ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUSC TCGA-18-3409 NDUFS8 SNP Silent 11 67800726 C T 32 50 LUSC TCGA-33-4583 NDUFS8 SNP Missense_Mutation 11 67799650 G A 39 75 LUSC TCGA-60-2720 NDUFS8 SNP Silent 11 67800460 G T 48 53 LUAD TCGA-67-3771 NDUFS8 SNP Missense_Mutation 11 67800450 G T 38 63 AML TCGA-AB-2814 NDUFS8 SNP Silent 11 67803776 T C 51 43 UCEC TCGA-AP-A059 NDUFS8 SNP Missense_Mutation 11 67800595 A G 11 87 UCEC TCGA-B5-A11E NDUFS8 SNP Splice_Site 11 67803719 G T 35 90 HNSC TCGA-BB-7862 NDUFS8 SNP Silent 11 67803773 C T 28 64 UCEC TCGA-BG-A0W2 NDUFS8 SNP Missense_Mutation 11 67803940 T G 63 42 KIRC TCGA-CJ-4923 NDUFS8 SNP Missense_Mutation 11 67799656 T A 55 60 HNSC TCGA-CR-7399 NDUFS8 SNP Missense_Mutation 11 67803822 G C 42 77 UCEC TCGA-D1-A103 NDUFS8 SNP Missense_Mutation 11 67803783 G A 37 92 BRCA TCGA-D8-A1XJ NDUFS8 SNP Missense_Mutation 11 67803732 G A 37 78