ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-005 RNF183 SNP Missense_Mutation 9 116060430 T C 54 82 DLBCL DLBCL-Ls2367 RNF183 SNP Missense_Mutation 9 116060167 G A 35 61 LUAD LUAD-5V8LT RNF183 SNP Silent 9 116060351 C G 21 57 MEL Mel_BRAFi_02_PRE RNF183 SNP Missense_Mutation 9 116059983 C T 27 62 PRAD PR-1701 RNF183 SNP Missense_Mutation 9 116059998 C T 27 68 LUAD TCGA-17-Z060 RNF183 SNP Silent 9 116060426 G A 42 51 LUAD TCGA-49-4487 RNF183 SNP Missense_Mutation 9 116060272 G T 34 79 BRCA TCGA-AC-A23E RNF183 SNP Missense_Mutation 9 116060076 G A 39 50 UCEC TCGA-AP-A051 RNF183 SNP Missense_Mutation 9 116060133 C T 27 86 UCEC TCGA-AP-A051 RNF183 SNP Missense_Mutation 9 116060145 C T 27 56