ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1154 PRKX SNP Silent 23 3530298 G A 36 52 ESO ESO-131 PRKX SNP Silent 23 3573435 G A 40 48 LUAD LUAD-CHTN-3090416 PRKX SNP Missense_Mutation 23 3592734 C A 29 86 MEL MEL-JWCI-14 PRKX SNP Missense_Mutation 23 3530362 G A 43 83 MEL MEL-JWCI-WGS-25 PRKX SNP Nonsense_Mutation 23 3533884 C T 21 83 MEL MEL-Ma-Mel-36 PRKX SNP Missense_Mutation 23 3533926 G A 38 71 LUAD TCGA-05-4384 PRKX SNP Missense_Mutation 23 3573373 C A 27 70 LUAD TCGA-05-4396 PRKX SNP Missense_Mutation 23 3592654 G T 39 85 GBM TCGA-26-5136 PRKX SNP Missense_Mutation 23 3573336 G C 33 52 LUSC TCGA-33-4583 PRKX SNP Missense_Mutation 23 3544547 G A 39 82 LUSC TCGA-66-2773 PRKX SNP Silent 23 3573384 G A 45 59 LUAD TCGA-75-6211 PRKX SNP Missense_Mutation 23 3592712 G T 35 85 CRC TCGA-AA-3947 PRKX SNP Missense_Mutation 23 3592724 C T 31 86 CRC TCGA-AA-3984 PRKX SNP Missense_Mutation 23 3533927 C T 26 83 UCEC TCGA-AP-A056 PRKX SNP Missense_Mutation 23 3530318 C T 31 83 UCEC TCGA-AX-A0J1 PRKX SNP Silent 23 3530337 G A 40 49 BRCA TCGA-B6-A0X1 PRKX SNP Missense_Mutation 23 3592796 A C 2 79 BRCA TCGA-BH-A201 PRKX SNP Missense_Mutation 23 3544506 G T 33 69 UCEC TCGA-BS-A0UJ PRKX SNP Missense_Mutation 23 3592717 A G 12 79 UCEC TCGA-D1-A103 PRKX SNP Silent 23 3559907 G A 37 53 UCEC TCGA-D1-A167 PRKX SNP Silent 23 3530280 G A 39 22 UCEC TCGA-D1-A17Q PRKX SNP Missense_Mutation 23 3559972 C T 31 86 HNSC TCGA-DQ-5631 PRKX SNP Silent 23 3573309 G A 37 39 HNSC TCGA-HD-7229 PRKX SNP Missense_Mutation 23 3592789 C G 23 86