ttype patient gene classification type chr pos ref_allele newbase context65 cons46 GBM TCGA-76-6661 GTF3C6 SNP Missense_Mutation 6 111288823 G T 33 65 CRC TCGA-AA-A010 GTF3C6 SNP Nonsense_Mutation 6 111283699 G T 33 81 UCEC TCGA-AP-A0LM GTF3C6 SNP Missense_Mutation 6 111281806 A C 1 59 UCEC TCGA-AP-A0LM GTF3C6 SNP Missense_Mutation 6 111288758 G A 37 71 UCEC TCGA-B5-A0K8 GTF3C6 DEL Frame_Shift_Del 6 111288854 T - 52 48 BRCA TCGA-C8-A27B GTF3C6 SNP Missense_Mutation 6 111280417 G T 33 84 HNSC TCGA-CR-6472 GTF3C6 SNP Missense_Mutation 6 111288781 C G 32 45 HNSC TCGA-CV-7435 GTF3C6 INS Frame_Shift_Ins 6 111288940 - T 16 54