Assay Details
Target Gene Details
Entrez Gene ID: | 166752 |
Gene Name: | FRAS1 related extracellular matrix 3 |
Gene Aliases: |
- |
Location: |
Chr.4:143577407-143700675 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FREM3 | NM_001168235.1 | NP_001161707.1 | ||
DR731220.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2759288 | Chr.4:143427140 - 144210439 on Build GRCh38 | Gain+Loss | GYPE LOC101927636 GAB1 LOC105377458 SMARCA5 GUSBP5 SMARCA5-AS1 FREM3 GYPB GYPA |
nsv830103 | Chr.4:143472245 - 143631892 on Build GRCh38 | Loss | GAB1 SMARCA5 GUSBP5 SMARCA5-AS1 FREM3 |
esv3894047 | Chr.4:143572032 - 144009062 on Build GRCh38 | Gain | GYPE LOC101927636 LOC105377458 FREM3 GYPB |
More Information
Additional Information:
For this assay, SNP(s) [rs80077470] 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 |