Product Details

Primer Sequences
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Primer Chromosome Location
Chr.8: 31066983-31067107 on Build GRCh38
Format
Each primer will be delivered in a single tube, dried-down
Quick Reference Guide
Primer Designer™ Tool Quick Reference
Ampliseq ID's

Gene Details

Gene Symbol
WRN
Entrez Gene ID
7486
Gene Name
Werner syndrome RecQ like helicase
Gene Aliases
RECQ3, RECQL2, RECQL3
UniGene
Hs.632050
Gene Chromosome Location
Chr.8: 31033262-31173761 on Build GRCh38
Transcripts
NM_000553.4 XM_011544639.2

Cosmic Detail

Cosmic ID Mutation AA Transcript Location
7254536 c.565C>A p.L189I Chr.8: 31067093-31067093 on Build GRCh38
5976821 c.548A>G p.H183R Chr.8: 31067076-31067076 on Build GRCh38
6485416 c.505-2A>T p.? Chr.8: 31067031-31067031 on Build GRCh38
6823362 c.558T>C p.G186G Chr.8: 31067086-31067086 on Build GRCh38
3785967 c.521C>T p.T174I Chr.8: 31067049-31067049 on Build GRCh38

SNP Detail

SNP ID Chromosome Location
rs772637078 Chr.8: 31067077-31067077 on Build GRCh38
rs777437332 Chr.8: 31067043-31067043 on Build GRCh38
rs576837409 Chr.8: 31067029-31067029 on Build GRCh38
rs746210769 Chr.8: 31067076-31067076 on Build GRCh38
rs748976035 Chr.8: 31067055-31067055 on Build GRCh38
rs780927874 Chr.8: 31067025-31067025 on Build GRCh38
rs765499420 Chr.8: 31067015-31067016 on Build GRCh38
rs752830087 Chr.8: 31067052-31067052 on Build GRCh38
rs770545798 Chr.8: 31067064-31067064 on Build GRCh38
rs1800389 Chr.8: 31067041-31067041 on Build GRCh38
rs367991517 Chr.8: 31067042-31067042 on Build GRCh38
rs774751582 Chr.8: 31067070-31067070 on Build GRCh38

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