ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0043 RNF217 SNP Missense_Mutation 6 125404031 A T 16 82 ESO ESO-682 RNF217 SNP Missense_Mutation 6 125397890 C T 23 78 MEL MEL-JWCI-WGS-29 RNF217 SNP Missense_Mutation 6 125404024 C T 30 89 MEL MEL-JWCI-WGS-3 RNF217 SNP Nonsense_Mutation 6 125379175 G T 35 98 MEL MEL-JWCI-WGS-7 RNF217 SNP Silent 6 125366410 C T 32 71 GBM TCGA-12-0615 RNF217 SNP Silent 6 125379096 C T 26 58 LUAD TCGA-50-6594 RNF217 SNP Missense_Mutation 6 125366429 G T 48 50 LUAD TCGA-64-5779 RNF217 SNP Splice_site 6 125404010 G T 44 89 UCEC TCGA-A5-A0GP RNF217 SNP Nonsense_Mutation 6 125404013 T G 61 82 CRC TCGA-AA-3525 RNF217 SNP Missense_Mutation 6 125379202 A C 7 77 CRC TCGA-AA-A00R RNF217 SNP Nonsense_Mutation 6 125397989 C T 27 60 CRC TCGA-AA-A010 RNF217 SNP Missense_Mutation 6 125404022 T G 64 82 UCEC TCGA-AP-A0LM RNF217 SNP Missense_Mutation 6 125366442 C T 19 100 UCEC TCGA-AX-A0J0 RNF217 SNP Missense_Mutation 6 125404022 T G 64 82 UCEC TCGA-B5-A0JY RNF217 SNP Missense_Mutation 6 125402605 C A 32 61 UCEC TCGA-B5-A11R RNF217 SNP Missense_Mutation 6 125366447 G C 45 100 BRCA TCGA-B6-A0X4 RNF217 SNP Nonsense_Mutation 6 125397899 C T 23 85 UCEC TCGA-BS-A0UF RNF217 SNP Silent 6 125379111 C T 31 49 BLCA TCGA-CU-A0YO RNF217 SNP Missense_Mutation 6 125366487 G A 40 75 KIRC TCGA-CZ-4854 RNF217 SNP Silent 6 125366368 C G 26 56