ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-LS4619 PSKH2 SNP Missense_Mutation 8 87060801 T A 54 57 ESO ESO-161 PSKH2 SNP Missense_Mutation 8 87081770 C T 23 42 LUAD LUAD-NYU847 PSKH2 SNP Missense_Mutation 8 87081832 C G 24 51 MEL MEL-13463 PSKH2 SNP Silent 8 87081690 C T 20 70 MEL MEL-JWCI-WGS-34 PSKH2 SNP Silent 8 87076404 A G 6 34 MEL MEL-Ma-Mel-114 PSKH2 SNP Silent 8 87076788 C T 32 82 MEL MEL-Ma-Mel-65 PSKH2 SNP Missense_Mutation 8 87076619 C T 24 75 MEL MEL-Ma-Mel-67 PSKH2 SNP Silent 8 87060979 G A 43 59 MEL MEL-Ma-Mel-67 PSKH2 SNP Missense_Mutation 8 87081679 C T 23 78 MM MM-0603 PSKH2 SNP Missense_Mutation 8 87060776 T C 56 65 OV TCGA-04-1336 PSKH2 SNP Missense_Mutation 8 87076291 G T 48 73 LUAD TCGA-05-4382 PSKH2 SNP Silent 8 87076623 G T 39 15 LUAD TCGA-05-4396 PSKH2 SNP Silent 8 87060837 G T 39 50 LUAD TCGA-05-4403 PSKH2 SNP Silent 8 87076326 G A 47 42 LUAD TCGA-05-4427 PSKH2 SNP Missense_Mutation 8 87076237 A T 3 86 LUAD TCGA-17-Z028 PSKH2 SNP Missense_Mutation 8 87076703 C A 18 83 LUAD TCGA-17-Z030 PSKH2 SNP Silent 8 87060979 G A 43 59 LUAD TCGA-17-Z042 PSKH2 SNP Missense_Mutation 8 87076366 T A 54 87 LUAD TCGA-17-Z060 PSKH2 SNP Missense_Mutation 8 87076698 G C 42 54 LUAD TCGA-17-Z062 PSKH2 SNP Missense_Mutation 8 87060802 C A 32 58 LUSC TCGA-18-3412 PSKH2 SNP Missense_Mutation 8 87076814 C A 17 55 LUSC TCGA-22-5489 PSKH2 SNP Nonsense_Mutation 8 87076589 C A 22 67 LUSC TCGA-34-2596 PSKH2 SNP Silent 8 87076470 A G 12 68 LUSC TCGA-34-5231 PSKH2 SNP Missense_Mutation 8 87081736 G C 38 59 LUAD TCGA-35-4122 PSKH2 SNP Missense_Mutation 8 87060752 C A 24 51 LUSC TCGA-43-2578 PSKH2 SNP Silent 8 87081732 G T 43 47 LUSC TCGA-46-3769 PSKH2 SNP Splice_site 8 87060998 T A 55 84 LUAD TCGA-50-5930 PSKH2 SNP Nonsense_Mutation 8 87076731 G T 38 52 LUAD TCGA-55-6712 PSKH2 SNP Missense_Mutation 8 87076709 G A 38 60 LUAD TCGA-64-1676 PSKH2 SNP Missense_Mutation 8 87076322 C A 25 81 LUAD TCGA-64-5775 PSKH2 SNP Silent 8 87081723 C A 27 38 LUSC TCGA-66-2792 PSKH2 SNP Missense_Mutation 8 87060971 G T 38 64 LUAD TCGA-67-4679 PSKH2 SNP Missense_Mutation 8 87060875 G T 46 55 LUAD TCGA-91-6831 PSKH2 SNP Missense_Mutation 8 87060894 A C 7 83 BRCA TCGA-A8-A07L PSKH2 SNP Silent 8 87076599 G C 45 58 BRCA TCGA-A8-A09I PSKH2 SNP Missense_Mutation 8 87060836 C T 31 51 CRC TCGA-AA-3672 PSKH2 SNP Missense_Mutation 8 87076537 C A 22 95 CRC TCGA-AA-3984 PSKH2 SNP Silent 8 87060823 C T 32 51 UCEC TCGA-AP-A056 PSKH2 SNP Silent 8 87076215 G A 46 59 UCEC TCGA-AP-A056 PSKH2 SNP Missense_Mutation 8 87076588 C T 30 97 UCEC TCGA-AX-A0J0 PSKH2 SNP Silent 8 87060919 T G 55 51 UCEC TCGA-B5-A0JY PSKH2 SNP Missense_Mutation 8 87060713 G A 37 63 UCEC TCGA-BS-A0TC PSKH2 SNP Silent 8 87076851 G T 45 61 UCEC TCGA-BS-A0UF PSKH2 SNP Silent 8 87076500 C T 30 54 UCEC TCGA-BS-A0UJ PSKH2 SNP Missense_Mutation 8 87076630 A G 7 75 BLCA TCGA-BT-A20J PSKH2 SNP Missense_Mutation 8 87076269 G C 41 61 KIRC TCGA-CJ-4907 PSKH2 SNP Nonsense_Mutation 8 87060713 G T 37 63 HNSC TCGA-CV-6935 PSKH2 SNP Missense_Mutation 8 87060915 C G 21 59 HNSC TCGA-CV-6948 PSKH2 SNP Silent 8 87076791 G T 47 60