NM_000059.4:c.7007+273G>A

  1. Home
  2. NM_000059.4:c.7007+273G>A

HGVS Expressions

  • NG_012772.3:g.36690G>A
  • NM_000059.4:c.7007+273G>A

Associated Genes

BRCA2 Gene
Back to search Result
Genomic Location

chr13:32347169

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

11571681

Clinvar

209718

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.28LebanonBenignBreast CancerJalkh et al, 2012 2 unrelated patients with breast cancer
Download Table

Contributors

  • Asha Deepthi: 10.06.2020

Edit History

  • Asha Deepthi: 11.06.2020
  • Asha Deepthi: 10.06.2020
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.