ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62506 FAM107A SNP Synonymous 3 58553031 G A 44 54 MEL ME035 FAM107A SNP Missense_Mutation 3 58552407 C T 32 56 MEL MEL-JWCI-WGS-12 FAM107A SNP Missense_Mutation 3 58555478 G A 43 97 MEL MEL-JWCI-WGS-4 FAM107A SNP Nonsense_Mutation 3 58555517 C T 21 97 MEL MEL-Ma-Mel-65 FAM107A SNP Missense_Mutation 3 58555548 C T 22 66 PRAD P04-2641 FAM107A SNP Nonsense_Mutation 3 58555516 C T 30 61 LUAD TCGA-17-Z042 FAM107A SNP Silent 3 58552961 G A 34 60 LUAD TCGA-17-Z060 FAM107A SNP Missense_Mutation 3 58555535 C T 23 79 LUAD TCGA-44-2668 FAM107A SNP Silent 3 58555486 C A 25 52 LUSC TCGA-66-2785 FAM107A SNP Missense_Mutation 3 58555429 C T 29 98 CRC TCGA-AA-3710 FAM107A SNP Missense_Mutation 3 58555562 C T 23 56 CRC TCGA-AA-3984 FAM107A SNP Missense_Mutation 3 58552356 G A 38 66 BRCA TCGA-BH-A18R FAM107A SNP Missense_Mutation 3 58552971 C G 28 62 UCEC TCGA-BS-A0UF FAM107A SNP Missense_Mutation 3 58555509 C T 30 97 HNSC TCGA-CR-7382 FAM107A SNP Silent 3 58555543 C G 29 50 UCEC TCGA-D1-A103 FAM107A SNP Missense_Mutation 3 58552895 C A 24 45 UCEC TCGA-D1-A167 FAM107A SNP Missense_Mutation 3 58552955 G A 40 69 UCEC TCGA-EY-A1GS FAM107A SNP Missense_Mutation 3 58555523 C T 32 70