ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-887 POU1F1 SNP Missense_Mutation 3 87309163 G C 33 86 LUAD LUAD-B01811 POU1F1 SNP Missense_Mutation 3 87313474 A T 2 89 MEL MEL-JWCI-WGS-38 POU1F1 SNP Silent 3 87313523 C T 21 41 MEL MEL-JWCI-WGS-7 POU1F1 SNP Missense_Mutation 3 87309064 C T 30 63 MM MM-0612 POU1F1 SNP Missense_Mutation 3 87309086 C A 32 59 LUAD TCGA-05-4432 POU1F1 SNP Missense_Mutation 3 87325585 C A 29 85 GBM TCGA-06-0744 POU1F1 SNP Silent 3 87325559 G A 40 51 LUSC TCGA-18-4086 POU1F1 SNP Missense_Mutation 3 87313626 T C 59 88 LUSC TCGA-21-1071 POU1F1 SNP Silent 3 87311291 G A 45 75 LUAD TCGA-49-4505 POU1F1 SNP Missense_Mutation 3 87311358 G T 42 99 LUAD TCGA-73-4659 POU1F1 SNP Missense_Mutation 3 87309058 G T 33 92 CRC TCGA-AA-3864 POU1F1 SNP Nonsense_Mutation 3 87322563 C A 24 66 CRC TCGA-AA-A010 POU1F1 SNP Missense_Mutation 3 87309052 A G 6 85 CRC TCGA-AA-A010 POU1F1 SNP Missense_Mutation 3 87310438 C T 31 95 CRC TCGA-AG-A002 POU1F1 SNP Missense_Mutation 3 87309109 G A 40 61 CRC TCGA-AG-A002 POU1F1 SNP Missense_Mutation 3 87313510 C A 32 98 UCEC TCGA-AX-A05Z POU1F1 SNP Nonsense_Mutation 3 87309172 C A 32 86 UCEC TCGA-AX-A0J0 POU1F1 SNP Nonsense_Mutation 3 87309172 C A 32 86 HNSC TCGA-BA-5149 POU1F1 SNP Splice_site 3 87322645 G C 41 72 KIRC TCGA-BP-4166 POU1F1 SNP Missense_Mutation 3 87322594 G C 33 60 UCEC TCGA-BS-A0UF POU1F1 SNP Missense_Mutation 3 87310438 C T 31 95 UCEC TCGA-BS-A0UL POU1F1 SNP Silent 3 87322579 C T 21 62 BRCA TCGA-C8-A26V POU1F1 SNP Missense_Mutation 3 87309075 G C 33 79 HNSC TCGA-CR-7371 POU1F1 SNP Silent 3 87325510 G A 33 65 HNSC TCGA-CR-7402 POU1F1 SNP Missense_Mutation 3 87313582 C A 26 53 UCEC TCGA-D1-A16X POU1F1 SNP Nonsense_Mutation 3 87313486 C A 32 97 UCEC TCGA-D1-A17Q POU1F1 SNP Nonsense_Mutation 3 87309193 C A 32 100 UCEC TCGA-FI-A2D2 POU1F1 DEL Frame_Shift_Del 3 87322643 G - 47 64