ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_00190 PHGDH SNP Synonymous 1 120285492 C T 23 39 LUAD LUAD-2GUGK PHGDH SNP Silent 1 120285585 A T 7 37 LUAD LUAD-S01315 PHGDH SNP Missense_Mutation 1 120278052 G T 41 97 MEL MEL-JWCI-WGS-7 PHGDH SNP Missense_Mutation 1 120278038 C T 26 75 MM MM-0297 PHGDH SNP Missense_Mutation 1 120286529 G A 40 66 LUAD TCGA-05-4244 PHGDH SNP Silent 1 120263891 T A 59 35 LUAD TCGA-05-4396 PHGDH SNP Silent 1 120263834 C A 23 35 LUAD TCGA-17-Z008 PHGDH SNP Missense_Mutation 1 120279825 G A 38 76 LUAD TCGA-17-Z042 PHGDH SNP Missense_Mutation 1 120277957 G T 43 83 LUAD TCGA-17-Z055 PHGDH SNP Splice_Site 1 120266066 T C 57 74 OV TCGA-25-1329 PHGDH SNP Silent 1 120284484 G A 45 50 GBM TCGA-27-2527 PHGDH SNP Missense_Mutation 1 120285535 C G 21 87 LUSC TCGA-66-2734 PHGDH SNP Missense_Mutation 1 120263815 G C 38 96 LUSC TCGA-66-2777 PHGDH SNP Missense_Mutation 1 120279815 G A 42 98 UCEC TCGA-A5-A0GP PHGDH SNP Missense_Mutation 1 120286511 C T 24 85 CRC TCGA-AA-3525 PHGDH SNP Silent 1 120277271 C T 18 65 CRC TCGA-AA-3811 PHGDH SNP Missense_Mutation 1 120277960 T C 59 89 CRC TCGA-AA-A022 PHGDH SNP Missense_Mutation 1 120284473 G A 48 63 KIRC TCGA-AK-3454 PHGDH SNP Missense_Mutation 1 120277939 T G 64 89 UCEC TCGA-AP-A051 PHGDH SNP Missense_Mutation 1 120254772 G T 34 66 UCEC TCGA-AP-A059 PHGDH SNP Silent 1 120286594 C A 32 64 UCEC TCGA-AP-A0LD PHGDH SNP Missense_Mutation 1 120269521 G A 39 99 UCEC TCGA-B5-A11E PHGDH SNP Silent 1 120269483 C T 22 53 UCEC TCGA-B5-A11H PHGDH SNP Missense_Mutation 1 120269703 G A 39 99 KIRC TCGA-B8-4153 PHGDH SNP Missense_Mutation 1 120254648 G A 47 88 UCEC TCGA-BS-A0TJ PHGDH SNP Missense_Mutation 1 120279801 C T 26 84 UCEC TCGA-BS-A0UF PHGDH SNP Silent 1 120279853 C T 31 21 UCEC TCGA-BS-A0UV PHGDH SNP Silent 1 120284439 C T 31 48 HNSC TCGA-CQ-5334 PHGDH DNP Nonsense_Mutation 1 120283058 GG AA 47 82 UCEC TCGA-D1-A103 PHGDH SNP Silent 1 120286531 G A 46 51 UCEC TCGA-FI-A2EW PHGDH SNP Silent 1 120263915 C T 23 21