Assay Details
Target Gene Details
Entrez Gene ID: | 57017 |
Gene Name: | coenzyme Q9 |
Gene Aliases: |
C16orf49, COQ10D5 |
Location: |
Chr.16:57447425-57461275 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| COQ9 | NM_020312.3 | 9 | 1442 | NP_064708.1 |
| AF161444.1 | 9 | 1376 | AAF29004.1 | |
| AL136884.1 | 4 | 876 | CAB66818.2 | |
| BC001478.2 | 7 | 1017 | AAH01478.2 | |
| BC054340.1 | 9 | 1376 | AAH54340.2 | |
| BC064946.1 | 9 | 1377 | AAH64946.1 | |
| DB513313.1 | 1 | 196 | ||
| DB562540.1 | 1 | 178 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833245 | Chr.16:57434073 - 57584619 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs112075830] 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: |
|

Genomic Map