Product Details

Primer Sequences
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Primer Chromosome Location
Chr.8: 31064921-31065052 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
6430149 c.365A>T p.Q122L Chr.8: 31064924-31064924 on Build GRCh38
5611175 c.406G>T p.A136S Chr.8: 31064965-31064965 on Build GRCh38
1099219 c.460A>G p.K154E Chr.8: 31065019-31065019 on Build GRCh38
6253918 c.412G>T p.V138L Chr.8: 31064971-31064971 on Build GRCh38
4741462 c.486A>T p.T162T Chr.8: 31065045-31065045 on Build GRCh38

SNP Detail

SNP ID Chromosome Location
rs267607008 Chr.8: 31064962-31064962 on Build GRCh38
rs773697397 Chr.8: 31064988-31064988 on Build GRCh38
rs766887542 Chr.8: 31064991-31064991 on Build GRCh38
rs548061402 Chr.8: 31064979-31064979 on Build GRCh38
rs61761625 Chr.8: 31065005-31065005 on Build GRCh38
rs752693894 Chr.8: 31065004-31065004 on Build GRCh38
rs867641943 Chr.8: 31064954-31064954 on Build GRCh38
rs17847582 Chr.8: 31064965-31064965 on Build GRCh38
rs752014453 Chr.8: 31064995-31064995 on Build GRCh38
rs758208189 Chr.8: 31065025-31065025 on Build GRCh38
rs771444804 Chr.8: 31064990-31064990 on Build GRCh38
rs951969651 Chr.8: 31064953-31064953 on Build GRCh38
rs200456571 Chr.8: 31065011-31065011 on Build GRCh38
rs769317785 Chr.8: 31064980-31064980 on Build GRCh38
rs925567153 Chr.8: 31065003-31065003 on Build GRCh38
rs767673195 Chr.8: 31065001-31065001 on Build GRCh38
rs878854139 Chr.8: 31064989-31064989 on Build GRCh38
rs587778753 Chr.8: 31065002-31065002 on Build GRCh38
rs916722009 Chr.8: 31065016-31065016 on Build GRCh38

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