NM_007294.4:c.5153-66T>A

HGVS Expressions

  • NG_005905.2:g.154545T>A
  • NM_007294.4:c.5153-66T>A

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43063439

Variant Type

Substitution

Clinvar

125789

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.20LebanonBreast CancerJalkh et al, 2012 44 unrelated patients with breast cancer
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