NM_006420.3:c.2776C>T

HGVS Expressions

  • NG_011490.2:g.72909C>T
  • NM_006420.3:c.2776C>T
  • NP_006411.2:p.Arg926Ter
  • NC_000020.11:g.48989646C>T
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CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608097.1.1Egypt2PathogenicPeriventricular Heterotopia With Microcephaly, Autosomal RecessiveMakrythanasis et al. 2014
608097.1.2Egypt2PathogenicPeriventricular Heterotopia With Microcephaly, Autosomal RecessiveMakrythanasis et al. 2014 Second-cousin of 608097.1.1
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