NC_012920.1:m.10899A>G

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HGVS Expressions

  • YP_003024035.1:p.Asn47Ser
  • NC_012920.1:m.10899A>G

Associated Genes

Complex I, Subunit ND4
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1603223010

Clinvar

693323

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
603041.1.2TunisiaUncertain SignificanceAmmar et al. 2022 Brother of 603041.1.1. Phenotypic variab...
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Contributors

  • Asha Deepthi: 12.03.2025

Edit History

  • Asha Deepthi: 12.03.2025
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© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.