Assay Details
Target Gene Details
Entrez Gene ID: | 57639 |
Gene Name: | coiled-coil domain containing 146 |
Gene Aliases: |
- |
Location: |
Chr.7:77122617-77295204 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CCDC146 | NM_020879.2 | NP_065930.2 | ||
| AK056542.1 | BAB71211.1 | |||
| AK292491.1 | ||||
| BC036053.1 | AAH36053.1 | |||
| BX649000.1 | ||||
| DB099681.1 | ||||
| HM370402.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv34102 | Chr.7:77003836 - 77225180 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs77056943] 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