NM_000089.4:c.2873G>A

HGVS Expressions

  • NG_007405.1:g.36227G>A
  • NM_000089.4:c.2873G>A
  • NP_000080.2:p.Gly958Asp
  • NC_000007.14:g.94425787G>A
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CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
166220.2Egypt1NAPathogenicOsteogenesis Imperfecta, Type IVMaddirevula et al. 2018 De novo mutation
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