NM_007294.4:c.1845T>C

HGVS Expressions

  • NG_005905.2:g.124298T>C
  • NM_007294.4:c.1845T>C
  • NP_009225.1:p.Ser615=
  • NC_000017.11:g.43093686A>G

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Likely Benign

Variant Type

Substitution

Clinvar

1551757

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.8LebanonBreast CancerJalkh et al, 2012 2 unrelated patients with breast cancer
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