NM_003235.5:c.2276A>G

HGVS Expressions

  • NG_015832.1:g.26124A>G
  • NM_003235.5:c.2276A>G
  • NP_003226.4:p.Tyr759Cys
  • NC_000008.11:g.132888083A>G

Associated Genes

Thyroglobulin
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

1028099

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
274700.5.1Yemen1Uncertain SignificanceThyroid Dyshormonogenesis 3Nicholas et al. 2016 The authors noted that the genotype asce...
274700.5.2Yemen1Uncertain SignificanceThyroid Dyshormonogenesis 3Nicholas et al. 2016 Identical twin sibling of 274700.5.1
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