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depmap_mutation_cancer_type

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text stringlengths 523 1.12M	SUBCLASS stringclasses 23 values
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 gen(...TRUNCATED)	BLCA
"The gene PERM1 has a mutation status of G75C, The gene MXRA8 has a mutation status of I430I, The ge(...TRUNCATED)	LUAD
"The gene PLEKHN1 has a mutation status of R154*, The gene PERM1 has a mutation status of S277S, The(...TRUNCATED)	LUAD

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