ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62739 CMPK2 SNP Splice_site 2 7003596 C A 23 41 MEL MEL-Ma-Mel-105 CMPK2 SNP Silent 2 6991787 G A 47 74 MEL MEL-Ma-Mel-79 CMPK2 SNP Missense_Mutation 2 6991671 G A 35 85 LUAD TCGA-05-4396 CMPK2 SNP Missense_Mutation 2 6991641 C A 23 99 LUAD TCGA-05-4424 CMPK2 SNP Missense_Mutation 2 6990087 T A 55 48 LUAD TCGA-05-5428 CMPK2 SNP Missense_Mutation 2 6991699 C G 29 69 LUSC TCGA-33-4538 CMPK2 SNP Missense_Mutation 2 7001388 A G 13 89 LUSC TCGA-37-4141 CMPK2 SNP Splice_site 2 6991813 A T 14 92 LUSC TCGA-39-5016 CMPK2 SNP Silent 2 7003614 G A 37 37 LUAD TCGA-64-5779 CMPK2 SNP Missense_Mutation 2 6991603 C A 26 54 LUSC TCGA-66-2773 CMPK2 SNP Silent 2 7003644 G A 41 58 LUSC TCGA-66-2783 CMPK2 SNP Missense_Mutation 2 7005270 C A 24 68 LUSC TCGA-66-2789 CMPK2 SNP Nonsense_Mutation 2 7001358 C A 31 82 LUAD TCGA-67-3771 CMPK2 SNP Missense_Mutation 2 7001425 G C 33 56 BRCA TCGA-A8-A07P CMPK2 SNP Nonsense_Mutation 2 6990088 G A 47 53 CRC TCGA-AG-A002 CMPK2 SNP Missense_Mutation 2 7001396 C A 32 97 UCEC TCGA-AP-A059 CMPK2 SNP Missense_Mutation 2 6991696 G T 35 52 UCEC TCGA-AP-A059 CMPK2 SNP Missense_Mutation 2 7003693 G T 35 95 UCEC TCGA-B5-A0JY CMPK2 SNP Missense_Mutation 2 6991587 C T 19 97 UCEC TCGA-B5-A11E CMPK2 SNP Missense_Mutation 2 6991642 G A 39 72 UCEC TCGA-BS-A0UF CMPK2 SNP Missense_Mutation 2 6990002 C A 32 48 UCEC TCGA-BS-A0UF CMPK2 SNP Nonsense_Mutation 2 6991612 C A 32 67