ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD_E00565 RCN2 SNP Missense_Mutation 15 77241495 C T 32 67 MEL MEL-Ma-Mel-37 RCN2 SNP Silent 15 77224776 C T 31 51 MM MM-0521 RCN2 SNP Missense_Mutation 15 77240834 G A 45 70 LUAD TCGA-50-5946 RCN2 SNP Missense_Mutation 15 77240793 G C 33 95 LUSC TCGA-60-2723 RCN2 SNP Missense_Mutation 15 77236139 A G 7 64 CRC TCGA-AA-A010 RCN2 SNP Missense_Mutation 15 77241474 C A 32 67 CRC TCGA-AG-A002 RCN2 SNP Splice_site 15 77241413 G A 38 52 UCEC TCGA-BG-A187 RCN2 SNP Missense_Mutation 15 77241491 G T 48 65 KIRC TCGA-BP-4985 RCN2 SNP Missense_Mutation 15 77241529 T G 54 91 BLCA TCGA-BT-A3PJ RCN2 SNP Missense_Mutation 15 77241555 G A 45 99 UCEC TCGA-D1-A177 RCN2 SNP Splice_site 15 77236099 C A 28 76