ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CRC CRC-0005 EPM2A SNP Missense 6 145956608 A C 12 91 ESO ESO-005 EPM2A SNP Missense_Mutation 6 145948794 G T 34 98 LUAD LUAD-CHTN-Z4716A EPM2A SNP Silent 6 145948681 C A 29 49 LUAD LUAD-S01315 EPM2A SNP Nonsense_Mutation 6 146007322 C A 29 98 MM MM-0530 EPM2A SNP Missense_Mutation 6 145956501 G C 48 82 GBM TCGA-06-6391 EPM2A SNP Missense_Mutation 6 145948736 C T 26 98 OV TCGA-36-1577 EPM2A SNP Missense 6 145956542 A C 4 91 LUAD TCGA-49-6767 EPM2A SNP Missense_Mutation 6 145948691 C T 26 99 LUSC TCGA-66-2782 EPM2A SNP Missense_Mutation 6 145948803 C A 18 98 KIRC TCGA-A3-3358 EPM2A SNP Missense_Mutation 6 145948647 G T 42 64 CRC TCGA-AA-A01Q EPM2A SNP Silent 6 145948827 G T 39 72 UCEC TCGA-AP-A056 EPM2A SNP Missense_Mutation 6 145948598 A C 1 90 BRCA TCGA-BH-A209 EPM2A SNP Splice_site 6 145956381 C A 24 97 CARC Carc-Asa16 EPM2A SNP Missense_Mutation 6 145948574 C T 19 57 CARC Carc-H54 EPM2A DEL Frame_Shift_Del 6 146056361 C - 30 62