MSH2 c.1386+3A>G

Variant ID: 2-47672799-A-G

NM_000251.2(MSH2):c.1386+3A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Spectrum and management of breast cancer patients with variant of uncertain significance mutations at a tertiary care centre in North India.

Ecancermedicalscience
Mittal, Abhenil A; Deo, S V S SVS; Gogia, Ajay A; Batra, Atul A; Kumar, Akash A; Bhoriwal, Sandeep S; Deb, Koushik Sinha KS; Dhamija, Ekta E; Ramprasad, V L VL; Olopade, Olufunmilayo O; Pramanik, Raja R
Publication Date: 2022

Variant appearance in text: MSH2: 1386+3A>G
PubMed Link: 36200007
Variant Present in the following documents:
  • can-16-1434.pdf
View BVdb publication page



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: MSH2: 1386+3A>G
PubMed Link: 24549055
Variant Present in the following documents:
  • Main text
View BVdb publication page