NM_021075.4:c.552dup

HGVS Expressions

  • NG_042281.1:g.15297dup
  • NM_021075.4:c.552dup
  • NP_066553.3:p.Leu185AlafsTer11
  • NC_000021.9:g.42903564dup
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CTGA Clinical Significance

Benign

Variant Type

Duplication

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608776.1United Arab Emirates2BenignAl-Shamsi et al. 2016
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