ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62237 SFT2D1 SNP Missense 6 166739628 C A 25 79 LUAD LUAD-NYU847 SFT2D1 SNP Missense_Mutation 6 166738050 T G 51 61 MEL ME020 SFT2D1 SNP Missense_Mutation 6 166743070 C T 30 58 GBM TCGA-06-0178 SFT2D1 SNP Missense_Mutation 6 166739646 T C 51 48 CRC TCGA-AA-3715 SFT2D1 SNP Silent 6 166741782 A G 5 49 CRC TCGA-AA-A00N SFT2D1 SNP Missense_Mutation 6 166743666 C T 19 46 CRC TCGA-AA-A010 SFT2D1 SNP Nonsense_Mutation 6 166743722 G T 45 65 AML TCGA-AB-2864 SFT2D1 SNP Splice_Site 6 166739657 T A 53 74 UCEC TCGA-B5-A0JY SFT2D1 SNP Silent 6 166743676 G A 37 52