NM_025074.7:c.2128A>T

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HGVS Expressions

  • NG_015812.2:g.266408A>T
  • NM_025074.7:c.2128A>T
  • NP_079350.5:p.Ile710Leu
  • NC_000004.12:g.78318977A>T

Associated Genes

FRAS1 Gene
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

345512

Clinvar

349691

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
618982.2Arab2BenignCook et al. 2020 North African Arab
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Contributors

  • Pratibha Nair: 22.02.2022

Edit History

  • Pratibha Nair: 22.02.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.