NM_007294.4:c.4837A>G

HGVS Expressions

  • NG_005905.2:g.146907A>G
  • NM_007294.4:c.4837A>G
  • NP_009225.1:p.Ser1613Gly

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43071077

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1799966

Clinvar

41827

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.21LebanonBenignBreast CancerJalkh et al, 2012 45 unrelated patients with breast cancer
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