NM_007294.4:c.2612C>T

HGVS Expressions

  • NG_005905.2:g.125065C>T
  • NM_007294.4:c.2612C>T
  • NP_009225.1:p.Pro871Leu

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43092919

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

799917

Clinvar

41812

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.23LebanonBenignBreast CancerJalkh et al, 2012 47 unrelated patients with breast cancer
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