ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls1620 POU5F2 SNP Silent 5 93076829 C G 21 55 HNSC HN_62814 POU5F2 SNP Missense 5 93076774 G C 39 55 LUAD LUAD-CHTN-MAD08-00104 POU5F2 SNP Silent 5 93076721 C A 25 59 LUAD LUAD-NYU776 POU5F2 SNP Missense_Mutation 5 93076372 C A 20 43 LUAD LUAD-RT-S01699 POU5F2 SNP Missense_Mutation 5 93076300 C T 22 59 MEL ME044 POU5F2 SNP Silent 5 93076967 C A 23 12 MEL ME049 POU5F2 SNP Silent 5 93076970 G A 41 53 MEL MEL-JWCI-WGS-33 POU5F2 SNP Silent 5 93076681 G A 33 68 MEL MEL-UKRV-Mel-24 POU5F2 SNP Nonsense_Mutation 5 93076762 G A 47 65 LUSC TCGA-33-4538 POU5F2 SNP Missense_Mutation 5 93077080 G T 41 45 LUSC TCGA-66-2785 POU5F2 SNP Missense_Mutation 5 93076968 G A 39 49 LUSC TCGA-70-6722 POU5F2 SNP Missense_Mutation 5 93077094 T G 58 55 LUAD TCGA-73-4666 POU5F2 SNP Missense_Mutation 5 93076803 C A 22 67 GBM TCGA-76-4929 POU5F2 SNP Missense_Mutation 5 93077142 C T 24 49 CRC TCGA-AG-3902 POU5F2 SNP Nonsense_Mutation 5 93076993 G A 38 56 CRC TCGA-AG-A002 POU5F2 SNP Silent 5 93077210 G A 42 42 CRC TCGA-AG-A02N POU5F2 SNP Missense_Mutation 5 93076585 A G 3 70 UCEC TCGA-AP-A0LM POU5F2 SNP Silent 5 93076769 G A 37 50 UCEC TCGA-AP-A0LT POU5F2 SNP Missense_Mutation 5 93076428 G A 42 55 UCEC TCGA-AX-A0J1 POU5F2 SNP Missense_Mutation 5 93077199 G A 39 59 HNSC TCGA-BA-6869 POU5F2 SNP Silent 5 93076445 C T 22 51 UCEC TCGA-BS-A0UV POU5F2 SNP Silent 5 93076769 G A 37 50 UCEC TCGA-D1-A103 POU5F2 SNP Silent 5 93076844 G A 36 58 BRCA TCGA-E2-A15R POU5F2 SNP Missense_Mutation 5 93077199 G A 39 59