ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-027 CPEB3 SNP Missense_Mutation 10 93811989 C G 19 79 HNSC HN_62421 CPEB3 SNP Missense 10 93902813 C T 29 89 HNSC HN_62506 CPEB3 SNP Missense 10 93870946 C A 25 100 LUAD LUAD-QY22Z CPEB3 SNP Missense_Mutation 10 93904831 C T 30 86 MEL ME009 CPEB3 SNP Missense_Mutation 10 93812118 G A 43 100 MEL MEL-13549 CPEB3 SNP Silent 10 93902868 G A 45 72 MEL MEL-JWCI-WGS-22 CPEB3 SNP Missense_Mutation 10 93812118 G A 43 100 NB NB-0462 CPEB3 SNP Missense_Mutation 10 93952380 G T 43 99 NB NB-3204 CPEB3 SNP Silent 10 93999253 C T 27 43 LUAD TCGA-17-Z046 CPEB3 SNP Silent 10 93999766 G T 46 56 LUAD TCGA-17-Z060 CPEB3 INS Frame_Shift_Ins 10 93999919 - G 23 54 OV TCGA-23-1122 CPEB3 SNP Synonymous 10 93812185 C T 28 100 LUSC TCGA-37-3789 CPEB3 SNP Missense_Mutation 10 93841226 C A 21 100 LUSC TCGA-39-5035 CPEB3 SNP Missense_Mutation 10 93999117 G C 33 68 LUAD TCGA-64-1680 CPEB3 SNP Splice_site 10 93851587 C T 21 79 CRC TCGA-AA-3525 CPEB3 SNP Silent 10 93812116 C T 19 47 CRC TCGA-AA-A00N CPEB3 SNP Missense_Mutation 10 93952356 G A 37 99 CRC TCGA-AA-A010 CPEB3 SNP Missense_Mutation 10 93851605 G T 41 100 CRC TCGA-AA-A01Q CPEB3 SNP Nonsense_Mutation 10 93812149 G T 42 67 CRC TCGA-AG-A02N CPEB3 SNP Missense_Mutation 10 94000105 C T 25 94 BRCA TCGA-AN-A0AR CPEB3 SNP Missense_Mutation 10 93952303 C G 24 99 UCEC TCGA-AP-A054 CPEB3 SNP Missense_Mutation 10 93904752 C T 27 100 UCEC TCGA-B5-A11E CPEB3 SNP Missense_Mutation 10 93940762 T G 64 79 UCEC TCGA-BS-A0UF CPEB3 SNP Missense_Mutation 10 93841238 C T 30 100 UCEC TCGA-BS-A0UV CPEB3 SNP Missense_Mutation 10 93904779 C T 27 88 UCEC TCGA-BS-A0UV CPEB3 SNP Silent 10 93999739 G A 33 64 HNSC TCGA-CR-6472 CPEB3 SNP Missense_Mutation 10 93902855 G A 37 100 UCEC TCGA-D1-A17H CPEB3 INS Frame_Shift_Ins 10 93999139 - A 41 63 BLCA TCGA-DK-A2I2 CPEB3 SNP Missense_Mutation 10 93952323 G C 36 83 UCEC TCGA-FI-A2F8 CPEB3 SNP Missense_Mutation 10 93870875 T G 60 55