ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62532 PRSS3 SNP Synonymous 9 33798019 C T 22 68 LUAD LUAD-S01345 PRSS3 SNP Missense_Mutation 9 33797870 G A 41 89 MEL MEL-JWCI-WGS-25 PRSS3 SNP Missense_Mutation 9 33796745 G A 39 67 GBM TCGA-06-0644 PRSS3 SNP Silent 9 33798043 C T 26 50 OV TCGA-13-0762 PRSS3 SNP Missense_Mutation 9 33799033 C T 32 89 LUSC TCGA-18-3406 PRSS3 SNP Missense_Mutation 9 33797929 G T 43 50 LUAD TCGA-38-4625 PRSS3 SNP Missense_Mutation 9 33797891 A C 5 47 LUSC TCGA-39-5024 PRSS3 SNP Missense_Mutation 9 33796728 C G 32 48 CRC TCGA-AA-A00K PRSS3 SNP Missense_Mutation 9 33799155 G T 41 43 CRC TCGA-AA-A01Q PRSS3 SNP Missense_Mutation 9 33796644 C T 28 75 AML TCGA-AB-2839 PRSS3 SNP Missense_Mutation 9 33795590 C T 24 61 UCEC TCGA-AP-A059 PRSS3 SNP Silent 9 33795589 C T 30 60 UCEC TCGA-AP-A059 PRSS3 SNP Missense_Mutation 9 33798495 G T 33 61 KIRC TCGA-B0-4710 PRSS3 DEL Frame_Shift_Del 9 33799094 T - 59 62 UCEC TCGA-B5-A0JY PRSS3 SNP Missense_Mutation 9 33797863 A C 3 36 KIRC TCGA-B8-4622 PRSS3 SNP Missense_Mutation 9 33798574 G A 34 71 KIRC TCGA-CJ-4644 PRSS3 SNP Splice_site 9 33798079 T C 59 50 KIRC TCGA-CJ-4892 PRSS3 SNP Silent 9 33797833 C T 30 89 HNSC TCGA-CR-7395 PRSS3 SNP Missense_Mutation 9 33798053 G A 39 89 HNSC TCGA-CR-7402 PRSS3 SNP Silent 9 33799064 C G 30 54 HNSC TCGA-CV-6961 PRSS3 SNP Silent 9 33796723 G A 45 66 BRCA TCGA-E9-A1R7 PRSS3 SNP Missense_Mutation 9 33797959 C G 29 62