NM_000769.4:c.636G>A

HGVS Expressions

  • NG_008384.3:g.22973G>A
  • NM_000769.4:c.636G>A
  • NP_000760.1:p.Trp212Ter
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Genomic Location

chr10:94780653

Clinvar Clinical Significance

Drug Response

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

4986893

Clinvar

16899

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
124020.1Lebanon10.003Drug ResponseDjaffar-Jureidini et al. 2011 Healthy Lebanese volunteer (from a study...
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