ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-105 CELF1 SNP Missense_Mutation 11 47498466 A G 16 93 ESO ESO-120 CELF1 SNP Missense_Mutation 11 47510470 G A 38 47 LUAD LUAD-B00731 CELF1 SNP Missense_Mutation 11 47504263 C A 30 77 LUAD LUAD-RT-S01707 CELF1 SNP Silent 11 47496958 C T 27 21 LUAD LUAD-RT-S01709 CELF1 SNP Missense_Mutation 11 47508730 T C 60 92 MEL MEL-Ma-Mel-102 CELF1 SNP Silent 11 47494704 G A 35 52 LUAD TCGA-05-4396 CELF1 SNP Missense_Mutation 11 47510421 C A 24 100 LUAD TCGA-05-4396 CELF1 SNP Missense_Mutation 11 47510469 C A 23 72 LUAD TCGA-05-4396 CELF1 SNP Silent 11 47510507 C A 21 67 OV TCGA-13-0751 CELF1 SNP Missense_Mutation 11 47500431 C A 30 76 LUAD TCGA-17-Z056 CELF1 SNP Missense_Mutation 11 47498401 C A 26 100 OV TCGA-23-1022 CELF1 SNP Missense_Mutation 11 47508323 C G 25 100 LUSC TCGA-33-4586 CELF1 SNP Missense_Mutation 11 47496998 G C 36 76 LUSC TCGA-37-3783 CELF1 SNP Missense_Mutation 11 47510421 C G 24 100 LUAD TCGA-44-3398 CELF1 SNP Missense_Mutation 11 47510459 G C 37 50 LUAD TCGA-64-5778 CELF1 SNP Missense_Mutation 11 47506016 T C 51 80 LUAD TCGA-75-5126 CELF1 SNP Missense_Mutation 11 47493789 G A 43 100 GBM TCGA-81-5910 CELF1 SNP Missense_Mutation 11 47496959 G A 38 100 CRC TCGA-AA-3710 CELF1 SNP Splice_Site 11 47498509 C A 24 88 CRC TCGA-AA-3811 CELF1 SNP Silent 11 47496958 C T 27 21 AML TCGA-AB-2828 CELF1 SNP Missense_Mutation 11 47496899 C T 28 100 UCEC TCGA-AP-A056 CELF1 SNP Missense_Mutation 11 47498893 G A 34 100 UCEC TCGA-B5-A0JY CELF1 SNP Silent 11 47494692 G A 37 53 UCEC TCGA-B5-A1MY CELF1 SNP Missense_Mutation 11 47508734 G T 45 100 UCEC TCGA-BS-A0UV CELF1 SNP Missense_Mutation 11 47506004 A G 2 93 BRCA TCGA-C8-A134 CELF1 SNP Missense_Mutation 11 47506035 C G 32 100 HNSC TCGA-CN-4728 CELF1 SNP Missense_Mutation 11 47508744 C G 32 78 HNSC TCGA-CV-7425 CELF1 SNP Missense_Mutation 11 47504267 G T 33 71 UCEC TCGA-D1-A15X CELF1 SNP Missense_Mutation 11 47504377 G A 34 100 UCEC TCGA-D1-A174 CELF1 SNP Missense_Mutation 11 47498872 G A 43 100 UCEC TCGA-D1-A17Q CELF1 SNP Missense_Mutation 11 47493807 G A 37 88 HNSC TCGA-D6-6516 CELF1 SNP Missense_Mutation 11 47510497 G A 41 100 BRCA TCGA-D8-A146 CELF1 SNP Silent 11 47498507 C A 18 55 BLCA TCGA-FD-A3N6 CELF1 SNP Nonsense_Mutation 11 47510398 G A 45 100