ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-NYU847 RABGGTB SNP Splice_Site 1 76253290 G T 48 96 LUAD LUAD-S01306 RABGGTB SNP Missense_Mutation 1 76259791 G T 47 100 MEL MEL-JWCI-WGS-11 RABGGTB SNP Splice_Site 1 76251961 T C 57 58 LUAD TCGA-05-4382 RABGGTB SNP Missense_Mutation 1 76254898 G A 36 98 LUAD TCGA-17-Z057 RABGGTB SNP Missense_Mutation 1 76260291 G A 33 100 LUAD TCGA-17-Z058 RABGGTB SNP Silent 1 76253196 G A 35 58 LUSC TCGA-18-3419 RABGGTB SNP Missense_Mutation 1 76259838 G T 45 100 OV TCGA-25-2400 RABGGTB SNP Silent 1 76260326 A G 15 52 LUAD TCGA-35-3621 RABGGTB SNP Missense_Mutation 1 76254867 G C 45 54 LUSC TCGA-43-5668 RABGGTB SNP Missense_Mutation 1 76254853 A T 16 75 LUAD TCGA-44-6145 RABGGTB SNP Splice_site 1 76253183 G T 42 96 CRC TCGA-AA-3864 RABGGTB SNP Missense_Mutation 1 76257984 C T 23 87 CRC TCGA-AA-3984 RABGGTB SNP Silent 1 76257952 A G 10 49 CRC TCGA-AA-A00J RABGGTB SNP Missense_Mutation 1 76260243 G A 43 88 CRC TCGA-AA-A00J RABGGTB SNP Silent 1 76260329 G A 45 68 CRC TCGA-AA-A022 RABGGTB SNP Missense_Mutation 1 76254926 G A 38 98 CRC TCGA-AG-A002 RABGGTB SNP Missense_Mutation 1 76257887 C A 32 66 UCEC TCGA-AP-A059 RABGGTB SNP Missense_Mutation 1 76254926 G A 38 98 UCEC TCGA-AX-A05S RABGGTB SNP Missense_Mutation 1 76255030 A G 15 89 UCEC TCGA-AX-A0J1 RABGGTB SNP Missense_Mutation 1 76259853 C T 27 71 KIRC TCGA-B0-5710 RABGGTB SNP Silent 1 76255648 G A 48 50 KIRC TCGA-BP-5183 RABGGTB SNP Missense_Mutation 1 76254935 G C 33 56 UCEC TCGA-BS-A0UV RABGGTB SNP Missense_Mutation 1 76253277 G T 33 67 HNSC TCGA-CN-4725 RABGGTB SNP Missense_Mutation 1 76260255 A G 12 56 HNSC TCGA-CR-7390 RABGGTB SNP Missense_Mutation 1 76257189 T C 60 91 HNSC TCGA-CV-5966 RABGGTB DEL Frame_Shift_Del 1 76255009 C - 30 98 BRCA TCGA-D8-A147 RABGGTB SNP Missense_Mutation 1 76254953 T A 64 89