NM_000106.6:c.836T>A

HGVS Expressions

  • NG_008376.3:g.6811T>A
  • NM_000106.6:c.836T>A
  • NP_000097.3:p.Met279Lys
  • NC_000022.11:g.42128181A>T
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Clinvar Clinical Significance

Drug Response

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

1135828

Clinvar

828887

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608902.G.1.3United Arab EmiratesDrug ResponseDrug Metabolism, Poor, CYP2D6-RelatedQumsieh et al. 2011 Subset of 608902.G.1.1. Number of subjec...
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