NM_000059.4:c.5744C>T

HGVS Expressions

  • NG_012772.3:g.29620C>T
  • NM_000059.4:c.5744C>T
  • NP_000050.3:p.Thr1915Met

Associated Genes

BRCA2 Gene
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Genomic Location

chr13:32340099

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association, Benign

Variant Type

Substitution

dbSNP

4987117

Clinvar

41556

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.28LebanonAssociationBreast CancerJalkh et al, 2017 Patient 'B22' from family 3 in the publi...
114480.G.1.27LebanonBenignBreast CancerJalkh et al, 2012 2 unrelated patients with breast cancer
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