ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CRC CRC-0010 IRF7 SNP Missense 11 613430 G A 39 63 ESO ESO-0590 IRF7 SNP Silent 11 613354 C T 26 39 ESO ESO-167 IRF7 SNP Missense_Mutation 11 615183 G C 34 54 HNSC HN_62505 IRF7 SNP Missense 11 613076 G A 40 50 MEL ME017 IRF7 SNP Splice_Site 11 614038 C T 24 64 MEL MEL-Ma-Mel-122 IRF7 SNP Silent 11 613810 G A 43 47 LUAD TCGA-05-4384 IRF7 SNP Missense_Mutation 11 614252 A G 8 50 LUAD TCGA-17-Z061 IRF7 INS Frame_Shift_Ins 11 613353 - C 42 48 LUSC TCGA-34-2596 IRF7 SNP Silent 11 612717 G A 33 49 UCEC TCGA-A5-A0VP IRF7 SNP Silent 11 613991 C T 31 37 KIRC TCGA-BP-5196 IRF7 SNP Silent 11 614301 G A 41 49 UCEC TCGA-BS-A0UF IRF7 SNP Silent 11 612681 G A 37 21 BLCA TCGA-C4-A0F1 IRF7 SNP Missense_Mutation 11 612784 C A 25 68 HNSC TCGA-CN-6013 IRF7 SNP Silent 11 613228 G A 37 40 HNSC TCGA-CQ-6218 IRF7 SNP Missense_Mutation 11 613301 C T 26 68 HNSC TCGA-CR-7370 IRF7 SNP Missense_Mutation 11 613308 C T 30 68 UCEC TCGA-D1-A17R IRF7 SNP Missense_Mutation 11 612704 C T 27 43 BRCA TCGA-D8-A1JI IRF7 SNP Missense_Mutation 11 615281 G A 33 44