ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0009 RTP3 SNP Missense_Mutation 3 46542381 G T 46 52 ESO ESO-0167 RTP3 SNP Missense_Mutation 3 46541971 A C 3 51 MEL MEL-Ma-Mel-105 RTP3 SNP Silent 3 46542035 G A 45 52 MEL MEL-Ma-Mel-114 RTP3 SNP Silent 3 46542332 C T 32 53 OV TCGA-13-0920 RTP3 SNP Missense_Mutation 3 46542220 C A 21 58 OV TCGA-13-1482 RTP3 SNP Silent 3 46539651 T A 62 41 GBM TCGA-19-5959 RTP3 SNP Silent 3 46542293 C T 19 67 LUSC TCGA-22-4599 RTP3 SNP Missense_Mutation 3 46542189 C A 17 52 LUSC TCGA-22-4604 RTP3 SNP Missense_Mutation 3 46542119 C G 32 48 LUSC TCGA-46-3769 RTP3 SNP Silent 3 46541960 C A 22 46 LUAD TCGA-50-5930 RTP3 SNP Silent 3 46542095 G A 35 48 OV TCGA-61-2088 RTP3 SNP Silent 3 46542042 C T 24 52 UCEC TCGA-B5-A0JY RTP3 SNP Missense_Mutation 3 46539614 C T 21 66 UCEC TCGA-B5-A0JY RTP3 SNP Missense_Mutation 3 46541892 C A 32 61 BLCA TCGA-BT-A20N RTP3 SNP Missense_Mutation 3 46542298 G A 46 39 HNSC TCGA-CN-5369 RTP3 SNP Missense_Mutation 3 46542332 C G 32 53 HNSC TCGA-CR-7399 RTP3 SNP Missense_Mutation 3 46542079 G A 33 52 HNSC TCGA-CV-6938 RTP3 SNP Missense_Mutation 3 46539589 C A 29 76