NM_203314.3:c.668G>A

HGVS Expressions

  • NM_203314.3:c.668G>A
  • NP_976059.1:p.Arg223His
  • NC_000003.12:g.197512259C>T
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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
603063.1.1Syria2Uncertain SignificanceReuter et al. 2017 Authors classified this gene variant as ...
603063.1.2Syria2Uncertain SignificanceReuter et al. 2017 Relative of 603063.1.1
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