ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62646 ELOVL6 SNP Synonymous 4 110980907 T G 49 53 LUAD TCGA-50-5049 ELOVL6 SNP Missense_Mutation 4 110972668 C A 21 58 LUSC TCGA-60-2724 ELOVL6 SNP Missense_Mutation 4 110980846 G T 46 100 UCEC TCGA-A5-A0GP ELOVL6 SNP Missense_Mutation 4 110980893 C T 31 100 BRCA TCGA-A8-A07C ELOVL6 SNP Missense_Mutation 4 110972768 G T 42 89 BRCA TCGA-A8-A09A ELOVL6 SNP Missense_Mutation 4 110980805 G C 46 100 CRC TCGA-AA-A022 ELOVL6 SNP Missense_Mutation 4 111026731 C T 23 84 UCEC TCGA-AP-A0LM ELOVL6 SNP Missense_Mutation 4 111119447 C A 28 62 UCEC TCGA-B5-A11E ELOVL6 SNP Nonsense_Mutation 4 110980894 G A 37 71 UCEC TCGA-B5-A11J ELOVL6 SNP Silent 4 110972773 C T 25 51 UCEC TCGA-BS-A0UF ELOVL6 SNP Missense_Mutation 4 110980799 G T 33 87 UCEC TCGA-BS-A0UV ELOVL6 SNP Silent 4 111026739 G A 37 53 HNSC TCGA-CN-5359 ELOVL6 SNP Missense_Mutation 4 110972591 C A 21 89 HNSC TCGA-CQ-6225 ELOVL6 SNP Missense_Mutation 4 110980810 C A 17 63 HNSC TCGA-CV-7235 ELOVL6 SNP Silent 4 110980841 T G 55 50 BRCA TCGA-E9-A1R3 ELOVL6 SNP Missense_Mutation 4 111026713 C G 31 98