ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CRC CRC-0005 VRK2 SNP Nonsense 2 58366926 A T 1 50 LUAD LUAD-D02326 VRK2 SNP Splice_Site 2 58359064 G C 36 100 LUAD LUAD-RT-S01699 VRK2 SNP Missense_Mutation 2 58276078 G C 47 84 LUAD LUAD-RT-S01699 VRK2 SNP Missense_Mutation 2 58350321 A T 8 93 LUAD TCGA-05-4396 VRK2 SNP Silent 2 58315576 C A 23 62 GBM TCGA-12-0688 VRK2 SNP Missense_Mutation 2 58373508 G A 37 57 LUAD TCGA-17-Z022 VRK2 SNP Silent 2 58276044 C A 25 46 LUAD TCGA-17-Z055 VRK2 SNP Silent 2 58315576 C A 23 62 LUSC TCGA-18-3409 VRK2 SNP Silent 2 58386588 T C 64 54 LUSC TCGA-21-5787 VRK2 SNP Missense_Mutation 2 58312046 G C 33 89 LUSC TCGA-22-4601 VRK2 SNP Missense_Mutation 2 58313518 C G 30 87 OV TCGA-24-1564 VRK2 SNP Missense_Mutation 2 58275998 T A 56 78 LUSC TCGA-33-4582 VRK2 SNP Missense_Mutation 2 58366957 A C 2 50 LUSC TCGA-34-5928 VRK2 SNP Splice_Site 2 58275961 G C 33 84 LUSC TCGA-51-4080 VRK2 SNP Missense_Mutation 2 58350361 G T 35 74 LUSC TCGA-60-2707 VRK2 SNP Splice_Site 2 58366799 A T 7 78 LUAD TCGA-64-1678 VRK2 SNP Missense_Mutation 2 58350345 G T 34 100 LUAD TCGA-91-6829 VRK2 SNP Nonsense_Mutation 2 58366863 C T 29 61 CRC TCGA-AA-3672 VRK2 SNP Missense_Mutation 2 58313492 G A 38 50 CRC TCGA-AA-3947 VRK2 SNP Missense_Mutation 2 58362286 G A 37 82 CRC TCGA-AA-A00N VRK2 SNP Missense_Mutation 2 58386638 G A 33 49 CRC TCGA-AG-3896 VRK2 SNP Missense_Mutation 2 58386817 T G 52 69 CRC TCGA-AG-A002 VRK2 SNP Nonsense_Mutation 2 58312046 G T 33 89 UCEC TCGA-AP-A051 VRK2 SNP Silent 2 58373543 C A 24 56 UCEC TCGA-AP-A0LI VRK2 SNP Missense_Mutation 2 58386671 T C 58 48 UCEC TCGA-AX-A0J0 VRK2 SNP Missense_Mutation 2 58312030 T G 51 82 KIRC TCGA-B8-4621 VRK2 DEL Frame_Shift_Del 2 58350342 C - 18 100 KIRC TCGA-B8-4621 VRK2 SNP Silent 2 58358987 C T 28 66 UCEC TCGA-BS-A0TE VRK2 SNP Missense_Mutation 2 58386545 G A 36 49 UCEC TCGA-BS-A0UF VRK2 SNP Missense_Mutation 2 58350346 C A 28 76 BRCA TCGA-C8-A12T VRK2 SNP Missense_Mutation 2 58350248 G C 33 100 HNSC TCGA-CN-4727 VRK2 SNP Silent 2 58276056 A T 14 45 HNSC TCGA-CN-4734 VRK2 SNP Missense_Mutation 2 58350334 A G 15 49 UCEC TCGA-D1-A103 VRK2 SNP Silent 2 58373534 C T 27 53 UCEC TCGA-D1-A167 VRK2 SNP Missense_Mutation 2 58386773 G A 38 54 HNSC TCGA-DQ-5629 VRK2 SNP Missense_Mutation 2 58373570 G T 35 46 HNSC TCGA-DQ-7595 VRK2 SNP Silent 2 58373462 A G 1 50