Product Details

Assay Reference Genome
Location

Chr.2:9603157 on build GRCh38
Cytoband
2p25.1
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs76963083] 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.

Target Gene Details

Entrez Gene ID
10971
Gene Symbol
YWHAQ
Gene Name
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta
Gene Aliases
14-3-3, 1C5, HS1
Location
Chr.2:9583967-9631055 on build GRCh38
Assay Gene Location
Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
YWHAQ NM_006826.3 NP_006817.1
AF070556.1 AAC28640.1
AK297624.1
AK302208.1
AK309462.1
AK316158.1
BC050601.1 AAH50601.1
BC056867.1 AAH56867.1
BC093019.1 AAH93019.1
BT020014.1 AAV38817.1
X56468.1 CAA39840.1
X57347.1 CAA40622.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv580915 Chr2:9168019 - 9704049 on Build GRCh38 Gain IAH1 ADAM17 YWHAQ ASAP2 LOC105373418 LOC101926982 CPSF3 ITGB1BP1

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