ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-E00934 IRF2 SNP Silent 4 185329364 C A 23 56 LUAD LUAD-S01474 IRF2 SNP Missense_Mutation 4 185340683 T C 53 54 MEL ME016 IRF2 SNP Missense_Mutation 4 185339712 G A 43 100 MEL MEL-JWCI-WGS-21 IRF2 SNP Missense_Mutation 4 185310000 G A 41 75 MEL MEL-JWCI-WGS-7 IRF2 SNP Missense_Mutation 4 185340662 T C 64 69 GBM TCGA-06-0145 IRF2 SNP Silent 4 185329382 A G 12 52 OV TCGA-10-0930 IRF2 SNP Missense_Mutation 4 185340638 A G 7 91 GBM TCGA-14-2554 IRF2 SNP Missense_Mutation 4 185310216 C T 23 65 OV TCGA-25-1632 IRF2 SNP Nonsense_Mutation 4 185339692 T A 61 87 LUAD TCGA-44-2655 IRF2 SNP Missense_Mutation 4 185310048 C A 21 88 LUAD TCGA-50-5044 IRF2 SNP Missense_Mutation 4 185320141 C T 29 92 LUSC TCGA-66-2767 IRF2 SNP Silent 4 185320124 C T 23 44 CRC TCGA-AA-3864 IRF2 SNP Silent 4 185350153 C T 23 19 CRC TCGA-AA-3979 IRF2 SNP Missense_Mutation 4 185339727 A C 10 91 CRC TCGA-AA-A010 IRF2 SNP Missense_Mutation 4 185339750 C A 32 56 CRC TCGA-AA-A010 IRF2 SNP Missense_Mutation 4 185340688 G A 38 99 AML TCGA-AB-2807 IRF2 SNP Missense_Mutation 4 185310179 C G 20 60 BRCA TCGA-AN-A0XN IRF2 SNP Missense_Mutation 4 185329410 G C 33 81 UCEC TCGA-AP-A051 IRF2 SNP Missense_Mutation 4 185339814 G A 38 100 UCEC TCGA-AP-A0LE IRF2 SNP Nonsense_Mutation 4 185320225 G A 48 74 UCEC TCGA-AX-A05Z IRF2 SNP Missense_Mutation 4 185339800 C G 27 99 UCEC TCGA-AX-A05Z IRF2 SNP Missense_Mutation 4 185340702 G A 41 51 UCEC TCGA-B5-A0JS IRF2 SNP Silent 4 185320124 C T 23 44 UCEC TCGA-BS-A0UA IRF2 SNP Missense_Mutation 4 185320080 G A 33 92 UCEC TCGA-BS-A0UV IRF2 SNP Silent 4 185339723 G A 44 62 HNSC TCGA-CN-4734 IRF2 SNP Splice_Site 4 185311904 C G 32 83 HNSC TCGA-CV-6953 IRF2 SNP Missense_Mutation 4 185339790 G A 41 69 HNSC TCGA-CV-7407 IRF2 SNP Silent 4 185340660 T C 56 54 UCEC TCGA-D1-A103 IRF2 SNP Missense_Mutation 4 185309950 T C 60 82 BLCA TCGA-DK-A3IU IRF2 SNP Splice_site 4 185340623 C T 24 99