Assay Details
Target Gene Details
Entrez Gene ID: | 23078 |
Gene Name: | von Willebrand factor A domain containing 8 |
Gene Aliases: |
KIAA0564 |
Location: |
Chr.13:41566825-41961111 on Build GRCh38 |
Assay Gene Location: | Within Intron 51 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
VWA8 | NM_015058.1 | NP_055873.1 | ||
XM_006719791.3 | XP_006719854.1 | |||
XM_017020469.1 | XP_016875958.1 | |||
XM_017020472.1 | XP_016875961.1 | |||
XM_017020473.1 | XP_016875962.1 | |||
AB011136.1 | BAA25490.1 | |||
AK025432.1 | ||||
AK308568.1 | ||||
BC131802.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv1634n100 | Chr.13:41408612 - 41936985 on Build GRCh38 | Gain | VWA8 OR7E37P MIR5006 RGCC |
nsv561539 | Chr.13:41522908 - 41951740 on Build GRCh38 | Gain | VWA8 MIR5006 |
More Information
Additional Information:
For this assay, SNP(s) [rs112887589] 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 Intronic Non-exonic DGV Variation |