NM_000106.6:c.1012G>A

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  2. NM_000106.6:c.1012G>A

HGVS Expressions

  • NG_008376.3:g.7384G>A
  • NM_000106.6:c.1012G>A
  • NP_000097.3:p.Val338Met
  • NC_000022.11:g.42127608C>T

Associated Genes

Cytochrome P450, Subfamily IID, Polypeptide 6
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Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

59421388

Clinvar

598263

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608902.G.1.4United Arab EmiratesDrug ResponseDrug Metabolism, Poor, CYP2D6-RelatedQumsieh et al. 2011 Subset of 608902.G.1.1. Number of subjec...
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Contributors

  • Pratibha Nair: 08.09.2021

Edit History

  • Sami Bizzari: 24.01.2024
  • Pratibha Nair: 08.09.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.