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 47 |
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 | |||
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 |
![]() ![]() ![]() ![]() |
nsv1160106 | Chr.13:41576436 - 41650277 on Build GRCh38 | Deletion |
![]() |
nsv455865 | Chr.13:41522908 - 41951740 on Build GRCh38 | Gain |
![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs73464917] 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: |
![]() ![]() ![]() ![]() |
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)