ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0025 KLRG1 SNP Missense_Mutation 12 9162088 C A 28 49 ESO ESO-838 KLRG1 SNP Missense_Mutation 12 9142242 G C 36 47 HNSC HN_62421 KLRG1 SNP Missense 12 9142292 G C 45 60 LUAD LUAD-5V8LT KLRG1 SNP Silent 12 9144881 G T 46 70 MEL MEL-JWCI-WGS-26 KLRG1 SNP Missense_Mutation 12 9144865 T C 60 67 MEL MEL-JWCI-WGS-43 KLRG1 SNP Missense_Mutation 12 9162098 C T 30 43 MEL MEL-Ma-Mel-102 KLRG1 SNP Missense_Mutation 12 9161653 C T 29 69 GBM TCGA-06-0649 KLRG1 DEL Frame_Shift_Del 12 9144889 A - 7 57 LUAD TCGA-17-Z000 KLRG1 SNP Nonsense_Mutation 12 9162084 C G 29 69 LUAD TCGA-17-Z031 KLRG1 SNP Missense_Mutation 12 9147751 G T 46 70 GBM TCGA-41-5651 KLRG1 SNP Missense_Mutation 12 9142272 C T 19 60 LUSC TCGA-66-2788 KLRG1 SNP Nonsense_Mutation 12 9147764 G A 41 70 UCEC TCGA-AP-A056 KLRG1 SNP Missense_Mutation 12 9147794 C A 32 51 UCEC TCGA-B5-A11Y KLRG1 SNP Silent 12 9147869 G A 39 46 HNSC TCGA-BA-4077 KLRG1 SNP Missense_Mutation 12 9161668 C T 29 68 HNSC TCGA-BA-5555 KLRG1 SNP Nonsense_Mutation 12 9162052 C A 27 47 KIRC TCGA-EU-5904 KLRG1 SNP Missense_Mutation 12 9144837 G A 42 54