NM_001715.3:c.530A>G

HGVS Expressions

  • NG_023543.2:g.65789A>G
  • NM_001715.3:c.530A>G
  • NP_001706.2:p.Tyr177Cys
  • NC_000008.11:g.11554800A>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
125853.23Qatar1Uncertain SignificanceType 2 Diabetes MellitusElashi et al. 2022
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