Assay Details
Target Gene Details
Entrez Gene ID: | 2778 |
Gene Name: | GNAS complex locus |
Gene Aliases: |
AHO, C20orf45, GNAS1, GPSA, GSA, GSP, NESP, POH, SCG6, SgVI |
Location: |
Chr.20:58839681-58911196 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GNAS | NM_001309861.1 | NP_001296790.1 | ||
NM_016592.3 | NP_057676.1 | |||
XM_017027815.1 | XP_016883304.1 | |||
XM_017027821.1 | XP_016883310.1 | |||
XM_017027822.1 | XP_016883311.1 | |||
AF105253.1 | AAF63226.1 | |||
AK122771.1 | ||||
AK315874.1 | ||||
CN273438.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv459031 | Chr.20:58846572 - 58904078 on Build GRCh38 | Loss | GNAS LOC101927932 GNAS-AS1 |
nsv828763 | Chr.20:58839788 - 58908828 on Build GRCh38 | Loss | GNAS LOC101927932 GNAS-AS1 |
More Information
Additional Information:
For this assay, SNP(s) [rs79020647] 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 |