ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-874 RNF169 SNP Missense_Mutation 11 74547153 A G 12 75 MEL MEL-JWCI-WGS-21 RNF169 SNP Nonsense_Mutation 11 74547506 C T 31 59 MEL MEL-Ma-Mel-114 RNF169 SNP Missense_Mutation 11 74528707 C T 31 78 NB NB-1744 RNF169 SNP Silent 11 74460417 T C 55 50 LUAD TCGA-05-4396 RNF169 SNP Silent 11 74528742 C A 24 67 GBM TCGA-06-0875 RNF169 SNP Missense_Mutation 11 74546969 C T 27 73 OV TCGA-13-0897 RNF169 SNP Missense_Mutation 11 74546864 A G 8 74 LUAD TCGA-17-Z035 RNF169 SNP Missense_Mutation 11 74546742 G A 40 95 LUAD TCGA-50-5044 RNF169 SNP Missense_Mutation 11 74546756 G C 45 95 CRC TCGA-AA-3680 RNF169 SNP Missense_Mutation 11 74546886 A G 2 87 CRC TCGA-AA-3869 RNF169 SNP Missense_Mutation 11 74528707 C T 31 78 CRC TCGA-AA-A010 RNF169 SNP Missense_Mutation 11 74547217 G T 33 60 CRC TCGA-AA-A01V RNF169 SNP Missense_Mutation 11 74546664 C T 31 95 CRC TCGA-AG-A002 RNF169 SNP Missense_Mutation 11 74546777 G A 37 95 BRCA TCGA-AO-A0JF RNF169 SNP Missense_Mutation 11 74546883 G A 38 95 BRCA TCGA-AO-A129 RNF169 SNP Missense_Mutation 11 74546847 G A 40 81 UCEC TCGA-AP-A051 RNF169 SNP Missense_Mutation 11 74547321 A T 3 52 UCEC TCGA-AX-A05Z RNF169 SNP Missense_Mutation 11 74545744 G T 35 90 UCEC TCGA-B5-A0JY RNF169 SNP Nonsense_Mutation 11 74521325 G T 45 78 BRCA TCGA-B6-A1KF RNF169 DEL In_Frame_Del 11 74547205 AAG - 1 50 BRCA TCGA-B6-A1KF RNF169 DEL Frame_Shift_Del 11 74547209 AGCAC - 15 68 KIRC TCGA-BP-5176 RNF169 SNP Silent 11 74546695 A T 14 43 UCEC TCGA-BS-A0UM RNF169 SNP Missense_Mutation 11 74546892 A T 2 38 UCEC TCGA-BS-A0UV RNF169 SNP Missense_Mutation 11 74546684 G A 37 95 BLCA TCGA-BT-A20U RNF169 SNP Missense_Mutation 11 74547657 G A 37 63 HNSC TCGA-CV-6961 RNF169 SNP Missense_Mutation 11 74546869 C G 29 54 UCEC TCGA-D1-A16X RNF169 SNP Nonsense_Mutation 11 74521238 G T 33 78 BRCA TCGA-E2-A10C RNF169 SNP Missense_Mutation 11 74500681 C G 29 64 BLCA TCGA-GD-A3OP RNF169 SNP Missense_Mutation 11 74545750 A G 7 63