NM_007294.4:c.2082C>T

HGVS Expressions

  • NG_005905.2:g.124535C>T
  • NM_007294.4:c.2082C>T
  • NP_009225.1:p.Ser694=

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43093449

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1799949

Clinvar

125536

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.24LebanonBenignBreast CancerJalkh et al, 2012 47 unrelated patients with breast cancer
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