ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW213 PHKG1 SNP Missense_Mutation 7 56156627 C A 23 61 DLBCL DLBCL-Ls3866 PHKG1 SNP Silent 7 56155412 G A 39 14 ESO ESO-224 PHKG1 SNP Missense_Mutation 7 56155334 C A 24 77 LUAD LUAD-NYU669 PHKG1 SNP Missense_Mutation 7 56154674 C A 21 66 LUAD LUAD-S01315 PHKG1 SNP Missense_Mutation 7 56149658 C A 30 47 MEL MEL-JWCI-WGS-12 PHKG1 SNP Silent 7 56149338 G A 43 48 LUAD TCGA-49-4487 PHKG1 SNP Missense_Mutation 7 56149336 C A 23 56 LUAD TCGA-50-5932 PHKG1 SNP Silent 7 56149703 G T 39 43 LUSC TCGA-66-2758 PHKG1 SNP Missense_Mutation 7 56149926 A T 13 91 LUSC TCGA-66-2793 PHKG1 SNP Missense_Mutation 7 56151350 C G 30 99 GBM TCGA-76-6656 PHKG1 SNP Missense_Mutation 7 56151084 T C 60 68 KIRC TCGA-AK-3445 PHKG1 SNP Missense_Mutation 7 56156620 C G 24 48 KIRC TCGA-AK-3454 PHKG1 SNP Missense_Mutation 7 56155465 C T 19 77 UCEC TCGA-AP-A051 PHKG1 SNP Missense_Mutation 7 56155321 G T 35 76 UCEC TCGA-AP-A051 PHKG1 SNP Missense_Mutation 7 56156559 G T 35 70 UCEC TCGA-AP-A059 PHKG1 SNP Silent 7 56154686 A T 3 57 UCEC TCGA-AP-A059 PHKG1 SNP Missense_Mutation 7 56156613 G A 42 100 UCEC TCGA-AX-A05Z PHKG1 SNP Nonsense_Mutation 7 56148854 G A 39 64 UCEC TCGA-B5-A0K3 PHKG1 SNP Missense_Mutation 7 56151072 C T 23 99 UCEC TCGA-B5-A11E PHKG1 SNP Missense_Mutation 7 56148986 C T 27 50 KIRC TCGA-BP-4777 PHKG1 SNP Missense_Mutation 7 56155438 G A 47 61 UCEC TCGA-BS-A0UF PHKG1 SNP Missense_Mutation 7 56151012 A C 1 91 UCEC TCGA-D1-A103 PHKG1 SNP Missense_Mutation 7 56148781 G T 42 85 UCEC TCGA-D1-A103 PHKG1 SNP Silent 7 56156593 C T 24 77 UCEC TCGA-D1-A16F PHKG1 SNP Silent 7 56149625 C T 27 32