NM_003978.5:c.203C>A

HGVS Expressions

  • NG_007526.1:g.28399C>A
  • NM_003978.5:c.203C>A
  • NP_003969.2:p.Thr68Lys
  • NC_000015.10:g.77018522C>A
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.29Lebanon1Uncertain SignificanceFamilial Mediterranean FeverUmar et al, 2020
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