Assay Details
Target Gene Details
Entrez Gene ID: | 101927347 |
Gene Name: | GRM7 antisense RNA 3 |
Gene Aliases: |
- |
Location: |
Chr.3:6632358-6805449 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GRM7-AS3 | NR_110123.1 | |||
BX113348.1 | ||||
DB447952.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1009743 | Chr.3:6640281 - 6683568 on Build GRCh38 | Loss | GRM7-AS3 |
nsv589567 | Chr.3:6638624 - 6726304 on Build GRCh38 | Loss | GRM7-AS3 LOC105376944 |
dgv4673n100 | Chr.3:6648983 - 6782709 on Build GRCh38 | Gain | GRM7-AS3 LOC105376944 |
esv3893652 | Chr.3:6500395 - 6763100 on Build GRCh38 | Loss | GRM7-AS3 LOC105376944 |
More Information
Additional Information:
For this assay, SNP(s) [rs202075462] 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 |