ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0027 COQ5 SNP Missense_Mutation 12 120960161 G C 45 74 LUAD LUAD-CHTN-MAD06-00668 COQ5 SNP Missense_Mutation 12 120966905 C T 23 51 LUAD LUAD-CHTN-MAD08-00104 COQ5 SNP Missense_Mutation 12 120966756 C G 32 56 MEL ME001 COQ5 SNP Silent 12 120942766 C G 22 45 LUAD TCGA-05-4396 COQ5 SNP Missense_Mutation 12 120941780 G T 39 100 LUAD TCGA-05-4396 COQ5 SNP Missense_Mutation 12 120941822 C A 21 100 LUAD TCGA-05-4396 COQ5 SNP Silent 12 120954392 G T 35 46 LUAD TCGA-05-4396 COQ5 SNP Missense_Mutation 12 120954454 C A 23 92 LUAD TCGA-17-Z022 COQ5 SNP Silent 12 120960072 G C 33 53 LUAD TCGA-17-Z031 COQ5 SNP Missense_Mutation 12 120960118 T C 50 93 OV TCGA-20-0990 COQ5 SNP Nonsense_Mutation 12 120941829 C A 21 80 LUSC TCGA-34-5239 COQ5 SNP Silent 12 120960138 C T 32 61 LUAD TCGA-35-3621 COQ5 SNP Missense_Mutation 12 120966926 A T 7 56 LUSC TCGA-39-5027 COQ5 SNP Silent 12 120966933 G A 39 62 LUAD TCGA-91-6836 COQ5 SNP Missense_Mutation 12 120954501 C A 21 100 UCEC TCGA-AP-A0LD COQ5 SNP Missense_Mutation 12 120954447 C T 19 40 HNSC TCGA-BA-6869 COQ5 SNP Silent 12 120947835 G C 45 60 BLCA TCGA-BT-A20N COQ5 SNP Silent 12 120942706 G C 45 51 BLCA TCGA-BT-A3PJ COQ5 SNP Missense_Mutation 12 120947870 C G 29 100 BLCA TCGA-C4-A0F6 COQ5 SNP Missense_Mutation 12 120966898 C T 22 67 KIRC TCGA-CJ-4913 COQ5 SNP Missense_Mutation 12 120966769 A T 6 84 KIRC TCGA-CJ-4920 COQ5 SNP Missense_Mutation 12 120954469 C T 32 59 HNSC TCGA-CV-6942 COQ5 SNP Missense_Mutation 12 120941685 C T 32 87 UCEC TCGA-D1-A17R COQ5 SNP Silent 12 120966825 A C 11 43 BRCA TCGA-E2-A1IF COQ5 SNP Missense_Mutation 12 120966842 C A 23 44