NM_007294.4:c.3548A>G

HGVS Expressions

  • NG_005905.2:g.126001A>G
  • NM_007294.4:c.3548A>G
  • NP_009225.1:p.Lys1183Arg

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43091983

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

16942

Clinvar

41818

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.17LebanonBenignBreast CancerJalkh et al, 2012 43 unrelated patients with breast cancer
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