ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-539 RNF146 SNP Missense_Mutation 6 127608404 G A 36 61 MEL MEL-JWCI-WGS-7 RNF146 SNP Missense_Mutation 6 127608357 G A 41 100 MM MM-0449 RNF146 SNP Missense_Mutation 6 127608815 C G 17 100 PRAD P04-594 RNF146 SNP Silent 6 127608574 A G 6 48 OV TCGA-24-1614 RNF146 SNP Missense_Mutation 6 127608473 G A 46 67 LUSC TCGA-33-4533 RNF146 SNP Missense_Mutation 6 127608771 G A 44 75 LUSC TCGA-66-2766 RNF146 SNP Silent 6 127608136 A G 3 67 CRC TCGA-AA-3977 RNF146 SNP Missense_Mutation 6 127608566 C A 29 82 CRC TCGA-AA-A010 RNF146 SNP Nonsense_Mutation 6 127608260 C T 27 58 UCEC TCGA-AP-A051 RNF146 SNP Missense_Mutation 6 127608246 G A 38 88 UCEC TCGA-AP-A056 RNF146 SNP Missense_Mutation 6 127608668 G A 46 69 UCEC TCGA-AP-A0LM RNF146 SNP Nonsense_Mutation 6 127608740 C T 31 67 UCEC TCGA-B5-A0JV RNF146 SNP Silent 6 127608679 C A 24 53 UCEC TCGA-B5-A0JY RNF146 SNP Missense_Mutation 6 127608617 G A 33 83 UCEC TCGA-BS-A0UV RNF146 SNP Nonsense_Mutation 6 127608731 C T 31 57 HNSC TCGA-CV-6940 RNF146 SNP Missense_Mutation 6 127607982 G A 37 88 UCEC TCGA-D1-A103 RNF146 SNP Silent 6 127608586 C T 25 62 UCEC TCGA-D1-A17Q RNF146 SNP Missense_Mutation 6 127608617 G A 33 83 BRCA TCGA-D8-A27H RNF146 SNP Missense_Mutation 6 127608175 A C 13 57