Assay Details
Target Gene Details
Entrez Gene ID: | 140686 |
Gene Name: | WAP four-disulfide core domain 3 |
Gene Aliases: |
WAP14, dJ447F3.3 |
Location: |
Chr.20:45708860-45791908 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 9 - Exon 10 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
WFDC3 | XM_017027668.1 | XP_016883157.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv586081 | Chr.20:45573240 - 45747557 on Build GRCh38 | Loss | WFDC3 WFDC9 WFDC10B MIR3617 WFDC10A WFDC8 WFDC13 SPINT4 WFDC11 |
dgv1247e212 | Chr.20:45708247 - 45752976 on Build GRCh38 | Loss | WFDC3 WFDC10B WFDC13 SPINT4 |
esv2751915 | Chr.20:45708077 - 45749572 on Build GRCh38 | Loss | WFDC3 WFDC10B WFDC13 SPINT4 |
More Information
Additional Information:
For this assay, SNP(s) [rs75748348] 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 Non-exonic DGV Variation |