Genomic Map
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Target Gene Details
Entrez Gene ID: | 83643 |
Gene Name: | coiled-coil domain containing 3 |
Gene Aliases: |
- |
Location: |
Chr.10:12896625-13099773 on Build GRCh38 |
Assay Gene Location: | Within Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CCDC3 | NM_001282658.1 | 7 | 2240 | NP_001269587.1 |
| NM_031455.3 | 3 | 1675 | NP_113643.1 | |
| AF190154.1 | 1 | 239 | AAQ13698.1 | |
| AK024578.1 | 1 | 658 | ||
| AK095792.1 | 7 | 2119 | ||
| AK123393.1 | 1 | 1816 | ||
| AK124195.1 | 1 | 1378 | ||
| AL136562.1 | 3 | 1591 | CAB66497.1 | |
| BC051334.1 | 3 | 1675 | AAH51334.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv971901 | Chr.10:12897050 - 12903518 on Build GRCh38 | Duplication |
 CCDC3
|
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Additional Information:
For this assay, SNP(s) [rs111965452] 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: |
Intragenic
Exonic
DGV Variation
|
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