2026-04-27T12:33:52Zhttps://uvadoc.uva.es/oai/request

oai:uvadoc.uva.es:10324/732812025-09-24T08:33:48Zcom_10324_1134com_10324_931com_10324_894col_10324_1213

00925njm 22002777a 4500 dc Velázquez Pérez, Carolina author Esteban Cardeñosa, Eva author Lastra, Enrique author Abella, Luis Enrique author de la Cruz, Virginia author Domínguez Lobatón, María Carmen author Duran Dominguez, María Mercedes author Infante Sanz, María Del Mar author 2019 BRIP1 is a component of the Fanconi Anemia/BRCA pathway responsible for DNA reparation via helicase activity. Some heterozygous variants in BRIP1 could contribute to Hereditary Breast Cancer through a defective DNA repair. The clinical utility of BRIP1 mutations in a familial cancer context is compromised by the conflicting interpretation of “variants of uncertain significance” (VUS). Defining the clinical significance of variants identified in genetic tests is a major challenge; therefore, studies that evaluate the biological effect of these variants are definitely necessary. To contribute to this purpose, we have characterized the variant c.550G>T of BRIP1, a missense mutation with little evidence about its pathogenicity. Since Human Splicing FinderTM predicts the creation of a new exonic splicing enhancer site we decided to perform cDNA analysis revealing that the c.550G>T mutation located in exon 6 led to an aberrant transcript causing exon 5 skipping. Our results demonstrate that the c.550G>T BRIP1 variant disrupts normal splicing, causing exon 5 skipping. Considering that the exon 5 encodes the helicase domain of BRIP1, it is expected an alteration of the function. This finding enhances the interpretation of this VUS, suggesting a potential pathogenic effect. Molecular Carcinogenesis,2019 Jan;58(1):156-160 0899-1987 https://uvadoc.uva.es/handle/10324/73281 10.1002/mc.22910 156 1 160 Molecular Carcinogenesis 58 1098-2744 Unraveling the molecular effect of a rare missense mutation in BRIP1 associated with inherited breast cancer