Assay Details
Target Gene Details
Entrez Gene ID: | 23174 |
Gene Name: | zinc finger CCHC-type containing 14 |
Gene Aliases: |
BDG-29, BDG29 |
Location: |
Chr.16:87406246-87492948 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ZCCHC14 | NM_015144.2 | 12 | 2540 | NP_055959.1 |
| XM_005255858.3 | 12 | 2731 | XP_005255915.2 | |
| XM_017023082.1 | 12 | 3490 | XP_016878571.1 | |
| AB011151.2 | 12 | 2398 | BAA25505.2 | |
| AB030243.1 | 12 | 2548 | BAB83129.1 | |
| AK289682.1 | 12 | 2731 | ||
| AL117532.1 | 9 | 2163 | CAB55981.1 | |
| BC101478.1 | 12 | 2547 | AAI01479.1 | |
| CN352228.1 | 1 | 458 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833320 | Chr.16:87315844 - 87501226 on Build GRCh38 | Gain |
|
| nsv428330 | Chr.16:87336922 - 87633082 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73238672] 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: |
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Genomic Map