ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_00190 MCEE SNP Missense 2 71337211 C G 32 72 MEL MEL-JWCI-WGS-12 MCEE DNP Missense_Mutation 2 71337123 GG AA 35 74 MM MM-0489 MCEE SNP Missense_Mutation 2 71357336 A G 7 51 MEL Mel_BRAFi_02_PRE MCEE SNP Missense_Mutation 2 71351406 C G 30 72 LUAD TCGA-05-4427 MCEE SNP Missense_Mutation 2 71351404 G T 40 50 OV TCGA-13-0726 MCEE SNP Silent 2 71351486 C T 23 49 LUSC TCGA-46-3769 MCEE SNP Missense_Mutation 2 71351516 C A 32 53 CRC TCGA-AA-3693 MCEE DNP Missense_Mutation 2 71351507 CA AG 21 53 CRC TCGA-AG-A002 MCEE SNP Missense_Mutation 2 71351592 G T 33 61 UCEC TCGA-AP-A0LM MCEE SNP Missense_Mutation 2 71351338 C T 31 92 KIRC TCGA-B0-5085 MCEE SNP Nonsense_Mutation 2 71351338 C A 31 92