ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62672 IRF2BP2 SNP Nonsense 1 234743107 C A 30 100 LUAD LUAD-5V8LT IRF2BP2 SNP Silent 1 234744707 C A 27 61 LUAD LUAD-B00731 IRF2BP2 SNP Silent 1 234744668 G A 45 49 LUAD LUAD-B00915 IRF2BP2 SNP Nonsense_Mutation 1 234743518 G A 47 100 LUAD LUAD-B01811 IRF2BP2 SNP Missense_Mutation 1 234743096 A T 4 73 LUAD LUAD-F00365 IRF2BP2 SNP Silent 1 234743135 C A 17 79 LUAD LUAD-NYU847 IRF2BP2 SNP Missense_Mutation 1 234743119 G A 47 100 LUAD LUAD-S01341 IRF2BP2 SNP Silent 1 234744314 C A 25 55 MED MD-146 IRF2BP2 SNP Missense_Mutation 1 234743061 A C 9 92 MEL MEL-Ma-Mel-94 IRF2BP2 DNP Missense_Mutation 1 234743375 GG AA 47 62 LUAD TCGA-05-4424 IRF2BP2 SNP Missense_Mutation 1 234743041 G T 48 86 LUAD TCGA-17-Z055 IRF2BP2 SNP Missense_Mutation 1 234742946 C G 25 100 LUSC TCGA-37-4133 IRF2BP2 SNP Missense_Mutation 1 234743448 G A 39 85 LUSC TCGA-46-6026 IRF2BP2 SNP Missense_Mutation 1 234743230 C T 32 97 LUSC TCGA-66-2794 IRF2BP2 SNP Missense_Mutation 1 234742956 C A 21 100 BRCA TCGA-A2-A0CU IRF2BP2 INS Frame_Shift_Ins 1 234743301 - A 41 100 BRCA TCGA-A2-A0T1 IRF2BP2 SNP Missense_Mutation 1 234744272 G T 46 73 CRC TCGA-AA-3518 IRF2BP2 SNP Silent 1 234743393 G A 43 51 UCEC TCGA-AP-A051 IRF2BP2 SNP Missense_Mutation 1 234743334 C A 20 59 UCEC TCGA-AX-A0J1 IRF2BP2 SNP Missense_Mutation 1 234743385 C T 26 86 KIRC TCGA-B0-4817 IRF2BP2 SNP Silent 1 234743339 C A 22 55 UCEC TCGA-B5-A11E IRF2BP2 SNP Missense_Mutation 1 234743164 C T 30 88 HNSC TCGA-BB-4228 IRF2BP2 DEL In_Frame_Del 1 234743346 TTG - 52 71 KIRC TCGA-BP-4998 IRF2BP2 SNP Missense_Mutation 1 234743247 C A 32 100 HNSC TCGA-CQ-5327 IRF2BP2 INS Frame_Shift_Ins 1 234743542 - CC 42 68 HNSC TCGA-CV-7095 IRF2BP2 SNP Nonsense_Mutation 1 234745081 C A 31 74 UCEC TCGA-D1-A161 IRF2BP2 INS Frame_Shift_Ins 1 234743516 - T 28 67 BLCA TCGA-G2-A2EO IRF2BP2 SNP Missense_Mutation 1 234744657 G A 37 62