ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0280 VSNL1 SNP Silent 2 17830862 C T 29 68 ESO ESO-173 VSNL1 SNP Missense_Mutation 2 17830732 A G 10 90 LUAD LUAD-RT-S01301 VSNL1 SNP Missense_Mutation 2 17773380 G A 47 99 LUAD LUAD-RT-S01769 VSNL1 SNP Missense_Mutation 2 17773430 G T 47 99 MEL ME016 VSNL1 SNP Missense_Mutation 2 17773439 G A 41 99 MEL MEL-Ma-Mel-35 VSNL1 SNP Silent 2 17773464 G A 41 55 LUAD TCGA-05-4396 VSNL1 SNP Silent 2 17830722 C A 23 61 LUSC TCGA-21-5787 VSNL1 SNP Nonsense_Mutation 2 17773402 G T 33 99 OV TCGA-25-1313 VSNL1 SNP Missense_Mutation 2 17773383 G T 35 65 LUAD TCGA-35-3621 VSNL1 SNP Missense_Mutation 2 17830762 G A 37 98 LUAD TCGA-38-4631 VSNL1 SNP Silent 2 17830709 C A 22 50 LUAD TCGA-44-2656 VSNL1 SNP Missense_Mutation 2 17836616 C A 27 71 LUAD TCGA-64-5781 VSNL1 SNP Missense_Mutation 2 17836575 G A 45 87 KIRC TCGA-A3-3387 VSNL1 SNP Silent 2 17773470 A G 13 58 UCEC TCGA-BS-A0UF VSNL1 SNP Missense_Mutation 2 17773444 C A 32 85 UCEC TCGA-BS-A0UF VSNL1 SNP Missense_Mutation 2 17836635 C A 20 87 HNSC TCGA-CN-6995 VSNL1 SNP Missense_Mutation 2 17836566 A T 9 92 BLCA TCGA-DK-A1A3 VSNL1 SNP Missense_Mutation 2 17773477 G C 37 99