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 Gene Details
Entrez Gene ID: | 10875 |
Gene Name: | fibrinogen like 2 |
Gene Aliases: |
T49, pT49 |
Location: |
Chr.7:77193371-77199833 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FGL2 | NM_006682.2 | 2 | 3867 | NP_006673.1 |
| CR626993.1 | 1 | 602 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv526097 | Chr.7:76803016 - 77197121 on Build GRCh38 | Gain |
|
| nsv428174 | Chr.7:76305019 - 77220062 on Build GRCh38 | Gain |
|
| nsv1034874 | Chr.7:76977978 - 77212740 on Build GRCh38 | Loss |
|
| nsv951363 | Chr.7:77186884 - 77200783 on Build GRCh38 | Duplication |
|
| esv34102 | Chr.7:77003836 - 77225180 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs79313675] 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