NM_000059.4:c.5645C>A

HGVS Expressions

  • NG_012772.3:g.29521C>A
  • NM_000059.4:c.5645C>A
  • NP_000050.3:p.Ser1882Ter
  • NC_000013.11:g.32340000C>A

Associated Genes

BRCA2 Gene
Back to search Result
Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Clinvar

37984

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
612555.4United Arab EmiratesLikely PathogenicBreast-Ovarian Cancer, Familial, Susceptibility To, 2Al-Ali et al. 2023
© CAGS 2024. All rights reserved.