Product Details

Assay Reference Genome
Location

Chr.8:31072457 on build GRCh38

Cytoband

8p12

Species

Homo sapiens

Variation Type

Copy Number

Additional Information

For this assay, SNP(s) [rs75027493] 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

7486

Gene Symbol

WRN

Gene Name

Werner syndrome RecQ like helicase

Gene Aliases

RECQ3, RECQL2, RECQL3

Location

Chr.8:31033262-31173761 on build GRCh38

Assay Gene Location

Within Intron 7

Gene Symbol	Transcript Accession	Exon Location	Assay Location	Protein ID
WRN	NM_000553.4			NP_000544.2
	XM_011544639.2			XP_011542941.1
	AF091214.1			AAC63361.1
	AY818673.1

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