ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0280 ELAVL4 SNP Missense_Mutation 1 50661241 A G 7 69 ESO ESO-752 ELAVL4 SNP Missense_Mutation 1 50642845 T C 54 92 HNSC HN_62338 ELAVL4 SNP Missense 1 50659530 C A 25 88 HNSC HN_62624 ELAVL4 SNP Missense 1 50572018 C T 32 85 LUAD LUAD-B00859 ELAVL4 SNP Silent 1 50610712 T C 58 68 LUAD LUAD-CHTN-3090415 ELAVL4 SNP Missense_Mutation 1 50661412 A G 5 94 MEL ME024 ELAVL4 SNP Missense_Mutation 1 50666752 G A 45 100 MEL MEL-JWCI-WGS-1 ELAVL4 SNP Missense_Mutation 1 50659521 G A 41 100 MEL MEL-JWCI-WGS-19 ELAVL4 SNP Splice_Site 1 50642760 G A 35 100 MEL MEL-JWCI-WGS-21 ELAVL4 SNP Missense_Mutation 1 50659567 G A 37 100 MEL MEL-JWCI-WGS-34 ELAVL4 SNP Missense_Mutation 1 50666563 G A 43 100 MEL MEL-Ma-Mel-05 ELAVL4 SNP Missense_Mutation 1 50610648 C T 24 85 MEL MEL-Ma-Mel-114 ELAVL4 SNP Missense_Mutation 1 50666588 G A 41 100 MEL MEL-Ma-Mel-119 ELAVL4 SNP Missense_Mutation 1 50666516 C T 22 59 MEL MEL-Ma-Mel-63 ELAVL4 SNP Silent 1 50610817 C T 31 59 MEL MEL-Ma-Mel-67 ELAVL4 SNP Missense_Mutation 1 50659521 G A 41 100 MM MM-0486 ELAVL4 SNP Silent 1 50661330 G A 39 43 LUAD TCGA-05-4427 ELAVL4 SNP Nonsense_Mutation 1 50610800 G T 33 100 LUAD TCGA-17-Z017 ELAVL4 SNP Missense_Mutation 1 50666503 C A 22 62 LUAD TCGA-17-Z023 ELAVL4 DNP Nonsense_Mutation 1 50610672 CC AA 30 84 LUAD TCGA-17-Z031 ELAVL4 SNP Silent 1 50610781 C A 22 71 LUAD TCGA-17-Z031 ELAVL4 SNP Missense_Mutation 1 50666560 G T 48 100 GBM TCGA-32-2494 ELAVL4 SNP Missense_Mutation 1 50610767 G A 40 100 LUSC TCGA-33-4533 ELAVL4 SNP Missense_Mutation 1 50661265 G A 45 100 LUAD TCGA-44-3918 ELAVL4 DEL Frame_Shift_Del 1 50659500 C - 30 100 LUSC TCGA-46-3769 ELAVL4 SNP Missense_Mutation 1 50642799 C G 30 100 LUAD TCGA-55-1592 ELAVL4 SNP Silent 1 50659526 G A 47 70 CRC TCGA-AA-3842 ELAVL4 SNP Silent 1 50663131 C T 27 86 CRC TCGA-AA-3977 ELAVL4 SNP Missense_Mutation 1 50666695 C T 31 100 CRC TCGA-AA-3994 ELAVL4 SNP Silent 1 50666631 C T 23 27 CRC TCGA-AA-A010 ELAVL4 SNP Missense_Mutation 1 50666606 T C 64 93 AML TCGA-AB-2928 ELAVL4 SNP Silent 1 50575630 G A 45 68 CRC TCGA-AG-3883 ELAVL4 SNP Silent 1 50666847 C A 24 80 UCEC TCGA-AP-A059 ELAVL4 SNP Missense_Mutation 1 50661235 G A 36 79 UCEC TCGA-AP-A0LM ELAVL4 SNP Missense_Mutation 1 50659482 C T 24 67 UCEC TCGA-AX-A0J0 ELAVL4 SNP Missense_Mutation 1 50661349 T G 60 94 KIRC TCGA-B0-4714 ELAVL4 SNP Silent 1 50610784 G A 33 64 UCEC TCGA-B5-A0JY ELAVL4 SNP Silent 1 50572035 C T 29 58 UCEC TCGA-B5-A11E ELAVL4 SNP Missense_Mutation 1 50666494 C T 18 57 UCEC TCGA-B5-A11E ELAVL4 SNP Missense_Mutation 1 50666546 G A 41 100 HNSC TCGA-BA-4078 ELAVL4 SNP Missense_Mutation 1 50659494 G A 39 100 BLCA TCGA-BT-A20J ELAVL4 SNP Missense_Mutation 1 50666507 C T 32 76 KIRC TCGA-CJ-4881 ELAVL4 SNP Missense_Mutation 1 50666792 G T 38 100 HNSC TCGA-CN-4736 ELAVL4 SNP Missense_Mutation 1 50659453 C T 23 100 HNSC TCGA-CR-6481 ELAVL4 SNP Splice_site 1 50574860 G A 33 72 HNSC TCGA-CR-7367 ELAVL4 SNP Missense_Mutation 1 50666696 G A 40 89 HNSC TCGA-CR-7374 ELAVL4 SNP Missense_Mutation 1 50661352 G T 46 100 HNSC TCGA-CR-7402 ELAVL4 INS Frame_Shift_Ins 1 50661318 - A 21 52 BLCA TCGA-CU-A0YN ELAVL4 SNP Silent 1 50666658 T C 63 36 HNSC TCGA-CV-6941 ELAVL4 SNP Silent 1 50666796 G T 47 72 HNSC TCGA-CV-7095 ELAVL4 SNP Missense_Mutation 1 50610702 A G 2 68 BLCA TCGA-DK-A1A5 ELAVL4 SNP Silent 1 50610766 C T 31 44 BLCA TCGA-DK-A1A6 ELAVL4 SNP Missense_Mutation 1 50642818 C T 26 100 BLCA TCGA-DK-A3IQ ELAVL4 SNP Nonsense_Mutation 1 50642770 T G 61 92 HNSC TCGA-DQ-7588 ELAVL4 SNP Silent 1 50642774 G T 44 70 UCEC TCGA-EO-A1Y5 ELAVL4 SNP Silent 1 50659454 G A 37 48 BLCA TCGA-G2-A2ES ELAVL4 SNP Missense_Mutation 1 50661283 G A 33 100 BLCA TCGA-G2-A3IB ELAVL4 SNP Missense_Mutation 1 50610812 C T 32 89 HNSC TCGA-HD-7832 ELAVL4 SNP Missense_Mutation 1 50663122 G A 47 100