ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls2258 TMEM39B SNP Missense_Mutation 1 32560443 G C 34 69 ESO ESO-1608 TMEM39B SNP Missense_Mutation 1 32568242 C T 22 54 LUAD LUAD-F00018 TMEM39B SNP Missense_Mutation 1 32560490 G T 45 100 MEL ME045 TMEM39B SNP Splice_site 1 32560572 C A 23 59 MEL MEL-13561 TMEM39B SNP Missense_Mutation 1 32568147 C T 31 100 MEL MEL-JWCI-WGS-12 TMEM39B SNP Silent 1 32542408 C T 31 43 MEL MEL-JWCI-WGS-25 TMEM39B SNP Silent 1 32542378 C T 31 52 MEL MEL-JWCI-WGS-38 TMEM39B SNP Missense_Mutation 1 32542795 C T 31 96 MEL MEL-Ma-Mel-67 TMEM39B SNP Missense_Mutation 1 32566147 C T 30 83 MM MM-0468 TMEM39B SNP Silent 1 32542807 C T 28 73 PRAD PR-06-1651 TMEM39B SNP Missense_Mutation 1 32557307 A T 9 87 LUAD TCGA-05-4398 TMEM39B SNP Missense_Mutation 1 32566053 G A 33 96 LUAD TCGA-05-4420 TMEM39B SNP Nonsense_Mutation 1 32557579 C A 20 55 GBM TCGA-06-0648 TMEM39B SNP Missense_Mutation 1 32541290 C G 21 96 LUAD TCGA-17-Z030 TMEM39B SNP Missense_Mutation 1 32542848 G T 41 96 LUSC TCGA-22-4613 TMEM39B SNP Silent 1 32542890 C T 24 61 OV TCGA-24-2288 TMEM39B SNP Missense_Mutation 1 32560520 G C 43 100 LUAD TCGA-49-4486 TMEM39B SNP Silent 1 32568034 C T 32 62 LUAD TCGA-50-6592 TMEM39B SNP Missense_Mutation 1 32557333 C G 32 56 UCEC TCGA-A5-A0GB TMEM39B SNP Missense_Mutation 1 32560409 T C 55 90 UCEC TCGA-AP-A051 TMEM39B SNP Missense_Mutation 1 32542820 G A 38 82 UCEC TCGA-AX-A060 TMEM39B SNP Missense_Mutation 1 32568213 T C 63 93 UCEC TCGA-AX-A0J0 TMEM39B SNP Missense_Mutation 1 32568173 T G 53 93 UCEC TCGA-AX-A0J1 TMEM39B SNP Silent 1 32557573 C T 27 47 UCEC TCGA-B5-A11E TMEM39B SNP Missense_Mutation 1 32542422 G A 38 96 UCEC TCGA-B5-A11E TMEM39B SNP Nonsense_Mutation 1 32542858 C T 23 74 UCEC TCGA-B5-A11E TMEM39B SNP Missense_Mutation 1 32568068 C A 24 80 BRCA TCGA-BH-A0AU TMEM39B SNP Silent 1 32568070 C T 30 37 KIRC TCGA-BP-5174 TMEM39B SNP Missense_Mutation 1 32557586 G T 42 96 UCEC TCGA-BS-A0UV TMEM39B SNP Missense_Mutation 1 32568247 G T 33 63 HNSC TCGA-CQ-5323 TMEM39B SNP Missense_Mutation 1 32542834 A G 6 88 HNSC TCGA-CR-7367 TMEM39B SNP Missense_Mutation 1 32557499 C T 23 98 HNSC TCGA-CV-5431 TMEM39B SNP Splice_Site 1 32542920 G A 40 96 KIRC TCGA-CZ-4862 TMEM39B SNP Missense_Mutation 1 32557363 G C 43 52 UCEC TCGA-D1-A103 TMEM39B SNP Missense_Mutation 1 32557412 C T 27 60 UCEC TCGA-D1-A17F TMEM39B INS Frame_Shift_Ins 1 32566131 - TCCCC 16 58