NM_000350.3:c.3623T>G

HGVS Expressions

  • NG_009073.1:g.88815T>G
  • NM_000350.3:c.3623T>G
  • NP_000341.2:p.Leu1208Arg
  • NC_000001.11:g.94037335A>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
248200.G.3United Arab Emirates4Likely PathogenicStargardt Disease 1Khan. 2020 2 related patients (cousins) with childh...
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