Assay Details
Target Gene Details
Entrez Gene ID: | 2788 |
Gene Name: | G protein subunit gamma 7 |
Gene Aliases: |
- |
Location: |
Chr.19:2511219-2702748 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GNG7 | NM_052847.2 | NP_443079.1 | ||
XM_017026606.1 | XP_016882095.1 | |||
AB010414.1 | BAA28348.1 | |||
AF493874.1 | AAM12588.1 | |||
AK311750.1 | ||||
BC014466.1 | AAH14466.1 | |||
BC053630.1 | AAH53630.1 | |||
DA106844.1 | ||||
DA247608.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1064930 | Chr.19:2380093 - 2592252 on Build GRCh38 | Gain | MIR7108 GADD45B TMPRSS9 LOC101929097 TIMM13 LOC101928602 GNG7 LMNB2 |
nsv509714 | Chr.19:2519629 - 2794403 on Build GRCh38 | Insertion | SLC39A3 THOP1 MIR7850 SGTA DIRAS1 GNG7 |
nsv953944 | Chr.19:2283702 - 2525802 on Build GRCh38 | Deletion | MIR7108 GADD45B TMPRSS9 LOC101929097 LINGO3 TIMM13 LOC101928602 GNG7 LMNB2 SPPL2B LSM7 |
More Information
Additional Information:
For this assay, SNP(s) [rs114492803] 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 |