NM_001673.5:c.224A>T

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HGVS Expressions

  • NG_033870.2:g.64630A>T
  • NM_001673.5:c.224A>T
  • NP_001664.3:p.Asn75Ile
  • NC_000007.14:g.97868933T>A

Associated Genes

Asparagine Synthetase
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Clinvar Clinical Significance

Likely Pathogenic, Uncertain Significance

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

dbSNP

747624770

Clinvar

1029362

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615574.6Saudi Arabia2PathogenicAsparagine Synthetase DeficiencyShaheen et al. 2019
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Contributors

  • Sayeeda Hana: 24.01.2022

Edit History

  • Sayeeda Hana: 25.01.2022
  • Sayeeda Hana: 24.01.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.