BRCA2 c.316+6T>A

Variant ID: 13-32893468-T-A

NM_000059.3(BRCA2):c.316+6T>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using BRCA2 Exon 3 as a Model System.

Cancer Research
Tubeuf, Hélène H; Caputo, Sandrine M SM; Sullivan, Teresa T; Rondeaux, Julie J; Krieger, Sophie S; Caux-Moncoutier, Virginie V; Hauchard, Julie J; Castelain, Gaia G; Fiévet, Alice A; Meulemans, Laëtitia L; Révillion, Françoise F; Léoné, Mélanie M; Boutry-Kryza, Nadia N; Delnatte, Capucine C; Guillaud-Bataille, Marine M; Cleveland, Linda L; Reid, Susan S; Southon, Eileen E; Soukarieh, Omar O; Drouet, Aurélie A; Di Giacomo, Daniela D; Vezain, Myriam M; Bonnet-Dorion, Françoise F; Bourdon, Violaine V; Larbre, Hélène H; Muller, Danièle D; Pujol, Pascal P; Vaz, Fátima F; Audebert-Bellanger, Séverine S; Colas, Chrystelle C; Venat-Bouvet, Laurence L; Solano, Angela R AR; Stoppa-Lyonnet, Dominique D; Houdayer, Claude C; Frebourg, Thierry T; Gaildrat, Pascaline P; Sharan, Shyam K SK; Martins, Alexandra A
Publication Date: 2020-09-01

Variant appearance in text: BRCA2: 316+6T>A
PubMed Link: 32641407
Variant Present in the following documents:
  • Main text
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