Assay Details
Target Gene Details
Entrez Gene ID: | 256987 |
Gene Name: | serine incorporator 5 |
Gene Aliases: |
C5orf12, TPO1 |
Location: |
Chr.5:80111227-80256082 on Build GRCh38 |
Assay Gene Location: | Within Intron 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SERINC5 | NM_001174071.2 | NP_001167542.1 | ||
NM_178276.6 | NP_840060.1 | |||
NR_126060.1 | ||||
NR_126061.1 | ||||
AF498273.1 | AAP06800.1 | |||
BC101280.2 | AAI01281.1 | |||
BC101283.2 | AAI01284.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv598744 | Chr.5:80092922 - 80127524 on Build GRCh38 | Gain | SERINC5 |
esv3605549 | Chr.5:80068073 - 80166801 on Build GRCh38 | Loss | THBS4 SERINC5 CTD-2201I18.1 |
More Information
Additional Information:
For this assay, SNP(s) [rs73125904,rs73125906] 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 |