Assay Details
Target Gene Details
Entrez Gene ID: | 284677 |
Gene Name: | chromosome 1 open reading frame 204 |
Gene Aliases: |
- |
Location: |
Chr.1:159834474-159855347 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
C1orf204 | NM_001134233.1 | NP_001127705.1 | ||
AK096506.1 |
Target Gene Details
Entrez Gene ID: | 391123 |
Gene Name: | V-set and immunoglobulin domain containing 8 |
Gene Aliases: |
- |
Location: |
Chr.1:159854316-159862657 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
VSIG8 | NM_001013661.1 | 7 | 1759 | NP_001013683.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1005195 | Chr.1:159482969 - 159940547 on Build GRCh38 | Gain | SLAMF8 DUSP23 VSIG8 IGSF9 FCRL6 CRP CFAP45 C1orf204 APCS MIR4259 OR10J5 TAGLN2 |
More Information
Additional Information:
For this assay, SNP(s) [rs74535973] 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 |