Assay Details
Target Gene Details
Entrez Gene ID: | 26658 |
Gene Name: | olfactory receptor family 7 subfamily C member 2 |
Gene Aliases: |
CIT-HSP-87M17, OR19-18, OR7C3 |
Location: |
Chr.19:14941489-14942448 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
OR7C2 | NM_012377.1 | 1 | 891 | NP_036509.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1063744 | Chr.19:14906349 - 14999775 on Build GRCh38 | Gain | SLC1A6 OR7C2 |
nsv510756 | Chr.19:14926456 - 14952143 on Build GRCh38 | Deletion | SLC1A6 OR7C2 |
nsv2424 | Chr.19:14934808 - 14978815 on Build GRCh38 | Deletion | SLC1A6 OR7C2 |
esv3893167 | Chr.19:14610447 - 14950404 on Build GRCh38 | Gain | SNORA104 OR7A17 CLEC17A OR7C1 ADGRE2 ADGRE3 ZNF333 SLC1A6 OR7A10 OR7A5 OR7C2 |
More Information
Additional Information:
For this assay, SNP(s) [rs74951519] 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 |