ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-682 GTF2H3 SNP Silent 12 124144734 G T 46 46 MEL MEL-13575 GTF2H3 SNP Missense_Mutation 12 124130012 C T 30 82 MM MM-0566 GTF2H3 SNP Missense_Mutation 12 124144769 A C 1 88 LUSC TCGA-33-4582 GTF2H3 SNP Missense_Mutation 12 124130034 G C 47 81 LUAD TCGA-50-6590 GTF2H3 SNP Missense_Mutation 12 124144730 C G 32 79 CRC TCGA-AA-3710 GTF2H3 SNP Missense_Mutation 12 124144076 C T 19 94 CRC TCGA-AA-3949 GTF2H3 INS Frame_Shift_Ins 12 124123861 - G 59 73 CRC TCGA-AA-3984 GTF2H3 SNP Missense_Mutation 12 124144728 T G 64 51 CRC TCGA-AA-A010 GTF2H3 SNP Missense_Mutation 12 124132613 G A 37 77 BRCA TCGA-AN-A0XW GTF2H3 SNP Silent 12 124144425 C T 32 99 UCEC TCGA-AX-A05Z GTF2H3 SNP Missense_Mutation 12 124144725 A C 1 65 BRCA TCGA-BH-A0DQ GTF2H3 SNP Splice_site 12 124144342 T A 59 89 UCEC TCGA-BS-A0UV GTF2H3 SNP Missense_Mutation 12 124132651 G T 33 56 BLCA TCGA-BT-A20J GTF2H3 SNP Missense_Mutation 12 124132646 G A 45 91 HNSC TCGA-CR-7370 GTF2H3 SNP Missense_Mutation 12 124144433 G A 37 86 HNSC TCGA-CV-6960 GTF2H3 DEL Frame_Shift_Del 12 124132650 A - 11 84 UCEC TCGA-D1-A103 GTF2H3 SNP Silent 12 124130037 G A 46 66 UCEC TCGA-D1-A16X GTF2H3 SNP Nonsense_Mutation 12 124144432 C T 31 59 UCEC TCGA-D1-A17B GTF2H3 SNP Missense_Mutation 12 124132581 T G 64 50