NM_007294.4:c.4956G>A

HGVS Expressions

  • NG_005905.2:g.147026G>A
  • NM_007294.4:c.4956G>A
  • NP_009225.1:p.Met1652Ile

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43070958

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1799967

Clinvar

41830

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.6LebanonBenignBreast CancerJalkh et al, 2012 2 unrelated patients with breast cancer
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