NM_004633.4:c.932T>C

HGVS Expressions

  • NM_004633.4:c.932T>C
  • NP_004624.1:p.Ile311Thr
  • NC_000002.12:g.102026155T>C
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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
249100.11Lebanon1Uncertain SignificanceUmar et al, 2020
249100.17Lebanon1Uncertain SignificanceUmar et al, 2020
249100.24Lebanon1Uncertain SignificanceFamilial Mediterranean FeverUmar et al, 2020
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