ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_00761 DPP7 SNP Missense 9 140008324 C T 23 90 MEL MEL-Ma-Mel-08a DPP7 SNP Missense_Mutation 9 140006572 C T 30 89 MM MM-0515 DPP7 SNP Silent 9 140008752 C A 23 47 LUAD TCGA-35-3621 DPP7 SNP Missense_Mutation 9 140005197 G A 38 54 OV TCGA-61-2113 DPP7 SNP Missense_Mutation 9 140007856 G A 46 70 CRC TCGA-AA-3516 DPP7 SNP Missense_Mutation 9 140005398 C T 23 38 CRC TCGA-AA-3666 DPP7 INS Splice_site 9 140006326 - C 6 27 UCEC TCGA-AP-A054 DPP7 SNP Missense_Mutation 9 140007889 G A 38 93 UCEC TCGA-AP-A0LH DPP7 INS Splice_site 9 140006205 - C 12 49 UCEC TCGA-AP-A0LM DPP7 SNP Missense_Mutation 9 140006195 C T 27 62 UCEC TCGA-BG-A0MQ DPP7 SNP Missense_Mutation 9 140007875 C T 27 93 BRCA TCGA-BH-A0HA DPP7 SNP Missense_Mutation 9 140006430 A G 2 71 HNSC TCGA-CR-6472 DPP7 SNP Missense_Mutation 9 140007428 G A 41 55 UCEC TCGA-D1-A17H DPP7 SNP Silent 9 140006600 G A 38 40 HNSC TCGA-DQ-7590 DPP7 SNP Missense_Mutation 9 140006472 C T 31 89