Assay Details
Target Gene Details
Entrez Gene ID: | 10418 |
Gene Name: | spondin 1 |
Gene Aliases: |
VSGP/F-spondin, f-spondin |
Location: |
Chr.11:13962637-14268133 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SPON1 | NM_006108.3 | NP_006099.2 | ||
AB051390.1 | BAB18461.1 | |||
AK074803.1 | BAC11217.1 | |||
AK291780.1 | ||||
BC136513.1 | ||||
BC136563.1 | ||||
DA965056.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3625418 | Chr.11:13962063 - 14027140 on Build GRCh38 | Loss | SPON1 |
esv2668036 | Chr.11:13962055 - 14027138 on Build GRCh38 | Deletion | SPON1 |
More Information
Additional Information:
For this assay, SNP(s) [rs73418492] 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 |