Assay Details
Target Gene Details
Entrez Gene ID: | 170712 |
Gene Name: | cytochrome c oxidase subunit 7B2 |
Gene Aliases: |
- |
Location: |
Chr.4:46734827-46909266 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
COX7B2 | NM_130902.2 | NP_570972.2 | ||
XM_005248056.4 | XP_005248113.1 | |||
XM_011513630.2 | XP_011511932.1 | |||
XM_011513631.2 | XP_011511933.1 | |||
XM_011513632.2 | XP_011511934.1 | |||
XM_011513633.2 | XP_011511935.1 | |||
XM_011513634.2 | XP_011511936.1 | |||
XM_011513635.2 | XP_011511937.1 | |||
XM_011513636.1 | XP_011511938.1 | |||
XM_011513637.2 | XP_011511939.1 | |||
XM_011513638.2 | XP_011511940.1 | |||
AF125109.1 | AAL75946.1 | |||
BC035923.1 | AAH35923.1 | |||
BC107855.1 | AAI07856.1 | |||
DB447854.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv594117 | Chr.4:46633150 - 46844025 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs116348321] 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:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)