ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-S01345 VSIG2 SNP Silent 11 124621343 C T 30 50 MEL MEL-JWCI-14 VSIG2 SNP Missense_Mutation 11 124619634 G A 41 61 MEL MEL-Ma-Mel-63 VSIG2 SNP Silent 11 124622022 G A 41 43 OV TCGA-04-1337 VSIG2 SNP Missense_Mutation 11 124617502 C G 22 65 LUAD TCGA-05-4395 VSIG2 SNP Splice_site 11 124621476 C T 22 76 LUAD TCGA-05-4396 VSIG2 SNP Silent 11 124618384 C A 21 66 LUAD TCGA-05-4417 VSIG2 SNP Silent 11 124619716 C A 21 56 LUAD TCGA-05-5715 VSIG2 SNP Missense_Mutation 11 124619682 C T 31 49 GBM TCGA-06-0185 VSIG2 SNP Missense_Mutation 11 124620786 G A 47 56 OV TCGA-13-0760 VSIG2 SNP Silent 11 124618354 G A 33 50 LUSC TCGA-18-3419 VSIG2 SNP Nonsense_Mutation 11 124617490 T A 56 72 OV TCGA-23-2077 VSIG2 SNP Missense_Mutation 11 124621997 G T 35 54 OV TCGA-24-1435 VSIG2 DEL Frame_Shift_Del 11 124620707 GTCA - 40 43 OV TCGA-24-1545 VSIG2 SNP Missense_Mutation 11 124618611 G A 37 81 GBM TCGA-26-5134 VSIG2 SNP Silent 11 124618351 G A 42 51 LUSC TCGA-37-3789 VSIG2 SNP Missense_Mutation 11 124617436 C A 19 65 LUAD TCGA-38-4631 VSIG2 SNP Missense_Mutation 11 124618406 C T 30 77 LUSC TCGA-60-2723 VSIG2 SNP Missense_Mutation 11 124620721 G T 36 66 CRC TCGA-AA-A010 VSIG2 SNP Missense_Mutation 11 124618358 G A 38 44 CRC TCGA-AG-A002 VSIG2 SNP Nonsense_Mutation 11 124620809 G T 36 53 UCEC TCGA-AP-A051 VSIG2 SNP Missense_Mutation 11 124621404 C T 25 76 KIRC TCGA-B0-5085 VSIG2 SNP Missense_Mutation 11 124619711 C T 26 75 UCEC TCGA-B5-A11N VSIG2 SNP Missense_Mutation 11 124620650 G T 33 66 UCEC TCGA-BS-A0UV VSIG2 SNP Splice_site 11 124618541 G A 39 48 HNSC TCGA-CN-4723 VSIG2 SNP Missense_Mutation 11 124621364 C G 20 58 HNSC TCGA-CN-5360 VSIG2 SNP Silent 11 124617497 G A 41 50 HNSC TCGA-CX-7082 VSIG2 SNP Missense_Mutation 11 124618415 C G 31 77 HNSC TCGA-DQ-5625 VSIG2 SNP Silent 11 124618357 C T 19 39 BLCA TCGA-FD-A3B5 VSIG2 SNP Silent 11 124620668 G T 45 45