NM_007294.4:c.466C>A

HGVS Expressions

  • NG_005905.2:g.118128C>A
  • NM_007294.4:c.466C>A
  • NP_009225.1:p.Leu156Ile

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43099856

Variant Type

Substitution

Clinvar

233464

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.2LebanonBreast CancerJalkh et al, 2012
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