ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0013 HNRNPA2B1 SNP Missense_Mutation 7 26236230 G A 34 89 HNSC HN_63080 HNRNPA2B1 SNP Missense 7 26232920 C G 32 65 HNSC HN_63080 HNRNPA2B1 SNP Missense 7 26232960 C G 30 100 LUAD LUAD-B00915 HNRNPA2B1 SNP Missense_Mutation 7 26236222 T C 53 81 LUAD LUAD-B02077 HNRNPA2B1 SNP Missense_Mutation 7 26233234 C A 22 85 LUAD LUAD-RT-S01707 HNRNPA2B1 SNP Missense_Mutation 7 26236074 C A 18 86 MM MM-0411 HNRNPA2B1 SNP Missense_Mutation 7 26236448 C T 29 100 LUAD TCGA-05-4396 HNRNPA2B1 SNP Missense_Mutation 7 26236973 C A 21 100 GBM TCGA-06-0155 HNRNPA2B1 DEL Splice_Site 7 26236176 CCT - 18 86 LUSC TCGA-22-5473 HNRNPA2B1 SNP Missense_Mutation 7 26236961 C G 29 100 OV TCGA-24-1103 HNRNPA2B1 SNP Silent 7 26233226 G C 34 74 LUSC TCGA-33-4566 HNRNPA2B1 SNP Missense_Mutation 7 26235514 C A 30 95 LUAD TCGA-38-4629 HNRNPA2B1 SNP Missense_Mutation 7 26235526 C G 30 95 LUAD TCGA-44-3918 HNRNPA2B1 SNP Missense_Mutation 7 26237076 C G 29 74 LUAD TCGA-44-6779 HNRNPA2B1 SNP Splice_site 7 26240191 C A 18 60 LUAD TCGA-55-1592 HNRNPA2B1 SNP Missense_Mutation 7 26236615 T G 51 81 LUAD TCGA-55-1592 HNRNPA2B1 SNP Missense_Mutation 7 26236626 T G 60 58 UCEC TCGA-A5-A0GB HNRNPA2B1 SNP Splice_Site 7 26232995 T C 53 89 BRCA TCGA-A8-A07G HNRNPA2B1 SNP Nonsense_Mutation 7 26233303 C A 21 98 CRC TCGA-AA-A010 HNRNPA2B1 SNP Missense_Mutation 7 26237050 C A 32 89 CRC TCGA-AG-3609 HNRNPA2B1 SNP Missense_Mutation 7 26236037 G T 36 53 UCEC TCGA-AP-A051 HNRNPA2B1 SNP Missense_Mutation 7 26237309 C T 28 89 KIRC TCGA-B0-5109 HNRNPA2B1 SNP Missense_Mutation 7 26235512 G T 40 72 UCEC TCGA-B5-A11E HNRNPA2B1 SNP Silent 7 26233223 G A 40 59 HNSC TCGA-BA-5558 HNRNPA2B1 SNP Missense_Mutation 7 26232925 T C 52 81 BRCA TCGA-BH-A0HP HNRNPA2B1 SNP Missense_Mutation 7 26237271 C G 31 80 UCEC TCGA-BS-A0UV HNRNPA2B1 SNP Splice_Site 7 26232994 C T 24 98 HNSC TCGA-CR-7364 HNRNPA2B1 INS Frame_Shift_Ins 7 26232884 - C 58 64 HNSC TCGA-CV-7248 HNRNPA2B1 SNP Silent 7 26236079 T G 59 23 HNSC TCGA-CV-7416 HNRNPA2B1 SNP Missense_Mutation 7 26233291 C T 23 77 UCEC TCGA-D1-A103 HNRNPA2B1 SNP Missense_Mutation 7 26235512 G A 40 72 BLCA TCGA-DK-A1AC HNRNPA2B1 SNP Splice_site 7 26240198 C T 31 53 HNSC TCGA-DQ-7588 HNRNPA2B1 SNP Missense_Mutation 7 26232879 T C 49 94