Assay Details
Target Gene Details
Entrez Gene ID: | 6002 |
Gene Name: | regulator of G-protein signaling 12 |
Gene Aliases: |
- |
Location: |
Chr.4:3292978-3439913 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RGS12 | XM_006713905.1 | XP_006713968.1 | ||
XM_006713906.2 | XP_006713969.1 | |||
XM_011513543.2 | XP_011511845.1 | |||
XM_017008529.1 | 1 | 787 | XP_016864018.1 | |
XM_017008530.1 | XP_016864019.1 | |||
AK310999.1 | ||||
BC028154.1 | AAH28154.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv8923n54 | Chr.4:3281695 - 3340410 on Build GRCh38 | Loss | RGS12 |
More Information
Additional Information:
For this assay, SNP(s) [rs71608266] 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 Exonic DGV Variation |