NM_003235.5:c.4930C>G

HGVS Expressions

  • NG_015832.1:g.71715C>G
  • NM_003235.5:c.4930C>G
  • NP_003226.4:p.Gln1644Glu
  • NC_000008.11:g.132933674C>G

Associated Genes

Thyroglobulin
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Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
274500.3United Arab Emirates1Nicholas et al. 2016
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