Assay Details
Target Gene Details
Entrez Gene ID: | 389941 |
Gene Name: | complement C1q like 3 |
Gene Aliases: |
C1QTNF13, C1ql, CTRP13, K100 |
Location: |
Chr.10:16513743-16522005 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
C1QL3 | NM_001010908.1 | NP_001010908.1 | ||
BC127716.1 | ||||
BC127717.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831797 | Chr.10:16514510 - 16690309 on Build GRCh38 | Loss | PTER C1QL3 RSU1 |
nsv1046833 | Chr.10:16385108 - 16530259 on Build GRCh38 | Gain | PTER C1QL3 |
More Information
Additional Information:
For this assay, SNP(s) [rs73595371] 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 |