NM_001283009.1:c.173C>G

HGVS Expressions

  • NG_033901.1:g.8559C>G
  • NM_001283009.1:c.173C>G
  • NP_001269938.1:p.Ala58Gly
  • NC_000020.11:g.63661368C>G
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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
219700.74United Arab Emirates1Uncertain SignificanceAlsamri et al. 2020
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