NM_000059.4:c.1365A>G

HGVS Expressions

  • NG_012772.3:g.22364A>G
  • NM_000059.4:c.1365A>G
  • NP_000050.3:p.Ser455=

Associated Genes

BRCA2 Gene
Back to search Result
Genomic Location

chr13:32332843

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1801439

Clinvar

125943

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.32LebanonBenignBreast CancerJalkh et al, 2012 6 unrelated patients with breast cancer
© CAGS 2024. All rights reserved.