NM_000059.4:c.658_659del

  1. Home
  2. NM_000059.4:c.658_659del

HGVS Expressions

  • NG_012772.3:g.18990_18991del
  • NM_000059.4:c.658_659del
  • NP_000050.3:p.Val220fs

Associated Genes

BRCA2 Gene
Back to search Result
Genomic Location

chr13:32329469-32329470

Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Deletion

dbSNP

80359604

Clinvar

9342

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.45LebanonPathogenicBreast CancerJalkh et al, 2017 Patient 'B41' from family 18 in the publ...
Download Table

Contributors

  • Asha Deepthi: 31.08.2020

Edit History

  • Sayeeda Hana: 05.10.2020
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 31.08.2020
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.