NM_000769.4:c.636G>A

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  2. 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

Associated Genes

Cytochrome P450, Subfamily IIC, Polypeptide 19
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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

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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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Contributors

  • Pratibha Nair: 31.05.2020

Edit History

  • Pratibha Nair: 31.05.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.