Product Details

Primer Sequences
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Primer Chromosome Location
Chr.8: 31059202-31059366 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
286547 c.172G>A p.D58N Chr.8: 31059228-31059228 on Build GRCh38
5976820 c.201A>G p.E67E Chr.8: 31059257-31059257 on Build GRCh38
3648342 c.156C>T p.S52S Chr.8: 31059212-31059212 on Build GRCh38
2958605 c.171C>T p.Y57Y Chr.8: 31059227-31059227 on Build GRCh38
3382218 c.184T>C p.C62R Chr.8: 31059240-31059240 on Build GRCh38
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SNP Detail

SNP ID Chromosome Location
rs868599739 Chr.8: 31059266-31059266 on Build GRCh38
rs752345825 Chr.8: 31059238-31059238 on Build GRCh38
rs951805442 Chr.8: 31059335-31059335 on Build GRCh38
rs756575284 Chr.8: 31059253-31059253 on Build GRCh38
rs764589321 Chr.8: 31059257-31059257 on Build GRCh38
rs372306347 Chr.8: 31059277-31059277 on Build GRCh38
rs754208761 Chr.8: 31059270-31059270 on Build GRCh38
rs949684941 Chr.8: 31059311-31059311 on Build GRCh38
rs576906241 Chr.8: 31059326-31059326 on Build GRCh38
rs757761103 Chr.8: 31059273-31059273 on Build GRCh38
rs745937507 Chr.8: 31059305-31059305 on Build GRCh38
rs993090076 Chr.8: 31059315-31059315 on Build GRCh38
rs758424926 Chr.8: 31059309-31059309 on Build GRCh38
rs866361372 Chr.8: 31059307-31059307 on Build GRCh38
rs747102789 Chr.8: 31059322-31059322 on Build GRCh38
rs759022881 Chr.8: 31059232-31059232 on Build GRCh38
rs767288688 Chr.8: 31059234-31059234 on Build GRCh38
rs1046605858 Chr.8: 31059312-31059312 on Build GRCh38
rs1024495075 Chr.8: 31059262-31059262 on Build GRCh38

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