ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-E01217 PGC SNP Missense_Mutation 6 41707563 C A 24 82 MEL ME009 PGC SNP Missense_Mutation 6 41704648 G A 41 54 MEL ME009 PGC SNP Missense_Mutation 6 41710133 C T 26 71 MEL ME033 PGC SNP Missense_Mutation 6 41704631 C T 31 94 MEL MEL-JWCI-WGS-1 PGC SNP Silent 6 41707630 G A 37 39 MEL MEL-JWCI-WGS-1 PGC SNP Missense_Mutation 6 41712503 C T 30 88 MEL MEL-JWCI-WGS-32 PGC SNP Silent 6 41704656 G A 41 73 MEL MEL-JWCI-WGS-32 PGC SNP Silent 6 41707555 C T 24 62 MEL MEL-Ma-Mel-65 PGC SNP Silent 6 41705498 G A 41 63 MEL MEL-Ma-Mel-65 PGC SNP Missense_Mutation 6 41712443 G A 39 54 MEL MEL-Ma-Mel-67 PGC SNP Missense_Mutation 6 41711064 G A 41 54 LUAD TCGA-17-Z055 PGC SNP Missense_Mutation 6 41712155 T C 57 72 LUAD TCGA-35-5375 PGC SNP Missense_Mutation 6 41708341 C A 22 50 LUSC TCGA-43-5668 PGC SNP Nonsense_Mutation 6 41704721 C A 22 78 LUSC TCGA-46-6026 PGC SNP Missense_Mutation 6 41708268 G A 35 66 LUSC TCGA-66-2785 PGC SNP Missense_Mutation 6 41704736 C A 23 47 LUAD TCGA-75-5146 PGC SNP Silent 6 41712181 G A 35 52 BRCA TCGA-A1-A0SD PGC SNP Missense_Mutation 6 41712443 G A 39 54 UCEC TCGA-A5-A0GB PGC SNP Silent 6 41710063 G T 43 52 CRC TCGA-AA-A00F PGC SNP Missense_Mutation 6 41710097 G A 44 60 CRC TCGA-AA-A010 PGC SNP Missense_Mutation 6 41704595 C T 27 56 CRC TCGA-AA-A010 PGC SNP Missense_Mutation 6 41710170 T C 57 41 CRC TCGA-AG-3726 PGC SNP Missense_Mutation 6 41712141 C T 26 72 CRC TCGA-AG-A02N PGC SNP Missense_Mutation 6 41712186 C T 23 94 UCEC TCGA-AP-A059 PGC SNP Silent 6 41704638 G A 39 49 UCEC TCGA-AP-A059 PGC SNP Splice_Site 6 41712253 C A 24 78 UCEC TCGA-AP-A0LM PGC SNP Missense_Mutation 6 41708820 T C 58 62 UCEC TCGA-AP-A0LM PGC SNP Missense_Mutation 6 41710065 C T 27 43 UCEC TCGA-AP-A0LT PGC SNP Missense_Mutation 6 41715044 C T 25 82 KIRC TCGA-B0-5115 PGC SNP Missense_Mutation 6 41712242 A C 1 60 UCEC TCGA-B5-A11E PGC SNP Missense_Mutation 6 41704667 C T 23 81 BLCA TCGA-BL-A3JM PGC SNP Silent 6 41708252 G C 33 51 UCEC TCGA-BS-A0TJ PGC SNP Missense_Mutation 6 41710161 C T 19 41 KIRC TCGA-CJ-4874 PGC SNP Silent 6 41711090 G T 35 52 HNSC TCGA-CV-5442 PGC SNP Missense_Mutation 6 41712219 G A 41 94 UCEC TCGA-D1-A103 PGC SNP Missense_Mutation 6 41710065 C T 27 43