ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-19 RNF181 SNP Missense_Mutation 2 85822945 G A 37 90 GBM TCGA-06-2563 RNF181 SNP Missense_Mutation 2 85824255 A G 11 85 LUSC TCGA-43-2578 RNF181 SNP Missense_Mutation 2 85823972 A T 9 86 UCEC TCGA-AP-A059 RNF181 SNP Missense_Mutation 2 85823694 G A 41 79 UCEC TCGA-AP-A059 RNF181 SNP Silent 2 85824144 G A 33 49 UCEC TCGA-B5-A11E RNF181 SNP Silent 2 85824199 G T 35 55 UCEC TCGA-BS-A0UJ RNF181 INS Splice_site 2 85824228 - A 17 92 HNSC TCGA-CV-7440 RNF181 DEL Frame_Shift_Del 2 85824002 TGCCT - 51 86 BLCA TCGA-FD-A3N5 RNF181 SNP Missense_Mutation 2 85823723 G T 33 62