Assay Details
Target Gene Details
Entrez Gene ID: | 353497 |
Gene Name: | DNA polymerase nu |
Gene Aliases: |
POL4P |
Location: |
Chr.4:2071958-2242164 on Build GRCh38 |
Assay Gene Location: | Within Intron 20 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
POLN | NM_181808.3 | NP_861524.2 | ||
AF044578.1 | AAD02338.1 | |||
AK131239.1 | BAD18421.1 | |||
AY136549.1 | AAN52116.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv291967 | Chr.4:2093111 - 2094363 on Build GRCh38 | Deletion | POLN |
esv2726835 | Chr.4:2019561 - 2959568 on Build GRCh38 | Deletion | ADD1 C4orf48 RNF4 ZFYVE28 NOP14-AS1 CFAP99 POLN HAUS3 FAM193A MFSD10 NAT8L NOP14 MXD4 TNIP2 MIR4800 SH3BP2 |
nsv4198 | Chr.4:2091126 - 2117779 on Build GRCh38 | Insertion | POLN |
More Information
Additional Information:
For this assay, SNP(s) [rs73799504] 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 |