Assay Details
Target Gene Details
Entrez Gene ID: | 132200 |
Gene Name: | chromosome 3 open reading frame 49 |
Gene Aliases: |
- |
Location: |
Chr.3:63819365-63848636 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 1 - Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
C3orf49 | NR_026866.1 | |||
CD636567.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1008751 | Chr.3:63595517 - 63862172 on Build GRCh38 | Gain | SYNPR SNTN LOC100130345 THOC7-AS1 C3orf49 THOC7 |
More Information
Additional Information:
For this assay, SNP(s) [rs114391175] 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 Non-exonic DGV Variation |