NM_000059.4:c.6841+80_6841+83delTTAA

  1. Home
  2. NM_000059.4:c.6841+80_6841+83delTTAA

HGVS Expressions

  • NG_012772.3:g.30797_30800del
  • NM_000059.4:c.6841+80_6841+83delTTAA

Associated Genes

BRCA2 Gene
Back to search Result
Genomic Location

chr13:32341276-32341279

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Deletion

dbSNP

11571661

Clinvar

126122

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.36LebanonBenignBreast CancerJalkh et al, 2012 10 unrelated patients with breast cancer
Download Table

Contributors

  • Asha Deepthi: 10.06.2020

Edit History

  • Sayeeda Hana: 04.10.2020
  • Asha Deepthi: 11.06.2020
  • Asha Deepthi: 10.06.2020
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.