ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DFCI_DLBCL_Goe05 EME2 SNP Silent 16 1823246 C A 23 53 HNSC HN_00443 EME2 SNP Missense 16 1825175 G A 39 47 LUAD TCGA-05-4398 EME2 SNP Silent 16 1826131 G T 38 60 LUAD TCGA-05-4424 EME2 SNP Missense_Mutation 16 1826213 G C 45 69 LUAD TCGA-38-4628 EME2 DNP Nonsense_Mutation 16 1825151 GC AA 46 47 LUSC TCGA-43-5668 EME2 DEL Frame_Shift_Del 16 1823398 GCAGG - 38 49 LUAD TCGA-91-6829 EME2 SNP Silent 16 1825092 C T 22 51 UCEC TCGA-AP-A059 EME2 SNP Missense_Mutation 16 1826099 C T 27 56 KIRC TCGA-CZ-4859 EME2 SNP Nonsense_Mutation 16 1825398 G T 41 49 UCEC TCGA-D1-A16J EME2 SNP Missense_Mutation 16 1825808 G A 41 89