NM_001098668.4:c.542A>G

HGVS Expressions

  • NG_013046.1:g.7994A>G
  • NM_001098668.4:c.542A>G
  • NP_001092138.1:p.Tyr181Cys
  • NC_000010.11:g.79557414T>C
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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
178500.5United Arab Emirates1Likely PathogenicInterstitial Lung Disease 2Alsamri et al. 2021
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