BRCA2 c.67+57A>C

Variant ID: 13-32890721-A-C

NM_000059.3(BRCA2):c.67+57A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study.

European Journal Of Human Genetics : Ejhg
Caux-Moncoutier, Virginie V; Pagès-Berhouet, Sabine S; Michaux, Dorothée D; Asselain, Bernard B; Castéra, Laurent L; De Pauw, Antoine A; Buecher, Bruno B; Gauthier-Villars, Marion M; Stoppa-Lyonnet, Dominique D; Houdayer, Claude C
Publication Date: 2009-11

Variant appearance in text: BRCA2: 67+57A>C
PubMed Link: 19471317
Variant Present in the following documents:
  • Main text
View BVdb publication page