ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-12 RBP2 SNP Silent 3 139181083 C T 24 54 LUAD TCGA-05-4396 RBP2 SNP Silent 3 139173577 C A 17 48 LUAD TCGA-05-4398 RBP2 SNP Missense_Mutation 3 139181102 A T 14 49 LUAD TCGA-17-Z026 RBP2 SNP Missense_Mutation 3 139173649 A T 8 50 LUAD TCGA-17-Z043 RBP2 SNP Missense_Mutation 3 139180964 C T 23 88 LUAD TCGA-17-Z049 RBP2 SNP Missense_Mutation 3 139173624 C T 30 99 LUSC TCGA-18-3421 RBP2 SNP Silent 3 139172003 C A 29 82 LUSC TCGA-18-5595 RBP2 SNP Nonsense_Mutation 3 139173596 C T 21 99 GBM TCGA-26-5135 RBP2 SNP Missense_Mutation 3 139195249 T C 54 76 LUSC TCGA-39-5027 RBP2 SNP Missense_Mutation 3 139195235 C A 26 80 LUAD TCGA-50-5049 RBP2 SNP Splice_site 3 139172010 T A 55 88 LUAD TCGA-50-5930 RBP2 SNP Silent 3 139173634 C A 25 54 LUAD TCGA-91-6836 RBP2 SNP Missense_Mutation 3 139181127 C T 29 87 UCEC TCGA-A5-A0GP RBP2 SNP Silent 3 139173580 C T 28 51 CRC TCGA-AA-A010 RBP2 SNP Missense_Mutation 3 139181100 G A 40 79 UCEC TCGA-AX-A05Z RBP2 SNP Missense_Mutation 3 139181123 A G 1 92 UCEC TCGA-BS-A0UF RBP2 SNP Silent 3 139195245 G A 34 69 BLCA TCGA-CU-A0YO RBP2 SNP Missense_Mutation 3 139181129 A G 4 92 HNSC TCGA-CV-7102 RBP2 SNP Nonsense_Mutation 3 139173605 C T 21 86