ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-2143 RRP8 SNP Missense_Mutation 11 6622755 G C 45 51 LUAD LUAD-5V8LT RRP8 SNP Missense_Mutation 11 6622616 C A 24 47 LUAD LUAD-S01306 RRP8 SNP Silent 11 6622759 G T 43 39 MEL ME010 RRP8 SNP Silent 11 6621946 G T 47 51 MEL MEL-JWCI-WGS-33 RRP8 SNP Missense_Mutation 11 6621720 G A 41 63 MEL MEL-Ma-Mel-35 RRP8 SNP Missense_Mutation 11 6621432 G A 42 56 MEL MEL-Ma-Mel-79 RRP8 SNP Missense_Mutation 11 6623337 C T 30 50 LUAD TCGA-05-4402 RRP8 SNP Missense_Mutation 11 6623441 G C 41 57 GBM TCGA-06-0128 RRP8 SNP Missense_Mutation 11 6622635 C G 32 65 LUSC TCGA-21-1070 RRP8 SNP Missense_Mutation 11 6622767 G A 43 48 LUSC TCGA-60-2720 RRP8 SNP Silent 11 6622567 T A 59 52 OV TCGA-61-2095 RRP8 SNP Silent 11 6624670 G T 33 49 LUSC TCGA-85-6561 RRP8 SNP Missense_Mutation 11 6621950 C T 30 94 CRC TCGA-AA-3715 RRP8 SNP Silent 11 6623320 G A 42 48 CRC TCGA-AG-A01Y RRP8 SNP Missense_Mutation 11 6622595 C T 23 77 CRC TCGA-AG-A036 RRP8 SNP Missense_Mutation 11 6622578 C T 28 68 UCEC TCGA-AP-A051 RRP8 SNP Missense_Mutation 11 6623432 C T 27 58 UCEC TCGA-AP-A059 RRP8 SNP Missense_Mutation 11 6622595 C T 23 77 UCEC TCGA-AP-A05N RRP8 SNP Missense_Mutation 11 6623126 G A 42 53 KIRC TCGA-B0-4852 RRP8 INS Frame_Shift_Ins 11 6621799 - T 20 60 UCEC TCGA-B5-A11H RRP8 SNP Missense_Mutation 11 6623129 T C 51 51 HNSC TCGA-BB-4223 RRP8 SNP Nonsense_Mutation 11 6621416 G C 45 57 UCEC TCGA-BS-A0TC RRP8 SNP Missense_Mutation 11 6623118 T G 64 59 HNSC TCGA-CV-7427 RRP8 SNP Missense_Mutation 11 6622653 C T 26 61 UCEC TCGA-D1-A103 RRP8 SNP Missense_Mutation 11 6622564 C A 28 55 BLCA TCGA-FD-A3N5 RRP8 SNP Missense_Mutation 11 6621449 C T 22 68