Assay Details
Target Gene Details
Entrez Gene ID: | 389136 |
Gene Name: | vestigial like family member 3 |
Gene Aliases: |
VGL-3, VGL3 |
Location: |
Chr.3:86937969-86991293 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
VGLL3 | NM_001320494.1 | NP_001307423.1 | ||
NM_016206.3 | NP_057290.2 | |||
XM_006713138.3 | XP_006713201.1 | |||
AF099505.1 | AAF00091.1 | |||
AK095826.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv527279 | Chr.3:86796784 - 87814130 on Build GRCh38 | Gain | MIR4795 HTR1F VGLL3 CHMP2B LINC00506 POU1F1 |
esv3596879 | Chr.3:86908792 - 86940260 on Build GRCh38 | Loss | VGLL3 |
nsv519148 | Chr.3:86781927 - 86945974 on Build GRCh38 | Gain | VGLL3 |
More Information
Additional Information:
For this assay, SNP(s) [rs114748581] 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 |