ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME029 GSG1 SNP Missense_Mutation 12 13240189 C T 22 100 MEL MEL-JWCI-WGS-11 GSG1 SNP Missense_Mutation 12 13243455 C T 30 83 MM MM-0581 GSG1 SNP Missense_Mutation 12 13243583 T C 58 54 LUAD TCGA-05-4382 GSG1 SNP Silent 12 13243462 G A 35 63 LUAD TCGA-05-4396 GSG1 SNP Missense_Mutation 12 13243512 C A 21 97 LUAD TCGA-17-Z022 GSG1 SNP Missense_Mutation 12 13238120 C G 19 19 LUAD TCGA-17-Z023 GSG1 SNP Missense_Mutation 12 13243530 G T 48 61 LUSC TCGA-39-5030 GSG1 SNP Silent 12 13243687 T C 59 56 CRC TCGA-AA-3877 GSG1 SNP Silent 12 13243456 C T 24 62 CRC TCGA-AA-3984 GSG1 SNP Missense_Mutation 12 13240110 A G 2 55 CRC TCGA-AA-A00A GSG1 SNP Missense_Mutation 12 13238141 C T 23 15 CRC TCGA-AA-A010 GSG1 SNP Missense_Mutation 12 13242166 A G 10 46 UCEC TCGA-AP-A0LM GSG1 SNP Missense_Mutation 12 13256415 A G 2 71 UCEC TCGA-AP-A0LM GSG1 SNP Translation_Start_Site 12 13256529 G A 40 45 UCEC TCGA-AX-A05Z GSG1 SNP Missense_Mutation 12 13243734 A C 3 44 UCEC TCGA-B5-A0JY GSG1 SNP Missense_Mutation 12 13256440 C A 31 50 UCEC TCGA-B5-A11E GSG1 SNP Missense_Mutation 12 13237901 A C 9 47 UCEC TCGA-B5-A11E GSG1 SNP Missense_Mutation 12 13238061 G A 39 54 HNSC TCGA-BA-5152 GSG1 SNP Missense_Mutation 12 13243458 C T 29 96 KIRC TCGA-BP-4807 GSG1 SNP Missense_Mutation 12 13241706 A G 9 58 UCEC TCGA-BS-A0TE GSG1 SNP Nonsense_Mutation 12 13238101 C A 30 84 UCEC TCGA-BS-A0UF GSG1 SNP Missense_Mutation 12 13238145 G A 38 61 BLCA TCGA-CF-A1HS GSG1 SNP Missense_Mutation 12 13256440 C G 31 50 HNSC TCGA-CV-7235 GSG1 SNP Silent 12 13243618 G A 43 61 HNSC TCGA-CV-7253 GSG1 SNP Missense_Mutation 12 13238169 C A 21 100 BLCA TCGA-GV-A3JZ GSG1 SNP Missense_Mutation 12 13243611 C T 31 67 BLCA TCGA-H4-A2HQ GSG1 SNP Missense_Mutation 12 13240941 G A 45 65