NM_004274.5:c.1874A>T

HGVS Expressions

  • NM_004274.5:c.1874A>T
  • NP_004265.3:p.Tyr625Phe
  • NC_000014.9:g.32546527A>T
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
604691.1Saudi Arabia1Likely PathogenicAKAP6-related Intellectual DisabilityMonies et al. 2017
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