation status of K459Q, The gene OSBPL10 has a mutation status of D133N, The gene DLEC1 has a mutation status of T611T, The gene MYRIP has a mutation status of D739D, The gene NKTR has a mutation status of T52K, The gene KIF15 has a mutation status of D748E, The gene PTPN23 has a mutation status of R1237C, The gene APEH has a mutation status of Q572H, The gene DOCK3 has a mutation status of N483K, The gene RRP9 has a mutation status of R140R, The gene STAB1 has a mutation status of F2542fs, The gene EOGT has a mutation status of H56R, The gene NAA50 has a mutation status of R21T, The gene DRD3 has a mutation status of H359H, The gene GTF2E1 has a mutation status of A18A, The gene SLC12A8 has a mutation status of N390N, The gene PLXNA1 has a mutation status of R942Q, The gene MGLL has a mutation status of V165V, The gene GP9 has a mutation status of A107S, The gene A4GNT has a mutation status of F36F, The gene ATR has a mutation status of D1915G, The gene IGSF10 has a mutation status of P1773S, The gene GPR149 has a mutation status of N423K, The gene PLCH1 has a mutation status of G436A, The gene SHOX2 has a mutation status of A296A, The gene IL12A has a mutation status of P60P, The gene KPNA4 has a mutation status of N39K, The gene SLITRK3 has a mutation status of S173S, The gene KCNMB3 has a mutation status of R249K, The gene YEATS2 has a mutation status of I339V, The gene YEATS2 has a mutation status of P1118L, The gene EIF4G1 has a mutation status of Y1401Y, The gene EPHB3 has a mutation status of A314A, The gene SENP2 has a mutation status of H537H, The gene ST6GAL1 has a mutation status of L326L, The gene MB21D2 has a mutation status of T135T, The gene CTBP1 has a mutation status of G197S, The gene NKX1-1 has a mutation status of P210A, The gene DOK7 has a mutation status of I48T, The gene LDB2 has a mutation status of D47V, The gene ADGRA3 has a mutation status of L1004H, The gene KLF3 has a mutation status of P120P, The gene TLR1 has a mutation status of G417V, The gene YIPF7 has a mutation status of T127S, The gene REST has a mutation status of T696A, The gene ODAM has a mutation status of Q68E, The gene SHROOM3 has a mutation status of A1002A, The gene SHROOM3 has a mutation status of H1237R, The gene FRAS1 has a mutation status of H3347Q, The gene GPRIN3 has a mutation status of S111*, The gene ADH7 has a mutation status of E239D, The gene CENPE has a mutation status of N391Y, The gene ZGRF1 has a mutation status of M2023T, The gene LARP7 has a mutation status of Q317H, The gene TNIP3 has a mutation status of P325L, The gene ADAD1 has a mutation status of T36M, The gene FAT4 has a mutation status of G4887V, The gene LRBA has a mutation status of A2546G, The gene RPS3A has a mutation status of T11T, The gene FSTL5 has a mutation status of T606I, The gene TENM3 has a mutation status of K1784M, The gene SORBS2 has a mutation status of N338K, The gene FAM149A has a mutation status of E187*, The gene PLEKHG4B has a mutation status of V1328V, The gene SEMA5A has a mutation status of Q438Q, The gene ATPSCKMT has a mutation status of R132Q, The gene ANKH has a mutation status of V87I, The gene FBXL7 has a mutation status of H98Y, The gene MYO10 has a mutation status of E1146K, The gene NIPBL has a mutation status of S1517*, The gene HCN1 has a mutation status of Y347Y, The gene ITGA2 has a mutation status of G793R, The gene ERBIN has a mutation status of N1083S, The gene MAST4 has a mutation status of S1870del, The gene OTP has a mutation status of A71V, The gene ADGRV1 has a mutation status of E2446K, The gene ADGRV1 has a mutation status of R4802Q, The gene AP3S1 has a mutation status of I182V, The gene LVRN has a mutation status of I766V, The gene ZNF474 has a mutation status of S78L, The gene TGFBI has a mutation status of P501T, The gene SLC4A9 has a mutation status of S614T, The gene PCDHB2 has a mutation status of V266D, The gene PCDHGA1 has a mutation status of A761A, The gene PCDHGA2 has a mutation status of D536Y, The gene SPINK14 has a mutation status of T53M, The gene AFAP1L1 has a mutation status of K714N, The gene HK3 has a mutation status of T895T, The gene IRF4 has a mutation status of T92T, The gene DSP has a mutation status of K1581E, The gene GCNT2 has a mutation status of E130G, The gene MYLIP has a mutation status of S354L, The gene H2BC7 has a mutation status of T91T, The gene H3C8 has a mutation status of L104L, The gene OR2B2 has a mutation status of R270G, The gene LTA has a mutation status of M1I, The gene PBX2 has a mutation status of E180K, The gene TBCC has a mutation status of I335V, The gene TBCC has a mutation status of T276I, The gene PTK7 has a mutation status of P698R, The gene ZNF318 has a mutation status of A1580T, The gene POLH has a mutation status of T478M, The gene GTPBP2 has a mutation status of V21A, The gene TMEM151B has a mutation status of G19G, The gene IMPG1 has a mutation status of K621K, The gene TTK has a mutation status of P468L, The gene TBX18 has a mutation status of E29K, The gene CDK19 has a mutation status of A38A, The gene GPRC6A has a mutation status of T253T, The gene STX7 has a mutation status of L76L, The gene HBS1L has a mutation status of M174V, The gene TXLNB has a mutation status of R243G, The gene RAET1E has a mutation status of L60L, The gene SYNE1 has a mutation status of T7356T, The gene SYNE1 has a mutation status of L6024L, The gene CNKSR3 has a mutation status of S306C, The gene ZDHHC14 has a mutation status of D116A, The gene SNX9 has a mutation status of I28L, The gene SYNJ2 has a mutation status of R744R, The gene ERMARD has a mutation status of A68A, The gene INTS1 has a mutation status of V1094A, The gene CHST12 has a mutation status of R222L, The gene AMZ1 has a mutation status of T343P, The gene RADIL has a mutation status of S56S, The gene RNF216 has a mutation status of E707Q, The gene PMS2 has a mutation status of Y313C, The gene THSD7A has a mutation status of P488T, The gene TMEM196 has a mutation status of E154D, The gene DNAH11 has a mutation status of W1733C, The gene DNAH11 has a mutation status of R2044Q, The gene STEAP1B has a mutation status of H32R, The gene TAX1BP1 has a mutation status of E618G, The gene PLEKHA8 has a mutation status of E269V, The gene UBE2D4 has a mutation status of C111S, The gene RAMP3 has a mutation status of N58K, The gene ASL has a mutation status of E50E, The gene SSC4D has a mutation status of G318R, The gene CCDC146 has a mutation status of E254K, The gene ABCB4 has a mutation status of A791S, The gene AKAP9 has a mutation status of L603L, The gene AKAP9 has a mutation status of K3276K, The gene COL1A2 has a mutation status of A765A, The gene PILRB has a mutation status of S30C, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T1234A, The gene MUC3A has a mutation status of P2041L, The gene SH2B2 has a mutation status of S612F, The gene COG5 has a mutation status of P788P, The gene PTPRZ1 has a mutation status of E1306Q, The gene FEZF1 has a mutation status of K203K, The gene GCC1 has a mutation status of A279A, The gene FLNC has a mutation status of T1880N, The gene IRF5 has a mutation status of K73K, The gene TCAF1 has a mutation status of V62M, The gene CNTNAP2 has a mutation status of G965G, The gene ZNF783 has a mutation status of Y168Y, The gene ZNF746 has a mutation status of I426I, The gene REPIN1 has a mutation status of R513R, The gene NUB1 has a mutation status of Q13R, The gene DPP6 has a mutation status of V650V, The gene CSMD1 has a mutation status of T295T, The gene BLK has a mutation status of Q392Q, The gene MTMR7 has a mutation status of I175T, The gene GFRA2 has a mutation status of A182V, The gene DOCK5 has a mutation status of Q1614H, The gene STMN4 has a mutation status of A188A, The gene INTS9 has a mutation status of V504G, The gene NSD3 has a mutation status of R1309T, The gene PDE7A has a mutation status of R65P, The gene MSC has a mutation status of R117H, The gene TRPA1 has a mutation status of Q1070R, The gene RGS22 has a mutation status of K429E, The gene COL14A1 has a mutation status of A1620A, The gene FAM83A has a mutation status of V60G, The gene ATAD2 has a mutation status of R295Q, The gene SCRIB has a mutation status of E1429*, The gene PLEC has a mutation status of A2194A, The gene MROH1 has a mutation status of D613A, The gene MROH1 has a mutation status of I874I, The gene MROH1 has a mutation status of P1321S, The gene MROH1 has a mutation status of A1497V, The gene KANK1 has a mutation status of A1203V, The gene KIAA2026 has a mutation status of T1259I, The gene RANBP6 has a mutation status of K547R, The gene MPDZ has a mutation status of I1011T, The gene CER1 has a mutation status of K53T, The gene CCDC171 has a mutation status of E363K, The gene ADAMTSL1 has a mutation status of V1265I, The gene CDKN2A has a mutation status of H15R, The gene AQP7 has a mutation status of L181L, The gene CNTNAP3 has a mutation status of A1182A, The gene NTRK2 has a mutation status of H300H, The gene ASPN has a mutation status of D46D, The gene ZNF484 has a mutation status of A812G, The gene WNK2 has a mutation status of V1035V, The gene PTCH1 has a mutation status of R893H, The gene TBC1D2 has a mutation status of A348T, The gene TBC1D2 has a mutation status of A257S, The gene PTPN3 has a mutation status of L384L, The gene ASTN2 has a mutation status of Y1060Y, The gene RABGAP1 has a mutation status of N1005Y, The gene LHX2 has a mutation status of A204E, The gene FAM102A has a mutation status of L146L, The gene SPTAN1 has a mutation status of A2140T, The gene RAPGEF1 has a mutation status of A487V, The gene SPACA9 has a mutation status of V104I, The gene STKLD1 has a mutation status of L631P, The gene DBH has a mutation status of T467M, The gene TMEM250 has a mutation status of A30T, The gene TRAF2 has a mutation status of T401T, The gene SLC34A3 has a mutation status of L204L, The gene ITIH2 has a mutation status of R464S, The gene ATP5F1C has a mutation status of R277C, The gene FRMD4A has a mutation status of S798S, The gene RSU1 has a mutation status of P217R, The gene MALRD1 has a mutation status of I1837L, The gene GPR158 has a mutation status of R525W, The gene SVIL has a mutation status of P659S, The gene FZD8 has a mutation status of T157P, The gene ZNF239 has a mutation status of K435R, The gene OR13A1 has a mutation status of L205V, The gene OGDHL has a mutation status of A533A, The gene CCAR1 has a mutation status of R327H, The gene DNAJB12 has a mutation status of E304K, The gene PLAU has a mutation status of P160S, The gene LDB3 has a mutation status of A282V, The gene CPEB3 has a mutation status of P16H, The gene CPEB3 has a mutation status of Q13K, The gene EXOC6 has a mutation status of T765A, The gene ZFYVE27 has a mutation status of P179H, The gene CPN1 has a mutation status of R24H, The gene GBF1 has a mutation status of S1357S, The gene PSD has a mutation status of P466P, The gene PNLIP has a mutation status of Y58H, The gene FGFR2 has a mutation status of F417V, The gene EBF3 has a mutation status of A397V, The gene LRRC56 has a mutation status of L143F, The gene DEAF1 has a mutation status of A436A, The gene PGAP2 has a mutation status of F93F, The gene TRIM68 has a mutation status of E111D, The gene DENND2B has a mutation status of P350P, The gene SCUBE2 has a mutation status of N405S, The gene ABCC8 has a mutation status of R1221Q, The gene OTOG has a mutation status of T1223P, The gene HPS5 has a mutation status of R184W, The gene NELL1 has a mutation status of C490G, The gene ANO3 has a mutation status of F183F, The gene KCNA4 has a mutation status of F228V, The gene MYBPC3 has a mutation status of K89Q, The gene NUP160 has a mutation status of P635P, The gene OR4C16 has a mutation status of W21fs, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene CD248 has a mutation status of D152D, The gene RIN1 has a mutation status of L360L, The gene RIN1 has a mutation status of E315*, The gene PC has a mutation status of S603N, The gene GAL has a mutation status of R107C, The gene PPFIA1 has a mutation status of L371L, The gene DHCR7 has a mutation status of A452T, The gene PAAF1 has a mutation status of G213A, The gene DLG2 has a mutation status of F55L, The gene FAT3 has a mutation status of Y2104Y, The gene FAT3 has a mutation status of K2936Q, The gene VPS11 has a mutation status of A451V, The gene TECTA has a mutation status of V1171M, The gene HSPA8 has a mutation status of K561N, The gene FEZ1 has a mutation status of H226H, The gene PRDM10 has a mutation status of N740N, The gene APLP2 has a mutation status of G295S, The gene CACNA1C has a mutation status of Q1964R, The gene C1S has a mutation status of P338A, The gene TAS2R7 has a mutation status of L29L, The gene PRB2 has a mutation status of P73R, The gene SLCO1B3 has a mutation status of C142F, The gene ITPR2 has a mutation status of V2074G, The gene PKP2 has a mutation status of L471L, The gene ADAMTS20 has a mutation status of E786fs, The gene SCAF11 has a mutation status of L1389L, The gene SLC38A1 has a mutation status of I399T, The gene CCNT1 has a mutation status of S475S, The gene KMT2D has a mutation status of P1097R, The gene SPATS2 has a mutation status of S507P, The gene FAIM2 has a mutation status of G44V, The gene MAP3K12 has a mutation status of L425M, The gene HOXC5 has a mutation status of H70P, The gene OR6C74 has a mutation status of D87V, The gene OR6C70 has a mutation status of S247S, The gene OR10P1 has a mutation status of T159I, The gene RDH5 has a mutation status of V14V, The gene ESYT1 has a mutation status of L302L, The gene STAT2 has a mutation status of L718L, The gene LRP1 has a mutation status of I3965I, The gene OTOGL has a mutation status of R1915P, The gene NTN4 has a mutation status of T572M, The gene NTN4 has a mutation status of E59K, The gene HAL has a mutation status of E115E, The gene TMPO has a mutation status of G80R, The gene PMCH has a mutation status of S87S, The gene NT5DC3 has a mutation status of S531S, The gene PRDM4 has a mutation status of L303F, The gene ATP2A2 has a mutation status of D886Y, The gene BRAP has a mutation status of V506I, The gene BRAP has a mutation status of V311V, The gene OAS2 has a mutation status of D508H, The gene DDX54 has a mutation status of R86H, The gene IQCD has a mutation status of K231E, The gene DNAH10 has a mutation status of V3620fs, The gene CCDC92 has a mutation status of T282P, The gene SFSWAP has a mutation status of F188I, The gene EP400 has a mutation status of S37P, The gene ATP8A2 has a mutation status of L256V, The gene FRY has a mutation status of S2432R, The gene SMAD9 has a mutation status of P145Q, The gene RB1 has a mutation status of H483R, The gene DACH1 has a mutation status of 81_82insGG, The gene DCT has a mutation status of V475V, The gene ABCC4 has a mutation status of G430G, The gene CLDN10 has a mutation status of L49L, The gene CLDN10 has a mutation status of S68T, The gene RNF113B has a mutation status of S89R, The gene FARP1 has a mutation status of H703P, The gene SLC15A1 has a mutation status of V450I, The gene NALCN has a mutation status of H1189N, The gene ERCC5 has a mutation status of E1181K, The gene ERCC5 has a mutation status of E1341K, The gene SLC10A2 has a mutation status of S35R, The gene ATP11A has a mutation status of K500T, The gene UPF3A has a mutation status of A66S, The gene OR4K15 has a mutation status of V270D, The gene RNASE13 has a mutation status of R7W, The gene ARHGEF40 has a mutation status of P1395A, The gene OR4E2 has a mutation status of R226*, The gene ADCY4 has a mutation status of K220K, The gene PRKD1 has a mutation status of G32G, The gene MIA2 has a mutation status of M1180T, The gene FANCM has a mutation status of H721R, The gene SYT16 has a mutation status of S291T, The gene SYNE2 has a mutation status of F1979F, The gene EXD2 has a mutation status of E92K, The gene SMOC1 has a mutation status of D309D, The gene CATSPERB has a mutation status of T323N, The gene TC2N has a mutation status of Q362fs, The gene COX8C has a mutation status of R5L, The gene BCL11B has a mutation status of N352T, The gene WARS1 has a mutation status of Y100Y, The gene RTL1 has a mutation status of P51L, The gene AHNAK2 has a mutation status of S245F, The gene LINC02203 has a mutation status of I259M, The gene VPS18 has a mutation status of A918A, The gene VPS39 has a mutation status of A248A, The gene GANC has a mutation status of R652Q, The gene CAPN3 has a mutation status of R315Q, The gene NEDD4 has a mutation status of Q60R, The gene HERC1 has a mutation status of R2997I, The gene DENND4A has a mutation status of N1109H, The gene SEMA7A has a mutation status of L308L, The gene PEX11A has a mutation status of E33K, The gene SYNM has a mutation status of R187Q, The gene LMF1 has a mutation status of G410R, The gene TPSB2 has a mutation status of H269Q, The gene EME2 has a mutation status of G279G, The gene TBL3 has a mutation status of T101P, The gene SRRM2 has a mutation status of P1278R, The gene SRRM2 has a mutation status of P2324S, The gene PRSS41 has a mutation status of P195P, The gene UBN1 has a mutation status of R117C, The gene TXNDC11 has a mutation status of H381H, The gene NPIPB2 has a mutation status of R94C, The gene CPPED1 has a mutation status of V72I, The gene XYLT1 has a mutation status of P721P, The gene PDILT has a mutation status of E519G, The gene VWA3A has a mutation status of N69N, The gene APOBR has a mutation status of S792S, The gene SRCAP has a mutation status of P2426P, The gene ITGAM has a mutation status of F457F, The gene ADCY7 has a mutation status of L774M, The gene TSNAXIP1 has a mutation status of F306del, The gene PDPR has a mutation status of Q205H, The gene PKD1L3 has a mutation status of Q616R, The gene PMFBP1 has a mutation status of M582I, The gene PMFBP1 has a mutation status of D567H, The gene GLG1 has a mutation status of G95G, The gene WDR59 has a mutation status of H70L, The gene TAF1C has a mutation status of Q805H, The gene ATP2C2 has a mutation status of A690A, The gene KLHL36 has a mutation status of A213A, The gene ANKRD11 has a mutation status of Y214Y, The gene AC092143.1 has a mutation status of T157P, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene NXN has a mutation status of V294G, The gene PRPF8 has a mutation status of S2205Y, The gene PRPF8 has a mutation status of I2199I, The gene OR1D2 has a mutation status of R292S, The gene ANKFY1 has a mutation status of V592A, The gene GGT6 has a mutation status of T423S, The gene CAMTA2 has a mutation status of D58D, The gene FBXO39 has a mutation status of I437I, The gene CD68 has a mutation status of A10T, The gene TP53 has a mutation status of R267W, The gene TP53 has a mutation status of E171del, The gene USP43 has a mutation status of G739R, The gene MYH13 has a mutation status of R1824W, The gene ARHGAP44 has a mutation status of A600A, The gene COX10 has a mutation status of E335K, The gene AC005324.3 has a mutation status of T120T, The gene EPN2 has a mutation status of S172P, The gene SLC13A2 has a mutation status of V533M, The gene EFCAB5 has a mutation status of G1073E, The gene ZNF207 has a mutation status of A294T, The gene SLC35G3 has a mutation status of A223A, The gene HEATR9 has a mutation status of M403I, The gene HEATR9 has a mutation status of E396K, The gene CCL4L2 has a mutation status of P67R, The gene GGNBP2 has a mutation status of E184K, The gene KRTAP9-2 has a mutation status of G106D, The gene CAVIN1 has a mutation status of D18D, The gene WNK4 has a mutation status of L619L, The gene NAGS has a mutation status of M169L, The gene GNGT2 has a mutation status of E7K, The gene ACE has a mutation status of M828T, The gene SDK2 has a mutation status of R1172C, The gene MYO15B has a mutation status of V2892G, The gene RECQL5 has a mutation status of V879V, The gene TMC6 has a mutation status of R783S, The gene TMEM235 has a mutation status of G183V, The gene DNAH17 has a mutation status of Y3712F, The gene DNAH17 has a mutation status of D3181D, The gene GAA has a mutation status of S940S, The gene AATK has a mutation status of T196T, The gene MYOM1 has a mutation status of D1053G, The gene NPC1 has a mutation status of S167S, The gene GALNT1 has a mutation status of L20V, The gene TPGS2 has a mutation status of G154G, The gene EPG5 has a mutation status of K257R, The gene ST8SIA3 has a mutation status of R188H, The gene LMAN1 has a mutation status of K159N, The gene RELCH has a mutation status of Q883H, The gene SERPINB13 has a mutation status of N157N, The gene CNDP1 has a mutation status of S135R, The gene GZMM has a mutation status of G254S, The gene BSG has a mutation status of D149E, The gene R3HDM4 has a mutation status of E15D, The gene SBNO2 has a mutation status of C686C, The gene SPPL2B has a mutation status of P517A, The gene RFX2 has a mutation status of T471T, The gene SLC25A23 has a mutation status of R11R, The gene LRRC8E has a mutation status of V169V, The gene FBN3 has a mutation status of G2133S, The gene PRAM1 has a mutation status of P27P, The gene MYO1F has a mutation status of R794R, The gene MYO1F has a mutation status of P786P, The gene EIF3G has a mutation status of P113P, The gene DOCK6 has a mutation status of A1267V, The gene EPOR has a mutation status of E84Q, The gene ZNF20 has a mutation status of Y434Y, The gene ZNF44 has a mutation status of P252P, The gene MAN2B1 has a mutation status of A957G, The gene MAST1 has a mutation status of P1498P, The gene EPS15L1 has a mutation status of T695M, The gene C19orf44 has a mutation status of S265S, The gene MYO9B has a mutation status of L1728R, The gene OCEL1 has a mutation status of R214R, The gene CCDC194 has a mutation status of G45V, The gene JAK3 has a mutation status of I213F, The gene UPF1 has a mutation status of L1035L, The gene DDX49 has a mutation status of R119Q, The gene ZNF254 has a mutation status of I286T, The gene PLEKHF1 has a mutation status of K106R, The gene PEPD has a mutation status of R314H, The gene ZNF30 has a mutation status of C543*, The gene AC020907.6 has a mutation status of H98fs, The gene GGN has a mutation status of P509P, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene FCGBP has a mutation status of D126H, The gene MAP3K10 has a mutation status of A310A, The gene PRX has a mutation status of S51S, The gene TMEM91 has a mutation status of A114V, The gene PSG7 has a mutation status of K371T, The gene CEACAM20 has a mutation status of P541fs, The gene KLC3 has a mutation status of A226A, The gene VASP has a mutation status of P77S, The gene GPR4 has a mutation status of S348S, The gene PGLYRP1 has a mutation status of L98L, The gene CCDC9 has a mutation status of G495S, The gene PLA2G4C has a mutation status of R430C, The gene RASIP1 has a mutation status of A603S, The gene CLEC11A has a mutation status of P104R, The gene CLEC11A has a mutation status of V127L, The gene KLK11 has a mutation status of G97S, The gene ZNF175 has a mutation status of D31D, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of 350_351insGY, The gene LILRA6 has a mutation status of Q350R, The gene NLRP11 has a mutation status of R534C, The gene ZIM2 has a mutation status of S320L, The gene PEG3 has a mutation status of L1134L, The gene TRAPPC2B has a mutation status of H87fs, The gene MZF1 has a mutation status of E642K, The gene C20orf96 has a mutation status of K184K, The gene SNPH has a mutation status of L264L, The gene SIRPA has a mutation status of L44S, The gene OXT has a mutation status of L101S, The gene CENPB has a mutation status of P151R, The gene PANK2 has a mutation status of L129L, The gene ISM1 has a mutation status of N50N, The gene SEC23B has a mutation status of S127F, The gene CFAP61 has a mutation status of R1115C, The gene TM9SF4 has a mutation status of G576R, The gene DNMT3B has a mutation status of A513V, The gene AAR2 has a mutation status of L298L, The gene MROH8 has a mutation status of N711H, The gene MROH8 has a mutation status of T290T, The gene ARHGAP40 has a mutation status of S136S, The gene LPIN3 has a mutation status of D477Y, The gene WFDC2 has a mutation status of A10A, The gene PLTP has a mutation status of V123V, The gene NFATC2 has a mutation status of P880L, The gene ZNF831 has a mutation status of A1037D, The gene FAM217B has a mutation status of N163N, The gene CDH26 has a mutation status of L74L, The gene EEF1A2 has a mutation status of A125A, The gene HELZ2 has a mutation status of R1988S, The gene ABHD16B has a mutation status of P313L, The gene ZNF512B has a mutation status of R585S, The gene KRTAP13-4 has a mutation status of S46P, The gene KRTAP11-1 has a mutation status of S6C, The gene URB1 has a mutation status of T1967T, The gene CBR1 has a mutation status of P213P, The gene DOP1B has a mutation status of S2264S, The gene RIPK4 has a mutation status of P584P, The gene C2CD2 has a mutation status of L599Q, The gene TRPM2 has a mutation status of R1454Q, The gene KRTAP10-8 has a mutation status of R214H, The gene ADARB1 has a mutation status of D503D, The gene PCBP3 has a mutation status of Q340Q, The gene PRMT2 has a mutation status of I223I, The gene DGCR6L has a mutation status of Q139Q, The gene ZNF280B has a mutation status of S225L, The gene GSTT4 has a mutation status of Q197R, The gene CABIN1 has a mutation status of P1741P, The gene MYO18B has a mutation status of Q1607Q, The gene SEZ6L has a mutation status of A551A, The gene MTFP1 has a mutation status of R76K, The gene SLC35E4 has a mutation status of A174T, The gene SMTN has a mutation status of S201S, The gene EIF4ENIF1 has a mutation status of A463A, The gene Z82190.2 has a mutation status of V288A, The gene HMGXB4 has a mutation status of K33R, The gene TRIOBP has a mutation status of P390L, The gene RPL3 has a mutation status of S304S, The gene ENTHD1 has a mutation status of L312L, The gene GRAP2 has a mutation status of H189P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene FAM118A has a mutation status of G289R, The gene TYMP has a mutation status of A14A, The gene CPT1B has a mutation status of F734F, The gene SHANK3 has a mutation status of P1214T, The gene IL3RA has a mutation status of R84Q, The gene WWC3 has a mutation status of C954R, The gene RS1 has a mutation status of P192P, The gene FAM47A has a mutation status of T764T, The gene CXorf38 has a mutation status of R69G, The gene SYN1 has a mutation status of G653G, The gene ZNF630 has a mutation status of K401T, The gene HDAC6 has a mutation status of P1033S, The gene KDM5C has a mutation status of V1463G, The gene GNL3L has a mutation status of Y351Y, The gene ALAS2 has a mutation status of G364A, The gene KLF8 has a mutation status of K171T, The gene AR has a mutation status of D354E, The gene EDA has a mutation status of P31P, The gene MED12 has a mutation status of L36P, The gene RLIM has a mutation status of R515T, The gene NEXMIF has a mutation status of G1093E, The gene DACH2 has a mutation status of S206S, The gene DIAPH2 has a mutation status of D882N, The gene GPRASP1 has a mutation status of R1167W, The gene IRS4 has a mutation status of H910D, The gene DOCK11 has a mutation status of L1522L, The gene TENM1 has a mutation status of L850H, The gene TENM1 has a mutation status of M516V, The gene CNGA2 has a mutation status of D662E, The gene OPN1LW has a mutation status of F287F, The gene MT-ND2 has a mutation status of T122A, The gene MT-CO2 has a mutation status of S94S, The gene MT-CO2 has a mutation status of S205S, The gene MT-CYB has a mutation status of G251S, The gene MT-CYB has a mutation status of V284V, The gene MT-CYB has a mutation status of I372V
PAAD
The gene ATAD3C has a mutation status of R245G, The gene FNDC10 has a mutation status of H225P, The gene AJAP1 has a mutation status of T348T, The gene RERE has a mutation status of L829L, The gene TNFRSF8 has a mutation status of L577L, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene FAM131C has a mutation status of S203T, The gene SPATA21 has a mutation status of D52A, The gene CROCC has a mutation status of Q1245H, The gene CROCC has a mutation status of E1959*, The gene ACTL8 has a mutation status of R156H, The gene MRTO4 has a mutation status of V75V, The gene VWA5B1 has a mutation status of S1031R, The gene HSPG2 has a mutation status of T3344P, The gene E2F2 has a mutation status of G419G, The gene FUCA1 has a mutation status of S8W, The gene OPRD1 has a mutation status of R146L, The gene CSMD2 has a mutation status of R837H, The gene MTF1 has a mutation status of P430P, The gene ACOT11 has a mutation status of L54L, The gene ST6GALNAC5 has a mutation status of R109R, The gene LRRC8B has a mutation status of W116*, The gene SPAG17 has a mutation status of R952P, The gene NBPF12 has a mutation status of R1042R, The gene NBPF11 has a mutation status of Q55H, The gene SCNM1 has a mutation status of R206Q, The gene FLG has a mutation status of S2087*, The gene SLC27A3 has a mutation status of R8G, The gene SLC27A3 has a mutation status of R22K, The gene USP21 has a mutation status of L9V, The gene SPATA46 has a mutation status of A229V, The gene TNN has a mutation status of A24P, The gene QSOX1 has a mutation status of G140G, The gene RGSL1 has a mutation status of H759C, The gene LAMC1 has a mutation status of A30G, The gene HMCN1 has a mutation status of S2858S, The gene HMCN1 has a mutation status of R3793C, The gene IGFN1 has a mutation status of P11S, The gene USH2A has a mutation status of S138F, The gene PCNX2 has a mutation status of R1122*, The gene TARBP1 has a mutation status of D1422E, The gene FMN2 has a mutation status of G58G, The gene MAP1LC3C has a mutation status of K6E, The gene SH3BP5L has a mutation status of V208G, The gene GDF7 has a mutation status of G336G, The gene APOB has a mutation status of F3161S, The gene PLB1 has a mutation status of W164C, The gene BIRC6 has a mutation status of E4123G, The gene CEBPZ has a mutation status of G180E, The gene C2orf74 has a mutation status of F40F, The gene CCT4 has a mutation status of V175G, The gene TET3 has a mutation status of G153R, The gene ITPRIPL1 has a mutation status of T236S, The gene CREG2 has a mutation status of Q237K, The gene NPHP1 has a mutation status of G533A, The gene MAP3K19 has a mutation status of K1264R, The gene RAB3GAP1 has a mutation status of K573K, The gene MBD5 has a mutation status of L1216S, The gene SCN9A has a mutation status of E1854Q, The gene HOXD1 has a mutation status of S130A, The gene TTN has a mutation status of E32948K, The gene TTN has a mutation status of V30338I, The gene CWC22 has a mutation status of H709R, The gene MYO1B has a mutation status of I416V, The gene HSPE1 has a mutation status of M1V, The gene PIKFYVE has a mutation status of V1292V, The gene UNC80 has a mutation status of E55K, The gene MYL1 has a mutation status of P54P, The gene PNKD has a mutation status of E295G, The gene SAG has a mutation status of P12L, The gene DGKD has a mutation status of V103I, The gene IL5RA has a mutation status of L214I, The gene RBMS3 has a mutation status of N125D, The gene STAC has a mutation status of I331T, The gene MLH1 has a mutation status of S99S, The gene SCN5A has a mutation status of G298S, The gene GASK1A has a mutation status of A348P, The gene APEH has a mutation status of P320L, The gene ERC2 has a mutation status of A724V, The gene PDZRN3 has a mutation status of R156H, The gene CNTN3 has a mutation status of D530G, The gene MYLK has a mutation status of G1639R, The gene KALRN has a mutation status of K228M, The gene MUC13 has a mutation status of R488M, The gene PLXNA1 has a mutation status of G1224G, The gene GRK7 has a mutation status of L324L, The gene GPR149 has a mutation status of R310H, The gene CCDC39 has a mutation status of N849K, The gene LIPH has a mutation status of G77E, The gene DGKG has a mutation status of M422T, The gene TNK2 has a mutation status of E763D, The gene LRCH3 has a mutation status of N159S, The gene ZNF141 has a mutation status of R30R, The gene MAN2B2 has a mutation status of R835C, The gene ABLIM2 has a mutation status of I337T, The gene FAM90A26 has a mutation status of P346L, The gene PACRGL has a mutation status of S59I, The gene SRP72 has a mutation status of P649T, The gene PRDM8 has a mutation status of G567G, The gene TET2 has a mutation status of L1229L, The gene RNF150 has a mutation status of V213I, The gene SFRP2 has a mutation status of R124Q, The gene GUCY1A1 has a mutation status of Q438Q, The gene SH3RF1 has a mutation status of G787G, The gene AHRR has a mutation status of P284P, The gene TRIO has a mutation status of G2305G, The gene SPEF2 has a mutation status of D702Y, The gene SPEF2 has a mutation status of R1410H, The gene SELENOP has a mutation status of Y159fs, The gene CCNO has a mutation status of T3P, The gene DEPDC1B has a mutation status of R36H, The gene ERBIN has a mutation status of K455Q, The gene MAST4 has a mutation status of Q1695*, The gene ZBED3 has a mutation status of L155A, The gene SLF1 has a mutation status of H601Y, The gene ACSL6 has a mutation status of A70G, The gene PROB1 has a mutation status of E110*, The gene SLC35A4 has a mutation status of L36W, The gene PCDHA6 has a mutation status of A484V, The gene PPP2R2B has a mutation status of R317H, The gene PDGFRB has a mutation status of L791L, The gene GRIA1 has a mutation status of H576Q, The gene RNF44 has a mutation status of G354A, The gene ZFP2 has a mutation status of T39P, The gene MGAT1 has a mutation status of R52W, The gene SIRT5 has a mutation status of V108G, The gene DEK has a mutation status of A7T, The gene CCHCR1 has a mutation status of L307M, The gene ATF6B has a mutation status of R588W, The gene CUTA has a mutation status of S34L, The gene ADGRF5 has a mutation status of T705A, The gene TRAM2 has a mutation status of E320G, The gene COL19A1 has a mutation status of G525C, The gene TTK has a mutation status of L608F, The gene AK9 has a mutation status of Y382H, The gene LAMA4 has a mutation status of H373Y, The gene FAM162B has a mutation status of G20V, The gene GINM1 has a mutation status of L19L, The gene THBS2 has a mutation status of S672S, The gene C6orf120 has a mutation status of Y149S, The gene AMZ1 has a mutation status of T343P, The gene SLC29A4 has a mutation status of G320R, The gene NPSR1 has a mutation status of E149K, The gene POLM has a mutation status of N456N, The gene POLM has a mutation status of S388G, The gene VWC2 has a mutation status of P65P, The gene IKZF1 has a mutation status of P353P, The gene ZNF727 has a mutation status of Y130H, The gene SEMA3C has a mutation status of E43E, The gene ZNF804B has a mutation status of K489N, The gene PPP1R35 has a mutation status of L110L, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene SPDYE6 has a mutation status of H337R, The gene IQUB has a mutation status of E436G, The gene KLF14 has a mutation status of P58S, The gene PLXNA4 has a mutation status of V1393M, The gene DGKI has a mutation status of A97V, The gene EPHA1 has a mutation status of D866A, The gene CNTNAP2 has a mutation status of S219S, The gene CNTNAP2 has a mutation status of S586R, The gene ZNF746 has a mutation status of E206D, The gene WDR60 has a mutation status of D59G, The gene MTMR9 has a mutation status of N14S, The gene FGF20 has a mutation status of Y210Y, The gene NEFM has a mutation status of F35F, The gene NUGGC has a mutation status of P792L, The gene ELP3 has a mutation status of K316*, The gene SNTG1 has a mutation status of A93V, The gene PXDNL has a mutation status of G732S, The gene HNF4G has a mutation status of S114S, The gene DCAF13 has a mutation status of N258S, The gene DPYS has a mutation status of V497V, The gene GPR20 has a mutation status of G232S, The gene EPPK1 has a mutation status of G1677S, The gene PLEC has a mutation status of A4604A, The gene RANBP6 has a mutation status of L651F, The gene FOCAD has a mutation status of D4N, The gene FOCAD has a mutation status of R256H, The gene CDKN2A has a mutation status of RALLEA29del, The gene GKAP1 has a mutation status of L98L, The gene NOL8 has a mutation status of K935R, The gene ANP32B has a mutation status of V42V, The gene TGFBR1 has a mutation status of N338S, The gene PALM2AKAP2 has a mutation status of D252D, The gene SVEP1 has a mutation status of V3422A, The gene COL27A1 has a mutation status of P204L, The gene LHX2 has a mutation status of H168R, The gene OLFML2A has a mutation status of Y534S, The gene HMCN2 has a mutation status of D514A, The gene BARHL1 has a mutation status of Q304R, The gene SLC2A6 has a mutation status of C152Y, The gene SEC16A has a mutation status of P234P, The gene ABCA2 has a mutation status of V1539G, The gene ANAPC2 has a mutation status of V303G, The gene ADARB2 has a mutation status of A385P, The gene ANKRD26 has a mutation status of E1466Q, The gene ATOH7 has a mutation status of F143L, The gene ECD has a mutation status of S534F, The gene WBP1L has a mutation status of H314P, The gene EIF3A has a mutation status of S1262A, The gene NSMCE4A has a mutation status of L92L, The gene GLRX3 has a mutation status of M165V, The gene DEAF1 has a mutation status of S48T, The gene SLC25A22 has a mutation status of L195L, The gene PIDD1 has a mutation status of D658E, The gene PNPLA2 has a mutation status of T349P, The gene OSBPL5 has a mutation status of C273W, The gene TUB has a mutation status of P540P, The gene MICAL2 has a mutation status of A1101A, The gene TP53I11 has a mutation status of T101P, The gene F2 has a mutation status of Q387*, The gene PTPRJ has a mutation status of V1173A, The gene OR4C13 has a mutation status of V245V, The gene OR10Q1 has a mutation status of L111H, The gene FAM111A has a mutation status of N246N, The gene TMEM132A has a mutation status of H166P, The gene TMEM132A has a mutation status of E735G, The gene ZNHIT2 has a mutation status of E14G, The gene PCNX3 has a mutation status of T599P, The gene C11orf80 has a mutation status of P480R, The gene CORO1B has a mutation status of H425P, The gene AIP has a mutation status of A322V, The gene CABP2 has a mutation status of R10H, The gene FGF3 has a mutation status of T169P, The gene TSKU has a mutation status of L253L, The gene TENM4 has a mutation status of L271L, The gene NAALAD2 has a mutation status of Y43C, The gene FAT3 has a mutation status of E1372K, The gene FAT3 has a mutation status of D4104A, The gene CEP295 has a mutation status of L82S, The gene KDM4E has a mutation status of R323C, The gene PPP2R1B has a mutation status of G3G, The gene BCL9L has a mutation status of G576V, The gene CCDC84 has a mutation status of L67L, The gene DCP1B has a mutation status of Q335*, The gene KRAS has a mutation status of G12D, The gene ADAMTS20 has a mutation status of F772F, The gene NELL2 has a mutation status of R135H, The gene PFKM has a mutation status of A225A, The gene KMT2D has a mutation status of T2131P, The gene SLC4A8 has a mutation status of L532P, The gene ITGB7 has a mutation status of S614G, The gene CMKLR1 has a mutation status of S11R, The gene DTX1 has a mutation status of A214T, The gene SFSWAP has a mutation status of E428Q, The gene POLE has a mutation status of L690V, The gene MEDAG has a mutation status of A4G, The gene COG3 has a mutation status of V43G, The gene ATP4B has a mutation status of R36Q, The gene RASA3 has a mutation status of E638*, The gene NKX2-8 has a mutation status of A157V, The gene TTC6 has a mutation status of R237R, The gene FANCM has a mutation status of Q1277Q, The gene PTGER2 has a mutation status of D53G, The gene ACOT4 has a mutation status of D113A, The gene RTF1 has a mutation status of N699S, The gene CASC4 has a mutation status of N67K, The gene SPPL2A has a mutation status of A200L, The gene TEX9 has a mutation status of T27I, The gene HERC1 has a mutation status of G125G, The gene RASL12 has a mutation status of L53F, The gene COMMD4 has a mutation status of V37G, The gene SH2D7 has a mutation status of R80G, The gene ADAMTS7 has a mutation status of P1152T, The gene C15orf40 has a mutation status of L2M, The gene WFIKKN1 has a mutation status of A145P, The gene BAIAP3 has a mutation status of P84P, The gene IFT140 has a mutation status of H209P, The gene EME2 has a mutation status of A253fs, The gene PPL has a mutation status of G62G, The gene CLEC16A has a mutation status of P787L, The gene GSG1L has a mutation status of R95L, The gene SHCBP1 has a mutation status of H508R, The gene CCDC102A has a mutation status of R258Q, The gene USB1 has a mutation status of G59G, The gene FHOD1 has a mutation status of E5G, The gene FA2H has a mutation status of H146P, The gene TAF1C has a mutation status of PIL180del, The gene GSE1 has a mutation status of T30P, The gene FOXC2 has a mutation status of R165Q, The gene ZZEF1 has a mutation status of T2954P, The gene CLDN7 has a mutation status of S172A, The gene TP53 has a mutation status of P151S, The gene GUCY2D has a mutation status of F355L, The gene DNAH9 has a mutation status of I1078S, The gene COX10 has a mutation status of H418P, The gene HS3ST3B1 has a mutation status of D73A, The gene AC005324.3 has a mutation status of T120T, The gene PLD6 has a mutation status of S171S, The gene FLII has a mutation status of H812P, The gene SEZ6 has a mutation status of R961P, The gene MLLT6 has a mutation status of G202G, The gene KRTAP9-6 has a mutation status of G106C, The gene HDAC5 has a mutation status of G411G, The gene PDK2 has a mutation status of A324A, The gene RNF43 has a mutation status of E174*, The gene SEPTIN4 has a mutation status of R333C, The gene PPM1E has a mutation status of E755E, The gene PPM1D has a mutation status of G122G, The gene LRRC37A3 has a mutation status of L1206L, The gene GNA13 has a mutation status of N120fs, The gene TTYH2 has a mutation status of A103A, The gene TTYH2 has a mutation status of V225V, The gene KCTD2 has a mutation status of P182P, The gene MRPS7 has a mutation status of K208K, The gene TSEN54 has a mutation status of V372M, The gene GALK1 has a mutation status of T375A, The gene ZACN has a mutation status of I259I, The gene FASN has a mutation status of R2233R, The gene FOXK2 has a mutation status of V502V, The gene THOC1 has a mutation status of P3P, The gene CCBE1 has a mutation status of F335L, The gene FBXO15 has a mutation status of I81M, The gene DIPK1C has a mutation status of Q408K, The gene ARID3A has a mutation status of T392P, The gene PCSK4 has a mutation status of V229I, The gene PCSK4 has a mutation status of V111G, The gene SLC25A41 has a mutation status of G135E, The gene ZNF557 has a mutation status of *431*, The gene PEX11G has a mutation status of E12*, The gene HNRNPM has a mutation status of G23G, The gene OR7G2 has a mutation status of P268P, The gene NOTCH3 has a mutation status of G1058G, The gene NOTCH3 has a mutation status of T328P, The gene BRD4 has a mutation status of P243P, The gene BRD4 has a mutation status of V242V, The gene RASAL3 has a mutation status of P14P, The gene INSL3 has a mutation status of T136T, The gene JAK3 has a mutation status of R984R, The gene JUND has a mutation status of E291D, The gene ZNF208 has a mutation status of N435K, The gene ZNF536 has a mutation status of T1191T, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene LTBP4 has a mutation status of T1556P, The gene LTBP4 has a mutation status of A1609A, The gene ZNF526 has a mutation status of G414R, The gene CIC has a mutation status of P2036P, The gene MEGF8 has a mutation status of T944P, The gene ERCC2 has a mutation status of T252P, The gene SPHK2 has a mutation status of S460S, The gene NTN5 has a mutation status of R219Q, The gene PNKP has a mutation status of A429G, The gene ACP4 has a mutation status of T306P, The gene LILRB3 has a mutation status of V574A, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of S205A, The gene KIR2DL1 has a mutation status of G283G, The gene ZNF579 has a mutation status of R216Q, The gene ZSCAN4 has a mutation status of P399T, The gene SLC9A8 has a mutation status of I74M, The gene KCNG1 has a mutation status of S14S, The gene LAMA5 has a mutation status of D1985A, The gene NKAIN4 has a mutation status of V26G, The gene TNFRSF6B has a mutation status of Q51P, The gene ZBTB46 has a mutation status of S110R, The gene NCAM2 has a mutation status of P499P, The gene SYNJ1 has a mutation status of V535I, The gene GART has a mutation status of E43E, The gene RUNX1 has a mutation status of G420D, The gene COL18A1 has a mutation status of P367L, The gene PCNT has a mutation status of F159F, The gene PCNT has a mutation status of Q645Q, The gene SEPTIN5 has a mutation status of D294D, The gene SMTN has a mutation status of S201S, The gene MPST has a mutation status of S183P, The gene CHADL has a mutation status of L541L, The gene TNFRSF13C has a mutation status of P156P, The gene TNFRSF13C has a mutation status of T155P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene GTPBP6 has a mutation status of G61R, The gene CFAP47 has a mutation status of R649H, The gene USP9X has a mutation status of E264Q, The gene FOXP3 has a mutation status of W26C, The gene CENPVL3 has a mutation status of F121L, The gene IQSEC2 has a mutation status of E222*, The gene GJB1 has a mutation status of V166G, The gene DIAPH2 has a mutation status of L237P, The gene AMOT has a mutation status of R331H, The gene CNGA2 has a mutation status of D662E, The gene MT-ATP8 has a mutation status of N32S, The gene MT-ATP8 has a mutation status of K49K, The gene MT-ND4 has a mutation status of W359R, The gene MT-CYB has a mutation status of A52A
PAAD
The gene PLCH2 has a mutation status of R166C, The gene GPR153 has a mutation status of S470S, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene GPN2 has a mutation status of Q220Q, The gene COL16A1 has a mutation status of P249T, The gene A3GALT2 has a mutation status of A131T, The gene IPP has a mutation status of C527C, The gene DOCK7 has a mutation status of R494K, The gene SSX2IP has a mutation status of H213Y, The gene ZNF326 has a mutation status of I295K, The gene ZNF326 has a mutation status of 296_297IE>KK, The gene BRDT has a mutation status of N72fs, The gene AMIGO1 has a mutation status of R84C, The gene KCNC4 has a mutation status of R368H, The gene NBPF20 has a mutation status of L4577L, The gene ANKRD34A has a mutation status of H433P, The gene NBPF9 has a mutation status of V918L, The gene AC242842.3 has a mutation status of V503L, The gene LCE1F has a mutation status of G74S, The gene FAM189B has a mutation status of T438P, The gene YY1AP1 has a mutation status of R517Q, The gene RXFP4 has a mutation status of V33V, The gene LMNA has a mutation status of I63L, The gene SMG5 has a mutation status of R637W, The gene IGSF8 has a mutation status of R315W, The gene LY9 has a mutation status of P13P, The gene NR1I3 has a mutation status of L238L, The gene POU2F1 has a mutation status of S84F, The gene TOR1AIP1 has a mutation status of H479Y, The gene IGFN1 has a mutation status of K1635E, The gene CAMK1G has a mutation status of S31L, The gene EPRS1 has a mutation status of R1333Q, The gene KIF26B has a mutation status of D165G, The gene NLRP3 has a mutation status of L346L, The gene OR2T1 has a mutation status of G305G, The gene ZNF672 has a mutation status of A286T, The gene ATAD2B has a mutation status of G509G, The gene ADGRF3 has a mutation status of Q55R, The gene STARD7 has a mutation status of V272V, The gene ANKRD36 has a mutation status of A586P, The gene ZRANB3 has a mutation status of T214T, The gene ACVR1 has a mutation status of W245*, The gene TTN has a mutation status of A32695F, The gene ANKAR has a mutation status of G458*, The gene FAM117B has a mutation status of G26G, The gene WNT6 has a mutation status of Q238*, The gene GRIP2 has a mutation status of P445P, The gene NBEAL2 has a mutation status of G1569S, The gene IP6K2 has a mutation status of H386Y, The gene CNTN3 has a mutation status of V359A, The gene ABI3BP has a mutation status of A833V, The gene ZBTB20 has a mutation status of P619fs, The gene AC131160.1 has a mutation status of M222V, The gene HTT has a mutation status of A274T, The gene CENPC has a mutation status of S155S, The gene UGT2B17 has a mutation status of Y99Y, The gene BANK1 has a mutation status of P196P, The gene NDST4 has a mutation status of L177L, The gene ELF2 has a mutation status of M159K, The gene TAS2R1 has a mutation status of Q286K, The gene HCN1 has a mutation status of 98_99insGFMQRQF, The gene GIN1 has a mutation status of R3C, The gene PCDHA12 has a mutation status of S417S, The gene RELL2 has a mutation status of L222M, The gene CSF1R has a mutation status of A95A, The gene ADAM19 has a mutation status of P739P, The gene CCNJL has a mutation status of T18T, The gene TMEM14B has a mutation status of 140_141CA>SP, The gene TNXB has a mutation status of S3324G, The gene C6orf132 has a mutation status of S449fs, The gene B3GAT2 has a mutation status of H141H, The gene SLC22A16 has a mutation status of 148_149CD>*H, The gene RWDD1 has a mutation status of Q128K, The gene FAM184A has a mutation status of K418K, The gene SYNJ2 has a mutation status of C389C, The gene PSMG3 has a mutation status of R113M, The gene NFE2L3 has a mutation status of S422del, The gene ABCA13 has a mutation status of K2269T, The gene TRRAP has a mutation status of P496P, The gene ZAN has a mutation status of TISPEKPTIPTEKPTIPTEKS711del, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene EXOC4 has a mutation status of A637A, The gene DENND2A has a mutation status of E558K, The gene PRSS1 has a mutation status of N77N, The gene CHPF2 has a mutation status of D570N, The gene RP1L1 has a mutation status of E2204A, The gene RP1L1 has a mutation status of P302P, The gene MTUS1 has a mutation status of Y155C, The gene TNFRSF10D has a mutation status of P71P, The gene FUT10 has a mutation status of L390V, The gene ADAM18 has a mutation status of P391R, The gene NSMAF has a mutation status of H248H, The gene NCALD has a mutation status of K96K, The gene THEM6 has a mutation status of A90fs, The gene EPPK1 has a mutation status of A2633del, The gene OPLAH has a mutation status of H870fs, The gene UNC13B has a mutation status of G408R, The gene HRCT1 has a mutation status of H104P, The gene ZCCHC7 has a mutation status of H54R, The gene CNTNAP3 has a mutation status of A1204T, The gene FRRS1L has a mutation status of R51A, The gene ZFP37 has a mutation status of C534Y, The gene LHX2 has a mutation status of A116G, The gene CDK9 has a mutation status of P197fs, The gene PKN3 has a mutation status of Y664Y, The gene CYSRT1 has a mutation status of T17I, The gene PFKP has a mutation status of P421L, The gene AKR1C8P has a mutation status of N172K, The gene DNMBP has a mutation status of S984C, The gene SORCS1 has a mutation status of A1151T, The gene OR8I2 has a mutation status of T191I, The gene OR9G1 has a mutation status of I196F, The gene OR9G4 has a mutation status of R302G, The gene GLYATL1 has a mutation status of I169T, The gene RCE1 has a mutation status of P21P, The gene KDM2A has a mutation status of G432V, The gene RSF1 has a mutation status of P712S, The gene CACNA1C has a mutation status of G1280G, The gene TEX52 has a mutation status of Q36P, The gene USP5 has a mutation status of P84S, The gene CLEC2D has a mutation status of G140D, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene ACVRL1 has a mutation status of R295R, The gene CFAP54 has a mutation status of M1234fs, The gene TDG has a mutation status of G343R, The gene CHD8 has a mutation status of N761fs, The gene EFS has a mutation status of P320P, The gene RABGGTA has a mutation status of A87S, The gene TTC6 has a mutation status of E252D, The gene L3HYPDH has a mutation status of I58M, The gene WDR89 has a mutation status of V369M, The gene SPTB has a mutation status of K1293K, The gene ABCD4 has a mutation status of T439M, The gene ITPK1 has a mutation status of P397S, The gene PPP4R4 has a mutation status of R862W, The gene HSP90AA1 has a mutation status of I491T, The gene ANKDD1A has a mutation status of L516L, The gene ADAMTS7 has a mutation status of C1516C, The gene GOLGA6L9 has a mutation status of R228S, The gene ASB7 has a mutation status of G80R, The gene NDUFB10 has a mutation status of K141E, The gene ATF7IP2 has a mutation status of A491A, The gene DNAH3 has a mutation status of A1377V, The gene VWA3A has a mutation status of R534W, The gene SETD1A has a mutation status of P1145P, The gene PHKB has a mutation status of T22T, The gene SLC12A4 has a mutation status of R483Q, The gene MARVELD3 has a mutation status of P85T, The gene NUP88 has a mutation status of V188I, The gene GPS2 has a mutation status of K54fs, The gene NLGN2 has a mutation status of S805fs, The gene ADORA2B has a mutation status of L96F, The gene PHF12 has a mutation status of Q326L, The gene CCL4L2 has a mutation status of P67R, The gene GJD3 has a mutation status of H175Y, The gene TMEM106A has a mutation status of S6N, The gene NAGS has a mutation status of N294D, The gene ARHGAP27 has a mutation status of K305E, The gene RGS9 has a mutation status of W299R, The gene ABCA9 has a mutation status of V162fs, The gene MYO15B has a mutation status of T538T, The gene DNAH17 has a mutation status of L56L, The gene FN3K has a mutation status of D274A, The gene MEP1B has a mutation status of T214fs, The gene NARS1 has a mutation status of T503M, The gene C2CD4C has a mutation status of N343S, The gene ABHD17A has a mutation status of A164A, The gene PTPRS has a mutation status of I1857I, The gene SLC25A23 has a mutation status of C321C, The gene MUC16 has a mutation status of R4208R, The gene PTGER1 has a mutation status of A37T, The gene NOTCH3 has a mutation status of S1580S, The gene BRD4 has a mutation status of P1012P, The gene ZNF737 has a mutation status of R240R, The gene ZNF729 has a mutation status of C908S, The gene ZNF536 has a mutation status of R381C, The gene RYR1 has a mutation status of R3550Q, The gene CCER2 has a mutation status of R54R, The gene DACT3 has a mutation status of L79P, The gene KLK7 has a mutation status of K197R, The gene CTU1 has a mutation status of S269L, The gene CTU1 has a mutation status of V267V, The gene ZNF610 has a mutation status of H366R, The gene ZNF415 has a mutation status of V11L, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene LILRB1 has a mutation status of E34E, The gene A1BG has a mutation status of G190C, The gene CSNK2A1 has a mutation status of V285V, The gene KAT14 has a mutation status of P740P, The gene RALGAPA2 has a mutation status of Q565P, The gene XKR7 has a mutation status of P533P, The gene EFCAB8 has a mutation status of G389V, The gene EFCAB8 has a mutation status of L525M, The gene RPN2 has a mutation status of I148I, The gene PABPC1L has a mutation status of R311R, The gene SNX21 has a mutation status of R203C, The gene ARFGEF2 has a mutation status of N1631S, The gene BCAS1 has a mutation status of T107T, The gene ZNF831 has a mutation status of C174C, The gene DGCR2 has a mutation status of G194V, The gene AC004997.1 has a mutation status of A276A, The gene EIF4ENIF1 has a mutation status of R632H, The gene TRIOBP has a mutation status of G1479fs, The gene CCDC134 has a mutation status of D58N, The gene SREBF2 has a mutation status of L212P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PARVB has a mutation status of G55G, The gene ZBED4 has a mutation status of A839T, The gene PLXNB2 has a mutation status of F229V, The gene SPIN3 has a mutation status of H248R, The gene DGAT2L6 has a mutation status of S133P, The gene HMGN5 has a mutation status of E276fs, The gene MAGEC1 has a mutation status of A9V, The gene MT-ND6 has a mutation status of T159M, The gene MT-ND6 has a mutation status of L104L
GBMLGG
The gene TTLL10 has a mutation status of P155P, The gene CFAP74 has a mutation status of T583P, The gene CFAP74 has a mutation status of Y463*, The gene PRAMEF13 has a mutation status of T257I, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene ECE1 has a mutation status of V603V, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene ARMH1 has a mutation status of S420S, The gene WDR63 has a mutation status of P612P, The gene ATP5PB has a mutation status of S16F, The gene NBPF11 has a mutation status of E333Q, The gene NBPF11 has a mutation status of Q55H, The gene NBPF11 has a mutation status of S9C, The gene RFX5 has a mutation status of R335P, The gene CD5L has a mutation status of K154N, The gene UHMK1 has a mutation status of V25G, The gene ASTN1 has a mutation status of Y803C, The gene ARHGEF33 has a mutation status of A624S, The gene EN1 has a mutation status of A163E, The gene TTN has a mutation status of A4853S, The gene EIF4E2 has a mutation status of V91V, The gene SYN2 has a mutation status of P105A, The gene ANKRD28 has a mutation status of H46Y, The gene TRIM71 has a mutation status of N545D, The gene CCR1 has a mutation status of L117F, The gene QRICH1 has a mutation status of T300T, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene ACAD11 has a mutation status of E493*, The gene MUC20 has a mutation status of 466_467EA>DT, The gene AP1AR has a mutation status of F10C, The gene DNAH5 has a mutation status of E1926Q, The gene C6 has a mutation status of C823C, The gene MCTP1 has a mutation status of Y261*, The gene ZNF608 has a mutation status of Y1245H, The gene PCDHB10 has a mutation status of S774*, The gene CD74 has a mutation status of Y155S, The gene CARMIL1 has a mutation status of S316S, The gene OR10C1 has a mutation status of T64P, The gene DDR1 has a mutation status of R78C, The gene HLA-C has a mutation status of T187L, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB1 has a mutation status of I248L, The gene GRM4 has a mutation status of S521N, The gene DNAH8 has a mutation status of L2579L, The gene FKBP6 has a mutation status of C263F, The gene AKAP9 has a mutation status of R2607G, The gene CYP3A43 has a mutation status of K488E, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene C7orf77 has a mutation status of G87G, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PRSS2 has a mutation status of V118I, The gene CNTNAP2 has a mutation status of S586R, The gene HR has a mutation status of N232K, The gene CEBPD has a mutation status of M219I, The gene LAPTM4B has a mutation status of M88K, The gene LAPTM4B has a mutation status of T90N, The gene CSMD3 has a mutation status of V3078V, The gene HAS2 has a mutation status of E224D, The gene FBXL6 has a mutation status of Q207Q, The gene FRMPD1 has a mutation status of A578fs, The gene HMCN2 has a mutation status of R819H, The gene HMCN2 has a mutation status of T1050T, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene CCDC187 has a mutation status of R294H, The gene FRMD4A has a mutation status of A762A, The gene PCDH15 has a mutation status of Y1786Y, The gene CASP7 has a mutation status of S199S, The gene CDHR5 has a mutation status of G546E, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of G1443R, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of I1961I, The gene MUC5AC has a mutation status of T4375S, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of A141A, The gene OR9G1 has a mutation status of I196F, The gene STIP1 has a mutation status of E255K, The gene PCNX3 has a mutation status of H1434P, The gene OVOL1 has a mutation status of T119P, The gene C1R has a mutation status of G313G, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PRB4 has a mutation status of R122G, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of E249R, The gene ENDOU has a mutation status of T88P, The gene MARS1 has a mutation status of A837A, The gene NTS has a mutation status of E27*, The gene AACS has a mutation status of I87I, The gene ITGBL1 has a mutation status of D148E, The gene TEP1 has a mutation status of W2180L, The gene G2E3 has a mutation status of Q109Q, The gene SERPINA1 has a mutation status of N53K, The gene LINC02203 has a mutation status of I259M, The gene TJP1 has a mutation status of A1418S, The gene MAP1A has a mutation status of C2623F, The gene SPATA5L1 has a mutation status of G367G, The gene PRTG has a mutation status of S267Y, The gene ANKDD1A has a mutation status of L516L, The gene TMEM266 has a mutation status of I166V, The gene GOLGA6L9 has a mutation status of R6H, The gene PDZD9 has a mutation status of Q104K, The gene TRPV3 has a mutation status of G640G, The gene CCL4L2 has a mutation status of P67R, The gene CCL4L2 has a mutation status of L88P, The gene SDK2 has a mutation status of A279S, The gene LOXHD1 has a mutation status of V2028G, The gene DIPK1C has a mutation status of Q408K, The gene DIPK1C has a mutation status of L407P, The gene ZNF407 has a mutation status of A2212T, The gene REXO1 has a mutation status of H665P, The gene NMRK2 has a mutation status of P112P, The gene PRR36 has a mutation status of P855L, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13007G, The gene MUC16 has a mutation status of T12336L, The gene COPE has a mutation status of V16L, The gene ZNF66 has a mutation status of L102L, The gene ZNF382 has a mutation status of N533D, The gene MAP3K10 has a mutation status of E358*, The gene KCNA7 has a mutation status of L224L, The gene PRR12 has a mutation status of G511G, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB2 has a mutation status of R295T, The gene LILRA4 has a mutation status of R399Y, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene LILRB1 has a mutation status of Y99I, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of P224S, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of N144S, The gene KIR2DL1 has a mutation status of G283G, The gene ZNF274 has a mutation status of R176W, The gene SIRPA has a mutation status of L44S, The gene ACSS1 has a mutation status of V431G, The gene ASXL1 has a mutation status of G645G, The gene BPIFB4 has a mutation status of T18P, The gene LAMA5 has a mutation status of H726P, The gene CLDN8 has a mutation status of C184C, The gene SON has a mutation status of I148V, The gene MICAL3 has a mutation status of M1437T, The gene DGCR2 has a mutation status of T193S, The gene TMPRSS6 has a mutation status of G402G, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene ARSF has a mutation status of R386L, The gene SCML1 has a mutation status of K89K, The gene SCML1 has a mutation status of L92I, The gene PLP2 has a mutation status of T122M, The gene KDM5C has a mutation status of L973L, The gene NOX1 has a mutation status of R287Q, The gene DRP2 has a mutation status of L63L, The gene RTL4 has a mutation status of F184L, The gene SLC25A5 has a mutation status of G121C, The gene SLC25A5 has a mutation status of T221R, The gene DCAF12L2 has a mutation status of V237G, The gene AIFM1 has a mutation status of E122E, The gene SLC6A8 has a mutation status of P528P, The gene PRKY has a mutation status of T115T, The gene DDX3Y has a mutation status of C221F, The gene MT-ND2 has a mutation status of V31A, The gene MT-ATP6 has a mutation status of A177T, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND4 has a mutation status of L197L, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L, The gene MT-CYB has a mutation status of M124V
KIPAN
The gene ATAD3C has a mutation status of E30*, The gene PLCH2 has a mutation status of T389fs, The gene CA6 has a mutation status of H141Y, The gene PRAMEF2 has a mutation status of P117C, The gene PRAMEF10 has a mutation status of 467_468KV>NM, The gene PRAMEF13 has a mutation status of V256G, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene TAS1R2 has a mutation status of V297M, The gene ZBTB40 has a mutation status of T1086M, The gene SRRM1 has a mutation status of KTRPRSRSRS273del, The gene KLF17 has a mutation status of R326H, The gene LRRIQ3 has a mutation status of I577R, The gene GBP1 has a mutation status of E147*, The gene RPAP2 has a mutation status of D262E, The gene AP4B1 has a mutation status of R28C, The gene AC253572.1 has a mutation status of T273S, The gene NBPF15 has a mutation status of L515L, The gene NBPF10 has a mutation status of L891V, The gene AC242842.3 has a mutation status of Q2070H, The gene CELF3 has a mutation status of F118F, The gene PKLR has a mutation status of D262N, The gene ASH1L has a mutation status of E515K, The gene CD1C has a mutation status of D106N, The gene IFI16 has a mutation status of F440L, The gene ATP1A4 has a mutation status of D685H, The gene ATF6 has a mutation status of V282V, The gene SEC16B has a mutation status of Q1034H, The gene CEP350 has a mutation status of D1901Y, The gene HMCN1 has a mutation status of R325G, The gene KCNT2 has a mutation status of R346K, The gene LRRN2 has a mutation status of R427Q, The gene TMCC2 has a mutation status of V74V, The gene CR2 has a mutation status of P963P, The gene LAMB3 has a mutation status of R1164H, The gene SLC35F3 has a mutation status of R427R, The gene RYR2 has a mutation status of D1298N, The gene RYR2 has a mutation status of E2769K, The gene OR2T4 has a mutation status of V109L, The gene OR2T6 has a mutation status of V213A, The gene NCAPH has a mutation status of P3P, The gene ANKRD36 has a mutation status of R405S, The gene MRPS9 has a mutation status of D309G, The gene TSN has a mutation status of R177H, The gene WDR33 has a mutation status of R974W, The gene GTDC1 has a mutation status of *459L, The gene SCN1A has a mutation status of N1027N, The gene ABCB11 has a mutation status of A75T, The gene PDE11A has a mutation status of F257L, The gene ITGAV has a mutation status of N488S, The gene FAM237A has a mutation status of V65I, The gene IKZF2 has a mutation status of Q144K, The gene VIL1 has a mutation status of Q323*, The gene VIL1 has a mutation status of Q343*, The gene DOCK10 has a mutation status of E1673K, The gene SYN2 has a mutation status of P105A, The gene SLC4A7 has a mutation status of *1215Q, The gene CCDC51 has a mutation status of Q376fs, The gene IP6K2 has a mutation status of A349A, The gene ABHD14B has a mutation status of A144A, The gene DNAH1 has a mutation status of G1949R, The gene SYNPR has a mutation status of S156L, The gene MAGI1 has a mutation status of R1405G, The gene MAGI1 has a mutation status of D1101G, The gene MAGI1 has a mutation status of G39G, The gene CLDND1 has a mutation status of E61K, The gene CFAP44 has a mutation status of F499F, The gene MYLK has a mutation status of E1414K, The gene SOX14 has a mutation status of N35N, The gene ARHGEF26 has a mutation status of K466N, The gene SMC4 has a mutation status of E60K, The gene KLHL6 has a mutation status of V541G, The gene TRMT44 has a mutation status of P199P, The gene WDR19 has a mutation status of L1136L, The gene CRACD has a mutation status of T1148S, The gene UGT2B28 has a mutation status of 119_120FH>LY, The gene ZGRF1 has a mutation status of F116S, The gene SPATA5 has a mutation status of F219fs, The gene SLC7A11 has a mutation status of E348K, The gene IQCM has a mutation status of S60F, The gene DCLK2 has a mutation status of R414K, The gene ASIC5 has a mutation status of H212R, The gene ADAMTS12 has a mutation status of V1443V, The gene SPEF2 has a mutation status of A389G, The gene GDNF has a mutation status of P32P, The gene LRRC70 has a mutation status of S33S, The gene BDP1 has a mutation status of I503V, The gene FAT2 has a mutation status of R3465*, The gene FAM153B has a mutation status of T141A, The gene PRSS16 has a mutation status of F238F, The gene H2AC14 has a mutation status of A41G, The gene LTB has a mutation status of T117T, The gene VWA7 has a mutation status of R80Q, The gene TTBK1 has a mutation status of P406L, The gene SLC35B2 has a mutation status of V70I, The gene MCM3 has a mutation status of A760A, The gene CILK1 has a mutation status of S626F, The gene BACH2 has a mutation status of P549P, The gene PRDM1 has a mutation status of G64G, The gene ARMC2 has a mutation status of C353*, The gene DSE has a mutation status of Y545Y, The gene SOGA3 has a mutation status of G86R, The gene AHI1 has a mutation status of Q294R, The gene AHI1 has a mutation status of M293I, The gene ADAT2 has a mutation status of T65T, The gene CCR6 has a mutation status of A150V, The gene AFDN has a mutation status of R1648*, The gene AFDN has a mutation status of K1650fs, The gene THBS2 has a mutation status of S281L, The gene SUN1 has a mutation status of P610S, The gene UNCX has a mutation status of K195K, The gene FOXK1 has a mutation status of T683A, The gene OSBPL3 has a mutation status of L835Q, The gene TAX1BP1 has a mutation status of N294K, The gene TAX1BP1 has a mutation status of T295S, The gene FKBP9 has a mutation status of R346K, The gene CAMK2B has a mutation status of Q500E, The gene FIGNL1 has a mutation status of W666*, The gene ERV3-1 has a mutation status of Q539K, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene WNT2 has a mutation status of R183T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene CALD1 has a mutation status of E186*, The gene TAS2R3 has a mutation status of R55S, The gene PRSS1 has a mutation status of N54R, The gene PRSS1 has a mutation status of N77N, The gene ZNF282 has a mutation status of P419P, The gene ZNF862 has a mutation status of L248P, The gene PTPRN2 has a mutation status of E42K, The gene ERI1 has a mutation status of E282Q, The gene SCARA5 has a mutation status of G318V, The gene FUT10 has a mutation status of A74V, The gene PAG1 has a mutation status of Q109Q, The gene PIP4P2 has a mutation status of V80V, The gene TRIQK has a mutation status of E85K, The gene FSBP has a mutation status of Q237Q, The gene VPS13B has a mutation status of E2395K, The gene NCALD has a mutation status of P139L, The gene AC100868.1 has a mutation status of E410E, The gene TG has a mutation status of R995H, The gene EPPK1 has a mutation status of A2633del, The gene CPSF1 has a mutation status of F600F, The gene C8orf82 has a mutation status of G6V, The gene BAG1 has a mutation status of I181T, The gene KLF9 has a mutation status of Y164F, The gene PRUNE2 has a mutation status of Q1801Q, The gene ZNF462 has a mutation status of D686Y, The gene MIGA2 has a mutation status of Q179E, The gene HMCN2 has a mutation status of R819H, The gene HMCN2 has a mutation status of G1098G, The gene WDR5 has a mutation status of E58K, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of R294H, The gene SKIDA1 has a mutation status of P750R, The gene APBB1IP has a mutation status of P512P, The gene ANKRD30A has a mutation status of R485V, The gene ZNF22 has a mutation status of E61E, The gene TIMM23 has a mutation status of S208L, The gene NCOA4 has a mutation status of N409K, The gene ANK3 has a mutation status of D3235D, The gene PTEN has a mutation status of L108R, The gene LIPM has a mutation status of R418R, The gene PKD2L1 has a mutation status of R796H, The gene CFAP43 has a mutation status of T264A, The gene GPAM has a mutation status of P681L, The gene PNLIPRP3 has a mutation status of N136S, The gene WDR11 has a mutation status of K155fs, The gene PWWP2B has a mutation status of R362W, The gene PWWP2B has a mutation status of S434S, The gene RIC8A has a mutation status of E242*, The gene PKP3 has a mutation status of D595V, The gene HRAS has a mutation status of E162K, The gene MUC6 has a mutation status of 1821_1822QT>HA, The gene MUC6 has a mutation status of S1763P, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of P1158P, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of I1961I, The gene MUC5AC has a mutation status of S3854R, The gene CRY2 has a mutation status of A17A, The gene DDB2 has a mutation status of I159I, The gene TRIM51GP has a mutation status of V357V, The gene OR8J3 has a mutation status of S243L, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene RAB3IL1 has a mutation status of P205R, The gene RAB3IL1 has a mutation status of V40A, The gene MEN1 has a mutation status of I402fs, The gene KLC2 has a mutation status of E215K, The gene CD248 has a mutation status of R225L, The gene FAM168A has a mutation status of T98T, The gene PGM2L1 has a mutation status of D536D, The gene GVQW3 has a mutation status of A137V, The gene CTSC has a mutation status of R442C, The gene MMP13 has a mutation status of T119T, The gene EXPH5 has a mutation status of S127F, The gene MPZL3 has a mutation status of G33A, The gene CACNA1C has a mutation status of R1207*, The gene TEX52 has a mutation status of L81F, The gene CD4 has a mutation status of K443K, The gene PTPN6 has a mutation status of V193V, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene GPR19 has a mutation status of R258Q, The gene LDHB has a mutation status of I38I, The gene GXYLT1 has a mutation status of C414H, The gene NCKAP5L has a mutation status of R1172H, The gene ANO4 has a mutation status of P920P, The gene SYCP3 has a mutation status of M186fs, The gene RIMBP2 has a mutation status of G990fs, The gene SPATA13 has a mutation status of L447P, The gene TMTC4 has a mutation status of R620K, The gene ADPRHL1 has a mutation status of E1726G, The gene ADPRHL1 has a mutation status of S686L, The gene DCUN1D2 has a mutation status of F259L, The gene SALL2 has a mutation status of A899V, The gene G2E3 has a mutation status of A168T, The gene MDGA2 has a mutation status of N233K, The gene LRRC9 has a mutation status of C86C, The gene PCNX1 has a mutation status of V829V, The gene GOLGA6L1 has a mutation status of R526R, The gene HERC2 has a mutation status of T1472M, The gene EIF2AK4 has a mutation status of E133*, The gene SPTBN5 has a mutation status of L1363L, The gene STRC has a mutation status of I1277V, The gene DUOX1 has a mutation status of E271K, The gene DTWD1 has a mutation status of D296G, The gene SLTM has a mutation status of R900R, The gene C2CD4B has a mutation status of A219S, The gene ANKDD1A has a mutation status of L516L, The gene GOLGA6L10 has a mutation status of C286R, The gene GOLGA6L9 has a mutation status of R6H, The gene HOMER2 has a mutation status of E264E, The gene ACAN has a mutation status of D200G, The gene PRR35 has a mutation status of P491L, The gene NHLRC4 has a mutation status of I82I, The gene NHLRC4 has a mutation status of L103L, The gene CACNA1H has a mutation status of M1933T, The gene SYNGR3 has a mutation status of F40L, The gene CASKIN1 has a mutation status of A107A, The gene SRRM2 has a mutation status of A382A, The gene OR1F1 has a mutation status of V280L, The gene ZNF75A has a mutation status of R27R, The gene ACSM2B has a mutation status of W35*, The gene ANKS4B has a mutation status of K210K, The gene TAOK2 has a mutation status of S894I, The gene ARL2BP has a mutation status of Y69Y, The gene CDH8 has a mutation status of P424T, The gene DDX19A has a mutation status of G364S, The gene ANKRD11 has a mutation status of D1261H, The gene ANKRD11 has a mutation status of E1203Q, The gene MYO1C has a mutation status of 144_145insRGRERRS, The gene SHPK has a mutation status of P415Q, The gene CHRNE has a mutation status of Y35H, The gene BORCS6 has a mutation status of V207V, The gene DNAH9 has a mutation status of P2446S, The gene VTN has a mutation status of F437L, The gene RNF135 has a mutation status of R56P, The gene CCL4L2 has a mutation status of P67R, The gene THRA has a mutation status of E343K, The gene KRT24 has a mutation status of V73G, The gene CAVIN1 has a mutation status of A371A, The gene GFAP has a mutation status of T180T, The gene KIF18B has a mutation status of C782Y, The gene OSBPL7 has a mutation status of M46I, The gene HSF5 has a mutation status of R20L, The gene PECAM1 has a mutation status of V513V, The gene TNRC6C has a mutation status of G914E, The gene C17orf99 has a mutation status of L161L, The gene SLC16A3 has a mutation status of H350Q, The gene L3MBTL4 has a mutation status of D234N, The gene L3MBTL4 has a mutation status of KA167del, The gene L3MBTL4 has a mutation status of L166F, The gene LAMA1 has a mutation status of Q3027K, The gene RAB12 has a mutation status of G19D, The gene ANKRD12 has a mutation status of I1102I, The gene CEP192 has a mutation status of P1466P, The gene ZNF521 has a mutation status of D880E, The gene SLC25A52 has a mutation status of K9N, The gene DTNA has a mutation status of R340S, The gene SMAD2 has a mutation status of L131L, The gene TSHZ1 has a mutation status of E1028K, The gene MED16 has a mutation status of R525W, The gene GPX4 has a mutation status of G181R, The gene TMPRSS9 has a mutation status of D250N, The gene TLE6 has a mutation status of S420C, The gene MFSD12 has a mutation status of A361V, The gene TUBB4A has a mutation status of R359C, The gene ZGLP1 has a mutation status of G183G, The gene C19orf57 has a mutation status of G501G, The gene MAP1S has a mutation status of S683S, The gene ZNF66 has a mutation status of A545A, The gene ZNF99 has a mutation status of G207C, The gene ZNF724 has a mutation status of E503D, The gene ZNF181 has a mutation status of H471Y, The gene GRAMD1A has a mutation status of R107Q, The gene KMT2B has a mutation status of R2712Q, The gene ZNF607 has a mutation status of H639Y, The gene SPRED3 has a mutation status of R84G, The gene SPTBN4 has a mutation status of Q2046H, The gene SPTBN4 has a mutation status of E2082K, The gene SPTBN4 has a mutation status of E2154Q, The gene PAFAH1B3 has a mutation status of L194L, The gene GRIN2D has a mutation status of L207L, The gene KCNC3 has a mutation status of D225N, The gene SIGLEC9 has a mutation status of A169A, The gene SIGLEC10 has a mutation status of P263R, The gene SIGLEC8 has a mutation status of G129R, The gene ZNF888 has a mutation status of L459V, The gene TSEN34 has a mutation status of T32T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of G175R, The gene KIR2DL3 has a mutation status of T287fs, The gene KIR2DL3 has a mutation status of R290S, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL4 has a mutation status of P102P, The gene MZF1 has a mutation status of L24I, The gene SIRPA has a mutation status of L44S, The gene SCP2D1 has a mutation status of K151E, The gene AAR2 has a mutation status of R348H, The gene ANKRD60 has a mutation status of C190F, The gene TAF4 has a mutation status of S543L, The gene LAMA5 has a mutation status of P1458S, The gene DIDO1 has a mutation status of A40A, The gene TPTE has a mutation status of T347I, The gene KRTAP6-3 has a mutation status of C98C, The gene GAB4 has a mutation status of R92C, The gene KIAA1671 has a mutation status of P818L, The gene DNAJB7 has a mutation status of G161G, The gene NAGA has a mutation status of A120A, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SHISAL1 has a mutation status of T74M, The gene GTPBP6 has a mutation status of G61R, The gene PPP2R3B has a mutation status of R288R, The gene CRLF2 has a mutation status of S323F, The gene ASMTL has a mutation status of R72Q, The gene FAM47C has a mutation status of S842F, The gene OTC has a mutation status of L42F, The gene CACNA1F has a mutation status of S1670S, The gene HEPH has a mutation status of R383Q, The gene FAM155B has a mutation status of S389S, The gene SLC25A5 has a mutation status of T221R, The gene TEX13C has a mutation status of G11E, The gene CXorf66 has a mutation status of D326Y, The gene MAGEC1 has a mutation status of D123E, The gene PASD1 has a mutation status of E202K, The gene ATP2B3 has a mutation status of M978V, The gene MT-ND6 has a mutation status of S132S, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A, The gene PERM1 has a mutation status of T274T, The gene CFAP74 has a mutation status of L1456L, The gene LRRC47 has a mutation status of G119C, The gene CA6 has a mutation status of H141Y, The gene PRAMEF13 has a mutation status of S245Y, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF33 has a mutation status of A342V, The gene TAS1R2 has a mutation status of V297M, The gene UBR4 has a mutation status of A684fs, The gene HSPG2 has a mutation status of G1243W, The gene ZBTB40 has a mutation status of T1086M, The gene HPCA has a mutation status of F193L, The gene CSMD2 has a mutation status of F1069V, The gene GNL2 has a mutation status of R152Q, The gene CDCA8 has a mutation status of L59L, The gene EPHA10 has a mutation status of V264G, The gene KLF17 has a mutation status of R326H, The gene ANKRD13C has a mutation status of G97D, The gene LRRIQ3 has a mutation status of I577R, The gene GBP1 has a mutation status of E147*, The gene RPAP2 has a mutation status of D262E, The gene PHTF1 has a mutation status of T325A, The gene AP4B1 has a mutation status of R28C, The gene NBPF15 has a mutation status of L515L, The gene AC242842.3 has a mutation status of Q2070H, The gene MSTO1 has a mutation status of W535L, The gene DAP3 has a mutation status of A33T, The gene CD1C has a mutation status of D106N, The gene AIM2 has a mutation status of D199N, The gene ATP1A4 has a mutation status of D685H, The gene ATF6 has a mutation status of V282V, The gene HMCN1 has a mutation status of R325G, The gene ZBTB41 has a mutation status of C639Y, The gene LRRN2 has a mutation status of R427Q, The gene FCMR has a mutation status of A327S, The gene FCMR has a mutation status of G324V, The gene CR2 has a mutation status of P963P, The gene LAMB3 has a mutation status of R1164H, The gene COQ8A has a mutation status of K358N, The gene OBSCN has a mutation status of F8902F, The gene TRIM67 has a mutation status of G144G, The gene SLC35F3 has a mutation status of R427R, The gene RYR2 has a mutation status of D1298N, The gene RYR2 has a mutation status of E2769K, The gene MYT1L has a mutation status of R922W, The gene NTSR2 has a mutation status of R64R, The gene GCKR has a mutation status of G607V, The gene TOGARAM2 has a mutation status of I707T, The gene CAPN14 has a mutation status of W317C, The gene CYP1B1 has a mutation status of G168G, The gene PPP1R21 has a mutation status of E120E, The gene ASPRV1 has a mutation status of V207L, The gene FBXO41 has a mutation status of V226G, The gene DNAH6 has a mutation status of R290C, The gene NCAPH has a mutation status of P3P, The gene MRPS9 has a mutation status of D309G, The gene WDR33 has a mutation status of R974W, The gene LRP1B has a mutation status of P78T, The gene GTDC1 has a mutation status of *459L, The gene KIF5C has a mutation status of E759E, The gene GRB14 has a mutation status of G59V, The gene SCN1A has a mutation status of N1027N, The gene ABCB11 has a mutation status of A75T, The gene TTN has a mutation status of T23046T, The gene TTN has a mutation status of F1466L, The gene ITGAV has a mutation status of N488S, The gene ALS2 has a mutation status of R547R, The gene ZDBF2 has a mutation status of D720H, The gene FAM237A has a mutation status of V65I, The gene IKZF2 has a mutation status of Q144K, The gene VIL1 has a mutation status of Q323*, The gene VIL1 has a mutation status of Q343*, The gene SPEG has a mutation status of A2522A, The gene CHPF has a mutation status of A542S, The gene OBSL1 has a mutation status of A222G, The gene DOCK10 has a mutation status of E1673K, The gene PID1 has a mutation status of A181T, The gene ATG16L1 has a mutation status of R258Q, The gene CROCC2 has a mutation status of A529E, The gene CROCC2 has a mutation status of R531R, The gene ATG4B has a mutation status of S68*, The gene RTP5 has a mutation status of P187L, The gene GRIP2 has a mutation status of V75I, The gene RARB has a mutation status of S96S, The gene SLC4A7 has a mutation status of *1215Q, The gene TRANK1 has a mutation status of G2903G, The gene OXSR1 has a mutation status of A37D, The gene SCN10A has a mutation status of Q363Q, The gene GASK1A has a mutation status of S295Y, The gene CCDC51 has a mutation status of R48G, The gene IP6K2 has a mutation status of A349A, The gene ABHD14B has a mutation status of A144A, The gene DNAH1 has a mutation status of G1949R, The gene ITIH4 has a mutation status of P676S, The gene ARHGEF3 has a mutation status of H398H, The gene ARHGEF3 has a mutation status of F384L, The gene SYNPR has a mutation status of S156L, The gene MAGI1 has a mutation status of R1405G, The gene MAGI1 has a mutation status of D1101G, The gene MAGI1 has a mutation status of G39G, The gene CLDND1 has a mutation status of E61K, The gene CCDC54 has a mutation status of L136I, The gene MYLK has a mutation status of E1414K, The gene HEG1 has a mutation status of R505R, The gene H1-8 has a mutation status of G120G, The gene C3orf36 has a mutation status of G121A, The gene EPHB1 has a mutation status of I358I, The gene SOX14 has a mutation status of N35N, The gene PLOD2 has a mutation status of V302F, The gene ARHGEF26 has a mutation status of K466N, The gene SMC4 has a mutation status of E60K, The gene TRIM59 has a mutation status of T205T, The gene KLHL6 has a mutation status of V541G, The gene TMEM175 has a mutation status of H484P, The gene TRMT44 has a mutation status of P199P, The gene USP17L26 has a mutation status of S5S, The gene HS3ST1 has a mutation status of F89F, The gene WDR19 has a mutation status of L1136L, The gene BEND4 has a mutation status of N255K, The gene NMU has a mutation status of R165W, The gene CRACD has a mutation status of T1148S, The gene UBA6 has a mutation status of S650F, The gene UGT2B28 has a mutation status of 119_120FH>LY, The gene ZGRF1 has a mutation status of F116S, The gene SPATA5 has a mutation status of F219fs, The gene SLC7A11 has a mutation status of E348K, The gene ABCE1 has a mutation status of I199V, The gene ZNF827 has a mutation status of C1093G, The gene DCLK2 has a mutation status of R414K, The gene ASIC5 has a mutation status of H212R, The gene FAT1 has a mutation status of I1125L, The gene ZFP42 has a mutation status of S90S, The gene SDHA has a mutation status of V4G, The gene AHRR has a mutation status of H473P, The gene SLC9A3 has a mutation status of V335V, The gene TRIP13 has a mutation status of G29S, The gene ADAMTS12 has a mutation status of V1443V, The gene SPEF2 has a mutation status of A389G, The gene GDNF has a mutation status of P32P, The gene BDP1 has a mutation status of I503V, The gene ADGRV1 has a mutation status of T1402S, The gene CAMLG has a mutation status of V16G, The gene PCDHB11 has a mutation status of R716K, The gene FAT2 has a mutation status of R3465*, The gene PWWP2A has a mutation status of E24*, The gene CCNJL has a mutation status of T274P, The gene FBLL1 has a mutation status of I239L, The gene TLX3 has a mutation status of A32A, The gene TLX3 has a mutation status of L108L, The gene C5orf47 has a mutation status of R94L, The gene FOXC1 has a mutation status of L518F, The gene SLC22A23 has a mutation status of D117Y, The gene PRSS16 has a mutation status of F238F, The gene H2AC14 has a mutation status of A41G, The gene HLA-C has a mutation status of R169R, The gene VWA7 has a mutation status of R80Q, The gene FKBPL has a mutation status of *350S, The gene DAAM2 has a mutation status of A196T, The gene TTBK1 has a mutation status of P406L, The gene SLC35B2 has a mutation status of V70I, The gene RUNX2 has a mutation status of L392M, The gene MCM3 has a mutation status of A760A, The gene MCM3 has a mutation status of G3G, The gene TRAM2 has a mutation status of E320G, The gene BACH2 has a mutation status of P549P, The gene PRDM1 has a mutation status of G64G, The gene DSE has a mutation status of Y545Y, The gene SOGA3 has a mutation status of G86R, The gene ADAT2 has a mutation status of T65T, The gene ARID1B has a mutation status of G587G, The gene SERAC1 has a mutation status of I392I, The gene CCR6 has a mutation status of A150V, The gene AFDN has a mutation status of R1648*, The gene AFDN has a mutation status of K1650fs, The gene THBS2 has a mutation status of S281L, The gene SUN1 has a mutation status of P610S, The gene UNCX has a mutation status of K195K, The gene ELFN1 has a mutation status of R119Q, The gene AMZ1 has a mutation status of D65N, The gene RADIL has a mutation status of R861W, The gene TNRC18 has a mutation status of A1478T, The gene ZNF853 has a mutation status of Q186K, The gene ZNF316 has a mutation status of G59G, The gene OSBPL3 has a mutation status of L835Q, The gene EVX1 has a mutation status of P318P, The gene FKBP9 has a mutation status of R346K, The gene EEPD1 has a mutation status of P550T, The gene CAMK2B has a mutation status of Q500E, The gene FIGNL1 has a mutation status of W666*, The gene HEPACAM2 has a mutation status of G323S, The gene SLC12A9 has a mutation status of R825L, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of S2046L, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene SPDYE6 has a mutation status of H337R, The gene SLC26A5 has a mutation status of E431*, The gene WNT2 has a mutation status of R183T, The gene CFTR has a mutation status of I148T, The gene IQUB has a mutation status of S69*, The gene EXOC4 has a mutation status of Y456Y, The gene CALD1 has a mutation status of E186*, The gene ZC3HAV1L has a mutation status of E98D, The gene TAS2R3 has a mutation status of R55S, The gene EPHB6 has a mutation status of N196N, The gene NOBOX has a mutation status of D369Y, The gene ZNF282 has a mutation status of P419P, The gene ZNF746 has a mutation status of Y442S, The gene ZNF862 has a mutation status of L248P, The gene AGAP3 has a mutation status of T243T, The gene ERI1 has a mutation status of E282Q, The gene PAG1 has a mutation status of Q109Q, The gene PSKH2 has a mutation status of C3G, The gene PIP4P2 has a mutation status of V80V, The gene TRIQK has a mutation status of E85K, The gene FSBP has a mutation status of Q237Q, The gene VPS13B has a mutation status of E2395K, The gene NCALD has a mutation status of P139L, The gene EMC2 has a mutation status of S5L, The gene SQLE has a mutation status of D427fs, The gene AC100868.1 has a mutation status of E410E, The gene TG has a mutation status of R995H, The gene ADGRB1 has a mutation status of Q325K, The gene ZC3H3 has a mutation status of R478R, The gene FAM83H has a mutation status of A387S, The gene PLEC has a mutation status of F1933V, The gene HSF1 has a mutation status of V172G, The gene CPSF1 has a mutation status of F600F, The gene TONSL has a mutation status of A724A, The gene CYHR1 has a mutation status of T109T, The gene C8orf82 has a mutation status of G6V, The gene KCNV2 has a mutation status of L214L, The gene KIAA2026 has a mutation status of G1663V, The gene FOCAD has a mutation status of G33V, The gene BAG1 has a mutation status of I181T, The gene APBA1 has a mutation status of R143C, The gene KLF9 has a mutation status of Y164F, The gene PRUNE2 has a mutation status of Q1801Q, The gene PSAT1 has a mutation status of D353D, The gene GAS1 has a mutation status of V163G, The gene WNK2 has a mutation status of Y1960S, The gene ZNF510 has a mutation status of E625E, The gene TBC1D2 has a mutation status of V376G, The gene ZNF462 has a mutation status of D686Y, The gene FRRS1L has a mutation status of R51A, The gene TNC has a mutation status of G203V, The gene NIBAN2 has a mutation status of T314N, The gene ODF2 has a mutation status of P27T, The gene WDR34 has a mutation status of L247L, The gene DOLK has a mutation status of Y360C, The gene MIGA2 has a mutation status of Q179E, The gene NTNG2 has a mutation status of S178P, The gene WDR5 has a mutation status of E58K, The gene COL5A1 has a mutation status of E677E, The gene PPP1R26 has a mutation status of P83P, The gene KCNT1 has a mutation status of A368A, The gene ABCA2 has a mutation status of V1665G, The gene FUT7 has a mutation status of P165P, The gene CYSRT1 has a mutation status of H117R, The gene PITRM1 has a mutation status of V12L, The gene SKIDA1 has a mutation status of P750R, The gene APBB1IP has a mutation status of P512P, The gene FZD8 has a mutation status of T158P, The gene ZNF22 has a mutation status of E61E, The gene ANK3 has a mutation status of D3235D, The gene TYSND1 has a mutation status of V37G, The gene PTEN has a mutation status of L108R, The gene LIPM has a mutation status of R418R, The gene PKD2L1 has a mutation status of R796H, The gene PSD has a mutation status of G52G, The gene WBP1L has a mutation status of H312P, The gene CFAP43 has a mutation status of T264A, The gene SMC3 has a mutation status of T1094I, The gene GPAM has a mutation status of P681L, The gene WDR11 has a mutation status of K155fs, The gene PWWP2B has a mutation status of R362W, The gene PWWP2B has a mutation status of S434S, The gene RIC8A has a mutation status of E242*, The gene HRAS has a mutation status of E162K, The gene MUC5AC has a mutation status of D95D, The gene MUC5AC has a mutation status of P3819T, The gene MUC5AC has a mutation status of S3854R, The gene MRGPRE has a mutation status of R213Q, The gene OR52B6 has a mutation status of F245F, The gene FAM160A2 has a mutation status of R922W, The gene TAF10 has a mutation status of G83G, The gene OTOG has a mutation status of P1523S, The gene CRY2 has a mutation status of A17A, The gene DDB2 has a mutation status of I159I, The gene OR4S1 has a mutation status of L152M, The gene OR8J3 has a mutation status of S243L, The gene OR9G1 has a mutation status of T62V, The gene TMEM132A has a mutation status of V635V, The gene RAB3IL1 has a mutation status of P205R, The gene RAB3IL1 has a mutation status of V40A, The gene MEN1 has a mutation status of I402fs, The gene KLC2 has a mutation status of E215K, The gene LRFN4 has a mutation status of E275K, The gene UNC93B1 has a mutation status of M1R, The gene ALDH3B1 has a mutation status of Y443S, The gene LRP5 has a mutation status of A1096T, The gene FAM168A has a mutation status of T98T, The gene PGM2L1 has a mutation status of D536D, The gene TPBGL has a mutation status of A19A, The gene MYO7A has a mutation status of L1714L, The gene CREBZF has a mutation status of E249D, The gene CTSC has a mutation status of R442C, The gene FAT3 has a mutation status of A4136P, The gene HEPHL1 has a mutation status of L1125F, The gene PGR has a mutation status of E466K, The gene MMP13 has a mutation status of T119T, The gene POGLUT3 has a mutation status of W35R, The gene EXPH5 has a mutation status of S127F, The gene MPZL3 has a mutation status of G33A, The gene TECTA has a mutation status of S2051F, The gene SORL1 has a mutation status of V205V, The gene CACNA1C has a mutation status of R1207*, The gene TEX52 has a mutation status of L81F, The gene LAG3 has a mutation status of H85P, The gene CD4 has a mutation status of K443K, The gene PTPN6 has a mutation status of V193V, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of H93fs, The gene TAS2R45 has a mutation status of I91fs, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene LDHB has a mutation status of I38I, The gene H3-5 has a mutation status of S11S, The gene RESF1 has a mutation status of I1671M, The gene HDAC7 has a mutation status of N631T, The gene KMT2D has a mutation status of Q3860H, The gene NCKAP5L has a mutation status of R1172H, The gene HOXC13 has a mutation status of A237P, The gene HOXC5 has a mutation status of H70P, The gene NFE2 has a mutation status of P216A, The gene ANO4 has a mutation status of P920P, The gene CHPT1 has a mutation status of V39G, The gene SYCP3 has a mutation status of M186fs, The gene HSP90B1 has a mutation status of I66M, The gene CHST11 has a mutation status of T95K, The gene RFLNA has a mutation status of T101P, The gene NCOR2 has a mutation status of G1843G, The gene RIMBP2 has a mutation status of G990fs, The gene SPATA13 has a mutation status of L447P, The gene ATP8A2 has a mutation status of S23*, The gene FARP1 has a mutation status of H702P, The gene FARP1 has a mutation status of H703P, The gene TMTC4 has a mutation status of R620K, The gene SOX1 has a mutation status of V166V, The gene DCUN1D2 has a mutation status of F259L, The gene TOX4 has a mutation status of S552F, The gene DHRS4 has a mutation status of E131A, The gene G2E3 has a mutation status of A168T, The gene HECTD1 has a mutation status of G94G, The gene MDGA2 has a mutation status of N233K, The gene ATL1 has a mutation status of Y223Y, The gene LRRC9 has a mutation status of C86C, The gene PCNX1 has a mutation status of V829V, The gene RPS6KL1 has a mutation status of T495P, The gene SAMD15 has a mutation status of E110K, The gene VRK1 has a mutation status of M286I, The gene SLC25A29 has a mutation status of G11G, The gene EXOC3L4 has a mutation status of I719I, The gene TNFAIP2 has a mutation status of R645W, The gene CEP170B has a mutation status of S692A, The gene JAG2 has a mutation status of G725V, The gene HERC2 has a mutation status of T1472M, The gene SPTBN5 has a mutation status of L1363L, The gene EPB42 has a mutation status of R366Q, The gene STRC has a mutation status of I1277V, The gene DTWD1 has a mutation status of D296G, The gene SLTM has a mutation status of R900R, The gene HOMER2 has a mutation status of E264E, The gene ACAN has a mutation status of D200G, The gene PRR35 has a mutation status of P491L, The gene NHLRC4 has a mutation status of I82I, The gene NHLRC4 has a mutation status of L103L, The gene MCRIP2 has a mutation status of A13E, The gene ANTKMT has a mutation status of A39G, The gene CACNA1H has a mutation status of T749T, The gene CACNA1H has a mutation status of V780F, The gene CACNA1H has a mutation status of S1110S, The gene CACNA1H has a mutation status of D1112A, The gene CACNA1H has a mutation status of M1933T, The gene ZNF598 has a mutation status of P698P, The gene CASKIN1 has a mutation status of A107A, The gene SRRM2 has a mutation status of A382A, The gene PAQR4 has a mutation status of R30R, The gene OR1F1 has a mutation status of V280L, The gene ANKS4B has a mutation status of K210K, The gene TAOK2 has a mutation status of S894I, The gene STX1B has a mutation status of N161S, The gene PYDC1 has a mutation status of V30M, The gene TRIM72 has a mutation status of Y427Y, The gene ARL2BP has a mutation status of Y69Y, The gene CNGB1 has a mutation status of S245F, The gene CDH8 has a mutation status of P424T, The gene DDX19A has a mutation status of G364S, The gene ANKRD11 has a mutation status of D1261H, The gene ANKRD11 has a mutation status of E1203Q, The gene SGSM2 has a mutation status of S535Y, The gene SHPK has a mutation status of P415Q, The gene ATP2A3 has a mutation status of A414A, The gene SPNS3 has a mutation status of A346T, The gene MINK1 has a mutation status of A520D, The gene CHRNE has a mutation status of Y35H, The gene CHRNB1 has a mutation status of L63L, The gene BORCS6 has a mutation status of V207V, The gene DNAH9 has a mutation status of L3777L, The gene ULK2 has a mutation status of V882G, The gene NOS2 has a mutation status of E145K, The gene TNFAIP1 has a mutation status of T166K, The gene VTN has a mutation status of F437L, The gene FOXN1 has a mutation status of L4L, The gene PHF12 has a mutation status of A968A, The gene EVI2B has a mutation status of S63S, The gene CCL4L2 has a mutation status of P67R, The gene THRA has a mutation status of E343K, The gene IGFBP4 has a mutation status of L6L, The gene CAVIN1 has a mutation status of A371A, The gene MEIOC has a mutation status of F543S, The gene GFAP has a mutation status of T180T, The gene KIF18B has a mutation status of C782Y, The gene MBTD1 has a mutation status of A411A, The gene HSF5 has a mutation status of R20L, The gene C17orf64 has a mutation status of K13N, The gene PECAM1 has a mutation status of V513V, The gene ABCA8 has a mutation status of V78I, The gene ABCA9 has a mutation status of Y749*, The gene KCNJ16 has a mutation status of G133G, The gene TRIM47 has a mutation status of H534L, The gene PRPSAP1 has a mutation status of P20T, The gene TNRC6C has a mutation status of G914E, The gene C17orf99 has a mutation status of L161L, The gene CANT1 has a mutation status of E284D, The gene LRRC45 has a mutation status of R602L, The gene FASN has a mutation status of F1728F, The gene SLC16A3 has a mutation status of H350Q, The gene L3MBTL4 has a mutation status of D234N, The gene L3MBTL4 has a mutation status of KA167del, The gene L3MBTL4 has a mutation status of L166F, The gene ANKRD12 has a mutation status of I1102I, The gene CEP192 has a mutation status of P1466P, The gene ZNF521 has a mutation status of D880E, The gene KCTD1 has a mutation status of G82G, The gene SLC25A52 has a mutation status of K9N, The gene DTNA has a mutation status of R340S, The gene RNF165 has a mutation status of T33P, The gene SMAD2 has a mutation status of L131L, The gene TSHZ1 has a mutation status of E1028K, The gene MED16 has a mutation status of R525W, The gene GPX4 has a mutation status of G17A, The gene GPX4 has a mutation status of G181R, The gene ABHD17A has a mutation status of E275E, The gene MKNK2 has a mutation status of Y256D, The gene PEAK3 has a mutation status of S366S, The gene LINGO3 has a mutation status of E55*, The gene TMPRSS9 has a mutation status of D250N, The gene TLE6 has a mutation status of S420C, The gene MFSD12 has a mutation status of A361V, The gene MFSD12 has a mutation status of V197G, The gene EBI3 has a mutation status of R136C, The gene TUBB4A has a mutation status of R359C, The gene RETN has a mutation status of S80S, The gene MUC16 has a mutation status of T13931T, The gene ZGLP1 has a mutation status of G183G, The gene SLC44A2 has a mutation status of G503A, The gene ECSIT has a mutation status of R115L, The gene ZNF564 has a mutation status of F430F, The gene CACNA1A has a mutation status of G950G, The gene PKN1 has a mutation status of T308P, The gene WIZ has a mutation status of I752L, The gene ANO8 has a mutation status of A31S, The gene MVB12A has a mutation status of S263R, The gene MAP1S has a mutation status of S683S, The gene SUGP1 has a mutation status of L347F, The gene ZNF99 has a mutation status of G207C, The gene ZNF724 has a mutation status of E503D, The gene ZNF181 has a mutation status of Q3E, The gene ZNF181 has a mutation status of H471Y, The gene GRAMD1A has a mutation status of R107Q, The gene KMT2B has a mutation status of P1931L, The gene KMT2B has a mutation status of R2712Q, The gene ZNF607 has a mutation status of H639Y, The gene SIRT2 has a mutation status of V360G, The gene PAK4 has a mutation status of S134R, The gene TIMM50 has a mutation status of P76S, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene SPTBN4 has a mutation status of A1492G, The gene SPTBN4 has a mutation status of L2010L, The gene SPTBN4 has a mutation status of E2154Q, The gene COQ8B has a mutation status of A495S, The gene DEDD2 has a mutation status of E316G, The gene PAFAH1B3 has a mutation status of L194L, The gene DACT3 has a mutation status of Q49H, The gene GRIN2D has a mutation status of L207L, The gene PRR12 has a mutation status of P778T, The gene KCNC3 has a mutation status of D225N, The gene SIGLEC9 has a mutation status of A169A, The gene SIGLEC8 has a mutation status of G129R, The gene MBOAT7 has a mutation status of A267S, The gene TSEN34 has a mutation status of T32T, The gene LILRB3 has a mutation status of H300Y, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL1 has a mutation status of P175T, The gene ZNF787 has a mutation status of I235L, The gene SNPH has a mutation status of V434V, The gene SIRPA has a mutation status of L44S, The gene AVP has a mutation status of V147G, The gene FAM83C has a mutation status of V23G, The gene ANKRD60 has a mutation status of C190F, The gene TAF4 has a mutation status of S543L, The gene LAMA5 has a mutation status of D1985A, The gene LAMA5 has a mutation status of P1458S, The gene DIDO1 has a mutation status of A40A, The gene KCNQ2 has a mutation status of T847P, The gene TPTE has a mutation status of T347I, The gene KRTAP6-3 has a mutation status of C98C, The gene RSPH1 has a mutation status of N165K, The gene KRTAP10-5 has a mutation status of C187F, The gene GAB4 has a mutation status of R92C, The gene KLHL22 has a mutation status of I344I, The gene THAP7 has a mutation status of R21L, The gene GSTT4 has a mutation status of Q197R, The gene KIAA1671 has a mutation status of P818L, The gene APOBEC3F has a mutation status of H4N, The gene ADSL has a mutation status of A47fs, The gene DNAJB7 has a mutation status of G161G, The gene TNFRSF13C has a mutation status of P156P, The gene NAGA has a mutation status of A120A, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PARVB has a mutation status of P12T, The gene SHISAL1 has a mutation status of T74M, The gene PLXNB2 has a mutation status of T636P, The gene SBF1 has a mutation status of D202Y, The gene CHKB has a mutation status of E96*, The gene ASMTL has a mutation status of G266G, The gene ASMTL has a mutation status of R72Q, The gene SHROOM2 has a mutation status of D865A, The gene FAM47C has a mutation status of S842F, The gene OTC has a mutation status of L42F, The gene PCSK1N has a mutation status of L82L, The gene CACNA1F has a mutation status of S1670S, The gene FOXP3 has a mutation status of G40V, The gene HEPH has a mutation status of R383Q, The gene AR has a mutation status of A417E, The gene FAM155B has a mutation status of S389S, The gene NHSL2 has a mutation status of T662K, The gene PHKA1 has a mutation status of L246L, The gene COL4A5 has a mutation status of L691F, The gene CXorf66 has a mutation status of D326Y, The gene MAGEC1 has a mutation status of D123E, The gene PASD1 has a mutation status of E202K, The gene PNMA6E has a mutation status of P578H, The gene ATP2B3 has a mutation status of M978V, The gene SRPK3 has a mutation status of I503I, The gene MT-ND3 has a mutation status of S90T, The gene MT-ND6 has a mutation status of S132S, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A
BRCA
The gene CDK11A has a mutation status of D752D, The gene CLSTN1 has a mutation status of A13V, The gene CLSTN1 has a mutation status of A6T, The gene PRAMEF9 has a mutation status of A24A, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene MAP3K6 has a mutation status of L25fs, The gene MAP3K6 has a mutation status of A22T, The gene RPA2 has a mutation status of D112D, The gene S100PBP has a mutation status of G185C, The gene ZSCAN20 has a mutation status of H897H, The gene SZT2 has a mutation status of D2327E, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene ACOT11 has a mutation status of Y504C, The gene GDAP2 has a mutation status of K422K, The gene NOTCH2 has a mutation status of K1641T, The gene NBPF12 has a mutation status of G1096R, The gene NBPF11 has a mutation status of L86L, The gene NBPF9 has a mutation status of E168K, The gene ENSA has a mutation status of G84A, The gene LCE3C has a mutation status of G82E, The gene NUP210L has a mutation status of Y1072H, The gene MGST3 has a mutation status of A133V, The gene KIFAP3 has a mutation status of V323A, The gene STX6 has a mutation status of R55Q, The gene ARL8A has a mutation status of V37I, The gene ARL8A has a mutation status of K33M, The gene ADORA1 has a mutation status of C131F, The gene LYST has a mutation status of M2742T, The gene LRATD1 has a mutation status of A134V, The gene ZNF638 has a mutation status of Q459L, The gene DYSF has a mutation status of R1625*, The gene ANKRD36 has a mutation status of R405S, The gene POLR1B has a mutation status of D753E, The gene RBMS1 has a mutation status of L123L, The gene LRP2 has a mutation status of R1643W, The gene CCDC173 has a mutation status of A107V, The gene TTN has a mutation status of S3280P, The gene FSIP2 has a mutation status of E1071E, The gene SF3B1 has a mutation status of P646P, The gene GPBAR1 has a mutation status of V325V, The gene HDAC4 has a mutation status of S400L, The gene DOCK3 has a mutation status of L278V, The gene DNAH12 has a mutation status of E2938E, The gene ZNF717 has a mutation status of T891T, The gene ROBO2 has a mutation status of S798S, The gene CRYBG3 has a mutation status of T641T, The gene OR5H6 has a mutation status of F202F, The gene HTT has a mutation status of A1831A, The gene EVC has a mutation status of A864D, The gene TBC1D1 has a mutation status of C178W, The gene KLB has a mutation status of A167D, The gene UGT2B17 has a mutation status of K287I, The gene UGT2B17 has a mutation status of K284I, The gene RAPGEF2 has a mutation status of E146G, The gene C5orf22 has a mutation status of D119D, The gene RAI14 has a mutation status of V821F, The gene TMEM167A has a mutation status of T12S, The gene PCDHB12 has a mutation status of P674L, The gene SLIT3 has a mutation status of A21V, The gene MAML1 has a mutation status of A86T, The gene ZKSCAN3 has a mutation status of T222I, The gene ATAT1 has a mutation status of S271P, The gene DDR1 has a mutation status of R337C, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Y42H, The gene HLA-DRB1 has a mutation status of I248L, The gene TRERF1 has a mutation status of Q1120K, The gene PTK7 has a mutation status of T635N, The gene DLK2 has a mutation status of C107Y, The gene MYMX has a mutation status of R39H, The gene CDC5L has a mutation status of L556L, The gene DST has a mutation status of S4072fs, The gene SESN1 has a mutation status of R548C, The gene MICAL1 has a mutation status of D312D, The gene TBC1D32 has a mutation status of K725N, The gene AHI1 has a mutation status of S462P, The gene ARFGEF3 has a mutation status of N95S, The gene RADIL has a mutation status of R212H, The gene TNRC18 has a mutation status of H733Q, The gene ZNF12 has a mutation status of E528D, The gene GRB10 has a mutation status of V267I, The gene SEPTIN14 has a mutation status of G50R, The gene PSPH has a mutation status of L68P, The gene GUSB has a mutation status of R327C, The gene NSUN5 has a mutation status of R172Q, The gene MAGI2 has a mutation status of D297G, The gene ZKSCAN5 has a mutation status of Q498K, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2046L, The gene MUC3A has a mutation status of FTSSITTTENATHSTPN2127del, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene MUC12 has a mutation status of P2099T, The gene TMEM168 has a mutation status of H642fs, The gene CAV1 has a mutation status of I139V, The gene KCP has a mutation status of R446W, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene TMEM213 has a mutation status of A19A, The gene OR2A12 has a mutation status of A200V, The gene ZNF786 has a mutation status of F657F, The gene XPO7 has a mutation status of M740V, The gene DOCK5 has a mutation status of Y1388*, The gene NSD3 has a mutation status of F34fs, The gene NSD3 has a mutation status of D32fs, The gene MRPL15 has a mutation status of A2A, The gene ZNF704 has a mutation status of P160P, The gene EPPK1 has a mutation status of S2669S, The gene EPPK1 has a mutation status of A2633del, The gene PTPRD has a mutation status of V1284D, The gene TMC1 has a mutation status of E517Q, The gene WNK2 has a mutation status of P1552S, The gene ALG2 has a mutation status of G80D, The gene FRRS1L has a mutation status of R51A, The gene PSMB7 has a mutation status of S5L, The gene QSOX2 has a mutation status of K692K, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene CCDC187 has a mutation status of T90M, The gene ITGA8 has a mutation status of R566R, The gene RBP3 has a mutation status of V757G, The gene ANK3 has a mutation status of N795N, The gene NPM3 has a mutation status of T5P, The gene PPRC1 has a mutation status of P962L, The gene RBM20 has a mutation status of V969L, The gene GRK5 has a mutation status of G209G, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of G1443R, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of I1961I, The gene MUC5AC has a mutation status of A2767V, The gene INSC has a mutation status of S147L, The gene PLEKHA7 has a mutation status of Y778C, The gene MRGPRX4 has a mutation status of R57C, The gene MADD has a mutation status of M1571T, The gene OR4C12 has a mutation status of I253I, The gene OR5D3P has a mutation status of S157*, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene APLNR has a mutation status of S56N, The gene OR1S1 has a mutation status of L143F, The gene SLC22A6 has a mutation status of L309L, The gene MACROD1 has a mutation status of S245N, The gene CCDC85B has a mutation status of D79N, The gene GAL3ST3 has a mutation status of G372G, The gene ALDH3B2 has a mutation status of P36L, The gene CCDC90B has a mutation status of L119L, The gene TNFRSF1A has a mutation status of Y236fs, The gene TNFRSF1A has a mutation status of R235fs, The gene SCNN1A has a mutation status of R204W, The gene TAS2R45 has a mutation status of I245V, The gene ARHGDIB has a mutation status of V59M, The gene OVCH1 has a mutation status of L216L, The gene SLC2A13 has a mutation status of N142S, The gene LRRK2 has a mutation status of Q1365R, The gene GXYLT1 has a mutation status of C414H, The gene MYO1A has a mutation status of R597*, The gene UHRF1BP1L has a mutation status of Y734*, The gene RAD9B has a mutation status of *342*, The gene KSR2 has a mutation status of A713T, The gene DNAH10 has a mutation status of D72V, The gene MTRF1 has a mutation status of K138R, The gene DGKH has a mutation status of T697N, The gene FARP1 has a mutation status of G442R, The gene TTC6 has a mutation status of E252D, The gene CLEC14A has a mutation status of A144A, The gene NIN has a mutation status of Q1587P, The gene PLEKHG3 has a mutation status of L910I, The gene RGS6 has a mutation status of V369V, The gene GALC has a mutation status of I102V, The gene BCL11B has a mutation status of R551R, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L1 has a mutation status of M518V, The gene GOLGA8S has a mutation status of I439V, The gene MTMR10 has a mutation status of S27L, The gene FBN1 has a mutation status of Q2477R, The gene SLTM has a mutation status of I247I, The gene ANKDD1A has a mutation status of L516L, The gene TMC3 has a mutation status of V1091V, The gene GOLGA6L10 has a mutation status of C286R, The gene GOLGA6L9 has a mutation status of R6H, The gene GOLGA6L9 has a mutation status of Q151E, The gene TEKT5 has a mutation status of I303N, The gene RBBP6 has a mutation status of K1780fs, The gene ITGAD has a mutation status of Q325*, The gene CHST6 has a mutation status of R359Q, The gene ADAMTS18 has a mutation status of Q612*, The gene JPH3 has a mutation status of G141G, The gene CPNE7 has a mutation status of V488L, The gene ENO3 has a mutation status of C356fs, The gene DVL2 has a mutation status of S594S, The gene TP53 has a mutation status of L265P, The gene VTN has a mutation status of V426L, The gene CCL4L2 has a mutation status of P67R, The gene TTC25 has a mutation status of L394L, The gene BRCA1 has a mutation status of H619N, The gene SOST has a mutation status of P48P, The gene UBE2Z has a mutation status of 335_336MD>IY, The gene B4GALNT2 has a mutation status of H368H, The gene UTP18 has a mutation status of P19P, The gene USP32 has a mutation status of Y110C, The gene ABCA8 has a mutation status of K624R, The gene BTBD17 has a mutation status of G36E, The gene MBD1 has a mutation status of E315K, The gene RNF152 has a mutation status of F16C, The gene SERPINB10 has a mutation status of R362*, The gene MPND has a mutation status of G59G, The gene PLIN4 has a mutation status of V1332G, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13007G, The gene MUC16 has a mutation status of N12654D, The gene MUC16 has a mutation status of G12642S, The gene AP1M2 has a mutation status of D24G, The gene SMARCA4 has a mutation status of E1499*, The gene ZNF14 has a mutation status of F484I, The gene ZNF66 has a mutation status of F97F, The gene ZNF681 has a mutation status of E628K, The gene TDRD12 has a mutation status of A963T, The gene GRAMD1A has a mutation status of D776N, The gene APLP1 has a mutation status of L485L, The gene LTBP4 has a mutation status of P460P, The gene CYP2S1 has a mutation status of R382Q, The gene CLASRP has a mutation status of H606H, The gene PPP1R37 has a mutation status of S561G, The gene PRR12 has a mutation status of P1517P, The gene SIGLEC10 has a mutation status of T318T, The gene LILRA2 has a mutation status of W163S, The gene LILRA1 has a mutation status of L268R, The gene LILRA1 has a mutation status of P271R, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene LILRB1 has a mutation status of Y99I, The gene LILRB1 has a mutation status of 171_172QP>HS, The gene PEG3 has a mutation status of A518A, The gene ZNF324 has a mutation status of L445F, The gene SIRPA has a mutation status of L44S, The gene LBP has a mutation status of R254H, The gene ZBP1 has a mutation status of R229C, The gene LAMA5 has a mutation status of S1800L, The gene KRTAP19-5 has a mutation status of S57G, The gene SH3BGR has a mutation status of L49W, The gene AIFM3 has a mutation status of G132G, The gene PDXP has a mutation status of E34Q, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TBC1D22A has a mutation status of T149A, The gene ZBED4 has a mutation status of Q774R, The gene SELENOO has a mutation status of V595M, The gene TUBGCP6 has a mutation status of L1171L, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene ARSH has a mutation status of A187D, The gene MAGEB10 has a mutation status of S105S, The gene MTMR8 has a mutation status of P565S, The gene SLC7A3 has a mutation status of R529I, The gene TENT5D has a mutation status of F266F, The gene RADX has a mutation status of R389R, The gene SLC25A5 has a mutation status of T221R, The gene DCAF12L2 has a mutation status of R335C, The gene SPANXB1 has a mutation status of Q42P, The gene AC236972.4 has a mutation status of P1394A, The gene MT-ND2 has a mutation status of G82G, The gene MT-CO1 has a mutation status of L283L, The gene MT-ATP6 has a mutation status of A20T, The gene MT-ATP6 has a mutation status of S188S, The gene MT-CO3 has a mutation status of G96G, The gene MT-ND5 has a mutation status of P198P, The gene MT-CYB has a mutation status of S172N, The gene MT-CYB has a mutation status of P247P, The gene MT-CYB has a mutation status of P346P
GBMLGG
The gene CDK11B has a mutation status of P663P, The gene CHD5 has a mutation status of D1363G, The gene PRAMEF1 has a mutation status of F280V, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene SPOCD1 has a mutation status of L47I, The gene FOXJ3 has a mutation status of S227I, The gene PPCS has a mutation status of R25P, The gene CYP4A22 has a mutation status of A124P, The gene NBPF14 has a mutation status of S1390N, The gene PRCC has a mutation status of K137E, The gene IGSF8 has a mutation status of E55K, The gene DYRK3 has a mutation status of L311S, The gene PIGR has a mutation status of D435D, The gene USH2A has a mutation status of E4461K, The gene GDF7 has a mutation status of L234M, The gene DNMT3A has a mutation status of C487Y, The gene ABHD1 has a mutation status of V43A, The gene PCARE has a mutation status of S517L, The gene XDH has a mutation status of S123G, The gene ABCG8 has a mutation status of R152H, The gene EPAS1 has a mutation status of D753E, The gene SPTBN1 has a mutation status of L240V, The gene ASTL has a mutation status of A49G, The gene MYO7B has a mutation status of K146K, The gene TTN has a mutation status of M28857T, The gene FAM171B has a mutation status of G506V, The gene ANKAR has a mutation status of Y734S, The gene SLC4A7 has a mutation status of E741G, The gene ARIH2OS has a mutation status of A153G, The gene DOCK3 has a mutation status of I444F, The gene SFMBT1 has a mutation status of P147L, The gene ROBO1 has a mutation status of L1273L, The gene COL8A1 has a mutation status of P248P, The gene ATP6V1A has a mutation status of A37G, The gene TEX55 has a mutation status of E457K, The gene KALRN has a mutation status of I1118V, The gene SLC25A36 has a mutation status of A223T, The gene RARRES1 has a mutation status of I191M, The gene ZBBX has a mutation status of A663S, The gene C3orf70 has a mutation status of R26R, The gene CCDC50 has a mutation status of R330S, The gene TFRC has a mutation status of F650F, The gene MAN2B2 has a mutation status of D38V, The gene RBPJ has a mutation status of P14L, The gene UGT2A3 has a mutation status of C280S, The gene PDE5A has a mutation status of A314V, The gene PCDH10 has a mutation status of G765S, The gene TMEM144 has a mutation status of A108E, The gene SLC6A19 has a mutation status of C166C, The gene C5orf49 has a mutation status of P33S, The gene HMGCS1 has a mutation status of G3R, The gene PCDHB11 has a mutation status of T756S, The gene RREB1 has a mutation status of G782R, The gene ZNF184 has a mutation status of P473S, The gene EHMT2 has a mutation status of R1145W, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DQB2 has a mutation status of L36V, The gene RPF2 has a mutation status of S300*, The gene RPS6KA2 has a mutation status of R633C, The gene DNAH11 has a mutation status of Q1132Q, The gene FAM126A has a mutation status of R510G, The gene GLI3 has a mutation status of P923P, The gene COBL has a mutation status of G898R, The gene AKAP9 has a mutation status of S2613N, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S326A, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of T433N, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of T1179P, The gene MUC3A has a mutation status of V1181V, The gene CTTNBP2 has a mutation status of I71S, The gene HYAL4 has a mutation status of P41S, The gene KLF14 has a mutation status of A39A, The gene PRSS2 has a mutation status of R68C, The gene TAS2R60 has a mutation status of M85L, The gene ZBED6CL has a mutation status of L13M, The gene SFRP1 has a mutation status of A118S, The gene SOX17 has a mutation status of V386E, The gene GGH has a mutation status of L162L, The gene NIPAL2 has a mutation status of I340V, The gene FAM83A has a mutation status of Q370H, The gene BOP1 has a mutation status of R158C, The gene BOP1 has a mutation status of N134N, The gene CPSF1 has a mutation status of R1019C, The gene PIGO has a mutation status of R664G, The gene OR2K2 has a mutation status of R143W, The gene CDK5RAP2 has a mutation status of D1377D, The gene CAMSAP1 has a mutation status of H969Q, The gene SEC16A has a mutation status of S1015R, The gene VIM has a mutation status of R364C, The gene ANKRD26 has a mutation status of G1386R, The gene DLG5 has a mutation status of N1758I, The gene INPP5F has a mutation status of S793F, The gene FUOM has a mutation status of S12F, The gene MUC5AC has a mutation status of T4319S, The gene KIAA1549L has a mutation status of L1855P, The gene OR4C15 has a mutation status of F101*, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR9I1 has a mutation status of V274M, The gene FAM86C1 has a mutation status of A25D, The gene KDM4F has a mutation status of I49V, The gene DDX10 has a mutation status of D412E, The gene KMT2A has a mutation status of R933W, The gene ARCN1 has a mutation status of S424S, The gene PDZD3 has a mutation status of V330V, The gene SIAE has a mutation status of S252C, The gene ARHGAP32 has a mutation status of L1454L, The gene C1S has a mutation status of E441K, The gene ABCC9 has a mutation status of T1053K, The gene KRT6C has a mutation status of I523L, The gene MARS1 has a mutation status of A837A, The gene CHST11 has a mutation status of T95K, The gene OAS2 has a mutation status of N416H, The gene ALG11 has a mutation status of A457T, The gene AL445989.1 has a mutation status of G53S, The gene HERC2 has a mutation status of S895A, The gene TP53BP1 has a mutation status of R376Q, The gene AC090517.4 has a mutation status of S99T, The gene MCTP2 has a mutation status of C449F, The gene CLCN7 has a mutation status of E732*, The gene KCTD5 has a mutation status of P11P, The gene ZNF213 has a mutation status of R132P, The gene CIITA has a mutation status of M210I, The gene MAPK3 has a mutation status of G73S, The gene SEPTIN1 has a mutation status of E111K, The gene ZNF48 has a mutation status of S66P, The gene SRCAP has a mutation status of P2821P, The gene BBS2 has a mutation status of D296G, The gene NUP93 has a mutation status of G315A, The gene CIAO2B has a mutation status of L146L, The gene NFATC3 has a mutation status of S975L, The gene IST1 has a mutation status of L65L, The gene CDT1 has a mutation status of A530T, The gene ZFP3 has a mutation status of F28L, The gene YBX2 has a mutation status of G340V, The gene MYOCD has a mutation status of C601F, The gene FLII has a mutation status of I777L, The gene SLC47A2 has a mutation status of E514G, The gene KIAA0100 has a mutation status of V481V, The gene RAB34 has a mutation status of I233V, The gene CCL4L2 has a mutation status of P67R, The gene GPR179 has a mutation status of A2333G, The gene THRA has a mutation status of K337R, The gene KRTAP4-11 has a mutation status of H136R, The gene KRT13 has a mutation status of S337S, The gene SEPTIN4 has a mutation status of P375S, The gene BPTF has a mutation status of D1334G, The gene ABCA8 has a mutation status of I1044I, The gene FBF1 has a mutation status of A919G, The gene FBF1 has a mutation status of E918G, The gene CDK3 has a mutation status of V230F, The gene DNAH17 has a mutation status of T1700T, The gene CCDC40 has a mutation status of E804D, The gene DSG2 has a mutation status of E820*, The gene SALL3 has a mutation status of A245V, The gene PLPP2 has a mutation status of S70L, The gene C2CD4C has a mutation status of P157H, The gene PTBP1 has a mutation status of G123D, The gene ZNF561 has a mutation status of E325G, The gene ZNF625 has a mutation status of D31D, The gene CYP4F2 has a mutation status of I299T, The gene SLC27A1 has a mutation status of E247K, The gene JAK3 has a mutation status of D130A, The gene ZNF728 has a mutation status of K525K, The gene ZNF850 has a mutation status of F16C, The gene SPTBN4 has a mutation status of L1921L, The gene ARHGEF1 has a mutation status of 683_684insDDLLL, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRB1 has a mutation status of P3S, The gene LILRB1 has a mutation status of Y99I, The gene ADAM33 has a mutation status of E438E, The gene ADAM33 has a mutation status of R383C, The gene BPIFB1 has a mutation status of R406R, The gene AL031681.3 has a mutation status of H178Q, The gene ZFP64 has a mutation status of F414L, The gene LAMA5 has a mutation status of V1602M, The gene FAM3B has a mutation status of V114V, The gene FTCD has a mutation status of R445R, The gene FTCD has a mutation status of G443G, The gene CCT8L2 has a mutation status of G55S, The gene DGCR8 has a mutation status of R262Q, The gene SSTR3 has a mutation status of T190P, The gene CACNA1I has a mutation status of H1042R, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ARSL has a mutation status of A239T, The gene MXRA5 has a mutation status of L2562F, The gene ACE2 has a mutation status of D292D, The gene MAGIX has a mutation status of S80I, The gene ARMCX1 has a mutation status of G248C, The gene RAB40AL has a mutation status of S33T, The gene ACSL4 has a mutation status of T268M, The gene SLC25A5 has a mutation status of T221R, The gene TENM1 has a mutation status of K2401R, The gene SPANXB1 has a mutation status of E80K
SARC
The gene SLC45A1 has a mutation status of T531A, The gene NPPB has a mutation status of R9W, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene CROCC has a mutation status of S840S, The gene UBR4 has a mutation status of L853L, The gene OTUD3 has a mutation status of Q97fs, The gene PLA2G2E has a mutation status of E90K, The gene PHACTR4 has a mutation status of V173V, The gene RLF has a mutation status of V1887A, The gene SPATA6 has a mutation status of T76A, The gene VCAM1 has a mutation status of K4fs, The gene KCNA3 has a mutation status of E262K, The gene CHIA has a mutation status of Y203C, The gene DENND2C has a mutation status of C618F, The gene VANGL1 has a mutation status of P498T, The gene TTF2 has a mutation status of T724fs, The gene ANKRD34A has a mutation status of I436L, The gene AC242842.3 has a mutation status of V503L, The gene RPRD2 has a mutation status of T1003I, The gene CGN has a mutation status of L798L, The gene FLG has a mutation status of H532H, The gene MNDA has a mutation status of T244I, The gene ATP1A4 has a mutation status of H501P, The gene ARHGAP30 has a mutation status of L706L, The gene F5 has a mutation status of R534Q, The gene RABGAP1L has a mutation status of R407H, The gene CACNA1S has a mutation status of F1187S, The gene SYT2 has a mutation status of R231H, The gene USH2A has a mutation status of R4392I, The gene DISP1 has a mutation status of T441M, The gene SRP9 has a mutation status of S67S, The gene OBSCN has a mutation status of E5517E, The gene OR2L13 has a mutation status of L129fs, The gene NBAS has a mutation status of T1410A, The gene EFR3B has a mutation status of A463V, The gene DPYSL5 has a mutation status of E41K, The gene PCARE has a mutation status of E1062Q, The gene SOCS5 has a mutation status of E153E, The gene USP34 has a mutation status of P497H, The gene OTX1 has a mutation status of M2I, The gene CLEC4F has a mutation status of M100I, The gene ZNF638 has a mutation status of S191F, The gene ANKRD23 has a mutation status of L126P, The gene AFF3 has a mutation status of R605R, The gene TBC1D8 has a mutation status of I205T, The gene SLC9A4 has a mutation status of S42fs, The gene ANAPC1 has a mutation status of V535V, The gene ANAPC1 has a mutation status of A193A, The gene LCT has a mutation status of F805F, The gene FASTKD1 has a mutation status of I200V, The gene FSIP2 has a mutation status of K6741K, The gene WDR75 has a mutation status of N204N, The gene KIAA2012 has a mutation status of A467V, The gene ABCB6 has a mutation status of I680I, The gene SPEG has a mutation status of R1617H, The gene SLC4A3 has a mutation status of I954I, The gene KCNE4 has a mutation status of V93V, The gene AQP12B has a mutation status of L28R, The gene FGD5 has a mutation status of F918F, The gene MON1A has a mutation status of H162fs, The gene NISCH has a mutation status of Y1169*, The gene CSNKA2IP has a mutation status of S163S, The gene IMPG2 has a mutation status of R131H, The gene DPPA2 has a mutation status of M216I, The gene GCSAM has a mutation status of Y82D, The gene ALDH1L1 has a mutation status of D149D, The gene COL6A5 has a mutation status of R273Q, The gene KNG1 has a mutation status of I26L, The gene ADIPOQ has a mutation status of D231V, The gene TMEM207 has a mutation status of F130V, The gene XXYLT1 has a mutation status of A121V, The gene NRROS has a mutation status of L112L, The gene PIGZ has a mutation status of L544L, The gene GRPEL1 has a mutation status of H175Y, The gene UBA6 has a mutation status of K991K, The gene CCDC158 has a mutation status of R402H, The gene MRPL1 has a mutation status of D261G, The gene WDFY3 has a mutation status of A3401V, The gene HPGDS has a mutation status of I21R, The gene ANK2 has a mutation status of T2250T, The gene ZNF827 has a mutation status of P319S, The gene RBM46 has a mutation status of E22*, The gene CCT5 has a mutation status of M29T, The gene CTNND2 has a mutation status of Y1019H, The gene PLCXD3 has a mutation status of F131F, The gene SREK1IP1 has a mutation status of L87K, The gene ZBED3 has a mutation status of L155A, The gene THBS4 has a mutation status of R206Q, The gene FBXL17 has a mutation status of S641G, The gene APC has a mutation status of M526L, The gene LMNB1 has a mutation status of R29W, The gene FNIP1 has a mutation status of S185S, The gene PCDHGC3 has a mutation status of R880C, The gene RBM27 has a mutation status of R174L, The gene SLC26A2 has a mutation status of R279W, The gene SLC6A7 has a mutation status of G119G, The gene CD74 has a mutation status of P163P, The gene FAT2 has a mutation status of V170L, The gene G3BP1 has a mutation status of E185Q, The gene WWC1 has a mutation status of E310D, The gene TBC1D9B has a mutation status of R171W, The gene MBOAT1 has a mutation status of P440T, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DQA1 has a mutation status of E73L, The gene ARMC12 has a mutation status of E303K, The gene MLIP has a mutation status of T81T, The gene COL12A1 has a mutation status of G2963E, The gene CRYBG1 has a mutation status of I1143S, The gene MFSD4B has a mutation status of L182Y, The gene FYN has a mutation status of E419fs, The gene LPA has a mutation status of T39T, The gene PRKN has a mutation status of Q347H, The gene PDE10A has a mutation status of I728M, The gene PDGFA has a mutation status of R189W, The gene MAD1L1 has a mutation status of F537L, The gene SDK1 has a mutation status of D1114N, The gene JAZF1 has a mutation status of F10del, The gene EEPD1 has a mutation status of D117D, The gene GLI3 has a mutation status of I1504V, The gene MRPL32 has a mutation status of R91W, The gene RFC2 has a mutation status of Y322C, The gene STEAP4 has a mutation status of Y420Y, The gene FAM133B has a mutation status of M147V, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S558T, The gene TES has a mutation status of P299T, The gene CFTR has a mutation status of L986V, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene WWP1 has a mutation status of K740N, The gene C8orf88 has a mutation status of Q69H, The gene UBR5 has a mutation status of QNK1404del, The gene CSMD3 has a mutation status of K2K, The gene MED30 has a mutation status of C103fs, The gene COL14A1 has a mutation status of Y1090*, The gene DENND3 has a mutation status of T121T, The gene TOP1MT has a mutation status of R21*, The gene EPPK1 has a mutation status of A2633del, The gene MROH1 has a mutation status of D885D, The gene NFIB has a mutation status of T505fs, The gene NFIB has a mutation status of W504fs, The gene MYORG has a mutation status of V457M, The gene FAM205C has a mutation status of E196*, The gene CNTNAP3B has a mutation status of D816D, The gene CNTNAP3B has a mutation status of P651P, The gene GAS1 has a mutation status of Y68Y, The gene BICD2 has a mutation status of E374K, The gene SUSD3 has a mutation status of S173S, The gene SMC2 has a mutation status of K1178N, The gene FRRS1L has a mutation status of R51A, The gene SVEP1 has a mutation status of P1775P, The gene SUSD1 has a mutation status of A8A, The gene HSPA5 has a mutation status of T203T, The gene ASB6 has a mutation status of A93T, The gene ADAMTSL2 has a mutation status of G421S, The gene NACC2 has a mutation status of AA155del, The gene CCDC187 has a mutation status of R945P, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of D12D, The gene PMPCA has a mutation status of V59A, The gene NOTCH1 has a mutation status of C254fs, The gene LCN12 has a mutation status of F129F, The gene FUT7 has a mutation status of G34G, The gene NDOR1 has a mutation status of T60S, The gene DIP2C has a mutation status of Q56Q, The gene CCDC7 has a mutation status of E807E, The gene FO681492.1 has a mutation status of S6L, The gene PCDH15 has a mutation status of R343K, The gene BICC1 has a mutation status of R700R, The gene SIRT1 has a mutation status of S535S, The gene TET1 has a mutation status of V1235L, The gene CFAP70 has a mutation status of N1118S, The gene SFTPA1 has a mutation status of P77L, The gene DNTT has a mutation status of T169A, The gene PIK3AP1 has a mutation status of D517D, The gene RRP12 has a mutation status of D616N, The gene TAF5 has a mutation status of R663R, The gene BCCIP has a mutation status of E11E, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of P1919L, The gene MUC5AC has a mutation status of T3668P, The gene ART1 has a mutation status of H144D, The gene CYB5R2 has a mutation status of I153T, The gene HIPK3 has a mutation status of N1032S, The gene OR9G1 has a mutation status of I196F, The gene GLYAT has a mutation status of K81E, The gene SPTBN2 has a mutation status of A1641V, The gene PC has a mutation status of S1086S, The gene C11orf24 has a mutation status of H73R, The gene DYNC2H1 has a mutation status of F948fs, The gene APOA5 has a mutation status of S212R, The gene CD3G has a mutation status of S148L, The gene OR10G9 has a mutation status of T13T, The gene CDON has a mutation status of S1225N, The gene GLB1L2 has a mutation status of T479T, The gene PZP has a mutation status of N1430N, The gene TAS2R9 has a mutation status of K110Q, The gene ADAMTS20 has a mutation status of A327D, The gene RAPGEF3 has a mutation status of G340D, The gene KRT79 has a mutation status of T242I, The gene OR10P1 has a mutation status of I289V, The gene TAFA2 has a mutation status of V85G, The gene LGR5 has a mutation status of L335S, The gene ZFC3H1 has a mutation status of A1913G, The gene PTPRQ has a mutation status of V537A, The gene CEP290 has a mutation status of E795K, The gene LTA4H has a mutation status of D258V, The gene PAH has a mutation status of I60T, The gene HCFC2 has a mutation status of G496S, The gene TCHP has a mutation status of E459del, The gene ACADS has a mutation status of A195A, The gene DNAH10 has a mutation status of E523fs, The gene NCOR2 has a mutation status of S168S, The gene GLT1D1 has a mutation status of A145A, The gene EP400 has a mutation status of R1401Q, The gene ZIC5 has a mutation status of P151P, The gene MRPL52 has a mutation status of S49*, The gene JPH4 has a mutation status of V68M, The gene STRN3 has a mutation status of I333L, The gene TXNDC16 has a mutation status of T485T, The gene PRIMA1 has a mutation status of V7fs, The gene CLMN has a mutation status of V60I, The gene TECPR2 has a mutation status of L393fs, The gene CDC42BPB has a mutation status of R570Q, The gene LINC02203 has a mutation status of I259M, The gene GOLGA6L2 has a mutation status of C715Y, The gene MAGEL2 has a mutation status of VHPPPPGTPM180del, The gene RYR3 has a mutation status of E2693Q, The gene SLC12A6 has a mutation status of V555M, The gene THBS1 has a mutation status of P622Q, The gene MGA has a mutation status of Q2151H, The gene TTBK2 has a mutation status of R164W, The gene UBR1 has a mutation status of S1178N, The gene CATSPER2 has a mutation status of R52H, The gene ANKDD1A has a mutation status of L516L, The gene DENND4A has a mutation status of D1191A, The gene RCN2 has a mutation status of E209del, The gene ANKRD34C has a mutation status of S223S, The gene CFAP161 has a mutation status of C222C, The gene BNC1 has a mutation status of E540E, The gene ADAMTSL3 has a mutation status of L476M, The gene ASB7 has a mutation status of L146V, The gene OR2C1 has a mutation status of R54W, The gene PLEKHG4 has a mutation status of A502S, The gene AC026464.3 has a mutation status of I150I, The gene ATXN1L has a mutation status of R610K, The gene DPEP1 has a mutation status of M1T, The gene TP53 has a mutation status of P152fs, The gene KDM6B has a mutation status of L702L, The gene MYH1 has a mutation status of K1621K, The gene MYH1 has a mutation status of L167M, The gene ABHD15 has a mutation status of E373E, The gene KRTAP4-1 has a mutation status of R85R, The gene CNTNAP1 has a mutation status of F598V, The gene LRRC37A2 has a mutation status of R1161R, The gene PRKAR1A has a mutation status of D227G, The gene CASKIN2 has a mutation status of A782A, The gene FAAP100 has a mutation status of R59G, The gene ALYREF has a mutation status of A9A, The gene AQP4 has a mutation status of M224T, The gene SLC39A6 has a mutation status of Q571Q, The gene RAX has a mutation status of K172K, The gene MFSD12 has a mutation status of R218Q, The gene MUC16 has a mutation status of S10497S, The gene BRD4 has a mutation status of P1012P, The gene HSH2D has a mutation status of P211L, The gene B3GNT3 has a mutation status of V257V, The gene ZNF599 has a mutation status of F572V, The gene MAP3K10 has a mutation status of P193A, The gene CYP2F1 has a mutation status of P368P, The gene CIC has a mutation status of K921N, The gene TSKS has a mutation status of A2V, The gene ZNF28 has a mutation status of T203T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRB2 has a mutation status of A468A, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q401L, The gene KIR3DL3 has a mutation status of R166H, The gene KIR2DL4 has a mutation status of P17L, The gene ZSCAN5A has a mutation status of V169L, The gene ZNF417 has a mutation status of K537*, The gene SIRPA has a mutation status of I374M, The gene RIN2 has a mutation status of T551T, The gene ASXL1 has a mutation status of R171R, The gene BPIFB2 has a mutation status of I397F, The gene BPIFB4 has a mutation status of A185T, The gene MYH7B has a mutation status of Q41E, The gene DLGAP4 has a mutation status of Q518H, The gene SOGA1 has a mutation status of K315R, The gene TGM2 has a mutation status of A459A, The gene TTPAL has a mutation status of L125V, The gene TP53TG5 has a mutation status of S83F, The gene SULF2 has a mutation status of H245H, The gene HELZ2 has a mutation status of F255F, The gene SLC2A4RG has a mutation status of R7H, The gene KRTAP19-5 has a mutation status of S57G, The gene IL10RB has a mutation status of V148M, The gene RIPK4 has a mutation status of L778F, The gene UBE2G2 has a mutation status of Y103Y, The gene CLTCL1 has a mutation status of S1057S, The gene EWSR1 has a mutation status of D352G, The gene SFI1 has a mutation status of V274I, The gene MICALL1 has a mutation status of A492T, The gene NPTXR has a mutation status of K488K, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PKDREJ has a mutation status of S1748C, The gene CRELD2 has a mutation status of S295A, The gene CSF2RA has a mutation status of T231M, The gene ITIH6 has a mutation status of T221S, The gene MTMR8 has a mutation status of W407C, The gene RLIM has a mutation status of Q335Q, The gene NEXMIF has a mutation status of W258C, The gene GPRASP1 has a mutation status of P961P, The gene CCDC160 has a mutation status of G276R, The gene IRAK1 has a mutation status of T152S, The gene TKTL1 has a mutation status of G296S, The gene MT-ND4 has a mutation status of S407T, The gene MT-ND5 has a mutation status of Y174Y, The gene MT-CYB has a mutation status of A191T, The gene NOL9 has a mutation status of G589fs, The gene NPPB has a mutation status of R9W, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene CROCC has a mutation status of S840S, The gene UBR4 has a mutation status of T2204S, The gene UBR4 has a mutation status of L853L, The gene PLA2G2E has a mutation status of E90K, The gene CELA3A has a mutation status of P65L, The gene CD52 has a mutation status of C59C, The gene ARID1A has a mutation status of S1000del, The gene PHACTR4 has a mutation status of V173V, The gene PHACTR4 has a mutation status of E319E, The gene RLF has a mutation status of V1887A, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene TAL1 has a mutation status of A264G, The gene SPATA6 has a mutation status of T76A, The gene AGBL4 has a mutation status of G53D, The gene DAB1 has a mutation status of H207H, The gene PATJ has a mutation status of N120S, The gene LRRC53 has a mutation status of L122Q, The gene SYDE2 has a mutation status of M1061V, The gene VCAM1 has a mutation status of K4fs, The gene KCNA3 has a mutation status of E262K, The gene CHIA has a mutation status of Y203C, The gene DENND2C has a mutation status of C618F, The gene VANGL1 has a mutation status of P498T, The gene TTF2 has a mutation status of T724fs, The gene RPRD2 has a mutation status of T1003I, The gene CGN has a mutation status of L798L, The gene FLG has a mutation status of H532H, The gene MNDA has a mutation status of T244I, The gene ATP1A4 has a mutation status of H501P, The gene ARHGAP30 has a mutation status of L706L, The gene PCP4L1 has a mutation status of A30V, The gene F5 has a mutation status of R534Q, The gene RABGAP1L has a mutation status of R407H, The gene IGFN1 has a mutation status of K1635E, The gene SYT2 has a mutation status of R231H, The gene USH2A has a mutation status of R4392I, The gene DISP1 has a mutation status of T441M, The gene SRP9 has a mutation status of S67S, The gene OBSCN has a mutation status of V1245L, The gene OBSCN has a mutation status of E5517E, The gene HEATR1 has a mutation status of F191F, The gene NBAS has a mutation status of T1410A, The gene EFR3B has a mutation status of A463V, The gene SOCS5 has a mutation status of E153E, The gene USP34 has a mutation status of P497H, The gene OTX1 has a mutation status of M2I, The gene CLEC4F has a mutation status of M100I, The gene EVA1A has a mutation status of G3S, The gene ANKRD23 has a mutation status of L126P, The gene AFF3 has a mutation status of R605R, The gene TBC1D8 has a mutation status of I205T, The gene ANAPC1 has a mutation status of L773fs, The gene ANAPC1 has a mutation status of A193A, The gene SFT2D3 has a mutation status of L161P, The gene AMER3 has a mutation status of L247F, The gene LRP1B has a mutation status of T3106T, The gene NEB has a mutation status of T328T, The gene GALNT13 has a mutation status of K377E, The gene SCN2A has a mutation status of I1772I, The gene STK39 has a mutation status of T292I, The gene FASTKD1 has a mutation status of I200V, The gene SP9 has a mutation status of C369C, The gene KIAA2012 has a mutation status of A467V, The gene SUMO1 has a mutation status of E54*, The gene INO80D has a mutation status of Q355*, The gene STK36 has a mutation status of L509L, The gene ABCB6 has a mutation status of I680I, The gene SPEG has a mutation status of R1617H, The gene SLC4A3 has a mutation status of I954I, The gene SP140L has a mutation status of P135P, The gene NCL has a mutation status of E267del, The gene RNPEPL1 has a mutation status of A3S, The gene AQP12B has a mutation status of L28R, The gene CROCC2 has a mutation status of Q1563R, The gene FGD5 has a mutation status of F918F, The gene BTD has a mutation status of E409K, The gene PLCL2 has a mutation status of G8D, The gene MON1A has a mutation status of H162fs, The gene NISCH has a mutation status of Y1169*, The gene IMPG2 has a mutation status of R131H, The gene DPPA2 has a mutation status of M216I, The gene GCSAM has a mutation status of Y82D, The gene IGSF11 has a mutation status of K394R, The gene ALDH1L1 has a mutation status of D149D, The gene KIAA1257 has a mutation status of A644V, The gene COL6A5 has a mutation status of R273Q, The gene SI has a mutation status of I311M, The gene KNG1 has a mutation status of I26L, The gene ADIPOQ has a mutation status of D231V, The gene TMEM207 has a mutation status of F130V, The gene XXYLT1 has a mutation status of A121V, The gene NRROS has a mutation status of L112L, The gene PIGZ has a mutation status of L544L, The gene NSG1 has a mutation status of F8C, The gene STK32B has a mutation status of G158R, The gene GRPEL1 has a mutation status of H175Y, The gene CLOCK has a mutation status of H821R, The gene CCDC158 has a mutation status of R402H, The gene MRPL1 has a mutation status of D261G, The gene WDFY3 has a mutation status of A3401V, The gene AP1AR has a mutation status of L220F, The gene ZNF827 has a mutation status of P319S, The gene CTNND2 has a mutation status of Y1019H, The gene MYO10 has a mutation status of S26T, The gene MROH2B has a mutation status of R390Q, The gene ZBED3 has a mutation status of L155A, The gene THBS4 has a mutation status of R206Q, The gene FBXL17 has a mutation status of S641G, The gene APC has a mutation status of M526L, The gene LMNB1 has a mutation status of R29W, The gene FNIP1 has a mutation status of S185S, The gene PCDHGC3 has a mutation status of R880C, The gene RBM27 has a mutation status of R174L, The gene SLC26A2 has a mutation status of R279W, The gene SLC6A7 has a mutation status of G119G, The gene CD74 has a mutation status of P163P, The gene FAT2 has a mutation status of V170L, The gene G3BP1 has a mutation status of E185Q, The gene GEMIN5 has a mutation status of L1431V, The gene WWC1 has a mutation status of E310D, The gene MAML1 has a mutation status of P420L, The gene TBC1D9B has a mutation status of R171W, The gene RIOK1 has a mutation status of P483S, The gene TXNDC5 has a mutation status of LL25del, The gene MBOAT1 has a mutation status of P440T, The gene HLA-C has a mutation status of T162S, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DQA1 has a mutation status of E73L, The gene ARMC12 has a mutation status of E303K, The gene MLIP has a mutation status of T81T, The gene EYS has a mutation status of N2473Y, The gene COL12A1 has a mutation status of G2963E, The gene BCKDHB has a mutation status of C106Y, The gene MDN1 has a mutation status of L3913L, The gene CASP8AP2 has a mutation status of W382L, The gene CRYBG1 has a mutation status of I1143S, The gene MFSD4B has a mutation status of L182Y, The gene FYN has a mutation status of E419fs, The gene PLAGL1 has a mutation status of A428V, The gene PLAGL1 has a mutation status of R414M, The gene AL357075.4 has a mutation status of G502S, The gene LPA has a mutation status of T39T, The gene PRKN has a mutation status of Q347H, The gene PDE10A has a mutation status of I728M, The gene MAD1L1 has a mutation status of F537L, The gene JAZF1 has a mutation status of F10del, The gene GLI3 has a mutation status of I1504V, The gene POM121C has a mutation status of I754V, The gene STEAP4 has a mutation status of Y420Y, The gene ZNF804B has a mutation status of H274Q, The gene ZNF804B has a mutation status of I1206V, The gene FAM133B has a mutation status of M147V, The gene NYAP1 has a mutation status of F327F, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T1594T, The gene MUC3A has a mutation status of V1672D, The gene SLC26A4 has a mutation status of G740V, The gene TES has a mutation status of P299T, The gene CFTR has a mutation status of L986V, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene ATG9B has a mutation status of P917L, The gene KMT2C has a mutation status of P3390S, The gene USP17L8 has a mutation status of A56G, The gene UNC5D has a mutation status of E173fs, The gene SNAI2 has a mutation status of W198G, The gene NCOA2 has a mutation status of P1336S, The gene C8orf88 has a mutation status of Q69H, The gene UBR5 has a mutation status of QNK1404del, The gene CSMD3 has a mutation status of K2K, The gene MED30 has a mutation status of C103fs, The gene COL14A1 has a mutation status of Y1090*, The gene TOP1MT has a mutation status of R21*, The gene IQANK1 has a mutation status of T558T, The gene EPPK1 has a mutation status of A2633del, The gene MROH1 has a mutation status of D885D, The gene IL33 has a mutation status of C58*, The gene NFIB has a mutation status of T505fs, The gene NFIB has a mutation status of W504fs, The gene MYORG has a mutation status of V457M, The gene CNTNAP3B has a mutation status of D816D, The gene CNTNAP3B has a mutation status of P651P, The gene GAS1 has a mutation status of Y68Y, The gene BICD2 has a mutation status of E374K, The gene SUSD3 has a mutation status of S173S, The gene TEX10 has a mutation status of L793fs, The gene FRRS1L has a mutation status of R51A, The gene SVEP1 has a mutation status of P1775P, The gene SUSD1 has a mutation status of A8A, The gene ORM2 has a mutation status of A2V, The gene CNTRL has a mutation status of L1491L, The gene HSPA5 has a mutation status of T203T, The gene ASB6 has a mutation status of A93T, The gene HMCN2 has a mutation status of G3045S, The gene ADAMTS13 has a mutation status of Q1419Q, The gene ADAMTSL2 has a mutation status of G421S, The gene NACC2 has a mutation status of AA155del, The gene LHX3 has a mutation status of T152T, The gene CCDC187 has a mutation status of G820G, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of Q431Q, The gene CCDC187 has a mutation status of R294H, The gene FUT7 has a mutation status of G34G, The gene NDOR1 has a mutation status of T60S, The gene DIP2C has a mutation status of Q56Q, The gene CAMK1D has a mutation status of D130D, The gene CCDC7 has a mutation status of E807E, The gene CHAT has a mutation status of V674V, The gene PCDH15 has a mutation status of R343K, The gene BICC1 has a mutation status of R700R, The gene SIRT1 has a mutation status of S535S, The gene TET1 has a mutation status of V1235L, The gene CFAP70 has a mutation status of N1118S, The gene SFTPA1 has a mutation status of P77L, The gene DNTT has a mutation status of T169A, The gene PIK3AP1 has a mutation status of D517D, The gene RRP12 has a mutation status of D616N, The gene SEMA4G has a mutation status of R521Q, The gene TAF5 has a mutation status of R663R, The gene SORCS1 has a mutation status of S57fs, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C843C, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of A1557T, The gene MUC5AC has a mutation status of T3668P, The gene ART1 has a mutation status of H144D, The gene RHOG has a mutation status of R66C, The gene CYB5R2 has a mutation status of I153T, The gene CAPRIN1 has a mutation status of *710*, The gene OR9G1 has a mutation status of I196F, The gene GLYAT has a mutation status of K81E, The gene CCDC86 has a mutation status of P118Q, The gene SPTBN2 has a mutation status of A1641V, The gene C11orf24 has a mutation status of H73R, The gene SHANK2 has a mutation status of E1283fs, The gene KCTD21 has a mutation status of E199del, The gene DYNC2H1 has a mutation status of F948fs, The gene APOA5 has a mutation status of S212R, The gene CD3G has a mutation status of S148L, The gene OR10G9 has a mutation status of T13T, The gene CDON has a mutation status of S1225N, The gene PZP has a mutation status of N1430N, The gene TAS2R9 has a mutation status of K110Q, The gene TMDD1 has a mutation status of L166P, The gene OR10P1 has a mutation status of I289V, The gene IKZF4 has a mutation status of T398N, The gene TAFA2 has a mutation status of V85G, The gene LGR5 has a mutation status of P154A, The gene LGR5 has a mutation status of L335S, The gene ZFC3H1 has a mutation status of A1913G, The gene PTPRQ has a mutation status of V537A, The gene PAH has a mutation status of I60T, The gene HCFC2 has a mutation status of G496S, The gene TCHP has a mutation status of E459del, The gene IQCD has a mutation status of E341del, The gene ACADS has a mutation status of A195A, The gene DNAH10 has a mutation status of E523fs, The gene NCOR2 has a mutation status of S168S, The gene EP400 has a mutation status of R1401Q, The gene MRPL52 has a mutation status of S49*, The gene JPH4 has a mutation status of V68M, The gene JPH4 has a mutation status of E38E, The gene FOXG1 has a mutation status of T87M, The gene DPF3 has a mutation status of E162*, The gene ACOT2 has a mutation status of T185V, The gene PRIMA1 has a mutation status of V7fs, The gene CLMN has a mutation status of V60I, The gene TECPR2 has a mutation status of L393fs, The gene CDC42BPB has a mutation status of R570Q, The gene GOLGA6L2 has a mutation status of C715Y, The gene MAGEL2 has a mutation status of VHPPPPGTPM180del, The gene GOLGA6L7 has a mutation status of R251R, The gene RYR3 has a mutation status of E2693Q, The gene SLC12A6 has a mutation status of V555M, The gene THBS1 has a mutation status of P622Q, The gene MGA has a mutation status of Q2151H, The gene TTBK2 has a mutation status of R164W, The gene UBR1 has a mutation status of S1178N, The gene TP53BP1 has a mutation status of L1551L, The gene ANKDD1A has a mutation status of L516L, The gene SLC24A1 has a mutation status of P631P, The gene DENND4A has a mutation status of D1191A, The gene RCN2 has a mutation status of E209del, The gene CFAP161 has a mutation status of C222C, The gene TMC3 has a mutation status of S763A, The gene ADAMTSL3 has a mutation status of L476M, The gene ASB7 has a mutation status of L146V, The gene NTN3 has a mutation status of R566W, The gene OR2C1 has a mutation status of R54W, The gene USP7 has a mutation status of Q430K, The gene AC099489.1 has a mutation status of R828W, The gene RRN3 has a mutation status of R470R, The gene PDILT has a mutation status of V205A, The gene ITFG1 has a mutation status of S206F, The gene TEPP has a mutation status of H42Y, The gene ZNF319 has a mutation status of E511K, The gene PLEKHG4 has a mutation status of A502S, The gene AC026464.3 has a mutation status of I150I, The gene SF3B3 has a mutation status of I642I, The gene ATP2C2 has a mutation status of I844del, The gene KLHL36 has a mutation status of D209N, The gene PIEZO1 has a mutation status of V590M, The gene DPEP1 has a mutation status of M1T, The gene VPS9D1 has a mutation status of A310T, The gene TP53 has a mutation status of P152fs, The gene KDM6B has a mutation status of L702L, The gene MYH1 has a mutation status of K1621K, The gene MYH1 has a mutation status of L167M, The gene TMEM238L has a mutation status of A52G, The gene ABHD15 has a mutation status of E373E, The gene CNTNAP1 has a mutation status of F598V, The gene LRRC37A2 has a mutation status of R1161R, The gene KCNH6 has a mutation status of R447C, The gene PRKAR1A has a mutation status of D227G, The gene GPR142 has a mutation status of P263P, The gene CASKIN2 has a mutation status of A782A, The gene SEC14L1 has a mutation status of I613I, The gene FAAP100 has a mutation status of R59G, The gene ALYREF has a mutation status of A9A, The gene AQP4 has a mutation status of M224T, The gene SLC39A6 has a mutation status of Q571Q, The gene DCC has a mutation status of T116P, The gene RAX has a mutation status of K172K, The gene MUC16 has a mutation status of S10497S, The gene HSH2D has a mutation status of P211L, The gene MED26 has a mutation status of G236V, The gene B3GNT3 has a mutation status of V257V, The gene ARRDC2 has a mutation status of A14A, The gene C19orf12 has a mutation status of G53R, The gene ZNF599 has a mutation status of F572V, The gene WDR62 has a mutation status of N182N, The gene SIPA1L3 has a mutation status of G542R, The gene MAP4K1 has a mutation status of T204T, The gene MAP3K10 has a mutation status of P193A, The gene CYP2F1 has a mutation status of P368P, The gene CIC has a mutation status of P153T, The gene PHLDB3 has a mutation status of G402R, The gene CLASRP has a mutation status of R322S, The gene MYPOP has a mutation status of R274Q, The gene PRR12 has a mutation status of N1146T, The gene TSKS has a mutation status of A2V, The gene SPACA6 has a mutation status of V172I, The gene ZNF28 has a mutation status of T203T, The gene VN1R2 has a mutation status of T351T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRB2 has a mutation status of A468A, The gene KIR3DL3 has a mutation status of R166H, The gene KIR2DL1 has a mutation status of V111L, The gene KIR2DL4 has a mutation status of P17L, The gene ZSCAN5A has a mutation status of V169L, The gene ZNF417 has a mutation status of K537*, The gene SIRPA has a mutation status of I374M, The gene BPIFB2 has a mutation status of I397F, The gene DLGAP4 has a mutation status of Q518H, The gene TGM2 has a mutation status of A459A, The gene TTPAL has a mutation status of L125V, The gene TP53TG5 has a mutation status of S83F, The gene SULF2 has a mutation status of H245H, The gene HELZ2 has a mutation status of F255F, The gene C20orf204 has a mutation status of P26L, The gene GABPA has a mutation status of L247L, The gene KRTAP19-5 has a mutation status of S57G, The gene UBE2G2 has a mutation status of Y103Y, The gene HIRA has a mutation status of L355F, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ATXN10 has a mutation status of I350L, The gene PKDREJ has a mutation status of S1748C, The gene ARSH has a mutation status of L133V, The gene WAS has a mutation status of H180N, The gene MTMR8 has a mutation status of W407C, The gene RLIM has a mutation status of Q335Q, The gene NEXMIF has a mutation status of W258C, The gene ATRX has a mutation status of 1841_1842insHSL, The gene PAK3 has a mutation status of C371G, The gene RNF113A has a mutation status of V193L, The gene IGSF1 has a mutation status of D475D, The gene GPC3 has a mutation status of G309G, The gene CCDC160 has a mutation status of G276R, The gene PNMA6E has a mutation status of R460H, The gene IRAK1 has a mutation status of T152S, The gene TKTL1 has a mutation status of G296S, The gene FAM50A has a mutation status of A8A, The gene MT-ND2 has a mutation status of A283A, The gene MT-ND5 has a mutation status of Y174Y, The gene MT-ND5 has a mutation status of G541S
SARC
The gene FNDC10 has a mutation status of H225P, The gene MIB2 has a mutation status of R14G, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene ZDHHC18 has a mutation status of I101V, The gene MANEAL has a mutation status of Y228H, The gene CITED4 has a mutation status of L173W, The gene GLIS1 has a mutation status of T6A, The gene NEXN has a mutation status of G29A, The gene PRMT6 has a mutation status of M285L, The gene NRAS has a mutation status of G12D, The gene PPIAL4H has a mutation status of N102I, The gene SEMA6C has a mutation status of D29E, The gene TRIM46 has a mutation status of V486G, The gene KIAA0040 has a mutation status of W81*, The gene LAMC1 has a mutation status of G81V, The gene HMCN1 has a mutation status of P702S, The gene DYRK3 has a mutation status of P520R, The gene C1orf116 has a mutation status of D71A, The gene SERTAD4 has a mutation status of A188T, The gene RPS6KC1 has a mutation status of M1V, The gene LIN9 has a mutation status of E381E, The gene FMN2 has a mutation status of S85S, The gene OR2M7 has a mutation status of P138T, The gene SNX17 has a mutation status of G402G, The gene SPDYA has a mutation status of M305I, The gene DHX57 has a mutation status of D840Y, The gene EPAS1 has a mutation status of D753E, The gene WDPCP has a mutation status of V621M, The gene RAB11FIP5 has a mutation status of T276P, The gene SMYD1 has a mutation status of V114G, The gene PDCL3 has a mutation status of G186S, The gene FOXD4L1 has a mutation status of E308E, The gene MBD5 has a mutation status of I784M, The gene NEB has a mutation status of W2631*, The gene ACVR1 has a mutation status of H320Y, The gene PRKRA has a mutation status of T204fs, The gene TTN has a mutation status of I32793T, The gene PMS1 has a mutation status of A755S, The gene NEMP2 has a mutation status of E25K, The gene KCTD18 has a mutation status of V227G, The gene SPAG16 has a mutation status of L243L, The gene ALPI has a mutation status of G62W, The gene UGT1A7 has a mutation status of N129R, The gene STK25 has a mutation status of D254A, The gene JAGN1 has a mutation status of L45V, The gene FGD5 has a mutation status of S458S, The gene NGLY1 has a mutation status of T43A, The gene PTH1R has a mutation status of S473F, The gene BSN has a mutation status of G2134R, The gene NEK4 has a mutation status of L79L, The gene FRMD4B has a mutation status of R719G, The gene SLC9C1 has a mutation status of L561V, The gene ZNF148 has a mutation status of D300N, The gene GAK has a mutation status of L482P, The gene SULT1E1 has a mutation status of E156G, The gene PLRG1 has a mutation status of H329H, The gene NPY5R has a mutation status of H178R, The gene SEMA5A has a mutation status of L148L, The gene OSMR has a mutation status of L643L, The gene OSMR has a mutation status of W645R, The gene PTGER4 has a mutation status of A463G, The gene ERCC8 has a mutation status of V161I, The gene KCNN2 has a mutation status of Q40H, The gene KCNN2 has a mutation status of I47V, The gene MEGF10 has a mutation status of C234C, The gene TAF7 has a mutation status of E221K, The gene ARHGAP26 has a mutation status of I40L, The gene HTR4 has a mutation status of I303F, The gene SLIT3 has a mutation status of I301V, The gene F12 has a mutation status of Y151H, The gene VARS1 has a mutation status of H463H, The gene HLA-DRB5 has a mutation status of Q220W, The gene DAXX has a mutation status of R182H, The gene ARMC12 has a mutation status of N102S, The gene STK38 has a mutation status of Q107*, The gene DNAH8 has a mutation status of K3553Q, The gene TREM1 has a mutation status of S74S, The gene TPBG has a mutation status of V105L, The gene AFDN has a mutation status of Q592P, The gene FOXK1 has a mutation status of T681P, The gene FOXK1 has a mutation status of T683P, The gene RADIL has a mutation status of L609L, The gene MIOS has a mutation status of D439V, The gene TAX1BP1 has a mutation status of S467A, The gene STX1A has a mutation status of E7K, The gene TRRAP has a mutation status of L1682L, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T452T, The gene MUC3A has a mutation status of S834T, The gene MUC17 has a mutation status of V1697A, The gene SPDYE6 has a mutation status of H337R, The gene PAX4 has a mutation status of R105C, The gene SND1 has a mutation status of R423S, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene HIPK2 has a mutation status of R497Q, The gene EZH2 has a mutation status of H279Y, The gene PDIA4 has a mutation status of V530M, The gene PAXIP1 has a mutation status of D774G, The gene RBM33 has a mutation status of Q600H, The gene CSMD1 has a mutation status of Y2428F, The gene SLC35G5 has a mutation status of S17S, The gene INTS9 has a mutation status of T88M, The gene KCNU1 has a mutation status of E1007A, The gene PRKDC has a mutation status of Y3114F, The gene SDR16C5 has a mutation status of I254T, The gene ZFHX4 has a mutation status of S1241L, The gene UBR5 has a mutation status of P634P, The gene NUDCD1 has a mutation status of P31A, The gene SLC39A4 has a mutation status of R251W, The gene INSL6 has a mutation status of R90W, The gene NPR2 has a mutation status of Q212K, The gene HRCT1 has a mutation status of H104P, The gene COL15A1 has a mutation status of P666L, The gene FRRS1L has a mutation status of R51A, The gene PDCL has a mutation status of T3T, The gene ENDOG has a mutation status of G275V, The gene BRD3 has a mutation status of S263S, The gene NACC2 has a mutation status of AA155del, The gene NOTCH1 has a mutation status of Q2459*, The gene PITRM1 has a mutation status of S934C, The gene NUDT13 has a mutation status of A275A, The gene TM9SF3 has a mutation status of S345S, The gene FBXL15 has a mutation status of N293T, The gene SORCS1 has a mutation status of Y273C, The gene PWWP2B has a mutation status of S436S, The gene CHID1 has a mutation status of A219S, The gene OR51I2 has a mutation status of A36T, The gene OR52L1 has a mutation status of V321M, The gene RBMXL2 has a mutation status of T111P, The gene ASCL3 has a mutation status of A137S, The gene DKK3 has a mutation status of A27T, The gene BBOX1 has a mutation status of C3F, The gene WT1 has a mutation status of P17P, The gene OR8U1 has a mutation status of N42N, The gene OR9G1 has a mutation status of T62V, The gene PRPF19 has a mutation status of A482T, The gene EEF1G has a mutation status of L303L, The gene PCNX3 has a mutation status of P600S, The gene GAL3ST3 has a mutation status of L23P, The gene LRP5 has a mutation status of T267N, The gene KLHL35 has a mutation status of G353S, The gene FAT3 has a mutation status of A4136P, The gene CNTN5 has a mutation status of P753P, The gene DYNC2H1 has a mutation status of R3326C, The gene DRD2 has a mutation status of R275R, The gene TNFRSF1A has a mutation status of N336T, The gene SLCO1B1 has a mutation status of G71R, The gene RECQL has a mutation status of E71K, The gene BHLHE41 has a mutation status of Y377S, The gene PTHLH has a mutation status of A19T, The gene SYT10 has a mutation status of I367I, The gene PRPH has a mutation status of G11A, The gene NR4A1 has a mutation status of V524G, The gene GDF11 has a mutation status of V43G, The gene ALX1 has a mutation status of A294S, The gene PLEKHG7 has a mutation status of F556L, The gene CCDC38 has a mutation status of L349L, The gene EP400 has a mutation status of N33P, The gene EP400 has a mutation status of P581M, The gene MTMR6 has a mutation status of L49L, The gene HSPH1 has a mutation status of L94L, The gene STARD13 has a mutation status of P598P, The gene RCBTB2 has a mutation status of G171E, The gene FARP1 has a mutation status of H702P, The gene FARP1 has a mutation status of H703P, The gene METTL21C has a mutation status of A89V, The gene UPF3A has a mutation status of S48L, The gene TEP1 has a mutation status of R1499C, The gene DHRS4 has a mutation status of T274P, The gene GZMH has a mutation status of R114H, The gene FOXG1 has a mutation status of S441S, The gene DAAM1 has a mutation status of K144N, The gene ASB2 has a mutation status of A278G, The gene KIF26A has a mutation status of H323P, The gene C14orf180 has a mutation status of H80R, The gene AHNAK2 has a mutation status of F151L, The gene LINC02203 has a mutation status of I259M, The gene MAGEL2 has a mutation status of P477P, The gene TLN2 has a mutation status of E2410V, The gene SLC24A1 has a mutation status of S274R, The gene KIF7 has a mutation status of V447I, The gene CCDC154 has a mutation status of V369M, The gene PKD1 has a mutation status of S3720A, The gene THOC6 has a mutation status of G158W, The gene VASN has a mutation status of V566I, The gene UBALD1 has a mutation status of H136P, The gene UQCRC2 has a mutation status of S215S, The gene APOBR has a mutation status of E618R, The gene ZNF48 has a mutation status of P173A, The gene TANGO6 has a mutation status of L873I, The gene GLG1 has a mutation status of G95G, The gene BCAR1 has a mutation status of A350S, The gene CDH13 has a mutation status of N519I, The gene SLC38A8 has a mutation status of L301F, The gene TAF1C has a mutation status of T657I, The gene FBXO31 has a mutation status of V129M, The gene CDT1 has a mutation status of V337A, The gene ANKRD11 has a mutation status of S1271W, The gene NXN has a mutation status of V294G, The gene INPP5K has a mutation status of G8G, The gene TRPV3 has a mutation status of V537V, The gene SPNS2 has a mutation status of G515G, The gene ENO3 has a mutation status of A171T, The gene PITPNM3 has a mutation status of D438A, The gene TEKT1 has a mutation status of F220L, The gene TP53 has a mutation status of T125T, The gene AURKB has a mutation status of P82P, The gene USP43 has a mutation status of G739R, The gene MYH13 has a mutation status of E219K, The gene SHISA6 has a mutation status of Q76E, The gene NT5M has a mutation status of T195P, The gene VTN has a mutation status of V426L, The gene CCL4L2 has a mutation status of P67R, The gene GPR179 has a mutation status of Y324H, The gene WIPF2 has a mutation status of E352D, The gene KRTAP4-1 has a mutation status of R85R, The gene BRIP1 has a mutation status of R762P, The gene KCNH6 has a mutation status of R517R, The gene LLGL2 has a mutation status of A307D, The gene RBFOX3 has a mutation status of R223R, The gene FOXK2 has a mutation status of GGGGS26del, The gene ALPK2 has a mutation status of I743N, The gene RNF152 has a mutation status of R196H, The gene ATP9B has a mutation status of E683Q, The gene DPP9 has a mutation status of Y835S, The gene SNAPC2 has a mutation status of L247L, The gene MUC16 has a mutation status of P12746L, The gene PKN1 has a mutation status of I52N, The gene AKAP8L has a mutation status of D303H, The gene MAST3 has a mutation status of H840P, The gene ATP13A1 has a mutation status of Q1061Q, The gene ZNF536 has a mutation status of T1191T, The gene WDR87 has a mutation status of EEEEER2264del, The gene CIC has a mutation status of A1665A, The gene PSG1 has a mutation status of P332Q, The gene PSG2 has a mutation status of L108L, The gene CKM has a mutation status of T313P, The gene RSPH6A has a mutation status of T609P, The gene RSPH6A has a mutation status of A605A, The gene GRWD1 has a mutation status of V177G, The gene PRRG2 has a mutation status of L175P, The gene PNKP has a mutation status of G18G, The gene SHANK1 has a mutation status of P1141P, The gene HAS1 has a mutation status of Q576H, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of W205Q, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene SIRPA has a mutation status of L44S, The gene KIF16B has a mutation status of I35I, The gene FOXA2 has a mutation status of G123G, The gene FAM83C has a mutation status of V23G, The gene LPIN3 has a mutation status of G305G, The gene NEURL2 has a mutation status of D89A, The gene NEURL2 has a mutation status of T86P, The gene ZNF831 has a mutation status of E5D, The gene LAMA5 has a mutation status of K312Q, The gene KCNQ2 has a mutation status of T847P, The gene ADAMTS1 has a mutation status of A68V, The gene ATP6V1E1 has a mutation status of T159N, The gene GSTT4 has a mutation status of Q197R, The gene HSCB has a mutation status of V12G, The gene MPST has a mutation status of P160R, The gene NOL12 has a mutation status of P155S, The gene MEI1 has a mutation status of T40P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TCF20 has a mutation status of G913D, The gene CELSR1 has a mutation status of M2455I, The gene PLXNB2 has a mutation status of T636P, The gene CHIC1 has a mutation status of L156L, The gene CSTF2 has a mutation status of A492A, The gene SERPINA7 has a mutation status of V199D, The gene TFDP3 has a mutation status of V57V, The gene GPC4 has a mutation status of L6F, The gene VGLL1 has a mutation status of A137A, The gene MT-ND1 has a mutation status of Q47Q, The gene MT-ND1 has a mutation status of Y228Y, The gene MT-CO1 has a mutation status of M277M, The gene MT-CO2 has a mutation status of G222G, The gene MT-ATP6 has a mutation status of L30F, The gene MT-CO3 has a mutation status of V247V, The gene MT-ND3 has a mutation status of I60I, The gene MT-ND4 has a mutation status of C52C, The gene MT-ND5 has a mutation status of M55M, The gene MT-ND5 has a mutation status of I356I, The gene MT-ND5 has a mutation status of I482V
DLBC
The gene SCNN1D has a mutation status of L363L, The gene CFAP74 has a mutation status of R835G, The gene GPR153 has a mutation status of C17Y, The gene CASZ1 has a mutation status of V403V, The gene MASP2 has a mutation status of Y401C, The gene HSPG2 has a mutation status of G2973D, The gene HIVEP3 has a mutation status of K79R, The gene B4GALT2 has a mutation status of Q233H, The gene SLC6A9 has a mutation status of W131*, The gene CYP4A11 has a mutation status of N234K, The gene C1orf52 has a mutation status of K145K, The gene GBP6 has a mutation status of A610V, The gene MTF2 has a mutation status of T442T, The gene AHCYL1 has a mutation status of P498L, The gene FLG has a mutation status of H2009N, The gene FAM189B has a mutation status of R529H, The gene LMNA has a mutation status of G608G, The gene NAXE has a mutation status of I217I, The gene CD1C has a mutation status of V173I, The gene ATP1A4 has a mutation status of N137N, The gene POU2F1 has a mutation status of E25fs, The gene ADCY10 has a mutation status of R1207W, The gene SLC19A2 has a mutation status of R96C, The gene RC3H1 has a mutation status of I909S, The gene TNN has a mutation status of R140H, The gene TNR has a mutation status of A460T, The gene HMCN1 has a mutation status of L3855F, The gene NR5A2 has a mutation status of G24R, The gene SLC45A3 has a mutation status of V346G, The gene PIGR has a mutation status of R192H, The gene LBR has a mutation status of Y321Y, The gene URB2 has a mutation status of L1478L, The gene SIPA1L2 has a mutation status of T1577T, The gene PCNX2 has a mutation status of R1450Q, The gene OR2L2 has a mutation status of Q6E, The gene PXDN has a mutation status of A555A, The gene ASAP2 has a mutation status of K905K, The gene NBAS has a mutation status of V2128L, The gene OSR1 has a mutation status of R136H, The gene TCF7L1 has a mutation status of N71N, The gene NEURL3 has a mutation status of Y221*, The gene MERTK has a mutation status of T795A, The gene STEAP3 has a mutation status of A182V, The gene SCN2A has a mutation status of K1260Q, The gene FAM171B has a mutation status of T482I, The gene ANKAR has a mutation status of L1292L, The gene PMS1 has a mutation status of P302fs, The gene KCTD18 has a mutation status of V227G, The gene ORC2 has a mutation status of H176Y, The gene RAPH1 has a mutation status of P618L, The gene WNT6 has a mutation status of A116P, The gene SLC4A3 has a mutation status of I1193I, The gene COL4A4 has a mutation status of L1381F, The gene SLC16A14 has a mutation status of N383N, The gene INPP5D has a mutation status of P1134L, The gene METTL6 has a mutation status of R143C, The gene CCR4 has a mutation status of I83V, The gene DCLK3 has a mutation status of G96R, The gene MLH1 has a mutation status of G276G, The gene HHATL has a mutation status of R248Q, The gene ZNF654 has a mutation status of S646C, The gene TFG has a mutation status of A274G, The gene ZNF80 has a mutation status of Q20*, The gene PIK3CB has a mutation status of A515T, The gene ATR has a mutation status of D836E, The gene TNIK has a mutation status of H305H, The gene LRCH3 has a mutation status of A594A, The gene NWD2 has a mutation status of P697S, The gene GABRG1 has a mutation status of R169*, The gene GABRB1 has a mutation status of D164A, The gene USO1 has a mutation status of E638del, The gene C4orf54 has a mutation status of T72P, The gene MYO10 has a mutation status of T1882T, The gene RGS7BP has a mutation status of S38S, The gene ZBED3 has a mutation status of L155A, The gene MCC has a mutation status of V223M, The gene RAD50 has a mutation status of N598I, The gene TRPC7 has a mutation status of R318*, The gene PSD2 has a mutation status of Q433E, The gene PCDHB11 has a mutation status of G730D, The gene PCDHB15 has a mutation status of R65W, The gene DELE1 has a mutation status of A69D, The gene OR2V1 has a mutation status of A255T, The gene DCDC2 has a mutation status of R452T, The gene H4C5 has a mutation status of L23L, The gene ZBED9 has a mutation status of T415T, The gene HLA-A has a mutation status of G314C, The gene MUCL3 has a mutation status of S224S, The gene TNXB has a mutation status of R4067R, The gene HLA-DRB5 has a mutation status of T262R, The gene ITPR3 has a mutation status of R1857C, The gene UBR2 has a mutation status of N997I, The gene RRP36 has a mutation status of E163D, The gene ABCC10 has a mutation status of L34P, The gene PNISR has a mutation status of I732M, The gene TRAF3IP2 has a mutation status of P336P, The gene PHACTR2 has a mutation status of S278N, The gene AKAP12 has a mutation status of F810C, The gene SYNJ2 has a mutation status of T1067T, The gene MAP3K4 has a mutation status of 1403_1404insVSRYFGVELHR, The gene SFT2D1 has a mutation status of W36*, The gene MMD2 has a mutation status of V22V, The gene TNRC18 has a mutation status of S1628G, The gene EIF2AK1 has a mutation status of K609Q, The gene HOXA2 has a mutation status of F272V, The gene AOAH has a mutation status of D105D, The gene GPR141 has a mutation status of V43V, The gene GLI3 has a mutation status of S1028I, The gene GTF2IRD1 has a mutation status of T345T, The gene ADAM22 has a mutation status of V104V, The gene LMTK2 has a mutation status of P349P, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of T1234A, The gene MUC3A has a mutation status of S1242N, The gene MUC3A has a mutation status of E1932K, The gene MUC3A has a mutation status of S3095S, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of T3202A, The gene ZNF800 has a mutation status of N271S, The gene MKLN1 has a mutation status of V490L, The gene AKR1B10 has a mutation status of L229L, The gene KIAA1549 has a mutation status of A768S, The gene TTC26 has a mutation status of V521V, The gene PRSS1 has a mutation status of N77N, The gene EPHA1 has a mutation status of T230A, The gene KMT2C has a mutation status of R3398Q, The gene MCPH1 has a mutation status of C222R, The gene ST18 has a mutation status of T647A, The gene ASPH has a mutation status of V740M, The gene UBR5 has a mutation status of C2761fs, The gene FER1L6 has a mutation status of K427M, The gene SCRIB has a mutation status of R1067L, The gene SLC39A4 has a mutation status of R251W, The gene DMRT2 has a mutation status of V440A, The gene IFNE has a mutation status of G100V, The gene ZBTB5 has a mutation status of M140K, The gene PCSK5 has a mutation status of D1811N, The gene PSAT1 has a mutation status of K110Q, The gene TRIM14 has a mutation status of L71L, The gene ERP44 has a mutation status of H357H, The gene COL27A1 has a mutation status of L842L, The gene LHX6 has a mutation status of Y149F, The gene OR1L6 has a mutation status of S149S, The gene DENND1A has a mutation status of P767L, The gene DBH has a mutation status of C283C, The gene PITRM1 has a mutation status of G392S, The gene MALRD1 has a mutation status of L708V, The gene LYZL2 has a mutation status of A109V, The gene ASAH2 has a mutation status of A346S, The gene NEUROG3 has a mutation status of F127F, The gene PTEN has a mutation status of I101T, The gene MUC5AC has a mutation status of A1431A, The gene LSP1 has a mutation status of D71D, The gene CARS1 has a mutation status of K533fs, The gene SCUBE2 has a mutation status of T451T, The gene C11orf58 has a mutation status of A155S, The gene OR4A16 has a mutation status of W44*, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene AP000781.2 has a mutation status of T222M, The gene GPR137 has a mutation status of T364P, The gene CARNS1 has a mutation status of G55V, The gene TCIRG1 has a mutation status of P511T, The gene GDPD5 has a mutation status of A538V, The gene C11orf97 has a mutation status of Q48Q, The gene KMT2A has a mutation status of M2602V, The gene PHLDB1 has a mutation status of R1184Q, The gene CCDC84 has a mutation status of V41G, The gene TBCEL has a mutation status of N351N, The gene GRAMD1B has a mutation status of R861S, The gene CACNA1C has a mutation status of S1498S, The gene FOXM1 has a mutation status of L697F, The gene CD163L1 has a mutation status of S765S, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of H93fs, The gene TAS2R45 has a mutation status of I91fs, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene OVCH1 has a mutation status of Y481Y, The gene GPR84 has a mutation status of F76L, The gene HECTD4 has a mutation status of P4004P, The gene PXN has a mutation status of S186R, The gene P2RX7 has a mutation status of I568N, The gene RIMBP2 has a mutation status of S721S, The gene RNF17 has a mutation status of T179M, The gene RB1 has a mutation status of R320*, The gene OR4K13 has a mutation status of C127Y, The gene HAUS4 has a mutation status of R363H, The gene CDH24 has a mutation status of T657T, The gene CARMIL3 has a mutation status of R1053Q, The gene TTC6 has a mutation status of N1461D, The gene PTGER2 has a mutation status of I306V, The gene DLGAP5 has a mutation status of P727H, The gene ACTR10 has a mutation status of E12G, The gene CCDC175 has a mutation status of R248H, The gene PCNX4 has a mutation status of R371*, The gene TRMT5 has a mutation status of R8M, The gene SYT16 has a mutation status of T77M, The gene SERPINA9 has a mutation status of R377R, The gene HHIPL1 has a mutation status of R687L, The gene CEP170B has a mutation status of S1513S, The gene GPR132 has a mutation status of R142Q, The gene GOLGA6L22 has a mutation status of I413T, The gene LPCAT4 has a mutation status of A336A, The gene SPINT1 has a mutation status of E177D, The gene TYRO3 has a mutation status of E509fs, The gene MGA has a mutation status of L664F, The gene FRMD5 has a mutation status of V215M, The gene ANKDD1A has a mutation status of L516L, The gene CYP1A1 has a mutation status of E256K, The gene GOLGA6L10 has a mutation status of L399P, The gene GOLGA6L10 has a mutation status of R385R, The gene FSD2 has a mutation status of N693N, The gene AC099489.1 has a mutation status of P524L, The gene AC099489.1 has a mutation status of A310D, The gene TNRC6A has a mutation status of T287A, The gene CD19 has a mutation status of L246L, The gene CNTNAP4 has a mutation status of A815A, The gene GSE1 has a mutation status of V1061I, The gene TP53 has a mutation status of Y236C, The gene CHD3 has a mutation status of H65Q, The gene USP43 has a mutation status of G739R, The gene MPRIP has a mutation status of S251R, The gene FLII has a mutation status of A553G, The gene FLII has a mutation status of E552G, The gene SARM1 has a mutation status of A78A, The gene SLFN12L has a mutation status of Y519Y, The gene ACACA has a mutation status of D1757E, The gene TANC2 has a mutation status of D757E, The gene SCN4A has a mutation status of M1753I, The gene HELZ has a mutation status of A1504A, The gene UNC13D has a mutation status of D206G, The gene LPIN2 has a mutation status of Y495Y, The gene NPC1 has a mutation status of P1007A, The gene KLHL14 has a mutation status of D226G, The gene LOXHD1 has a mutation status of V800E, The gene APC2 has a mutation status of A1828D, The gene ZNF763 has a mutation status of V212F, The gene OR7A5 has a mutation status of H269L, The gene NOTCH3 has a mutation status of L1547V, The gene OR10H3 has a mutation status of C142F, The gene SYNE4 has a mutation status of R321Q, The gene SPRED3 has a mutation status of L252L, The gene SIRT2 has a mutation status of R163H, The gene EML2 has a mutation status of I108N, The gene NOP53 has a mutation status of R36R, The gene CRX has a mutation status of A121A, The gene TRPM4 has a mutation status of L1075P, The gene ZNF432 has a mutation status of E83Q, The gene LILRB3 has a mutation status of Q270R, The gene LENG9 has a mutation status of C32*, The gene EPS8L1 has a mutation status of A126G, The gene UBE2S has a mutation status of L15L, The gene SIRPA has a mutation status of L44S, The gene ATRN has a mutation status of A375A, The gene ANKEF1 has a mutation status of P651L, The gene ANKEF1 has a mutation status of S682*, The gene OVOL2 has a mutation status of T112T, The gene TGIF2-RAB5IF has a mutation status of S4S, The gene TGM2 has a mutation status of P345L, The gene RALGAPB has a mutation status of L866L, The gene SPO11 has a mutation status of R145G, The gene NPEPL1 has a mutation status of L79Q, The gene GNAS has a mutation status of H353P, The gene TUBB1 has a mutation status of D128D, The gene CHRNA4 has a mutation status of T545T, The gene ZNF512B has a mutation status of R681C, The gene NPBWR2 has a mutation status of V123I, The gene BRWD1 has a mutation status of R1441Q, The gene RIPK4 has a mutation status of T601M, The gene KLHL22 has a mutation status of V147E, The gene GSTT4 has a mutation status of Q197R, The gene SRRD has a mutation status of E304*, The gene ASCC2 has a mutation status of E544fs, The gene TNFRSF13C has a mutation status of G64V, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PANX2 has a mutation status of P595P, The gene GTPBP6 has a mutation status of M181L, The gene REPS2 has a mutation status of P656L, The gene MAP3K15 has a mutation status of A830P, The gene SH3KBP1 has a mutation status of V395I, The gene CFAP47 has a mutation status of Q2422Q, The gene ZNF41 has a mutation status of L706F, The gene MED12 has a mutation status of H1822Q, The gene MED12 has a mutation status of R1871*, The gene AMOT has a mutation status of T300A, The gene MAGEC3 has a mutation status of M270K, The gene MT-CO3 has a mutation status of H231H, The gene MT-ND3 has a mutation status of G29S, The gene MT-ND5 has a mutation status of S99S, The gene MT-ND6 has a mutation status of G131G
GBMLGG
The gene PERM1 has a mutation status of T274T, The gene CCDC27 has a mutation status of Q479K, The gene CEP104 has a mutation status of G18V, The gene VPS13D has a mutation status of D3451G, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF20 has a mutation status of T330N, The gene HSPG2 has a mutation status of T3909P, The gene HSPG2 has a mutation status of Y3908P, The gene MYOM3 has a mutation status of Q84P, The gene EXTL1 has a mutation status of R31H, The gene CRYBG2 has a mutation status of N564T, The gene EPB41 has a mutation status of M395V, The gene CSMD2 has a mutation status of H226R, The gene HIVEP3 has a mutation status of T437P, The gene SZT2 has a mutation status of A2337A, The gene PRKAA2 has a mutation status of A191V, The gene C8B has a mutation status of L358L, The gene TM2D1 has a mutation status of L51F, The gene CACHD1 has a mutation status of Y408Y, The gene FPGT-TNNI3K has a mutation status of V818A, The gene AMPD2 has a mutation status of R33fs, The gene AMPD2 has a mutation status of G34G, The gene NGF has a mutation status of *242C, The gene TTF2 has a mutation status of R584*, The gene ZNF697 has a mutation status of R448H, The gene SRGAP2C has a mutation status of N158N, The gene FAM189B has a mutation status of D342Y, The gene YY1AP1 has a mutation status of A5G, The gene MEX3A has a mutation status of G64G, The gene INSRR has a mutation status of V596I, The gene KCNJ10 has a mutation status of E177G, The gene ADCY10 has a mutation status of D37Y, The gene IER5 has a mutation status of P72P, The gene SWT1 has a mutation status of T620I, The gene RO60 has a mutation status of S79S, The gene LHX9 has a mutation status of R132S, The gene ZNF281 has a mutation status of T64P, The gene MYBPH has a mutation status of G101G, The gene CHIT1 has a mutation status of A183V, The gene LRRN2 has a mutation status of T585P, The gene PACC1 has a mutation status of F83F, The gene LYPLAL1 has a mutation status of T216S, The gene SUSD4 has a mutation status of Y394D, The gene OBSCN has a mutation status of D1110G, The gene ARV1 has a mutation status of R6G, The gene GGPS1 has a mutation status of S145N, The gene OR2T4 has a mutation status of V109L, The gene GDF7 has a mutation status of G336G, The gene GDF7 has a mutation status of G338G, The gene EIF2B4 has a mutation status of R88P, The gene C2orf16 has a mutation status of E3942A, The gene WDR43 has a mutation status of D609G, The gene HNRNPLL has a mutation status of Y186N, The gene THUMPD2 has a mutation status of E157del, The gene RTN4 has a mutation status of V745V, The gene CLHC1 has a mutation status of E292fs, The gene ZNF638 has a mutation status of Q1057Q, The gene REG1A has a mutation status of V73V, The gene POLR1A has a mutation status of T779P, The gene PTCD3 has a mutation status of I396T, The gene KDM3A has a mutation status of D187E, The gene RNF103 has a mutation status of R663W, The gene AFF3 has a mutation status of R629Q, The gene PSD4 has a mutation status of T819P, The gene ORC4 has a mutation status of D301G, The gene HOXD13 has a mutation status of A57G, The gene ZNF385B has a mutation status of K44T, The gene NCKAP1 has a mutation status of T29P, The gene CAVIN2 has a mutation status of V172V, The gene PARD3B has a mutation status of Q637H, The gene CDK5R2 has a mutation status of T127P, The gene RESP18 has a mutation status of G145V, The gene SPEG has a mutation status of P614R, The gene MFF has a mutation status of R255C, The gene SCYGR4 has a mutation status of M1V, The gene TRPM8 has a mutation status of E402D, The gene SH3BP4 has a mutation status of K644R, The gene OTOS has a mutation status of Q87E, The gene CAPN10 has a mutation status of V432G, The gene CAPN10 has a mutation status of V437G, The gene TRNT1 has a mutation status of I155V, The gene CRBN has a mutation status of H17P, The gene RAF1 has a mutation status of A42I, The gene TMEM40 has a mutation status of R209C, The gene RBSN has a mutation status of T214P, The gene CLASP2 has a mutation status of L915F, The gene TRANK1 has a mutation status of M2744I, The gene DLEC1 has a mutation status of V1308G, The gene SCN5A has a mutation status of A1147T, The gene KLHL40 has a mutation status of R48C, The gene GASK1A has a mutation status of T163K, The gene TOPAZ1 has a mutation status of I1595V, The gene ARIH2OS has a mutation status of A153G, The gene DOCK3 has a mutation status of H1979P, The gene GRM2 has a mutation status of V716G, The gene ITIH4 has a mutation status of P373P, The gene CACNA2D3 has a mutation status of E111G, The gene PCNP has a mutation status of T66S, The gene SLC35A5 has a mutation status of R145H, The gene CCDC80 has a mutation status of G617A, The gene GOLGB1 has a mutation status of C3197F, The gene MED12L has a mutation status of V1018V, The gene MED12L has a mutation status of R2052R, The gene GMPS has a mutation status of S378C, The gene TIPARP has a mutation status of R605S, The gene NAALADL2 has a mutation status of R700R, The gene EIF4G1 has a mutation status of P502P, The gene CLDN16 has a mutation status of L145P, The gene SLBP has a mutation status of H122Q, The gene ABLIM2 has a mutation status of S334S, The gene USP17L10 has a mutation status of K290K, The gene MED28 has a mutation status of P4P, The gene SLC30A9 has a mutation status of W258C, The gene ANKRD17 has a mutation status of G106G, The gene MEPE has a mutation status of A324A, The gene NAP1L5 has a mutation status of A172P, The gene METAP1 has a mutation status of R374*, The gene LRAT has a mutation status of V110V, The gene C4orf45 has a mutation status of T37N, The gene GPM6A has a mutation status of T76A, The gene C4orf47 has a mutation status of S234Y, The gene TLR3 has a mutation status of L159F, The gene SLC9A3 has a mutation status of F437F, The gene TAF11L2 has a mutation status of R93M, The gene LIFR has a mutation status of A985S, The gene F2R has a mutation status of P136P, The gene PJA2 has a mutation status of L471L, The gene PGGT1B has a mutation status of T198T, The gene PKD2L2 has a mutation status of T26K, The gene PSD2 has a mutation status of T652P, The gene PCDHB12 has a mutation status of S543S, The gene LARS1 has a mutation status of D500D, The gene LCP2 has a mutation status of P280S, The gene OR2V2 has a mutation status of L223V, The gene HUS1B has a mutation status of D144G, The gene HLA-F has a mutation status of S113A, The gene HLA-A has a mutation status of K292E, The gene TNXB has a mutation status of H1086P, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DQA1 has a mutation status of E73L, The gene AL669918.1 has a mutation status of G47G, The gene PI16 has a mutation status of S48P, The gene PI16 has a mutation status of P423L, The gene PGC has a mutation status of V6G, The gene MEP1A has a mutation status of P23P, The gene CD109 has a mutation status of I434N, The gene CEP162 has a mutation status of D178D, The gene SOGA3 has a mutation status of P91P, The gene L3MBTL3 has a mutation status of P225S, The gene TULP4 has a mutation status of L400L, The gene IGF2R has a mutation status of S1048*, The gene SLC22A1 has a mutation status of L192I, The gene TMEM184A has a mutation status of V264F, The gene GRIFIN has a mutation status of L132R, The gene FOXK1 has a mutation status of T602P, The gene FOXK1 has a mutation status of T683P, The gene HOXA5 has a mutation status of N120K, The gene CPVL has a mutation status of M133I, The gene TBX20 has a mutation status of V171G, The gene POU6F2 has a mutation status of T705P, The gene SUGCT has a mutation status of K263K, The gene GLI3 has a mutation status of Y858S, The gene POM121L12 has a mutation status of D85A, The gene GALNT17 has a mutation status of F330F, The gene PCLO has a mutation status of S4293C, The gene RUNDC3B has a mutation status of I161V, The gene ZNF804B has a mutation status of V1128V, The gene ZKSCAN5 has a mutation status of S833N, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene MUC17 has a mutation status of A68T, The gene MUC17 has a mutation status of P1361L, The gene MYL10 has a mutation status of V13V, The gene NAMPT has a mutation status of V266I, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PRSS1 has a mutation status of N77N, The gene KRBA1 has a mutation status of E25G, The gene REPIN1 has a mutation status of T76P, The gene AGAP3 has a mutation status of T243T, The gene GINS4 has a mutation status of L173L, The gene KCNB2 has a mutation status of E592K, The gene CSMD3 has a mutation status of R395Q, The gene MTSS1 has a mutation status of E516D, The gene TG has a mutation status of A519A, The gene COL22A1 has a mutation status of A1490V, The gene LY6D has a mutation status of L106F, The gene TIGD5 has a mutation status of W532*, The gene FAM83H has a mutation status of V429G, The gene SCRIB has a mutation status of A1069V, The gene NRBP2 has a mutation status of Q465P, The gene SPATC1 has a mutation status of E20G, The gene FAM205A has a mutation status of Y1314S, The gene TESK1 has a mutation status of V82I, The gene ANKRD18A has a mutation status of L264P, The gene PGM5 has a mutation status of Y70D, The gene WNK2 has a mutation status of H863P, The gene ZNF782 has a mutation status of E531E, The gene TBC1D2 has a mutation status of L471L, The gene PALM2AKAP2 has a mutation status of K46I, The gene ECPAS has a mutation status of T115M, The gene GSN has a mutation status of T598P, The gene CRB2 has a mutation status of H119Q, The gene NUP188 has a mutation status of Y1074S, The gene PPP1R26 has a mutation status of P496L, The gene CCDC187 has a mutation status of A321T, The gene INPP5E has a mutation status of S518A, The gene ABCA2 has a mutation status of L345V, The gene DPP7 has a mutation status of R307L, The gene AKR1C3 has a mutation status of M151V, The gene SLC39A12 has a mutation status of Y140N, The gene FRMPD2 has a mutation status of P226P, The gene AIFM2 has a mutation status of G324D, The gene ADAMTS14 has a mutation status of T26P, The gene ADAMTS14 has a mutation status of A952T, The gene ARHGAP19 has a mutation status of H133H, The gene ARMH3 has a mutation status of F50F, The gene NFKB2 has a mutation status of G634G, The gene NEURL1 has a mutation status of R181C, The gene TACC2 has a mutation status of T18I, The gene DMBT1 has a mutation status of G516G, The gene ADGRA1 has a mutation status of H189P, The gene CDHR5 has a mutation status of A376A, The gene MUC5AC has a mutation status of S3630P, The gene TOLLIP has a mutation status of V33G, The gene CD81 has a mutation status of S177L, The gene OR51A4 has a mutation status of R264C, The gene FAM160A2 has a mutation status of V389I, The gene RBMXL2 has a mutation status of R335L, The gene MICAL2 has a mutation status of V15G, The gene DCDC1 has a mutation status of S125A, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of M155V, The gene OR8U1 has a mutation status of I282L, The gene OR9G1 has a mutation status of T62V, The gene P2RX3 has a mutation status of T202P, The gene CCDC88B has a mutation status of E235D, The gene KAT5 has a mutation status of D164A, The gene ANO1 has a mutation status of N290T, The gene RPS3 has a mutation status of P249P, The gene MAP6 has a mutation status of A42P, The gene B3GNT6 has a mutation status of A172fs, The gene NOX4 has a mutation status of H342P, The gene FAT3 has a mutation status of A4136P, The gene ENDOD1 has a mutation status of V481F, The gene PCSK7 has a mutation status of G702G, The gene NECTIN1 has a mutation status of S363G, The gene APLP2 has a mutation status of G136G, The gene GLB1L3 has a mutation status of F21F, The gene IQSEC3 has a mutation status of A263G, The gene GALNT8 has a mutation status of R161R, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PIK3C2G has a mutation status of N87S, The gene CPNE8 has a mutation status of D526E, The gene H1-7 has a mutation status of S19R, The gene LMBR1L has a mutation status of R333*, The gene AQP2 has a mutation status of S10S, The gene SMAGP has a mutation status of S27F, The gene ACVR1B has a mutation status of P26S, The gene NR4A1 has a mutation status of G544G, The gene HOXC11 has a mutation status of D164A, The gene PMEL has a mutation status of I209T, The gene MYL6B has a mutation status of D53H, The gene MDM1 has a mutation status of S363N, The gene GNPTAB has a mutation status of N524D, The gene APPL2 has a mutation status of I322I, The gene SDS has a mutation status of L320V, The gene ZNF664 has a mutation status of H47Q, The gene ULK1 has a mutation status of L967L, The gene P2RX2 has a mutation status of T135P, The gene SETDB2 has a mutation status of Q174K, The gene SLITRK5 has a mutation status of H791P, The gene FARP1 has a mutation status of H702P, The gene FARP1 has a mutation status of H703P, The gene STK24 has a mutation status of E221K, The gene IRS2 has a mutation status of G206G, The gene NYNRIN has a mutation status of L925L, The gene SYNE2 has a mutation status of Y6444H, The gene PLEKHG3 has a mutation status of S1081L, The gene YLPM1 has a mutation status of Y8*, The gene KCNK10 has a mutation status of A247A, The gene TTC7B has a mutation status of I839T, The gene CCDC88C has a mutation status of S572L, The gene RIN3 has a mutation status of V371A, The gene BTBD7 has a mutation status of G360E, The gene PPP1R13B has a mutation status of T810P, The gene APBA2 has a mutation status of A57V, The gene FMN1 has a mutation status of P726P, The gene JMJD7-PLA2G4B has a mutation status of P778P, The gene AC090517.4 has a mutation status of C249F, The gene CGNL1 has a mutation status of T1041K, The gene CHRNA3 has a mutation status of Y236C, The gene AGBL1 has a mutation status of L941F, The gene FURIN has a mutation status of S685P, The gene PKD1 has a mutation status of Q3955P, The gene TIGD7 has a mutation status of A106T, The gene CLUAP1 has a mutation status of P334P, The gene CORO7 has a mutation status of V582G, The gene LAT has a mutation status of P71P, The gene PRRT2 has a mutation status of P203P, The gene SRCAP has a mutation status of P2426P, The gene BCL7C has a mutation status of G84G, The gene LONP2 has a mutation status of A345S, The gene NUP93 has a mutation status of S592S, The gene CDH16 has a mutation status of G352G, The gene CENPT has a mutation status of H80R, The gene MARVELD3 has a mutation status of A342G, The gene HPR has a mutation status of K157K, The gene DHX38 has a mutation status of Q759K, The gene FA2H has a mutation status of H146P, The gene CHST5 has a mutation status of R15*, The gene DBNDD1 has a mutation status of N101K, The gene ITGAE has a mutation status of L474L, The gene PELP1 has a mutation status of EE902del, The gene PELP1 has a mutation status of G23G, The gene CXCL16 has a mutation status of S107L, The gene NLRP1 has a mutation status of L1218L, The gene AC004706.3 has a mutation status of G775V, The gene TP53 has a mutation status of V147D, The gene MYH10 has a mutation status of G1094D, The gene DNAH9 has a mutation status of G2556R, The gene ZNF18 has a mutation status of Q224K, The gene ATPAF2 has a mutation status of S24R, The gene AKAP10 has a mutation status of S269P, The gene ASIC2 has a mutation status of L128F, The gene TOP2A has a mutation status of S1392*, The gene STAT5A has a mutation status of S746P, The gene VAT1 has a mutation status of D101A, The gene DCAKD has a mutation status of Y202S, The gene PPP1R9B has a mutation status of V704G, The gene RNF43 has a mutation status of V627A, The gene KCNH6 has a mutation status of F700fs, The gene KCNH6 has a mutation status of SFW703del, The gene DDX5 has a mutation status of G136V, The gene CDC42EP4 has a mutation status of S322G, The gene CD300LD has a mutation status of W2G, The gene CCDC40 has a mutation status of R587R, The gene ANKRD12 has a mutation status of R1734T, The gene LAMA3 has a mutation status of D1548G, The gene WDR7 has a mutation status of Y81C, The gene FECH has a mutation status of *424C, The gene FECH has a mutation status of T419P, The gene PHLPP1 has a mutation status of P1692P, The gene ZNF407 has a mutation status of T1697A, The gene CTDP1 has a mutation status of T391P, The gene MFSD12 has a mutation status of V384I, The gene TBXA2R has a mutation status of G56G, The gene STAP2 has a mutation status of T150T, The gene LONP1 has a mutation status of K572K, The gene SLC25A23 has a mutation status of C321C, The gene TNFSF14 has a mutation status of T70P, The gene PNPLA6 has a mutation status of R337R, The gene MUC16 has a mutation status of G5009G, The gene DOCK6 has a mutation status of Q1550R, The gene FBXW9 has a mutation status of T55T, The gene ZSWIM4 has a mutation status of L896L, The gene ADGRL1 has a mutation status of G1322G, The gene BABAM1 has a mutation status of I205I, The gene IQCN has a mutation status of S492S, The gene CRLF1 has a mutation status of T152P, The gene GMIP has a mutation status of A955T, The gene HSPB6 has a mutation status of A151P, The gene ARHGAP33 has a mutation status of S964S, The gene LRFN3 has a mutation status of S237S, The gene WDR62 has a mutation status of G24G, The gene WDR62 has a mutation status of V25G, The gene KCNK6 has a mutation status of V75G, The gene CAPN12 has a mutation status of F367L, The gene LGALS4 has a mutation status of G244S, The gene MAP3K10 has a mutation status of E423G, The gene EXOSC5 has a mutation status of A184A, The gene CLASRP has a mutation status of A358A, The gene EML2 has a mutation status of C747C, The gene QPCTL has a mutation status of R8R, The gene QPCTL has a mutation status of C167S, The gene DMWD has a mutation status of S225L, The gene KPTN has a mutation status of E40G, The gene NOP53 has a mutation status of R36R, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of H203R, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of T333A, The gene ZNF256 has a mutation status of H210Y, The gene DEFB132 has a mutation status of T91T, The gene TGM6 has a mutation status of T539P, The gene ATRN has a mutation status of Y1037C, The gene EFCAB8 has a mutation status of Q194R, The gene SNTA1 has a mutation status of A367P, The gene EDEM2 has a mutation status of L16L, The gene EMILIN3 has a mutation status of S296S, The gene RIMS4 has a mutation status of A41T, The gene ZNF334 has a mutation status of E514*, The gene ZMYND8 has a mutation status of S650S, The gene HRH3 has a mutation status of Y167Y, The gene COL9A3 has a mutation status of V84G, The gene COL20A1 has a mutation status of P213L, The gene KCNQ2 has a mutation status of G850G, The gene KCNQ2 has a mutation status of R691C, The gene RUNX1 has a mutation status of R49S, The gene MORC3 has a mutation status of Q913*, The gene BRWD1 has a mutation status of L1179V, The gene RIPK4 has a mutation status of G31G, The gene SUMO3 has a mutation status of R97C, The gene RTL10 has a mutation status of E286D, The gene PPIL2 has a mutation status of T157P, The gene GSTT4 has a mutation status of Q197R, The gene GGT1 has a mutation status of P169P, The gene KIAA1671 has a mutation status of P818L, The gene TRIOBP has a mutation status of K428R, The gene MICALL1 has a mutation status of S644P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene PACSIN2 has a mutation status of F120L, The gene SBF1 has a mutation status of V1457G, The gene MAPK8IP2 has a mutation status of A544G, The gene NHS has a mutation status of L215P, The gene SSX3 has a mutation status of P145A, The gene ZMYM3 has a mutation status of L85V, The gene CSTF2 has a mutation status of G3G, The gene RTL9 has a mutation status of S615S, The gene TRPC5 has a mutation status of G962G, The gene ZNF280C has a mutation status of S69S, The gene SLC10A3 has a mutation status of S270G, The gene MT-ND4L has a mutation status of E70E, The gene MT-CYB has a mutation status of A330T
OV
The gene SCNN1D has a mutation status of R57Q, The gene CCNL2 has a mutation status of R93P, The gene SKI has a mutation status of P352L, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene RCC2 has a mutation status of G465R, The gene HTR6 has a mutation status of V369V, The gene CLIC4 has a mutation status of D161Y, The gene CATSPER4 has a mutation status of G155S, The gene EVA1B has a mutation status of P141L, The gene TIE1 has a mutation status of E151E, The gene PCSK9 has a mutation status of G117D, The gene DAB1 has a mutation status of G527E, The gene BCAR3 has a mutation status of P74H, The gene KIAA1324 has a mutation status of H339D, The gene CELSR2 has a mutation status of R2015K, The gene NBPF20 has a mutation status of A48A, The gene RPRD2 has a mutation status of P329P, The gene FCRLA has a mutation status of T32M, The gene KIF14 has a mutation status of P220L, The gene CR1 has a mutation status of P1322T, The gene MIA3 has a mutation status of L504F, The gene LBR has a mutation status of A301V, The gene DISC1 has a mutation status of R233G, The gene LYST has a mutation status of A3723T, The gene GREM2 has a mutation status of I30L, The gene MYCN has a mutation status of P44L, The gene C2orf16 has a mutation status of Q1094R, The gene SPDYA has a mutation status of R219Q, The gene TOGARAM2 has a mutation status of P202P, The gene SLC30A6 has a mutation status of P130P, The gene BIRC6 has a mutation status of D60G, The gene CHAC2 has a mutation status of S36R, The gene C2orf81 has a mutation status of T247P, The gene SMYD1 has a mutation status of V114G, The gene FER1L5 has a mutation status of F1070L, The gene HS6ST1 has a mutation status of V26G, The gene FBLN2 has a mutation status of P409S, The gene SLC6A6 has a mutation status of L8L, The gene ZNF197 has a mutation status of N387K, The gene EXOSC7 has a mutation status of F149V, The gene LARS2 has a mutation status of S80L, The gene NBEAL2 has a mutation status of P444P, The gene NBEAL2 has a mutation status of L971L, The gene BSN has a mutation status of S746R, The gene CAMKV has a mutation status of Q195K, The gene DOCK3 has a mutation status of D1966A, The gene DCAF1 has a mutation status of Y480C, The gene ITIH1 has a mutation status of A494T, The gene SIDT1 has a mutation status of R289*, The gene ROPN1B has a mutation status of W36*, The gene C3orf56 has a mutation status of S231S, The gene GATA2 has a mutation status of H460P, The gene IFT122 has a mutation status of A663A, The gene PTX3 has a mutation status of D21G, The gene CHRD has a mutation status of E267K, The gene TMEM175 has a mutation status of H484P, The gene BOD1L1 has a mutation status of G42G, The gene PPARGC1A has a mutation status of T691A, The gene RFC1 has a mutation status of S621C, The gene FAT4 has a mutation status of S173F, The gene FAT4 has a mutation status of Q3460P, The gene ADAMTS16 has a mutation status of V958G, The gene DNAH5 has a mutation status of R3079*, The gene PDZD2 has a mutation status of Q942K, The gene C7 has a mutation status of K771Q, The gene SNX18 has a mutation status of L133P, The gene FOXD1 has a mutation status of R240R, The gene SLF1 has a mutation status of T809K, The gene MCTP1 has a mutation status of L130P, The gene EPB41L4A has a mutation status of L682L, The gene SOWAHA has a mutation status of S37R, The gene PURA has a mutation status of A50G, The gene PURA has a mutation status of P51P, The gene APBB3 has a mutation status of G306A, The gene DIAPH1 has a mutation status of S264Y, The gene DPYSL3 has a mutation status of R440R, The gene HMGXB3 has a mutation status of H797Y, The gene HMMR has a mutation status of A484T, The gene BTNL8 has a mutation status of E94G, The gene CARMIL1 has a mutation status of R1246Q, The gene H3C8 has a mutation status of K37R, The gene ZBED9 has a mutation status of R54C, The gene DDR1 has a mutation status of H43R, The gene HLA-DRB1 has a mutation status of T106N, The gene LGSN has a mutation status of I339I, The gene EPHA7 has a mutation status of T169T, The gene HS3ST5 has a mutation status of K225Q, The gene HSF2 has a mutation status of V501V, The gene AKAP7 has a mutation status of Y87C, The gene FRMD1 has a mutation status of H244R, The gene FAM120B has a mutation status of R488W, The gene GARS1 has a mutation status of A255A, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of T987I, The gene WNT16 has a mutation status of T95P, The gene RNF133 has a mutation status of R94*, The gene FLNC has a mutation status of G1548G, The gene FLNC has a mutation status of V2661I, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene CSMD1 has a mutation status of A2957T, The gene LYN has a mutation status of A455T, The gene FAM83A has a mutation status of P393P, The gene FREM1 has a mutation status of S5C, The gene CDKN2A has a mutation status of A36G, The gene ACO1 has a mutation status of A433S, The gene MYORG has a mutation status of D354N, The gene FAM205A has a mutation status of Y1314S, The gene PHF2 has a mutation status of T479P, The gene MIGA2 has a mutation status of V331M, The gene SURF2 has a mutation status of V56G, The gene CCDC187 has a mutation status of A321T, The gene NOTCH1 has a mutation status of T701P, The gene ABCA2 has a mutation status of V1665G, The gene EXD3 has a mutation status of A687D, The gene TASOR2 has a mutation status of D2607E, The gene ANXA8 has a mutation status of G114S, The gene CCDC6 has a mutation status of G43G, The gene NRG3 has a mutation status of Q360K, The gene CFAP46 has a mutation status of Y1615S, The gene PHRF1 has a mutation status of P348L, The gene USP47 has a mutation status of V1169A, The gene DBX1 has a mutation status of P59P, The gene NELL1 has a mutation status of Q123Q, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TMEM132A has a mutation status of H166P, The gene TMEM132A has a mutation status of E735G, The gene VEGFB has a mutation status of D153A, The gene NAALAD2 has a mutation status of S565F, The gene FAT3 has a mutation status of R3760H, The gene FUT4 has a mutation status of W143G, The gene CCDC84 has a mutation status of V41G, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene CDKN1B has a mutation status of C99fs, The gene DDX11 has a mutation status of R522Q, The gene HDAC7 has a mutation status of G75V, The gene TUBA1C has a mutation status of S62C, The gene KRT84 has a mutation status of A418V, The gene KRT5 has a mutation status of G570G, The gene PRIM1 has a mutation status of T133A, The gene R3HDM2 has a mutation status of F456V, The gene TRHDE has a mutation status of V114G, The gene APPL2 has a mutation status of R524W, The gene PCDH8 has a mutation status of G546G, The gene PCDH8 has a mutation status of T289P, The gene FARP1 has a mutation status of H703P, The gene FNTB has a mutation status of C345Y, The gene PGF has a mutation status of V59G, The gene GALC has a mutation status of L6I, The gene ASB2 has a mutation status of H515P, The gene CEP170B has a mutation status of P1511P, The gene LINC02203 has a mutation status of I259M, The gene GJD2 has a mutation status of E271E, The gene TGM7 has a mutation status of R511H, The gene MAP1A has a mutation status of S2961R, The gene IGDCC4 has a mutation status of S463Y, The gene PIAS1 has a mutation status of F407fs, The gene NOX5 has a mutation status of R174P, The gene ISLR2 has a mutation status of N474D, The gene CCDC33 has a mutation status of N71D, The gene ULK3 has a mutation status of G395R, The gene ULK3 has a mutation status of R115H, The gene GOLGA6L9 has a mutation status of R228S, The gene CHSY1 has a mutation status of D450N, The gene NME4 has a mutation status of V69G, The gene NME4 has a mutation status of M71V, The gene SOX8 has a mutation status of Y288S, The gene NME3 has a mutation status of G39C, The gene TRAF7 has a mutation status of C403C, The gene CASKIN1 has a mutation status of L1205P, The gene NTN3 has a mutation status of T345P, The gene ZNF205 has a mutation status of T402P, The gene CIITA has a mutation status of A506A, The gene SPN has a mutation status of G217R, The gene ZNF646 has a mutation status of S906N, The gene ZNF319 has a mutation status of V507G, The gene MON1B has a mutation status of L109I, The gene JPH3 has a mutation status of L460L, The gene JPH3 has a mutation status of R462R, The gene BANP has a mutation status of P322P, The gene PIEZO1 has a mutation status of G169G, The gene ZNF276 has a mutation status of G485D, The gene DPH1 has a mutation status of I370L, The gene TP53 has a mutation status of V272M, The gene MYH3 has a mutation status of D1887G, The gene RHBDL3 has a mutation status of L99V, The gene UNC45B has a mutation status of R15W, The gene CCL4L2 has a mutation status of P67R, The gene KRT32 has a mutation status of P427I, The gene KLHL10 has a mutation status of V203G, The gene CSH2 has a mutation status of L127M, The gene ABCA6 has a mutation status of E783E, The gene MYOM1 has a mutation status of V896V, The gene CFAP53 has a mutation status of E428*, The gene ZADH2 has a mutation status of P58P, The gene C2CD4C has a mutation status of S220S, The gene POLRMT has a mutation status of Q331*, The gene ZNF77 has a mutation status of S337L, The gene FZR1 has a mutation status of T300P, The gene DNMT1 has a mutation status of V1539M, The gene HOOK2 has a mutation status of E260G, The gene BRD4 has a mutation status of E1246E, The gene ATP4A has a mutation status of V435G, The gene FCGBP has a mutation status of GP1230del, The gene FCGBP has a mutation status of S1228fs, The gene PSG5 has a mutation status of L237P, The gene PSG9 has a mutation status of R345H, The gene VASP has a mutation status of P211L, The gene ARHGAP35 has a mutation status of L1222L, The gene GYS1 has a mutation status of Q203K, The gene TRPM4 has a mutation status of P750P, The gene CNOT3 has a mutation status of L190Q, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q50Q, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of H290N, The gene FAM83D has a mutation status of L108M, The gene MATN4 has a mutation status of P139P, The gene NEURL2 has a mutation status of D89A, The gene STX16 has a mutation status of L169L, The gene MTG2 has a mutation status of P58P, The gene PAXBP1 has a mutation status of V8G, The gene RIPK4 has a mutation status of A136P, The gene PFKL has a mutation status of T770P, The gene IL17RA has a mutation status of V669M, The gene HSCB has a mutation status of V12G, The gene TMPRSS6 has a mutation status of A700S, The gene MSL3 has a mutation status of S2T, The gene ACE2 has a mutation status of H34H, The gene KDM5C has a mutation status of G1124fs, The gene ZNF711 has a mutation status of T656T, The gene FRMPD3 has a mutation status of A280V, The gene AFF2 has a mutation status of R927H, The gene CNGA2 has a mutation status of D662E, The gene IL9R has a mutation status of G447G, The gene MT-CO2 has a mutation status of L75L, The gene MT-ND5 has a mutation status of V92V
DLBC
The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of M105L, The gene SPEN has a mutation status of T1258S, The gene SPEN has a mutation status of R1959G, The gene KLHDC7A has a mutation status of Q335K, The gene NKAIN1 has a mutation status of R60W, The gene PPCS has a mutation status of R25P, The gene ZFYVE9 has a mutation status of V864V, The gene LRRC7 has a mutation status of R920C, The gene SEMA6C has a mutation status of F238Y, The gene RAB13 has a mutation status of N121S, The gene ATP1A4 has a mutation status of R985*, The gene SELP has a mutation status of T683T, The gene PRDX6 has a mutation status of F28L, The gene NAV1 has a mutation status of 1785_1786insGPP, The gene PLXNA2 has a mutation status of C826G, The gene CDC42BPA has a mutation status of G292R, The gene NID1 has a mutation status of C769C, The gene OR2T12 has a mutation status of A179T, The gene FEZ2 has a mutation status of N92N, The gene EPAS1 has a mutation status of D753E, The gene ANKRD36C has a mutation status of S746C, The gene GPR39 has a mutation status of R197C, The gene RBMS1 has a mutation status of T62T, The gene FAM171B has a mutation status of I364T, The gene OSGEPL1 has a mutation status of V126M, The gene AOX1 has a mutation status of D1200H, The gene PARD3B has a mutation status of Q687K, The gene COL4A4 has a mutation status of G1039G, The gene EAF1 has a mutation status of P222L, The gene CTDSPL has a mutation status of L251R, The gene HYAL2 has a mutation status of R379C, The gene ADAMTS9 has a mutation status of K1725I, The gene ROBO2 has a mutation status of V645L, The gene EPHA3 has a mutation status of C366C, The gene SENP7 has a mutation status of C980G, The gene KALRN has a mutation status of R907C, The gene C3orf33 has a mutation status of R287H, The gene AP2M1 has a mutation status of G127D, The gene CLCN2 has a mutation status of E721K, The gene SLC2A9 has a mutation status of V77M, The gene BOD1L1 has a mutation status of G1536G, The gene GRXCR1 has a mutation status of T152T, The gene ADAM29 has a mutation status of Q796P, The gene ING2 has a mutation status of L82L, The gene DNAH5 has a mutation status of R3885*, The gene DNAH5 has a mutation status of T1684T, The gene C9 has a mutation status of R271Q, The gene MAP1B has a mutation status of S1609C, The gene CMYA5 has a mutation status of E1275E, The gene CAST has a mutation status of R273C, The gene SLCO6A1 has a mutation status of D490N, The gene PCDHB8 has a mutation status of L641L, The gene CAMK2A has a mutation status of V73I, The gene TRIM10 has a mutation status of R331*, The gene NELFE has a mutation status of I11I, The gene TNFRSF21 has a mutation status of T291I, The gene CASP8AP2 has a mutation status of Y914S, The gene HBS1L has a mutation status of D548N, The gene ECT2L has a mutation status of A880A, The gene RAET1E has a mutation status of T262T, The gene AMZ1 has a mutation status of D371H, The gene ABCA13 has a mutation status of H1863H, The gene PSPH has a mutation status of L68P, The gene RFC2 has a mutation status of L344L, The gene ANKIB1 has a mutation status of S884Y, The gene SRRT has a mutation status of R17K, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S342G, The gene MUC3A has a mutation status of S830S, The gene MUC3A has a mutation status of S834T, The gene MUC3A has a mutation status of T987I, The gene MUC3A has a mutation status of P3036L, The gene WNT16 has a mutation status of K63R, The gene ESCO2 has a mutation status of H34N, The gene FZD3 has a mutation status of R167Q, The gene TEX15 has a mutation status of G3075R, The gene SGK3 has a mutation status of I446S, The gene ZFHX4 has a mutation status of G1755S, The gene ZFHX4 has a mutation status of P2678A, The gene DECR1 has a mutation status of V115D, The gene DPY19L4 has a mutation status of A192V, The gene MATN2 has a mutation status of V76V, The gene RNF19A has a mutation status of T240T, The gene LRATD2 has a mutation status of Q52H, The gene DENND3 has a mutation status of R462fs, The gene GPAA1 has a mutation status of V232fs, The gene TAF1L has a mutation status of P516H, The gene NUTM2F has a mutation status of L28L, The gene FKTN has a mutation status of Y31fs, The gene CAMSAP1 has a mutation status of C848S, The gene NOTCH1 has a mutation status of L1593P, The gene AKR1C8P has a mutation status of N172K, The gene JCAD has a mutation status of S1307N, The gene ALOX5 has a mutation status of A307D, The gene PSAP has a mutation status of D340V, The gene CDHR1 has a mutation status of A617T, The gene MUC5B has a mutation status of S1986P, The gene OR51I2 has a mutation status of C32C, The gene WEE1 has a mutation status of P240L, The gene ACCSL has a mutation status of T519T, The gene OR9G1 has a mutation status of T62V, The gene OR5B21 has a mutation status of N63N, The gene DDB1 has a mutation status of I1068M, The gene BAD has a mutation status of S136T, The gene BAD has a mutation status of W133G, The gene MAP3K11 has a mutation status of M32V, The gene RELA has a mutation status of P369A, The gene RELA has a mutation status of E362*, The gene USP35 has a mutation status of G839G, The gene MED17 has a mutation status of A452E, The gene ROBO4 has a mutation status of P923P, The gene ST14 has a mutation status of P132T, The gene WNK1 has a mutation status of Q201E, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PRB2 has a mutation status of Q90Q, The gene ABCC9 has a mutation status of 1188_1189FR>LG, The gene SPATS2 has a mutation status of Q435H, The gene KRT71 has a mutation status of L137L, The gene KRT1 has a mutation status of S631C, The gene KRT1 has a mutation status of T507K, The gene TNS2 has a mutation status of Y1044*, The gene HOXC8 has a mutation status of K205E, The gene TIMELESS has a mutation status of L810P, The gene LRIG3 has a mutation status of R569H, The gene CHST11 has a mutation status of T95K, The gene SRRM4 has a mutation status of R485R, The gene P2RX7 has a mutation status of I568N, The gene HSPH1 has a mutation status of E800E, The gene TSC22D1 has a mutation status of Q568K, The gene CBY2 has a mutation status of G11G, The gene AL445989.1 has a mutation status of T38S, The gene FBXL3 has a mutation status of M329K, The gene TTC6 has a mutation status of I1866S, The gene SAMD4A has a mutation status of I113T, The gene ABCD4 has a mutation status of P526L, The gene FAM181A has a mutation status of S96Y, The gene APBA2 has a mutation status of P535S, The gene TYRO3 has a mutation status of K235fs, The gene TYRO3 has a mutation status of E509fs, The gene MGA has a mutation status of K1978R, The gene CD276 has a mutation status of V42V, The gene RCCD1 has a mutation status of Q267R, The gene NME4 has a mutation status of M73I, The gene PDP2 has a mutation status of A493G, The gene EDC4 has a mutation status of L16M, The gene EDC4 has a mutation status of L22M, The gene PSKH1 has a mutation status of P229L, The gene NFATC3 has a mutation status of I1047S, The gene CNTNAP4 has a mutation status of G388R, The gene SLC43A2 has a mutation status of S425S, The gene ZFP3 has a mutation status of Y449Y, The gene CD68 has a mutation status of S280S, The gene USP43 has a mutation status of G739R, The gene GAS7 has a mutation status of E412G, The gene MYOCD has a mutation status of C601F, The gene SEZ6 has a mutation status of R454W, The gene TMEM132E has a mutation status of R174G, The gene CCL4L2 has a mutation status of P67R, The gene LHX1 has a mutation status of T206P, The gene HIGD1B has a mutation status of M1T, The gene MRC2 has a mutation status of R899H, The gene MARCHF10 has a mutation status of V305M, The gene PECAM1 has a mutation status of S104S, The gene SMURF2 has a mutation status of Q63Q, The gene USH1G has a mutation status of G338R, The gene MYO15B has a mutation status of G474A, The gene FOXJ1 has a mutation status of P109A, The gene CCDC57 has a mutation status of D1027D, The gene TGIF1 has a mutation status of K44K, The gene ARHGAP45 has a mutation status of E1030A, The gene ATP8B3 has a mutation status of N152K, The gene THOP1 has a mutation status of F109L, The gene DNM2 has a mutation status of R361*, The gene CILP2 has a mutation status of G120G, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene GEMIN7 has a mutation status of F129L, The gene SIGLEC10 has a mutation status of P235T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of N187T, The gene LILRA6 has a mutation status of L11L, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene TGM6 has a mutation status of R252H, The gene PLCB1 has a mutation status of K975N, The gene BPIFB3 has a mutation status of G169D, The gene PCK1 has a mutation status of T92M, The gene ABHD16B has a mutation status of S115S, The gene ADAMTS1 has a mutation status of D202H, The gene TRMT2A has a mutation status of V482L, The gene CCDC116 has a mutation status of R380R, The gene RAB36 has a mutation status of L257M, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene KIAA0930 has a mutation status of N326N, The gene RIBC2 has a mutation status of N138H, The gene PPP6R2 has a mutation status of S413F, The gene CHST7 has a mutation status of S114S, The gene HUWE1 has a mutation status of N2241S, The gene DGAT2L6 has a mutation status of T240M, The gene ZMAT1 has a mutation status of D335Y, The gene LONRF3 has a mutation status of V228M, The gene SLC25A5 has a mutation status of T221R, The gene SASH3 has a mutation status of H181R, The gene MBNL3 has a mutation status of S116P, The gene SLITRK2 has a mutation status of V692V, The gene MAGEA3 has a mutation status of Y145Y, The gene PLXNB3 has a mutation status of P213S, The gene PLXNB3 has a mutation status of D372D, The gene UTY has a mutation status of S451S, The gene MT-ND1 has a mutation status of A4V, The gene MT-ND2 has a mutation status of N289N, The gene MT-ND5 has a mutation status of V92V
DLBC
The gene FNDC10 has a mutation status of H225P, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF15 has a mutation status of N442K, The gene AKR7A2 has a mutation status of H302Y, The gene FAM43B has a mutation status of G106R, The gene ZSCAN20 has a mutation status of P827S, The gene CSMD2 has a mutation status of N1056D, The gene SFPQ has a mutation status of P132P, The gene SFPQ has a mutation status of S128P, The gene PPCS has a mutation status of V37G, The gene SZT2 has a mutation status of Q154L, The gene ASB17 has a mutation status of Y57*, The gene PTGFRN has a mutation status of R152R, The gene ARNT has a mutation status of V610I, The gene NCSTN has a mutation status of G6G, The gene F5 has a mutation status of N1562N, The gene YOD1 has a mutation status of G35G, The gene RAB3GAP2 has a mutation status of A1254V, The gene CDC42BPA has a mutation status of L435V, The gene IRF2BP2 has a mutation status of K164K, The gene HEATR1 has a mutation status of I755F, The gene HS1BP3 has a mutation status of P181S, The gene LDAH has a mutation status of A86V, The gene TET3 has a mutation status of D177E, The gene C2orf81 has a mutation status of T247P, The gene WDR54 has a mutation status of R141Q, The gene ST3GAL5 has a mutation status of R388L, The gene RGPD6 has a mutation status of T19P, The gene THSD7B has a mutation status of N1443N, The gene LRP2 has a mutation status of Q3770K, The gene LRP2 has a mutation status of G2470V, The gene TTN has a mutation status of R29784C, The gene DNAH7 has a mutation status of L357L, The gene AC053503.6 has a mutation status of H101P, The gene OBSL1 has a mutation status of A1085E, The gene INPP5D has a mutation status of L234M, The gene IQCA1 has a mutation status of V753M, The gene ESPNL has a mutation status of A84D, The gene GPC1 has a mutation status of P537S, The gene NEU4 has a mutation status of V476V, The gene SYN2 has a mutation status of P105A, The gene GASK1A has a mutation status of W185L, The gene COL7A1 has a mutation status of G762G, The gene LAMB2 has a mutation status of A1206A, The gene FLNB has a mutation status of H2355P, The gene MYH15 has a mutation status of E1040Q, The gene BOC has a mutation status of R839W, The gene ARHGAP31 has a mutation status of R426G, The gene ZNF148 has a mutation status of A381A, The gene MSL2 has a mutation status of P389A, The gene FOXL2 has a mutation status of G40G, The gene KPNA4 has a mutation status of N39K, The gene PLD1 has a mutation status of S59fs, The gene B3GNT5 has a mutation status of Y353*, The gene AHSG has a mutation status of A313A, The gene UTS2B has a mutation status of S25F, The gene IQCG has a mutation status of R138W, The gene TMEM175 has a mutation status of H484P, The gene BOD1L1 has a mutation status of D1737G, The gene PAICS has a mutation status of I96T, The gene HNRNPDL has a mutation status of L42S, The gene ARHGAP24 has a mutation status of R460K, The gene GUCY1A1 has a mutation status of G35G, The gene GPM6A has a mutation status of G87G, The gene MRPL36 has a mutation status of L56V, The gene CPLANE1 has a mutation status of N1755H, The gene NUP155 has a mutation status of K1197I, The gene CCNB1 has a mutation status of N12K, The gene ARHGEF28 has a mutation status of E209E, The gene MCTP1 has a mutation status of H128L, The gene LOX has a mutation status of Y190Y, The gene ACSL6 has a mutation status of A70G, The gene SEPTIN8 has a mutation status of H149H, The gene PCDHA6 has a mutation status of Y492H, The gene CDX1 has a mutation status of Y14S, The gene FLT4 has a mutation status of T618P, The gene BPHL has a mutation status of T127T, The gene PPT2 has a mutation status of L126V, The gene HLA-DRB5 has a mutation status of Q220W, The gene HLA-DRB5 has a mutation status of Q38W, The gene DNAH8 has a mutation status of R3635R, The gene NCR2 has a mutation status of V156V, The gene TBCC has a mutation status of V244L, The gene CUL7 has a mutation status of Y257*, The gene FABP7 has a mutation status of V84I, The gene SOGA3 has a mutation status of P29P, The gene CCDC170 has a mutation status of R393R, The gene SYNJ2 has a mutation status of T797P, The gene SOD2 has a mutation status of S93F, The gene INTS1 has a mutation status of W1368*, The gene BRAT1 has a mutation status of V425G, The gene FOXK1 has a mutation status of T683P, The gene SLC29A4 has a mutation status of H416P, The gene EIF2AK1 has a mutation status of T297A, The gene EGFR has a mutation status of Y240Y, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S543N, The gene MUC3A has a mutation status of 544_545AG>DR, The gene MUC3A has a mutation status of S568Y, The gene KCP has a mutation status of R1259W, The gene KLF14 has a mutation status of P58S, The gene MKRN1 has a mutation status of A369A, The gene PRSS1 has a mutation status of N77N, The gene CLCN1 has a mutation status of R894R, The gene CLDN23 has a mutation status of V5G, The gene TNKS has a mutation status of V195M, The gene MTUS1 has a mutation status of T234fs, The gene MCMDC2 has a mutation status of K22K, The gene SULF1 has a mutation status of A75T, The gene JPH1 has a mutation status of S258S, The gene GPR20 has a mutation status of L243L, The gene CYP11B1 has a mutation status of P485A, The gene PLEC has a mutation status of A2272T, The gene WDR97 has a mutation status of A1281T, The gene BOP1 has a mutation status of N134N, The gene TONSL has a mutation status of L945H, The gene ANKRD18B has a mutation status of E367*, The gene TRPM6 has a mutation status of R1784K, The gene TDRD7 has a mutation status of S229P, The gene TBC1D2 has a mutation status of V376G, The gene FRRS1L has a mutation status of R51A, The gene PRPF4 has a mutation status of C299S, The gene AKNA has a mutation status of H620P, The gene GLT6D1 has a mutation status of S127I, The gene CCDC187 has a mutation status of A286S, The gene ATP5F1C has a mutation status of G183G, The gene ADAMTS14 has a mutation status of V667M, The gene CDH23 has a mutation status of D2695A, The gene RPP30 has a mutation status of K72T, The gene LBX1 has a mutation status of H22P, The gene SORCS1 has a mutation status of T868T, The gene PDCD4 has a mutation status of Q435*, The gene PNLIP has a mutation status of W5G, The gene WDR11 has a mutation status of A663T, The gene FGFR2 has a mutation status of T137T, The gene FAM53B has a mutation status of A327P, The gene FAM53B has a mutation status of T249T, The gene PAOX has a mutation status of A24V, The gene RASSF7 has a mutation status of T129P, The gene MUC5AC has a mutation status of A497V, The gene MUC5AC has a mutation status of A5353K, The gene SPON1 has a mutation status of A111T, The gene PEX16 has a mutation status of E273G, The gene FOLH1 has a mutation status of A365A, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene SLC43A3 has a mutation status of G3V, The gene DTX4 has a mutation status of N374fs, The gene CHRM1 has a mutation status of R320Q, The gene EHBP1L1 has a mutation status of V893F, The gene NADSYN1 has a mutation status of D361G, The gene TRIM49 has a mutation status of F422V, The gene FOXM1 has a mutation status of T548N, The gene TSPAN9 has a mutation status of A239T, The gene TAS2R45 has a mutation status of I33T, The gene PDE3A has a mutation status of V193G, The gene PDE3A has a mutation status of V194G, The gene RAPGEF3 has a mutation status of R664G, The gene KRT76 has a mutation status of Q220*, The gene ITGB7 has a mutation status of A124A, The gene HOXC12 has a mutation status of P37P, The gene ITGA5 has a mutation status of S714S, The gene TRHDE has a mutation status of G112G, The gene TMPO has a mutation status of T74P, The gene WASHC4 has a mutation status of R14R, The gene RNF17 has a mutation status of A970V, The gene ATP4B has a mutation status of N146K, The gene ARID4A has a mutation status of N815I, The gene ZC3H14 has a mutation status of P346L, The gene CEP170B has a mutation status of P1511P, The gene OIP5 has a mutation status of L120P, The gene TYRO3 has a mutation status of G251S, The gene SPTBN5 has a mutation status of E913G, The gene SMAD6 has a mutation status of S158R, The gene IQCH has a mutation status of P892L, The gene TLE3 has a mutation status of P396P, The gene ACSBG1 has a mutation status of C11S, The gene CHRNB4 has a mutation status of T215P, The gene LMF1 has a mutation status of G335V, The gene ALG1 has a mutation status of I222V, The gene RABEP2 has a mutation status of P250S, The gene NPIPB11 has a mutation status of 169_170HD>QH, The gene MAZ has a mutation status of A163P, The gene SEZ6L2 has a mutation status of P127P, The gene CDH16 has a mutation status of G352G, The gene SNTB2 has a mutation status of V118G, The gene DHX38 has a mutation status of L25L, The gene ADAMTS18 has a mutation status of N339N, The gene TAF1C has a mutation status of A545E, The gene TAF1C has a mutation status of N481K, The gene COTL1 has a mutation status of Q140fs, The gene ZFPM1 has a mutation status of A791A, The gene ZFP3 has a mutation status of C227*, The gene LLGL1 has a mutation status of V404A, The gene CCL4L2 has a mutation status of P67R, The gene LHX1 has a mutation status of T206P, The gene KRT32 has a mutation status of P427I, The gene ANKFN1 has a mutation status of A1054A, The gene CYB561 has a mutation status of R73R, The gene MYO15B has a mutation status of P2480P, The gene FN3K has a mutation status of K269N, The gene LRRC30 has a mutation status of T246N, The gene VAPA has a mutation status of A2S, The gene SALL3 has a mutation status of A185L, The gene STAP2 has a mutation status of T150T, The gene CAMSAP3 has a mutation status of F684T, The gene CLEC4G has a mutation status of L157P, The gene TSPAN16 has a mutation status of D167N, The gene HOOK2 has a mutation status of E260G, The gene GCDH has a mutation status of R88C, The gene BRD4 has a mutation status of P757P, The gene UPK1A has a mutation status of T147P, The gene KIRREL2 has a mutation status of N338T, The gene PSG8 has a mutation status of R73K, The gene BICRA has a mutation status of A573A, The gene BICRA has a mutation status of P858L, The gene SLC6A16 has a mutation status of M148L, The gene GPR32 has a mutation status of A98fs, The gene GPR32 has a mutation status of M99V, The gene ZNF888 has a mutation status of Q253E, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA1 has a mutation status of R296T, The gene LILRB4 has a mutation status of K362P, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene ISOC2 has a mutation status of V146G, The gene CENPB has a mutation status of T150P, The gene XKR7 has a mutation status of G124G, The gene NECAB3 has a mutation status of R376R, The gene PIGU has a mutation status of L188F, The gene PABPC1L has a mutation status of P454T, The gene PREX1 has a mutation status of L1650I, The gene OGFR has a mutation status of V249G, The gene HELZ2 has a mutation status of H1468P, The gene ADAMTS5 has a mutation status of V319M, The gene PRDM15 has a mutation status of E222*, The gene PDE9A has a mutation status of L540R, The gene CCT8L2 has a mutation status of G474W, The gene PPIL2 has a mutation status of T157P, The gene GSTT4 has a mutation status of Q197R, The gene GSTT4 has a mutation status of I19M, The gene RNF215 has a mutation status of L218W, The gene MCM5 has a mutation status of T166P, The gene EIF3L has a mutation status of H26Q, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene POLDIP3 has a mutation status of S405F, The gene MXRA5 has a mutation status of A1655T, The gene DCAF8L1 has a mutation status of P117P, The gene FAM47B has a mutation status of R4L, The gene KCND1 has a mutation status of S79S, The gene FAM120C has a mutation status of R1028W, The gene EDA has a mutation status of P31P, The gene NHSL2 has a mutation status of L143L, The gene FGF16 has a mutation status of S111S, The gene GPRASP1 has a mutation status of S520S, The gene BCORL1 has a mutation status of L1132P, The gene PNMA6E has a mutation status of E626E, The gene PDZD4 has a mutation status of T513P, The gene MT-CO3 has a mutation status of H103H, The gene MT-ND4 has a mutation status of C52C, The gene MT-ND5 has a mutation status of A459V, The gene MT-ND5 has a mutation status of G460E, The gene MT-CYB has a mutation status of A380T
DLBC
The gene PERM1 has a mutation status of G51V, The gene SKI has a mutation status of E490K, The gene CCDC27 has a mutation status of Q479K, The gene ESPN has a mutation status of E820G, The gene CLSTN1 has a mutation status of D283D, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene E2F2 has a mutation status of R82R, The gene CNR2 has a mutation status of R302Q, The gene LDLRAP1 has a mutation status of S245R, The gene SLC30A2 has a mutation status of E26G, The gene ADGRB2 has a mutation status of G747G, The gene TMEM39B has a mutation status of Q484H, The gene GJA4 has a mutation status of A301G, The gene RRAGC has a mutation status of P23P, The gene TIE1 has a mutation status of G299E, The gene PATJ has a mutation status of V1516G, The gene TNNI3K has a mutation status of M817V, The gene TGFBR3 has a mutation status of V605L, The gene BTBD8 has a mutation status of S1489S, The gene NTNG1 has a mutation status of S242F, The gene EPS8L3 has a mutation status of P176L, The gene KCND3 has a mutation status of A248A, The gene MAB21L3 has a mutation status of W203G, The gene IGSF3 has a mutation status of P1107A, The gene CD101 has a mutation status of Q194K, The gene TCHH has a mutation status of K1190T, The gene ARHGEF2 has a mutation status of G69V, The gene IQGAP3 has a mutation status of H753Y, The gene SPTA1 has a mutation status of E1115*, The gene AIM2 has a mutation status of E220E, The gene CD84 has a mutation status of K258N, The gene PPOX has a mutation status of G155G, The gene POGK has a mutation status of Y511*, The gene ILDR2 has a mutation status of R367R, The gene MROH9 has a mutation status of D237D, The gene TNN has a mutation status of G1132D, The gene ASTN1 has a mutation status of M1068I, The gene RASAL2 has a mutation status of A1025V, The gene TPR has a mutation status of T1503R, The gene LGR6 has a mutation status of I146T, The gene PLXNA2 has a mutation status of D1025Y, The gene TGFB2 has a mutation status of L366L, The gene HHIPL2 has a mutation status of G502R, The gene ENAH has a mutation status of E206G, The gene NBAS has a mutation status of A1299P, The gene GDF7 has a mutation status of A135G, The gene APOB has a mutation status of P1067L, The gene FAM228B has a mutation status of Q303fs, The gene PREB has a mutation status of Q117Q, The gene RASGRP3 has a mutation status of K8N, The gene SLC3A1 has a mutation status of V490L, The gene EML6 has a mutation status of D314E, The gene ALMS1 has a mutation status of A1410S, The gene DCTN1 has a mutation status of I1113I, The gene AUP1 has a mutation status of T109T, The gene PTCD3 has a mutation status of G17A, The gene SMYD1 has a mutation status of A107G, The gene CNNM4 has a mutation status of L579I, The gene SEMA4C has a mutation status of A617G, The gene GPR45 has a mutation status of A123P, The gene RGPD4 has a mutation status of S18F, The gene RGPD4 has a mutation status of D1127N, The gene IL1F10 has a mutation status of Q129H, The gene CNTNAP5 has a mutation status of S500T, The gene MYO7B has a mutation status of E13G, The gene LRP2 has a mutation status of C1601C, The gene HOXD1 has a mutation status of P164P, The gene ALS2 has a mutation status of R998R, The gene UNC80 has a mutation status of I794I, The gene ABCA12 has a mutation status of A1283G, The gene XRCC5 has a mutation status of E645K, The gene TNS1 has a mutation status of R117*, The gene VIL1 has a mutation status of T684A, The gene ZNF142 has a mutation status of G1684V, The gene ZNF142 has a mutation status of A278P, The gene RNF25 has a mutation status of E449Q, The gene FEV has a mutation status of V83G, The gene FEV has a mutation status of F75V, The gene EIF4E2 has a mutation status of Q235*, The gene USP40 has a mutation status of R1039R, The gene UGT1A9 has a mutation status of R88W, The gene MTERF4 has a mutation status of R24K, The gene IL17RC has a mutation status of V25L, The gene ATP2B2 has a mutation status of R694P, The gene CTDSPL has a mutation status of H200Y, The gene ULK4 has a mutation status of Q1271K, The gene SCAP has a mutation status of Y407*, The gene CELSR3 has a mutation status of E1857G, The gene NISCH has a mutation status of A693V, The gene DNASE1L3 has a mutation status of T144T, The gene C3orf67 has a mutation status of A577V, The gene GOLGB1 has a mutation status of L3093W, The gene NPHP3 has a mutation status of S79S, The gene TOPBP1 has a mutation status of T861T, The gene PCOLCE2 has a mutation status of D269N, The gene TSC22D2 has a mutation status of S538S, The gene GPR171 has a mutation status of L14V, The gene GFM1 has a mutation status of A641S, The gene SLC49A3 has a mutation status of A357S, The gene MFSD10 has a mutation status of S94S, The gene RBM47 has a mutation status of M161I, The gene AMBN has a mutation status of T404I, The gene SCD5 has a mutation status of T314T, The gene FAT4 has a mutation status of A43A, The gene FAT4 has a mutation status of V2783I, The gene PCDH10 has a mutation status of R964C, The gene PCDH18 has a mutation status of A836P, The gene NKD2 has a mutation status of A157T, The gene ADCY2 has a mutation status of L244L, The gene MTRR has a mutation status of L245L, The gene DNAH5 has a mutation status of L861F, The gene UGT3A2 has a mutation status of A405P, The gene ERBIN has a mutation status of Y1336*, The gene MAST4 has a mutation status of E1934D, The gene MBLAC2 has a mutation status of S2S, The gene ERAP2 has a mutation status of V55L, The gene PAM has a mutation status of G3G, The gene FBN2 has a mutation status of M631V, The gene SLC22A5 has a mutation status of S190L, The gene CATSPER3 has a mutation status of G147A, The gene SLC25A48 has a mutation status of L177fs, The gene KLHL3 has a mutation status of G347G, The gene PCDHGC3 has a mutation status of V800G, The gene PCDHGC3 has a mutation status of L801V, The gene GRIA1 has a mutation status of R708W, The gene HAND1 has a mutation status of S141N, The gene FAM193B has a mutation status of G632G, The gene FOXC1 has a mutation status of 518_519LN>FY, The gene GFOD1 has a mutation status of T52L, The gene RANBP9 has a mutation status of N578S, The gene NHLRC1 has a mutation status of T125A, The gene ZKSCAN4 has a mutation status of R3K, The gene GABBR1 has a mutation status of R923L, The gene DDR1 has a mutation status of C203W, The gene EGFL8 has a mutation status of C132C, The gene NOTCH4 has a mutation status of S210P, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of L246L, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DQB2 has a mutation status of V37Y, The gene AL669918.1 has a mutation status of A514G, The gene HLA-DOA has a mutation status of S45S, The gene HLA-DOA has a mutation status of A44P, The gene ITPR3 has a mutation status of F244V, The gene ITPR3 has a mutation status of L2635V, The gene TBC1D22B has a mutation status of R421L, The gene FRS3 has a mutation status of V112V, The gene CUL7 has a mutation status of P663A, The gene FBXO9 has a mutation status of R85P, The gene RNGTT has a mutation status of G17A, The gene MDN1 has a mutation status of D3304G, The gene RWDD1 has a mutation status of L75L, The gene MCM9 has a mutation status of R132L, The gene NHSL1 has a mutation status of S688T, The gene OPRM1 has a mutation status of T39T, The gene NOX3 has a mutation status of C327A, The gene NOX3 has a mutation status of W53L, The gene IGF2R has a mutation status of C830F, The gene THBS2 has a mutation status of V6G, The gene GRID2IP has a mutation status of E534E, The gene NACAD has a mutation status of A622P, The gene EGFR has a mutation status of R264G, The gene SEPTIN14 has a mutation status of T168A, The gene PSPH has a mutation status of L68P, The gene ZNF273 has a mutation status of H224R, The gene GALNT17 has a mutation status of P424P, The gene NSUN5 has a mutation status of E319Q, The gene ELN has a mutation status of A309P, The gene POR has a mutation status of E237K, The gene AKAP9 has a mutation status of S248N, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of P3036L, The gene MUC12 has a mutation status of T4425T, The gene VGF has a mutation status of G250V, The gene SPDYE6 has a mutation status of H337R, The gene LSM8 has a mutation status of T2T, The gene LRRC4 has a mutation status of P485P, The gene FLNC has a mutation status of V231G, The gene KLF14 has a mutation status of P58S, The gene PRSS1 has a mutation status of N77N, The gene EPHA1 has a mutation status of V257G, The gene MYOM2 has a mutation status of L1346V, The gene RP1L1 has a mutation status of R23P, The gene ENTPD4 has a mutation status of F392L, The gene ZNF703 has a mutation status of R580R, The gene ADGRA2 has a mutation status of G391S, The gene RB1CC1 has a mutation status of N251N, The gene DNAJC5B has a mutation status of H46H, The gene NCOA2 has a mutation status of P1066P, The gene ZBTB10 has a mutation status of R140C, The gene CDH17 has a mutation status of Y131N, The gene RIMS2 has a mutation status of R1234G, The gene COL22A1 has a mutation status of A1077A, The gene NAPRT has a mutation status of P266P, The gene PLEC has a mutation status of A761G, The gene PARP10 has a mutation status of G942A, The gene OPLAH has a mutation status of M746I, The gene MROH1 has a mutation status of E260G, The gene KANK1 has a mutation status of R1215Q, The gene GLDC has a mutation status of G421G, The gene TYRP1 has a mutation status of D343D, The gene CDKN2A has a mutation status of 19_20insTA, The gene VCP has a mutation status of F682F, The gene SHB has a mutation status of A214D, The gene WNK2 has a mutation status of L1399L, The gene ECPAS has a mutation status of K846R, The gene FKBP15 has a mutation status of D503D, The gene ALAD has a mutation status of A93T, The gene ASTN2 has a mutation status of V777V, The gene CRB2 has a mutation status of L156L, The gene CRB2 has a mutation status of H157Y, The gene CRB2 has a mutation status of H1099H, The gene FPGS has a mutation status of L545L, The gene ABL1 has a mutation status of G1079D, The gene AL162417.1 has a mutation status of C249W, The gene NOTCH1 has a mutation status of A811A, The gene TMEM203 has a mutation status of G13S, The gene NELFB has a mutation status of G593V, The gene CUBN has a mutation status of S2228Y, The gene ITGB1 has a mutation status of F252F, The gene HKDC1 has a mutation status of G265R, The gene ZSWIM8 has a mutation status of D625D, The gene ZSWIM8 has a mutation status of L628V, The gene CAMK2G has a mutation status of T495P, The gene DLG5 has a mutation status of D45G, The gene GHITM has a mutation status of V333I, The gene ANKRD1 has a mutation status of K153I, The gene CYP26C1 has a mutation status of E204G, The gene RRP12 has a mutation status of D742N, The gene MMS19 has a mutation status of R861Q, The gene CNNM2 has a mutation status of Y478*, The gene GPR26 has a mutation status of V263M, The gene TCERG1L has a mutation status of P266L, The gene ZNF511 has a mutation status of G53G, The gene RNH1 has a mutation status of H398P, The gene RASSF7 has a mutation status of P101L, The gene TIMM10B has a mutation status of S103S, The gene DCHS1 has a mutation status of A2574G, The gene SPON1 has a mutation status of Q344Q, The gene NAV2 has a mutation status of C1842W, The gene DGKZ has a mutation status of P287H, The gene OR5D13 has a mutation status of D123N, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene ZFP91 has a mutation status of E397E, The gene INCENP has a mutation status of A130G, The gene MTA2 has a mutation status of Y70*, The gene INTS5 has a mutation status of V913G, The gene INTS5 has a mutation status of S727F, The gene MACROD1 has a mutation status of Q293E, The gene B4GAT1 has a mutation status of L109L, The gene MRGPRD has a mutation status of R214Q, The gene LRRC32 has a mutation status of L145V, The gene KDM4E has a mutation status of R443R, The gene MAML2 has a mutation status of T980T, The gene COLCA2 has a mutation status of K14N, The gene TMEM225 has a mutation status of S134N, The gene HEPACAM has a mutation status of L71V, The gene ADAMTS8 has a mutation status of Y703*, The gene IGSF9B has a mutation status of T249P, The gene GLB1L3 has a mutation status of T395I, The gene SCNN1A has a mutation status of R204W, The gene CLEC7A has a mutation status of S91P, The gene KRAS has a mutation status of G12V, The gene LRRK2 has a mutation status of N202Y, The gene TMEM106C has a mutation status of R46G, The gene NDUFA4L2 has a mutation status of G3G, The gene LRRIQ1 has a mutation status of A1339G, The gene STAB2 has a mutation status of G921A, The gene CHST11 has a mutation status of F182N, The gene ACACB has a mutation status of L541L, The gene SRRM4 has a mutation status of R39R, The gene PITPNM2 has a mutation status of A1166G, The gene SLC15A4 has a mutation status of T438P, The gene ULK1 has a mutation status of K237M, The gene MIPEP has a mutation status of L197P, The gene SUCLA2 has a mutation status of S60N, The gene FNDC3A has a mutation status of S22P, The gene IPO5 has a mutation status of R59K, The gene CCDC168 has a mutation status of S2S, The gene IRS2 has a mutation status of N201D, The gene ADPRHL1 has a mutation status of S1367Y, The gene TMEM255B has a mutation status of C186W, The gene TEP1 has a mutation status of E1011D, The gene ZFHX2 has a mutation status of A122T, The gene NKX2-8 has a mutation status of R84S, The gene FBXO34 has a mutation status of Y660C, The gene PSMA3 has a mutation status of I190I, The gene SIX6 has a mutation status of Y71C, The gene SIX4 has a mutation status of R211G, The gene GALNT16 has a mutation status of S491C, The gene SERPINA4 has a mutation status of T410T, The gene PPP1R13B has a mutation status of A1090T, The gene KIF26A has a mutation status of H1652Q, The gene INF2 has a mutation status of G771A, The gene JAG2 has a mutation status of R575R, The gene TUBGCP5 has a mutation status of E452K, The gene FMN1 has a mutation status of E51G, The gene LTK has a mutation status of G154G, The gene TYRO3 has a mutation status of 554_555insDIIAST, The gene MAPK6 has a mutation status of C440F, The gene MYO5C has a mutation status of Q9Q, The gene RORA has a mutation status of N114S, The gene ALPK3 has a mutation status of S235I, The gene ALPK3 has a mutation status of V1273A, The gene NTRK3 has a mutation status of T392M, The gene PEX11A has a mutation status of M43T, The gene CACNA1H has a mutation status of A7T, The gene PKD1 has a mutation status of Q4216K, The gene E4F1 has a mutation status of G312G, The gene PKMYT1 has a mutation status of G159A, The gene CLUAP1 has a mutation status of P334P, The gene UBALD1 has a mutation status of T105P, The gene ZNF500 has a mutation status of L168L, The gene SEC14L5 has a mutation status of E348V, The gene TVP23A has a mutation status of L143V, The gene RMI2 has a mutation status of S126C, The gene SRCAP has a mutation status of T1715S, The gene KAT8 has a mutation status of E350E, The gene ABCC11 has a mutation status of V584I, The gene PLLP has a mutation status of S13G, The gene PLLP has a mutation status of R11W, The gene KATNB1 has a mutation status of C250W, The gene DDX19B has a mutation status of D305D, The gene TAT has a mutation status of R57G, The gene DHX38 has a mutation status of R674P, The gene ADAMTS18 has a mutation status of A870fs, The gene RFLNB has a mutation status of A132A, The gene SGSM2 has a mutation status of S37T, The gene SPNS3 has a mutation status of T352I, The gene PITPNM3 has a mutation status of E445Q, The gene TP53 has a mutation status of T125T, The gene WRAP53 has a mutation status of S234Y, The gene PIK3R6 has a mutation status of E253E, The gene PIK3R5 has a mutation status of T774T, The gene GAS7 has a mutation status of A283A, The gene CDRT4 has a mutation status of R140R, The gene MIEF2 has a mutation status of S273R, The gene ULK2 has a mutation status of T844T, The gene MAP2K3 has a mutation status of Y214*, The gene PHF12 has a mutation status of L998L, The gene TMEM132E has a mutation status of S76S, The gene CCL4L2 has a mutation status of S29R, The gene CCL4L2 has a mutation status of P67R, The gene THRA has a mutation status of A382P, The gene KRT24 has a mutation status of T405T, The gene KRTAP4-9 has a mutation status of S133R, The gene KRT19 has a mutation status of Y61S, The gene GPATCH8 has a mutation status of R973K, The gene TSPOAP1 has a mutation status of V258L, The gene RNF43 has a mutation status of R330fs, The gene MTMR4 has a mutation status of R1026W, The gene HELZ has a mutation status of E760G, The gene COG1 has a mutation status of E408E, The gene SDK2 has a mutation status of W1447G, The gene CYGB has a mutation status of A82P, The gene CYGB has a mutation status of H81P, The gene TNRC6C has a mutation status of A1449S, The gene ENGASE has a mutation status of S520T, The gene SIRT7 has a mutation status of K310N, The gene NOTUM has a mutation status of Q465R, The gene FASN has a mutation status of Y891*, The gene RNMT has a mutation status of P422S, The gene ASXL3 has a mutation status of A1463P, The gene ASXL3 has a mutation status of S1523S, The gene SIGLEC15 has a mutation status of S126*, The gene EPG5 has a mutation status of E1412K, The gene ZBTB7C has a mutation status of C369*, The gene ONECUT2 has a mutation status of H297P, The gene CDH20 has a mutation status of H571P, The gene SERPINB8 has a mutation status of Y220H, The gene TMX3 has a mutation status of D323E, The gene PLPPR3 has a mutation status of S31F, The gene ABCA7 has a mutation status of L1403fs, The gene MOB3A has a mutation status of H165H, The gene TJP3 has a mutation status of S112S, The gene PRR36 has a mutation status of H513H, The gene FBN3 has a mutation status of F2468S, The gene MUC16 has a mutation status of S11018T, The gene ANGPTL6 has a mutation status of G378C, The gene TYK2 has a mutation status of S430P, The gene TYK2 has a mutation status of D429P, The gene ZNF442 has a mutation status of R583H, The gene BRD4 has a mutation status of H829P, The gene SIN3B has a mutation status of D829A, The gene SIN3B has a mutation status of A1000V, The gene CPAMD8 has a mutation status of V433M, The gene FCHO1 has a mutation status of E511E, The gene JAK3 has a mutation status of D130A, The gene ELL has a mutation status of P371P, The gene NCAN has a mutation status of F344F, The gene NCAN has a mutation status of S346P, The gene ZNF100 has a mutation status of H331D, The gene KMT2B has a mutation status of P1953P, The gene ALKBH6 has a mutation status of D144Y, The gene LRFN1 has a mutation status of T190T, The gene NUMBL has a mutation status of P541P, The gene NUMBL has a mutation status of P506P, The gene MEGF8 has a mutation status of T944P, The gene MEGF8 has a mutation status of E2614G, The gene ZNF226 has a mutation status of F428L, The gene DHX34 has a mutation status of N888K, The gene RUVBL2 has a mutation status of V389L, The gene CCDC155 has a mutation status of V54G, The gene MYBPC2 has a mutation status of R677Q, The gene ZNF613 has a mutation status of Y400Y, The gene ZNF813 has a mutation status of T447M, The gene PRPF31 has a mutation status of V295G, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of H300Y, The gene LILRB3 has a mutation status of M21V, The gene LILRB2 has a mutation status of A596P, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene EPS8L1 has a mutation status of S310S, The gene PTPRH has a mutation status of P608P, The gene ISOC2 has a mutation status of V146G, The gene NLRP4 has a mutation status of K128N, The gene ZNF8 has a mutation status of T370S, The gene ZNF324B has a mutation status of R152H, The gene SIRPA has a mutation status of L44S, The gene TGM6 has a mutation status of Y266*, The gene LZTS3 has a mutation status of E607G, The gene LZTS3 has a mutation status of P180S, The gene RRBP1 has a mutation status of H666P, The gene DNMT3B has a mutation status of V700L, The gene TRPC4AP has a mutation status of P706A, The gene ARHGAP40 has a mutation status of Q293K, The gene PREX1 has a mutation status of P765L, The gene ZNFX1 has a mutation status of R1354R, The gene PHACTR3 has a mutation status of D179N, The gene LAMA5 has a mutation status of R2953R, The gene LAMA5 has a mutation status of A2375G, The gene GATA5 has a mutation status of A324P, The gene ADAMTS1 has a mutation status of E58G, The gene GRIK1 has a mutation status of A106G, The gene CRYZL1 has a mutation status of I135I, The gene DSCAM has a mutation status of Y763*, The gene COL18A1 has a mutation status of S1388S, The gene MCM3AP has a mutation status of F1584L, The gene PCNT has a mutation status of D801H, The gene ESS2 has a mutation status of V244A, The gene GSTT4 has a mutation status of Q197R, The gene MYO18B has a mutation status of L1392P, The gene LIF has a mutation status of N31N, The gene SMTN has a mutation status of V330L, The gene SLC5A4 has a mutation status of V243I, The gene MPST has a mutation status of F189L, The gene SLC16A8 has a mutation status of V283L, The gene SGSM3 has a mutation status of H494H, The gene ACO2 has a mutation status of G312G, The gene PARVG has a mutation status of A86G, The gene PPARA has a mutation status of C248C, The gene DENND6B has a mutation status of D178fs, The gene NLGN4X has a mutation status of P11S, The gene FAM9A has a mutation status of M301I, The gene CLTRN has a mutation status of L8L, The gene ZRSR2 has a mutation status of R467G, The gene MAGEB3 has a mutation status of N147I, The gene MAGEB1 has a mutation status of Q23*, The gene MAOB has a mutation status of A19G, The gene TBC1D25 has a mutation status of G93R, The gene TFE3 has a mutation status of T313T, The gene TFE3 has a mutation status of A312P, The gene CCDC120 has a mutation status of T355P, The gene MAGIX has a mutation status of P297L, The gene FGD1 has a mutation status of Q631Q, The gene ZXDA has a mutation status of T310A, The gene AMER1 has a mutation status of F685S, The gene ZC3H12B has a mutation status of Y742*, The gene NHSL2 has a mutation status of Y715*, The gene CYSLTR1 has a mutation status of I123T, The gene CYLC1 has a mutation status of S296C, The gene COL4A6 has a mutation status of L9V, The gene PAK3 has a mutation status of E96*, The gene GPR101 has a mutation status of N100T, The gene DKC1 has a mutation status of R138G, The gene MT-CO1 has a mutation status of A122T, The gene MT-CO3 has a mutation status of G113G, The gene MT-ND3 has a mutation status of G40S, The gene MT-ND4 has a mutation status of A131A
PAAD
The gene TTLL10 has a mutation status of P604T, The gene ACAP3 has a mutation status of N415N, The gene MIB2 has a mutation status of V816M, The gene NADK has a mutation status of H89H, The gene PANK4 has a mutation status of P433P, The gene NPHP4 has a mutation status of S621S, The gene PIK3CD has a mutation status of T739P, The gene TMEM51 has a mutation status of H102P, The gene SPEN has a mutation status of R1859W, The gene CROCC has a mutation status of L340L, The gene KLHDC7A has a mutation status of D606A, The gene UBXN10 has a mutation status of M34V, The gene VWA5B1 has a mutation status of R879H, The gene EIF4G3 has a mutation status of Q16Q, The gene CNR2 has a mutation status of S69S, The gene ARID1A has a mutation status of F1924fs, The gene SYTL1 has a mutation status of Q3H, The gene DCDC2B has a mutation status of L26L, The gene SYNC has a mutation status of T278A, The gene KIAA1522 has a mutation status of S114P, The gene TMEM54 has a mutation status of V71I, The gene DLGAP3 has a mutation status of D753D, The gene C1orf216 has a mutation status of Q190R, The gene CLSPN has a mutation status of L619L, The gene POU3F1 has a mutation status of A429A, The gene NFYC has a mutation status of R252R, The gene SLC6A9 has a mutation status of P524T, The gene ERI3 has a mutation status of G232G, The gene MYSM1 has a mutation status of P760L, The gene MYSM1 has a mutation status of D382fs, The gene KANK4 has a mutation status of G682S, The gene WDR78 has a mutation status of V554I, The gene LRRC7 has a mutation status of A721T, The gene ERICH3 has a mutation status of D139G, The gene ST6GALNAC5 has a mutation status of P36S, The gene ADGRL4 has a mutation status of S81S, The gene SYDE2 has a mutation status of D173Y, The gene SYDE2 has a mutation status of R70L, The gene CLCA4 has a mutation status of L299L, The gene ZNF644 has a mutation status of S65S, The gene ABCD3 has a mutation status of R266S, The gene SLC44A3 has a mutation status of M424T, The gene OLFM3 has a mutation status of H415fs, The gene TMEM167B has a mutation status of I10I, The gene DCLRE1B has a mutation status of P459A, The gene PTGFRN has a mutation status of R152R, The gene CHD1L has a mutation status of Y871*, The gene NBPF9 has a mutation status of N855D, The gene RFX5 has a mutation status of R328R, The gene POGZ has a mutation status of R1008R, The gene FLG has a mutation status of V4006V, The gene IVL has a mutation status of L483Q, The gene PGLYRP4 has a mutation status of T224I, The gene S100A9 has a mutation status of E99K, The gene DCST2 has a mutation status of T455T, The gene IQGAP3 has a mutation status of R630W, The gene TTC24 has a mutation status of D328Y, The gene NCSTN has a mutation status of A570A, The gene ARHGAP30 has a mutation status of Q213Q, The gene RC3H1 has a mutation status of L970L, The gene TNR has a mutation status of R899Q, The gene PAPPA2 has a mutation status of P1679T, The gene ABL2 has a mutation status of P109L, The gene KIAA1614 has a mutation status of L208L, The gene KIAA1614 has a mutation status of H214Y, The gene BRINP3 has a mutation status of E421K, The gene CFHR5 has a mutation status of G450G, The gene ASCL5 has a mutation status of H206N, The gene IGFN1 has a mutation status of G2851G, The gene AVPR1B has a mutation status of P139P, The gene CR2 has a mutation status of T67S, The gene C1orf74 has a mutation status of Y183C, The gene FAM71A has a mutation status of I39M, The gene FLVCR1 has a mutation status of R301W, The gene LYPLAL1 has a mutation status of R136I, The gene MTARC1 has a mutation status of C119C, The gene NVL has a mutation status of S121S, The gene TMEM63A has a mutation status of N368S, The gene OBSCN has a mutation status of W8228R, The gene H3-4 has a mutation status of K37Q, The gene H2BU1 has a mutation status of S57S, The gene CAPN9 has a mutation status of A661G, The gene MTR has a mutation status of S574S, The gene KMO has a mutation status of I224V, The gene EXO1 has a mutation status of A671V, The gene OR2G3 has a mutation status of A99A, The gene OR2T27 has a mutation status of A110A, The gene EIPR1 has a mutation status of L296M, The gene FKBP1B has a mutation status of E4D, The gene FKBP1B has a mutation status of T86T, The gene ADCY3 has a mutation status of K501N, The gene ALK has a mutation status of M1478T, The gene THADA has a mutation status of S1933T, The gene PRKCE has a mutation status of N108K, The gene LHCGR has a mutation status of T521T, The gene B3GNT2 has a mutation status of L146L, The gene CYP26B1 has a mutation status of C148R, The gene CCDC142 has a mutation status of Y113fs, The gene CCDC142 has a mutation status of A112V, The gene FOXI3 has a mutation status of R338H, The gene TMEM131 has a mutation status of P494R, The gene VWA3B has a mutation status of R1207R, The gene LONRF2 has a mutation status of Q210H, The gene ST6GAL2 has a mutation status of L321L, The gene PSD4 has a mutation status of T819P, The gene MARCO has a mutation status of D233N, The gene CLASP1 has a mutation status of I1453I, The gene ARHGEF4 has a mutation status of P829T, The gene TANC1 has a mutation status of D1703G, The gene FIGN has a mutation status of P723T, The gene SCN7A has a mutation status of A1282V, The gene TLK1 has a mutation status of A222A, The gene MAP3K20 has a mutation status of S599P, The gene CDCA7 has a mutation status of C75C, The gene AGPS has a mutation status of P29T, The gene TTN has a mutation status of T26116T, The gene TTN has a mutation status of V24360I, The gene TTN has a mutation status of I12472M, The gene FSIP2 has a mutation status of K6771K, The gene OSGEPL1 has a mutation status of T44I, The gene DNAH7 has a mutation status of S3568S, The gene C2CD6 has a mutation status of K1122I, The gene CRYGA has a mutation status of P83S, The gene IDH1 has a mutation status of L209L, The gene BARD1 has a mutation status of S241C, The gene FN1 has a mutation status of I1807I, The gene TNS1 has a mutation status of G615S, The gene CFAP65 has a mutation status of L1204F, The gene ANKZF1 has a mutation status of S517N, The gene AC053503.6 has a mutation status of C100S, The gene AC053503.6 has a mutation status of H101P, The gene OBSL1 has a mutation status of G1284S, The gene COL4A4 has a mutation status of V260V, The gene SLC19A3 has a mutation status of S381T, The gene NGEF has a mutation status of R110*, The gene USP40 has a mutation status of A523T, The gene UGT1A4 has a mutation status of P10P, The gene PER2 has a mutation status of V175L, The gene CAND2 has a mutation status of A499I, The gene SLC22A13 has a mutation status of G504G, The gene SCN5A has a mutation status of D1656D, The gene KIF15 has a mutation status of N1016N, The gene SCAP has a mutation status of A1067T, The gene PLXNB1 has a mutation status of V1767M, The gene PLXNB1 has a mutation status of G858G, The gene COL7A1 has a mutation status of A1071T, The gene NICN1 has a mutation status of I135fs, The gene BSN has a mutation status of Q240Q, The gene RNF123 has a mutation status of F435V, The gene RBM15B has a mutation status of V182V, The gene DNAH1 has a mutation status of R2928H, The gene ITIH3 has a mutation status of P26R, The gene ADAMTS9 has a mutation status of S259S, The gene PDZRN3 has a mutation status of D561D, The gene CIP2A has a mutation status of K582M, The gene MORC1 has a mutation status of P759P, The gene MORC1 has a mutation status of V758V, The gene CFAP44 has a mutation status of N1721K, The gene GATA2 has a mutation status of H51Y, The gene TRH has a mutation status of D175E, The gene RYK has a mutation status of L35L, The gene FOXL2 has a mutation status of H291P, The gene SLC9A9 has a mutation status of F88F, The gene SMC4 has a mutation status of R191R, The gene SMC4 has a mutation status of R827fs, The gene SLC2A2 has a mutation status of R432P, The gene GHSR has a mutation status of R357Q, The gene TBCCD1 has a mutation status of R360G, The gene IL1RAP has a mutation status of I302V, The gene MELTF has a mutation status of S59Y, The gene MSX1 has a mutation status of R157S, The gene EVC has a mutation status of L886V, The gene C4orf50 has a mutation status of T1444I, The gene SORCS2 has a mutation status of V881I, The gene SLC2A9 has a mutation status of P222P, The gene HS3ST1 has a mutation status of R205C, The gene BOD1L1 has a mutation status of G45G, The gene FAM184B has a mutation status of P370P, The gene LCORL has a mutation status of G1642R, The gene PGM2 has a mutation status of A329T, The gene ALB has a mutation status of E392E, The gene MAPK10 has a mutation status of L14L, The gene OTUD4 has a mutation status of V317A, The gene MND1 has a mutation status of K70M, The gene ANXA10 has a mutation status of A130T, The gene CEP44 has a mutation status of G30F, The gene WDR17 has a mutation status of A499S, The gene IRF2 has a mutation status of K31K, The gene CCDC110 has a mutation status of S775I, The gene CCDC127 has a mutation status of V199F, The gene AHRR has a mutation status of A300S, The gene AHRR has a mutation status of R365Q, The gene ZDHHC11B has a mutation status of P65P, The gene CPLANE1 has a mutation status of A579V, The gene FYB1 has a mutation status of Q328K, The gene C5orf34 has a mutation status of P29L, The gene HTR1A has a mutation status of K412E, The gene TNPO1 has a mutation status of 357_358insD, The gene VCAN has a mutation status of D2895H, The gene ADGRV1 has a mutation status of G1589R, The gene ARRDC3 has a mutation status of L278L, The gene KIAA0825 has a mutation status of H779R, The gene MCTP1 has a mutation status of G45G, The gene MCC has a mutation status of S674A, The gene DMXL1 has a mutation status of D1597N, The gene SMIM32 has a mutation status of L20V, The gene PCDHA1 has a mutation status of G8G, The gene PCDHA9 has a mutation status of A452E, The gene PCDHA11 has a mutation status of D409Y, The gene GPR151 has a mutation status of C136Y, The gene PDGFRB has a mutation status of R685C, The gene NDST1 has a mutation status of A707V, The gene LCP2 has a mutation status of A137E, The gene HRH2 has a mutation status of Y78*, The gene NSD1 has a mutation status of V2618I, The gene COL23A1 has a mutation status of A67S, The gene HNRNPH1 has a mutation status of G410G, The gene RASGEF1C has a mutation status of G132G, The gene FLT4 has a mutation status of K732K, The gene GMPR has a mutation status of R34C, The gene H1-4 has a mutation status of G56G, The gene H1-3 has a mutation status of K137K, The gene GABBR1 has a mutation status of R494H, The gene HLA-DRB5 has a mutation status of A244A, The gene HLA-DRB1 has a mutation status of W38E, The gene RNF8 has a mutation status of M25G, The gene VEGFA has a mutation status of A28G, The gene ADGRF1 has a mutation status of T721M, The gene MCM3 has a mutation status of G437V, The gene COL19A1 has a mutation status of I133M, The gene MMS22L has a mutation status of I948V, The gene CRYBG1 has a mutation status of R940H, The gene METTL24 has a mutation status of D166D, The gene MAN1A1 has a mutation status of I236M, The gene LAMA2 has a mutation status of Y240H, The gene AKAP7 has a mutation status of E197A, The gene ENPP1 has a mutation status of N179S, The gene VNN2 has a mutation status of N189N, The gene MAS1 has a mutation status of V324V, The gene PRR18 has a mutation status of P226A, The gene DLL1 has a mutation status of T610T, The gene MRM2 has a mutation status of G73S, The gene SNX8 has a mutation status of A18S, The gene FOXK1 has a mutation status of T683P, The gene RADIL has a mutation status of L653L, The gene KDELR2 has a mutation status of D177D, The gene PHF14 has a mutation status of Q640Q, The gene AGR3 has a mutation status of T127A, The gene ABCB5 has a mutation status of H345H, The gene DNAH11 has a mutation status of E566D, The gene FAM126A has a mutation status of N417T, The gene HOXA11 has a mutation status of PSA97del, The gene NOD1 has a mutation status of A687T, The gene SPDYE1 has a mutation status of M304I, The gene ABCA13 has a mutation status of Q1005*, The gene ABCA13 has a mutation status of D3067G, The gene CLIP2 has a mutation status of L419M, The gene GNAI1 has a mutation status of I78I, The gene CALCR has a mutation status of V310V, The gene TECPR1 has a mutation status of A378D, The gene EPHB4 has a mutation status of V228A, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of L1361P, The gene MUC3A has a mutation status of I3082I, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene SPDYE6 has a mutation status of H337R, The gene PRKRIP1 has a mutation status of R127*, The gene LAMB4 has a mutation status of N1574K, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene AKR1B15 has a mutation status of A67T, The gene EPHA1 has a mutation status of T177P, The gene AOC1 has a mutation status of V192L, The gene GALNT11 has a mutation status of D197Y, The gene PTPRN2 has a mutation status of N793N, The gene VIPR2 has a mutation status of T396P, The gene USP17L7 has a mutation status of K234Q, The gene ZNF703 has a mutation status of H421P, The gene ASH2L has a mutation status of H538R, The gene ADAM9 has a mutation status of R465Q, The gene SPIDR has a mutation status of V643M, The gene SOX17 has a mutation status of K107K, The gene TGS1 has a mutation status of S96G, The gene CHD7 has a mutation status of 123_125MGV>I, The gene SULF1 has a mutation status of T314T, The gene XKR9 has a mutation status of F313F, The gene NECAB1 has a mutation status of N107D, The gene PDP1 has a mutation status of N477N, The gene SPAG1 has a mutation status of Y158Y, The gene UBR5 has a mutation status of V842A, The gene COL14A1 has a mutation status of K1376K, The gene ZNF572 has a mutation status of R289C, The gene SQLE has a mutation status of L435L, The gene OPLAH has a mutation status of E724K, The gene HGH1 has a mutation status of V159G, The gene MROH1 has a mutation status of A1153A, The gene SCRT1 has a mutation status of S16P, The gene FREM1 has a mutation status of D947Y, The gene HAUS6 has a mutation status of S409S, The gene IFNA17 has a mutation status of A42G, The gene GDA has a mutation status of G40G, The gene PRUNE2 has a mutation status of T815I, The gene AUH has a mutation status of R87L, The gene CARD19 has a mutation status of L118L, The gene DNAJC25 has a mutation status of E281D, The gene ASTN2 has a mutation status of Y1193H, The gene DAB2IP has a mutation status of L1020M, The gene SLC25A25 has a mutation status of A198A, The gene SPACA9 has a mutation status of L103V, The gene LCN9 has a mutation status of D19N, The gene TMEM250 has a mutation status of V10G, The gene CCDC187 has a mutation status of A321T, The gene PFKP has a mutation status of S771S, The gene ITIH5 has a mutation status of A552V, The gene EBLN1 has a mutation status of G28W, The gene MAP3K8 has a mutation status of R59C, The gene PARD3 has a mutation status of R294Q, The gene BMS1 has a mutation status of P414P, The gene BMS1 has a mutation status of G440G, The gene OR13A1 has a mutation status of L319F, The gene WDFY4 has a mutation status of S859S, The gene WDFY4 has a mutation status of A2990A, The gene ERCC6 has a mutation status of R735L, The gene OGDHL has a mutation status of A630V, The gene ASAH2 has a mutation status of F394S, The gene STOX1 has a mutation status of G763G, The gene UNC5B has a mutation status of R269C, The gene DNAJB12 has a mutation status of E304K, The gene KAT6B has a mutation status of K1243R, The gene KCNMA1 has a mutation status of A560A, The gene TMEM254 has a mutation status of R92R, The gene KIF20B has a mutation status of N1213N, The gene NOC3L has a mutation status of A122V, The gene PIK3AP1 has a mutation status of E551K, The gene SLIT1 has a mutation status of T1480M, The gene RRP12 has a mutation status of S429L, The gene HPSE2 has a mutation status of S243C, The gene SEMA4G has a mutation status of R415S, The gene FAM160B1 has a mutation status of Y111C, The gene ABRAXAS2 has a mutation status of Q183*, The gene SCART1 has a mutation status of S658*, The gene MUC5AC has a mutation status of T4991P, The gene TRPM5 has a mutation status of G541V, The gene OR52J3 has a mutation status of R82C, The gene OR2AG2 has a mutation status of S109S, The gene OLFML1 has a mutation status of S320S, The gene SCUBE2 has a mutation status of R456C, The gene MICAL2 has a mutation status of P1732T, The gene PARVA has a mutation status of L68L, The gene OTOG has a mutation status of G2808G, The gene TMEM86A has a mutation status of G169R, The gene NAV2 has a mutation status of S140S, The gene PAMR1 has a mutation status of S473S, The gene LRP4 has a mutation status of H1322P, The gene LRP4 has a mutation status of N94N, The gene MADD has a mutation status of E1337D, The gene RAPSN has a mutation status of G47D, The gene AGBL2 has a mutation status of P177S, The gene TRIM48 has a mutation status of A208V, The gene OR5I1 has a mutation status of A119T, The gene OR9G1 has a mutation status of I196F, The gene CTNND1 has a mutation status of I747V, The gene OR6Q1 has a mutation status of A190T, The gene OR9Q1 has a mutation status of F168del, The gene OR10Q1 has a mutation status of L157fs, The gene MS4A14 has a mutation status of A309S, The gene DDB1 has a mutation status of L1000V, The gene MYRF has a mutation status of I628I, The gene ZBTB3 has a mutation status of A335P, The gene GPR137 has a mutation status of P421L, The gene CCDC88B has a mutation status of L63L, The gene SF1 has a mutation status of P473P, The gene PACS1 has a mutation status of V499L, The gene CD248 has a mutation status of G172G, The gene TBX10 has a mutation status of H183H, The gene LRP5 has a mutation status of V600V, The gene P2RY6 has a mutation status of V102F, The gene THRSP has a mutation status of P76S, The gene GRM5 has a mutation status of R26R, The gene FAT3 has a mutation status of E136Q, The gene HEPHL1 has a mutation status of C366Y, The gene NCAM1 has a mutation status of C235C, The gene NXPE4 has a mutation status of N279T, The gene SIK3 has a mutation status of A322T, The gene C2CD2L has a mutation status of P497S, The gene BSX has a mutation status of P92S, The gene VWA5A has a mutation status of S197S, The gene IGSF9B has a mutation status of P1286P, The gene KCNA1 has a mutation status of P109P, The gene SCNN1A has a mutation status of S518S, The gene USP5 has a mutation status of E438E, The gene PDE3A has a mutation status of Y149S, The gene PDE3A has a mutation status of G953F, The gene KRAS has a mutation status of G12V, The gene KMT2D has a mutation status of V5180V, The gene KRT5 has a mutation status of G570G, The gene KRT76 has a mutation status of L450L, The gene HNRNPA1 has a mutation status of V159L, The gene OR6C6 has a mutation status of C139Y, The gene OR6C6 has a mutation status of L67S, The gene RDH16 has a mutation status of S312N, The gene LRP1 has a mutation status of E153E, The gene AGAP2 has a mutation status of G171S, The gene AVIL has a mutation status of R230C, The gene XPOT has a mutation status of R778L, The gene LRRC10 has a mutation status of A151A, The gene TRHDE has a mutation status of S365S, The gene ACSS3 has a mutation status of L294L, The gene HSP90B1 has a mutation status of R116R, The gene DTX1 has a mutation status of R440C, The gene DDX54 has a mutation status of Y243Y, The gene BICDL1 has a mutation status of D233Y, The gene ACADS has a mutation status of P85S, The gene ACADS has a mutation status of L96L, The gene DNAH10 has a mutation status of R2911H, The gene PIWIL1 has a mutation status of S726P, The gene ZNF605 has a mutation status of T97A, The gene PARP4 has a mutation status of L427F, The gene FLT3 has a mutation status of P336L, The gene FRY has a mutation status of T24T, The gene KL has a mutation status of D202D, The gene SMAD9 has a mutation status of P145Q, The gene SLC25A15 has a mutation status of V156L, The gene THSD1 has a mutation status of Q351Q, The gene ACOD1 has a mutation status of L128F, The gene SLAIN1 has a mutation status of S181*, The gene SLITRK6 has a mutation status of I621T, The gene PCCA has a mutation status of T8T, The gene TMTC4 has a mutation status of F160C, The gene NALCN has a mutation status of A276A, The gene COL4A1 has a mutation status of Q985H, The gene OR4K5 has a mutation status of Y193F, The gene RNASE11 has a mutation status of A134S, The gene ARHGEF40 has a mutation status of G1476G, The gene CARMIL3 has a mutation status of L304L, The gene PRKD1 has a mutation status of Q876*, The gene NKX2-8 has a mutation status of E29Q, The gene L2HGDH has a mutation status of I392V, The gene SAMD4A has a mutation status of T53P, The gene GPR135 has a mutation status of A461G, The gene RTN1 has a mutation status of S408S, The gene SYT16 has a mutation status of S230S, The gene SPTB has a mutation status of L567Q, The gene FUT8 has a mutation status of P72P, The gene DCAF4 has a mutation status of R35Q, The gene NEK9 has a mutation status of T123T, The gene IRF2BPL has a mutation status of L579V, The gene ADCK1 has a mutation status of G20G, The gene RTL1 has a mutation status of P51L, The gene EXOC3L4 has a mutation status of S380G, The gene CEP170B has a mutation status of K284K, The gene NDN has a mutation status of A74A, The gene NPAP1 has a mutation status of I797V, The gene TRPM1 has a mutation status of V1604V, The gene SLC12A6 has a mutation status of G322S, The gene KNL1 has a mutation status of R1006K, The gene TTBK2 has a mutation status of P487A, The gene DUOX1 has a mutation status of T1030T, The gene MYO5A has a mutation status of A1821T, The gene VPS13C has a mutation status of L86L, The gene LACTB has a mutation status of M5I, The gene CILP has a mutation status of W155*, The gene HCN4 has a mutation status of P882P, The gene LOXL1 has a mutation status of A140A, The gene TMC3 has a mutation status of K310R, The gene ACAN has a mutation status of Q497L, The gene ACAN has a mutation status of A948P, The gene IGF1R has a mutation status of P190P, The gene RHBDL1 has a mutation status of S5*, The gene CHTF18 has a mutation status of E175Q, The gene PKD1 has a mutation status of V3752G, The gene GPR139 has a mutation status of S21S, The gene IGSF6 has a mutation status of G168S, The gene MAZ has a mutation status of P32L, The gene RNF40 has a mutation status of R702C, The gene SETD1A has a mutation status of F820F, The gene CHD9 has a mutation status of I317M, The gene CHD9 has a mutation status of V2078I, The gene CDH16 has a mutation status of G352G, The gene ZNF19 has a mutation status of E217K, The gene ATMIN has a mutation status of M309V, The gene JPH3 has a mutation status of T465T, The gene ANKRD11 has a mutation status of Y2438C, The gene ANKRD11 has a mutation status of Y2015S, The gene WDR81 has a mutation status of R786M, The gene HIC1 has a mutation status of A510T, The gene PELP1 has a mutation status of P478L, The gene KIF1C has a mutation status of R912W, The gene NLRP1 has a mutation status of T878T, The gene ELP5 has a mutation status of G26S, The gene PLSCR3 has a mutation status of F66fs, The gene TP53 has a mutation status of P153fs, The gene DNAH2 has a mutation status of S312S, The gene ALOX12B has a mutation status of L187L, The gene HES7 has a mutation status of P200S, The gene GLP2R has a mutation status of R261H, The gene MYH8 has a mutation status of W133C, The gene MYH4 has a mutation status of R1254C, The gene MYH3 has a mutation status of R704C, The gene CDRT15 has a mutation status of K4N, The gene TRPV2 has a mutation status of L479R, The gene SLC47A1 has a mutation status of E275K, The gene NOS2 has a mutation status of V925V, The gene SARM1 has a mutation status of A234P, The gene SPAG5 has a mutation status of T309I, The gene ABHD15 has a mutation status of S235R, The gene CCL4L2 has a mutation status of P67R, The gene MSL1 has a mutation status of H410H, The gene IGFBP4 has a mutation status of A36A, The gene KRT9 has a mutation status of G146D, The gene MEOX1 has a mutation status of Q13H, The gene FAM171A2 has a mutation status of S664S, The gene ADAM11 has a mutation status of G356G, The gene OSBPL7 has a mutation status of C453G, The gene ANKFN1 has a mutation status of I596F, The gene MRC2 has a mutation status of P66L, The gene TANC2 has a mutation status of S69N, The gene SLC39A11 has a mutation status of T119T, The gene CD300C has a mutation status of V127A, The gene OTOP2 has a mutation status of T394I, The gene OTOP2 has a mutation status of P442P, The gene FOXJ1 has a mutation status of D58Y, The gene AATK has a mutation status of P1033L, The gene FAAP100 has a mutation status of P61P, The gene LRRC45 has a mutation status of L177M, The gene ZNF750 has a mutation status of G606A, The gene PIEZO2 has a mutation status of Y975Y, The gene LOXHD1 has a mutation status of G628D, The gene ST8SIA5 has a mutation status of E353E, The gene SMAD4 has a mutation status of E442*, The gene ZNF236 has a mutation status of V432I, The gene CTDP1 has a mutation status of A687A, The gene MISP has a mutation status of A392V, The gene KISS1R has a mutation status of N208N, The gene ARID3A has a mutation status of G37S, The gene PCSK4 has a mutation status of V111G, The gene PLK5 has a mutation status of G134G, The gene ADAT3 has a mutation status of R120R, The gene AMH has a mutation status of R123Q, The gene S1PR4 has a mutation status of V297I, The gene STAP2 has a mutation status of E307E, The gene INSR has a mutation status of Y1361C, The gene CLEC4G has a mutation status of D65E, The gene FBN3 has a mutation status of Q1473R, The gene ACTL9 has a mutation status of T77N, The gene COL5A3 has a mutation status of R525R, The gene CACNA1A has a mutation status of T665M, The gene CCDC130 has a mutation status of D302D, The gene PODNL1 has a mutation status of E440*, The gene MISP3 has a mutation status of P8P, The gene ADGRL1 has a mutation status of G1322G, The gene SLC1A6 has a mutation status of L271L, The gene C19orf44 has a mutation status of D346E, The gene ANKLE1 has a mutation status of S509S, The gene UPF1 has a mutation status of T616T, The gene CILP2 has a mutation status of M952I, The gene ZNF676 has a mutation status of K311fs, The gene TDRD12 has a mutation status of Q1129K, The gene SLC7A10 has a mutation status of S56S, The gene ZFP14 has a mutation status of T279T, The gene ZNF420 has a mutation status of G683S, The gene ZNF585B has a mutation status of N525H, The gene ACP7 has a mutation status of S199T, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene ATP1A3 has a mutation status of A592A, The gene CLASRP has a mutation status of A358A, The gene PPP1R37 has a mutation status of P562P, The gene IGFL4 has a mutation status of L44L, The gene FKRP has a mutation status of Y88S, The gene BICRA has a mutation status of A573A, The gene TMEM143 has a mutation status of T273P, The gene LMTK3 has a mutation status of A880A, The gene PRR12 has a mutation status of H1334R, The gene SCAF1 has a mutation status of R928S, The gene ACP4 has a mutation status of T306P, The gene CD33 has a mutation status of I198M, The gene CD33 has a mutation status of V294L, The gene SIGLEC5 has a mutation status of L334I, The gene SIGLEC5 has a mutation status of S333Y, The gene PRPF31 has a mutation status of L366L, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene NLRP2 has a mutation status of A131V, The gene PTPRH has a mutation status of A661A, The gene KMT5C has a mutation status of G275G, The gene ZNF865 has a mutation status of G784G, The gene SIRPA has a mutation status of L44S, The gene PANK2 has a mutation status of R165R, The gene PLCB1 has a mutation status of Q593K, The gene MACROD2 has a mutation status of M64I, The gene DZANK1 has a mutation status of Q279*, The gene FOXS1 has a mutation status of R67R, The gene PDRG1 has a mutation status of D50N, The gene EFCAB8 has a mutation status of A1106A, The gene BPIFB3 has a mutation status of V60F, The gene BPIFB4 has a mutation status of L81F, The gene C20orf144 has a mutation status of R89R, The gene GSS has a mutation status of T299S, The gene LPIN3 has a mutation status of D477Y, The gene PTPRT has a mutation status of P489S, The gene SLC2A10 has a mutation status of Q338H, The gene SALL4 has a mutation status of G117R, The gene GNAS has a mutation status of L20M, The gene NELFCD has a mutation status of A32A, The gene SYCP2 has a mutation status of D1341D, The gene CDH26 has a mutation status of R368T, The gene CDH4 has a mutation status of T414T, The gene LAMA5 has a mutation status of P1847P, The gene MYT1 has a mutation status of L901L, The gene KRTAP27-1 has a mutation status of R10I, The gene KRTAP19-5 has a mutation status of Y66Y, The gene RCAN1 has a mutation status of V28G, The gene KRTAP10-8 has a mutation status of V11V, The gene PCNT has a mutation status of D2148D, The gene BCL2L13 has a mutation status of A2A, The gene BID has a mutation status of N53N, The gene CLDN5 has a mutation status of V32G, The gene SLC7A4 has a mutation status of C494Y, The gene GSTT4 has a mutation status of Q197R, The gene GGT5 has a mutation status of H43H, The gene GUCD1 has a mutation status of W33L, The gene KIAA1671 has a mutation status of T681T, The gene SEZ6L has a mutation status of Y648Y, The gene HPS4 has a mutation status of P247P, The gene NF2 has a mutation status of A405A, The gene MYH9 has a mutation status of P633P, The gene KCNJ4 has a mutation status of G102G, The gene CACNA1I has a mutation status of Q1798P, The gene MEI1 has a mutation status of T40P, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TCF20 has a mutation status of R26R, The gene PRR5 has a mutation status of R256C, The gene TTLL8 has a mutation status of P29L, The gene KLHDC7B has a mutation status of P1172T, The gene AKAP17A has a mutation status of K307K, The gene KLHL15 has a mutation status of Y91*, The gene GPR82 has a mutation status of S226R, The gene CHST7 has a mutation status of A362A, The gene RGN has a mutation status of A177V, The gene ELK1 has a mutation status of A260A, The gene PRICKLE3 has a mutation status of G208G, The gene USP51 has a mutation status of T223N, The gene TAF1 has a mutation status of R1029H, The gene DACH2 has a mutation status of S357C, The gene COL4A5 has a mutation status of P1094S, The gene RBMXL3 has a mutation status of R273H, The gene BCORL1 has a mutation status of H1014H, The gene CD99L2 has a mutation status of S195C, The gene CNGA2 has a mutation status of D662E, The gene FLNA has a mutation status of N931D, The gene LAGE3 has a mutation status of I121T, The gene MT-ND1 has a mutation status of G120G, The gene MT-CO1 has a mutation status of Y409Y, The gene MT-CO2 has a mutation status of P145P, The gene MT-ATP6 has a mutation status of T146T, The gene MT-CO3 has a mutation status of G30G, The gene MT-CO3 has a mutation status of L206L, The gene MT-ND5 has a mutation status of T251T, The gene MT-ND6 has a mutation status of P23P
PAAD
The gene MXRA8 has a mutation status of V214G, The gene FNDC10 has a mutation status of H225P, The gene TNFRSF25 has a mutation status of C141Y, The gene AGTRAP has a mutation status of L98L, The gene C1orf167 has a mutation status of L854L, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of M105L, The gene ZBTB17 has a mutation status of P473A, The gene SH2D5 has a mutation status of V64I, The gene WASF2 has a mutation status of P260S, The gene SPOCD1 has a mutation status of E632A, The gene GJB3 has a mutation status of T238P, The gene CAP1 has a mutation status of R313G, The gene PTPRF has a mutation status of L1128P, The gene C8B has a mutation status of T342fs, The gene KANK4 has a mutation status of A593S, The gene LRRC7 has a mutation status of G896G, The gene AMPD2 has a mutation status of G34G, The gene AP4B1 has a mutation status of H446L, The gene TRIM33 has a mutation status of Y974H, The gene GJA8 has a mutation status of D3N, The gene PIP5K1A has a mutation status of L165fs, The gene PIP5K1A has a mutation status of L165L, The gene S100A7A has a mutation status of Q101R, The gene PBXIP1 has a mutation status of G184G, The gene ADAM15 has a mutation status of P22P, The gene RXFP4 has a mutation status of V243G, The gene IGSF8 has a mutation status of E394Q, The gene TEDDM1 has a mutation status of L92L, The gene RGL1 has a mutation status of E692V, The gene NIBAN1 has a mutation status of K62N, The gene HMCN1 has a mutation status of R1522C, The gene RGS2 has a mutation status of I110V, The gene ASPM has a mutation status of Y1146C, The gene PTPRC has a mutation status of L830F, The gene NUAK2 has a mutation status of R268W, The gene CR2 has a mutation status of G540R, The gene KIF26B has a mutation status of E995D, The gene KIF26B has a mutation status of L996P, The gene GREB1 has a mutation status of P295L, The gene DTNB has a mutation status of T556P, The gene EMILIN1 has a mutation status of R706S, The gene ZNF513 has a mutation status of R523W, The gene EHD3 has a mutation status of A534S, The gene CYP1B1 has a mutation status of R175R, The gene DNAH6 has a mutation status of R1153G, The gene SMYD1 has a mutation status of V114G, The gene SMYD1 has a mutation status of E115G, The gene AL845331.2 has a mutation status of R39R, The gene ST6GAL2 has a mutation status of V261V, The gene LRP1B has a mutation status of V4301V, The gene RIF1 has a mutation status of G2317G, The gene NEB has a mutation status of E7717G, The gene NEB has a mutation status of T3361T, The gene SCN1A has a mutation status of L1606V, The gene TTN has a mutation status of M1187I, The gene KCTD18 has a mutation status of V227G, The gene CYP20A1 has a mutation status of C334S, The gene TNS1 has a mutation status of T1227P, The gene STK11IP has a mutation status of S8Y, The gene TRIP12 has a mutation status of E323Q, The gene NMUR1 has a mutation status of H206H, The gene ASB18 has a mutation status of A327G, The gene KLHL30 has a mutation status of T544P, The gene CNTN6 has a mutation status of G678S, The gene SRGAP3 has a mutation status of P886P, The gene ATG7 has a mutation status of P426L, The gene SLC4A7 has a mutation status of S695N, The gene OSBPL10 has a mutation status of E719E, The gene SCN10A has a mutation status of N812T, The gene CSPG5 has a mutation status of R398S, The gene PLXNB1 has a mutation status of D236G, The gene UBA7 has a mutation status of H229H, The gene DNAH1 has a mutation status of D811D, The gene NISCH has a mutation status of V861L, The gene ZNF654 has a mutation status of T922I, The gene BBX has a mutation status of A397V, The gene CD200R1L has a mutation status of G181V, The gene ADPRH has a mutation status of W289L, The gene LRRIQ4 has a mutation status of T473T, The gene NLGN1 has a mutation status of R280H, The gene MUC20 has a mutation status of 466_467EA>DT, The gene RUBCN has a mutation status of V652F, The gene TMEM175 has a mutation status of H484P, The gene MSANTD1 has a mutation status of R76H, The gene EVC2 has a mutation status of R698*, The gene BOD1L1 has a mutation status of E2853E, The gene SLIT2 has a mutation status of F1354Y, The gene DTHD1 has a mutation status of K856K, The gene KIAA1109 has a mutation status of S4120S, The gene FAT4 has a mutation status of D609D, The gene SMARCA5 has a mutation status of G35S, The gene LRBA has a mutation status of L849R, The gene FHDC1 has a mutation status of L754M, The gene TKTL2 has a mutation status of G470E, The gene TRIM75P has a mutation status of C97C, The gene ADCY2 has a mutation status of G385G, The gene SNX18 has a mutation status of G186G, The gene RGS7BP has a mutation status of R85R, The gene FAM151B has a mutation status of A75S, The gene ANKRD34B has a mutation status of T442A, The gene VCAN has a mutation status of S599S, The gene ADAMTS19 has a mutation status of P113P, The gene SLC35A4 has a mutation status of L64L, The gene SPINK1 has a mutation status of I6I, The gene WWC1 has a mutation status of L6L, The gene OR2V2 has a mutation status of M165I, The gene FOXC1 has a mutation status of L518F, The gene RPP40 has a mutation status of I125T, The gene DSP has a mutation status of A2148S, The gene CAP2 has a mutation status of V353A, The gene H1-2 has a mutation status of K184E, The gene TRIM39 has a mutation status of R238Q, The gene HLA-C has a mutation status of L294C, The gene HLA-C has a mutation status of T187E, The gene HLA-DRB1 has a mutation status of S66N, The gene GCM1 has a mutation status of E89E, The gene GFRAL has a mutation status of A329E, The gene ZNF451 has a mutation status of F221C, The gene TTK has a mutation status of R414G, The gene PRDM13 has a mutation status of Y288S, The gene FRK has a mutation status of P402P, The gene SERINC1 has a mutation status of M61I, The gene TAAR5 has a mutation status of P68L, The gene GRM1 has a mutation status of L865L, The gene OPRM1 has a mutation status of R55T, The gene MAP3K4 has a mutation status of S764I, The gene THBS2 has a mutation status of L1152L, The gene FAM120B has a mutation status of R105S, The gene ELFN1 has a mutation status of R240P, The gene FOXK1 has a mutation status of T682P, The gene TNRC18 has a mutation status of G304G, The gene UBE2D4 has a mutation status of T11I, The gene IKZF1 has a mutation status of H351Q, The gene EGFR has a mutation status of L813R, The gene ZNF736 has a mutation status of F6I, The gene POM121C has a mutation status of S802del, The gene COPS6 has a mutation status of A6G, The gene COPS6 has a mutation status of A7G, The gene AGFG2 has a mutation status of G18S, The gene FBXO24 has a mutation status of L50F, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene SPDYE6 has a mutation status of H337R, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene NDUFB2 has a mutation status of C8S, The gene NOBOX has a mutation status of D154H, The gene REPIN1 has a mutation status of T76P, The gene RBM33 has a mutation status of Q600H, The gene VIPR2 has a mutation status of T396P, The gene DLGAP2 has a mutation status of D300D, The gene MYOM2 has a mutation status of R101*, The gene TRIM35 has a mutation status of S65S, The gene PTK2B has a mutation status of N883S, The gene YTHDF3 has a mutation status of P86R, The gene VCPIP1 has a mutation status of S65S, The gene RALYL has a mutation status of R171S, The gene TRAPPC9 has a mutation status of A340V, The gene PTP4A3 has a mutation status of P112T, The gene HRCT1 has a mutation status of 104_105insHHHHHP, The gene PRUNE2 has a mutation status of L318I, The gene WNK2 has a mutation status of V461G, The gene TLR4 has a mutation status of D194D, The gene OR1L4 has a mutation status of T215S, The gene SLC27A4 has a mutation status of V435I, The gene FCN2 has a mutation status of D4N, The gene PPP1R26 has a mutation status of R294W, The gene WDR37 has a mutation status of L425L, The gene ASB13 has a mutation status of K261N, The gene GAD2 has a mutation status of S13S, The gene CCNY has a mutation status of L84V, The gene FZD8 has a mutation status of L262L, The gene FUT11 has a mutation status of V8G, The gene BLNK has a mutation status of R106R, The gene PIK3AP1 has a mutation status of A364V, The gene CALHM1 has a mutation status of G87S, The gene COL17A1 has a mutation status of Y1337Y, The gene GSTO2 has a mutation status of E76*, The gene RBM20 has a mutation status of N80T, The gene HSPA12A has a mutation status of G630G, The gene INPP5F has a mutation status of R69Q, The gene CHST15 has a mutation status of N441S, The gene PWWP2B has a mutation status of T97P, The gene RNH1 has a mutation status of D47Y, The gene MUC6 has a mutation status of S278P, The gene MUC6 has a mutation status of Y277S, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of P1158P, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of T2793K, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4116S, The gene MUC5AC has a mutation status of T4781T, The gene TOLLIP has a mutation status of V33G, The gene BRSK2 has a mutation status of I49I, The gene KCNQ1 has a mutation status of R401R, The gene OR52R1 has a mutation status of I314L, The gene HBB has a mutation status of T88P, The gene UEVLD has a mutation status of F44S, The gene BBOX1 has a mutation status of S359T, The gene PEX16 has a mutation status of E273G, The gene TRIM51 has a mutation status of H245H, The gene OR9G1 has a mutation status of T62V, The gene DTX4 has a mutation status of T375K, The gene SYT7 has a mutation status of A382T, The gene CCDC88B has a mutation status of R246G, The gene CCDC88B has a mutation status of A741A, The gene MRGPRD has a mutation status of S270S, The gene NADSYN1 has a mutation status of L229L, The gene NADSYN1 has a mutation status of D361G, The gene ARHGEF17 has a mutation status of G257A, The gene MAP6 has a mutation status of H39P, The gene RSF1 has a mutation status of S1364T, The gene MMP3 has a mutation status of R316H, The gene PAFAH1B2 has a mutation status of I118I, The gene TMPRSS13 has a mutation status of Q83R, The gene OAF has a mutation status of V134G, The gene FKBP4 has a mutation status of P119S, The gene GALNT8 has a mutation status of E387V, The gene KCNA6 has a mutation status of E168E, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PDE3A has a mutation status of Y149S, The gene ANO6 has a mutation status of A616A, The gene FAIM2 has a mutation status of C223F, The gene DIP2B has a mutation status of Q876R, The gene MAP3K12 has a mutation status of G660G, The gene NFE2 has a mutation status of R323H, The gene LRIG3 has a mutation status of P69P, The gene LRIG3 has a mutation status of L68L, The gene KCNC2 has a mutation status of E136K, The gene GLIPR1L1 has a mutation status of P110A, The gene TMTC2 has a mutation status of A134S, The gene CFAP54 has a mutation status of T2256R, The gene HCFC2 has a mutation status of E384Q, The gene TXNRD1 has a mutation status of L455L, The gene GIT2 has a mutation status of R142I, The gene CUX2 has a mutation status of A755T, The gene OAS3 has a mutation status of V456I, The gene ZCCHC8 has a mutation status of A667V, The gene AL445989.1 has a mutation status of T38S, The gene MYCBP2 has a mutation status of V1136I, The gene HS6ST3 has a mutation status of V468G, The gene CUL4A has a mutation status of N383D, The gene ISM2 has a mutation status of R454W, The gene SLC24A4 has a mutation status of P346R, The gene TRAF3 has a mutation status of V47M, The gene GOLGA8S has a mutation status of R472C, The gene AVEN has a mutation status of A249A, The gene RPAP1 has a mutation status of A967V, The gene SLC12A1 has a mutation status of N166S, The gene SNX1 has a mutation status of S229del, The gene FBXO22 has a mutation status of S273S, The gene ACSBG1 has a mutation status of S159S, The gene ADAMTS7 has a mutation status of S1031S, The gene TLNRD1 has a mutation status of T223I, The gene TICRR has a mutation status of S1623S, The gene WDR93 has a mutation status of H236L, The gene MESP2 has a mutation status of K254N, The gene WDR90 has a mutation status of T1626T, The gene CLCN7 has a mutation status of V630G, The gene CCNF has a mutation status of T442P, The gene VPS35L has a mutation status of M73R, The gene GP2 has a mutation status of 483_484insL, The gene ACSM2A has a mutation status of Q363E, The gene SULT1A4 has a mutation status of T7P, The gene CDIPT has a mutation status of L62L, The gene CORO1A has a mutation status of T193P, The gene DRC7 has a mutation status of S327T, The gene CMTM2 has a mutation status of P141T, The gene SLC12A4 has a mutation status of C781F, The gene CRISPLD2 has a mutation status of Y373*, The gene NXN has a mutation status of Y199D, The gene BCL6B has a mutation status of P368Q, The gene NTN1 has a mutation status of T375P, The gene ATPAF2 has a mutation status of S24R, The gene ATPAF2 has a mutation status of G22G, The gene LLGL1 has a mutation status of R734*, The gene EFCAB5 has a mutation status of G1117E, The gene GOSR1 has a mutation status of R112R, The gene ASIC2 has a mutation status of L128F, The gene CCL4L2 has a mutation status of P67R, The gene LHX1 has a mutation status of T206P, The gene TTC25 has a mutation status of E543E, The gene ATP6V0A1 has a mutation status of E107K, The gene COL1A1 has a mutation status of R865R, The gene ABCA5 has a mutation status of E449K, The gene C17orf80 has a mutation status of D601N, The gene SDK2 has a mutation status of W1447G, The gene NUP85 has a mutation status of D580D, The gene MYO15B has a mutation status of V2892G, The gene ZBTB14 has a mutation status of A434A, The gene DSG4 has a mutation status of M148V, The gene ASXL3 has a mutation status of F1023Y, The gene ATP8B1 has a mutation status of V997M, The gene DIPK1C has a mutation status of Q408K, The gene SALL3 has a mutation status of A185L, The gene NFATC1 has a mutation status of P66P, The gene RBFA has a mutation status of G6G, The gene TPGS1 has a mutation status of D223Y, The gene ATP8B3 has a mutation status of S781*, The gene NFIC has a mutation status of T384M, The gene TBXA2R has a mutation status of G56G, The gene DPP9 has a mutation status of Y835S, The gene PTPRS has a mutation status of F1147L, The gene C3 has a mutation status of K1375Q, The gene MYO1F has a mutation status of F525L, The gene MUC16 has a mutation status of S9540A, The gene CACNA1A has a mutation status of L1701P, The gene CACNA1A has a mutation status of Q1673K, The gene NWD1 has a mutation status of V1278V, The gene SLC25A42 has a mutation status of R276Q, The gene ZNF431 has a mutation status of R571K, The gene TSHZ3 has a mutation status of T824M, The gene KIRREL2 has a mutation status of N338T, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene NOVA2 has a mutation status of P127P, The gene PNKP has a mutation status of N425T, The gene ZNF841 has a mutation status of L129F, The gene CACNG7 has a mutation status of E68E, The gene LILRB3 has a mutation status of M21V, The gene PTPRH has a mutation status of C245F, The gene NLRP11 has a mutation status of N813S, The gene RPS5 has a mutation status of E98K, The gene SIGLEC1 has a mutation status of R578W, The gene PLCB1 has a mutation status of P238P, The gene VSX1 has a mutation status of F300I, The gene RIMS4 has a mutation status of R217P, The gene PREX1 has a mutation status of L1467L, The gene SLC9A8 has a mutation status of F391V, The gene OSBPL2 has a mutation status of V239I, The gene LAMA5 has a mutation status of G92G, The gene NTSR1 has a mutation status of V302M, The gene MYT1 has a mutation status of E354E, The gene LTN1 has a mutation status of D1370G, The gene KRTAP19-5 has a mutation status of Y13Y, The gene SCAF4 has a mutation status of 718_719insP, The gene SYNJ1 has a mutation status of Y724C, The gene BRWD1 has a mutation status of D570D, The gene KRTAP10-7 has a mutation status of G248S, The gene FAM207A has a mutation status of T85T, The gene COL6A1 has a mutation status of G452G, The gene IL17RA has a mutation status of E186K, The gene GSTT4 has a mutation status of Q197R, The gene MN1 has a mutation status of A1226T, The gene NPTXR has a mutation status of A172P, The gene XRCC6 has a mutation status of G138R, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SCUBE1 has a mutation status of I353I, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene CLCN4 has a mutation status of T728M, The gene TLR7 has a mutation status of S827S, The gene CNKSR2 has a mutation status of E445E, The gene FAM47B has a mutation status of H294H, The gene DGKK has a mutation status of S1112S, The gene BMP15 has a mutation status of F314L, The gene HUWE1 has a mutation status of R1676H, The gene PHF8 has a mutation status of T757T, The gene WNK3 has a mutation status of A536T, The gene CXorf65 has a mutation status of Y74Y, The gene ARMCX1 has a mutation status of G126W, The gene CT47B1 has a mutation status of V153L, The gene MBNL3 has a mutation status of S122A, The gene HS6ST2 has a mutation status of T25P, The gene SPANXN2 has a mutation status of A36A, The gene F8 has a mutation status of L646*, The gene MT-ND2 has a mutation status of T226T, The gene MT-ND4L has a mutation status of L40L, The gene MT-ND4 has a mutation status of L351L, The gene MT-ND5 has a mutation status of G582D
LUAD
The gene PLEKHN1 has a mutation status of G606G, The gene SCNN1D has a mutation status of E419K, The gene INTS11 has a mutation status of H226H, The gene PRXL2B has a mutation status of G10G, The gene CHD5 has a mutation status of D1363G, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF14 has a mutation status of C388C, The gene PRAMEF14 has a mutation status of R386S, The gene ARHGEF10L has a mutation status of D276V, The gene PAQR7 has a mutation status of L328I, The gene PAQR7 has a mutation status of I327S, The gene PTPRU has a mutation status of S1185S, The gene TMEM234 has a mutation status of ASAGLQR28del, The gene CSMD2 has a mutation status of G46G, The gene GJB3 has a mutation status of V84I, The gene ERMAP has a mutation status of R216Q, The gene MPL has a mutation status of V124V, The gene NASP has a mutation status of A203A, The gene IPP has a mutation status of I392M, The gene MAST2 has a mutation status of G1703G, The gene GLIS1 has a mutation status of N603S, The gene PARS2 has a mutation status of A280A, The gene TTC22 has a mutation status of A151A, The gene FYB2 has a mutation status of S727S, The gene C8A has a mutation status of L9S, The gene LRRIQ3 has a mutation status of F35C, The gene DIPK1A has a mutation status of P14P, The gene AMY2A has a mutation status of R95S, The gene FNDC7 has a mutation status of S239S, The gene GSTM2 has a mutation status of N59S, The gene ST7L has a mutation status of P496S, The gene LRIG2 has a mutation status of L124L, The gene ANKRD35 has a mutation status of E266D, The gene BCL9 has a mutation status of N799D, The gene BCAN has a mutation status of R321R, The gene SPTA1 has a mutation status of V2410I, The gene FCRLA has a mutation status of I81I, The gene PRRC2C has a mutation status of V1323V, The gene RGS16 has a mutation status of A154A, The gene ASPM has a mutation status of Y2245H, The gene PTPRC has a mutation status of Y455Y, The gene PLEKHA6 has a mutation status of P871P, The gene IKBKE has a mutation status of T483M, The gene C1orf115 has a mutation status of H38H, The gene CDC42BPA has a mutation status of R1275C, The gene CDC42BPA has a mutation status of C678C, The gene AGT has a mutation status of A434V, The gene CHML has a mutation status of D10D, The gene EXO1 has a mutation status of R93K, The gene OR14K1 has a mutation status of P180P, The gene OR2T4 has a mutation status of A120T, The gene MBOAT2 has a mutation status of T468A, The gene ASAP2 has a mutation status of R835C, The gene LPIN1 has a mutation status of P398A, The gene DDX1 has a mutation status of K535T, The gene RAD51AP2 has a mutation status of E901*, The gene PSME4 has a mutation status of V106L, The gene BMP10 has a mutation status of A417A, The gene C2orf78 has a mutation status of E310K, The gene PSD4 has a mutation status of P434P, The gene SAP130 has a mutation status of V721F, The gene UGGT1 has a mutation status of V993I, The gene ZRANB3 has a mutation status of R272L, The gene LRP1B has a mutation status of V3868M, The gene G6PC2 has a mutation status of G114R, The gene TTC30A has a mutation status of G3G, The gene PJVK has a mutation status of L88V, The gene ITGAV has a mutation status of R618L, The gene CXCR1 has a mutation status of S327I, The gene SLC11A1 has a mutation status of L393L, The gene USP37 has a mutation status of R348K, The gene RNF25 has a mutation status of G429S, The gene CYP27A1 has a mutation status of K134T, The gene CFAP65 has a mutation status of A1177A, The gene DNAJB2 has a mutation status of L126P, The gene SPEG has a mutation status of P852P, The gene UGT1A5 has a mutation status of R241R, The gene COL6A3 has a mutation status of D1293E, The gene KLHL30 has a mutation status of E68K, The gene ITPR1 has a mutation status of M945I, The gene TMEM43 has a mutation status of Y371H, The gene NR1D2 has a mutation status of N326N, The gene VILL has a mutation status of E448K, The gene MOBP has a mutation status of S13S, The gene ENTPD3 has a mutation status of A13E, The gene ULK4 has a mutation status of T60S, The gene NKTR has a mutation status of Q322R, The gene ZNF662 has a mutation status of R55G, The gene CAMP has a mutation status of R49W, The gene DALRD3 has a mutation status of Q213E, The gene LAMB2 has a mutation status of R1267H, The gene STAB1 has a mutation status of G2479G, The gene NEK4 has a mutation status of P2P, The gene CACNA1D has a mutation status of V1250I, The gene TASOR has a mutation status of V1456F, The gene IL17RD has a mutation status of K72K, The gene BBX has a mutation status of S178S, The gene BOC has a mutation status of G309R, The gene POGLUT1 has a mutation status of L285L, The gene SEMA5B has a mutation status of G888W, The gene TRIM42 has a mutation status of R94H, The gene SI has a mutation status of D671E, The gene BCHE has a mutation status of L456R, The gene LRRC31 has a mutation status of G408V, The gene HTR3D has a mutation status of T447T, The gene CHRD has a mutation status of G15V, The gene LRCH3 has a mutation status of P212S, The gene GAK has a mutation status of G1115S, The gene DGKQ has a mutation status of G378R, The gene DOK7 has a mutation status of H445N, The gene CCKAR has a mutation status of S424L, The gene NFXL1 has a mutation status of D194D, The gene PDGFRA has a mutation status of S1013S, The gene KDR has a mutation status of L912L, The gene KDR has a mutation status of A775A, The gene NOA1 has a mutation status of L73L, The gene IGFBP7 has a mutation status of T188S, The gene EPHA5 has a mutation status of S673T, The gene CXCL6 has a mutation status of L47L, The gene FRAS1 has a mutation status of S2190F, The gene AFF1 has a mutation status of G152S, The gene ANK2 has a mutation status of V3174M, The gene TRAM1L1 has a mutation status of L202R, The gene DDX60L has a mutation status of P1366S, The gene ADCY2 has a mutation status of M693I, The gene ADAMTS12 has a mutation status of K617K, The gene MTREX has a mutation status of G32G, The gene ELOVL7 has a mutation status of N260N, The gene BDP1 has a mutation status of R94S, The gene BDP1 has a mutation status of Y2397D, The gene ADGRV1 has a mutation status of A602T, The gene WDR36 has a mutation status of P688P, The gene TRPC7 has a mutation status of K677I, The gene PURA has a mutation status of R150R, The gene SH3TC2 has a mutation status of R77W, The gene RANBP17 has a mutation status of H970Q, The gene STC2 has a mutation status of R154Q, The gene ZNF354C has a mutation status of K438N, The gene MAML1 has a mutation status of H549Y, The gene MGAT4B has a mutation status of K59R, The gene FLT4 has a mutation status of K732K, The gene FLT4 has a mutation status of E336K, The gene OR2Y1 has a mutation status of R90H, The gene H2AC8 has a mutation status of E62E, The gene H3C6 has a mutation status of T23A, The gene BTN3A2 has a mutation status of L227L, The gene UBD has a mutation status of H102H, The gene HLA-B has a mutation status of Y140L, The gene BAG6 has a mutation status of P388H, The gene MSH5 has a mutation status of G676G, The gene SRPK1 has a mutation status of T341M, The gene CD109 has a mutation status of A138A, The gene FILIP1 has a mutation status of A923A, The gene TENT5A has a mutation status of G76D, The gene BACH2 has a mutation status of G778R, The gene GPRC6A has a mutation status of V608I, The gene TRDN has a mutation status of S667T, The gene NCOA7 has a mutation status of D300N, The gene PTPRK has a mutation status of A6E, The gene LATS1 has a mutation status of R174C, The gene SNX9 has a mutation status of F148F, The gene CHST12 has a mutation status of S211S, The gene SLC29A4 has a mutation status of F81F, The gene ANKMY2 has a mutation status of K146K, The gene DNAH11 has a mutation status of P2198L, The gene DNAH11 has a mutation status of T4219T, The gene OGDH has a mutation status of Y417Y, The gene PKD1L1 has a mutation status of S1948S, The gene VWC2 has a mutation status of A126V, The gene COBL has a mutation status of H533H, The gene POM121 has a mutation status of P738P, The gene FZD9 has a mutation status of G434G, The gene DTX2 has a mutation status of L274R, The gene SLC25A40 has a mutation status of S105N, The gene PPP1R9A has a mutation status of R917C, The gene ZAN has a mutation status of C2301R, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T303V, The gene MUC3A has a mutation status of M384T, The gene MUC3A has a mutation status of S395T, The gene MUC3A has a mutation status of T1234A, The gene RELN has a mutation status of L1696L, The gene LAMB4 has a mutation status of V1506V, The gene PNPLA8 has a mutation status of Y483H, The gene WNT16 has a mutation status of I70I, The gene HTR5A has a mutation status of R67H, The gene MYOM2 has a mutation status of L1022F, The gene DEFB1 has a mutation status of S32S, The gene RP1L1 has a mutation status of L87P, The gene PDGFRL has a mutation status of E315D, The gene MTUS1 has a mutation status of T58T, The gene PLPP5 has a mutation status of W51L, The gene ADAM9 has a mutation status of Y412Y, The gene CYP7A1 has a mutation status of N233S, The gene ZFHX4 has a mutation status of G1952D, The gene ZFHX4 has a mutation status of N3248K, The gene ATP6V0D2 has a mutation status of L49R, The gene SLC26A7 has a mutation status of G200E, The gene RBM12B has a mutation status of R267W, The gene RGS22 has a mutation status of *1084R, The gene PKHD1L1 has a mutation status of G1737G, The gene FER1L6 has a mutation status of C1021C, The gene TG has a mutation status of S1450R, The gene KHDRBS3 has a mutation status of R164R, The gene KCNK9 has a mutation status of V221M, The gene MAPK15 has a mutation status of S447S, The gene SCRIB has a mutation status of A1277T, The gene PLEC has a mutation status of H3717H, The gene PLEC has a mutation status of R3600H, The gene PARP10 has a mutation status of A800V, The gene MROH1 has a mutation status of A1497V, The gene RECQL4 has a mutation status of Y1177Y, The gene RCL1 has a mutation status of D40N, The gene FOCAD has a mutation status of I1477V, The gene MELK has a mutation status of S486*, The gene NTRK2 has a mutation status of Y175Y, The gene LPAR1 has a mutation status of I352T, The gene BSPRY has a mutation status of D270D, The gene TNC has a mutation status of A1055D, The gene OR1J4 has a mutation status of L15Q, The gene SH2D3C has a mutation status of V285V, The gene ZDHHC12 has a mutation status of R111W, The gene NUP188 has a mutation status of H152H, The gene USP20 has a mutation status of T62T, The gene LAMC3 has a mutation status of R785H, The gene DDX31 has a mutation status of F14L, The gene MYMK has a mutation status of S119L, The gene PPP1R26 has a mutation status of S180N, The gene NACC2 has a mutation status of A153A, The gene NOTCH1 has a mutation status of C456C, The gene CACNA1B has a mutation status of L1642L, The gene CACNA1B has a mutation status of P1738P, The gene KLF6 has a mutation status of R198R, The gene SKIDA1 has a mutation status of E422E, The gene ABI1 has a mutation status of G304A, The gene ARMC4 has a mutation status of N664S, The gene NCOA4 has a mutation status of V407F, The gene ANK3 has a mutation status of D2775N, The gene BMPR1A has a mutation status of Q3P, The gene EXOSC1 has a mutation status of G101E, The gene TACC2 has a mutation status of P1147L, The gene DMBT1 has a mutation status of A165V, The gene EDRF1 has a mutation status of P13P, The gene C10orf90 has a mutation status of D114fs, The gene VENTX has a mutation status of E101K, The gene PNPLA2 has a mutation status of P269L, The gene MUC5AC has a mutation status of L4460fs, The gene KCNQ1 has a mutation status of A370A, The gene OR52I2 has a mutation status of L17F, The gene OR52A5 has a mutation status of G18R, The gene OR51B5 has a mutation status of V248I, The gene UBQLN3 has a mutation status of H95Q, The gene OVCH2 has a mutation status of P328A, The gene ARNTL has a mutation status of E217E, The gene MRGPRX2 has a mutation status of R61G, The gene NELL1 has a mutation status of Q454E, The gene DCDC1 has a mutation status of N544N, The gene QSER1 has a mutation status of A1171V, The gene KIAA1549L has a mutation status of A1047A, The gene ABTB2 has a mutation status of R711G, The gene AGBL2 has a mutation status of A478A, The gene OR4A15 has a mutation status of I172T, The gene OR5I1 has a mutation status of R263W, The gene OR8K5 has a mutation status of R20Q, The gene OR5J2 has a mutation status of A237A, The gene OR9G1 has a mutation status of T62V, The gene MPEG1 has a mutation status of D177N, The gene OR4D10 has a mutation status of A188T, The gene TMEM109 has a mutation status of R37Q, The gene HNRNPUL2 has a mutation status of G340A, The gene CHRM1 has a mutation status of Q165Q, The gene PCNX3 has a mutation status of L1208L, The gene SF3B2 has a mutation status of F505F, The gene PC has a mutation status of S293S, The gene SYT12 has a mutation status of R207W, The gene SYT12 has a mutation status of E232K, The gene KDM2A has a mutation status of S104G, The gene ALDH3B1 has a mutation status of G301S, The gene RNF121 has a mutation status of L24F, The gene CLPB has a mutation status of P45P, The gene GAB2 has a mutation status of T609T, The gene CCDC89 has a mutation status of E329V, The gene SLC36A4 has a mutation status of R75T, The gene KDM4D has a mutation status of D499E, The gene BIRC2 has a mutation status of S131A, The gene NPAT has a mutation status of R230Q, The gene RDX has a mutation status of D298H, The gene CCDC153 has a mutation status of V109G, The gene GRIK4 has a mutation status of R262C, The gene JHY has a mutation status of D72N, The gene OR8D4 has a mutation status of L144L, The gene OR8G5 has a mutation status of S53F, The gene ROBO4 has a mutation status of T404A, The gene KCNJ5 has a mutation status of L215L, The gene TMEM45B has a mutation status of I181I, The gene ERC1 has a mutation status of K615Q, The gene LRTM2 has a mutation status of I149M, The gene A2M has a mutation status of H358Y, The gene STYK1 has a mutation status of H249H, The gene TAS2R31 has a mutation status of 150_151KE>NQ, The gene BORCS5 has a mutation status of R182W, The gene BCAT1 has a mutation status of E61A, The gene GXYLT1 has a mutation status of C414H, The gene DDN has a mutation status of G525A, The gene LARP4 has a mutation status of T116A, The gene KRT79 has a mutation status of Y234*, The gene WSCD2 has a mutation status of R238C, The gene FAM222A has a mutation status of A176V, The gene TPCN1 has a mutation status of T675N, The gene VSIG10 has a mutation status of P252T, The gene MORN3 has a mutation status of E228A, The gene TCTN2 has a mutation status of Q306*, The gene ADGRD1 has a mutation status of H435H, The gene POLE has a mutation status of K1550R, The gene CDX2 has a mutation status of L249S, The gene TSC22D1 has a mutation status of H2H, The gene COG3 has a mutation status of Y133S, The gene LCP1 has a mutation status of T89S, The gene CLDN10 has a mutation status of A71P, The gene SLC15A1 has a mutation status of T281T, The gene CARS2 has a mutation status of G60R, The gene ATP11A has a mutation status of I79T, The gene UPF3A has a mutation status of H372R, The gene RIPK3 has a mutation status of L242fs, The gene RIPK3 has a mutation status of S241*, The gene AKAP6 has a mutation status of D235N, The gene RALGAPA1 has a mutation status of S1322F, The gene VCPKMT has a mutation status of E6Q, The gene CDKL1 has a mutation status of I33M, The gene TBPL2 has a mutation status of Y21*, The gene OTX2 has a mutation status of P27H, The gene DCAF4 has a mutation status of I258I, The gene NPAP1 has a mutation status of I141T, The gene ATP10A has a mutation status of R717R, The gene ARHGAP11A has a mutation status of A423T, The gene RPUSD2 has a mutation status of R302W, The gene INO80 has a mutation status of S3L, The gene TGM5 has a mutation status of M285I, The gene CKMT1B has a mutation status of R340H, The gene TERB2 has a mutation status of *221Q, The gene VPS13C has a mutation status of H1100L, The gene PML has a mutation status of L146L, The gene DNAJA4 has a mutation status of P125P, The gene AGBL1 has a mutation status of F910L, The gene AEN has a mutation status of P224P, The gene GNG13 has a mutation status of E33Q, The gene RPS2 has a mutation status of V282M, The gene C16orf71 has a mutation status of R210C, The gene PPL has a mutation status of E1334K, The gene MYH11 has a mutation status of D623G, The gene PDILT has a mutation status of T60S, The gene NPIPB11 has a mutation status of H49Q, The gene GNAO1 has a mutation status of D201D, The gene OGFOD1 has a mutation status of K380K, The gene CMTM3 has a mutation status of G50R, The gene PLA2G15 has a mutation status of A81V, The gene CDH1 has a mutation status of PIFVPP484del, The gene HYDIN has a mutation status of R2520C, The gene ZFHX3 has a mutation status of K3259E, The gene FA2H has a mutation status of H146P, The gene TMEM170A has a mutation status of A16A, The gene ADAMTS18 has a mutation status of P262P, The gene MLYCD has a mutation status of L401L, The gene WFDC1 has a mutation status of S166T, The gene ZCCHC14 has a mutation status of T519P, The gene VPS9D1 has a mutation status of A562T, The gene SPIRE2 has a mutation status of Y149Y, The gene MYO1C has a mutation status of R224Q, The gene DPH1 has a mutation status of R47Q, The gene HIC1 has a mutation status of E463D, The gene CHRNB1 has a mutation status of M344T, The gene ZBTB4 has a mutation status of K344K, The gene TP53 has a mutation status of R248Q, The gene ARHGAP44 has a mutation status of P732L, The gene ANKRD13B has a mutation status of N352S, The gene CCL4L2 has a mutation status of T39T, The gene CCL4L2 has a mutation status of P67R, The gene LASP1 has a mutation status of Y57Y, The gene RAPGEFL1 has a mutation status of R142W, The gene CNP has a mutation status of R19C, The gene DGKE has a mutation status of T538T, The gene RNF43 has a mutation status of T58S, The gene AC127029.3 has a mutation status of A250T, The gene KPNA2 has a mutation status of A523T, The gene ABCA9 has a mutation status of D383N, The gene ABCA6 has a mutation status of L1543L, The gene GRB2 has a mutation status of Y52N, The gene EVPL has a mutation status of A1032A, The gene MFSD11 has a mutation status of I94I, The gene AATK has a mutation status of P1080P, The gene TBCD has a mutation status of R320C, The gene TUBB8B has a mutation status of R320C, The gene LAMA1 has a mutation status of D1247N, The gene RBBP8 has a mutation status of M99T, The gene ATP8B1 has a mutation status of S1232W, The gene NETO1 has a mutation status of V512I, The gene ABCA7 has a mutation status of N58K, The gene ZNF554 has a mutation status of S420S, The gene UBXN6 has a mutation status of R80Q, The gene PLIN5 has a mutation status of R134W, The gene ZNRF4 has a mutation status of R162C, The gene CATSPERD has a mutation status of D339D, The gene ZNF557 has a mutation status of S183N, The gene CACNA1A has a mutation status of R1056C, The gene C19orf53 has a mutation status of A19T, The gene PRKACA has a mutation status of G127G, The gene NWD1 has a mutation status of M503V, The gene SSBP4 has a mutation status of G217S, The gene SUGP2 has a mutation status of R81T, The gene ZNF99 has a mutation status of K124M, The gene ZNF91 has a mutation status of P1163S, The gene ZNF30 has a mutation status of C543*, The gene ZNF570 has a mutation status of K244K, The gene RYR1 has a mutation status of P1773S, The gene NFKBIB has a mutation status of A2V, The gene MRPS12 has a mutation status of T15I, The gene FCGBP has a mutation status of TCRPSGGSL1234del, The gene ZNF227 has a mutation status of P450S, The gene GPR4 has a mutation status of S348S, The gene DHX34 has a mutation status of R806W, The gene TMEM143 has a mutation status of G187V, The gene PLEKHA4 has a mutation status of R91R, The gene SLC6A16 has a mutation status of S25fs, The gene AP2A1 has a mutation status of A157A, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of W205Q, The gene LILRB3 has a mutation status of T201M, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene TNNT1 has a mutation status of R265R, The gene ZNF460 has a mutation status of V9F, The gene SIRPA has a mutation status of L44S, The gene FASTKD5 has a mutation status of L91L, The gene PAX1 has a mutation status of G390A, The gene CCM2L has a mutation status of Q88K, The gene DNMT3B has a mutation status of Y681Y, The gene RPN2 has a mutation status of T507T, The gene PLCG1 has a mutation status of D315G, The gene ZSWIM3 has a mutation status of E639K, The gene ZNFX1 has a mutation status of V1106V, The gene APCDD1L has a mutation status of A333T, The gene DIDO1 has a mutation status of V763I, The gene C21orf91 has a mutation status of I203V, The gene SYNJ1 has a mutation status of Q1250R, The gene IL10RB has a mutation status of A255T, The gene DONSON has a mutation status of T410I, The gene CBR1 has a mutation status of R74L, The gene MORC3 has a mutation status of Y917Y, The gene MX1 has a mutation status of R402R, The gene KRTAP10-6 has a mutation status of C25R, The gene ADARB1 has a mutation status of E485E, The gene ADARB1 has a mutation status of G593G, The gene ADA2 has a mutation status of Y453H, The gene BCL2L13 has a mutation status of S80fs, The gene PI4KA has a mutation status of S347F, The gene SSTR3 has a mutation status of A211A, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene CERK has a mutation status of R96H, The gene TBL1X has a mutation status of G217D, The gene POLA1 has a mutation status of V1301I, The gene MAGEB10 has a mutation status of C217R, The gene DIPK2B has a mutation status of L271I, The gene GNL3L has a mutation status of Y351Y, The gene ATP7A has a mutation status of I1464V, The gene NRK has a mutation status of L1280L, The gene RADX has a mutation status of D803V, The gene COL4A6 has a mutation status of G1434G, The gene SLC25A5 has a mutation status of G121C, The gene SLC25A5 has a mutation status of T221R, The gene SLC25A5 has a mutation status of N277S, The gene ATP1B4 has a mutation status of R18H, The gene BCORL1 has a mutation status of G1682fs, The gene MT-ATP6 has a mutation status of A126T, The gene MT-ND4 has a mutation status of Y152Y
STES
The gene CAMTA1 has a mutation status of L1080L, The gene DISP3 has a mutation status of R135W, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene AGMAT has a mutation status of Q264K, The gene SPEN has a mutation status of R1488I, The gene UBR4 has a mutation status of R1394H, The gene PHACTR4 has a mutation status of E523D, The gene RLF has a mutation status of T30S, The gene TMEM125 has a mutation status of P140A, The gene SZT2 has a mutation status of D2816D, The gene PTCH2 has a mutation status of I533T, The gene CYP4A22 has a mutation status of G417D, The gene PRKAA2 has a mutation status of P371T, The gene NFIA has a mutation status of T434P, The gene AMPD2 has a mutation status of R789H, The gene MAB21L3 has a mutation status of R105R, The gene CD2 has a mutation status of C217Y, The gene FAM72B has a mutation status of I131T, The gene NBPF15 has a mutation status of M70I, The gene NBPF20 has a mutation status of L4577L, The gene NBPF11 has a mutation status of L86L, The gene MCL1 has a mutation status of E110del, The gene FCRL3 has a mutation status of L457L, The gene SPTA1 has a mutation status of Q1581H, The gene OR10J1 has a mutation status of T158T, The gene CLEC20A has a mutation status of E386K, The gene COLGALT2 has a mutation status of V475I, The gene HMCN1 has a mutation status of R3635Q, The gene PLA2G4A has a mutation status of H442Q, The gene KCNT2 has a mutation status of I909I, The gene KLHDC8A has a mutation status of S277G, The gene DNAH14 has a mutation status of Q3535K, The gene EPHX1 has a mutation status of V392A, The gene TRIM11 has a mutation status of R37H, The gene OR2T33 has a mutation status of F111F, The gene AGBL5 has a mutation status of R487P, The gene SULT6B1 has a mutation status of A108A, The gene ATL2 has a mutation status of G437G, The gene LHCGR has a mutation status of D564N, The gene BMP10 has a mutation status of G336G, The gene ACOXL has a mutation status of S321N, The gene DDX18 has a mutation status of G41R, The gene TUBA3E has a mutation status of W346C, The gene ARHGEF4 has a mutation status of T441R, The gene SCN3A has a mutation status of E946G, The gene SP3 has a mutation status of G428S, The gene MFSD6 has a mutation status of E777A, The gene ZNF142 has a mutation status of R1165H, The gene SLC4A3 has a mutation status of D458fs, The gene TEX44 has a mutation status of T265T, The gene UGT1A6 has a mutation status of S444I, The gene ATG4B has a mutation status of D200fs, The gene SLC22A13 has a mutation status of A432T, The gene TCAIM has a mutation status of A263V, The gene RRP9 has a mutation status of R8G, The gene BAP1 has a mutation status of Q261*, The gene DNAH12 has a mutation status of E2938E, The gene GPR15 has a mutation status of V252L, The gene KALRN has a mutation status of Y972Y, The gene RARRES1 has a mutation status of S200F, The gene GOLIM4 has a mutation status of A284L, The gene MAP3K13 has a mutation status of P682P, The gene RTP1 has a mutation status of R124S, The gene MB21D2 has a mutation status of H46H, The gene PIGZ has a mutation status of S361fs, The gene SH3TC1 has a mutation status of R354W, The gene NFXL1 has a mutation status of P459A, The gene PDGFRA has a mutation status of T1052T, The gene NOA1 has a mutation status of Q579R, The gene CXCL9 has a mutation status of T125A, The gene KIAA1109 has a mutation status of P1455S, The gene LRBA has a mutation status of Q1459Q, The gene TRIM61 has a mutation status of A448E, The gene TLL1 has a mutation status of L594L, The gene PDCD6 has a mutation status of G123C, The gene C5orf34 has a mutation status of S266R, The gene MAP3K1 has a mutation status of D1369D, The gene ZNF608 has a mutation status of R1326Q, The gene CTNNA1 has a mutation status of Q678*, The gene PCDHB15 has a mutation status of A719V, The gene ADRB2 has a mutation status of E62D, The gene SLC36A1 has a mutation status of R40C, The gene UNC5A has a mutation status of R267W, The gene GMCL2 has a mutation status of K247fs, The gene PPP1R3G has a mutation status of R19Q, The gene GMPR has a mutation status of E167K, The gene LY6G6F-LY6G6D has a mutation status of P192R, The gene SKIV2L has a mutation status of L183V, The gene PRRT1 has a mutation status of A94T, The gene HLA-DRB5 has a mutation status of A244A, The gene HLA-DRB5 has a mutation status of A244T, The gene HLA-DRB5 has a mutation status of Q38W, The gene HSD17B8 has a mutation status of V158L, The gene B3GALT4 has a mutation status of V180A, The gene DNAH8 has a mutation status of R114W, The gene TTBK1 has a mutation status of S1232I, The gene SDHAF4 has a mutation status of P88P, The gene CYB5R4 has a mutation status of D371Y, The gene CEP85L has a mutation status of S33P, The gene REPS1 has a mutation status of V501V, The gene SAMD5 has a mutation status of R173H, The gene DACT2 has a mutation status of V184M, The gene GPNMB has a mutation status of S547I, The gene EVX1 has a mutation status of R319Q, The gene ANKIB1 has a mutation status of R743C, The gene ERVW-1 has a mutation status of Q260*, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of TSHSTPGFTSSITTTET2232del, The gene MUC3A has a mutation status of V2475S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene FLNC has a mutation status of D205Y, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene TBXAS1 has a mutation status of R85W, The gene CNTNAP2 has a mutation status of T968S, The gene GIMAP5 has a mutation status of I148F, The gene ABCB8 has a mutation status of A648G, The gene PAXIP1 has a mutation status of F491C, The gene MFHAS1 has a mutation status of R556H, The gene SGCZ has a mutation status of L57F, The gene PEBP4 has a mutation status of R149P, The gene ADRA1A has a mutation status of G40W, The gene CHRNA2 has a mutation status of A258T, The gene BRF2 has a mutation status of T321T, The gene ZBTB10 has a mutation status of A91V, The gene ENPP2 has a mutation status of R284Q, The gene TOP1MT has a mutation status of S420S, The gene EPPK1 has a mutation status of A2633del, The gene EPPK1 has a mutation status of R1965W, The gene SCRT1 has a mutation status of A133S, The gene SLC39A4 has a mutation status of R251W, The gene NFX1 has a mutation status of V7V, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene PRSS3 has a mutation status of G208R, The gene FRMPD1 has a mutation status of G572D, The gene TRMT10B has a mutation status of Y289L, The gene ABCA1 has a mutation status of C1933C, The gene FRRS1L has a mutation status of R51A, The gene COL27A1 has a mutation status of A92A, The gene CIZ1 has a mutation status of L859L, The gene DNM1 has a mutation status of P816S, The gene ADAMTSL2 has a mutation status of E408K, The gene CCDC187 has a mutation status of L747L, The gene DIP2C has a mutation status of V1264M, The gene AKR1C8P has a mutation status of N172K, The gene ITIH2 has a mutation status of E417K, The gene TAF3 has a mutation status of P366fs, The gene STAM has a mutation status of L314L, The gene ENKUR has a mutation status of D135V, The gene ANKRD26 has a mutation status of P483S, The gene CCNY has a mutation status of G2W, The gene A1CF has a mutation status of T316S, The gene ANK3 has a mutation status of G4220G, The gene ADAMTS14 has a mutation status of G930G, The gene IFIT3 has a mutation status of M1I, The gene AVPI1 has a mutation status of Q32*, The gene HPSE2 has a mutation status of V331V, The gene SORCS1 has a mutation status of K223N, The gene ATRNL1 has a mutation status of N861T, The gene MUC6 has a mutation status of R2392H, The gene NUP98 has a mutation status of G1652V, The gene SMPD1 has a mutation status of S191P, The gene SMPD1 has a mutation status of A194P, The gene IPO7 has a mutation status of A923S, The gene MICAL2 has a mutation status of T1324P, The gene MRGPRX3 has a mutation status of L146L, The gene DNAJC24 has a mutation status of S103fs, The gene SLC39A13 has a mutation status of P127P, The gene PTPRJ has a mutation status of H1104D, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR1S1 has a mutation status of F215I, The gene STIP1 has a mutation status of K60N, The gene ZNHIT2 has a mutation status of A59P, The gene C11orf97 has a mutation status of G46G, The gene OR8G1 has a mutation status of S291fs, The gene ACAD8 has a mutation status of R7R, The gene TAS2R13 has a mutation status of N149S, The gene TAS2R19 has a mutation status of L235R, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PRB4 has a mutation status of R122G, The gene C12orf71 has a mutation status of D43D, The gene SLC2A13 has a mutation status of S15I, The gene LRRK2 has a mutation status of N202N, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of V28K, The gene PPHLN1 has a mutation status of V118M, The gene ADAMTS20 has a mutation status of Y1176C, The gene KCNH3 has a mutation status of P214S, The gene KRT1 has a mutation status of G116S, The gene ZC3H10 has a mutation status of G35R, The gene PAN2 has a mutation status of E373fs, The gene HSD17B6 has a mutation status of A6V, The gene NAB2 has a mutation status of D68D, The gene INHBE has a mutation status of R62T, The gene PPP1R12A has a mutation status of Q767H, The gene LUM has a mutation status of R315H, The gene ACADS has a mutation status of S10S, The gene MLXIP has a mutation status of I575I, The gene HCAR1 has a mutation status of N56fs, The gene DHX37 has a mutation status of I985M, The gene NOC4L has a mutation status of R344C, The gene SMAD9 has a mutation status of A163T, The gene FREM2 has a mutation status of L1034P, The gene MYCBP2 has a mutation status of S3013Y, The gene GPR180 has a mutation status of T32N, The gene COL4A1 has a mutation status of T1449A, The gene ATP4B has a mutation status of A2V, The gene MYH6 has a mutation status of R1398Q, The gene NFKBIA has a mutation status of R143fs, The gene FSCB has a mutation status of E407E, The gene DCAF5 has a mutation status of Y671Y, The gene SLC10A1 has a mutation status of S162P, The gene TMEM63C has a mutation status of F347L, The gene DGLUCY has a mutation status of T613T, The gene PPP4R4 has a mutation status of R558C, The gene WARS1 has a mutation status of E455D, The gene GABRG3 has a mutation status of K425E, The gene STARD9 has a mutation status of S348G, The gene STARD9 has a mutation status of P863S, The gene ANKDD1A has a mutation status of L516L, The gene PDCD7 has a mutation status of P471R, The gene LINGO1 has a mutation status of I595I, The gene TSC2 has a mutation status of D1327D, The gene ADCY9 has a mutation status of R580C, The gene C16orf96 has a mutation status of T567T, The gene AC099489.1 has a mutation status of T1899S, The gene SMG1 has a mutation status of K3583Q, The gene CCP110 has a mutation status of P293R, The gene CHP2 has a mutation status of L122F, The gene KIAA0556 has a mutation status of R1087Q, The gene TMEM219 has a mutation status of L200V, The gene ZNF423 has a mutation status of A44T, The gene NOD2 has a mutation status of A211A, The gene PDPR has a mutation status of Y547F, The gene TMEM231 has a mutation status of E264A, The gene ADAT1 has a mutation status of Q417R, The gene ZNF469 has a mutation status of W3316*, The gene AC092143.1 has a mutation status of A553A, The gene PRPF8 has a mutation status of S2278S, The gene RTN4RL1 has a mutation status of A42A, The gene SPEM3 has a mutation status of P376S, The gene TP53 has a mutation status of G108del, The gene CNTROB has a mutation status of R527W, The gene LLGL1 has a mutation status of L522L, The gene NOS2 has a mutation status of A679S, The gene SLFN5 has a mutation status of G107V, The gene SLFN11 has a mutation status of L595S, The gene RASL10B has a mutation status of V52M, The gene TBC1D3B has a mutation status of S510G, The gene KRT25 has a mutation status of L90L, The gene KRT20 has a mutation status of G164R, The gene KRT19 has a mutation status of L245L, The gene ITGB3 has a mutation status of P433P, The gene TRIM47 has a mutation status of F561fs, The gene NDUFAF8 has a mutation status of A24A, The gene CTIF has a mutation status of V389L, The gene MBD2 has a mutation status of G93C, The gene TNFRSF11A has a mutation status of A576A, The gene TSHZ1 has a mutation status of D497D, The gene ZNF516 has a mutation status of K158N, The gene TPGS1 has a mutation status of V122L, The gene ADAT3 has a mutation status of E36D, The gene CD70 has a mutation status of F152F, The gene MUC16 has a mutation status of T12336L, The gene CYP4F3 has a mutation status of Q377E, The gene PLVAP has a mutation status of K215K, The gene TMEM161A has a mutation status of E85L, The gene ZNF66 has a mutation status of F97F, The gene ZNF676 has a mutation status of H555R, The gene PEPD has a mutation status of G257R, The gene SRRM5 has a mutation status of A410V, The gene ZNF227 has a mutation status of 518_519KR>N*, The gene ZNF229 has a mutation status of Y377S, The gene BICRA has a mutation status of P651H, The gene MYBPC2 has a mutation status of P730L, The gene ZNF808 has a mutation status of Y595*, The gene PRPF31 has a mutation status of R365W, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of H290H, The gene LILRA6 has a mutation status of H290N, The gene LILRA4 has a mutation status of S407T, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene LILRB1 has a mutation status of Y99I, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of G283G, The gene SOX12 has a mutation status of P206P, The gene SIRPA has a mutation status of L44S, The gene TGM6 has a mutation status of L531L, The gene PLCB1 has a mutation status of A743A, The gene BPIFB1 has a mutation status of L409L, The gene TOX2 has a mutation status of R272Q, The gene SLC2A10 has a mutation status of V84A, The gene TRPM2 has a mutation status of E263E, The gene KRTAP10-4 has a mutation status of C387F, The gene SEC14L4 has a mutation status of L106L, The gene MYH9 has a mutation status of H1401del, The gene APOBEC3B has a mutation status of R144H, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene SBF1 has a mutation status of R888H, The gene ZNF674 has a mutation status of E85K, The gene HUWE1 has a mutation status of R481K, The gene ITIH6 has a mutation status of P76L, The gene ZXDA has a mutation status of E447G, The gene TAF1 has a mutation status of L1098L, The gene RPS4X has a mutation status of E97Q, The gene PCDH11X has a mutation status of L515Q, The gene ARMCX3 has a mutation status of V301F, The gene PLS3 has a mutation status of D485A, The gene SLC25A5 has a mutation status of Y165C, The gene TEX13C has a mutation status of L650L, The gene AC236972.4 has a mutation status of P1394A, The gene AC236972.4 has a mutation status of A1486fs, The gene ATP2B3 has a mutation status of P566P, The gene PLXNB3 has a mutation status of Y1336Y, The gene MT-CO2 has a mutation status of G115G, The gene MT-ND4 has a mutation status of L4L, The gene MT-ND5 has a mutation status of S402P, The gene MT-ND6 has a mutation status of V164M
BRCA
The gene TNFRSF18 has a mutation status of P32T, The gene TNFRSF18 has a mutation status of P28H, The gene PRKCZ has a mutation status of D358D, The gene FBXO44 has a mutation status of E59K, The gene CLCN6 has a mutation status of L262L, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene KAZN has a mutation status of L401L, The gene PLEKHM2 has a mutation status of A652A, The gene KDM1A has a mutation status of K705R, The gene PTPRU has a mutation status of P614P, The gene PPCS has a mutation status of R25P, The gene LURAP1 has a mutation status of F223F, The gene NDC1 has a mutation status of L65L, The gene C1orf87 has a mutation status of E200*, The gene LRRIQ3 has a mutation status of T387S, The gene TGFBR3 has a mutation status of M491I, The gene CDC14A has a mutation status of V221A, The gene COL11A1 has a mutation status of R352W, The gene ALX3 has a mutation status of G256V, The gene ALX3 has a mutation status of G253V, The gene NGF has a mutation status of R95S, The gene PPIAL4H has a mutation status of N102I, The gene NBPF12 has a mutation status of K581R, The gene HRNR has a mutation status of G1002E, The gene FLG2 has a mutation status of H938H, The gene LCE2D has a mutation status of G67G, The gene DENND4B has a mutation status of K1407N, The gene ARHGEF2 has a mutation status of R761M, The gene IQGAP3 has a mutation status of H755N, The gene SLAMF7 has a mutation status of I13V, The gene COLGALT2 has a mutation status of P612L, The gene PLEKHA6 has a mutation status of P105P, The gene CD34 has a mutation status of L257L, The gene LBR has a mutation status of Y273Y, The gene JMJD4 has a mutation status of L20I, The gene OBSCN has a mutation status of R7418R, The gene RYR2 has a mutation status of F4306S, The gene OR2L2 has a mutation status of R219W, The gene OR2T4 has a mutation status of V109L, The gene KIDINS220 has a mutation status of D118D, The gene MYCN has a mutation status of P109Q, The gene RAD51AP2 has a mutation status of M1150I, The gene MFSD2B has a mutation status of G351W, The gene ALK has a mutation status of T1312I, The gene DHX57 has a mutation status of R630Q, The gene EPAS1 has a mutation status of D753E, The gene DYSF has a mutation status of F1153L, The gene ZNF2 has a mutation status of Q296Q, The gene ADRA2B has a mutation status of E301E, The gene TMEM127 has a mutation status of A52A, The gene TMEM127 has a mutation status of P51H, The gene COL5A2 has a mutation status of Q224H, The gene ERBB4 has a mutation status of V391I, The gene SNORC has a mutation status of P20T, The gene HES6 has a mutation status of T212T, The gene HES6 has a mutation status of L211L, The gene GRM7 has a mutation status of I593V, The gene IL17RC has a mutation status of E186K, The gene EMC3 has a mutation status of D41H, The gene RBSN has a mutation status of A301A, The gene ANKRD28 has a mutation status of V509A, The gene ITIH3 has a mutation status of L373L, The gene DENND6A has a mutation status of R15S, The gene FLNB has a mutation status of H2355P, The gene MAGI1 has a mutation status of G933G, The gene MYH15 has a mutation status of G137R, The gene ESYT3 has a mutation status of F87V, The gene TRIM42 has a mutation status of R107C, The gene ZNF721 has a mutation status of K784N, The gene GAK has a mutation status of A535A, The gene NSD2 has a mutation status of E1241*, The gene HAUS3 has a mutation status of K558N, The gene FRAS1 has a mutation status of V2518M, The gene TET2 has a mutation status of F1041fs, The gene TBCK has a mutation status of R530L, The gene SEC24D has a mutation status of D24N, The gene PGRMC2 has a mutation status of R77fs, The gene INPP4B has a mutation status of Q814Q, The gene ARHGAP10 has a mutation status of H375N, The gene FNIP2 has a mutation status of G921V, The gene TENM3 has a mutation status of A2517S, The gene IRX2 has a mutation status of S236*, The gene DNAH5 has a mutation status of V3783V, The gene TAF9 has a mutation status of T159T, The gene HMGCR has a mutation status of L11L, The gene DDX46 has a mutation status of L865L, The gene PPARGC1B has a mutation status of F17L, The gene EBF1 has a mutation status of S438S, The gene DBN1 has a mutation status of P343T, The gene ADAMTS2 has a mutation status of P219S, The gene HIVEP1 has a mutation status of D2236N, The gene BTN2A2 has a mutation status of P252P, The gene BTN3A1 has a mutation status of G228S, The gene HLA-B has a mutation status of Y140L, The gene LTB has a mutation status of L19H, The gene MSH5 has a mutation status of C580G, The gene VWA7 has a mutation status of S774Y, The gene AGER has a mutation status of T256A, The gene HLA-DRB5 has a mutation status of Q220W, The gene LRRC73 has a mutation status of G15S, The gene CRYBG1 has a mutation status of W406L, The gene CRYBG1 has a mutation status of M409I, The gene CRYBG1 has a mutation status of A1022V, The gene DDO has a mutation status of R193Q, The gene TAAR6 has a mutation status of I126T, The gene ARFGEF3 has a mutation status of V1901G, The gene ADAT2 has a mutation status of L145P, The gene ULBP1 has a mutation status of K147T, The gene PLEKHG1 has a mutation status of H1296Y, The gene ARID1B has a mutation status of Q693Q, The gene TBXT has a mutation status of L270I, The gene INTS1 has a mutation status of T255T, The gene SNX8 has a mutation status of Q379H, The gene SLC29A4 has a mutation status of M1L, The gene COL28A1 has a mutation status of G713G, The gene FERD3L has a mutation status of E78K, The gene MACC1 has a mutation status of R190C, The gene SP8 has a mutation status of T167N, The gene HOXA3 has a mutation status of Y6C, The gene ANLN has a mutation status of I1121V, The gene MYO1G has a mutation status of E304*, The gene RFC2 has a mutation status of A150V, The gene FGL2 has a mutation status of C191Y, The gene SMURF1 has a mutation status of R7H, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S3321S, The gene CFTR has a mutation status of A62A, The gene FLNC has a mutation status of P2186T, The gene BRAF has a mutation status of V600E, The gene MGAM2 has a mutation status of P214P, The gene PRSS1 has a mutation status of N77N, The gene KRBA1 has a mutation status of E19*, The gene DPP6 has a mutation status of V438L, The gene SLC35G5 has a mutation status of P6H, The gene KIF13B has a mutation status of E1319*, The gene ADGRA2 has a mutation status of A1078A, The gene WWP1 has a mutation status of K536E, The gene RIPK2 has a mutation status of M515T, The gene RGS22 has a mutation status of Q96Q, The gene ZFAT has a mutation status of E1179Q, The gene ZFAT has a mutation status of A1173E, The gene GPIHBP1 has a mutation status of G18V, The gene PLEC has a mutation status of A4418V, The gene SHARPIN has a mutation status of P345H, The gene MROH1 has a mutation status of R1015Q, The gene SMARCA2 has a mutation status of R346L, The gene PUM3 has a mutation status of C576G, The gene RCL1 has a mutation status of S244S, The gene TTC39B has a mutation status of Q39*, The gene MELK has a mutation status of L596L, The gene ZCCHC7 has a mutation status of D307H, The gene TSTD2 has a mutation status of V144M, The gene MUSK has a mutation status of A454T, The gene FKBP15 has a mutation status of S548Y, The gene AMBP has a mutation status of K311T, The gene AKNA has a mutation status of V473L, The gene MEGF9 has a mutation status of G81W, The gene GARNL3 has a mutation status of N780K, The gene NAIF1 has a mutation status of A162A, The gene RAPGEF1 has a mutation status of R666M, The gene AK8 has a mutation status of G469V, The gene PAXX has a mutation status of S99*, The gene TUBAL3 has a mutation status of G373W, The gene SKIDA1 has a mutation status of G892S, The gene PARD3 has a mutation status of H426R, The gene RBP3 has a mutation status of P1241Q, The gene RBP3 has a mutation status of L1243L, The gene ANXA8 has a mutation status of T207M, The gene COL13A1 has a mutation status of P195Q, The gene KAT6B has a mutation status of S417T, The gene SAMD8 has a mutation status of L216L, The gene CDHR1 has a mutation status of P372S, The gene CYP26A1 has a mutation status of G470G, The gene NEURL1 has a mutation status of G176G, The gene SMC3 has a mutation status of R967*, The gene WDR11 has a mutation status of L1116L, The gene STK32C has a mutation status of H214N, The gene MUC5AC has a mutation status of S4844Y, The gene MUC5AC has a mutation status of V4847I, The gene OR51M1 has a mutation status of P266H, The gene OR52W1 has a mutation status of G93W, The gene USP47 has a mutation status of S1203P, The gene SPON1 has a mutation status of P69P, The gene PSMC3 has a mutation status of L342I, The gene OR4A15 has a mutation status of L99R, The gene OR8I2 has a mutation status of G16V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TM7SF2 has a mutation status of A49V, The gene RELA has a mutation status of L207L, The gene SPTBN2 has a mutation status of N1224S, The gene KDM2A has a mutation status of S104G, The gene FGF4 has a mutation status of S182N, The gene SERPINH1 has a mutation status of A87E, The gene SERPINH1 has a mutation status of A93D, The gene PICALM has a mutation status of P584Q, The gene AMOTL1 has a mutation status of Q583K, The gene AMOTL1 has a mutation status of Q589K, The gene KDM4D has a mutation status of D499E, The gene DYNC2H1 has a mutation status of Q4304R, The gene DDX10 has a mutation status of Q528K, The gene SORL1 has a mutation status of R793C, The gene CLMP has a mutation status of D55N, The gene ZNF202 has a mutation status of R133Q, The gene GLB1L2 has a mutation status of L152L, The gene PLEKHG6 has a mutation status of Q642Q, The gene LPAR5 has a mutation status of A288T, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of N76C, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene GUCY2C has a mutation status of Y397*, The gene PIK3C2G has a mutation status of G350W, The gene ADAMTS20 has a mutation status of E1424V, The gene KMT2D has a mutation status of R5501*, The gene KMT2D has a mutation status of R5432W, The gene NCKAP5L has a mutation status of G702V, The gene KRT72 has a mutation status of A63D, The gene ITGA7 has a mutation status of T661M, The gene PAN2 has a mutation status of K459R, The gene DPY19L2 has a mutation status of A462T, The gene NR2C1 has a mutation status of S278S, The gene MORN3 has a mutation status of R153C, The gene HCAR1 has a mutation status of F55L, The gene SBNO1 has a mutation status of N768D, The gene EP400 has a mutation status of P581M, The gene EP400 has a mutation status of A1008A, The gene MICU2 has a mutation status of K306L, The gene THSD1 has a mutation status of P679P, The gene PCDH8 has a mutation status of L439L, The gene ANKRD10 has a mutation status of P46P, The gene MCF2L has a mutation status of L794L, The gene GRK1 has a mutation status of L145I, The gene AJUBA has a mutation status of G42R, The gene RNF31 has a mutation status of E32*, The gene GPR135 has a mutation status of D456G, The gene L3HYPDH has a mutation status of G38V, The gene PLEKHH1 has a mutation status of L38L, The gene RIOX1 has a mutation status of Q23H, The gene EML5 has a mutation status of K768K, The gene ASB2 has a mutation status of H515P, The gene DYNC1H1 has a mutation status of E58*, The gene KIF26A has a mutation status of R1222S, The gene LINC02203 has a mutation status of I259M, The gene ZFYVE19 has a mutation status of P177Q, The gene SPINT1 has a mutation status of E110*, The gene MGA has a mutation status of P608T, The gene MGA has a mutation status of P611T, The gene SPTBN5 has a mutation status of E2562K, The gene PLA2G4F has a mutation status of V816G, The gene SLC12A1 has a mutation status of V277V, The gene TLN2 has a mutation status of M160I, The gene HERC1 has a mutation status of P4024S, The gene CORO2B has a mutation status of W253L, The gene CHRNA3 has a mutation status of S340S, The gene UNC45A has a mutation status of P13P, The gene RGS11 has a mutation status of Q323H, The gene NPW has a mutation status of L89I, The gene PKMYT1 has a mutation status of G309W, The gene IL4R has a mutation status of F395L, The gene SBK1 has a mutation status of T248T, The gene ITGAM has a mutation status of S827S, The gene SLC5A2 has a mutation status of P626Q, The gene SLC5A2 has a mutation status of L628I, The gene CNGB1 has a mutation status of E229D, The gene JPH3 has a mutation status of R348C, The gene ANKRD11 has a mutation status of I433R, The gene CPNE7 has a mutation status of K431N, The gene GEMIN4 has a mutation status of P932H, The gene MYO1C has a mutation status of N770D, The gene ASGR1 has a mutation status of Q29K, The gene SHBG has a mutation status of E133*, The gene KDM6B has a mutation status of R1209Q, The gene DNAH9 has a mutation status of S3830S, The gene SREBF1 has a mutation status of V226V, The gene SLC47A2 has a mutation status of R246S, The gene CPD has a mutation status of V856G, The gene TMEM132E has a mutation status of A169A, The gene PLXDC1 has a mutation status of R105R, The gene PLXDC1 has a mutation status of H103Q, The gene KRT39 has a mutation status of L206L, The gene KRT37 has a mutation status of I259I, The gene KRT37 has a mutation status of F257L, The gene KRT32 has a mutation status of P427I, The gene WNK4 has a mutation status of P38S, The gene PTGES3L has a mutation status of C81C, The gene DBF4B has a mutation status of V89M, The gene FMNL1 has a mutation status of L644L, The gene MRC2 has a mutation status of L300F, The gene SDK2 has a mutation status of P1402T, The gene SDK2 has a mutation status of A536A, The gene GGA3 has a mutation status of S299P, The gene LLGL2 has a mutation status of P955R, The gene LAMA1 has a mutation status of T2617M, The gene PTPN2 has a mutation status of S307G, The gene ATP5F1A has a mutation status of Q286K, The gene POLI has a mutation status of R202L, The gene ONECUT2 has a mutation status of R9L, The gene RAX has a mutation status of E78D, The gene SERPINB8 has a mutation status of L92V, The gene GZMM has a mutation status of Q74*, The gene PRTN3 has a mutation status of A196D, The gene TCF3 has a mutation status of P211H, The gene HDGFL2 has a mutation status of L503L, The gene DPP9 has a mutation status of P602H, The gene CAMSAP3 has a mutation status of S646Y, The gene MUC16 has a mutation status of E1706K, The gene CDKN2D has a mutation status of R25L, The gene RAB3D has a mutation status of F38fs, The gene SAMD1 has a mutation status of G241C, The gene SLC27A1 has a mutation status of G159V, The gene MAP1S has a mutation status of P694P, The gene PIK3R2 has a mutation status of P184L, The gene ZNF536 has a mutation status of T325T, The gene RASGRP4 has a mutation status of R570S, The gene CAPN12 has a mutation status of T663P, The gene PSG8 has a mutation status of R252R, The gene PSG6 has a mutation status of I210T, The gene SPHK2 has a mutation status of Y342S, The gene SPHK2 has a mutation status of L343P, The gene SPHK2 has a mutation status of *596*, The gene PRR12 has a mutation status of A8D, The gene SCAF1 has a mutation status of P1059P, The gene JOSD2 has a mutation status of S99S, The gene KLK5 has a mutation status of D153N, The gene SIGLEC8 has a mutation status of L191Q, The gene CEACAM18 has a mutation status of W63C, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of N187T, The gene LILRA1 has a mutation status of R296T, The gene ZNF628 has a mutation status of G22G, The gene ZSCAN1 has a mutation status of L395L, The gene SLC4A11 has a mutation status of P334P, The gene POFUT1 has a mutation status of W29L, The gene CNBD2 has a mutation status of Y8H, The gene SOGA1 has a mutation status of E534*, The gene TGM2 has a mutation status of L673M, The gene AURKA has a mutation status of A17G, The gene PRELID3B has a mutation status of T5N, The gene HELZ2 has a mutation status of A102A, The gene CLTCL1 has a mutation status of K806K, The gene KREMEN1 has a mutation status of P332L, The gene SLC35E4 has a mutation status of G97E, The gene MFNG has a mutation status of Q98K, The gene CDC42EP1 has a mutation status of E356K, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TTLL8 has a mutation status of R668C, The gene SBF1 has a mutation status of P271S, The gene FAM9B has a mutation status of D115D, The gene SHROOM2 has a mutation status of D824D, The gene DMD has a mutation status of R563C, The gene DMD has a mutation status of L167L, The gene H2AP has a mutation status of S30I, The gene EBP has a mutation status of V163A, The gene GPKOW has a mutation status of E44D, The gene MED12 has a mutation status of L36P, The gene PDZD4 has a mutation status of P491H, The gene PDZD4 has a mutation status of S490G, The gene IRAK1 has a mutation status of R366C, The gene MECP2 has a mutation status of P379P, The gene FAM50A has a mutation status of A244T, The gene PLXNA3 has a mutation status of R290R, The gene MT-ND4 has a mutation status of A287A
LAML
The gene TTLL10 has a mutation status of R83R, The gene TAS1R3 has a mutation status of T709T, The gene FBXO6 has a mutation status of F198F, The gene PRAMEF11 has a mutation status of P418P, The gene HNRNPCL1 has a mutation status of R92Q, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF15 has a mutation status of L400L, The gene SPEN has a mutation status of K1600*, The gene ARHGEF10L has a mutation status of P881P, The gene UBXN11 has a mutation status of L107L, The gene ZMYM6 has a mutation status of C1141F, The gene MACF1 has a mutation status of N714S, The gene HIVEP3 has a mutation status of S1895S, The gene FOXD2 has a mutation status of F355F, The gene PTGER3 has a mutation status of C208G, The gene TGFBR3 has a mutation status of A72V, The gene NBPF14 has a mutation status of Y1393Y, The gene SETDB1 has a mutation status of P5S, The gene FLG2 has a mutation status of S1062F, The gene PAQR6 has a mutation status of L128L, The gene ISG20L2 has a mutation status of S88T, The gene LY9 has a mutation status of T73I, The gene IER5 has a mutation status of V224G, The gene RNASEL has a mutation status of P85L, The gene CACNA1S has a mutation status of S177L, The gene TMEM9 has a mutation status of R136C, The gene IGFN1 has a mutation status of P11S, The gene PLXNA2 has a mutation status of I1865I, The gene PLXNA2 has a mutation status of C826G, The gene RAB3GAP2 has a mutation status of E577V, The gene CDC42BPA has a mutation status of Q1324E, The gene CDC42BPA has a mutation status of G260G, The gene URB2 has a mutation status of L1422L, The gene CAPN9 has a mutation status of A661G, The gene TRIM67 has a mutation status of D461A, The gene C1orf131 has a mutation status of R249T, The gene EGLN1 has a mutation status of A140V, The gene TARBP1 has a mutation status of I419F, The gene ZBTB18 has a mutation status of L176S, The gene KIF26B has a mutation status of S1006S, The gene TMEM18 has a mutation status of S84*, The gene DNMT3A has a mutation status of R635W, The gene CYP1B1 has a mutation status of S112L, The gene THADA has a mutation status of K1118N, The gene SPTBN1 has a mutation status of S1458S, The gene EML6 has a mutation status of V45G, The gene C2orf74 has a mutation status of F40F, The gene XPO1 has a mutation status of L625L, The gene ALMS1 has a mutation status of V950V, The gene C2orf81 has a mutation status of V229G, The gene HK2 has a mutation status of Q771R, The gene NEURL3 has a mutation status of G252G, The gene KIAA1211L has a mutation status of A486A, The gene GLI2 has a mutation status of H991N, The gene THSD7B has a mutation status of N572S, The gene LRP1B has a mutation status of K3585Q, The gene SCN3A has a mutation status of V1564V, The gene SP5 has a mutation status of D186N, The gene TTN has a mutation status of A2962P, The gene ITGAV has a mutation status of R333H, The gene MYO1B has a mutation status of N146H, The gene KCTD18 has a mutation status of V227G, The gene UNC80 has a mutation status of R489H, The gene TNS1 has a mutation status of S971C, The gene DES has a mutation status of P148S, The gene OBSL1 has a mutation status of Q225P, The gene MRPL44 has a mutation status of V299V, The gene PER2 has a mutation status of T409T, The gene GPC1 has a mutation status of Q385K, The gene LMCD1 has a mutation status of A293A, The gene RAF1 has a mutation status of A118fs, The gene FGD5 has a mutation status of R575R, The gene GASK1A has a mutation status of D279E, The gene PFKFB4 has a mutation status of G122V, The gene CACNA1D has a mutation status of Q1355*, The gene ERC2 has a mutation status of I851I, The gene ZNF80 has a mutation status of R124C, The gene GAP43 has a mutation status of Q203K, The gene ALDH1L1 has a mutation status of A107V, The gene PLXNA1 has a mutation status of R630L, The gene C3orf56 has a mutation status of S231S, The gene KPNA4 has a mutation status of N39K, The gene AC131160.1 has a mutation status of T34P, The gene RTP2 has a mutation status of K17K, The gene RPL35A has a mutation status of L5M, The gene FGFRL1 has a mutation status of G27S, The gene TAPT1 has a mutation status of K272R, The gene FAM184B has a mutation status of W26C, The gene PCDH7 has a mutation status of L814F, The gene SDAD1 has a mutation status of K209E, The gene SCARB2 has a mutation status of S20T, The gene HERC5 has a mutation status of V52G, The gene TACR3 has a mutation status of T389A, The gene NPNT has a mutation status of V417I, The gene DNAH5 has a mutation status of C1191Y, The gene SNX18 has a mutation status of G131G, The gene ANKRD55 has a mutation status of L567V, The gene RNF180 has a mutation status of D287N, The gene ADGRV1 has a mutation status of G5337G, The gene MAN2A1 has a mutation status of N738S, The gene NRG2 has a mutation status of V4G, The gene PCDHA10 has a mutation status of S508S, The gene PCDHB16 has a mutation status of S704S, The gene CCDC69 has a mutation status of H163Q, The gene GRIA1 has a mutation status of E451E, The gene PDLIM7 has a mutation status of V110V, The gene COL23A1 has a mutation status of D246Y, The gene FOXC1 has a mutation status of L518F, The gene CARMIL1 has a mutation status of L349V, The gene ZNF165 has a mutation status of H110R, The gene MDC1 has a mutation status of Q1333Q, The gene AGER has a mutation status of R77P, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q220W, The gene TEAD3 has a mutation status of C53C, The gene TBC1D22B has a mutation status of R345R, The gene DNAH8 has a mutation status of G2031V, The gene CUL9 has a mutation status of T630T, The gene ENPP5 has a mutation status of L335fs, The gene PKHD1 has a mutation status of D3540G, The gene HTR1B has a mutation status of C8C, The gene CRYBG1 has a mutation status of G1722S, The gene ZBTB24 has a mutation status of F378S, The gene RPF2 has a mutation status of L4R, The gene MCM9 has a mutation status of P718L, The gene EPB41L2 has a mutation status of A125S, The gene AHI1 has a mutation status of R548S, The gene SMIM28 has a mutation status of W9C, The gene GPR31 has a mutation status of L141L, The gene AMZ1 has a mutation status of T343P, The gene FOXK1 has a mutation status of T683P, The gene SLC29A4 has a mutation status of G414G, The gene VWDE has a mutation status of V1097L, The gene GLI3 has a mutation status of S1028I, The gene PHKG1 has a mutation status of R330W, The gene SSC4D has a mutation status of V256V, The gene TECPR1 has a mutation status of G852W, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of E725K, The gene MUC3A has a mutation status of T730I, The gene MUC3A has a mutation status of T1624T, The gene SPDYE6 has a mutation status of H337R, The gene CREB3L2 has a mutation status of G7W, The gene FASTK has a mutation status of D449A, The gene CHPF2 has a mutation status of V696G, The gene SHH has a mutation status of G297C, The gene SHH has a mutation status of G296W, The gene DLGAP2 has a mutation status of D391E, The gene REEP4 has a mutation status of I107V, The gene POLR3D has a mutation status of D306N, The gene C8orf58 has a mutation status of R345W, The gene SCARA5 has a mutation status of G214C, The gene KIF13B has a mutation status of A1576A, The gene CHRNB3 has a mutation status of V335I, The gene OPRK1 has a mutation status of W132*, The gene OPRK1 has a mutation status of A4V, The gene CDH17 has a mutation status of G297R, The gene GEM has a mutation status of S104S, The gene SNTB1 has a mutation status of G16G, The gene FER1L6 has a mutation status of P425P, The gene CYP11B2 has a mutation status of D335D, The gene MROH6 has a mutation status of P488P, The gene MROH6 has a mutation status of A372T, The gene EPPK1 has a mutation status of L805L, The gene ERMP1 has a mutation status of N421S, The gene MPDZ has a mutation status of E702M, The gene CDKN2A has a mutation status of A36G, The gene NFX1 has a mutation status of S977S, The gene SIGMAR1 has a mutation status of W11L, The gene CCIN has a mutation status of V118A, The gene WNK2 has a mutation status of P726P, The gene FBP2 has a mutation status of Y259Y, The gene ZNF189 has a mutation status of C178Y, The gene FRRS1L has a mutation status of R51A, The gene GSN has a mutation status of V44G, The gene TTLL11 has a mutation status of G146V, The gene TTLL11 has a mutation status of E142*, The gene CRB2 has a mutation status of S807S, The gene DENND1A has a mutation status of P819H, The gene PTRH1 has a mutation status of G128W, The gene PRDM12 has a mutation status of E170K, The gene VAV2 has a mutation status of I656M, The gene OBP2A has a mutation status of A92V, The gene SAPCD2 has a mutation status of L69L, The gene TOR4A has a mutation status of R40H, The gene AKR1C8P has a mutation status of N172K, The gene USP6NL has a mutation status of E10D, The gene ARHGAP21 has a mutation status of Q719R, The gene MKX has a mutation status of V71G, The gene FZD8 has a mutation status of V382G, The gene ANTXRL has a mutation status of H61N, The gene ANTXRL has a mutation status of T303N, The gene CCAR1 has a mutation status of Q71K, The gene DDX50 has a mutation status of P16P, The gene CDH23 has a mutation status of D2695A, The gene TNKS2 has a mutation status of G10G, The gene CPEB3 has a mutation status of R270L, The gene FRAT1 has a mutation status of G187W, The gene ABCC2 has a mutation status of R529W, The gene LBX1 has a mutation status of H22P, The gene FBXL15 has a mutation status of W20L, The gene NKX1-2 has a mutation status of D226N, The gene CFAP46 has a mutation status of V645G, The gene KNDC1 has a mutation status of T644T, The gene MUC6 has a mutation status of T1071P, The gene MUC5B has a mutation status of P57P, The gene SMPD1 has a mutation status of S263N, The gene DNHD1 has a mutation status of P3322H, The gene C1QTNF4 has a mutation status of F77Y, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene RAB3IL1 has a mutation status of Y346C, The gene GAL3ST3 has a mutation status of A377S, The gene CTTN has a mutation status of V536G, The gene SESN3 has a mutation status of R318Q, The gene KMT2A has a mutation status of K1751*, The gene IQSEC3 has a mutation status of P124P, The gene VWF has a mutation status of N2546Y, The gene SMCO2 has a mutation status of L179M, The gene GXYLT1 has a mutation status of E32K, The gene ARID2 has a mutation status of N178N, The gene SPATS2 has a mutation status of R254W, The gene SMARCD1 has a mutation status of A5V, The gene LARP4 has a mutation status of T30T, The gene KRT5 has a mutation status of G570G, The gene KRT72 has a mutation status of A381T, The gene TNS2 has a mutation status of Y1044*, The gene NCKAP1L has a mutation status of R214Q, The gene METAP2 has a mutation status of G3G, The gene OASL has a mutation status of I343I, The gene NCOR2 has a mutation status of D559D, The gene ZMYM5 has a mutation status of I83V, The gene TSC22D1 has a mutation status of Q568K, The gene CCDC168 has a mutation status of D4207E, The gene IPO4 has a mutation status of V31F, The gene FOXA1 has a mutation status of G378S, The gene FAM161B has a mutation status of G206G, The gene VSX2 has a mutation status of P49Q, The gene TMEM63C has a mutation status of H294P, The gene KIF26A has a mutation status of P348Q, The gene JAG2 has a mutation status of T708P, The gene FMN1 has a mutation status of S272A, The gene CHST14 has a mutation status of P76P, The gene RPUSD2 has a mutation status of E167A, The gene SPTBN5 has a mutation status of Q2569K, The gene PLA2G4D has a mutation status of A742A, The gene STARD9 has a mutation status of L4099I, The gene LDHAL6B has a mutation status of V185fs, The gene CHRNB4 has a mutation status of Q211H, The gene ZNF592 has a mutation status of P1085L, The gene FES has a mutation status of E287G, The gene SYNM has a mutation status of K701R, The gene TM2D3 has a mutation status of E185G, The gene CACNA1H has a mutation status of S1110S, The gene CACNA1H has a mutation status of D1112A, The gene SLC9A3R2 has a mutation status of V199G, The gene NTN3 has a mutation status of T345P, The gene ZNF75A has a mutation status of P113Q, The gene RBFOX1 has a mutation status of P307S, The gene GRIN2A has a mutation status of L98L, The gene EIF3C has a mutation status of R288C, The gene TAOK2 has a mutation status of N721S, The gene INO80E has a mutation status of P164P, The gene CCDC189 has a mutation status of P62T, The gene CNGB1 has a mutation status of S1017T, The gene MMP15 has a mutation status of V620G, The gene CARMIL2 has a mutation status of G941G, The gene SNTB2 has a mutation status of V116G, The gene WWOX has a mutation status of P217S, The gene PLCG2 has a mutation status of E165K, The gene ZNF469 has a mutation status of G47C, The gene ZNF469 has a mutation status of R49S, The gene CDT1 has a mutation status of L314M, The gene CDH15 has a mutation status of *815C, The gene FANCA has a mutation status of E1451K, The gene PITPNA has a mutation status of K5N, The gene SPEM3 has a mutation status of I1099T, The gene SHISA6 has a mutation status of R73R, The gene FLCN has a mutation status of N184K, The gene FLII has a mutation status of E552G, The gene MAPK7 has a mutation status of Y741Y, The gene FOXN1 has a mutation status of T497P, The gene FNDC8 has a mutation status of G203G, The gene UNC45B has a mutation status of A678T, The gene CCL4L2 has a mutation status of P67R, The gene CCDC47 has a mutation status of E329D, The gene BPTF has a mutation status of P67P, The gene CASKIN2 has a mutation status of P884Q, The gene CASKIN2 has a mutation status of S880P, The gene FOXJ1 has a mutation status of W38L, The gene RHBDF2 has a mutation status of V11G, The gene TMC6 has a mutation status of G242C, The gene OXLD1 has a mutation status of P51T, The gene CD7 has a mutation status of D213G, The gene TBCD has a mutation status of G31G, The gene GREB1L has a mutation status of D1108G, The gene FHOD3 has a mutation status of T1528P, The gene SETBP1 has a mutation status of P1539H, The gene MBD1 has a mutation status of R352H, The gene FECH has a mutation status of T419P, The gene MALT1 has a mutation status of A23D, The gene DSEL has a mutation status of 1127_1128LL>FM, The gene MED16 has a mutation status of P705Q, The gene MED16 has a mutation status of G197R, The gene GRIN3B has a mutation status of G981V, The gene ABCA7 has a mutation status of G72G, The gene ABCA7 has a mutation status of T2023P, The gene PCSK4 has a mutation status of V111G, The gene DIRAS1 has a mutation status of V18G, The gene ANKRD24 has a mutation status of P227P, The gene SH3GL1 has a mutation status of L29L, The gene CHAF1A has a mutation status of E391G, The gene MICOS13 has a mutation status of G109C, The gene PNPLA6 has a mutation status of S1285*, The gene TYK2 has a mutation status of E824*, The gene DOCK6 has a mutation status of E1052K, The gene HOOK2 has a mutation status of E260G, The gene SYDE1 has a mutation status of P399P, The gene SYDE1 has a mutation status of R574S, The gene BRD4 has a mutation status of L866L, The gene BRD4 has a mutation status of P777P, The gene GTPBP3 has a mutation status of T53P, The gene B3GNT3 has a mutation status of P106R, The gene TMEM59L has a mutation status of P34T, The gene HOMER3 has a mutation status of R325L, The gene ZNF257 has a mutation status of A414P, The gene WTIP has a mutation status of E44*, The gene LSR has a mutation status of H63P, The gene PROSER3 has a mutation status of E340K, The gene CAPN12 has a mutation status of T663P, The gene FCGBP has a mutation status of Q2163E, The gene FCGBP has a mutation status of TCRPSGGSL1234del, The gene FCGBP has a mutation status of S1228fs, The gene PRX has a mutation status of S51S, The gene SPTBN4 has a mutation status of V1105P, The gene MEGF8 has a mutation status of P1411P, The gene RELB has a mutation status of P314Q, The gene VASP has a mutation status of P172P, The gene PRKD2 has a mutation status of T328I, The gene CCDC114 has a mutation status of M192V, The gene PRR12 has a mutation status of E1823*, The gene PNKP has a mutation status of E13Q, The gene ZNF480 has a mutation status of D31D, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA5 has a mutation status of V19M, The gene LILRA1 has a mutation status of R296T, The gene EPS8L1 has a mutation status of P470T, The gene LZTS3 has a mutation status of G595G, The gene ADAM33 has a mutation status of T701P, The gene C20orf27 has a mutation status of *175*, The gene ENTPD6 has a mutation status of T121P, The gene SUN5 has a mutation status of T352I, The gene ASIP has a mutation status of A104A, The gene TGM2 has a mutation status of S212P, The gene NEURL2 has a mutation status of F55I, The gene SLC12A5 has a mutation status of D30A, The gene CTSZ has a mutation status of G228R, The gene CDH26 has a mutation status of V641L, The gene CHODL has a mutation status of V30G, The gene IFNAR1 has a mutation status of A17V, The gene SON has a mutation status of 1229_1230insYSVSASDPSVLVSEAAVT, The gene TRPM2 has a mutation status of A553A, The gene KRTAP10-4 has a mutation status of V272M, The gene DIP2A has a mutation status of D1300A, The gene GSTT4 has a mutation status of Q197R, The gene GSTT4 has a mutation status of E126K, The gene SEC14L2 has a mutation status of I264fs, The gene APOBEC3F has a mutation status of N31D, The gene MGAT3 has a mutation status of V204G, The gene TTC38 has a mutation status of L299P, The gene PPP6R2 has a mutation status of A486L, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene MXRA5 has a mutation status of G2458G, The gene MXRA5 has a mutation status of W7L, The gene DCAF8L1 has a mutation status of L188L, The gene BCOR has a mutation status of D1718Y, The gene USP11 has a mutation status of V647V, The gene HDAC6 has a mutation status of A133A, The gene CCDC120 has a mutation status of T355P, The gene NUDT11 has a mutation status of G50W, The gene HUWE1 has a mutation status of G1749D, The gene NLGN3 has a mutation status of E61*, The gene CSTF2 has a mutation status of G3G, The gene RADX has a mutation status of I532T, The gene SOX3 has a mutation status of L28L, The gene TREX2 has a mutation status of R156H, The gene PLXNB3 has a mutation status of P108Q, The gene MT-ATP6 has a mutation status of D224N
LAML
The gene PERM1 has a mutation status of T274T, The gene HSPG2 has a mutation status of S2888Y, The gene ZBTB40 has a mutation status of P979S, The gene RUNX3 has a mutation status of T222K, The gene IFI6 has a mutation status of P65P, The gene CSMD2 has a mutation status of L730P, The gene SFPQ has a mutation status of G265D, The gene TFAP2E has a mutation status of A8S, The gene MANEAL has a mutation status of P88H, The gene DMAP1 has a mutation status of Y196S, The gene CMPK1 has a mutation status of L32L, The gene ST6GALNAC3 has a mutation status of G231S, The gene WDR47 has a mutation status of A259A, The gene EPS8L3 has a mutation status of A216T, The gene LRIG2 has a mutation status of I425V, The gene TTF2 has a mutation status of P337T, The gene NOTCH2 has a mutation status of H1160R, The gene NBPF11 has a mutation status of V159F, The gene POGZ has a mutation status of L411R, The gene FCRL5 has a mutation status of R658H, The gene UFC1 has a mutation status of N166N, The gene FCGR2B has a mutation status of L135V, The gene DUSP12 has a mutation status of P192A, The gene ALDH9A1 has a mutation status of N37S, The gene CEP350 has a mutation status of Q2887Q, The gene HMCN1 has a mutation status of Q5345R, The gene PPP1R12B has a mutation status of L77L, The gene PPP1R12B has a mutation status of V550I, The gene PPP1R15B has a mutation status of E446E, The gene SLC26A9 has a mutation status of H703H, The gene PLXNA2 has a mutation status of C826G, The gene LAMB3 has a mutation status of V753G, The gene OBSCN has a mutation status of P5025P, The gene ARV1 has a mutation status of R6G, The gene ARV1 has a mutation status of S7G, The gene PCNX2 has a mutation status of R1450Q, The gene ARID4B has a mutation status of L60L, The gene RYR2 has a mutation status of A165D, The gene ZNF124 has a mutation status of P134H, The gene PUM2 has a mutation status of R393C, The gene TDRD15 has a mutation status of V1251L, The gene C2orf16 has a mutation status of P5013P, The gene XDH has a mutation status of L398P, The gene STON1 has a mutation status of YKLELGSDQEIPSDW653del, The gene UGP2 has a mutation status of V448A, The gene SLC4A5 has a mutation status of P23P, The gene AFF3 has a mutation status of G99G, The gene CREG2 has a mutation status of Q237K, The gene IWS1 has a mutation status of E279K, The gene PLEKHB2 has a mutation status of L162V, The gene FMNL2 has a mutation status of P527P, The gene FMNL2 has a mutation status of F107F, The gene KCNJ3 has a mutation status of T90N, The gene FIGN has a mutation status of L374V, The gene TTN has a mutation status of Y7962F, The gene CCDC150 has a mutation status of T90fs, The gene FN1 has a mutation status of V276A, The gene CXCR2 has a mutation status of R288H, The gene PAX3 has a mutation status of R270C, The gene EIF4E2 has a mutation status of R140Q, The gene CCDC174 has a mutation status of K308K, The gene FGD5 has a mutation status of S458S, The gene CLASP2 has a mutation status of T920T, The gene TTC21A has a mutation status of G321G, The gene ARIH2OS has a mutation status of A153G, The gene DNAH12 has a mutation status of L2786L, The gene ADAMTS9 has a mutation status of V692V, The gene PDZRN3 has a mutation status of K81R, The gene ZPLD1 has a mutation status of A173A, The gene BOC has a mutation status of S247N, The gene CFAP44 has a mutation status of A555V, The gene GOLGB1 has a mutation status of N2286T, The gene IFT122 has a mutation status of M971I, The gene ATR has a mutation status of C742C, The gene CHST2 has a mutation status of S462S, The gene NMD3 has a mutation status of V96L, The gene TNIK has a mutation status of G34R, The gene CLCN2 has a mutation status of P615P, The gene ZNF595 has a mutation status of I357M, The gene EVC2 has a mutation status of I549V, The gene TLR10 has a mutation status of K318R, The gene TLR1 has a mutation status of D30G, The gene GUF1 has a mutation status of R18G, The gene CEP135 has a mutation status of L1033L, The gene CXCL5 has a mutation status of V11V, The gene SHROOM3 has a mutation status of L756L, The gene ARHGAP24 has a mutation status of S439G, The gene SLC9B1 has a mutation status of S334T, The gene NR3C2 has a mutation status of A976A, The gene GLRA3 has a mutation status of D113D, The gene TENM3 has a mutation status of S653S, The gene CFAP97 has a mutation status of S115S, The gene FAT1 has a mutation status of N3919N, The gene PDZD2 has a mutation status of S341S, The gene CPLANE1 has a mutation status of T175T, The gene DHX29 has a mutation status of G660V, The gene DEPDC1B has a mutation status of A308V, The gene ARSB has a mutation status of L336fs, The gene DHFR has a mutation status of T147T, The gene KCNN2 has a mutation status of R835Q, The gene FTMT has a mutation status of G185D, The gene DND1 has a mutation status of R327Q, The gene PCDHB7 has a mutation status of A305V, The gene PCDHB7 has a mutation status of G778G, The gene RBM27 has a mutation status of G739D, The gene FAM71B has a mutation status of E391D, The gene TENM2 has a mutation status of G2421S, The gene TENM2 has a mutation status of L2438L, The gene NSD1 has a mutation status of A1728A, The gene TBC1D9B has a mutation status of Q652R, The gene GFPT2 has a mutation status of N549K, The gene NUP153 has a mutation status of V1097A, The gene AGER has a mutation status of R77P, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of Q38W, The gene COL11A2 has a mutation status of R742W, The gene LHFPL5 has a mutation status of D204G, The gene BRPF3 has a mutation status of S959S, The gene FBXO9 has a mutation status of R85P, The gene LCA5 has a mutation status of D367D, The gene DOP1A has a mutation status of Q1174Q, The gene NR2E1 has a mutation status of S74S, The gene AK9 has a mutation status of V117V, The gene KIAA0408 has a mutation status of P278S, The gene ENPP1 has a mutation status of D175N, The gene SYNE1 has a mutation status of L4415I, The gene FNDC1 has a mutation status of S671P, The gene USP42 has a mutation status of I522L, The gene USP42 has a mutation status of N697H, The gene BBS9 has a mutation status of W10C, The gene PGAM2 has a mutation status of S189C, The gene SSC4D has a mutation status of R419L, The gene NYAP1 has a mutation status of G99G, The gene FBXO24 has a mutation status of E83E, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S568Y, The gene MUC3A has a mutation status of T1351S, The gene MUC3A has a mutation status of P1354T, The gene MUC3A has a mutation status of L3196L, The gene MUC3A has a mutation status of T3202A, The gene SPDYE6 has a mutation status of H337R, The gene LAMB1 has a mutation status of E1395K, The gene ASZ1 has a mutation status of T301T, The gene PRSS1 has a mutation status of N77N, The gene TAS2R41 has a mutation status of N173K, The gene CDK5 has a mutation status of R120C, The gene H2BE1 has a mutation status of V115A, The gene DLC1 has a mutation status of Q303R, The gene CCAR2 has a mutation status of Q689E, The gene CEBPD has a mutation status of T73fs, The gene SLCO5A1 has a mutation status of K497*, The gene PSKH2 has a mutation status of Y281C, The gene PKHD1L1 has a mutation status of T866N, The gene FER1L6 has a mutation status of P961L, The gene ASAP1 has a mutation status of A570T, The gene MROH1 has a mutation status of S1333S, The gene DGAT1 has a mutation status of V301G, The gene TRMT10B has a mutation status of M133T, The gene CNTNAP3 has a mutation status of A1182A, The gene SEMA4D has a mutation status of P538R, The gene ROR2 has a mutation status of S393S, The gene NUTM2F has a mutation status of E255E, The gene FANCC has a mutation status of M350V, The gene FAM102A has a mutation status of T322M, The gene USP20 has a mutation status of L247L, The gene USP20 has a mutation status of R714H, The gene SETX has a mutation status of K1889K, The gene ADAMTSL2 has a mutation status of A840A, The gene BRD3 has a mutation status of P23T, The gene WDR5 has a mutation status of T18P, The gene NOTCH1 has a mutation status of N685T, The gene NELFB has a mutation status of V497L, The gene RSU1 has a mutation status of L245H, The gene CUBN has a mutation status of E1096K, The gene KIAA1217 has a mutation status of D922D, The gene GPR158 has a mutation status of G238S, The gene SVIL has a mutation status of S1970S, The gene HNRNPF has a mutation status of D110N, The gene ANXA8 has a mutation status of D314H, The gene CHAT has a mutation status of D250G, The gene ANK3 has a mutation status of Y1494*, The gene SH2D4B has a mutation status of R391S, The gene BAG3 has a mutation status of H212H, The gene CHST15 has a mutation status of L44L, The gene DPYSL4 has a mutation status of H107H, The gene CFAP46 has a mutation status of S2463I, The gene ADAM8 has a mutation status of P748P, The gene MUC5AC has a mutation status of C1146F, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of R3992H, The gene OR51D1 has a mutation status of T150K, The gene OR51E1 has a mutation status of T13I, The gene OR5P2 has a mutation status of V109V, The gene SPTY2D1 has a mutation status of T111A, The gene MADD has a mutation status of I1349K, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene BTBD18 has a mutation status of A44E, The gene DTX4 has a mutation status of N374fs, The gene ZP1 has a mutation status of P140L, The gene PLCB3 has a mutation status of Q677*, The gene NRXN2 has a mutation status of R6P, The gene TMEM262 has a mutation status of G71E, The gene KAT5 has a mutation status of N206N, The gene KLC2 has a mutation status of A475P, The gene SHANK2 has a mutation status of Y145*, The gene B3GNT6 has a mutation status of A172G, The gene B3GNT6 has a mutation status of E173G, The gene PCF11 has a mutation status of G1280G, The gene PRSS23 has a mutation status of H175D, The gene MTMR2 has a mutation status of Y93Y, The gene MTMR2 has a mutation status of A28fs, The gene MMP10 has a mutation status of T350T, The gene CARD17 has a mutation status of C69R, The gene GUCY1A2 has a mutation status of Q156K, The gene FGF23 has a mutation status of R175W, The gene ATN1 has a mutation status of Y530*, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene KRAS has a mutation status of G12D, The gene GALNT6 has a mutation status of T95T, The gene ANKRD33 has a mutation status of A450A, The gene AGAP2 has a mutation status of S249P, The gene LRIG3 has a mutation status of L86S, The gene SLC6A15 has a mutation status of L243V, The gene CFAP54 has a mutation status of R951R, The gene HVCN1 has a mutation status of M71T, The gene CIT has a mutation status of K1191R, The gene HIP1R has a mutation status of N345S, The gene GOLGA3 has a mutation status of A483D, The gene MPHOSPH8 has a mutation status of P246S, The gene PARP4 has a mutation status of L283L, The gene RNF17 has a mutation status of H878P, The gene RB1 has a mutation status of C590C, The gene KPNA3 has a mutation status of F331fs, The gene THSD1 has a mutation status of R460W, The gene SLC10A2 has a mutation status of P290L, The gene CARS2 has a mutation status of A501A, The gene OR4K2 has a mutation status of P261S, The gene LMLN2 has a mutation status of G209G, The gene STRN3 has a mutation status of Y371Y, The gene AKAP6 has a mutation status of E1394E, The gene SPTB has a mutation status of R814Q, The gene SIPA1L1 has a mutation status of A555A, The gene RGS6 has a mutation status of I97I, The gene FAM161B has a mutation status of L277L, The gene PGF has a mutation status of V38G, The gene ANKRD9 has a mutation status of D149H, The gene ASPG has a mutation status of Y510H, The gene GOLGA8S has a mutation status of I439V, The gene PDIA3 has a mutation status of D41Y, The gene WDR72 has a mutation status of S375S, The gene SCAPER has a mutation status of I1217T, The gene ALPK3 has a mutation status of V26G, The gene KIF7 has a mutation status of L235L, The gene MESP1 has a mutation status of V113A, The gene BLM has a mutation status of D64V, The gene PERCC1 has a mutation status of R127Q, The gene PKD1 has a mutation status of S3720A, The gene ECI1 has a mutation status of T262T, The gene ABCA3 has a mutation status of R1174H, The gene AC099489.1 has a mutation status of S3226I, The gene UBFD1 has a mutation status of V71G, The gene FHOD1 has a mutation status of I438T, The gene SLC7A6 has a mutation status of N149K, The gene PITPNM3 has a mutation status of G255G, The gene CLDN7 has a mutation status of S172A, The gene CLDN7 has a mutation status of A170G, The gene TP53 has a mutation status of G360V, The gene TP53 has a mutation status of G245S, The gene TRAPPC1 has a mutation status of C115C, The gene MYH4 has a mutation status of F1453C, The gene DNAH9 has a mutation status of G3992R, The gene LLGL1 has a mutation status of A406A, The gene PRPSAP2 has a mutation status of I125V, The gene SPECC1 has a mutation status of K153R, The gene WSB1 has a mutation status of P410A, The gene GSDMB has a mutation status of A307A, The gene HDAC5 has a mutation status of G411G, The gene KIF18B has a mutation status of R482H, The gene HEATR6 has a mutation status of A1021fs, The gene ICAM2 has a mutation status of G184G, The gene CEP112 has a mutation status of H72R, The gene WDR45B has a mutation status of Q267R, The gene TUBB8B has a mutation status of N348N, The gene LAMA1 has a mutation status of E883Q, The gene GATA6 has a mutation status of L3F, The gene RBBP8 has a mutation status of S534*, The gene TMEM241 has a mutation status of L159F, The gene TPGS2 has a mutation status of I27M, The gene TPGS2 has a mutation status of T25A, The gene CELF4 has a mutation status of P40P, The gene ZNF532 has a mutation status of A515A, The gene DAZAP1 has a mutation status of P198L, The gene APC2 has a mutation status of P1559P, The gene NCLN has a mutation status of R263S, The gene LONP1 has a mutation status of T644P, The gene MCOLN1 has a mutation status of Y355D, The gene MUC16 has a mutation status of L14460F, The gene ADGRL1 has a mutation status of T1366P, The gene ANKLE1 has a mutation status of G189R, The gene FCHO1 has a mutation status of S454R, The gene ARHGAP33 has a mutation status of A108G, The gene RYR1 has a mutation status of R2248C, The gene LIPE has a mutation status of W543C, The gene SIX5 has a mutation status of G11V, The gene OSCAR has a mutation status of R58Q, The gene CNOT3 has a mutation status of P559L, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of L156L, The gene ZSCAN5B has a mutation status of K446E, The gene SIRPA has a mutation status of S154S, The gene GPCPD1 has a mutation status of P176R, The gene RIN2 has a mutation status of S378S, The gene MYLK2 has a mutation status of K42R, The gene BPIFB3 has a mutation status of L237I, The gene EDEM2 has a mutation status of N119I, The gene ARHGAP40 has a mutation status of Q293K, The gene TTC3 has a mutation status of V48V, The gene DSCAM has a mutation status of G1325G, The gene DSCAM has a mutation status of E1274K, The gene PRDM15 has a mutation status of G473S, The gene PFKL has a mutation status of E692K, The gene KRTAP10-1 has a mutation status of V248I, The gene PI4KA has a mutation status of Y1628S, The gene SNAP29 has a mutation status of V128G, The gene ZNRF3 has a mutation status of E649G, The gene NIPSNAP1 has a mutation status of L108L, The gene SFI1 has a mutation status of R644S, The gene SLC16A8 has a mutation status of P234L, The gene KCNJ4 has a mutation status of G98G, The gene POLDIP3 has a mutation status of T256A, The gene GTPBP6 has a mutation status of G61R, The gene ASB11 has a mutation status of M1V, The gene CFAP47 has a mutation status of D1351Y, The gene PHF8 has a mutation status of R983S, The gene AMER1 has a mutation status of A150G, The gene AMER1 has a mutation status of G149G, The gene DLG3 has a mutation status of S813F, The gene CDX4 has a mutation status of S135A, The gene CT45A10 has a mutation status of G83R, The gene SAGE1 has a mutation status of D766N, The gene FATE1 has a mutation status of S15S, The gene ATP2B3 has a mutation status of L552V, The gene MT-ND5 has a mutation status of I283V, The gene MT-CYB has a mutation status of R100Q
PAAD
The gene RNF223 has a mutation status of A239D, The gene SCNN1D has a mutation status of E42*, The gene CCNL2 has a mutation status of L92P, The gene CAMTA1 has a mutation status of A408A, The gene TNFRSF1B has a mutation status of A20E, The gene PRAMEF13 has a mutation status of S245Y, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene PTPRU has a mutation status of H68H, The gene LCK has a mutation status of E176E, The gene LSM10 has a mutation status of V104fs, The gene DNALI1 has a mutation status of N142K, The gene RIMKLA has a mutation status of R12H, The gene TRABD2B has a mutation status of R306C, The gene CLCA1 has a mutation status of R93I, The gene CLCA4 has a mutation status of E709G, The gene SYPL2 has a mutation status of G255G, The gene ADORA3 has a mutation status of L270M, The gene CD2 has a mutation status of G262G, The gene CD2 has a mutation status of H339L, The gene NBPF20 has a mutation status of L4577L, The gene MINDY1 has a mutation status of A205A, The gene MUC1 has a mutation status of R99Q, The gene THBS3 has a mutation status of L13L, The gene MTX1 has a mutation status of D20Y, The gene SYT11 has a mutation status of D366N, The gene SMG5 has a mutation status of R637Q, The gene BCAN has a mutation status of Y676Y, The gene NES has a mutation status of N1541S, The gene ATP1A4 has a mutation status of I117V, The gene LY9 has a mutation status of D331D, The gene USF1 has a mutation status of Y116Y, The gene NOS1AP has a mutation status of D130N, The gene TNN has a mutation status of A24P, The gene TNR has a mutation status of E839D, The gene RNASEL has a mutation status of Q619Q, The gene F13B has a mutation status of R147R, The gene IGFN1 has a mutation status of R2510S, The gene NFASC has a mutation status of R937W, The gene IKBKE has a mutation status of R525Q, The gene LAMB3 has a mutation status of V753G, The gene CENPF has a mutation status of R300H, The gene CAPN2 has a mutation status of N275K, The gene ENAH has a mutation status of P429Q, The gene OBSCN has a mutation status of A5326D, The gene OBSCN has a mutation status of T8578I, The gene PGBD5 has a mutation status of A51T, The gene ARV1 has a mutation status of R6G, The gene ARV1 has a mutation status of S7G, The gene WDR64 has a mutation status of R348W, The gene SCCPDH has a mutation status of P7L, The gene FAM110C has a mutation status of T299T, The gene TMEM18 has a mutation status of I98V, The gene MYT1L has a mutation status of A694A, The gene SOX11 has a mutation status of A277A, The gene HEATR5B has a mutation status of G289S, The gene CCDC88A has a mutation status of L1215M, The gene OTX1 has a mutation status of Q352E, The gene ALMS1 has a mutation status of I3785V, The gene CTNNA2 has a mutation status of A337A, The gene AL845331.2 has a mutation status of V210G, The gene ADRA2B has a mutation status of E301E, The gene CNOT11 has a mutation status of R12R, The gene MAP4K4 has a mutation status of Q402R, The gene SH3RF3 has a mutation status of R179Q, The gene FIGN has a mutation status of P723P, The gene SLC25A12 has a mutation status of R624H, The gene TTN has a mutation status of I7990I, The gene NCKAP1 has a mutation status of Y428Y, The gene CFAP65 has a mutation status of L33H, The gene NYAP2 has a mutation status of H83Q, The gene NMUR1 has a mutation status of W122R, The gene HRH1 has a mutation status of M451V, The gene EAF1 has a mutation status of P26Q, The gene EOMES has a mutation status of F316L, The gene SCN11A has a mutation status of A630V, The gene AC109583.1 has a mutation status of R165K, The gene EPHA6 has a mutation status of R268C, The gene SMC4 has a mutation status of R107C, The gene AHSG has a mutation status of A44D, The gene ATP13A4 has a mutation status of F1036L, The gene CFAP99 has a mutation status of A91D, The gene CRMP1 has a mutation status of A67S, The gene HTRA3 has a mutation status of I317I, The gene HMX1 has a mutation status of R212S, The gene LCORL has a mutation status of C1815Y, The gene SEL1L3 has a mutation status of V877A, The gene RFC1 has a mutation status of S1145L, The gene UGT2B15 has a mutation status of S172R, The gene FRAS1 has a mutation status of Q1325H, The gene EGF has a mutation status of R221T, The gene FAT4 has a mutation status of F4337fs, The gene FAT4 has a mutation status of R4796K, The gene IQCM has a mutation status of E17K, The gene PALLD has a mutation status of S199P, The gene CFAP97 has a mutation status of F353L, The gene MTRR has a mutation status of H128R, The gene RICTOR has a mutation status of G407A, The gene SRFBP1 has a mutation status of E12Q, The gene CSNK1G3 has a mutation status of L247F, The gene MINAR2 has a mutation status of E115Q, The gene PSD2 has a mutation status of G486R, The gene SGCD has a mutation status of K24K, The gene FBLL1 has a mutation status of L198M, The gene ZFP2 has a mutation status of C160Y, The gene RUFY1 has a mutation status of G27D, The gene SQSTM1 has a mutation status of T221T, The gene FLT4 has a mutation status of N612N, The gene TRIM7 has a mutation status of G9R, The gene FAM8A1 has a mutation status of G134I, The gene FAM8A1 has a mutation status of A140T, The gene C6orf62 has a mutation status of S6C, The gene H3C1 has a mutation status of D82H, The gene HLA-DRB5 has a mutation status of T262R, The gene HLA-DRB5 has a mutation status of H260Q, The gene HLA-DRB5 has a mutation status of I248L, The gene HLA-DRB5 has a mutation status of L246L, The gene HLA-DRB5 has a mutation status of Q38W, The gene MOCS1 has a mutation status of T236I, The gene RHAG has a mutation status of M269I, The gene EYS has a mutation status of Q601fs, The gene SLC22A16 has a mutation status of K530*, The gene FRK has a mutation status of A401A, The gene TAAR2 has a mutation status of F66F, The gene TXLNB has a mutation status of C635C, The gene STXBP5 has a mutation status of R860W, The gene CCDC170 has a mutation status of Q285E, The gene TULP4 has a mutation status of V301F, The gene LPA has a mutation status of R860Q, The gene PRR18 has a mutation status of A112A, The gene AFDN has a mutation status of D1769D, The gene ELFN1 has a mutation status of P338P, The gene IQCE has a mutation status of R394*, The gene POU6F2 has a mutation status of P228P, The gene IKZF1 has a mutation status of H351Q, The gene IKZF1 has a mutation status of Y435Y, The gene PSPH has a mutation status of L68P, The gene SRRM3 has a mutation status of A114A, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene SPDYE6 has a mutation status of H337R, The gene SLC37A3 has a mutation status of V23V, The gene H2BE1 has a mutation status of S33Y, The gene CLDN23 has a mutation status of E211*, The gene MTUS1 has a mutation status of G628R, The gene DDHD2 has a mutation status of S377S, The gene THAP1 has a mutation status of P103A, The gene SPIDR has a mutation status of S49L, The gene RB1CC1 has a mutation status of Q43H, The gene CRH has a mutation status of Q39*, The gene RNF19A has a mutation status of Y811C, The gene FAM83A has a mutation status of V53G, The gene FAM83A has a mutation status of L54V, The gene LY6K has a mutation status of C100*, The gene PLEC has a mutation status of T4553M, The gene KDM4C has a mutation status of N704T, The gene WNK2 has a mutation status of P1004H, The gene GABBR2 has a mutation status of R797H, The gene FRRS1L has a mutation status of R51A, The gene SUSD1 has a mutation status of S212N, The gene DAB2IP has a mutation status of L83L, The gene LHX2 has a mutation status of H183H, The gene CCDC187 has a mutation status of R294H, The gene MAMDC4 has a mutation status of G843G, The gene MAN1B1 has a mutation status of I102L, The gene TUBB8 has a mutation status of D88D, The gene RHOBTB1 has a mutation status of L540L, The gene PSAP has a mutation status of G74G, The gene KAT6B has a mutation status of L985L, The gene LIPK has a mutation status of M291R, The gene PANK1 has a mutation status of A98V, The gene BTAF1 has a mutation status of E99E, The gene PDZD7 has a mutation status of S764I, The gene CFAP43 has a mutation status of T59T, The gene TDRD1 has a mutation status of V413V, The gene MGMT has a mutation status of R9C, The gene PNPLA2 has a mutation status of G483W, The gene MUC5AC has a mutation status of T3668P, The gene LSP1 has a mutation status of H453H, The gene MRGPRG has a mutation status of A111A, The gene OR51V1 has a mutation status of L43L, The gene CAVIN3 has a mutation status of P131H, The gene SMPD1 has a mutation status of Y244H, The gene AMPD3 has a mutation status of A763G, The gene ANO3 has a mutation status of A770V, The gene KIAA1549L has a mutation status of R1396Q, The gene EXT2 has a mutation status of V363M, The gene LRP4 has a mutation status of D113D, The gene OR4C16 has a mutation status of L280L, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene PRPF19 has a mutation status of H273R, The gene PLAAT3 has a mutation status of A96V, The gene PYGM has a mutation status of A365V, The gene ACTN3 has a mutation status of M1I, The gene CORO1B has a mutation status of H425P, The gene GPR152 has a mutation status of E190K, The gene PDE2A has a mutation status of L381L, The gene GAB2 has a mutation status of M465I, The gene FAT3 has a mutation status of R3256R, The gene CEP164 has a mutation status of S566T, The gene SLC37A4 has a mutation status of S22R, The gene IQSEC3 has a mutation status of A454A, The gene FBXL14 has a mutation status of S242L, The gene ACSM4 has a mutation status of I563I, The gene SOX5 has a mutation status of M686T, The gene TMTC1 has a mutation status of V507V, The gene IGFBP6 has a mutation status of E46D, The gene ITGA7 has a mutation status of G292G, The gene MBD6 has a mutation status of P880L, The gene TRHDE has a mutation status of P204P, The gene CFAP54 has a mutation status of V933G, The gene BTBD11 has a mutation status of K375K, The gene SVOP has a mutation status of T67N, The gene FOXN4 has a mutation status of P152P, The gene GCN1 has a mutation status of R1803W, The gene SIRT4 has a mutation status of R178R, The gene ADGRD1 has a mutation status of T790M, The gene ZMYM2 has a mutation status of N1317N, The gene CENPJ has a mutation status of P1104T, The gene RGCC has a mutation status of G8C, The gene PCDH9 has a mutation status of S79S, The gene DACH1 has a mutation status of P47fs, The gene ACOD1 has a mutation status of R331H, The gene LAMP1 has a mutation status of N249K, The gene PCK2 has a mutation status of P107P, The gene GZMB has a mutation status of G83S, The gene NOVA1 has a mutation status of T382A, The gene EAPP has a mutation status of E54E, The gene ARMH4 has a mutation status of Y733Y, The gene KCNH5 has a mutation status of S699R, The gene SYNE2 has a mutation status of P4240S, The gene SYNE2 has a mutation status of K4749K, The gene RAB15 has a mutation status of A172V, The gene TRIP11 has a mutation status of P1879P, The gene PAPOLA has a mutation status of P365S, The gene CCDC85C has a mutation status of R34R, The gene EXOC3L4 has a mutation status of G232G, The gene KLC1 has a mutation status of N524N, The gene PPP1R13B has a mutation status of P834P, The gene KIF26A has a mutation status of S1437F, The gene AHNAK2 has a mutation status of T230T, The gene DPH6 has a mutation status of L187F, The gene TLN2 has a mutation status of A451A, The gene NOX5 has a mutation status of Q679H, The gene CSPG4 has a mutation status of S1596S, The gene GOLGA6L10 has a mutation status of R385R, The gene KIF7 has a mutation status of L235L, The gene PRC1 has a mutation status of R281W, The gene SV2B has a mutation status of I212T, The gene RGS11 has a mutation status of Y334C, The gene CHTF18 has a mutation status of L310V, The gene LMF1 has a mutation status of F139F, The gene CRAMP1 has a mutation status of G19C, The gene PKD1 has a mutation status of V2782M, The gene PKMYT1 has a mutation status of P362P, The gene PDXDC1 has a mutation status of E775D, The gene TMC5 has a mutation status of A121V, The gene ACSM1 has a mutation status of G508V, The gene ZKSCAN2 has a mutation status of Q860Q, The gene KIAA0556 has a mutation status of P920P, The gene MMP15 has a mutation status of T313P, The gene CDH16 has a mutation status of G352G, The gene SMPD3 has a mutation status of S527S, The gene CFDP1 has a mutation status of E242E, The gene OSGIN1 has a mutation status of Q418R, The gene ZCCHC14 has a mutation status of P990H, The gene ZFPM1 has a mutation status of R703R, The gene DPEP1 has a mutation status of R348M, The gene VPS9D1 has a mutation status of P252T, The gene CLUH has a mutation status of K172R, The gene ITGAE has a mutation status of C236R, The gene TP53 has a mutation status of R248W, The gene NOS2 has a mutation status of P918P, The gene TRAF4 has a mutation status of R173Q, The gene NUFIP2 has a mutation status of T584A, The gene MMP28 has a mutation status of P453S, The gene CCL4L2 has a mutation status of P67R, The gene DUSP3 has a mutation status of G127V, The gene DUSP3 has a mutation status of K79R, The gene AXIN2 has a mutation status of D90D, The gene USH1G has a mutation status of A139A, The gene FBF1 has a mutation status of R895W, The gene BAHCC1 has a mutation status of P330H, The gene OXLD1 has a mutation status of E69G, The gene EPB41L3 has a mutation status of A920D, The gene PIEZO2 has a mutation status of H1102Y, The gene ZNF532 has a mutation status of A730A, The gene CCDC102B has a mutation status of K419E, The gene TSHZ1 has a mutation status of P693P, The gene TMEM259 has a mutation status of F348L, The gene PWWP3A has a mutation status of A670S, The gene IZUMO4 has a mutation status of V150V, The gene AC005551.1 has a mutation status of F143L, The gene DAPK3 has a mutation status of A333A, The gene FBN3 has a mutation status of T761R, The gene KANK3 has a mutation status of A558S, The gene MUC16 has a mutation status of A643S, The gene ZNF266 has a mutation status of H385Q, The gene ZNF560 has a mutation status of R536Q, The gene CARM1 has a mutation status of A517S, The gene ZNF433 has a mutation status of R470S, The gene MAST1 has a mutation status of V986V, The gene RFX1 has a mutation status of V786A, The gene USHBP1 has a mutation status of Y356H, The gene ZNF536 has a mutation status of Q356K, The gene FXYD5 has a mutation status of R145R, The gene RBM42 has a mutation status of P6A, The gene FCGBP has a mutation status of N2927N, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene LIPE has a mutation status of S275S, The gene PSG3 has a mutation status of S192S, The gene APOE has a mutation status of H158N, The gene APOE has a mutation status of H158Q, The gene CLASRP has a mutation status of D139D, The gene CLASRP has a mutation status of D196D, The gene PPP1R37 has a mutation status of A600S, The gene SCAF1 has a mutation status of P720A, The gene MYBPC2 has a mutation status of R1057C, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of N187T, The gene C19orf85 has a mutation status of *223*, The gene PEG3 has a mutation status of E1444K, The gene ZNF132 has a mutation status of S471S, The gene TRIM28 has a mutation status of A455A, The gene NRSN2 has a mutation status of G14V, The gene DTD1 has a mutation status of D156E, The gene RIN2 has a mutation status of L724F, The gene PAX1 has a mutation status of G501G, The gene TPX2 has a mutation status of C364F, The gene POFUT1 has a mutation status of P118P, The gene UBE2C has a mutation status of S87R, The gene FAM217B has a mutation status of R248L, The gene C21orf91 has a mutation status of V98M, The gene HUNK has a mutation status of A231A, The gene GSTT4 has a mutation status of E126K, The gene TTC28 has a mutation status of R24L, The gene SYN3 has a mutation status of Q428H, The gene APOL6 has a mutation status of D68E, The gene TRIOBP has a mutation status of W56C, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene FBLN1 has a mutation status of A5A, The gene KLHDC7B has a mutation status of G169W, The gene CSF2RA has a mutation status of R84H, The gene NLGN4X has a mutation status of R753S, The gene CFAP47 has a mutation status of S1684S, The gene TRO has a mutation status of N1296K, The gene ZXDA has a mutation status of A130T, The gene MED12 has a mutation status of A1558A, The gene TCEAL6 has a mutation status of G179G, The gene SLC25A5 has a mutation status of T221R, The gene IDH3G has a mutation status of G184G, The gene MT-ND1 has a mutation status of K58K, The gene MT-CO1 has a mutation status of E119E, The gene MT-ATP6 has a mutation status of A177T, The gene MT-CO3 has a mutation status of L164L, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND4 has a mutation status of G242G, The gene MT-ND4 has a mutation status of L361L, The gene MT-ND5 has a mutation status of I468I, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L, The gene MT-CYB has a mutation status of A380T
PRAD
The gene PRAMEF4 has a mutation status of V117F, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene UBR4 has a mutation status of H3100H, The gene EPHA8 has a mutation status of V826M, The gene CRYBG2 has a mutation status of T581M, The gene PTPRU has a mutation status of R618C, The gene S100PBP has a mutation status of L350F, The gene HOOK1 has a mutation status of H710R, The gene AMPD1 has a mutation status of D241D, The gene NOTCH2 has a mutation status of D661E, The gene NBPF12 has a mutation status of R1042R, The gene AC242842.3 has a mutation status of V503L, The gene S100A10 has a mutation status of Q93H, The gene SH2D2A has a mutation status of G66E, The gene DNM3 has a mutation status of R271Q, The gene KLHL20 has a mutation status of V225I, The gene PIK3C2B has a mutation status of C1285C, The gene PIK3C2B has a mutation status of L1283*, The gene USH2A has a mutation status of L2135V, The gene HLX has a mutation status of A166V, The gene DNAH14 has a mutation status of V1826I, The gene DISC1 has a mutation status of C239C, The gene DISC1 has a mutation status of M291T, The gene ARID4B has a mutation status of Y608Y, The gene PLD5 has a mutation status of E303K, The gene OR2T12 has a mutation status of T6N, The gene OR2T4 has a mutation status of V109L, The gene LYPD8 has a mutation status of Q24P, The gene KIDINS220 has a mutation status of I1237V, The gene RASGRP3 has a mutation status of H159Y, The gene TMEM247 has a mutation status of A156A, The gene EHBP1 has a mutation status of R863W, The gene VPS54 has a mutation status of M50L, The gene RNF149 has a mutation status of K277T, The gene RGPD4 has a mutation status of S1305A, The gene POLR1B has a mutation status of R523P, The gene IWS1 has a mutation status of E175K, The gene KIF5C has a mutation status of A638A, The gene NEB has a mutation status of N7760D, The gene CYBRD1 has a mutation status of L81P, The gene DLX1 has a mutation status of A154P, The gene SP3 has a mutation status of S389C, The gene PLCL1 has a mutation status of Q770L, The gene PNKD has a mutation status of Y293H, The gene CHPF has a mutation status of L749L, The gene TRPM8 has a mutation status of L509L, The gene KIF1A has a mutation status of L1327I, The gene SATB1 has a mutation status of P39P, The gene NGLY1 has a mutation status of N444Y, The gene CACNA1D has a mutation status of A1285T, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene DNAH12 has a mutation status of D2383E, The gene ZNF717 has a mutation status of 21_22insISFEDVAVHFTWEEWQDLDNAQRTLYRD, The gene DZIP1L has a mutation status of Q627H, The gene MRAS has a mutation status of G25G, The gene ZIC4 has a mutation status of Y58*, The gene MED12L has a mutation status of I1618I, The gene VEPH1 has a mutation status of R782G, The gene VEPH1 has a mutation status of L219L, The gene PIK3CA has a mutation status of C420R, The gene ZNF718 has a mutation status of V88L, The gene CRACD has a mutation status of Q84K, The gene ADGRL3 has a mutation status of R906R, The gene ANTXR2 has a mutation status of G136V, The gene METAP1 has a mutation status of M329V, The gene NDST3 has a mutation status of D584E, The gene ASIC5 has a mutation status of S44Y, The gene ADAM29 has a mutation status of T800M, The gene TRAPPC11 has a mutation status of K510N, The gene CFAP97 has a mutation status of T60A, The gene F11 has a mutation status of S495F, The gene FAT1 has a mutation status of V2202V, The gene TRIML1 has a mutation status of A293G, The gene SLC6A19 has a mutation status of T228M, The gene ZSWIM6 has a mutation status of I109L, The gene ZSWIM6 has a mutation status of W112*, The gene ERBIN has a mutation status of A1125A, The gene ZBED3 has a mutation status of L155A, The gene PPIP5K2 has a mutation status of Q396E, The gene SLC22A5 has a mutation status of V135V, The gene PCDHB4 has a mutation status of P677P, The gene PCDHB11 has a mutation status of A570T, The gene PCDHB13 has a mutation status of S534T, The gene HAVCR1 has a mutation status of M116L, The gene HLA-A has a mutation status of K292E, The gene PRR3 has a mutation status of N8S, The gene DDX39B has a mutation status of I353I, The gene C6orf132 has a mutation status of P183P, The gene SENP6 has a mutation status of E39*, The gene EPHA7 has a mutation status of Y365*, The gene MFSD4B has a mutation status of L182Y, The gene CEP85L has a mutation status of K223T, The gene MYCT1 has a mutation status of R23I, The gene SCAF8 has a mutation status of A32fs, The gene PDE10A has a mutation status of A86T, The gene IQCE has a mutation status of V547V, The gene SKAP2 has a mutation status of T296I, The gene GTF2IRD1 has a mutation status of V406I, The gene ZNF804B has a mutation status of I1059I, The gene TRRAP has a mutation status of A1894G, The gene PCOLCE has a mutation status of S78S, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S395T, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene CTAGE6 has a mutation status of Q429G, The gene OR2A25 has a mutation status of C233F, The gene EZH2 has a mutation status of P193R, The gene GOT1L1 has a mutation status of H369L, The gene ARFGEF1 has a mutation status of N203N, The gene GSDMD has a mutation status of E143E, The gene SCRIB has a mutation status of A1414V, The gene EPPK1 has a mutation status of V5016V, The gene MROH1 has a mutation status of E322fs, The gene ARHGAP39 has a mutation status of A550T, The gene BNC2 has a mutation status of S165S, The gene CAAP1 has a mutation status of T65T, The gene MYORG has a mutation status of D442N, The gene ZNF462 has a mutation status of R528R, The gene SVEP1 has a mutation status of G1028R, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of R294H, The gene AKR1C4 has a mutation status of M120V, The gene PCDH15 has a mutation status of L1670L, The gene HKDC1 has a mutation status of Q607H, The gene HK1 has a mutation status of R398H, The gene CDH23 has a mutation status of A1616T, The gene INA has a mutation status of Y315H, The gene CCDC186 has a mutation status of E645E, The gene EBF3 has a mutation status of G511S, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of C903C, The gene MUC5AC has a mutation status of R1187R, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of S1927S, The gene MUC5AC has a mutation status of T3364S, The gene MUC5AC has a mutation status of T3367T, The gene MUC5AC has a mutation status of R3590R, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of A4396A, The gene MUC5AC has a mutation status of STTSASTA4496del, The gene TUB has a mutation status of D347D, The gene TRIM51 has a mutation status of L127F, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene OR10Q1 has a mutation status of A195S, The gene AHNAK has a mutation status of R102C, The gene C11orf95 has a mutation status of L336L, The gene CCDC88B has a mutation status of A445V, The gene CCDC88B has a mutation status of D886S, The gene SLC22A12 has a mutation status of G335G, The gene CCDC87 has a mutation status of P346L, The gene PITPNM1 has a mutation status of G800G, The gene ACY3 has a mutation status of Q63Q, The gene SHANK2 has a mutation status of T626T, The gene HSPA8 has a mutation status of L599L, The gene VSIG10L2 has a mutation status of R172W, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R31 has a mutation status of G253K, The gene TAS2R46 has a mutation status of 296_297HV>QM, The gene TAS2R46 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PTPRO has a mutation status of I1164F, The gene SLCO1B3 has a mutation status of T531T, The gene RACGAP1 has a mutation status of R18Q, The gene LRP1 has a mutation status of C2342C, The gene SETD1B has a mutation status of K938E, The gene NBEA has a mutation status of Y957F, The gene OXGR1 has a mutation status of L75V, The gene PCID2 has a mutation status of D225N, The gene ADPRHL1 has a mutation status of P1482P, The gene TFDP1 has a mutation status of P389P, The gene AKAP6 has a mutation status of A2067P, The gene RPL10L has a mutation status of W171L, The gene FOS has a mutation status of S260G, The gene INF2 has a mutation status of L165L, The gene LPCAT4 has a mutation status of A375V, The gene RPUSD2 has a mutation status of R214H, The gene ITPKA has a mutation status of N152N, The gene ANKDD1A has a mutation status of L516L, The gene SMAD3 has a mutation status of S222S, The gene GOLGA6L10 has a mutation status of R300H, The gene GOLGA6L10 has a mutation status of R272C, The gene WDR90 has a mutation status of A786V, The gene PPL has a mutation status of R1047R, The gene ABCC6 has a mutation status of A1303P, The gene FUS has a mutation status of R441R, The gene CYLD has a mutation status of F672F, The gene DOK4 has a mutation status of G113G, The gene PLD2 has a mutation status of R765R, The gene NLGN2 has a mutation status of P802L, The gene TP53 has a mutation status of E271fs, The gene ALOX15B has a mutation status of F344L, The gene NF1 has a mutation status of Q347H, The gene MYO1D has a mutation status of D79N, The gene CCL4L2 has a mutation status of P67R, The gene C17orf78 has a mutation status of T169S, The gene ARHGAP23 has a mutation status of E955G, The gene KRTAP4-6 has a mutation status of R106H, The gene KCNH4 has a mutation status of T330A, The gene DCAKD has a mutation status of R108C, The gene MAP3K14 has a mutation status of E767G, The gene PHB has a mutation status of Q187Q, The gene SGCA has a mutation status of T208I, The gene NOG has a mutation status of P84H, The gene LPO has a mutation status of R21Q, The gene SMARCD2 has a mutation status of A207A, The gene PECAM1 has a mutation status of V513V, The gene RGS9 has a mutation status of I3I, The gene SDK2 has a mutation status of A814F, The gene TTYH2 has a mutation status of N475N, The gene NPC1 has a mutation status of T1066T, The gene RNF165 has a mutation status of F143F, The gene MC4R has a mutation status of L263L, The gene DSEL has a mutation status of Q659R, The gene POLRMT has a mutation status of A777V, The gene POLRMT has a mutation status of R253W, The gene CNN2 has a mutation status of M249T, The gene PLIN4 has a mutation status of C801fs, The gene MICOS13 has a mutation status of P68A, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T12336L, The gene BRD4 has a mutation status of N1088N, The gene ZNF737 has a mutation status of P521L, The gene FCGBP has a mutation status of V4112L, The gene ZNF546 has a mutation status of I322T, The gene ZNF235 has a mutation status of S311fs, The gene NTN5 has a mutation status of P462T, The gene TEAD2 has a mutation status of T344T, The gene ZNF600 has a mutation status of A549A, The gene ZNF160 has a mutation status of T812T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M21V, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Y99I, The gene LILRB1 has a mutation status of 171_172QP>HS, The gene LILRB1 has a mutation status of Q401L, The gene KIR2DL3 has a mutation status of G12A, The gene KIR2DL3 has a mutation status of P224S, The gene KIR2DL1 has a mutation status of T91K, The gene KIR2DL1 has a mutation status of N144S, The gene SSC5D has a mutation status of S1140F, The gene ZNF329 has a mutation status of L186fs, The gene RRBP1 has a mutation status of S222F, The gene SEC23B has a mutation status of F702F, The gene EPB41L1 has a mutation status of G73S, The gene ARHGAP40 has a mutation status of A517A, The gene LPIN3 has a mutation status of Y3Y, The gene PLTP has a mutation status of R372H, The gene PREX1 has a mutation status of I454F, The gene PTGIS has a mutation status of T327K, The gene RIPOR3 has a mutation status of L640L, The gene MOCS3 has a mutation status of G445G, The gene ZNF217 has a mutation status of Y17F, The gene HELZ2 has a mutation status of L2444L, The gene HELZ2 has a mutation status of H1783Y, The gene SON has a mutation status of V646G, The gene TSPEAR has a mutation status of Y416S, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene TUBGCP6 has a mutation status of L1171L, The gene SBF1 has a mutation status of R1557H, The gene GTPBP6 has a mutation status of M181L, The gene GTPBP6 has a mutation status of G61R, The gene AKAP17A has a mutation status of K523K, The gene SHROOM2 has a mutation status of A898A, The gene FANCB has a mutation status of N746N, The gene FANCB has a mutation status of L744L, The gene TXLNG has a mutation status of T334K, The gene CFAP47 has a mutation status of N2532D, The gene JADE3 has a mutation status of E75A, The gene CDK16 has a mutation status of P28P, The gene WDR13 has a mutation status of V278fs, The gene GRIPAP1 has a mutation status of K530K, The gene ARHGEF9 has a mutation status of Y170F, The gene AMER1 has a mutation status of D233G, The gene FAM236C has a mutation status of T34T, The gene ARMCX2 has a mutation status of Q503Q, The gene SLC25A5 has a mutation status of T221R, The gene UPF3B has a mutation status of D86E, The gene THOC2 has a mutation status of S485N, The gene ARHGAP36 has a mutation status of A496S, The gene CD40LG has a mutation status of H125N, The gene AC236972.4 has a mutation status of S1611S, The gene MT-ND1 has a mutation status of E202E, The gene MT-ND2 has a mutation status of F342F, The gene MT-CO1 has a mutation status of T181T, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A
BRCA
The gene TMEM52 has a mutation status of A172A, The gene ARHGEF16 has a mutation status of A79V, The gene CCDC27 has a mutation status of E327*, The gene RNF207 has a mutation status of R578T, The gene KLHL21 has a mutation status of R275L, The gene SLC2A5 has a mutation status of A113A, The gene UBE4B has a mutation status of E983D, The gene CASZ1 has a mutation status of A1273P, The gene PRAMEF13 has a mutation status of S245Y, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene CROCC has a mutation status of Q917*, The gene CROCC has a mutation status of R918L, The gene ARHGEF10L has a mutation status of A164G, The gene ARHGEF10L has a mutation status of A1199T, The gene HSPG2 has a mutation status of P2142T, The gene RSRP1 has a mutation status of R169fs, The gene RHCE has a mutation status of Q25*, The gene TRIM63 has a mutation status of R112Q, The gene ZDHHC18 has a mutation status of A239V, The gene GMEB1 has a mutation status of N365N, The gene PTPRU has a mutation status of E979G, The gene GJA4 has a mutation status of G283R, The gene COL8A2 has a mutation status of Y605*, The gene MAP7D1 has a mutation status of E711G, The gene KCNQ4 has a mutation status of A402G, The gene HIVEP3 has a mutation status of R1891W, The gene PTCH2 has a mutation status of A517G, The gene TOE1 has a mutation status of L53L, The gene CC2D1B has a mutation status of V619V, The gene ORC1 has a mutation status of L790L, The gene PARS2 has a mutation status of A271S, The gene LHX8 has a mutation status of E23K, The gene AC093155.3 has a mutation status of N298N, The gene ARHGAP29 has a mutation status of I281V, The gene ATP1A1 has a mutation status of V329L, The gene NOTCH2 has a mutation status of A21S, The gene NBPF26 has a mutation status of R237W, The gene NBPF12 has a mutation status of R1042R, The gene ACP6 has a mutation status of D44Y, The gene RFX5 has a mutation status of T364K, The gene CRNN has a mutation status of R424L, The gene S100A7 has a mutation status of L55P, The gene SPTA1 has a mutation status of V184G, The gene DCAF8 has a mutation status of R225R, The gene USP21 has a mutation status of H314N, The gene RGS4 has a mutation status of G24S, The gene LHX4 has a mutation status of S336N, The gene KDM5B has a mutation status of N756T, The gene CHIT1 has a mutation status of A149S, The gene SLC30A1 has a mutation status of K479Q, The gene USH2A has a mutation status of S4143L, The gene USH2A has a mutation status of Y586Y, The gene ENAH has a mutation status of I651T, The gene CDC42BPA has a mutation status of D1224D, The gene MRPL55 has a mutation status of T63P, The gene GALNT2 has a mutation status of V133G, The gene SIPA1L2 has a mutation status of S1288T, The gene OR2T4 has a mutation status of V109L, The gene OR2G6 has a mutation status of S67S, The gene HS1BP3 has a mutation status of Q360Q, The gene UBXN2A has a mutation status of V4I, The gene FAM228A has a mutation status of I52I, The gene KIF3C has a mutation status of G283G, The gene PRR30 has a mutation status of H19Q, The gene C2orf16 has a mutation status of C1412Y, The gene OXER1 has a mutation status of P123P, The gene MSH2 has a mutation status of M688I, The gene GCFC2 has a mutation status of D261D, The gene CNGA3 has a mutation status of A619V, The gene GPR45 has a mutation status of L172L, The gene SH3RF3 has a mutation status of S350S, The gene PLA2R1 has a mutation status of P598P, The gene KCNH7 has a mutation status of E372E, The gene SCN2A has a mutation status of N1196K, The gene TTC30B has a mutation status of R280R, The gene TTN has a mutation status of D20086H, The gene ITGA4 has a mutation status of A78P, The gene COL3A1 has a mutation status of G1050D, The gene MSTN has a mutation status of L156I, The gene IKZF2 has a mutation status of Y175Y, The gene TNS1 has a mutation status of Q666*, The gene SPEG has a mutation status of L2352R, The gene GMPPA has a mutation status of A274G, The gene CHPF has a mutation status of G280G, The gene OBSL1 has a mutation status of Q1809P, The gene OBSL1 has a mutation status of L1806F, The gene STK11IP has a mutation status of L1035V, The gene USP40 has a mutation status of T711T, The gene RBM44 has a mutation status of T945A, The gene PER2 has a mutation status of Y482*, The gene MTERF4 has a mutation status of R24K, The gene STK25 has a mutation status of N9S, The gene XPC has a mutation status of A902G, The gene BTD has a mutation status of L324L, The gene ZBTB47 has a mutation status of E573E, The gene ANO10 has a mutation status of Y203*, The gene LRRC2 has a mutation status of K364N, The gene SETD2 has a mutation status of E972K, The gene SCAP has a mutation status of A465A, The gene UBA7 has a mutation status of R29S, The gene TMEM115 has a mutation status of S320R, The gene RBM15B has a mutation status of P268P, The gene RFT1 has a mutation status of A287G, The gene RFT1 has a mutation status of T276T, The gene ERC2 has a mutation status of N53S, The gene C3orf49 has a mutation status of M276I, The gene RIOX2 has a mutation status of I290V, The gene OR5H15 has a mutation status of Q207K, The gene ABI3BP has a mutation status of M615T, The gene NXPE3 has a mutation status of A279D, The gene NECTIN3 has a mutation status of S295L, The gene CASR has a mutation status of Q934Q, The gene PARP9 has a mutation status of N676S, The gene ADCY5 has a mutation status of S532R, The gene CFAP100 has a mutation status of R125R, The gene MCM2 has a mutation status of R870P, The gene H1-8 has a mutation status of R87W, The gene MSL2 has a mutation status of P425R, The gene STAG1 has a mutation status of N565N, The gene ESYT3 has a mutation status of R186H, The gene TFDP2 has a mutation status of T308T, The gene PAQR9 has a mutation status of Y278P, The gene EEF1AKMT4-ECE2 has a mutation status of L137L, The gene RTP1 has a mutation status of F113L, The gene IL1RAP has a mutation status of E384K, The gene MSX1 has a mutation status of R157S, The gene ABLIM2 has a mutation status of I337T, The gene ARAP2 has a mutation status of R136K, The gene C4orf19 has a mutation status of D36D, The gene KCTD8 has a mutation status of P262A, The gene ATP10D has a mutation status of V194V, The gene ATP10D has a mutation status of R1030G, The gene CXCL6 has a mutation status of L47L, The gene FAT4 has a mutation status of A43A, The gene FAT4 has a mutation status of R4227Q, The gene IQCM has a mutation status of K316E, The gene CPE has a mutation status of A226D, The gene DDX60L has a mutation status of T1141A, The gene IRF2 has a mutation status of P213L, The gene PLEKHG4B has a mutation status of V1117L, The gene ADCY2 has a mutation status of L244L, The gene FASTKD3 has a mutation status of V392M, The gene PDZD2 has a mutation status of A2058P, The gene SPEF2 has a mutation status of D1584D, The gene MROH2B has a mutation status of D867D, The gene ERBIN has a mutation status of Y1336*, The gene WDR41 has a mutation status of L412L, The gene LNPEP has a mutation status of G388D, The gene TNFAIP8 has a mutation status of T13K, The gene JADE2 has a mutation status of E148G, The gene JADE2 has a mutation status of A332A, The gene PROB1 has a mutation status of L950L, The gene PCDHB8 has a mutation status of R725R, The gene PCDHB10 has a mutation status of Q11*, The gene ARAP3 has a mutation status of R433C, The gene TCOF1 has a mutation status of P744P, The gene NUDCD2 has a mutation status of A53A, The gene SFXN1 has a mutation status of I191V, The gene CLTB has a mutation status of N81S, The gene UNC5A has a mutation status of A798V, The gene TMED9 has a mutation status of A32G, The gene RUFY1 has a mutation status of S586T, The gene MAML1 has a mutation status of P771Q, The gene EXOC2 has a mutation status of T594M, The gene MYLK4 has a mutation status of S298S, The gene RREB1 has a mutation status of P159P, The gene DSP has a mutation status of R105Q, The gene H1-2 has a mutation status of A116G, The gene H2AC15 has a mutation status of A15A, The gene IER3 has a mutation status of S62N, The gene BAG6 has a mutation status of S623F, The gene NOTCH4 has a mutation status of R1410H, The gene TAP1 has a mutation status of A609G, The gene BRD2 has a mutation status of E503E, The gene COL11A2 has a mutation status of V841V, The gene FANCE has a mutation status of R134H, The gene UBR2 has a mutation status of T588T, The gene CUL7 has a mutation status of P663A, The gene PTK7 has a mutation status of P507P, The gene SLC22A7 has a mutation status of T515T, The gene POLH has a mutation status of T471P, The gene TDRD6 has a mutation status of K164N, The gene TNFRSF21 has a mutation status of T66I, The gene CRISP1 has a mutation status of L206I, The gene PKHD1 has a mutation status of G604V, The gene PAQR8 has a mutation status of Y55*, The gene COL21A1 has a mutation status of P762fs, The gene GABRR2 has a mutation status of R354C, The gene TBC1D32 has a mutation status of W676L, The gene LAMA2 has a mutation status of C1060F, The gene VNN1 has a mutation status of S306S, The gene PBOV1 has a mutation status of P33Q, The gene ARFGEF3 has a mutation status of R1966K, The gene NHSL1 has a mutation status of Y80*, The gene UTRN has a mutation status of Q3230R, The gene STXBP5 has a mutation status of S17L, The gene STXBP5 has a mutation status of S19L, The gene SASH1 has a mutation status of Y659Y, The gene TBXT has a mutation status of V110V, The gene PRR18 has a mutation status of S123L, The gene GET4 has a mutation status of S55fs, The gene PHF14 has a mutation status of S296I, The gene HDAC9 has a mutation status of G866G, The gene YAE1 has a mutation status of T191T, The gene INHBA has a mutation status of T125T, The gene TNS3 has a mutation status of F1121F, The gene PSPH has a mutation status of L68P, The gene FZD9 has a mutation status of Y52*, The gene AKAP9 has a mutation status of Q2730R, The gene EPO has a mutation status of L13F, The gene EPHB4 has a mutation status of P840A, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T650M, The gene MUC3A has a mutation status of P654P, The gene MUC3A has a mutation status of T1379P, The gene MUC3A has a mutation status of P3166P, The gene MUC3A has a mutation status of G3182G, The gene AP1S1 has a mutation status of F67F, The gene VGF has a mutation status of H463P, The gene MET has a mutation status of M636V, The gene ASB15 has a mutation status of T3I, The gene ZC3HC1 has a mutation status of A65V, The gene KLF14 has a mutation status of A39A, The gene CLCN1 has a mutation status of E950K, The gene EPHA1 has a mutation status of V257G, The gene ZNF467 has a mutation status of R224H, The gene ZNF467 has a mutation status of C218Y, The gene KCNH2 has a mutation status of L315F, The gene ATG9B has a mutation status of E874E, The gene PAXIP1 has a mutation status of D177D, The gene LMBR1 has a mutation status of C202Y, The gene TNKS has a mutation status of H12N, The gene C8orf48 has a mutation status of R135C, The gene LPL has a mutation status of A5A, The gene PTK2B has a mutation status of P645A, The gene KIF13B has a mutation status of A1605V, The gene KCNU1 has a mutation status of P728L, The gene RAB11FIP1 has a mutation status of G8G, The gene ANK1 has a mutation status of V1223A, The gene ZFHX4 has a mutation status of L1077L, The gene ZFHX4 has a mutation status of P2061P, The gene DECR1 has a mutation status of A104A, The gene TSPYL5 has a mutation status of E184G, The gene ENPP2 has a mutation status of P325S, The gene FER1L6 has a mutation status of S1339S, The gene MTSS1 has a mutation status of C103R, The gene FAM83H has a mutation status of V429G, The gene WDR97 has a mutation status of P1544P, The gene SCRT1 has a mutation status of P338S, The gene ADCK5 has a mutation status of N324S, The gene FOXH1 has a mutation status of G267G, The gene SIGMAR1 has a mutation status of F37F, The gene STOML2 has a mutation status of S21F, The gene RUSC2 has a mutation status of I1061I, The gene ZCCHC7 has a mutation status of R150Q, The gene FRMPD1 has a mutation status of F655F, The gene EXOSC3 has a mutation status of P91T, The gene SHB has a mutation status of E285G, The gene SPATA31A6 has a mutation status of A1200A, The gene AL358113.1 has a mutation status of A776S, The gene MAMDC2 has a mutation status of L21P, The gene TRPM6 has a mutation status of E1638fs, The gene PCSK5 has a mutation status of V1396A, The gene PRUNE2 has a mutation status of D3081V, The gene FOXB2 has a mutation status of A224V, The gene WNK2 has a mutation status of A1828V, The gene TEX10 has a mutation status of R660R, The gene ELP1 has a mutation status of F631L, The gene DENND1A has a mutation status of Q528fs, The gene IER5L has a mutation status of A210A, The gene HMCN2 has a mutation status of A3911D, The gene FUBP3 has a mutation status of D209E, The gene RAPGEF1 has a mutation status of D1022N, The gene SETX has a mutation status of A2596G, The gene ADAMTSL2 has a mutation status of S337S, The gene CCDC187 has a mutation status of T90M, The gene TRAF2 has a mutation status of Y388*, The gene ABCA2 has a mutation status of S1094N, The gene RNF224 has a mutation status of G144A, The gene NELFB has a mutation status of E457G, The gene DIP2C has a mutation status of A444P, The gene DIP2C has a mutation status of D443A, The gene ADARB2 has a mutation status of A385P, The gene ITGA8 has a mutation status of V799F, The gene KIAA1217 has a mutation status of P691P, The gene GPR158 has a mutation status of R525W, The gene MPP7 has a mutation status of P87fs, The gene AGAP9 has a mutation status of G294G, The gene PCDH15 has a mutation status of K1023N, The gene STOX1 has a mutation status of G763G, The gene TBATA has a mutation status of I326T, The gene TBATA has a mutation status of L224F, The gene CDH23 has a mutation status of R90R, The gene DLG5 has a mutation status of Y226Y, The gene ANXA11 has a mutation status of V179V, The gene SHLD2 has a mutation status of E282K, The gene SLC35G1 has a mutation status of V348L, The gene SLIT1 has a mutation status of E1451K, The gene CHUK has a mutation status of P239L, The gene CALHM3 has a mutation status of A316A, The gene MXI1 has a mutation status of E131E, The gene DUSP5 has a mutation status of P365L, The gene RBM20 has a mutation status of G181R, The gene HABP2 has a mutation status of Y195C, The gene AL603764.2 has a mutation status of I41V, The gene DHX32 has a mutation status of G112S, The gene B4GALNT4 has a mutation status of A716S, The gene IRF7 has a mutation status of A400P, The gene GATD1 has a mutation status of R164P, The gene MUC6 has a mutation status of D1097G, The gene MUC6 has a mutation status of T1071P, The gene MUC5B has a mutation status of V824M, The gene MUC5B has a mutation status of A1131G, The gene MUC5B has a mutation status of T3533S, The gene OR52B4 has a mutation status of I143N, The gene OR56A4 has a mutation status of L282L, The gene ILK has a mutation status of D21G, The gene OLFML1 has a mutation status of A281P, The gene OVCH2 has a mutation status of I3T, The gene DENND2B has a mutation status of E257G, The gene KIAA1549L has a mutation status of A2V, The gene CAPRIN1 has a mutation status of S642L, The gene LRRC4C has a mutation status of I512L, The gene C1QTNF4 has a mutation status of A192S, The gene TRIM64C has a mutation status of N367I, The gene OR5I1 has a mutation status of S114A, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene SLC43A3 has a mutation status of H212L, The gene INCENP has a mutation status of A130G, The gene SLC22A6 has a mutation status of D282D, The gene BAD has a mutation status of A136S, The gene TM7SF2 has a mutation status of V226G, The gene PCNX3 has a mutation status of R576G, The gene MUS81 has a mutation status of L189F, The gene MRPL11 has a mutation status of D158H, The gene AP002748.5 has a mutation status of R233W, The gene PITPNM1 has a mutation status of P812T, The gene INPPL1 has a mutation status of G1191W, The gene STARD10 has a mutation status of G277G, The gene WNT11 has a mutation status of R255H, The gene USP35 has a mutation status of R30R, The gene FAT3 has a mutation status of G4404N, The gene DYNC2H1 has a mutation status of G2370E, The gene EXPH5 has a mutation status of L1898S, The gene ANKK1 has a mutation status of R581R, The gene PCSK7 has a mutation status of G358E, The gene VPS11 has a mutation status of R904K, The gene ADAMTS15 has a mutation status of S906S, The gene THYN1 has a mutation status of R99P, The gene MANSC1 has a mutation status of K32K, The gene KCNJ8 has a mutation status of R352W, The gene KRAS has a mutation status of G12R, The gene DDX11 has a mutation status of S853S, The gene GXYLT1 has a mutation status of C414H, The gene ENDOU has a mutation status of F299F, The gene OR5BS1P has a mutation status of P183P, The gene LETMD1 has a mutation status of C320F, The gene FIGNL2 has a mutation status of R267H, The gene KRT80 has a mutation status of R275Q, The gene KRT80 has a mutation status of D247Y, The gene KRT75 has a mutation status of I73V, The gene KRT73 has a mutation status of I104I, The gene OR10P1 has a mutation status of S196S, The gene AGAP2 has a mutation status of G171S, The gene MSRB3 has a mutation status of L11F, The gene HELB has a mutation status of K149R, The gene TMCC3 has a mutation status of N201S, The gene ELK3 has a mutation status of N135N, The gene STAB2 has a mutation status of G1392A, The gene TDG has a mutation status of 131_132insI, The gene GIT2 has a mutation status of P527T, The gene GIT2 has a mutation status of Y516Y, The gene ATXN2 has a mutation status of D632D, The gene RNFT2 has a mutation status of L171M, The gene SRRM4 has a mutation status of T566M, The gene ACADS has a mutation status of V401G, The gene WDR66 has a mutation status of M721I, The gene ATP6V0A2 has a mutation status of Q102R, The gene DDX51 has a mutation status of S140R, The gene ANHX has a mutation status of V156V, The gene BRCA2 has a mutation status of G2044V, The gene DGKH has a mutation status of E252*, The gene TSC22D1 has a mutation status of S37R, The gene PCDH8 has a mutation status of G738R, The gene PCDH9 has a mutation status of T56T, The gene RNF113B has a mutation status of S89R, The gene TMTC4 has a mutation status of R481L, The gene MYO16 has a mutation status of P1639P, The gene CARS2 has a mutation status of E442Q, The gene OR4K2 has a mutation status of C97R, The gene TEP1 has a mutation status of L1140V, The gene RPGRIP1 has a mutation status of Y864Y, The gene PPP1R3E has a mutation status of L172V, The gene AP1G2 has a mutation status of P750S, The gene AP1G2 has a mutation status of A64T, The gene PCK2 has a mutation status of F217F, The gene DHRS1 has a mutation status of A259A, The gene DHRS1 has a mutation status of R80G, The gene RALGAPA1 has a mutation status of E514K, The gene SEC23A has a mutation status of A740A, The gene PYGL has a mutation status of E707G, The gene FRMD6 has a mutation status of R140Q, The gene ACTR10 has a mutation status of N58D, The gene PCNX4 has a mutation status of R429C, The gene SYNE2 has a mutation status of P8S, The gene RAD51B has a mutation status of H302H, The gene SIPA1L1 has a mutation status of S1262S, The gene SYNDIG1L has a mutation status of *239Y, The gene TTLL5 has a mutation status of M1205V, The gene GSTZ1 has a mutation status of I29I, The gene VIPAS39 has a mutation status of P355P, The gene NRXN3 has a mutation status of T1475T, The gene CPSF2 has a mutation status of I563I, The gene MOAP1 has a mutation status of P98Q, The gene BCL11B has a mutation status of P420P, The gene GOLGA8S has a mutation status of I439V, The gene SNRPN has a mutation status of A168S, The gene ATP10A has a mutation status of R85H, The gene ACTC1 has a mutation status of L351L, The gene LTK has a mutation status of G154G, The gene MGA has a mutation status of L28V, The gene SPTBN5 has a mutation status of R1460W, The gene SERINC4 has a mutation status of G237G, The gene DUOX2 has a mutation status of Y838*, The gene VPS13C has a mutation status of L2572L, The gene MAP2K1 has a mutation status of Q10K, The gene UACA has a mutation status of R372I, The gene MPI has a mutation status of L362L, The gene C15orf39 has a mutation status of E795K, The gene COMMD4 has a mutation status of E160G, The gene GOLGA6L9 has a mutation status of Q151E, The gene TICRR has a mutation status of K523E, The gene IQGAP1 has a mutation status of H1124Y, The gene IQGAP1 has a mutation status of I1429I, The gene FURIN has a mutation status of H248H, The gene RGS11 has a mutation status of D69N, The gene RHOT2 has a mutation status of P549T, The gene PTX4 has a mutation status of S165fs, The gene PRSS27 has a mutation status of V110G, The gene PAQR4 has a mutation status of R40P, The gene IL32 has a mutation status of A59A, The gene VASN has a mutation status of Q87R, The gene PPL has a mutation status of K36R, The gene SEC14L5 has a mutation status of H513N, The gene EEF2KMT has a mutation status of S28Y, The gene SLC5A11 has a mutation status of L428L, The gene NPIPB7 has a mutation status of R4C, The gene SEZ6L2 has a mutation status of G842A, The gene SLC5A2 has a mutation status of P502L, The gene OGFOD1 has a mutation status of W43G, The gene SETD6 has a mutation status of V32G, The gene LRRC29 has a mutation status of L118F, The gene FHOD1 has a mutation status of E453K, The gene LCAT has a mutation status of Q387fs, The gene LCAT has a mutation status of R386P, The gene AC026464.3 has a mutation status of F122L, The gene MLKL has a mutation status of G289R, The gene KARS1 has a mutation status of C463C, The gene ADAMTS18 has a mutation status of A870fs, The gene SLC38A8 has a mutation status of H232R, The gene MBTPS1 has a mutation status of S182N, The gene FBXO31 has a mutation status of A201P, The gene FBXO31 has a mutation status of K200R, The gene CDH15 has a mutation status of G659G, The gene CPNE7 has a mutation status of P71H, The gene TRPV1 has a mutation status of N619T, The gene MYBBP1A has a mutation status of A7P, The gene MINK1 has a mutation status of Q914H, The gene PFN1 has a mutation status of Q139Q, The gene CAMTA2 has a mutation status of C123W, The gene TP53 has a mutation status of R282W, The gene DNAH2 has a mutation status of A1987V, The gene ALOX12B has a mutation status of L379L, The gene SHISA6 has a mutation status of R518C, The gene COX10 has a mutation status of A303A, The gene PRPSAP2 has a mutation status of A236G, The gene KIAA0100 has a mutation status of W1995L, The gene SUPT6H has a mutation status of L1394R, The gene TAOK1 has a mutation status of Q786K, The gene SPACA3 has a mutation status of L9L, The gene GAS2L2 has a mutation status of R814R, The gene TAF15 has a mutation status of D440D, The gene CCL4L2 has a mutation status of P67R, The gene GPR179 has a mutation status of E1948K, The gene GPR179 has a mutation status of E1461Q, The gene CDC6 has a mutation status of H69R, The gene KRTAP4-7 has a mutation status of P67H, The gene KRTAP4-11 has a mutation status of H136R, The gene KRT34 has a mutation status of V356M, The gene KRT9 has a mutation status of G146D, The gene HROB has a mutation status of Y572C, The gene RUNDC3A has a mutation status of A356P, The gene GJC1 has a mutation status of R165R, The gene SLC35B1 has a mutation status of G265S, The gene RNF43 has a mutation status of S607S, The gene HSF5 has a mutation status of L94L, The gene MRC2 has a mutation status of I1023I, The gene SDK2 has a mutation status of T1470S, The gene OTOP2 has a mutation status of S472S, The gene GGA3 has a mutation status of Q209K, The gene MYO15B has a mutation status of P2016P, The gene GALK1 has a mutation status of A198V, The gene TRIM65 has a mutation status of Q150*, The gene TRIM65 has a mutation status of Q149L, The gene FBF1 has a mutation status of S641S, The gene MGAT5B has a mutation status of R176H, The gene TMC6 has a mutation status of G530G, The gene TMC8 has a mutation status of Y411*, The gene DNAH17 has a mutation status of R4395W, The gene DNAH17 has a mutation status of V672I, The gene GAA has a mutation status of P86R, The gene RNF213 has a mutation status of D2915D, The gene NOTUM has a mutation status of A385P, The gene NOTUM has a mutation status of A383P, The gene LRRC45 has a mutation status of E309E, The gene FASN has a mutation status of Y891*, The gene CSNK1D has a mutation status of R358Q, The gene DLGAP1 has a mutation status of M49I, The gene CDH2 has a mutation status of S26F, The gene TRAPPC8 has a mutation status of P1194P, The gene MOCOS has a mutation status of S376S, The gene EPG5 has a mutation status of E1412K, The gene HDHD2 has a mutation status of G226G, The gene MBD1 has a mutation status of H77L, The gene CCDC68 has a mutation status of K220R, The gene CCDC102B has a mutation status of T237T, The gene DOK6 has a mutation status of S327P, The gene MIDN has a mutation status of P376P, The gene PCSK4 has a mutation status of P193T, The gene CELF5 has a mutation status of L288L, The gene PIP5K1C has a mutation status of A335G, The gene STAP2 has a mutation status of L412F, The gene CATSPERD has a mutation status of I247I, The gene GPR108 has a mutation status of R89Q, The gene PNPLA6 has a mutation status of R627H, The gene PRR36 has a mutation status of A373V, The gene MUC16 has a mutation status of T7276S, The gene ZNF560 has a mutation status of N687N, The gene FDX2 has a mutation status of A5A, The gene FDX2 has a mutation status of M4T, The gene KEAP1 has a mutation status of G9R, The gene DOCK6 has a mutation status of A876A, The gene ZNF823 has a mutation status of R566H, The gene BEST2 has a mutation status of M386R, The gene ADGRL1 has a mutation status of A1272A, The gene OR7C1 has a mutation status of Y60Y, The gene CPAMD8 has a mutation status of P530P, The gene AC008397.2 has a mutation status of S228S, The gene UPF1 has a mutation status of T616T, The gene TM6SF2 has a mutation status of A130T, The gene CILP2 has a mutation status of V521G, The gene GPATCH1 has a mutation status of R463G, The gene GGN has a mutation status of A537G, The gene RASGRP4 has a mutation status of A501P, The gene RINL has a mutation status of P26S, The gene C19orf47 has a mutation status of A333A, The gene RABAC1 has a mutation status of V71M, The gene GSK3A has a mutation status of G325W, The gene MEGF8 has a mutation status of M1514I, The gene GEMIN7 has a mutation status of F129L, The gene VASP has a mutation status of T76T, The gene EML2 has a mutation status of Y63*, The gene GNG8 has a mutation status of M27R, The gene KDELR1 has a mutation status of G184G, The gene HRC has a mutation status of W14C, The gene TBC1D17 has a mutation status of A163P, The gene MYH14 has a mutation status of R1241Q, The gene KLK3 has a mutation status of R250Q, The gene KLK11 has a mutation status of P66H, The gene ZNF816 has a mutation status of Q604*, The gene LILRB3 has a mutation status of M21V, The gene BRSK1 has a mutation status of P25H, The gene TMEM150B has a mutation status of S228P, The gene ZNF628 has a mutation status of G912G, The gene TRIM28 has a mutation status of Q451Q, The gene SIGLEC1 has a mutation status of L992Q, The gene SIGLEC1 has a mutation status of L989H, The gene PLCB1 has a mutation status of P209P, The gene ANKEF1 has a mutation status of N216N, The gene SLC24A3 has a mutation status of K85N, The gene RALGAPA2 has a mutation status of K11M, The gene SSTR4 has a mutation status of F275L, The gene MAP1LC3A has a mutation status of E19E, The gene EPB41L1 has a mutation status of P206A, The gene ZNF335 has a mutation status of Y881*, The gene PREX1 has a mutation status of E1369G, The gene ZNFX1 has a mutation status of S1448P, The gene ADNP has a mutation status of V962D, The gene ADNP has a mutation status of D961D, The gene SALL4 has a mutation status of G340S, The gene ZFP64 has a mutation status of L418L, The gene CASS4 has a mutation status of V176M, The gene LAMA5 has a mutation status of A2375G, The gene LAMA5 has a mutation status of E2031E, The gene LAMA5 has a mutation status of E2031Q, The gene NKAIN4 has a mutation status of V26G, The gene KCNQ2 has a mutation status of C429Y, The gene RTEL1 has a mutation status of G1220G, The gene HUNK has a mutation status of R318C, The gene RSPH1 has a mutation status of A253D, The gene RRP1B has a mutation status of N559T, The gene ITGB2 has a mutation status of P6P, The gene COL18A1 has a mutation status of P1448H, The gene COL6A2 has a mutation status of G845G, The gene XKR3 has a mutation status of C45Y, The gene UFD1 has a mutation status of P200P, The gene DERL3 has a mutation status of R138L, The gene SLC2A11 has a mutation status of T49T, The gene SLC2A11 has a mutation status of P95P, The gene SLC2A11 has a mutation status of R259Q, The gene CABIN1 has a mutation status of G765G, The gene TPST2 has a mutation status of A200A, The gene PISD has a mutation status of R102G, The gene Z82190.2 has a mutation status of L23L, The gene Z82190.2 has a mutation status of G114G, The gene PLA2G6 has a mutation status of A268A, The gene SGSM3 has a mutation status of E672G, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ARFGAP3 has a mutation status of S451A, The gene MIOX has a mutation status of V77M, The gene MAPK8IP2 has a mutation status of A544G, The gene ASMTL has a mutation status of L339L, The gene CLCN4 has a mutation status of R604R, The gene MAGEB17 has a mutation status of G20C, The gene NHS has a mutation status of R1484Q, The gene CXorf58 has a mutation status of S39L, The gene DDX3X has a mutation status of L397L, The gene NDP has a mutation status of G20R, The gene CFP has a mutation status of Q365H, The gene ZNF81 has a mutation status of Q313Q, The gene ZC3H12B has a mutation status of Y742*, The gene EDA has a mutation status of A30G, The gene GJB1 has a mutation status of Y171S, The gene NHSL2 has a mutation status of Y715*, The gene BTK has a mutation status of R615R, The gene ARMCX1 has a mutation status of W29L, The gene TBC1D8B has a mutation status of K351K, The gene GRIA3 has a mutation status of V75I, The gene ZNF280C has a mutation status of N720S, The gene OR13H1 has a mutation status of C188Y, The gene MECP2 has a mutation status of G232A, The gene DNASE1L1 has a mutation status of R49P, The gene LAGE3 has a mutation status of I121T, The gene USP9Y has a mutation status of R211C, The gene USP9Y has a mutation status of P2109P, The gene NLGN4Y has a mutation status of E161E, The gene MT-ND4 has a mutation status of V313I
PAAD
The gene CHD5 has a mutation status of P895P, The gene ESPN has a mutation status of S312L, The gene PLEKHG5 has a mutation status of T916P, The gene RERE has a mutation status of R1179L, The gene C1orf127 has a mutation status of Q551Q, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF17 has a mutation status of V425A, The gene PRAMEF17 has a mutation status of L430L, The gene PADI6 has a mutation status of R221fs, The gene HIVEP3 has a mutation status of P534A, The gene PPCS has a mutation status of R133W, The gene CC2D1B has a mutation status of Q756H, The gene CC2D1B has a mutation status of Q756K, The gene RBMXL1 has a mutation status of R368R, The gene NRAS has a mutation status of Q61K, The gene NBPF20 has a mutation status of L5403L, The gene NBPF10 has a mutation status of V1509V, The gene NBPF12 has a mutation status of I17T, The gene NBPF11 has a mutation status of P133P, The gene FLG has a mutation status of Q2551E, The gene ASH1L has a mutation status of Q472H, The gene LRRC52 has a mutation status of A258A, The gene CEP350 has a mutation status of R171P, The gene RAB7B has a mutation status of G53D, The gene PACC1 has a mutation status of L77L, The gene WDR26 has a mutation status of K381E, The gene EPHX1 has a mutation status of E453fs, The gene URB2 has a mutation status of D534D, The gene PCNX2 has a mutation status of D1425E, The gene HNRNPU has a mutation status of S798N, The gene MYT1L has a mutation status of M448T, The gene DYSF has a mutation status of Q253Q, The gene EVA1A has a mutation status of G56R, The gene AL845331.2 has a mutation status of V210M, The gene NCKAP5 has a mutation status of G317S, The gene LRP2 has a mutation status of Q3516R, The gene TTN has a mutation status of V9899V, The gene RNF25 has a mutation status of G108G, The gene SYN2 has a mutation status of P105A, The gene TRANK1 has a mutation status of V1499V, The gene SFMBT1 has a mutation status of A691V, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of M2733V, The gene CRYBG3 has a mutation status of R2900Q, The gene ARHGAP31 has a mutation status of E586D, The gene ARHGAP31 has a mutation status of A1197D, The gene ARHGAP31 has a mutation status of E1223G, The gene GOLGB1 has a mutation status of E942D, The gene MCM2 has a mutation status of A112T, The gene DZIP1L has a mutation status of K741K, The gene HLTF has a mutation status of Y19D, The gene DNAJB11 has a mutation status of L355L, The gene TP63 has a mutation status of I675I, The gene STK32B has a mutation status of R27R, The gene AFAP1 has a mutation status of R476H, The gene UGT2B28 has a mutation status of V196V, The gene NPNT has a mutation status of G353*, The gene DDX60 has a mutation status of D716Y, The gene ADAMTS16 has a mutation status of V958G, The gene SV2C has a mutation status of E80fs, The gene FER has a mutation status of S65S, The gene PCDHGC4 has a mutation status of H770N, The gene FAT2 has a mutation status of D2950E, The gene ZNF346 has a mutation status of D152E, The gene HLA-A has a mutation status of K292E, The gene CGAS has a mutation status of Y470Y, The gene MFSD4B has a mutation status of I298M, The gene MED23 has a mutation status of Q740*, The gene STEAP1B has a mutation status of Y200C, The gene HOXA4 has a mutation status of H309fs, The gene FKBP9 has a mutation status of A555G, The gene SUGCT has a mutation status of L321P, The gene GRM3 has a mutation status of E111G, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T1853M, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P2915S, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene COPG2 has a mutation status of T552T, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PRSS1 has a mutation status of N54R, The gene PRSS2 has a mutation status of R68C, The gene OR9A2 has a mutation status of R118R, The gene KCNH2 has a mutation status of P1157P, The gene CYP7B1 has a mutation status of A26V, The gene WWP1 has a mutation status of V417F, The gene PUF60 has a mutation status of A338S, The gene EPPK1 has a mutation status of A2633del, The gene MROH1 has a mutation status of D1021D, The gene KIAA2026 has a mutation status of V158L, The gene DNAJA1 has a mutation status of G121A, The gene CNTNAP3B has a mutation status of G811R, The gene AL358113.1 has a mutation status of A1152F, The gene FRRS1L has a mutation status of R51A, The gene ZFP37 has a mutation status of E23E, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of R294H, The gene GDI2 has a mutation status of A217V, The gene FBH1 has a mutation status of Y567Y, The gene UBE2D1 has a mutation status of S83N, The gene CDHR1 has a mutation status of V121A, The gene OPN4 has a mutation status of I405V, The gene PNPLA2 has a mutation status of G483R, The gene MUC6 has a mutation status of A1593P, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of G1443R, The gene MUC5AC has a mutation status of P1480A, The gene MRGPRE has a mutation status of V180G, The gene RPL27A has a mutation status of Y108H, The gene PAX6 has a mutation status of T393T, The gene ABTB2 has a mutation status of T797N, The gene AGBL2 has a mutation status of T363N, The gene PTPRJ has a mutation status of V908A, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MPEG1 has a mutation status of Q293H, The gene ZP1 has a mutation status of V287F, The gene RPS6KA4 has a mutation status of K732K, The gene EHD1 has a mutation status of I390I, The gene MUS81 has a mutation status of P534T, The gene FGF19 has a mutation status of E174V, The gene SLC36A4 has a mutation status of A133V, The gene FOXR1 has a mutation status of R260H, The gene OR6X1 has a mutation status of M57I, The gene SCNN1A has a mutation status of R204W, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene PRB4 has a mutation status of R122G, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of E249R, The gene DDN has a mutation status of V615M, The gene NXPH4 has a mutation status of G205G, The gene MON2 has a mutation status of A1465V, The gene CEP290 has a mutation status of R1762H, The gene KERA has a mutation status of L124L, The gene BTBD11 has a mutation status of V348A, The gene TCHP has a mutation status of N110Y, The gene AMER2 has a mutation status of G221E, The gene B3GLCT has a mutation status of I81I, The gene DHRS2 has a mutation status of Y265Y, The gene PSMA3 has a mutation status of L212L, The gene ARID4A has a mutation status of A994G, The gene CEP128 has a mutation status of K944R, The gene INF2 has a mutation status of V557G, The gene GOLGA6L1 has a mutation status of R526R, The gene GOLGA6L1 has a mutation status of M518V, The gene GOLGA8S has a mutation status of I439V, The gene MAGEL2 has a mutation status of G1098R, The gene TJP1 has a mutation status of S751Y, The gene CAPN3 has a mutation status of K211R, The gene MYO1E has a mutation status of T137T, The gene ANKDD1A has a mutation status of L516L, The gene CX3CL1 has a mutation status of Q233K, The gene PIEZO1 has a mutation status of Q1519P, The gene NCBP3 has a mutation status of D185N, The gene UBE2G1 has a mutation status of H115H, The gene MINK1 has a mutation status of V298G, The gene EPN2 has a mutation status of T179P, The gene CCL4L2 has a mutation status of P67R, The gene KRT31 has a mutation status of S55I, The gene ZNF385C has a mutation status of K155Q, The gene RPS6KB1 has a mutation status of P474P, The gene ERN1 has a mutation status of A305S, The gene WIPI1 has a mutation status of G53R, The gene SOX9 has a mutation status of E63V, The gene MYO15B has a mutation status of G470D, The gene MYO15B has a mutation status of G474A, The gene MYO15B has a mutation status of S620H, The gene OGFOD3 has a mutation status of V128I, The gene LOXHD1 has a mutation status of G103C, The gene ZADH2 has a mutation status of Y27C, The gene FUT3 has a mutation status of D164N, The gene MCOLN1 has a mutation status of F117F, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of H12873R, The gene MUC16 has a mutation status of T12336L, The gene ZNF763 has a mutation status of P370L, The gene CIC has a mutation status of R2377R, The gene SIGLEC12 has a mutation status of G480A, The gene LILRB3 has a mutation status of Q270R, The gene LILRA6 has a mutation status of N187T, The gene LILRB1 has a mutation status of E34E, The gene KIR2DL1 has a mutation status of T91K, The gene KIR2DL1 has a mutation status of K237E, The gene ZNF865 has a mutation status of G770G, The gene GDF5 has a mutation status of L309M, The gene RALGAPB has a mutation status of L656M, The gene PREX1 has a mutation status of R23W, The gene TAF4 has a mutation status of A367A, The gene TAF4 has a mutation status of T360T, The gene TCFL5 has a mutation status of R472L, The gene RIPK4 has a mutation status of A645A, The gene PCNT has a mutation status of R1903F, The gene GAB4 has a mutation status of Q155K, The gene GSC2 has a mutation status of H129R, The gene DGCR8 has a mutation status of H343H, The gene SEZ6L has a mutation status of L302fs, The gene SSTR3 has a mutation status of S171L, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene GTPBP6 has a mutation status of M181L, The gene SHOX has a mutation status of P245L, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene VCX3B has a mutation status of *247Y, The gene DCAF8L2 has a mutation status of S608S, The gene MED14 has a mutation status of V97I, The gene STARD8 has a mutation status of S247G, The gene GCNA has a mutation status of S329S, The gene ARMCX4 has a mutation status of G1814R, The gene RTL9 has a mutation status of V1164M, The gene AC236972.4 has a mutation status of S1611S, The gene CCNQ has a mutation status of A209A, The gene KDM5D has a mutation status of P985P, The gene MT-ND1 has a mutation status of A82A, The gene MT-ND1 has a mutation status of I105I, The gene MT-ND2 has a mutation status of V118V, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A
SARC
The gene SAMD11 has a mutation status of S677P, The gene PLCH2 has a mutation status of R241H, The gene ARHGEF16 has a mutation status of E291K, The gene CASZ1 has a mutation status of A1273P, The gene EXOSC10 has a mutation status of V25V, The gene NPPA has a mutation status of G71E, The gene NECAP2 has a mutation status of N172N, The gene UBR4 has a mutation status of V4738G, The gene EMC1 has a mutation status of K201R, The gene KIF17 has a mutation status of K194E, The gene CELA3A has a mutation status of G60V, The gene SRRM1 has a mutation status of P666Q, The gene HDAC1 has a mutation status of F241L, The gene COL8A2 has a mutation status of Y605*, The gene BMP8A has a mutation status of G400A, The gene MYCL has a mutation status of P259H, The gene HIVEP3 has a mutation status of L818F, The gene P3H1 has a mutation status of R74P, The gene BEST4 has a mutation status of D356A, The gene CYP4B1 has a mutation status of Q210*, The gene USP24 has a mutation status of E1955K, The gene DDAH1 has a mutation status of L252L, The gene CELSR2 has a mutation status of R2015K, The gene PROK1 has a mutation status of H61P, The gene WDR3 has a mutation status of T922I, The gene NBPF15 has a mutation status of V594M, The gene RFX5 has a mutation status of T364K, The gene GLMP has a mutation status of A140G, The gene ISG20L2 has a mutation status of L34L, The gene INSRR has a mutation status of R1266Q, The gene USP21 has a mutation status of H314N, The gene DCAF6 has a mutation status of V112E, The gene PKP1 has a mutation status of K260K, The gene MYBPH has a mutation status of Q53fs, The gene CR1 has a mutation status of A35A, The gene CNIH3 has a mutation status of L93M, The gene DNAH14 has a mutation status of C1545C, The gene LBR has a mutation status of G298G, The gene ITPKB has a mutation status of S879R, The gene OBSCN has a mutation status of L717M, The gene SLC35F3 has a mutation status of H297P, The gene IRF2BP2 has a mutation status of A246A, The gene AHCTF1 has a mutation status of S2261N, The gene OR2M2 has a mutation status of I158I, The gene GREB1 has a mutation status of A380A, The gene KIF3C has a mutation status of F661S, The gene FAM166C has a mutation status of Y26D, The gene ALK has a mutation status of R41G, The gene SULT6B1 has a mutation status of G125S, The gene PLEKHH2 has a mutation status of Q1017L, The gene RAB11FIP5 has a mutation status of L1305A, The gene TET3 has a mutation status of P728L, The gene WDR54 has a mutation status of I224V, The gene AC092835.1 has a mutation status of E414E, The gene CNNM4 has a mutation status of L558L, The gene CNNM4 has a mutation status of L579I, The gene TMEM131 has a mutation status of A1779fs, The gene EPB41L5 has a mutation status of M229T, The gene CLASP1 has a mutation status of E1408G, The gene AMER3 has a mutation status of V849G, The gene ARHGEF4 has a mutation status of T683T, The gene MBD5 has a mutation status of M327T, The gene PLA2R1 has a mutation status of S1071*, The gene SLC25A12 has a mutation status of A675P, The gene NRP2 has a mutation status of Y356*, The gene MARCHF4 has a mutation status of A227G, The gene ATG9A has a mutation status of I608V, The gene PTPRN has a mutation status of A686G, The gene COL4A4 has a mutation status of P225T, The gene RNPEPL1 has a mutation status of A406D, The gene PASK has a mutation status of G117W, The gene NR2C2 has a mutation status of R402Q, The gene GLB1 has a mutation status of A564T, The gene ITGA9 has a mutation status of M777V, The gene SCN5A has a mutation status of A123V, The gene PTPN23 has a mutation status of P1124P, The gene PLXNB1 has a mutation status of W16*, The gene TREX1 has a mutation status of R114P, The gene BSN has a mutation status of S3455P, The gene BSN has a mutation status of A3904P, The gene RNF123 has a mutation status of L842V, The gene CACNA1D has a mutation status of R1510M, The gene MAGI1 has a mutation status of Q1238K, The gene OR5K1 has a mutation status of G233*, The gene RETNLB has a mutation status of C93fs, The gene GTPBP8 has a mutation status of G9G, The gene BOC has a mutation status of L124L, The gene SPICE1 has a mutation status of N147K, The gene ATP6V1A has a mutation status of A37G, The gene MYLK has a mutation status of P203Q, The gene TXNRD3 has a mutation status of G61G, The gene CEP63 has a mutation status of N190S, The gene EPHB1 has a mutation status of T29N, The gene ZIC1 has a mutation status of A19E, The gene GFM1 has a mutation status of E509G, The gene OPA1 has a mutation status of I523F, The gene GAK has a mutation status of P966L, The gene MAN2B2 has a mutation status of T159T, The gene SLIT2 has a mutation status of R680G, The gene CCKAR has a mutation status of V133L, The gene PTTG2 has a mutation status of T3N, The gene CHIC2 has a mutation status of Q21K, The gene SHROOM3 has a mutation status of P979Q, The gene LIN54 has a mutation status of R435Q, The gene PRDM5 has a mutation status of M326V, The gene FAT4 has a mutation status of L14L, The gene PABPC4L has a mutation status of L68L, The gene ZNF827 has a mutation status of D631D, The gene SFRP2 has a mutation status of I153I, The gene PDGFC has a mutation status of R217K, The gene SPATA4 has a mutation status of A3G, The gene MTNR1A has a mutation status of L197L, The gene PLEKHG4B has a mutation status of D781A, The gene CCDC127 has a mutation status of A140A, The gene RETREG1 has a mutation status of A146A, The gene NPR3 has a mutation status of A159G, The gene LIFR has a mutation status of G818L, The gene FYB1 has a mutation status of G230E, The gene ITGA2 has a mutation status of G1015G, The gene ERBIN has a mutation status of Y1336*, The gene BDP1 has a mutation status of H2379Y, The gene FOXD1 has a mutation status of P90Q, The gene HAPLN1 has a mutation status of Y348C, The gene SLC22A5 has a mutation status of W62C, The gene SHROOM1 has a mutation status of L347F, The gene TCF7 has a mutation status of H140P, The gene SLC35A4 has a mutation status of G322A, The gene PCDHA10 has a mutation status of F190V, The gene PCDHB3 has a mutation status of E386E, The gene CSF1R has a mutation status of F715F, The gene TTC1 has a mutation status of A76V, The gene WWC1 has a mutation status of E830G, The gene ERGIC1 has a mutation status of R246R, The gene CLTB has a mutation status of A46A, The gene DOK3 has a mutation status of D50N, The gene TRIM41 has a mutation status of L476L, The gene HIVEP1 has a mutation status of A873T, The gene SIRT5 has a mutation status of R119C, The gene MOG has a mutation status of I55V, The gene TRIM26 has a mutation status of T3M, The gene HLA-C has a mutation status of S140L, The gene HLA-C has a mutation status of R132R, The gene HLA-B has a mutation status of Y140L, The gene C6orf47 has a mutation status of L3P, The gene C4A has a mutation status of T1138S, The gene HLA-DRB1 has a mutation status of S66N, The gene AL669918.1 has a mutation status of V467I, The gene COL11A2 has a mutation status of R151H, The gene TAPBP has a mutation status of H299H, The gene ITPR3 has a mutation status of G1950A, The gene KCNK16 has a mutation status of A248G, The gene RPL7L1 has a mutation status of V222M, The gene SLC22A7 has a mutation status of G363S, The gene ZNF318 has a mutation status of G780G, The gene ZNF318 has a mutation status of T598T, The gene PKHD1 has a mutation status of G604G, The gene ZNF451 has a mutation status of H277Y, The gene IMPG1 has a mutation status of E707E, The gene CASP8AP2 has a mutation status of S1721N, The gene SMPD2 has a mutation status of G347G, The gene AHI1 has a mutation status of R472W, The gene ARFGEF3 has a mutation status of R1966K, The gene HIVEP2 has a mutation status of S629C, The gene GRM1 has a mutation status of S317I, The gene AGPAT4 has a mutation status of F313V, The gene TBP has a mutation status of T106A, The gene DNAAF5 has a mutation status of G531C, The gene ADAP1 has a mutation status of Q124E, The gene LFNG has a mutation status of Y224*, The gene TRIL has a mutation status of H251P, The gene POU6F2 has a mutation status of A537S, The gene CAMK2B has a mutation status of D404G, The gene COBL has a mutation status of S191R, The gene EGFR has a mutation status of R264G, The gene POM121 has a mutation status of G953G, The gene STYXL1 has a mutation status of Y138C, The gene DTX2 has a mutation status of S205R, The gene TECPR1 has a mutation status of V226A, The gene GPC2 has a mutation status of C260W, The gene EPHB4 has a mutation status of V301A, The gene SLC12A9 has a mutation status of L21P, The gene MUC3A has a mutation status of S123L, The gene NAT16 has a mutation status of G239V, The gene FLNC has a mutation status of I285M, The gene CPA1 has a mutation status of R27*, The gene BRAF has a mutation status of P490fs, The gene BRAF has a mutation status of L485fs, The gene PRSS1 has a mutation status of N77N, The gene EPHA1 has a mutation status of V257G, The gene CNTNAP2 has a mutation status of A1309A, The gene PDIA4 has a mutation status of R435Q, The gene KRBA1 has a mutation status of Y347*, The gene AGAP3 has a mutation status of T243T, The gene ARHGEF10 has a mutation status of S1138A, The gene SOX7 has a mutation status of R117L, The gene BMP1 has a mutation status of L831L, The gene EPHX2 has a mutation status of T151T, The gene ZNF395 has a mutation status of E352K, The gene PXDNL has a mutation status of R293*, The gene VXN has a mutation status of D113A, The gene RMDN1 has a mutation status of T269R, The gene FZD6 has a mutation status of Q464E, The gene CSMD3 has a mutation status of G3469R, The gene ASAP1 has a mutation status of S819R, The gene JRK has a mutation status of C405S, The gene TIGD5 has a mutation status of V379L, The gene FAM83H has a mutation status of P560T, The gene FAM83H has a mutation status of V429G, The gene PLEC has a mutation status of Y2914*, The gene PLEC has a mutation status of A761G, The gene HSF1 has a mutation status of E171G, The gene SLC39A4 has a mutation status of E480*, The gene RECQL4 has a mutation status of E936G, The gene DOCK8 has a mutation status of I920V, The gene DOCK8 has a mutation status of S1145S, The gene DMRT3 has a mutation status of R428H, The gene RANBP6 has a mutation status of P482R, The gene CCDC171 has a mutation status of R1120C, The gene ADAMTSL1 has a mutation status of V551V, The gene IFNA8 has a mutation status of D101D, The gene C9orf24 has a mutation status of S252P, The gene FAM166B has a mutation status of D141D, The gene TESK1 has a mutation status of G461G, The gene GBA2 has a mutation status of R734H, The gene PRKACG has a mutation status of R195C, The gene WNK2 has a mutation status of L1399L, The gene TBC1D2 has a mutation status of Q135E, The gene STX17 has a mutation status of A98V, The gene C9orf152 has a mutation status of E24G, The gene SVEP1 has a mutation status of S2880R, The gene PRPF4 has a mutation status of R5G, The gene CDK5RAP2 has a mutation status of T980I, The gene OR1J2 has a mutation status of L185L, The gene OR1N1 has a mutation status of R163P, The gene DENND1A has a mutation status of G771D, The gene NR5A1 has a mutation status of K150R, The gene TRUB2 has a mutation status of P43T, The gene CERCAM has a mutation status of R429R, The gene HMCN2 has a mutation status of P1686R, The gene LAMC3 has a mutation status of A1504D, The gene GFI1B has a mutation status of V135A, The gene RXRA has a mutation status of T143P, The gene NACC2 has a mutation status of Y330*, The gene DHTKD1 has a mutation status of Q320*, The gene PHYH has a mutation status of G228E, The gene BMS1 has a mutation status of R1200R, The gene WDFY4 has a mutation status of R584W, The gene SRGN has a mutation status of F129L, The gene MCU has a mutation status of Y289H, The gene MRPS16 has a mutation status of A37G, The gene CHCHD1 has a mutation status of A11G, The gene CAMK2G has a mutation status of T495P, The gene ZNF503 has a mutation status of S2T, The gene MYOF has a mutation status of K2055R, The gene SLIT1 has a mutation status of T978P, The gene SLC25A28 has a mutation status of G42G, The gene PPRC1 has a mutation status of R1288L, The gene WBP1L has a mutation status of G202G, The gene WBP1L has a mutation status of E205G, The gene EBF3 has a mutation status of Q525K, The gene EBF3 has a mutation status of P469P, The gene CFAP46 has a mutation status of H223Q, The gene ZNF511 has a mutation status of A31G, The gene EPS8L2 has a mutation status of A641S, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of R3992H, The gene LSP1 has a mutation status of G417G, The gene KCNQ1 has a mutation status of F127L, The gene TPP1 has a mutation status of H298N, The gene DCHS1 has a mutation status of A2574G, The gene INSC has a mutation status of T111P, The gene MRGPRX2 has a mutation status of Q292H, The gene KIAA1549L has a mutation status of N1516T, The gene MADD has a mutation status of I673T, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene TMEM132A has a mutation status of E832K, The gene B3GAT3 has a mutation status of L10V, The gene FERMT3 has a mutation status of E404E, The gene FRMD8 has a mutation status of S387S, The gene LTBP3 has a mutation status of S598P, The gene B4GAT1 has a mutation status of A23T, The gene PC has a mutation status of D712A, The gene TBX10 has a mutation status of S274R, The gene LRP5 has a mutation status of A1097A, The gene RNF169 has a mutation status of L601M, The gene B3GNT6 has a mutation status of A172G, The gene B3GNT6 has a mutation status of E173G, The gene USP35 has a mutation status of R30R, The gene USP35 has a mutation status of G839G, The gene MAML2 has a mutation status of Q596Q, The gene DYNC2H1 has a mutation status of G967A, The gene ALKBH8 has a mutation status of A485G, The gene HSPB2 has a mutation status of A177P, The gene TMPRSS5 has a mutation status of P93L, The gene NXPE1 has a mutation status of D417H, The gene TMEM225 has a mutation status of L63L, The gene HEPACAM has a mutation status of L71V, The gene ADAMTS15 has a mutation status of P45fs, The gene ADAMTS15 has a mutation status of D169Y, The gene THYN1 has a mutation status of R99P, The gene FGF6 has a mutation status of A2V, The gene MANSC4 has a mutation status of M167I, The gene HDAC7 has a mutation status of P37P, The gene SMARCD1 has a mutation status of R360W, The gene CERS5 has a mutation status of P24T, The gene GRASP has a mutation status of L78M, The gene KRT75 has a mutation status of Y502*, The gene KRT77 has a mutation status of 431_432insSLLSSW, The gene ANKRD52 has a mutation status of C733W, The gene KIF5A has a mutation status of P411P, The gene SLC26A10 has a mutation status of 180_181CF>WL, The gene LRRIQ1 has a mutation status of A1339G, The gene PLXNC1 has a mutation status of R78R, The gene DAO has a mutation status of A49G, The gene ACACB has a mutation status of S1620R, The gene ATP2A2 has a mutation status of S555R, The gene SETD1B has a mutation status of E1634K, The gene TMEM132C has a mutation status of N250N, The gene SLC15A4 has a mutation status of D314N, The gene PARP4 has a mutation status of L283L, The gene ATP12A has a mutation status of V1008G, The gene PDS5B has a mutation status of A460A, The gene CKAP2 has a mutation status of Q250*, The gene AL445989.1 has a mutation status of T38S, The gene SLITRK5 has a mutation status of R343H, The gene ERCC5 has a mutation status of E1560V, The gene MYO16 has a mutation status of Y234*, The gene C13orf46 has a mutation status of G130*, The gene TEP1 has a mutation status of L1140V, The gene ZNF219 has a mutation status of T146P, The gene SSTR1 has a mutation status of L60L, The gene NID2 has a mutation status of P653S, The gene CNIH1 has a mutation status of F3L, The gene WDHD1 has a mutation status of T657R, The gene MPP5 has a mutation status of H296H, The gene SLC8A3 has a mutation status of V243M, The gene SEL1L has a mutation status of V549V, The gene RIN3 has a mutation status of T830S, The gene INF2 has a mutation status of N375K, The gene ATP10A has a mutation status of D534N, The gene CCDC9B has a mutation status of E54K, The gene BAHD1 has a mutation status of S335S, The gene FBN1 has a mutation status of D1191N, The gene SHC4 has a mutation status of I262M, The gene SLC27A2 has a mutation status of V125G, The gene CILP has a mutation status of Y522*, The gene IGDCC4 has a mutation status of A249G, The gene NPTN has a mutation status of A198V, The gene PML has a mutation status of A125G, The gene EDC3 has a mutation status of P482P, The gene PPCDC has a mutation status of V67V, The gene C15orf39 has a mutation status of A730T, The gene PSTPIP1 has a mutation status of T68S, The gene ANKRD34C has a mutation status of L423P, The gene AP3B2 has a mutation status of L563L, The gene BTBD1 has a mutation status of A8S, The gene AKAP13 has a mutation status of A1258G, The gene AKAP13 has a mutation status of V2525V, The gene KIF7 has a mutation status of D916G, The gene FURIN has a mutation status of P266A, The gene FURIN has a mutation status of A267D, The gene RHBDL1 has a mutation status of Y347Y, The gene CLCN7 has a mutation status of F174S, The gene CCNF has a mutation status of T327K, The gene CCNF has a mutation status of L718F, The gene C16orf90 has a mutation status of R24C, The gene ADCY9 has a mutation status of S900S, The gene EMP2 has a mutation status of A66T, The gene NUBP1 has a mutation status of C8*, The gene AC099489.1 has a mutation status of V1298G, The gene TXNDC11 has a mutation status of A689G, The gene FOPNL has a mutation status of A70A, The gene CCP110 has a mutation status of R656W, The gene DNAH3 has a mutation status of N3804N, The gene FBRS has a mutation status of A733D, The gene TRIM72 has a mutation status of D231E, The gene SLC38A7 has a mutation status of T320T, The gene CARMIL2 has a mutation status of A212G, The gene AC026464.3 has a mutation status of Y106*, The gene AARS1 has a mutation status of E189E, The gene PHLPP2 has a mutation status of A941T, The gene DHX38 has a mutation status of R674P, The gene RFWD3 has a mutation status of S735S, The gene TAF1C has a mutation status of G582V, The gene ZNF469 has a mutation status of P3689P, The gene ZNF469 has a mutation status of L3940L, The gene SMG6 has a mutation status of Q741K, The gene SLC25A11 has a mutation status of T138T, The gene DERL2 has a mutation status of E9G, The gene NLRP1 has a mutation status of T389P, The gene SLC16A13 has a mutation status of L163V, The gene SLC16A13 has a mutation status of S164R, The gene ACADVL has a mutation status of D269D, The gene TP53 has a mutation status of R273H, The gene DNAH9 has a mutation status of S237P, The gene ZNF18 has a mutation status of G397G, The gene MYOCD has a mutation status of V542G, The gene NCOR1 has a mutation status of R1445H, The gene PLD6 has a mutation status of S171S, The gene FLCN has a mutation status of V505I, The gene MYO15A has a mutation status of S2351T, The gene MAP2K3 has a mutation status of G76V, The gene NOS2 has a mutation status of S81Y, The gene NEK8 has a mutation status of E536G, The gene MYO18A has a mutation status of A1897G, The gene C17orf75 has a mutation status of S35P, The gene CCL4L2 has a mutation status of P67R, The gene MRM1 has a mutation status of V149P, The gene SRCIN1 has a mutation status of P707Q, The gene KRTAP16-1 has a mutation status of V323A, The gene GHDC has a mutation status of A357P, The gene STAT3 has a mutation status of P327A, The gene RUNDC1 has a mutation status of P455P, The gene VAT1 has a mutation status of R96K, The gene TMEM101 has a mutation status of A168G, The gene GFAP has a mutation status of E332G, The gene HOXB8 has a mutation status of Y88*, The gene TSPOAP1 has a mutation status of C83F, The gene CSH2 has a mutation status of E114G, The gene DDX5 has a mutation status of S2L, The gene PRKAR1A has a mutation status of E291*, The gene BTBD17 has a mutation status of G60G, The gene HID1 has a mutation status of C85W, The gene TSEN54 has a mutation status of Q236H, The gene UNC13D has a mutation status of A356G, The gene EVPL has a mutation status of L1801L, The gene DNAH17 has a mutation status of T4311T, The gene SLC38A10 has a mutation status of A900P, The gene FASN has a mutation status of Y891*, The gene HEXD has a mutation status of A251P, The gene METRNL has a mutation status of F240L, The gene DLGAP1 has a mutation status of N264T, The gene TMEM200C has a mutation status of D163D, The gene LOXHD1 has a mutation status of V941G, The gene ZNF532 has a mutation status of T450N, The gene FBXO15 has a mutation status of L107L, The gene NFATC1 has a mutation status of A55P, The gene PLEKHJ1 has a mutation status of E101G, The gene OAZ1 has a mutation status of G137A, The gene ZFR2 has a mutation status of R537R, The gene UBXN6 has a mutation status of A55P, The gene GTF2F1 has a mutation status of E48G, The gene MCOLN1 has a mutation status of S559S, The gene ADAMTS10 has a mutation status of P257R, The gene PDE4A has a mutation status of A471G, The gene CARM1 has a mutation status of Y155*, The gene EPOR has a mutation status of A496A, The gene CACNA1A has a mutation status of D2077E, The gene ZSWIM4 has a mutation status of P132S, The gene C19orf57 has a mutation status of P569P, The gene NWD1 has a mutation status of R315C, The gene SIN3B has a mutation status of E583G, The gene JAK3 has a mutation status of V619A, The gene ARMC6 has a mutation status of N311T, The gene FXYD5 has a mutation status of T52T, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene LTBP4 has a mutation status of E1205G, The gene CIC has a mutation status of P1861S, The gene MEGF8 has a mutation status of A2666A, The gene FBXO46 has a mutation status of L467V, The gene SIX5 has a mutation status of T564P, The gene NPAS1 has a mutation status of E122D, The gene CCDC9 has a mutation status of H496P, The gene CA11 has a mutation status of R176R, The gene PLEKHA4 has a mutation status of G642V, The gene CCDC155 has a mutation status of Q157K, The gene PRR12 has a mutation status of H46P, The gene PRR12 has a mutation status of P980P, The gene KLK6 has a mutation status of H95P, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene NLRP2 has a mutation status of T421P, The gene SNRPB has a mutation status of T158P, The gene DDRGK1 has a mutation status of E136*, The gene AL035461.4 has a mutation status of L387fs, The gene CST9L has a mutation status of R45P, The gene XKR7 has a mutation status of P157T, The gene BPIFA3 has a mutation status of D132H, The gene SGK2 has a mutation status of P232P, The gene GDAP1L1 has a mutation status of I65D, The gene ADA has a mutation status of V178L, The gene PREX1 has a mutation status of P1479A, The gene ARFGEF2 has a mutation status of S1337Y, The gene LAMA5 has a mutation status of H1084P, The gene SLCO4A1 has a mutation status of D647G, The gene OGFR has a mutation status of V168F, The gene ADAMTS5 has a mutation status of A65E, The gene TCP10L has a mutation status of A35G, The gene SIM2 has a mutation status of V117G, The gene PKNOX1 has a mutation status of D52N, The gene PFKL has a mutation status of F229V, The gene COL18A1 has a mutation status of G846S, The gene ESS2 has a mutation status of K86T, The gene PI4KA has a mutation status of Y1628S, The gene GSTT4 has a mutation status of Q197R, The gene CABIN1 has a mutation status of A1183V, The gene KIAA1671 has a mutation status of G213G, The gene RASL10A has a mutation status of G118V, The gene MCM5 has a mutation status of D601A, The gene TNRC6B has a mutation status of K24K, The gene ADSL has a mutation status of A143S, The gene SGSM3 has a mutation status of S677R, The gene MRTFA has a mutation status of P688P, The gene SHANK3 has a mutation status of E768G, The gene SHANK3 has a mutation status of A772V, The gene MXRA5 has a mutation status of V2629G, The gene WWC3 has a mutation status of A807A, The gene PTCHD1 has a mutation status of V5G, The gene MED14 has a mutation status of P1013P, The gene CCDC22 has a mutation status of S446A, The gene CCNB3 has a mutation status of A739P, The gene SHROOM4 has a mutation status of N923T, The gene SHROOM4 has a mutation status of A518P, The gene ZC3H12B has a mutation status of Y742*, The gene AWAT1 has a mutation status of E95*, The gene KIF4A has a mutation status of E495K, The gene TEX11 has a mutation status of R680Q, The gene NLGN3 has a mutation status of S479S, The gene ZMYM3 has a mutation status of G329G, The gene NHSL2 has a mutation status of Y715*, The gene RAB40A has a mutation status of P137A, The gene SLC25A53 has a mutation status of V236A, The gene COL4A6 has a mutation status of L9V, The gene CAPN6 has a mutation status of Q304E, The gene RBMXL3 has a mutation status of W317C, The gene SLC25A5 has a mutation status of T221R, The gene DCAF12L1 has a mutation status of G192G, The gene SPANXD has a mutation status of P26P, The gene MT-CO2 has a mutation status of R82H, The gene MT-ATP6 has a mutation status of L208L, The gene MT-ND3 has a mutation status of V88V, The gene MT-CYB has a mutation status of I189I
LUAD
The gene DISP3 has a mutation status of G491R, The gene PRAMEF1 has a mutation status of R375C, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene PRAMEF20 has a mutation status of R4P, The gene RSC1A1 has a mutation status of N158D, The gene PLEKHM2 has a mutation status of S733S, The gene SPEN has a mutation status of E662G, The gene ARID1A has a mutation status of G272V, The gene THRAP3 has a mutation status of T954I, The gene TACSTD2 has a mutation status of T122T, The gene DNAJC6 has a mutation status of G250V, The gene NBPF14 has a mutation status of S1390N, The gene GATAD2B has a mutation status of R264C, The gene PRCC has a mutation status of P69P, The gene OR6Y1 has a mutation status of P267A, The gene ITLN1 has a mutation status of Y223C, The gene ITLN2 has a mutation status of S45S, The gene ODR4 has a mutation status of D156N, The gene C1orf116 has a mutation status of T8A, The gene SLC30A1 has a mutation status of P432P, The gene USH2A has a mutation status of E5070K, The gene USH2A has a mutation status of I4295I, The gene ARID4B has a mutation status of S159S, The gene RYR2 has a mutation status of G2945A, The gene LPIN1 has a mutation status of R671W, The gene ATAD2B has a mutation status of V1122V, The gene CRIPT has a mutation status of G69R, The gene PNPT1 has a mutation status of D518N, The gene TMEM131 has a mutation status of A1276A, The gene VWA3B has a mutation status of H505R, The gene IL1RL2 has a mutation status of T573T, The gene PRPF40A has a mutation status of A255A, The gene SCN1A has a mutation status of L867L, The gene CAVIN2 has a mutation status of V180M, The gene C2CD6 has a mutation status of H1762N, The gene KIAA2012 has a mutation status of Q266*, The gene NBEAL1 has a mutation status of T652M, The gene CATIP has a mutation status of R311W, The gene WNT6 has a mutation status of F109F, The gene NEU4 has a mutation status of S57N, The gene FGD5 has a mutation status of T352P, The gene TRANK1 has a mutation status of S2711F, The gene FYCO1 has a mutation status of G1385A, The gene SMARCC1 has a mutation status of P1094P, The gene CCDC66 has a mutation status of K230N, The gene SLC12A8 has a mutation status of E457*, The gene KIAA1257 has a mutation status of R1059*, The gene PLXND1 has a mutation status of T512T, The gene RASA2 has a mutation status of E165E, The gene LRRC15 has a mutation status of F289F, The gene EVC2 has a mutation status of L1195S, The gene WFS1 has a mutation status of A684A, The gene FAM90A26 has a mutation status of K115T, The gene SLIT2 has a mutation status of Q483E, The gene AFP has a mutation status of I284I, The gene FAT4 has a mutation status of G3016*, The gene TTC29 has a mutation status of P3P, The gene CEP44 has a mutation status of I186V, The gene LRRC14B has a mutation status of R459H, The gene SDHA has a mutation status of A45T, The gene CWC27 has a mutation status of V335G, The gene CWC27 has a mutation status of E336K, The gene BDP1 has a mutation status of P2381L, The gene IQGAP2 has a mutation status of L687V, The gene RAD50 has a mutation status of D967V, The gene GABRA6 has a mutation status of 71_72insKY, The gene GABRA6 has a mutation status of D72fs, The gene PTK7 has a mutation status of P272L, The gene TFAP2D has a mutation status of M156R, The gene OR2A4 has a mutation status of R96R, The gene OR2A4 has a mutation status of A94A, The gene TNFAIP3 has a mutation status of Q784K, The gene UTRN has a mutation status of E1160Q, The gene TPST1 has a mutation status of D185G, The gene TMEM248 has a mutation status of E105E, The gene STEAP4 has a mutation status of G387R, The gene PON1 has a mutation status of Y207H, The gene C7orf61 has a mutation status of W123R, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of FTSSITTTENATHSTPN2127del, The gene MUC3A has a mutation status of P3166P, The gene MUC17 has a mutation status of L1751L, The gene WNT2 has a mutation status of L15F, The gene CTTNBP2 has a mutation status of S1005T, The gene KCP has a mutation status of R136S, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene ZNF777 has a mutation status of C223C, The gene FAM90A14P has a mutation status of S231T, The gene KAT6A has a mutation status of S510C, The gene SPAG1 has a mutation status of L845V, The gene PABPC1 has a mutation status of P362P, The gene DEPTOR has a mutation status of H56fs, The gene SQLE has a mutation status of F78Y, The gene EPPK1 has a mutation status of A2633del, The gene MROH1 has a mutation status of W1292fs, The gene RECQL4 has a mutation status of L499L, The gene UHRF2 has a mutation status of R772R, The gene PTPRD has a mutation status of V253I, The gene CCDC171 has a mutation status of V534M, The gene FRMD3 has a mutation status of E218*, The gene ROR2 has a mutation status of K489N, The gene ZNF782 has a mutation status of Q11H, The gene ZNF462 has a mutation status of V877E, The gene FRRS1L has a mutation status of R51A, The gene ZFP37 has a mutation status of T436T, The gene TNC has a mutation status of K1011K, The gene FCN2 has a mutation status of KN268del, The gene USP6NL has a mutation status of P584S, The gene ARHGAP21 has a mutation status of R1296G, The gene SIRT1 has a mutation status of S535S, The gene ASCC1 has a mutation status of H109R, The gene PDZD8 has a mutation status of F304Y, The gene MCMBP has a mutation status of L268L, The gene TACC2 has a mutation status of P1979P, The gene KNDC1 has a mutation status of L331L, The gene SLC22A18 has a mutation status of Q2Q, The gene OR51G1 has a mutation status of A231T, The gene SYT9 has a mutation status of V152V, The gene EIF3M has a mutation status of A217A, The gene LRP4 has a mutation status of Y1792C, The gene LRP4 has a mutation status of E856D, The gene TRIM64C has a mutation status of A253E, The gene OR5M8 has a mutation status of C140C, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene NRXN2 has a mutation status of P684H, The gene CCDC83 has a mutation status of T346T, The gene UBE4A has a mutation status of A802T, The gene KIRREL3 has a mutation status of G154G, The gene NANOGNB has a mutation status of A13A, The gene FAM90A1 has a mutation status of K115T, The gene EIF2S3B has a mutation status of V64I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene PUS7L has a mutation status of I301M, The gene KRT84 has a mutation status of V587I, The gene MIP has a mutation status of P38P, The gene PRDM4 has a mutation status of T479T, The gene KSR2 has a mutation status of P537L, The gene P2RX7 has a mutation status of I568N, The gene MPHOSPH8 has a mutation status of L441I, The gene FRY has a mutation status of K2396K, The gene PDS5B has a mutation status of G1335G, The gene ERICH6B has a mutation status of E138V, The gene ERICH6B has a mutation status of E135G, The gene TUBGCP3 has a mutation status of P189P, The gene CUL4A has a mutation status of D3E, The gene CFL2 has a mutation status of K110R, The gene MIPOL1 has a mutation status of H376R, The gene TOGARAM1 has a mutation status of T64I, The gene FERMT2 has a mutation status of M316fs, The gene TBPL2 has a mutation status of *376G, The gene ASB2 has a mutation status of D562G, The gene ADSS1 has a mutation status of A69T, The gene SNRPN has a mutation status of R65R, The gene TYRO3 has a mutation status of K235fs, The gene JMJD7-PLA2G4B has a mutation status of 468_469insQGYF*L, The gene EHD4 has a mutation status of F371L, The gene FBN1 has a mutation status of H1877R, The gene CGNL1 has a mutation status of G765G, The gene PIF1 has a mutation status of T427T, The gene ANKDD1A has a mutation status of L516L, The gene PDIA2 has a mutation status of D404E, The gene TMC5 has a mutation status of S915T, The gene GTF3C1 has a mutation status of E623G, The gene BCKDK has a mutation status of S57L, The gene KAT8 has a mutation status of W192C, The gene MBTPS1 has a mutation status of L930F, The gene FANCA has a mutation status of T1161M, The gene ANKFY1 has a mutation status of M14L, The gene CLEC10A has a mutation status of A89V, The gene TP53 has a mutation status of R213*, The gene CCL4L2 has a mutation status of P67R, The gene KRTAP9-6 has a mutation status of G106C, The gene ARHGAP27 has a mutation status of F184C, The gene RSAD1 has a mutation status of D249H, The gene FADS6 has a mutation status of P6P, The gene MYO15B has a mutation status of P1782L, The gene RECQL5 has a mutation status of N505K, The gene ITGB4 has a mutation status of G449S, The gene GAA has a mutation status of R591Q, The gene RNF213 has a mutation status of R2269Q, The gene RNMT has a mutation status of I315V, The gene CELF4 has a mutation status of G262G, The gene ZNF407 has a mutation status of M2I, The gene KISS1R has a mutation status of G26A, The gene SBNO2 has a mutation status of P1337S, The gene MIDN has a mutation status of H275H, The gene SEMA6B has a mutation status of A673S, The gene MCOLN1 has a mutation status of G112R, The gene MUC16 has a mutation status of S9145P, The gene F2RL3 has a mutation status of R92Q, The gene ZNF730 has a mutation status of H410Q, The gene TBCB has a mutation status of S17N, The gene CYP2A6 has a mutation status of E419K, The gene CEACAM21 has a mutation status of N50N, The gene EML2 has a mutation status of T122T, The gene DMPK has a mutation status of A268T, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA1 has a mutation status of R296T, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of G283G, The gene NLRP8 has a mutation status of V632A, The gene ZSCAN18 has a mutation status of Y469Y, The gene SIRPA has a mutation status of L44S, The gene EIF6 has a mutation status of A103T, The gene DIDO1 has a mutation status of S1471F, The gene MYH9 has a mutation status of V353I, The gene TMPRSS6 has a mutation status of H439H, The gene C1QTNF6 has a mutation status of H81Y, The gene ELFN2 has a mutation status of A252T, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene HDAC10 has a mutation status of R104Q, The gene DHRSX has a mutation status of L103L, The gene ASB11 has a mutation status of A277T, The gene PHEX has a mutation status of R658R, The gene DMD has a mutation status of A2020P, The gene ARAF has a mutation status of A475P, The gene SPANXN5 has a mutation status of L67L, The gene TRO has a mutation status of F1009C, The gene ATP7A has a mutation status of S1473F, The gene HDX has a mutation status of N414K, The gene SATL1 has a mutation status of VQQPG198del, The gene MID2 has a mutation status of C658R, The gene CCNQ has a mutation status of E226E, The gene SLC6A8 has a mutation status of R278P, The gene MT-CO3 has a mutation status of I217I, The gene MT-ND4 has a mutation status of G239V, The gene MT-ND4 has a mutation status of G240C, The gene MT-CYB has a mutation status of I27T
DLBC
The gene PLCH2 has a mutation status of P1114S, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene RPS6KA1 has a mutation status of P393A, The gene ARID1A has a mutation status of G1255E, The gene SFPQ has a mutation status of Q70H, The gene PDE4B has a mutation status of G458G, The gene NEGR1 has a mutation status of P89L, The gene TGFBR3 has a mutation status of G798R, The gene PHTF1 has a mutation status of G173E, The gene ITGA10 has a mutation status of G922R, The gene NBPF10 has a mutation status of C1535W, The gene NBPF10 has a mutation status of Y680*, The gene H2AC21 has a mutation status of D91E, The gene DCST1 has a mutation status of S657S, The gene CLK2 has a mutation status of R417H, The gene MAEL has a mutation status of I114N, The gene RNF2 has a mutation status of G35D, The gene PRG4 has a mutation status of P358H, The gene LHX9 has a mutation status of T24P, The gene IGFN1 has a mutation status of E1628fs, The gene ZP4 has a mutation status of S71S, The gene CHRM3 has a mutation status of A72T, The gene SNX17 has a mutation status of L162L, The gene VWA3B has a mutation status of G1048S, The gene LONRF2 has a mutation status of T737T, The gene RANBP2 has a mutation status of S1422N, The gene KIF5C has a mutation status of S622G, The gene KIF5C has a mutation status of S681G, The gene GALNT5 has a mutation status of N362N, The gene COL3A1 has a mutation status of Q1127H, The gene MARS2 has a mutation status of G570R, The gene C2CD6 has a mutation status of R1411R, The gene NRP2 has a mutation status of A262V, The gene ABCA12 has a mutation status of Q727Q, The gene C2orf72 has a mutation status of G276W, The gene QRICH1 has a mutation status of Q163Q, The gene USP19 has a mutation status of H458H, The gene GRM2 has a mutation status of V241V, The gene CACNA1D has a mutation status of P1888L, The gene ERC2 has a mutation status of S340N, The gene ABI3BP has a mutation status of L15V, The gene POLQ has a mutation status of G1871D, The gene CCDC14 has a mutation status of H13Y, The gene AADACL2 has a mutation status of M64I, The gene LRRC31 has a mutation status of E173G, The gene FBXO45 has a mutation status of N219S, The gene EPHA5 has a mutation status of I378I, The gene GYPA has a mutation status of S66Y, The gene C9 has a mutation status of P56H, The gene MAN2A1 has a mutation status of S1081I, The gene HMGXB3 has a mutation status of H1013R, The gene SYNPO has a mutation status of I114T, The gene FAT2 has a mutation status of A1856A, The gene SLC34A1 has a mutation status of W576*, The gene PPP1R3G has a mutation status of R353C, The gene RREB1 has a mutation status of A429T, The gene HLA-C has a mutation status of S140L, The gene HLA-DRB5 has a mutation status of Q220W, The gene SYNGAP1 has a mutation status of E582E, The gene ANKS1A has a mutation status of R130W, The gene RAB44 has a mutation status of V988L, The gene DNAH8 has a mutation status of G3442R, The gene PRPH2 has a mutation status of D338G, The gene ECHDC1 has a mutation status of G189G, The gene SAMD3 has a mutation status of R89L, The gene MED23 has a mutation status of V959V, The gene ADGB has a mutation status of P1359P, The gene TULP4 has a mutation status of D188N, The gene PLG has a mutation status of P159T, The gene PDE10A has a mutation status of Q13Q, The gene EIF3B has a mutation status of L711P, The gene ELMO1 has a mutation status of D382H, The gene NPC1L1 has a mutation status of R268H, The gene UPP1 has a mutation status of R130W, The gene SRRM3 has a mutation status of K361K, The gene SRRM3 has a mutation status of R387R, The gene PEX1 has a mutation status of R762H, The gene OCM2 has a mutation status of E82E, The gene GJC3 has a mutation status of L71I, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2046L, The gene HYAL4 has a mutation status of K318K, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene PARP12 has a mutation status of D657N, The gene PRSS1 has a mutation status of N77N, The gene SHH has a mutation status of R232L, The gene RP1L1 has a mutation status of W548*, The gene RP1L1 has a mutation status of A138T, The gene PSD3 has a mutation status of G423V, The gene CHRNA2 has a mutation status of S42Y, The gene GOLGA7 has a mutation status of Q100R, The gene PXDNL has a mutation status of P990L, The gene NPBWR1 has a mutation status of L295L, The gene ZBTB10 has a mutation status of E864K, The gene SLC7A13 has a mutation status of I211F, The gene SLC7A13 has a mutation status of G106E, The gene ODF1 has a mutation status of P229S, The gene PLEC has a mutation status of A2547L, The gene SCRT1 has a mutation status of A133S, The gene TUSC1 has a mutation status of G37S, The gene ACO1 has a mutation status of R802C, The gene FBXO10 has a mutation status of R687*, The gene ZNF782 has a mutation status of G309V, The gene FRRS1L has a mutation status of R51A, The gene GARNL3 has a mutation status of A663T, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene LCN15 has a mutation status of D165Y, The gene ITGA8 has a mutation status of H562N, The gene TMEM236 has a mutation status of *352Y, The gene CDH23 has a mutation status of R27Q, The gene ZSWIM8 has a mutation status of R404H, The gene SLIT1 has a mutation status of A754S, The gene TACC2 has a mutation status of G2532D, The gene CPXM2 has a mutation status of L401M, The gene EDRF1 has a mutation status of A1198V, The gene CEND1 has a mutation status of K6N, The gene MUC5AC has a mutation status of H680H, The gene MUC5AC has a mutation status of Q718E, The gene SLC22A18AS has a mutation status of I22V, The gene OR52E5 has a mutation status of A66G, The gene SMPD1 has a mutation status of T298N, The gene OVCH2 has a mutation status of S387R, The gene PLEKHA7 has a mutation status of F698I, The gene PIK3C2A has a mutation status of A1007A, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene MPEG1 has a mutation status of S389L, The gene CD5 has a mutation status of H461C, The gene CPSF7 has a mutation status of P210R, The gene FIBP has a mutation status of P74S, The gene GPR152 has a mutation status of R250K, The gene KDM4D has a mutation status of Q77H, The gene TTC12 has a mutation status of G264G, The gene DSCAML1 has a mutation status of R1537Q, The gene PRH1 has a mutation status of P163L, The gene SLCO1C1 has a mutation status of E313E, The gene KRT3 has a mutation status of P518L, The gene ITGA7 has a mutation status of E25G, The gene LRP1 has a mutation status of A2676T, The gene FRS2 has a mutation status of R238R, The gene NAA25 has a mutation status of S226C, The gene HSPB8 has a mutation status of E84D, The gene P2RX7 has a mutation status of I568N, The gene TMEM132C has a mutation status of L599Q, The gene DDX51 has a mutation status of D201D, The gene ZNF84 has a mutation status of S109N, The gene CDK8 has a mutation status of P232Q, The gene DCT has a mutation status of Y182Y, The gene ABCC4 has a mutation status of L1235L, The gene CLDN10 has a mutation status of P149R, The gene EFS has a mutation status of S298P, The gene JPH4 has a mutation status of Q47K, The gene TTC6 has a mutation status of E252D, The gene SLC35F4 has a mutation status of N45N, The gene SYT16 has a mutation status of Q193L, The gene SMOC1 has a mutation status of A234T, The gene TMEM63C has a mutation status of L679L, The gene EXOC3L4 has a mutation status of F576fs, The gene GOLGA6L6 has a mutation status of 548_549insHD, The gene HERC2 has a mutation status of V395V, The gene MAPKBP1 has a mutation status of G1212V, The gene JMJD7-PLA2G4B has a mutation status of R239K, The gene PLA2G4F has a mutation status of L505S, The gene DUOX2 has a mutation status of P225A, The gene ANKDD1A has a mutation status of L516L, The gene DPP8 has a mutation status of K817M, The gene WHAMM has a mutation status of W78C, The gene RAB11FIP3 has a mutation status of D56N, The gene PRR35 has a mutation status of A16A, The gene MAPK8IP3 has a mutation status of I1105I, The gene SRRM2 has a mutation status of D1141V, The gene NLRC3 has a mutation status of L408R, The gene AC099489.1 has a mutation status of Q2789H, The gene SHISA9 has a mutation status of G43R, The gene FOPNL has a mutation status of A112T, The gene EEF2K has a mutation status of M723T, The gene KDM8 has a mutation status of P8P, The gene GTF3C1 has a mutation status of R1863H, The gene MAZ has a mutation status of A90A, The gene FBRS has a mutation status of A387G, The gene DRC7 has a mutation status of H737H, The gene EDC4 has a mutation status of P342P, The gene GSE1 has a mutation status of C777C, The gene ANKRD11 has a mutation status of E1378K, The gene ASGR2 has a mutation status of Q28*, The gene MYH3 has a mutation status of Y1853C, The gene MPRIP has a mutation status of E143Q, The gene CCL4L2 has a mutation status of P67R, The gene MYO19 has a mutation status of I168V, The gene PGAP3 has a mutation status of A14A, The gene PLEKHM1 has a mutation status of R628G, The gene KANSL1 has a mutation status of S784Y, The gene PITPNC1 has a mutation status of V193I, The gene RTTN has a mutation status of P1277P, The gene POLR2E has a mutation status of Y8Y, The gene GIPC3 has a mutation status of A19A, The gene KDM4B has a mutation status of P527L, The gene PODNL1 has a mutation status of E493D, The gene ATP13A1 has a mutation status of G952G, The gene ZNF507 has a mutation status of V305D, The gene PRX has a mutation status of D79D, The gene ZNF229 has a mutation status of L308P, The gene GFY has a mutation status of P347L, The gene NOSIP has a mutation status of G189V, The gene SPACA6 has a mutation status of M167T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of L140L, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of V111V, The gene KIR2DL1 has a mutation status of H203R, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene AL121899.2 has a mutation status of S695S, The gene C20orf194 has a mutation status of R33Q, The gene RALGAPA2 has a mutation status of H1752R, The gene BPIFB4 has a mutation status of M539K, The gene NRIP1 has a mutation status of S972I, The gene PCNT has a mutation status of Q1588*, The gene GAB4 has a mutation status of S315S, The gene CLTCL1 has a mutation status of N653S, The gene HPS4 has a mutation status of P101S, The gene MYH9 has a mutation status of Y106C, The gene CDC42EP1 has a mutation status of P255fs, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene NCAPH2 has a mutation status of D436G, The gene HDAC6 has a mutation status of A946G, The gene HUWE1 has a mutation status of V3984F, The gene DIAPH2 has a mutation status of E1052V, The gene ARMCX2 has a mutation status of Q503Q, The gene TEX13A has a mutation status of L267L, The gene THOC2 has a mutation status of S53P, The gene BCORL1 has a mutation status of P482L, The gene MAGEC1 has a mutation status of Q234fs, The gene MT-CO1 has a mutation status of H291H, The gene MT-ND4L has a mutation status of M9M, The gene MT-ND5 has a mutation status of Y159H
OV
The gene TTLL10 has a mutation status of R379C, The gene MIB2 has a mutation status of Q495R, The gene HES3 has a mutation status of Q78H, The gene PRAMEF13 has a mutation status of T257I, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene EIF4G3 has a mutation status of D1162V, The gene ADGRB2 has a mutation status of E470*, The gene LDLRAD1 has a mutation status of A51S, The gene ACOT11 has a mutation status of T263T, The gene SERBP1 has a mutation status of V12V, The gene C1orf146 has a mutation status of N45T, The gene NRAS has a mutation status of Q61K, The gene IGSF3 has a mutation status of G295G, The gene CD101 has a mutation status of R233K, The gene KPRP has a mutation status of H373H, The gene KCNN3 has a mutation status of L66Q, The gene KCNN3 has a mutation status of P63Q, The gene SELL has a mutation status of C316F, The gene FMO3 has a mutation status of C197Y, The gene CYB5R1 has a mutation status of R34R, The gene BTG2 has a mutation status of L35L, The gene PACC1 has a mutation status of F83F, The gene MTARC2 has a mutation status of S318L, The gene TPO has a mutation status of H805H, The gene KIDINS220 has a mutation status of T590T, The gene GPN1 has a mutation status of D333E, The gene ATL2 has a mutation status of R104H, The gene EPAS1 has a mutation status of D753E, The gene EIF2AK3 has a mutation status of A50D, The gene DPP10 has a mutation status of D542N, The gene AMER3 has a mutation status of L342R, The gene RAB6D has a mutation status of D182D, The gene TTC30A has a mutation status of G3G, The gene TTN has a mutation status of V31138F, The gene TTN has a mutation status of D27951Y, The gene TTN has a mutation status of T23978A, The gene ABCA12 has a mutation status of M1074V, The gene TNS1 has a mutation status of N319N, The gene CUL3 has a mutation status of D698G, The gene USP40 has a mutation status of A1093T, The gene VILL has a mutation status of A753A, The gene PLCD1 has a mutation status of V75L, The gene AC006059.2 has a mutation status of S672C, The gene LAMB2 has a mutation status of R1267H, The gene IMPG2 has a mutation status of L827L, The gene CD200R1 has a mutation status of H346P, The gene BOC has a mutation status of Q331K, The gene GAP43 has a mutation status of G152D, The gene GAP43 has a mutation status of T217P, The gene GOLGB1 has a mutation status of H1361R, The gene H1-8 has a mutation status of R76K, The gene PLXND1 has a mutation status of M851V, The gene SLC9A9 has a mutation status of P482R, The gene NMD3 has a mutation status of V96L, The gene MCCC1 has a mutation status of R281*, The gene DGKQ has a mutation status of C204C, The gene HTRA3 has a mutation status of T96N, The gene HTRA3 has a mutation status of C101F, The gene BOD1L1 has a mutation status of G1536G, The gene GRXCR1 has a mutation status of Q234Q, The gene MANBA has a mutation status of L757L, The gene ALPK1 has a mutation status of V1032I, The gene MAML3 has a mutation status of Q491Q, The gene FGA has a mutation status of W795*, The gene SDHA has a mutation status of Y205*, The gene RICTOR has a mutation status of N1166K, The gene NNT has a mutation status of E849Q, The gene ADGRV1 has a mutation status of S2089R, The gene SRP19 has a mutation status of S69C, The gene TRPC7 has a mutation status of A546D, The gene LRRTM2 has a mutation status of T32T, The gene SH3TC2 has a mutation status of A461F, The gene SYNPO has a mutation status of S153R, The gene H2AC8 has a mutation status of L86L, The gene HLA-DMB has a mutation status of M61V, The gene KCNK17 has a mutation status of P197P, The gene AARS2 has a mutation status of V59G, The gene DEFB112 has a mutation status of C42R, The gene CILK1 has a mutation status of L48F, The gene FBXO9 has a mutation status of R85P, The gene GCM1 has a mutation status of R272*, The gene PHIP has a mutation status of Y16*, The gene FRMD1 has a mutation status of C578F, The gene GPR146 has a mutation status of P134L, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T1234A, The gene KCND2 has a mutation status of T280A, The gene ASB15 has a mutation status of P534P, The gene TPK1 has a mutation status of G212R, The gene ZNF783 has a mutation status of R407Q, The gene NUDT18 has a mutation status of V45V, The gene LGI3 has a mutation status of F315L, The gene SNX31 has a mutation status of M206V, The gene ANKRD20A4P has a mutation status of C404Y, The gene SPOUT1 has a mutation status of D238E, The gene SOHLH1 has a mutation status of M1V, The gene CAMSAP1 has a mutation status of H969Q, The gene NOTCH1 has a mutation status of T701P, The gene ARMC3 has a mutation status of T420A, The gene ANKRD30A has a mutation status of K1136I, The gene NRG3 has a mutation status of V609I, The gene OR51B5 has a mutation status of L220L, The gene NLRP14 has a mutation status of R159K, The gene PPFIBP2 has a mutation status of L13M, The gene RAG1 has a mutation status of E806E, The gene MTCH2 has a mutation status of G11D, The gene MTCH2 has a mutation status of V8M, The gene OR4C11 has a mutation status of K231N, The gene OR9G1 has a mutation status of T62V, The gene OR10W1 has a mutation status of Q149K, The gene GPR137 has a mutation status of T364P, The gene MYO7A has a mutation status of P1633S, The gene FAT3 has a mutation status of C3952C, The gene KDM4D has a mutation status of D499E, The gene MMP20 has a mutation status of W149*, The gene PHLDB1 has a mutation status of L352R, The gene PHLDB1 has a mutation status of E684E, The gene NECTIN1 has a mutation status of R380W, The gene B4GALNT3 has a mutation status of T153A, The gene KCNA5 has a mutation status of V303V, The gene CD9 has a mutation status of F55V, The gene TAS2R45 has a mutation status of I274A, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of L193I, The gene TAS2R45 has a mutation status of R154W, The gene TAS2R45 has a mutation status of I33T, The gene TAS2R45 has a mutation status of A28A, The gene ITPR2 has a mutation status of V2074G, The gene KMT2D has a mutation status of S2597fs, The gene SP1 has a mutation status of L550L, The gene PAH has a mutation status of Y351H, The gene HECTD4 has a mutation status of P3797P, The gene KDM2B has a mutation status of P1020S, The gene ULK1 has a mutation status of E15E, The gene ATP11A has a mutation status of R585Q, The gene F7 has a mutation status of L149V, The gene GRK1 has a mutation status of L83Q, The gene MDGA2 has a mutation status of G351V, The gene KTN1 has a mutation status of A456S, The gene FNTB has a mutation status of R291R, The gene NRDE2 has a mutation status of M339V, The gene CEP170B has a mutation status of R1080Q, The gene KNL1 has a mutation status of L1917V, The gene TYRO3 has a mutation status of V233fs, The gene TGM7 has a mutation status of G277A, The gene GOLGA6A has a mutation status of A195A, The gene ALDH1A3 has a mutation status of G257G, The gene UNKL has a mutation status of F540F, The gene ZNF598 has a mutation status of A109A, The gene CREBBP has a mutation status of D1435E, The gene SMG1 has a mutation status of A1817T, The gene TMC5 has a mutation status of L435L, The gene CNGB1 has a mutation status of V755V, The gene MMP15 has a mutation status of N272N, The gene E2F4 has a mutation status of E35E, The gene FHOD1 has a mutation status of R949H, The gene ESRP2 has a mutation status of P565P, The gene SLC13A5 has a mutation status of A222T, The gene MYH1 has a mutation status of E1183E, The gene ZSWIM7 has a mutation status of A2V, The gene AC134669.1 has a mutation status of S25N, The gene CCL4L2 has a mutation status of P67R, The gene TMEM92 has a mutation status of E107E, The gene LLGL2 has a mutation status of P955R, The gene EVPL has a mutation status of M46I, The gene SEH1L has a mutation status of R5P, The gene RNF125 has a mutation status of S12P, The gene BCL2 has a mutation status of A42V, The gene COL5A3 has a mutation status of P1507L, The gene NR2F6 has a mutation status of T91P, The gene UNC13A has a mutation status of P1420Q, The gene JAK3 has a mutation status of D130A, The gene FKBP8 has a mutation status of R374R, The gene FCGBP has a mutation status of Y1197fs, The gene FCGBP has a mutation status of 1163_1196ESACREGCVCDAGFVLSGDTCVPVGQCGCLHDDR>G, The gene ATP1A3 has a mutation status of M31V, The gene MEGF8 has a mutation status of T2231P, The gene LMTK3 has a mutation status of A381V, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of M117T, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene KIR2DL1 has a mutation status of P175T, The gene ZNF579 has a mutation status of V291G, The gene SIRPA has a mutation status of L44S, The gene ANKEF1 has a mutation status of N216N, The gene PAX1 has a mutation status of G390A, The gene BPIFB3 has a mutation status of S145L, The gene GNAS has a mutation status of S95I, The gene GNAS has a mutation status of A331V, The gene KRTAP19-5 has a mutation status of S57G, The gene TPST2 has a mutation status of R101L, The gene SHISA8 has a mutation status of V395F, The gene PLXNB2 has a mutation status of F988L, The gene NR0B1 has a mutation status of C43C, The gene TFE3 has a mutation status of A455A, The gene EDA has a mutation status of Y310Y, The gene ERCC6L has a mutation status of Q401L, The gene ATRX has a mutation status of K1169Q, The gene COL4A5 has a mutation status of G542R, The gene IL13RA2 has a mutation status of Y12H, The gene TENM1 has a mutation status of A437S, The gene DCAF12L1 has a mutation status of A279V, The gene BCORL1 has a mutation status of L1132P, The gene MAGEC1 has a mutation status of R954C, The gene FMR1 has a mutation status of K299Q, The gene MT-ND1 has a mutation status of V260I, The gene MT-ND5 has a mutation status of V92V, The gene MT-ND5 has a mutation status of S574P, The gene MT-CYB has a mutation status of F18L
DLBC
The gene MMEL1 has a mutation status of I192V, The gene RPL22 has a mutation status of F78F, The gene PRAMEF12 has a mutation status of V361K, The gene PRAMEF1 has a mutation status of R213F, The gene PRAMEF1 has a mutation status of R375C, The gene PRAMEF2 has a mutation status of M28V, The gene PRAMEF2 has a mutation status of G208Q, The gene PRAMEF2 has a mutation status of N293M, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of M105L, The gene AGMAT has a mutation status of D278D, The gene CROCC has a mutation status of L612Q, The gene CROCC has a mutation status of L1756L, The gene ARHGEF10L has a mutation status of L454L, The gene UBR4 has a mutation status of R1463H, The gene EPHA8 has a mutation status of E462G, The gene EPHA8 has a mutation status of T674T, The gene TMEM222 has a mutation status of T32T, The gene MAP3K6 has a mutation status of S581S, The gene PTPRU has a mutation status of S1371N, The gene ADPRS has a mutation status of K362N, The gene PRKAA2 has a mutation status of L467L, The gene EFCAB7 has a mutation status of E141V, The gene ERICH3 has a mutation status of D139G, The gene NEXN has a mutation status of E332K, The gene SYDE2 has a mutation status of N1040S, The gene GBP6 has a mutation status of M581V, The gene SLC44A3 has a mutation status of F109L, The gene PLPPR4 has a mutation status of V411I, The gene CELSR2 has a mutation status of P1277L, The gene SLC6A17 has a mutation status of S164N, The gene OVGP1 has a mutation status of G594G, The gene CAPZA1 has a mutation status of N44S, The gene PTGFRN has a mutation status of L720L, The gene NOTCH2 has a mutation status of R1260H, The gene NBPF12 has a mutation status of A187S, The gene RFX5 has a mutation status of E523E, The gene RFX5 has a mutation status of R16G, The gene LCE2D has a mutation status of G69G, The gene LCE2A has a mutation status of C52C, The gene LCE2A has a mutation status of S54P, The gene SPRR3 has a mutation status of T156M, The gene ASH1L has a mutation status of K1796K, The gene ASH1L has a mutation status of N1653N, The gene GON4L has a mutation status of E1943D, The gene RAB25 has a mutation status of V91M, The gene IQGAP3 has a mutation status of L1425P, The gene INSRR has a mutation status of S197S, The gene FCRL1 has a mutation status of I103K, The gene CD5L has a mutation status of P135S, The gene SLAMF8 has a mutation status of A38A, The gene USP21 has a mutation status of R130H, The gene SUCO has a mutation status of G20S, The gene COP1 has a mutation status of R295T, The gene SEC16B has a mutation status of Q791H, The gene CFH has a mutation status of E961D, The gene CFHR5 has a mutation status of G450G, The gene CAMSAP2 has a mutation status of P958L, The gene ATP2B4 has a mutation status of P894S, The gene CAPN2 has a mutation status of S329R, The gene ITPKB has a mutation status of S176P, The gene OBSCN has a mutation status of N7390S, The gene H3-4 has a mutation status of F68*, The gene HEATR1 has a mutation status of L1741Q, The gene RYR2 has a mutation status of L297V, The gene SDCCAG8 has a mutation status of R19R, The gene SNTG2 has a mutation status of R258W, The gene EIPR1 has a mutation status of H137H, The gene ATP6V1C2 has a mutation status of V118L, The gene PUM2 has a mutation status of Q274Q, The gene APOB has a mutation status of G3511G, The gene ADCY3 has a mutation status of V845M, The gene TOGARAM2 has a mutation status of A290A, The gene ALK has a mutation status of M1478T, The gene XDH has a mutation status of N1109T, The gene AC007040.2 has a mutation status of S100S, The gene SPR has a mutation status of V214V, The gene TBC1D8 has a mutation status of I856V, The gene MAP4K4 has a mutation status of H532H, The gene IL1R2 has a mutation status of S62R, The gene IL18R1 has a mutation status of G423R, The gene GCC2 has a mutation status of M1098V, The gene GLI2 has a mutation status of A896V, The gene IWS1 has a mutation status of E202del, The gene LRP1B has a mutation status of I761V, The gene PKP4 has a mutation status of P216P, The gene FIGN has a mutation status of T49T, The gene PARD3B has a mutation status of T738N, The gene PIKFYVE has a mutation status of Q84*, The gene CFAP65 has a mutation status of F647S, The gene PTPRN has a mutation status of S149S, The gene ACSL3 has a mutation status of S402N, The gene SH3BP4 has a mutation status of D130H, The gene MLPH has a mutation status of T56A, The gene CAND2 has a mutation status of I483M, The gene EOMES has a mutation status of R295R, The gene GADL1 has a mutation status of E457D, The gene SUSD5 has a mutation status of I460T, The gene MLH1 has a mutation status of I32V, The gene SLC22A13 has a mutation status of R377C, The gene ZNF445 has a mutation status of M234T, The gene KIAA1143 has a mutation status of Y9S, The gene CDCP1 has a mutation status of S398del, The gene QRICH1 has a mutation status of G615G, The gene BSN has a mutation status of S746R, The gene UBA7 has a mutation status of A955V, The gene PRKCD has a mutation status of N183S, The gene FLNB has a mutation status of S1159L, The gene FRMD4B has a mutation status of L331F, The gene RETNLB has a mutation status of D37N, The gene SLC9C1 has a mutation status of H244Q, The gene GAP43 has a mutation status of Q203K, The gene B4GALT4 has a mutation status of A44E, The gene IQCB1 has a mutation status of V225I, The gene KALRN has a mutation status of N914S, The gene HPS3 has a mutation status of C784Y, The gene IGSF10 has a mutation status of R2216*, The gene KCNAB1 has a mutation status of P212L, The gene LIPH has a mutation status of C212S, The gene ST6GAL1 has a mutation status of L392L, The gene MUC4 has a mutation status of D678D, The gene TNK2 has a mutation status of N335N, The gene UVSSA has a mutation status of R330H, The gene ZNF518B has a mutation status of G732R, The gene LRRC66 has a mutation status of N422N, The gene KIT has a mutation status of N91Y, The gene UGT2A1 has a mutation status of I256I, The gene HPSE has a mutation status of L13M, The gene PDLIM5 has a mutation status of G36G, The gene PDLIM5 has a mutation status of G37G, The gene ADH5 has a mutation status of Y264C, The gene ABHD18 has a mutation status of R354G, The gene MAML3 has a mutation status of A127A, The gene NR3C2 has a mutation status of C308G, The gene NR3C2 has a mutation status of C73Y, The gene LRBA has a mutation status of S2350I, The gene FHDC1 has a mutation status of T439T, The gene DCHS2 has a mutation status of T2805S, The gene DCHS2 has a mutation status of P2800Q, The gene TMA16 has a mutation status of R80S, The gene PRIMPOL has a mutation status of A196A, The gene TRIML1 has a mutation status of S254R, The gene EXOC3 has a mutation status of T207T, The gene TERT has a mutation status of Y122Y, The gene NSUN2 has a mutation status of H451H, The gene NNT has a mutation status of S385S, The gene SNX18 has a mutation status of P308Q, The gene PDE4D has a mutation status of T183S, The gene MAP1B has a mutation status of L2123P, The gene HEXB has a mutation status of F77F, The gene ARRDC3 has a mutation status of L278L, The gene SLC25A46 has a mutation status of L186L, The gene ALDH7A1 has a mutation status of V141V, The gene APBB3 has a mutation status of M1T, The gene TMCO6 has a mutation status of V439I, The gene PCDHA8 has a mutation status of G275E, The gene RGS14 has a mutation status of Q261R, The gene GRM6 has a mutation status of V304V, The gene RASGEF1C has a mutation status of D94E, The gene ZNF391 has a mutation status of I242T, The gene GABBR1 has a mutation status of F645L, The gene ZFP57 has a mutation status of R38Q, The gene RNF39 has a mutation status of E189E, The gene PPP1R10 has a mutation status of A294A, The gene STK19 has a mutation status of P120P, The gene HLA-DQB2 has a mutation status of A28G, The gene FANCE has a mutation status of R343Q, The gene PEX6 has a mutation status of R137Q, The gene CUL7 has a mutation status of R1564W, The gene GSTA4 has a mutation status of T163A, The gene GCLC has a mutation status of R66W, The gene COX7A2 has a mutation status of A52T, The gene HTR1B has a mutation status of D259Y, The gene FUT9 has a mutation status of H109N, The gene TSPYL4 has a mutation status of G6A, The gene ARFGEF3 has a mutation status of V1901G, The gene ADGRG6 has a mutation status of S642S, The gene HIVEP2 has a mutation status of T1646A, The gene FBXO30 has a mutation status of F527L, The gene TFB1M has a mutation status of I138I, The gene TBXT has a mutation status of K145E, The gene SNX8 has a mutation status of N420N, The gene DNAH11 has a mutation status of V2112L, The gene NOD1 has a mutation status of S51S, The gene PKD1L1 has a mutation status of C1914Y, The gene PKD1L1 has a mutation status of D1867N, The gene C7orf57 has a mutation status of E151Q, The gene PTPN12 has a mutation status of N764S, The gene RUNDC3B has a mutation status of T445K, The gene CYP51A1 has a mutation status of G239G, The gene PDK4 has a mutation status of S83P, The gene TFR2 has a mutation status of S64S, The gene ZAN has a mutation status of EKLTIPT869del, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of S834T, The gene MUC17 has a mutation status of S2037fs, The gene IFT22 has a mutation status of L112L, The gene CDHR3 has a mutation status of R235S, The gene PIK3CG has a mutation status of Q778P, The gene CFTR has a mutation status of I506I, The gene CFTR has a mutation status of Y917C, The gene CPED1 has a mutation status of P8S, The gene SLC37A3 has a mutation status of L153L, The gene BRAF has a mutation status of V600E, The gene OR6V1 has a mutation status of M96V, The gene OR2A14 has a mutation status of F94L, The gene TMUB1 has a mutation status of T48A, The gene MFHAS1 has a mutation status of D327G, The gene PCM1 has a mutation status of M12V, The gene GFRA2 has a mutation status of E19K, The gene FAM160B2 has a mutation status of S575C, The gene NEFL has a mutation status of T21M, The gene NEFL has a mutation status of Y18C, The gene SCARA5 has a mutation status of 179_180DT>EP, The gene DUSP26 has a mutation status of I189I, The gene RAB11FIP1 has a mutation status of L504L, The gene BAG4 has a mutation status of G143D, The gene DDHD2 has a mutation status of L390I, The gene PXDNL has a mutation status of R1303S, The gene TRIM55 has a mutation status of P404S, The gene MSC has a mutation status of S153P, The gene ZFHX4 has a mutation status of H1969H, The gene PKHD1L1 has a mutation status of D3401G, The gene TAF2 has a mutation status of A82A, The gene DOCK8 has a mutation status of V278I, The gene FOCAD has a mutation status of R1099H, The gene CREB3 has a mutation status of L74P, The gene SPATA31A6 has a mutation status of P393P, The gene TMC1 has a mutation status of R759C, The gene GCNT1 has a mutation status of V31I, The gene WNK2 has a mutation status of A1779A, The gene TEX10 has a mutation status of L873L, The gene OR13C2 has a mutation status of S18F, The gene CTNNAL1 has a mutation status of M696I, The gene FKBP15 has a mutation status of L178L, The gene AKNA has a mutation status of G876G, The gene CRB2 has a mutation status of D1113D, The gene AL441992.3 has a mutation status of R387Q, The gene IER5L has a mutation status of G319G, The gene CFAP77 has a mutation status of H283P, The gene STKLD1 has a mutation status of M335V, The gene SARDH has a mutation status of A364fs, The gene CAMSAP1 has a mutation status of H969Q, The gene NACC2 has a mutation status of A155T, The gene AKR1E2 has a mutation status of F188L, The gene ZNF438 has a mutation status of A599A, The gene ZEB1 has a mutation status of N81S, The gene CCNY has a mutation status of A320T, The gene CHAT has a mutation status of A217A, The gene PCDH15 has a mutation status of S1747R, The gene RUFY2 has a mutation status of L597P, The gene HKDC1 has a mutation status of I577L, The gene SGPL1 has a mutation status of R190S, The gene KCNMA1 has a mutation status of A1004A, The gene SFTPD has a mutation status of R292C, The gene WAPL has a mutation status of E653Q, The gene MYOF has a mutation status of S965S, The gene TCTN3 has a mutation status of A426A, The gene CPN1 has a mutation status of Y134Y, The gene PSD has a mutation status of T896P, The gene SH3PXD2A has a mutation status of L718L, The gene CCDC186 has a mutation status of D276D, The gene TDRD1 has a mutation status of Q551Q, The gene EIF3A has a mutation status of R611R, The gene ADAM12 has a mutation status of P685P, The gene INPP5A has a mutation status of T260T, The gene KNDC1 has a mutation status of P401P, The gene MUC6 has a mutation status of T1071P, The gene MUC5B has a mutation status of V5047I, The gene TOLLIP has a mutation status of V33G, The gene NUP98 has a mutation status of N1144S, The gene OR2AG1 has a mutation status of M258T, The gene MRVI1 has a mutation status of E276D, The gene SPON1 has a mutation status of T545M, The gene OR8U1 has a mutation status of L131M, The gene OR9G1 has a mutation status of T62V, The gene OR9G1 has a mutation status of I196F, The gene GLYATL2 has a mutation status of P135P, The gene VPS51 has a mutation status of F556F, The gene CST6 has a mutation status of D109N, The gene PC has a mutation status of R243Q, The gene TMEM134 has a mutation status of I156V, The gene C2CD3 has a mutation status of E800Q, The gene USP35 has a mutation status of A973A, The gene TENM4 has a mutation status of M2255I, The gene CCDC89 has a mutation status of T16A, The gene AMOTL1 has a mutation status of T877T, The gene CCDC82 has a mutation status of K128R, The gene SDHD has a mutation status of Y93S, The gene TMPRSS13 has a mutation status of Q78R, The gene TMPRSS13 has a mutation status of A77G, The gene MPZL2 has a mutation status of Q74*, The gene PDZD3 has a mutation status of R73P, The gene OR8G5 has a mutation status of L14V, The gene IGSF9B has a mutation status of T178M, The gene PLEKHG6 has a mutation status of L593L, The gene MANSC1 has a mutation status of K32K, The gene C2CD5 has a mutation status of R186R, The gene LRMP has a mutation status of R14R, The gene OVCH1 has a mutation status of P794P, The gene ACVRL1 has a mutation status of L99L, The gene KRT7 has a mutation status of F111L, The gene KRT6B has a mutation status of T377T, The gene KRT2 has a mutation status of P169P, The gene KRT76 has a mutation status of K188N, The gene KRT78 has a mutation status of A371V, The gene KRT8 has a mutation status of R23C, The gene SLC39A5 has a mutation status of A182V, The gene BAZ2A has a mutation status of P1485T, The gene KIF5A has a mutation status of I442fs, The gene IRAK3 has a mutation status of Y180*, The gene NAV3 has a mutation status of P1028L, The gene OTOGL has a mutation status of P1961P, The gene TMTC3 has a mutation status of L113V, The gene HAL has a mutation status of I555M, The gene NEDD1 has a mutation status of N520K, The gene UHRF1BP1L has a mutation status of C476Y, The gene GLT8D2 has a mutation status of T270A, The gene NUAK1 has a mutation status of L181L, The gene BTBD11 has a mutation status of A775A, The gene ACACB has a mutation status of R2282H, The gene RBM19 has a mutation status of F450L, The gene VSIG10 has a mutation status of G425V, The gene ABCB9 has a mutation status of A408A, The gene NCOR2 has a mutation status of H289H, The gene TEX26 has a mutation status of P11P, The gene CCDC122 has a mutation status of K243Q, The gene OR4K2 has a mutation status of C97R, The gene ARHGEF40 has a mutation status of R1447C, The gene OR10G2 has a mutation status of S72S, The gene RBM23 has a mutation status of 392_393insP, The gene L2HGDH has a mutation status of I392V, The gene TTLL5 has a mutation status of R444C, The gene DGLUCY has a mutation status of G195G, The gene CCDC88C has a mutation status of S1985C, The gene GOLGA5 has a mutation status of P134R, The gene SERPINA3 has a mutation status of M414V, The gene EXOC3L4 has a mutation status of R216S, The gene INF2 has a mutation status of A1155V, The gene TRPM1 has a mutation status of V1604V, The gene AVEN has a mutation status of T332T, The gene RASGRP1 has a mutation status of T267T, The gene RTF1 has a mutation status of R501R, The gene ZNF106 has a mutation status of V898M, The gene CDAN1 has a mutation status of E356K, The gene DUOX2 has a mutation status of R376Q, The gene SHC4 has a mutation status of P56L, The gene USP8 has a mutation status of S315fs, The gene FEM1B has a mutation status of V506V, The gene STOML1 has a mutation status of P182P, The gene UBL7 has a mutation status of P97S, The gene C15orf39 has a mutation status of R962K, The gene MAN2C1 has a mutation status of V230V, The gene SNUPN has a mutation status of P239P, The gene ODF3L1 has a mutation status of T171T, The gene CEMIP has a mutation status of G104R, The gene AP3B2 has a mutation status of E252G, The gene NTRK3 has a mutation status of P22S, The gene MESP1 has a mutation status of T22S, The gene PRC1 has a mutation status of S146L, The gene CHSY1 has a mutation status of E487E, The gene MRPL28 has a mutation status of P72P, The gene TELO2 has a mutation status of A728A, The gene NTHL1 has a mutation status of A162A, The gene RNPS1 has a mutation status of S100S, The gene PAQR4 has a mutation status of S36S, The gene ADCY9 has a mutation status of F125F, The gene COG7 has a mutation status of V302M, The gene ZNF629 has a mutation status of P568P, The gene CDH16 has a mutation status of S614S, The gene WWP2 has a mutation status of I813V, The gene CMC2 has a mutation status of T11S, The gene FBXO31 has a mutation status of D165D, The gene PRPF8 has a mutation status of Y1028Y, The gene TRPV1 has a mutation status of G93G, The gene NLRP1 has a mutation status of L694L, The gene FBXO39 has a mutation status of W29R, The gene TEKT1 has a mutation status of K311N, The gene GPS2 has a mutation status of T306A, The gene CD68 has a mutation status of T75M, The gene MYH8 has a mutation status of N605K, The gene MYH1 has a mutation status of I993V, The gene MYOCD has a mutation status of P188S, The gene WSB1 has a mutation status of D322N, The gene VTN has a mutation status of P251L, The gene DHRS13 has a mutation status of Y20Y, The gene ADAP2 has a mutation status of R98fs, The gene GPR179 has a mutation status of R1170Q, The gene LPO has a mutation status of E181K, The gene TEX14 has a mutation status of L163L, The gene SMG8 has a mutation status of G3G, The gene VMP1 has a mutation status of V372V, The gene INTS2 has a mutation status of S364P, The gene ICAM2 has a mutation status of G184G, The gene BPTF has a mutation status of V2680M, The gene PRKAR1A has a mutation status of T182T, The gene CDC42EP4 has a mutation status of G152G, The gene RNF157 has a mutation status of A73S, The gene SRSF2 has a mutation status of R61R, The gene TNRC6C has a mutation status of N317H, The gene DNAH17 has a mutation status of A2130V, The gene GAA has a mutation status of P444P, The gene RNF213 has a mutation status of L2405F, The gene BAIAP2 has a mutation status of A357A, The gene BAHCC1 has a mutation status of P310R, The gene FASN has a mutation status of A1376V, The gene LAMA1 has a mutation status of D2814D, The gene SEH1L has a mutation status of R5P, The gene POTEC has a mutation status of K380R, The gene CTAGE1 has a mutation status of R526R, The gene LAMA3 has a mutation status of Y1057Y, The gene KIAA1328 has a mutation status of S269S, The gene WDR7 has a mutation status of V476L, The gene CDH20 has a mutation status of Y72H, The gene RTTN has a mutation status of N278S, The gene ZNF554 has a mutation status of E224K, The gene ZBTB7A has a mutation status of A359A, The gene VMAC has a mutation status of S2S, The gene SH2D3A has a mutation status of G98G, The gene COL5A3 has a mutation status of L1060L, The gene ANGPTL6 has a mutation status of G435S, The gene PPAN-P2RY11 has a mutation status of G358V, The gene ZNF878 has a mutation status of H441R, The gene ZNF333 has a mutation status of E182K, The gene IQCN has a mutation status of T1118S, The gene ZNF93 has a mutation status of S466S, The gene ZNF430 has a mutation status of G547G, The gene ZNF729 has a mutation status of A496P, The gene ZNF573 has a mutation status of K613E, The gene RYR1 has a mutation status of P1773S, The gene IFNL2 has a mutation status of R74K, The gene ATP1A3 has a mutation status of Q427Q, The gene MEGF8 has a mutation status of P681P, The gene ZNF225 has a mutation status of S551T, The gene CBLC has a mutation status of A59D, The gene GEMIN7 has a mutation status of F129L, The gene SLC1A5 has a mutation status of S491S, The gene LMTK3 has a mutation status of G1008G, The gene NUP62 has a mutation status of A260S, The gene ZNF320 has a mutation status of Y41C, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of R169C, The gene KIR2DL3 has a mutation status of Y207Y, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL3 has a mutation status of E295D, The gene KIR2DL1 has a mutation status of H203R, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of G283G, The gene ZNF628 has a mutation status of V294M, The gene ZNF419 has a mutation status of Y227Y, The gene SNPH has a mutation status of S397S, The gene SIRPA has a mutation status of L44S, The gene TMC2 has a mutation status of I659T, The gene PRND has a mutation status of N75Y, The gene KAT14 has a mutation status of A516T, The gene CFAP61 has a mutation status of G894A, The gene DEFB116 has a mutation status of I13N, The gene MYLK2 has a mutation status of G393R, The gene CTSZ has a mutation status of G5W, The gene CDH4 has a mutation status of S335S, The gene KCNQ2 has a mutation status of F802V, The gene PRPF6 has a mutation status of D832D, The gene TPTE has a mutation status of S155P, The gene NRIP1 has a mutation status of K1105E, The gene USP25 has a mutation status of Q524L, The gene CXADR has a mutation status of P343L, The gene TMPRSS15 has a mutation status of E641K, The gene BACH1 has a mutation status of R685R, The gene HUNK has a mutation status of H55H, The gene DOP1B has a mutation status of G1340S, The gene TRPM2 has a mutation status of Q1500*, The gene IL17RA has a mutation status of S298S, The gene ATP6V1E1 has a mutation status of K82R, The gene CRKL has a mutation status of T26T, The gene CABIN1 has a mutation status of P1741P, The gene SEZ6L has a mutation status of N956I, The gene SFI1 has a mutation status of G1197G, The gene FOXRED2 has a mutation status of G451S, The gene CBX6 has a mutation status of P364P, The gene PNPLA3 has a mutation status of R79W, The gene MLC1 has a mutation status of P294P, The gene PHEX has a mutation status of R166H, The gene DMD has a mutation status of M439V, The gene FAM47A has a mutation status of L387I, The gene FAM47A has a mutation status of L125L, The gene SSX5 has a mutation status of R181H, The gene ZMYM3 has a mutation status of G84G, The gene DIAPH2 has a mutation status of G559G, The gene ZNF449 has a mutation status of P170P, The gene ADGRG4 has a mutation status of T1020T, The gene ADGRG4 has a mutation status of T1877I, The gene MAGEA3 has a mutation status of E102G, The gene SRY has a mutation status of S155S, The gene MT-ATP8 has a mutation status of P36P, The gene MT-CYB has a mutation status of I78T
GBMLGG
The gene CHD5 has a mutation status of T1713M, The gene MTOR has a mutation status of Q1718Q, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of W98R, The gene PADI1 has a mutation status of Y602Y, The gene UBR4 has a mutation status of D5033D, The gene KIF17 has a mutation status of Q865Q, The gene ALPL has a mutation status of A514V, The gene SYTL1 has a mutation status of S35S, The gene DCDC2B has a mutation status of H293Q, The gene TMEM35B has a mutation status of Q62Q, The gene MANEAL has a mutation status of I302K, The gene HIVEP3 has a mutation status of R323C, The gene TSPAN1 has a mutation status of V179I, The gene FOXE3 has a mutation status of T146T, The gene C8B has a mutation status of P572L, The gene LEPR has a mutation status of V9A, The gene NEGR1 has a mutation status of P138H, The gene HFM1 has a mutation status of E779G, The gene BTBD8 has a mutation status of S1199S, The gene DBT has a mutation status of L312V, The gene NBPF15 has a mutation status of L515L, The gene NBPF10 has a mutation status of L891V, The gene BCL9 has a mutation status of P744P, The gene NBPF11 has a mutation status of Q55H, The gene IVL has a mutation status of C75Y, The gene PYGO2 has a mutation status of G316W, The gene APOA2 has a mutation status of P97A, The gene DDR2 has a mutation status of G466R, The gene SLC9C2 has a mutation status of G42E, The gene CACNA1E has a mutation status of V210V, The gene F13B has a mutation status of P581Q, The gene C1orf53 has a mutation status of Q111*, The gene IGFN1 has a mutation status of M951V, The gene C4BPA has a mutation status of E541D, The gene DISC1 has a mutation status of C502Y, The gene RYR2 has a mutation status of R2772H, The gene OR2G6 has a mutation status of F73Y, The gene PCARE has a mutation status of E1062Q, The gene NLRC4 has a mutation status of G889fs, The gene PRKD3 has a mutation status of L582L, The gene MSH6 has a mutation status of P673Q, The gene FAM161A has a mutation status of E240E, The gene PROKR1 has a mutation status of R307C, The gene ASPRV1 has a mutation status of A72A, The gene CTNNA2 has a mutation status of N351H, The gene DNAH6 has a mutation status of V3223M, The gene SEMA4C has a mutation status of S369L, The gene SLC9A2 has a mutation status of G756G, The gene ST6GAL2 has a mutation status of R220C, The gene CNTNAP5 has a mutation status of D495N, The gene POTEI has a mutation status of D165D, The gene MBD5 has a mutation status of D1198G, The gene GRB14 has a mutation status of G482R, The gene LRP2 has a mutation status of Y3217C, The gene PHOSPHO2 has a mutation status of S227A, The gene EVX2 has a mutation status of A402T, The gene TTN has a mutation status of T8925M, The gene TTN has a mutation status of P1728L, The gene GTF3C3 has a mutation status of T882A, The gene ADAM23 has a mutation status of P788P, The gene FAM237A has a mutation status of L21L, The gene ABCA12 has a mutation status of G2187S, The gene STK36 has a mutation status of K316R, The gene CFAP65 has a mutation status of L1017del, The gene DAW1 has a mutation status of H260D, The gene DNER has a mutation status of R168H, The gene DGKD has a mutation status of Q1068E, The gene TRPM8 has a mutation status of A28T, The gene COL6A3 has a mutation status of T525M, The gene AQP12B has a mutation status of A191T, The gene NEU4 has a mutation status of P298P, The gene GRM7 has a mutation status of A836A, The gene SYN2 has a mutation status of 67_68insPAPQ, The gene SYN2 has a mutation status of P105A, The gene IQSEC1 has a mutation status of E369D, The gene ITGA9 has a mutation status of E623D, The gene CX3CR1 has a mutation status of E181K, The gene MAP4 has a mutation status of D1416fs, The gene BSN has a mutation status of P3692L, The gene ACY1 has a mutation status of L128L, The gene PBRM1 has a mutation status of S205S, The gene SLMAP has a mutation status of S724C, The gene DNASE1L3 has a mutation status of T224M, The gene FOXP1 has a mutation status of T41M, The gene DCBLD2 has a mutation status of A341T, The gene BBX has a mutation status of H428R, The gene MORC1 has a mutation status of I377I, The gene CCDC80 has a mutation status of A340G, The gene BOC has a mutation status of P571A, The gene ARHGAP31 has a mutation status of T116T, The gene ROPN1B has a mutation status of C9Y, The gene UROC1 has a mutation status of R14W, The gene MCM2 has a mutation status of R133C, The gene EFCC1 has a mutation status of R130P, The gene COL6A6 has a mutation status of G1452V, The gene PRR23A has a mutation status of T51I, The gene AADAC has a mutation status of N37N, The gene SLC66A1L has a mutation status of T57I, The gene RSRC1 has a mutation status of S280fs, The gene DGKG has a mutation status of H272H, The gene FGFR3 has a mutation status of P402P, The gene LYAR has a mutation status of R273W, The gene CLNK has a mutation status of P180P, The gene AASDH has a mutation status of E112G, The gene UGT2A3 has a mutation status of T133M, The gene UGT2B28 has a mutation status of A346T, The gene PPBP has a mutation status of L24R, The gene NUP54 has a mutation status of V443V, The gene PAQR3 has a mutation status of W140R, The gene ARHGAP24 has a mutation status of L335V, The gene AFF1 has a mutation status of V1049L, The gene SLC9B1 has a mutation status of M207I, The gene COL25A1 has a mutation status of G452fs, The gene GPM6A has a mutation status of T145T, The gene AGA has a mutation status of D248N, The gene TRIO has a mutation status of T2787S, The gene BRIX1 has a mutation status of D125V, The gene SPEF2 has a mutation status of R789C, The gene UGT3A1 has a mutation status of H335Y, The gene ZBED3 has a mutation status of L155A, The gene BHMT has a mutation status of G297G, The gene TTC37 has a mutation status of Y1410H, The gene EPB41L4A has a mutation status of T27I, The gene PCDHA1 has a mutation status of R287H, The gene PCDH1 has a mutation status of A5A, The gene JAKMIP2 has a mutation status of T319T, The gene ABLIM3 has a mutation status of R442Q, The gene GPX3 has a mutation status of L10L, The gene UBLCP1 has a mutation status of D228D, The gene SLC35B3 has a mutation status of F303F, The gene MUC22 has a mutation status of K567N, The gene AL645922.1 has a mutation status of Q71*, The gene HLA-DRB5 has a mutation status of T262R, The gene HLA-DRB5 has a mutation status of H260Q, The gene HLA-DRB5 has a mutation status of Q220W, The gene CUL9 has a mutation status of V1743V, The gene DEFB133 has a mutation status of I3T, The gene FAM83B has a mutation status of K222Q, The gene COL21A1 has a mutation status of G907V, The gene KHDC1L has a mutation status of E18K, The gene PHIP has a mutation status of E614E, The gene TTK has a mutation status of G531G, The gene STX7 has a mutation status of E113E, The gene SLC2A12 has a mutation status of A501T, The gene AKAP12 has a mutation status of R1038W, The gene GTF2H5 has a mutation status of D40N, The gene IGF2BP3 has a mutation status of E303Q, The gene IGF2BP3 has a mutation status of K294T, The gene MINDY4 has a mutation status of F438fs, The gene NPSR1 has a mutation status of I158I, The gene ASNS has a mutation status of S434F, The gene ACTL6B has a mutation status of A46V, The gene ZAN has a mutation status of A168T, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of 205_206insS, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC3A has a mutation status of P3166P, The gene MUC12 has a mutation status of A1844A, The gene CLDN15 has a mutation status of A117A, The gene HBP1 has a mutation status of H213H, The gene DOCK4 has a mutation status of Y1444Y, The gene WNT2 has a mutation status of R299W, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene MGAM has a mutation status of N1585N, The gene NOBOX has a mutation status of C159F, The gene WDR86 has a mutation status of E57K, The gene WDR60 has a mutation status of A1057T, The gene SGCZ has a mutation status of L7L, The gene TUSC3 has a mutation status of L329L, The gene STC1 has a mutation status of R139*, The gene DOCK5 has a mutation status of E1295K, The gene DPYSL2 has a mutation status of T177M, The gene ZFHX4 has a mutation status of P839S, The gene EPPK1 has a mutation status of A2633del, The gene SHARPIN has a mutation status of G336G, The gene CPSF1 has a mutation status of V1172M, The gene TONSL has a mutation status of A280T, The gene COMMD5 has a mutation status of D154fs, The gene TAF1L has a mutation status of I330V, The gene TAF1L has a mutation status of Y315F, The gene CBWD6 has a mutation status of D159N, The gene FAM189A2 has a mutation status of H523R, The gene SECISBP2 has a mutation status of M498fs, The gene SEMA4D has a mutation status of V699V, The gene GRIN3A has a mutation status of P20P, The gene FRRS1L has a mutation status of R51A, The gene COL27A1 has a mutation status of A92A, The gene CNTRL has a mutation status of L894P, The gene CNTRL has a mutation status of V983M, The gene PBX3 has a mutation status of G128A, The gene ZBTB43 has a mutation status of D34D, The gene SLC2A8 has a mutation status of P60L, The gene ST6GALNAC6 has a mutation status of D90D, The gene NUP214 has a mutation status of I310V, The gene RXRA has a mutation status of R182Q, The gene PPP1R26 has a mutation status of R933*, The gene DIP2C has a mutation status of V789V, The gene WDR37 has a mutation status of T180M, The gene ASB13 has a mutation status of S243*, The gene PARD3 has a mutation status of S428L, The gene RBP3 has a mutation status of H808Q, The gene SFTPD has a mutation status of N336T, The gene SH2D4B has a mutation status of H200Y, The gene PTEN has a mutation status of R15I, The gene IDE has a mutation status of D977D, The gene ZNF518A has a mutation status of Q818Q, The gene ZNF518A has a mutation status of E828E, The gene ADD3 has a mutation status of G326A, The gene RBM20 has a mutation status of G284R, The gene DHX32 has a mutation status of A251V, The gene TUBGCP2 has a mutation status of P542P, The gene DRD4 has a mutation status of P326S, The gene MUC6 has a mutation status of K193K, The gene MUC5AC has a mutation status of T3668P, The gene MUC5AC has a mutation status of N5017N, The gene TRIM66 has a mutation status of E905Q, The gene ACCS has a mutation status of R120C, The gene OR5F1 has a mutation status of T20K, The gene OR9G1 has a mutation status of I196F, The gene OR4D9 has a mutation status of A119V, The gene TCN1 has a mutation status of N259S, The gene ASRGL1 has a mutation status of V197I, The gene SLC3A2 has a mutation status of R562H, The gene CTSF has a mutation status of L170F, The gene FGF3 has a mutation status of R210W, The gene P2RY2 has a mutation status of L160L, The gene ARHGEF17 has a mutation status of R1715R, The gene THRSP has a mutation status of L42V, The gene FAT3 has a mutation status of Y2383Y, The gene DYNC2H1 has a mutation status of L1457I, The gene SIDT2 has a mutation status of D204N, The gene NLRX1 has a mutation status of R347H, The gene RPUSD4 has a mutation status of A8V, The gene AKAP3 has a mutation status of A478S, The gene RECQL has a mutation status of Y441fs, The gene ABCC9 has a mutation status of W1306C, The gene ABCC9 has a mutation status of E519E, The gene OR6C74 has a mutation status of D87N, The gene RBMS2 has a mutation status of I60M, The gene AGAP2 has a mutation status of R122L, The gene TMTC3 has a mutation status of A540E, The gene GCN1 has a mutation status of L11L, The gene ANAPC5 has a mutation status of R298W, The gene PITPNM2 has a mutation status of G1343R, The gene POLE has a mutation status of E1240K, The gene GEMIN2 has a mutation status of L233L, The gene CCDC198 has a mutation status of G231V, The gene SERPINA10 has a mutation status of L443F, The gene AMN has a mutation status of H64Y, The gene FAN1 has a mutation status of A686A, The gene LPCAT4 has a mutation status of G17R, The gene CEP152 has a mutation status of N321S, The gene DMXL2 has a mutation status of R1081H, The gene GCNT3 has a mutation status of G72G, The gene ANKDD1A has a mutation status of L516L, The gene CYP11A1 has a mutation status of T172M, The gene HMG20A has a mutation status of D54Y, The gene CEMIP has a mutation status of C997S, The gene BNC1 has a mutation status of L635S, The gene BNC1 has a mutation status of K379Q, The gene CACNA1H has a mutation status of F289F, The gene NAA60 has a mutation status of P39S, The gene UBN1 has a mutation status of K715E, The gene PPL has a mutation status of L880M, The gene ABCC6 has a mutation status of I1297I, The gene INO80E has a mutation status of A104fs, The gene ITGAD has a mutation status of L214L, The gene CNTNAP4 has a mutation status of C624fs, The gene CNTNAP4 has a mutation status of R743W, The gene TAF1C has a mutation status of G89V, The gene SPG7 has a mutation status of M684L, The gene CDK10 has a mutation status of E28Q, The gene VPS53 has a mutation status of P749P, The gene HIC1 has a mutation status of R523R, The gene USP6 has a mutation status of W84R, The gene FBXO39 has a mutation status of R291W, The gene TP53 has a mutation status of R175H, The gene VTN has a mutation status of R463C, The gene NF1 has a mutation status of K92fs, The gene NF1 has a mutation status of K92N, The gene TMEM132E has a mutation status of H28Q, The gene MMP28 has a mutation status of K129E, The gene LHX1 has a mutation status of P301P, The gene ARHGAP23 has a mutation status of L858L, The gene ZPBP2 has a mutation status of L7L, The gene KRTAP4-8 has a mutation status of CISSCCRPSCCVSSCCKPQCCQSVCCQPNCCRPSC95del, The gene KRTAP9-6 has a mutation status of G106C, The gene KRT34 has a mutation status of R388C, The gene KRT31 has a mutation status of E96E, The gene SKAP1 has a mutation status of R163W, The gene ABCA5 has a mutation status of Y394C, The gene FADS6 has a mutation status of P6P, The gene AC015802.6 has a mutation status of G274V, The gene ENGASE has a mutation status of G442R, The gene CCDC40 has a mutation status of R739Q, The gene EPB41L3 has a mutation status of G501R, The gene MTCL1 has a mutation status of V816M, The gene POTEC has a mutation status of K40R, The gene GATA6 has a mutation status of A17V, The gene FHOD3 has a mutation status of T14T, The gene SERPINB10 has a mutation status of D301D, The gene APC2 has a mutation status of K1753K, The gene ATP8B3 has a mutation status of R159R, The gene LRRC8E has a mutation status of T11T, The gene SNAPC2 has a mutation status of R39W, The gene ZNF266 has a mutation status of F568L, The gene TYK2 has a mutation status of S431R, The gene COLGALT1 has a mutation status of R221C, The gene INSL3 has a mutation status of V39G, The gene ZNF536 has a mutation status of R193H, The gene ZNF850 has a mutation status of Q648*, The gene LRFN1 has a mutation status of A16G, The gene ZNF226 has a mutation status of L280V, The gene CCDC114 has a mutation status of L105P, The gene PIH1D1 has a mutation status of F54Y, The gene PRR12 has a mutation status of P798P, The gene TSKS has a mutation status of P285L, The gene SHANK1 has a mutation status of A1868T, The gene LILRB3 has a mutation status of G349G, The gene LILRB3 has a mutation status of Q270R, The gene LILRB3 has a mutation status of M21V, The gene LILRA6 has a mutation status of I88M, The gene LILRA5 has a mutation status of V19M, The gene LILRA1 has a mutation status of R296T, The gene ZNF787 has a mutation status of T87M, The gene ZBTB45 has a mutation status of R485R, The gene SNPH has a mutation status of K143R, The gene ADAM33 has a mutation status of P673T, The gene JAG1 has a mutation status of G327M, The gene RIN2 has a mutation status of Y834F, The gene ASXL1 has a mutation status of Q1448Q, The gene SLC32A1 has a mutation status of I189I, The gene PPP1R16B has a mutation status of N531S, The gene CHD6 has a mutation status of L279L, The gene CHD6 has a mutation status of K97R, The gene ZSWIM3 has a mutation status of E86K, The gene BCAS1 has a mutation status of P562T, The gene HRH3 has a mutation status of T304N, The gene ZBTB21 has a mutation status of F655F, The gene AIFM3 has a mutation status of R446*, The gene SEZ6L has a mutation status of P224H, The gene SREBF2 has a mutation status of L25L, The gene SLC25A6 has a mutation status of A125A, The gene RPS6KA3 has a mutation status of S17S, The gene ASB12 has a mutation status of Q214R, The gene FOXO4 has a mutation status of D373N, The gene ATP7A has a mutation status of D101G, The gene USP26 has a mutation status of N794I, The gene USP26 has a mutation status of T130A, The gene SAGE1 has a mutation status of R113H, The gene MAGEA6 has a mutation status of V251L, The gene UTY has a mutation status of E34G, The gene MT-ND1 has a mutation status of K58K, The gene MT-CO1 has a mutation status of D4N, The gene MT-CO3 has a mutation status of L164L, The gene MT-CO3 has a mutation status of L252L, The gene MT-ND3 has a mutation status of W77W, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4 has a mutation status of I34I, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND5 has a mutation status of T544M, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L, The gene MT-CYB has a mutation status of D171N, The gene MT-CYB has a mutation status of L234L
GBMLGG
The gene PRAMEF2 has a mutation status of N293M, The gene PRAMEF18 has a mutation status of N268Y, The gene PRAMEF18 has a mutation status of L218P, The gene PRAMEF18 has a mutation status of V171V, The gene PRAMEF18 has a mutation status of R132R, The gene PRAMEF18 has a mutation status of W98R, The gene PRAMEF33 has a mutation status of L344L, The gene LACTBL1 has a mutation status of L405L, The gene TSSK3 has a mutation status of D42H, The gene ZSCAN20 has a mutation status of E534Q, The gene KLF18 has a mutation status of 861_862insALYGGQNMMTSTGNQ, The gene CACHD1 has a mutation status of Y499H, The gene COL11A1 has a mutation status of G1575*, The gene COL11A1 has a mutation status of G506R, The gene SPAG17 has a mutation status of M114L, The gene NBPF26 has a mutation status of K1096K, The gene NBPF15 has a mutation status of L515L, The gene POLR3C has a mutation status of R533K, The gene NBPF10 has a mutation status of L891V, The gene PPIAL4H has a mutation status of N102I, The gene NBPF11 has a mutation status of E759Q, The gene C1orf56 has a mutation status of C248*, The gene ILF2 has a mutation status of A252G, The gene IQGAP3 has a mutation status of F485L, The gene SLAMF8 has a mutation status of I157I, The gene F5 has a mutation status of A1573A, The gene METTL18 has a mutation status of V346L, The gene METTL18 has a mutation status of E343K, The gene METTL18 has a mutation status of G188G, The gene FMO1 has a mutation status of P470A, The gene QSOX1 has a mutation status of E186D, The gene HMCN1 has a mutation status of R3759R, The gene B3GALT2 has a mutation status of S194S, The gene CFHR5 has a mutation status of S174C, The gene IGFN1 has a mutation status of G1615G, The gene IGFN1 has a mutation status of K1635E, The gene PLXNA2 has a mutation status of T943M, The gene H3-3A has a mutation status of R129C, The gene ARID4B has a mutation status of L60L, The gene CHML has a mutation status of E174A, The gene OR2W3 has a mutation status of A34T, The gene TOGARAM2 has a mutation status of H205H, The gene XDH has a mutation status of A370A, The gene TTC27 has a mutation status of I265T, The gene PSME4 has a mutation status of I172I, The gene ASPRV1 has a mutation status of K244K, The gene INO80B has a mutation status of Q280L, The gene EN1 has a mutation status of T149A, The gene KIF5C has a mutation status of Q440Q, The gene NEB has a mutation status of K636M, The gene TTN has a mutation status of V7074I, The gene TTN has a mutation status of K4194R, The gene SF3B1 has a mutation status of G225G, The gene CXCR2 has a mutation status of A91V, The gene PLCD4 has a mutation status of L273L, The gene WNT10A has a mutation status of H235N, The gene RESP18 has a mutation status of L215I, The gene ALPI has a mutation status of A505A, The gene UGT1A5 has a mutation status of D87D, The gene WDR48 has a mutation status of V596V, The gene CACNA2D2 has a mutation status of S303S, The gene DNAH12 has a mutation status of E2938E, The gene DNAH12 has a mutation status of L2786L, The gene TRMT10C has a mutation status of S294S, The gene MYH15 has a mutation status of S760C, The gene PLXND1 has a mutation status of G154S, The gene PLSCR4 has a mutation status of C202F, The gene PIK3CA has a mutation status of E542K, The gene PEX5L has a mutation status of N547K, The gene DGKQ has a mutation status of E695K, The gene FAM184B has a mutation status of V977L, The gene ADGRA3 has a mutation status of S161L, The gene FRYL has a mutation status of G1516E, The gene COQ2 has a mutation status of P205R, The gene WDFY3 has a mutation status of N826H, The gene PTPN13 has a mutation status of S1521S, The gene NDST3 has a mutation status of I225I, The gene LARP1B has a mutation status of S472F, The gene FSTL5 has a mutation status of Q486H, The gene DUX4 has a mutation status of A419D, The gene DROSHA has a mutation status of P155L, The gene DEPDC1B has a mutation status of V145M, The gene LHFPL2 has a mutation status of L153L, The gene FBXL17 has a mutation status of G235A, The gene KIF20A has a mutation status of F305F, The gene TENM2 has a mutation status of M405L, The gene PANK3 has a mutation status of E43E, The gene BTNL3 has a mutation status of G276R, The gene H3C6 has a mutation status of A136A, The gene OR11A1 has a mutation status of T311N, The gene MUC22 has a mutation status of S763S, The gene AL662899.4 has a mutation status of P121P, The gene HLA-DRB5 has a mutation status of T262R, The gene HLA-DRB1 has a mutation status of W38E, The gene HLA-DRB1 has a mutation status of K5T, The gene BEND6 has a mutation status of T26I, The gene KIAA1586 has a mutation status of N759S, The gene QRSL1 has a mutation status of V258V, The gene GJA1 has a mutation status of A315G, The gene NHSL1 has a mutation status of D111E, The gene AP5Z1 has a mutation status of D234Y, The gene PMS2 has a mutation status of C297S, The gene SOSTDC1 has a mutation status of V184I, The gene NEUROD6 has a mutation status of P296P, The gene NT5C3A has a mutation status of C108Y, The gene PKD1L1 has a mutation status of D1666E, The gene PTPN12 has a mutation status of F591F, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S123L, The gene MUC3A has a mutation status of S2488S, The gene MUC3A has a mutation status of S2495L, The gene MUC12 has a mutation status of Q50*, The gene MUC12 has a mutation status of S53T, The gene SH2B2 has a mutation status of A368P, The gene PTPRZ1 has a mutation status of S299L, The gene FEZF1 has a mutation status of F260F, The gene FLNC has a mutation status of E1137Q, The gene CPA5 has a mutation status of W208*, The gene KLF14 has a mutation status of P58S, The gene KLF14 has a mutation status of A39A, The gene DGKI has a mutation status of E682D, The gene RAB19 has a mutation status of L155L, The gene FGL1 has a mutation status of T276M, The gene TTI2 has a mutation status of G190V, The gene ZNF703 has a mutation status of G344S, The gene HGSNAT has a mutation status of R247R, The gene SOX17 has a mutation status of G28V, The gene LAPTM4B has a mutation status of M88K, The gene LAPTM4B has a mutation status of T90N, The gene DPYS has a mutation status of H217H, The gene POU5F1B has a mutation status of P78fs, The gene SLC39A4 has a mutation status of R251W, The gene BNC2 has a mutation status of T600N, The gene EQTN has a mutation status of N58fs, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of D105N, The gene PRSS3 has a mutation status of R122H, The gene CBWD6 has a mutation status of D159N, The gene CNTNAP3B has a mutation status of L968L, The gene AL358113.1 has a mutation status of R1112S, The gene FGD3 has a mutation status of R326T, The gene WNK2 has a mutation status of G1100G, The gene GRIN3A has a mutation status of I295S, The gene FRRS1L has a mutation status of R51A, The gene CCDC187 has a mutation status of R1071R, The gene CCDC187 has a mutation status of G1067G, The gene CCDC187 has a mutation status of E1017E, The gene CCDC187 has a mutation status of L747L, The gene CCDC187 has a mutation status of A321T, The gene CCDC187 has a mutation status of T90M, The gene SAPCD2 has a mutation status of A180A, The gene SAPCD2 has a mutation status of L96L, The gene IL15RA has a mutation status of T250S, The gene ALOX5 has a mutation status of L642L, The gene TET1 has a mutation status of A1760A, The gene ECD has a mutation status of T556I, The gene FRAT1 has a mutation status of V44L, The gene CFAP58 has a mutation status of D514N, The gene CCDC186 has a mutation status of N232S, The gene BNIP3 has a mutation status of H238Y, The gene SCART1 has a mutation status of V169V, The gene MUC5AC has a mutation status of G651G, The gene MUC5AC has a mutation status of S1378S, The gene MUC5AC has a mutation status of A1431A, The gene MUC5AC has a mutation status of G1443R, The gene MUC5AC has a mutation status of P1480A, The gene MUC5AC has a mutation status of L4000I, The gene MUC5AC has a mutation status of G5113V, The gene CHRNA10 has a mutation status of R27C, The gene HPS5 has a mutation status of G658V, The gene EXT2 has a mutation status of P341P, The gene CKAP5 has a mutation status of A596D, The gene OR4A16 has a mutation status of K22Q, The gene OR4A16 has a mutation status of N132T, The gene OR4A16 has a mutation status of I319A, The gene OR4P4 has a mutation status of N20N, The gene OR8U1 has a mutation status of N42N, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene OR9G1 has a mutation status of I196F, The gene AP006333.1 has a mutation status of *675*, The gene MAP4K2 has a mutation status of R279W, The gene SPTBN2 has a mutation status of Y2247H, The gene ALG8 has a mutation status of L303F, The gene C11orf65 has a mutation status of F32Y, The gene EXPH5 has a mutation status of R1594K, The gene TAS2R31 has a mutation status of I274A, The gene TAS2R46 has a mutation status of I245V, The gene TAS2R45 has a mutation status of I245V, The gene TAS2R45 has a mutation status of R154W, The gene LRMP has a mutation status of F290L, The gene GXYLT1 has a mutation status of C414H, The gene GXYLT1 has a mutation status of E249R, The gene GXYLT1 has a mutation status of I220G, The gene GXYLT1 has a mutation status of S212Y, The gene NR4A1 has a mutation status of D24E, The gene KRT8 has a mutation status of M378I, The gene KRT18 has a mutation status of T103N, The gene SMARCC2 has a mutation status of T484T, The gene APPL2 has a mutation status of N610Y, The gene TCTN1 has a mutation status of F151L, The gene OGFOD2 has a mutation status of A91S, The gene MTUS2 has a mutation status of T804K, The gene DGKH has a mutation status of S1028F, The gene ZC3H13 has a mutation status of N1627T, The gene TRIM13 has a mutation status of R153C, The gene INTS6 has a mutation status of N246D, The gene CCDC168 has a mutation status of P6314P, The gene ANKRD10 has a mutation status of D244D, The gene OR6S1 has a mutation status of R264Q, The gene GALNT16 has a mutation status of V228G, The gene PCNX1 has a mutation status of P930P, The gene KCNK10 has a mutation status of P46P, The gene GOLGA6L1 has a mutation status of R491W, The gene GOLGA6L2 has a mutation status of W501Q, The gene GOLGA6L2 has a mutation status of L500M, The gene SPTBN5 has a mutation status of A1294A, The gene WDR72 has a mutation status of A798S, The gene LDHAL6B has a mutation status of E361E, The gene LDHAL6B has a mutation status of H364P, The gene LACTB has a mutation status of V41G, The gene LACTB has a mutation status of G43G, The gene ANKDD1A has a mutation status of L516L, The gene GOLGA6L10 has a mutation status of C286R, The gene NOMO3 has a mutation status of V493M, The gene MVP has a mutation status of A584A, The gene SLC9A5 has a mutation status of R621H, The gene TERF2IP has a mutation status of M29L, The gene WWOX has a mutation status of R104R, The gene ZC3H18 has a mutation status of A723T, The gene SGSM2 has a mutation status of Q854K, The gene SPAG5 has a mutation status of V260V, The gene TAOK1 has a mutation status of R413K, The gene CCL4L2 has a mutation status of S29R, The gene CCL4L2 has a mutation status of P67R, The gene RPL23 has a mutation status of A79A, The gene TNS4 has a mutation status of P373L, The gene KRT10 has a mutation status of G543G, The gene KRT19 has a mutation status of E346*, The gene KLHL11 has a mutation status of Y242C, The gene EFTUD2 has a mutation status of T395S, The gene TSPOAP1 has a mutation status of G305R, The gene USP32 has a mutation status of F1574F, The gene MRC2 has a mutation status of D1471H, The gene CEP112 has a mutation status of D689D, The gene ZACN has a mutation status of V222V, The gene LAMA1 has a mutation status of R2362I, The gene APCDD1 has a mutation status of R213Q, The gene ANKRD62 has a mutation status of S470L, The gene CABLES1 has a mutation status of L197L, The gene SKOR2 has a mutation status of H250P, The gene FECH has a mutation status of A10G, The gene SERPINB13 has a mutation status of T105T, The gene PNPLA6 has a mutation status of R36P, The gene MUC16 has a mutation status of G13530S, The gene MUC16 has a mutation status of V13518L, The gene MUC16 has a mutation status of T12336L, The gene ZNF823 has a mutation status of S487C, The gene DNAJB1 has a mutation status of D313N, The gene RASAL3 has a mutation status of L808V, The gene NIBAN3 has a mutation status of Y385*, The gene ZNF85 has a mutation status of K195K, The gene IFNL1 has a mutation status of M1K, The gene FCGBP has a mutation status of P1883P, The gene HIPK4 has a mutation status of R353C, The gene PSG9 has a mutation status of I151S, The gene ZNF224 has a mutation status of R672S, The gene LILRB3 has a mutation status of Y290H, The gene LILRB3 has a mutation status of R288P, The gene LILRB3 has a mutation status of T201M, The gene LILRB3 has a mutation status of M21V, The gene LILRA2 has a mutation status of W163S, The gene LILRB1 has a mutation status of E34E, The gene LILRB1 has a mutation status of Q41Q, The gene LILRB1 has a mutation status of Y99I, The gene KIR2DL3 has a mutation status of P37R, The gene KIR2DL3 has a mutation status of E63E, The gene KIR2DL3 has a mutation status of K82K, The gene KIR2DL3 has a mutation status of E237K, The gene KIR2DL1 has a mutation status of D184N, The gene KIR2DL1 has a mutation status of K237E, The gene KIR2DL1 has a mutation status of G283G, The gene KIR2DL1 has a mutation status of T333A, The gene TMEM150B has a mutation status of Q214*, The gene FIZ1 has a mutation status of F60F, The gene SIRPA has a mutation status of L44S, The gene TGM6 has a mutation status of F499L, The gene LTN1 has a mutation status of E1243K, The gene KRTAP19-3 has a mutation status of Y64C, The gene LRRC3 has a mutation status of G182G, The gene GAB4 has a mutation status of I242L, The gene TSSK2 has a mutation status of A24T, The gene SLC7A4 has a mutation status of L104V, The gene OSM has a mutation status of V184G, The gene CYP2D6 has a mutation status of S486T, The gene CYP2D6 has a mutation status of V136V, The gene ATXN10 has a mutation status of L320L, The gene GTPBP6 has a mutation status of M181L, The gene GTPBP6 has a mutation status of G61R, The gene CRLF2 has a mutation status of V313V, The gene CRLF2 has a mutation status of P308P, The gene ASB11 has a mutation status of G219E, The gene BX276092.9 has a mutation status of P333S, The gene FAM236C has a mutation status of T34T, The gene KLHL4 has a mutation status of N151N, The gene TCEAL9 has a mutation status of R91H, The gene PWWP3B has a mutation status of V616V, The gene SLC25A5 has a mutation status of T221R, The gene UBE2A has a mutation status of I109I, The gene MAGEA3 has a mutation status of E102D, The gene AC236972.4 has a mutation status of P1394A, The gene MT-ND2 has a mutation status of T334T, The gene MT-CO2 has a mutation status of P145P, The gene MT-ATP8 has a mutation status of P36P, The gene MT-ATP6 has a mutation status of A177T, The gene MT-ATP6 has a mutation status of T189T, The gene MT-CO3 has a mutation status of L164L, The gene MT-ND4L has a mutation status of M27M, The gene MT-ND4 has a mutation status of T180T, The gene MT-ND4 has a mutation status of K206K, The gene MT-ND6 has a mutation status of E169E, The gene MT-CYB has a mutation status of F18L
LUAD