ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-D01751 RAP2A SNP Missense_Mutation 13 98116583 G T 38 98 MEL ME009 RAP2A SNP Splice_site 13 98086723 C T 19 66 MEL MEL-JWCI-WGS-34 RAP2A DNP Missense_Mutation 13 98086804 CC TT 18 91 MM MM-0493 RAP2A SNP Silent 13 98086964 C G 31 45 GBM TCGA-32-4208 RAP2A SNP Missense_Mutation 13 98086962 C G 24 92 LUSC TCGA-66-2758 RAP2A SNP Silent 13 98086847 C T 25 69 CRC TCGA-AA-3984 RAP2A SNP Missense_Mutation 13 98116607 G A 37 98 BRCA TCGA-AO-A03P RAP2A SNP Nonsense_Mutation 13 98086995 C T 21 79 UCEC TCGA-AP-A051 RAP2A SNP Missense_Mutation 13 98116647 C T 28 99 UCEC TCGA-AX-A05S RAP2A SNP Missense_Mutation 13 98116573 G T 47 98 HNSC TCGA-BA-5152 RAP2A SNP Silent 13 98086811 C T 31 62 BLCA TCGA-BT-A2LB RAP2A SNP Silent 13 98086808 C T 29 91 HNSC TCGA-CR-6472 RAP2A SNP Silent 13 98086796 G C 45 67