ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-F00018 GFM2 SNP Missense_Mutation 5 74017589 C T 31 85 MEL ME009 GFM2 SNP Splice_site 5 74046404 C T 24 100 MM MM-0332 GFM2 SNP Synonymous 5 74043597 A C 11 49 MM MM-0526 GFM2 SNP Missense_Mutation 5 74041516 G A 42 83 GBM TCGA-02-0047 GFM2 SNP Missense_Mutation 5 74028894 G A 38 74 GBM TCGA-02-0047 GFM2 SNP Silent 5 74041590 T C 56 57 LUAD TCGA-05-4396 GFM2 SNP Missense_Mutation 5 74026139 C A 23 97 GBM TCGA-27-1832 GFM2 SNP Splice_Site 5 74056813 T C 53 64 LUAD TCGA-75-6206 GFM2 SNP Silent 5 74032775 G C 47 48 LUAD TCGA-91-6836 GFM2 SNP Missense_Mutation 5 74034397 C T 18 99 BRCA TCGA-A8-A083 GFM2 SNP Missense_Mutation 5 74026192 A G 16 89 CRC TCGA-AA-3821 GFM2 SNP Silent 5 74026212 A G 6 65 CRC TCGA-AA-A01I GFM2 SNP Missense_Mutation 5 74046462 C T 23 89 CRC TCGA-AG-A002 GFM2 SNP Missense_Mutation 5 74021496 A C 4 86 CRC TCGA-AG-A002 GFM2 SNP Missense_Mutation 5 74026188 C A 32 56 UCEC TCGA-AP-A051 GFM2 SNP Missense_Mutation 5 74034435 G A 46 99 UCEC TCGA-AX-A0J0 GFM2 SNP Missense_Mutation 5 74043556 C T 31 85 UCEC TCGA-B5-A11E GFM2 SNP Missense_Mutation 5 74021912 A G 6 77 UCEC TCGA-B5-A11Y GFM2 SNP Missense_Mutation 5 74028873 C T 20 91 UCEC TCGA-BS-A0UV GFM2 SNP Nonsense_Mutation 5 74041628 C A 32 73 BRCA TCGA-C8-A274 GFM2 SNP Missense_Mutation 5 74047198 G A 48 100 HNSC TCGA-CN-5360 GFM2 SNP Silent 5 74017519 A G 12 58 HNSC TCGA-CV-5442 GFM2 SNP Missense_Mutation 5 74018254 G A 37 100 UCEC TCGA-D1-A16Y GFM2 SNP Silent 5 74021922 T G 56 50 BRCA TCGA-D8-A1JP GFM2 SNP Missense_Mutation 5 74047238 T C 57 71 BLCA TCGA-H4-A2HQ GFM2 SNP Missense_Mutation 5 74054712 C T 32 98