The intronic BRCA1 c.5407-25T>A variant causing partly skipping of exon 23—a likely pathogenic variant with reduced penetrance?

Rare sequence variants in the non-coding part of the BRCA genes are often reported as variants of uncertain significance (VUS), which leave patients and doctors in a challenging position. The aim of this study was to determine the pathogenicity of the BRCA1 c.5407-25T>A variant found in 20 famili...

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Detalles Bibliográficos
Autores principales: Høberg-Vetti, Hildegunn, Ognedal, Elisabet, Buisson, Adrien, Vamre, Tone Bøe Aaman, Ariansen, Sarah, Hoover, Jacqueline M., Eide, Geir Egil, Houge, Gunnar, Fiskerstrand, Torunn, Haukanes, Bjørn Ivar, Bjorvatn, Cathrine, Knappskog, Per Morten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382492/
https://www.ncbi.nlm.nih.gov/pubmed/32203205
http://dx.doi.org/10.1038/s41431-020-0612-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382492/
https://www.ncbi.nlm.nih.gov/pubmed/32203205
http://dx.doi.org/10.1038/s41431-020-0612-1

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