ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0280 PEX14 SNP Missense_Mutation 1 10689718 G A 37 95 LUAD LUAD-B00523 PEX14 SNP Nonsense_Mutation 1 10689985 G T 37 92 LUAD LUAD-B01811 PEX14 SNP Missense_Mutation 1 10689978 G T 33 67 LUAD LUAD-CHTN-MAD06-00668 PEX14 SNP Nonsense_Mutation 1 10689632 G A 47 81 MEL MEL-JWCI-WGS-12 PEX14 SNP Splice_Site 1 10596269 G A 33 96 MEL MEL-JWCI-WGS-35 PEX14 SNP Silent 1 10683087 C T 30 66 MEL MEL-Ma-Mel-119 PEX14 SNP Missense_Mutation 1 10678460 C T 29 80 MEL MEL-Ma-Mel-35 PEX14 SNP Silent 1 10683097 C T 24 48 LUAD TCGA-05-4420 PEX14 SNP Silent 1 10690005 G A 42 53 GBM TCGA-14-1825 PEX14 SNP Missense_Mutation 1 10683104 G T 42 96 GBM TCGA-14-2554 PEX14 SNP Missense_Mutation 1 10555347 G A 41 56 LUSC TCGA-22-4593 PEX14 SNP Missense_Mutation 1 10689653 C A 23 66 LUAD TCGA-44-2662 PEX14 SNP Missense_Mutation 1 10555367 C G 31 79 GBM TCGA-76-4928 PEX14 SNP Missense_Mutation 1 10555343 C G 30 78 BRCA TCGA-A2-A25A PEX14 SNP Silent 1 10596278 G T 39 44 CRC TCGA-AA-3672 PEX14 SNP Missense_Mutation 1 10678421 G A 38 81 CRC TCGA-AA-A01Q PEX14 SNP Silent 1 10678450 A C 8 43 CRC TCGA-AA-A01Q PEX14 SNP Missense_Mutation 1 10683079 T C 49 88 BRCA TCGA-AN-A0XN PEX14 SNP Silent 1 10678420 C T 27 42 UCEC TCGA-AX-A0J0 PEX14 SNP Silent 1 10683165 C T 27 51 HNSC TCGA-CN-5369 PEX14 SNP Silent 1 10659377 A C 6 46 HNSC TCGA-CR-7388 PEX14 SNP Missense_Mutation 1 10659315 G A 45 71 HNSC TCGA-CV-5440 PEX14 SNP Missense_Mutation 1 10690033 G C 45 92 UCEC TCGA-D1-A17Q PEX14 SNP Splice_site 1 10687419 C T 31 68