| sample_id,chromosome,position,reference_allele,variant_allele,mutation_type,pathogenicity_score,clinical_significance,variant_allele_frequency,read_depth | |
| ONC-001,chr1,115256529,T,A,Missense,0.92,Pathogenic,0.45,450 | |
| ONC-002,chr7,55242465,G,C,Missense,0.88,Likely_Pathogenic,0.32,380 | |
| ONC-003,chr13,32890664,C,T,Nonsense,0.98,Pathogenic,0.51,520 | |
| ONC-004,chr17,7577121,G,A,Frameshift,0.95,Pathogenic,0.28,290 | |
| ONC-005,chr10,89623101,A,G,Splice_Site,0.81,VUS,0.12,180 | |
| ONC-006,chrX,153295431,T,C,Synonymous,0.05,Benign,0.48,610 | |
| ONC-007,chr2,209113112,C,G,Missense,0.42,VUS,0.15,405 | |
| ONC-008,chr4,153245452,G,T,Missense,0.76,Likely_Pathogenic,0.38,325 | |
| ONC-009,chr11,108115622,A,C,Stop_Loss,0.91,Pathogenic,0.42,485 | |
| ONC-010,chr12,25398284,C,T,Missense,0.94,Pathogenic,0.55,540 | |
| ONC-011,chr1,156108521,G,A,Intronic,0.02,Benign,0.50,600 | |
| ONC-012,chr14,105235684,T,G,Missense,0.55,VUS,0.18,255 | |
| ONC-013,chr9,133748283,A,T,Nonsense,0.99,Pathogenic,0.35,310 | |
| ONC-014,chr5,112175231,C,G,Missense,0.85,Pathogenic,0.44,475 | |
| ONC-015,chr19,11025232,G,C,Frameshift,0.97,Pathogenic,0.22,340 | |
| ONC-016,chr3,178936091,T,A,Missense,0.89,Pathogenic,0.39,415 | |
| ONC-017,chr16,2115243,C,T,Splice_Site,0.78,Likely_Pathogenic,0.25,280 | |
| ONC-018,chr20,62345672,A,G,Missense,0.12,Benign,0.49,580 | |
| ONC-019,chr22,29083745,G,A,Missense,0.68,VUS,0.29,360 | |
| ONC-020,chr6,152453671,C,T,Intronic,0.01,Benign,0.52,650 | |
| ONC-021,chr8,128748315,A,C,Missense,0.93,Pathogenic,0.41,490 | |
| ONC-022,chr15,40654321,T,G,Nonsense,0.96,Pathogenic,0.33,395 | |
| ONC-023,chr18,48575123,C,A,Missense,0.48,VUS,0.14,210 | |
| ONC-024,chr21,36254189,G,T,Frameshift,0.99,Pathogenic,0.20,330 | |
| ONC-025,chr7,116412043,A,G,Missense,0.82,Likely_Pathogenic,0.36,420 | |
| ONC-026,chr10,123241567,T,C,Synonymous,0.04,Benign,0.46,590 | |
| ONC-027,chr12,121804703,C,G,Missense,0.72,Likely_Pathogenic,0.27,355 | |
| ONC-028,chr17,37844393,G,A,Missense,0.95,Pathogenic,0.40,505 | |
| ONC-029,chr2,204123567,A,T,Intronic,0.03,Benign,0.51,620 | |
| ONC-030,chr4,1807218,C,G,Missense,0.98,Pathogenic,0.47,445 | |
| ONC-031,chr1,24895642,T,C,Missense,0.51,VUS,0.19,275 |