ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62426 PDHX SNP Synonymous 11 35016506 G A 45 52 LUAD LUAD-CHTN-MAD06-00668 PDHX SNP Missense_Mutation 11 35016545 G T 44 52 MEL MEL-Ma-Mel-37 PDHX SNP Missense_Mutation 11 34999724 C T 24 89 LUAD TCGA-17-Z012 PDHX SNP Silent 11 35016541 G T 43 98 LUAD TCGA-17-Z031 PDHX SNP Missense_Mutation 11 34988231 C A 18 56 LUAD TCGA-17-Z044 PDHX SNP Missense_Mutation 11 34978962 G T 44 84 LUSC TCGA-21-1070 PDHX SNP Missense_Mutation 11 34988317 C T 26 68 LUSC TCGA-46-6025 PDHX SNP Silent 11 34988250 A G 7 54 LUSC TCGA-46-6026 PDHX SNP Silent 11 34938280 A G 15 50 LUAD TCGA-67-3771 PDHX SNP Splice_Site 11 34969155 T C 57 84 CRC TCGA-AA-A010 PDHX SNP Missense_Mutation 11 34981990 G A 38 94 CRC TCGA-AA-A010 PDHX SNP Missense_Mutation 11 35016492 G A 37 98 CRC TCGA-AG-A002 PDHX SNP Silent 11 34999702 C A 29 57 UCEC TCGA-AP-A056 PDHX SNP Missense_Mutation 11 35006231 G T 33 64 UCEC TCGA-AP-A059 PDHX SNP Missense_Mutation 11 34979121 G A 43 69 UCEC TCGA-AP-A0LM PDHX SNP Missense_Mutation 11 34978943 A C 3 50 UCEC TCGA-AX-A05Z PDHX SNP Missense_Mutation 11 34991801 C T 28 90 UCEC TCGA-AX-A0J0 PDHX SNP Missense_Mutation 11 34969146 A C 1 65 UCEC TCGA-AX-A0J1 PDHX SNP Nonsense_Mutation 11 34988347 C T 17 60 KIRC TCGA-B0-4843 PDHX SNP Missense_Mutation 11 35016578 A C 3 56 UCEC TCGA-B5-A0JY PDHX SNP Missense_Mutation 11 34991821 G T 33 57 UCEC TCGA-B5-A0JY PDHX SNP Missense_Mutation 11 35006231 G T 33 64 UCEC TCGA-B5-A11E PDHX SNP Silent 11 35016488 C T 31 64 BRCA TCGA-BH-A18T PDHX SNP Missense_Mutation 11 34981989 C G 23 70 UCEC TCGA-BS-A0UF PDHX SNP Silent 11 34991719 C A 31 56 UCEC TCGA-BS-A0UF PDHX SNP Missense_Mutation 11 35016654 G A 37 83 UCEC TCGA-BS-A0UV PDHX SNP Silent 11 35016488 C T 31 64 UCEC TCGA-BS-A0WQ PDHX SNP Missense_Mutation 11 34938234 C T 23 46 HNSC TCGA-CQ-6221 PDHX SNP Missense_Mutation 11 34978997 G C 33 85 HNSC TCGA-CR-6484 PDHX SNP Missense_Mutation 11 34982054 A G 16 50 HNSC TCGA-CR-7364 PDHX SNP Missense_Mutation 11 34988233 G A 37 80 HNSC TCGA-CV-6940 PDHX SNP Missense_Mutation 11 34988327 C T 21 80 KIRC TCGA-CZ-4862 PDHX SNP Silent 11 35016594 C T 20 68 UCEC TCGA-D1-A167 PDHX SNP Silent 11 35016594 C T 20 68 UCEC TCGA-D1-A16X PDHX SNP Nonsense_Mutation 11 35016492 G T 37 98 BLCA TCGA-G2-A3IE PDHX SNP Missense_Mutation 11 35006268 C G 32 76