ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-MAYO_DLBCL_234 ELAVL1 SNP Missense_Mutation 19 8038675 C T 19 80 HNSC HN_62469 ELAVL1 SNP Synonymous 19 8028550 C T 19 59 MEL MEL-Ma-Mel-92 ELAVL1 SNP Missense_Mutation 19 8038723 C T 27 94 LUAD TCGA-05-4396 ELAVL1 SNP Missense_Mutation 19 8056648 C A 23 81 LUAD TCGA-05-4432 ELAVL1 SNP Missense_Mutation 19 8038675 C G 19 80 GBM TCGA-06-0879 ELAVL1 SNP Missense_Mutation 19 8028639 G A 42 73 LUAD TCGA-17-Z023 ELAVL1 SNP Missense_Mutation 19 8032642 C G 29 99 LUAD TCGA-17-Z060 ELAVL1 SNP Missense_Mutation 19 8028472 C A 29 98 LUSC TCGA-18-3416 ELAVL1 SNP Splice_Site 19 8045966 C A 18 96 LUAD TCGA-50-5051 ELAVL1 SNP Silent 19 8028583 G A 39 49 LUSC TCGA-66-2771 ELAVL1 SNP Silent 19 8032655 C A 19 51 UCEC TCGA-A5-A0VP ELAVL1 SNP Missense_Mutation 19 8046013 G A 38 97 CRC TCGA-AA-3543 ELAVL1 SNP Silent 19 8028661 G A 38 47 CRC TCGA-AA-3710 ELAVL1 SNP Missense_Mutation 19 8028533 T C 52 77 CRC TCGA-AA-3715 ELAVL1 SNP Missense_Mutation 19 8046013 G A 38 97 CRC TCGA-AA-3812 ELAVL1 SNP Missense_Mutation 19 8028686 G A 41 98 CRC TCGA-AA-A010 ELAVL1 SNP Silent 19 8032484 G A 37 48 AML TCGA-AB-2828 ELAVL1 SNP Missense_Mutation 19 8032461 G A 38 99 BRCA TCGA-AN-A0FK ELAVL1 SNP Missense_Mutation 19 8032461 G A 38 99 UCEC TCGA-AP-A05N ELAVL1 SNP Splice_Site 19 8045966 C T 18 96 UCEC TCGA-AX-A0J0 ELAVL1 SNP Splice_Site 19 8032675 C A 24 85 UCEC TCGA-B5-A0JY ELAVL1 SNP Missense_Mutation 19 8056543 G A 37 84 UCEC TCGA-BG-A0MG ELAVL1 SNP Nonsense_Mutation 19 8032492 G A 38 53 BRCA TCGA-BH-A0HW ELAVL1 SNP Missense_Mutation 19 8056669 C T 31 75 UCEC TCGA-BS-A0TJ ELAVL1 DEL Frame_Shift_Del 19 8046014 CT - 28 97 UCEC TCGA-BS-A0UV ELAVL1 SNP Silent 19 8046030 C T 31 42 BLCA TCGA-BT-A20Q ELAVL1 SNP Silent 19 8046039 G A 40 51 HNSC TCGA-CV-6941 ELAVL1 SNP Missense_Mutation 19 8032636 G A 40 66 UCEC TCGA-D1-A0ZS ELAVL1 SNP Silent 19 8028622 G A 39 36 UCEC TCGA-D1-A16B ELAVL1 SNP Missense_Mutation 19 8032470 T C 59 77 UCEC TCGA-D1-A17Q ELAVL1 SNP Missense_Mutation 19 8046018 C A 32 61 BRCA TCGA-E9-A1RF ELAVL1 SNP Silent 19 8032481 T G 54 62 BLCA TCGA-G2-A2EO ELAVL1 SNP Missense_Mutation 19 8032455 C G 32 98 BLCA TCGA-GD-A3OP ELAVL1 SNP Splice_Site 19 8056716 C G 32 86