Bibliome.ai browser hg19
Search
About
Stats
FAQ
BRCA2 c.2627del ;(p.N876Ifs*19)
Variant ID: 13-32911117-CA-C
NM_000059.3(
BRCA2
):c.2627del;(p.N876Ifs*19)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes.
European Journal Of Human Genetics : Ejhg
Castéra, Laurent L; Krieger, Sophie S; Rousselin, Antoine A; Legros, Angélina A; Baumann, Jean-Jacques JJ; Bruet, Olivia O; Brault, Baptiste B; Fouillet, Robin R; Goardon, Nicolas N; Letac, Olivier O; Baert-Desurmont, Stéphanie S; Tinat, Julie J; Bera, Odile O; Dugast, Catherine C; Berthet, Pascaline P; Polycarpe, Florence F; Layet, Valérie V; Hardouin, Agnes A; Frébourg, Thierry T; Vaur, Dominique D
Publication Date: 2014-11
Variant appearance in text: BRCA2: 2627del; Asn876Ilefs*19
PubMed Link:
24549055
Variant Present in the following documents:
Main text
View BVdb publication page