Assay Details
Target Gene Details
Entrez Gene ID: | 148641 |
Gene Name: | solute carrier family 35 member F3 |
Gene Aliases: |
- |
Location: |
Chr.1:233904712-234324518 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC35F3 | NM_173508.3 | NP_775779.1 | ||
AK095031.1 | BAC04479.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832892 | Chr.1:233784001 - 233964848 on Build GRCh38 | Loss | SLC35F3 |
More Information
Additional Information:
For this assay, SNP(s) [rs200053843] 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 |