Assay Details
Target Gene Details
Entrez Gene ID: | 8110 |
Gene Name: | double PHD fingers 3 |
Gene Aliases: |
BAF45C, CERD4 |
Location: |
Chr.14:72609032-72894116 on Build GRCh38 |
Assay Gene Location: | Within Exon 19 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DPF3 | XM_017021670.1 | 11 | 3645 | XP_016877159.1 |
AK024141.1 | BAB14838.1 |
Target Gene Details
Entrez Gene ID: | 9628 |
Gene Name: | regulator of G-protein signaling 6 |
Gene Aliases: |
GAP |
Location: |
Chr.14:71932100-72632478 on Build GRCh38 |
Assay Gene Location: | Within Intron 34 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RGS6 | XM_017021825.1 | XP_016877314.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv456338 | Chr.14:72603947 - 72656563 on Build GRCh38 | Loss | RGS6 DPF3 |
nsv565046 | Chr.14:72595825 - 72622005 on Build GRCh38 | Loss | RGS6 DPF3 |
esv3892558 | Chr.14:72255497 - 72756402 on Build GRCh38 | Gain | RGS6 DPF3 MIR7843 |
More Information
Additional Information:
For this assay, SNP(s) [rs78914547] 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 Intronic Non-exonic DGV Variation |