Genomic Map
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Target Gene Details
Entrez Gene ID: | 55800 |
Gene Name: | sodium voltage-gated channel beta subunit 3 |
Gene Aliases: |
ATFB16, BRGDA7, HSA243396, SCNB3 |
Location: |
Chr.11:123629187-123654607 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SCN3B | NM_001040151.1 | NP_001035241.1 | ||
| NM_018400.3 | NP_060870.1 | |||
| XM_011542897.1 | XP_011541199.1 | |||
| AB032984.1 | ||||
| AJ243396.2 | CAB76825.1 | |||
| AK314513.1 | ||||
| AL136589.1 | CAB66524.1 | |||
| BC117282.1 | ||||
| BC126265.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2759868 | Chr.11:123408487 - 123674087 on Build GRCh38 | Loss |
 GRAMD1B
SCN3B
|
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Additional Information:
For this assay, SNP(s) [rs112754044,rs78564934] 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
|
Panther Classification:
Gene Ontology Categories:
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