NM_007294.4:c.1772T>C

HGVS Expressions

  • NG_005905.2:g.124225T>C
  • NM_007294.4:c.1772T>C
  • NP_009225.1:p.Ile591Thr
  • NC_000017.11:g.43093759A>G

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

54345

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.74LebanonUncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage II lobular carcinoma
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