| Literature DB >> 35277653 |
Mélanie Eyries1, Olivier Ariste2, Gaelle Legrand3, Noémie Basset3, Erell Guillerm3, Alexandre Perrier3, Caroline Duros4, Odile Cohen-Haguenauer4, Pierre de la Grange2, Florence Coulet3.
Abstract
Despite routine analysis of a large panel of genes, pathogenic variants are only detected in approximately 20% of families with hereditary breast and/or ovarian cancer. Mobile element insertions (MEI) are known to cause genetic diseases in humans, but remain challenging to detect. Retrospective analysis of targeted next-generation sequencing (NGS) data from 359 patients was performed using a dedicated MEI detection pipeline. We detected one MEI in exon 9 of the PALB2 gene in a woman with a family history of breast cancer. The pathogenic variant, c.2872_2888delins114AluL2, disrupts the PALB2 coding sequence and leads to the production of a truncated protein, p.(Gln958Valfs*38). This is the first report of a pathogenic MEI in PALB2. This study illustrates that MEI analysis may help to improve molecular diagnostic yield and can be performed from targeted NGS data used for routine diagnosis.Entities:
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Year: 2022 PMID: 35277653 PMCID: PMC9553905 DOI: 10.1038/s41431-022-01064-3
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 5.351