ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62897 COQ3 SNP Missense 6 99825294 C T 29 94 LUAD LUAD-5V8LT COQ3 SNP Missense_Mutation 6 99823974 C G 29 97 LUAD LUAD_E00565 COQ3 SNP Missense_Mutation 6 99828184 T A 64 38 LUAD TCGA-05-4396 COQ3 SNP Missense_Mutation 6 99817545 C A 24 48 LUAD TCGA-05-4396 COQ3 SNP Nonsense_Mutation 6 99817670 C A 24 96 LUAD TCGA-05-4396 COQ3 SNP Missense_Mutation 6 99823932 G C 35 67 LUAD TCGA-17-Z028 COQ3 SNP Splice_Site 6 99825363 T A 56 82 UCEC TCGA-AP-A051 COQ3 SNP Missense_Mutation 6 99823892 G A 34 80 UCEC TCGA-AP-A056 COQ3 SNP Missense_Mutation 6 99817482 C A 32 65 UCEC TCGA-AP-A059 COQ3 SNP Missense_Mutation 6 99817597 G T 34 95 BRCA TCGA-BH-A0DZ COQ3 SNP Missense_Mutation 6 99817588 G A 41 74 BLCA TCGA-BT-A3PJ COQ3 SNP Silent 6 99823966 G A 41 53 UCEC TCGA-D1-A103 COQ3 SNP Missense_Mutation 6 99828173 T C 58 87 UCEC TCGA-D1-A167 COQ3 SNP Missense_Mutation 6 99828081 T C 54 60 BRCA TCGA-D8-A1X9 COQ3 SNP Missense_Mutation 6 99842022 C A 22 47