Assay Details
Target Gene Details
Entrez Gene ID: | 51426 |
Gene Name: | polymerase (DNA) kappa |
Gene Aliases: |
DINB1, DINP, POLQ |
Location: |
Chr.5:75511832-75602576 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
POLK | NM_016218.2 | NP_057302.1 | ||
XM_005248534.4 | XP_005248591.1 | |||
XM_011543464.2 | XP_011541766.1 | |||
XM_011543467.2 | XP_011541769.1 | |||
XM_017009561.1 | XP_016865050.1 | |||
XM_017009562.1 | XP_016865051.1 | |||
XM_017009564.1 | XP_016865053.1 | |||
AF163570.1 | AAF02540.1 | |||
AF194973.1 | AAF23270.1 | |||
AF318313.1 | AAN15781.1 | |||
AK091659.1 | BAC03714.1 | |||
AK314610.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv9883n54 | Chr.5:75521024 - 75535790 on Build GRCh38 | Loss | POLK |
More Information
Additional Information:
For this assay, SNP(s) [rs114634982] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |