NM_007294.4:c.2077G>A

HGVS Expressions

  • NG_005905.2:g.124530G>A
  • NM_007294.4:c.2077G>A
  • NP_009225.1:p.Asp693Asn

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43093454

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

4986850

Clinvar

41808

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.13LebanonBenignBreast CancerJalkh et al, 2012 11 unrelated patients with breast cancer
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