ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0071 VARS2 SNP Missense_Mutation 6 30887973 C T 24 58 ESO ESO-555 VARS2 SNP Splice_Site 6 30890482 G A 35 92 LUAD LUAD-S01302 VARS2 SNP Nonsense_Mutation 6 30891158 G A 47 94 MED MD-050 VARS2 SNP Missense_Mutation 6 30891170 G A 38 83 MEL ME012 VARS2 SNP Missense_Mutation 6 30892296 C T 22 91 MEL MEL-JWCI-WGS-25 VARS2 SNP Silent 6 30892214 C T 30 50 MEL MEL-Ma-Mel-05 VARS2 SNP Silent 6 30893421 C T 22 51 MEL MEL-UKRV-Mel-6 VARS2 SNP Missense_Mutation 6 30887556 C T 31 51 LUAD TCGA-05-4396 VARS2 SNP Missense_Mutation 6 30883140 G T 47 53 LUAD TCGA-05-4396 VARS2 SNP Missense_Mutation 6 30883192 C A 23 56 LUAD TCGA-05-4396 VARS2 SNP Silent 6 30884929 G T 39 34 LUAD TCGA-05-4396 VARS2 SNP Missense_Mutation 6 30887544 G T 39 87 LUAD TCGA-05-4396 VARS2 SNP Missense_Mutation 6 30890693 G T 39 93 LUAD TCGA-05-4396 VARS2 SNP Missense_Mutation 6 30890741 C A 21 75 LUAD TCGA-05-4426 VARS2 SNP Missense_Mutation 6 30884943 G T 39 91 LUAD TCGA-05-4427 VARS2 SNP Missense_Mutation 6 30888132 G T 39 88 GBM TCGA-06-5417 VARS2 SNP Missense_Mutation 6 30893483 A G 14 56 LUAD TCGA-17-Z028 VARS2 SNP Silent 6 30882661 G A 45 58 LUSC TCGA-18-3409 VARS2 SNP Missense_Mutation 6 30891143 C T 30 55 LUSC TCGA-21-5786 VARS2 SNP Silent 6 30892295 C A 22 46 OV TCGA-23-1110 VARS2 SNP Missense_Mutation 6 30890956 G T 38 71 OV TCGA-24-1464 VARS2 SNP Missense_Mutation 6 30892146 G A 40 57 GBM TCGA-27-2518 VARS2 SNP Missense_Mutation 6 30883807 G T 46 75 LUSC TCGA-43-5668 VARS2 SNP Missense_Mutation 6 30888132 G T 39 88 OV TCGA-59-2355 VARS2 SNP Missense_Mutation 6 30890923 G A 37 96 OV TCGA-61-1998 VARS2 SNP Synonymous 6 30887984 C T 20 52 LUAD TCGA-64-5779 VARS2 SNP Missense_Mutation 6 30884915 C T 27 76 UCEC TCGA-A5-A0GP VARS2 SNP Silent 6 30883636 C T 31 42 CRC TCGA-AA-3518 VARS2 SNP Missense_Mutation 6 30882949 T A 52 50 CRC TCGA-AA-3544 VARS2 SNP Missense_Mutation 6 30886682 C T 31 90 CRC TCGA-AA-3664 VARS2 DEL Frame_Shift_Del 6 30892136 T - 55 49 CRC TCGA-AA-3811 VARS2 SNP Missense_Mutation 6 30889969 G A 38 91 CRC TCGA-AA-3939 VARS2 SNP Missense_Mutation 6 30884991 C T 31 90 CRC TCGA-AA-3947 VARS2 SNP Missense_Mutation 6 30889394 G A 39 69 CRC TCGA-AA-3952 VARS2 SNP Silent 6 30883004 T A 59 48 AML TCGA-AB-2806 VARS2 SNP Missense_Mutation 6 30890321 T A 59 51 AML TCGA-AB-2806 VARS2 SNP Missense_Mutation 6 30890708 G C 47 93 AML TCGA-AB-2920 VARS2 SNP Silent 6 30886617 G A 47 43 AML TCGA-AB-2938 VARS2 SNP Missense_Mutation 6 30887907 G A 45 68 CRC TCGA-AG-3582 VARS2 SNP Silent 6 30886629 A C 5 36 CRC TCGA-AG-A032 VARS2 SNP Silent 6 30889937 G A 39 43 KIRC TCGA-B0-5096 VARS2 SNP Missense_Mutation 6 30884693 G A 44 91 KIRC TCGA-B0-5096 VARS2 SNP Silent 6 30884694 T C 59 47 UCEC TCGA-B5-A11E VARS2 SNP Missense_Mutation 6 30882985 A C 9 54 BLCA TCGA-BT-A2LB VARS2 SNP Missense_Mutation 6 30884903 G A 45 91 BLCA TCGA-DK-A1A5 VARS2 SNP Missense_Mutation 6 30882669 C T 29 54 HNSC TCGA-IQ-7632 VARS2 SNP Nonsense_Mutation 6 30888896 C T 25 62