ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME011 RNF2 SNP Missense_Mutation 1 185060723 G A 33 99 MEL MEL-Ma-Mel-85 RNF2 SNP Missense_Mutation 1 185067364 A G 13 75 LUAD TCGA-05-4382 RNF2 SNP Missense_Mutation 1 185069342 G T 42 85 GBM TCGA-06-5411 RNF2 SNP Missense_Mutation 1 185069006 G A 34 73 LUAD TCGA-38-4631 RNF2 SNP Missense_Mutation 1 185060780 A T 4 90 BRCA TCGA-A2-A0SW RNF2 SNP Silent 1 185060756 C T 32 68 CRC TCGA-AA-3710 RNF2 SNP Missense_Mutation 1 185067316 A T 15 87 CRC TCGA-AA-A00Z RNF2 SNP Missense_Mutation 1 185062312 A C 8 89 CRC TCGA-AG-A002 RNF2 SNP Missense_Mutation 1 185056762 G A 37 86 CRC TCGA-AG-A002 RNF2 SNP Nonsense_Mutation 1 185069002 C T 31 77 UCEC TCGA-AP-A051 RNF2 SNP Missense_Mutation 1 185056767 C T 18 99 UCEC TCGA-AX-A060 RNF2 SNP Splice_site 1 185060871 G A 43 98 BLCA TCGA-BT-A2LB RNF2 SNP Nonsense_Mutation 1 185056735 G A 47 98 HNSC TCGA-CR-6481 RNF2 SNP Missense_Mutation 1 185062311 C T 29 97