ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME024 RAB6B SNP Missense_Mutation 3 133557052 C G 17 92 LUAD TCGA-05-4396 RAB6B SNP Missense_Mutation 3 133583484 C A 23 87 LUAD TCGA-17-Z015 RAB6B SNP Missense_Mutation 3 133547660 G T 39 70 LUAD TCGA-17-Z037 RAB6B SNP Missense_Mutation 3 133558368 G A 40 84 LUSC TCGA-34-2608 RAB6B SNP Missense_Mutation 3 133560150 C T 17 92 LUSC TCGA-60-2713 RAB6B SNP Silent 3 133560496 C T 30 51 LUSC TCGA-66-2785 RAB6B SNP Missense_Mutation 3 133547652 C G 31 97 UCEC TCGA-A5-A0VP RAB6B SNP Missense_Mutation 3 133560458 C T 27 92 CRC TCGA-AA-A00N RAB6B SNP Silent 3 133558427 G A 37 44 CRC TCGA-AG-3881 RAB6B SNP Splice_site 3 133583485 G A 37 50 UCEC TCGA-AP-A051 RAB6B SNP Missense_Mutation 3 133560186 G T 35 79 UCEC TCGA-AP-A056 RAB6B SNP Silent 3 133557034 C T 31 22 UCEC TCGA-B5-A0JY RAB6B SNP Missense_Mutation 3 133553450 C A 21 94 UCEC TCGA-B5-A0JY RAB6B SNP Missense_Mutation 3 133614276 C A 32 79 UCEC TCGA-B5-A11E RAB6B SNP Missense_Mutation 3 133557013 C A 28 59 UCEC TCGA-BG-A0M4 RAB6B SNP Missense_Mutation 3 133557074 C T 27 92 KIRC TCGA-BP-4770 RAB6B SNP Missense_Mutation 3 133558406 C G 22 60 UCEC TCGA-BS-A0UV RAB6B SNP Nonsense_Mutation 3 133553425 C A 32 94 HNSC TCGA-CR-6481 RAB6B SNP Nonsense_Mutation 3 133553479 G A 37 80 UCEC TCGA-D1-A167 RAB6B SNP Missense_Mutation 3 133614253 C T 22 79