ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0014 SERINC5 SNP Missense_Mutation 5 79498793 C T 27 100 DLBCL DLBCL-Ls3245 SERINC5 SNP Missense_Mutation 5 79473802 C T 20 100 ESO ESO-155 SERINC5 SNP Missense_Mutation 5 79473826 C A 18 100 ESO ESO-913 SERINC5 SNP Silent 5 79462288 C A 23 37 LUAD LUAD-B00859 SERINC5 SNP Missense_Mutation 5 79442027 C G 30 82 MEL MEL-JWCI-WGS-1 SERINC5 SNP Missense_Mutation 5 79473883 G A 41 100 MEL MEL-JWCI-WGS-22 SERINC5 SNP Missense_Mutation 5 79473882 G A 35 87 MEL MEL-Ma-Mel-119 SERINC5 SNP Missense_Mutation 5 79446751 G A 37 61 MEL MEL-Ma-Mel-120 SERINC5 SNP Missense_Mutation 5 79446751 G A 37 61 MEL MEL-Ma-Mel-28 SERINC5 SNP Silent 5 79498744 G A 45 66 MEL MEL-Ma-Mel-67 SERINC5 SNP Missense_Mutation 5 79462284 G A 34 51 LUAD TCGA-05-4382 SERINC5 SNP Missense_Mutation 5 79454738 C A 21 71 LUAD TCGA-17-Z054 SERINC5 SNP Silent 5 79498750 G A 34 63 LUSC TCGA-22-5471 SERINC5 SNP Silent 5 79442032 C T 24 50 OV TCGA-24-2030 SERINC5 SNP Missense_Mutation 5 79446708 C A 21 51 LUAD TCGA-50-5933 SERINC5 SNP Missense_Mutation 5 79473158 C A 32 82 LUAD TCGA-50-5946 SERINC5 SNP Missense_Mutation 5 79473874 C G 29 58 UCEC TCGA-A5-A0GB SERINC5 SNP Silent 5 79498729 G T 39 28 UCEC TCGA-A5-A0GP SERINC5 SNP Missense_Mutation 5 79473811 C T 19 100 AML TCGA-AB-2863 SERINC5 SNP Missense_Mutation 5 79470852 G A 42 84 KIRC TCGA-AK-3431 SERINC5 SNP Splice_Region 5 79462203 T C 61 58 UCEC TCGA-AP-A0LM SERINC5 SNP Silent 5 79465315 C T 27 0 UCEC TCGA-B5-A0JY SERINC5 SNP Missense_Mutation 5 79473808 A G 14 91 KIRC TCGA-BP-4758 SERINC5 SNP Missense_Mutation 5 79465263 A G 13 90 UCEC TCGA-BS-A0UV SERINC5 SNP Nonsense_Mutation 5 79473793 C A 21 100 UCEC TCGA-BS-A0UV SERINC5 SNP Missense_Mutation 5 79473804 C A 32 66 BRCA TCGA-C8-A1HN SERINC5 SNP Missense_Mutation 5 79473765 C G 17 55 HNSC TCGA-CR-7395 SERINC5 SNP Missense_Mutation 5 79473837 C T 17 100 HNSC TCGA-CR-7398 SERINC5 SNP Silent 5 79498804 G C 43 48 HNSC TCGA-CR-7402 SERINC5 SNP Missense_Mutation 5 79470855 C T 30 98 HNSC TCGA-CV-6955 SERINC5 SNP Missense_Mutation 5 79473175 C T 30 96 HNSC TCGA-DQ-7595 SERINC5 SNP Missense_Mutation 5 79462247 T G 57 92 KIRC TCGA-EU-5906 SERINC5 SNP Missense_Mutation 5 79473191 C G 22 73