Genomic Map
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Target Gene Details
Entrez Gene ID: | 6747 |
Gene Name: | signal sequence receptor subunit 3 |
Gene Aliases: |
TRAPG |
Location: |
Chr.3:156539553-156555200 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SSR3 | NM_001308197.1 | 5 | 2712 | NP_001295126.1 |
| NM_001308204.1 | 5 | 2538 | NP_001295133.1 | |
| NM_001308205.1 | 5 | 2562 | NP_001295134.1 | |
| NM_007107.4 | 5 | 2673 | NP_009038.1 | |
| AF110647.1 | 5 | 2618 | AAD48587.1 | |
| CX786292.1 | 1 | 73 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv829764 | Chr.3:156457035 - 156629985 on Build GRCh38 | Gain |
 KCNAB1
SSR3
|
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Additional Information:
For this assay, SNP(s) [rs200179482] 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
DGV Variation
|
Gene Ontology Categories:
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