Assay Details
Target Gene Details
Entrez Gene ID: | 56655 |
Gene Name: | DNA polymerase epsilon 4, accessory subunit |
Gene Aliases: |
YHHQ1, p12 |
Location: |
Chr.2:74958648-74969732 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
POLE4 | NM_019896.2 | NP_063949.2 | ||
AY034104.1 | ||||
BC031331.1 | AAH31331.1 | |||
CA454961.1 | ||||
CF529348.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv998145 | Chr.2:74969670 - 75241030 on Build GRCh38 | Loss |
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nsv834262 | Chr.2:74907892 - 75062072 on Build GRCh38 | Gain |
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esv2751900 | Chr.2:74722905 - 75041937 on Build GRCh38 | Gain |
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esv3575258 | Chr.2:74925505 - 75012498 on Build GRCh38 | Gain |
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dgv3872n100 | Chr.2:74917558 - 75013442 on Build GRCh38 | Gain |
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nsv526995 | Chr.2:74916957 - 75012498 on Build GRCh38 | Gain |
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nsv582217 | Chr.2:74736541 - 74993869 on Build GRCh38 | Gain |
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nsv1001495 | Chr.2:74598036 - 75093218 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs115218561] 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: |
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Panther Classification:
Gene Ontology Categories:
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