ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-5V8LT PDCL3 SNP Splice_site 2 101183090 G C 47 43 LUAD LUAD-NYU408 PDCL3 SNP Nonsense_Mutation 2 101183061 G T 33 72 MEL MEL-JWCI-WGS-21 PDCL3 SNP Missense_Mutation 2 101183022 C T 22 54 MEL MEL-JWCI-WGS-39 PDCL3 SNP Silent 2 101183021 C T 22 51 LUAD TCGA-17-Z017 PDCL3 SNP Missense_Mutation 2 101183005 A G 1 74 LUAD TCGA-17-Z033 PDCL3 SNP Missense_Mutation 2 101188240 G A 42 99 LUSC TCGA-37-5819 PDCL3 SNP Splice_Site 2 101188050 A G 15 92 LUSC TCGA-43-6647 PDCL3 SNP Missense_Mutation 2 101188144 G T 46 98 LUSC TCGA-66-2789 PDCL3 SNP Silent 2 101185427 G T 47 50 LUSC TCGA-66-2789 PDCL3 SNP Nonsense_Mutation 2 101185428 G T 41 74 UCEC TCGA-A5-A0VQ PDCL3 SNP Missense_Mutation 2 101192915 G A 38 57 CRC TCGA-AA-3930 PDCL3 SNP Missense_Mutation 2 101186042 G A 39 74 CRC TCGA-AA-A022 PDCL3 SNP Missense_Mutation 2 101192826 G T 41 95 AML TCGA-AB-2948 PDCL3 INS Frame_Shift_Ins 2 101183018 - C 14 58 UCEC TCGA-AP-A051 PDCL3 SNP Missense_Mutation 2 101192845 G A 34 95 UCEC TCGA-AP-A059 PDCL3 SNP Nonsense_Mutation 2 101183040 G T 33 91 UCEC TCGA-B5-A11E PDCL3 SNP Missense_Mutation 2 101186042 G A 39 74 BRCA TCGA-BH-A1EV PDCL3 SNP Missense_Mutation 2 101188161 G C 45 99 UCEC TCGA-BS-A0UV PDCL3 SNP Missense_Mutation 2 101186103 G T 33 57 HNSC TCGA-CN-5374 PDCL3 SNP Silent 2 101188229 G A 47 62 HNSC TCGA-CQ-5331 PDCL3 SNP Missense_Mutation 2 101188255 G C 33 55 UCEC TCGA-D1-A16J PDCL3 SNP Missense_Mutation 2 101186146 G A 37 65 UCEC TCGA-D1-A16X PDCL3 SNP Splice_Site 2 101188051 G T 33 100 BLCA TCGA-DK-A3IN PDCL3 SNP Silent 2 101188178 G A 37 28