ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MM MM-0497 H1FX SNP Silent 3 129034595 G A 34 83 MM MM-0546 H1FX SNP Missense_Mutation 3 129034285 G A 41 53 LUAD TCGA-17-Z058 H1FX SNP Silent 3 129034608 G T 46 65 OV TCGA-61-2000 H1FX SNP Missense_Mutation 3 129034682 T G 58 51 UCEC TCGA-AP-A059 H1FX SNP Silent 3 129034620 C T 32 64 HNSC TCGA-CR-7376 H1FX DEL Frame_Shift_Del 3 129034495 T - 52 81 BLCA TCGA-CU-A0YN H1FX SNP Missense_Mutation 3 129034521 C G 32 74 BLCA TCGA-CU-A0YN H1FX SNP Missense_Mutation 3 129034529 C T 31 64 KIRC TCGA-CW-6093 H1FX SNP Missense_Mutation 3 129034182 C G 32 70