Assay Details
Target Gene Details
Entrez Gene ID: | 896 |
Gene Name: | cyclin D3 |
Gene Aliases: |
- |
Location: |
Chr.6:41934933-42048894 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CCND3 | NM_001136017.3 | NP_001129489.1 | ||
| NM_001136126.2 | NP_001129598.1 | |||
| NM_001287434.1 | NP_001274363.1 | |||
| XM_011514972.1 | XP_011513274.1 | |||
| AB209825.1 | BAD93062.1 | |||
| AK057206.1 | ||||
| AK096276.1 | ||||
| AK097856.1 | ||||
| AK303452.1 | ||||
| DA069566.1 | ||||
| DA999482.1 | ||||
| DB001987.1 | ||||
| DB104254.1 | ||||
| DB110132.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3576144 | Chr.6:41934304 - 41947781 on Build GRCh38 | Gain |
|
| nsv830646 | Chr.6:41916050 - 42096473 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs78915271] 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