NM_000059.4:c.262_263del

  1. Home
  2. NM_000059.4:c.262_263del

HGVS Expressions

  • NG_012772.3:g.8790CT[1]
  • NM_000059.4:c.262_263del
  • NP_000050.3:p.Leu88AlafsTer12
  • NC_000013.11:g.32319271_32319272del

Associated Genes

BRCA2 Gene
Back to search Result
Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Microsatellite

dbSNP

276174825

Clinvar

51317

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
612555.1United Arab EmiratesLikely PathogenicBreast-Ovarian Cancer, Familial, Susceptibility To, 2Al-Ali et al. 2023
612555.2United Arab EmiratesLikely PathogenicBreast-Ovarian Cancer, Familial, Susceptibility To, 2Al-Ali et al. 2023
Download Table

Contributors

  • Pratibha Nair: 24.01.2024

Edit History

  • Pratibha Nair: 24.01.2024
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.