ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1872 PHYH SNP Splice_site 10 13337497 G A 37 47 LUAD LUAD-NYU1051S PHYH SNP Missense_Mutation 10 13330521 G A 43 100 LUAD LUAD-NYU259 PHYH SNP Silent 10 13330414 C A 25 54 LUAD LUAD-TJW61 PHYH SNP Silent 10 13325786 G C 43 51 LUAD LUAD-YINHD PHYH SNP Missense_Mutation 10 13323023 C T 24 51 MEL MEL-JWCI-WGS-5 PHYH SNP Missense_Mutation 10 13336511 A G 16 53 MEL MEL-JWCI-WGS-7 PHYH SNP Silent 10 13323093 G A 37 49 LUSC TCGA-18-3409 PHYH SNP Splice_site 10 13323110 C T 26 56 LUSC TCGA-18-3409 PHYH SNP Splice_Site 10 13323111 C G 24 98 LUSC TCGA-21-1081 PHYH SNP Missense_Mutation 10 13330441 G C 45 43 LUAD TCGA-44-2655 PHYH INS Frame_Shift_Ins 10 13325834 - C 54 40 LUAD TCGA-64-5779 PHYH SNP Silent 10 13325783 C A 22 27 LUSC TCGA-66-2778 PHYH SNP Missense_Mutation 10 13330464 C T 27 56 LUSC TCGA-66-2794 PHYH SNP Missense_Mutation 10 13330438 G T 42 62 LUAD TCGA-91-6836 PHYH SNP Missense_Mutation 10 13325784 C A 23 79 CRC TCGA-AA-A00E PHYH SNP Silent 10 13336482 C T 24 63 CRC TCGA-AA-A00N PHYH SNP Missense_Mutation 10 13320332 C T 31 59 CRC TCGA-AA-A00N PHYH SNP Missense_Mutation 10 13337568 C A 32 85 CRC TCGA-AG-3892 PHYH SNP Silent 10 13336521 C T 31 43 BRCA TCGA-AO-A0J2 PHYH SNP Silent 10 13325816 G A 40 50 UCEC TCGA-AP-A051 PHYH SNP Missense_Mutation 10 13325728 G T 47 100 UCEC TCGA-AP-A059 PHYH SNP Silent 10 13323039 G A 37 35 UCEC TCGA-AP-A059 PHYH SNP Missense_Mutation 10 13330526 C T 19 87 UCEC TCGA-AP-A0LM PHYH SNP Missense_Mutation 10 13323083 C T 31 50 UCEC TCGA-B5-A11N PHYH SNP Missense_Mutation 10 13337568 C A 32 85 UCEC TCGA-BS-A0UF PHYH SNP Missense_Mutation 10 13325814 C A 22 100 HNSC TCGA-CQ-5327 PHYH SNP Missense_Mutation 10 13323083 C T 31 50 HNSC TCGA-CV-6941 PHYH SNP Missense_Mutation 10 13337587 C A 19 50 KIRC TCGA-CZ-5456 PHYH SNP Missense_Mutation 10 13325777 G T 44 72 UCEC TCGA-D1-A0ZO PHYH SNP Missense_Mutation 10 13330428 C T 23 100 UCEC TCGA-D1-A103 PHYH SNP Missense_Mutation 10 13330479 C T 31 54 UCEC TCGA-D1-A16X PHYH SNP Missense_Mutation 10 13325800 C T 31 72 UCEC TCGA-D1-A16X PHYH SNP Missense_Mutation 10 13336522 G A 37 54 UCEC TCGA-D1-A174 PHYH SNP Missense_Mutation 10 13330437 G A 39 48 UCEC TCGA-DI-A0WH PHYH SNP Silent 10 13330465 G A 38 48 BRCA TCGA-E2-A14V PHYH SNP Missense_Mutation 10 13320306 G C 33 76 BRCA TCGA-E2-A155 PHYH SNP Silent 10 13325695 G T 39 55