ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-175 VPS26B SNP Silent 11 134115431 C T 24 63 LUAD LUAD-LC15C VPS26B SNP Missense_Mutation 11 134113026 G A 33 99 MEL ME009 VPS26B SNP Missense_Mutation 11 134114843 C T 22 100 GBM TCGA-32-1991 VPS26B SNP Silent 11 134104939 G T 45 56 LUAD TCGA-38-4629 VPS26B SNP Missense_Mutation 11 134095109 C T 19 48 LUAD TCGA-44-2657 VPS26B SNP Missense_Mutation 11 134095068 G T 37 98 LUSC TCGA-46-3765 VPS26B SNP Missense_Mutation 11 134114844 C T 23 100 LUAD TCGA-50-6594 VPS26B SNP Missense_Mutation 11 134104877 G T 42 72 LUSC TCGA-60-2724 VPS26B SNP Missense_Mutation 11 134114850 G T 39 100 UCEC TCGA-A5-A0GW VPS26B SNP Missense_Mutation 11 134110010 A G 11 92 CRC TCGA-AA-3516 VPS26B SNP Nonsense_Mutation 11 134113185 C T 27 60 CRC TCGA-AA-3543 VPS26B SNP Missense_Mutation 11 134109979 A G 9 92 CRC TCGA-AA-3672 VPS26B SNP Missense_Mutation 11 134104835 G A 44 100 CRC TCGA-AA-3984 VPS26B SNP Silent 11 134095130 C T 30 59 AML TCGA-AB-2833 VPS26B SNP Missense_Mutation 11 134115390 A T 7 76 AML TCGA-AB-2859 VPS26B SNP Missense_Mutation 11 134095072 C G 25 83 UCEC TCGA-AP-A059 VPS26B SNP Missense_Mutation 11 134114838 C A 30 100 UCEC TCGA-AP-A0LM VPS26B SNP Missense_Mutation 11 134095170 C A 24 66 KIRC TCGA-B0-4846 VPS26B SNP Missense_Mutation 11 134095128 T G 64 90 UCEC TCGA-B5-A0JY VPS26B SNP Missense_Mutation 11 134109908 G A 34 73 UCEC TCGA-B5-A0JY VPS26B SNP Missense_Mutation 11 134115410 C T 27 65 HNSC TCGA-BA-6871 VPS26B SNP Silent 11 134095034 C T 31 57 BRCA TCGA-BH-A18K VPS26B SNP Silent 11 134114938 G C 45 60 BRCA TCGA-D8-A1XW VPS26B SNP Missense_Mutation 11 134115368 G A 40 97 BLCA TCGA-DK-A1AG VPS26B SNP Missense_Mutation 11 134114848 C G 30 87 BRCA TCGA-GI-A2C8 VPS26B SNP Silent 11 134104810 G T 41 52 BLCA TCGA-GV-A3JZ VPS26B SNP Missense_Mutation 11 134113161 G C 37 99