Assay Details
Target Gene Details
Entrez Gene ID: | 7485 |
Gene Name: | tryptophan rich basic protein |
Gene Aliases: |
CHD5, GET1 |
Location: |
Chr.21:39380287-39397889 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 1 - Exon 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
WRB | NM_001146218.1 | NP_001139690.1 | ||
NM_004627.4 | NP_004618.2 | |||
AK293113.1 | ||||
AK293866.1 | ||||
AK297186.1 | ||||
AK299144.1 | ||||
AK299245.1 | ||||
AK310268.1 | ||||
BC012415.1 | AAH12415.1 | |||
BC111393.1 | ||||
DB498697.1 | ||||
DB500750.1 | ||||
Y12478.1 | CAA73081.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv4433n100 | Chr.21:39369967 - 39418271 on Build GRCh38 | Gain | WRB WRB-SH3BGR LCA5L |
nsv1061454 | Chr.21:39386047 - 39893479 on Build GRCh38 | Gain | IGSF5 WRB PCP4 SH3BGR MIR6508 B3GALT5 B3GALT5-AS1 WRB-SH3BGR LCA5L |
More Information
Additional Information:
For this assay, SNP(s) [rs114798465] 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 |