ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-250 RBM17 SNP Missense_Mutation 10 6146945 G A 45 100 LUAD LUAD-NYU201 RBM17 SNP Missense_Mutation 10 6147005 G A 41 100 LUAD LUAD-NYU408 RBM17 SNP Splice_site 10 6154173 G T 43 39 LUAD LUAD-S01405 RBM17 SNP Missense_Mutation 10 6139113 C G 29 98 MEL MEL-JWCI-WGS-1 RBM17 SNP Silent 10 6146905 C T 21 52 MEL MEL-Ma-Mel-92 RBM17 SNP Silent 10 6143347 G A 45 47 LUAD TCGA-17-Z026 RBM17 SNP Missense_Mutation 10 6148146 A T 10 54 LUAD TCGA-17-Z030 RBM17 SNP Silent 10 6154179 G T 39 34 GBM TCGA-32-2491 RBM17 SNP Silent 10 6143245 G T 37 48 LUSC TCGA-39-5031 RBM17 SNP Nonsense_Mutation 10 6155486 C G 29 82 LUAD TCGA-44-3918 RBM17 SNP Missense_Mutation 10 6143252 A G 3 76 LUAD TCGA-64-1676 RBM17 SNP Missense_Mutation 10 6157491 G C 35 96 CRC TCGA-AA-A01Q RBM17 SNP Missense_Mutation 10 6154312 G A 38 63 CRC TCGA-AA-A01R RBM17 SNP Missense_Mutation 10 6154291 G A 39 98 UCEC TCGA-AP-A059 RBM17 SNP Missense_Mutation 10 6156025 C T 27 81 BRCA TCGA-AR-A0U4 RBM17 SNP Missense_Mutation 10 6157483 C G 17 64 UCEC TCGA-AX-A05S RBM17 SNP Missense_Mutation 10 6154289 G A 42 98 UCEC TCGA-AX-A05Z RBM17 SNP Splice_Site 10 6156011 G T 33 99 KIRC TCGA-B0-5692 RBM17 SNP Silent 10 6143320 C T 17 59 UCEC TCGA-BS-A0UV RBM17 SNP Missense_Mutation 10 6146974 T G 52 51 UCEC TCGA-BS-A0UV RBM17 SNP Missense_Mutation 10 6151957 G T 33 61 BLCA TCGA-BT-A0YX RBM17 SNP Silent 10 6143281 G A 45 46 HNSC TCGA-CN-4740 RBM17 SNP Nonsense_Mutation 10 6139143 C T 29 98 HNSC TCGA-CR-7390 RBM17 SNP Silent 10 6148125 A G 3 48 BLCA TCGA-CU-A0YN RBM17 SNP Missense_Mutation 10 6155497 C G 30 97 KIRC TCGA-CZ-5985 RBM17 SNP Missense_Mutation 10 6147033 G A 33 100 UCEC TCGA-D1-A103 RBM17 SNP Silent 10 6143329 G A 38 21