ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0049 PHF14 SNP Missense_Mutation 7 11150987 T C 51 92 HNSC HN_00190 PHF14 SNP Missense 7 11076118 G T 47 100 HNSC HN_62897 PHF14 SNP Missense 7 11053504 T A 51 63 LUAD LUAD-B01811 PHF14 DNP Nonsense_Mutation 7 11091341 GG TT 35 62 LUAD LUAD-NYU776 PHF14 SNP Silent 7 11076098 A G 12 49 LUAD LUAD-RT-S01832 PHF14 SNP Silent 7 11022609 T C 51 57 LUAD LUAD-S01473 PHF14 SNP Missense_Mutation 7 11022513 G T 35 52 LUAD LUAD_E00522 PHF14 SNP Nonsense_Mutation 7 11151071 G T 41 100 MEL MEL-JWCI-WGS-12 PHF14 SNP Splice_Site 7 11021998 G A 33 89 MEL MEL-JWCI-WGS-12 PHF14 SNP Missense_Mutation 7 11022362 C T 28 72 MEL MEL-Ma-Mel-65 PHF14 SNP Missense_Mutation 7 11075400 C T 29 100 MEL MEL-Ma-Mel-92 PHF14 SNP Silent 7 11075351 C T 32 57 MEL MEL-UKRV-Mel-24 PHF14 SNP Silent 7 11101659 A G 13 48 MM MM-0455 PHF14 SNP Missense_Mutation 7 11022392 C T 19 54 MM MM-0571 PHF14 SNP Missense_Mutation 7 11022030 T A 51 51 PRAD PR-3026 PHF14 SNP Missense_Mutation 7 11076181 T C 51 92 LUAD TCGA-17-Z041 PHF14 SNP Silent 7 11022138 T G 55 52 LUAD TCGA-17-Z053 PHF14 SNP Nonsense_Mutation 7 11022706 A T 13 61 LUSC TCGA-33-4532 PHF14 SNP Missense_Mutation 7 11078436 G A 36 60 LUAD TCGA-44-2656 PHF14 SNP Nonsense_Mutation 7 11022088 G T 33 80 LUAD TCGA-44-2656 PHF14 SNP Silent 7 11068427 A T 7 54 LUAD TCGA-44-2659 PHF14 SNP Missense_Mutation 7 11068363 G T 48 100 LUSC TCGA-46-3769 PHF14 SNP Nonsense_Mutation 7 11022091 G T 33 80 LUSC TCGA-46-3769 PHF14 SNP Silent 7 11078410 A G 14 48 LUAD TCGA-49-6742 PHF14 SNP Missense_Mutation 7 11068332 C T 31 100 LUAD TCGA-50-6590 PHF14 SNP Splice_site 7 11068308 G T 41 100 LUSC TCGA-66-2758 PHF14 SNP Missense_Mutation 7 11075331 A G 3 94 LUAD TCGA-67-3771 PHF14 SNP Missense_Mutation 7 11022767 C T 32 94 BRCA TCGA-A7-A13D PHF14 SNP Silent 7 11022150 A G 3 59 CRC TCGA-AA-3715 PHF14 SNP Missense_Mutation 7 11022763 C A 24 71 CRC TCGA-AA-3715 PHF14 SNP Missense_Mutation 7 11053482 G A 48 99 CRC TCGA-AA-3949 PHF14 SNP Missense_Mutation 7 11068366 A T 12 92 AML TCGA-AB-2823 PHF14 SNP Missense_Mutation 7 11022113 T A 57 53 CRC TCGA-AG-3902 PHF14 SNP Missense_Mutation 7 11022332 C G 28 57 CRC TCGA-AG-A002 PHF14 SNP Missense_Mutation 7 11062550 G T 45 100 UCEC TCGA-AP-A051 PHF14 SNP Missense_Mutation 7 11022400 G A 38 43 UCEC TCGA-AP-A054 PHF14 DEL Frame_Shift_Del 7 11075380 AG - 3 78 UCEC TCGA-AP-A056 PHF14 SNP Nonsense_Mutation 7 11022148 G T 33 79 UCEC TCGA-AP-A056 PHF14 SNP Missense_Mutation 7 11022692 A C 3 75 UCEC TCGA-AP-A056 PHF14 SNP Missense_Mutation 7 11075334 G T 33 100 UCEC TCGA-AP-A056 PHF14 SNP Missense_Mutation 7 11078433 G A 37 93 UCEC TCGA-AP-A059 PHF14 SNP Missense_Mutation 7 11053398 G T 36 99 UCEC TCGA-AP-A0LM PHF14 SNP Missense_Mutation 7 11014563 G A 33 96 UCEC TCGA-AP-A0LM PHF14 SNP Silent 7 11022276 A G 1 50 UCEC TCGA-AP-A0LM PHF14 SNP Missense_Mutation 7 11076623 C T 27 84 UCEC TCGA-AX-A05Z PHF14 SNP Missense_Mutation 7 11091322 G A 37 86 KIRC TCGA-B0-4827 PHF14 SNP Missense_Mutation 7 11078422 T G 51 61 UCEC TCGA-B5-A11E PHF14 SNP Silent 7 11022276 A G 1 50 UCEC TCGA-B5-A11H PHF14 DEL In_Frame_Del 7 11082323 AAG - 13 78 UCEC TCGA-B5-A11H PHF14 SNP Nonsense_Mutation 7 11151056 G T 39 100 UCEC TCGA-B5-A11N PHF14 SNP Missense_Mutation 7 11078433 G A 37 93 UCEC TCGA-BS-A0UJ PHF14 SNP Missense_Mutation 7 11082384 T C 56 91 BRCA TCGA-C8-A12Q PHF14 SNP Missense_Mutation 7 11030350 G C 33 73 KIRC TCGA-CZ-5459 PHF14 SNP Missense_Mutation 7 11076624 G C 38 99 UCEC TCGA-D1-A103 PHF14 SNP Nonsense_Mutation 7 11022292 G T 33 77 UCEC TCGA-D1-A103 PHF14 SNP Missense_Mutation 7 11022400 G A 38 43 UCEC TCGA-D1-A103 PHF14 SNP Missense_Mutation 7 11022706 A G 13 61 UCEC TCGA-D1-A16N PHF14 DEL In_Frame_Del 7 11068419 CTG - 32 59 UCEC TCGA-D1-A174 PHF14 SNP Silent 7 11030443 G A 36 83 UCEC TCGA-D1-A17M PHF14 SNP Nonsense_Mutation 7 11022445 C T 19 59 BRCA TCGA-D8-A13Y PHF14 SNP Silent 7 11022484 C T 28 74 BLCA TCGA-FD-A3N6 PHF14 SNP Missense_Mutation 7 11076172 G A 40 100