ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_00076 RRAS2 SNP Missense 11 14380346 C T 26 84 LUAD LUAD-NYU847 RRAS2 SNP Silent 11 14380330 C A 27 58 LUAD LUAD-RT-S01707 RRAS2 SNP Missense_Mutation 11 14303157 C T 23 100 MEL MEL-JWCI-WGS-13 RRAS2 SNP Silent 11 14303171 G A 41 69 LUSC TCGA-37-4141 RRAS2 DEL Frame_Shift_Del 11 14380349 C - 26 72 LUSC TCGA-43-6771 RRAS2 SNP Missense_Mutation 11 14316390 T A 63 92 LUAD TCGA-49-4505 RRAS2 SNP Missense_Mutation 11 14316111 T C 49 60 CRC TCGA-AA-3984 RRAS2 SNP Missense_Mutation 11 14316076 G A 37 66 CRC TCGA-AG-A002 RRAS2 SNP Missense_Mutation 11 14317365 C A 32 94 UCEC TCGA-AX-A05Z RRAS2 SNP Silent 11 14316023 T C 64 48 UCEC TCGA-B5-A0K4 RRAS2 SNP Missense_Mutation 11 14316389 T A 56 79 UCEC TCGA-BG-A0M4 RRAS2 SNP Missense_Mutation 11 14316390 T A 63 92 UCEC TCGA-BG-A0YU RRAS2 SNP Missense_Mutation 11 14316389 T G 56 79 HNSC TCGA-CV-7430 RRAS2 SNP Missense_Mutation 11 14316390 T A 63 92 UCEC TCGA-D1-A17U RRAS2 SNP Missense_Mutation 11 14303235 C T 23 100 CARC Carc-DFCI-184 RRAS2 SNP Splice_Site 11 14316304 A C 2 69