NM_000773.3:c.-1295G>C

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HGVS Expressions

  • NG_008383.1:g.3739G>C
  • NM_000773.3:c.-1295G>C
  • NC_000010.11:g.133526101G>C

Associated Genes

Cytochrome P450, Subfamily IIE
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CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

3813867

Clinvar

132775

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
124040.G.1Lebanon0.015Drug ResponseOssaily and Zgheib. 2014
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Contributors

  • Pratibha Nair: 29.06.2020

Edit History

  • Asha Deepthi: 19.01.2021
  • Pratibha Nair: 29.06.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.