Pathogenic Intronic Splice-Affecting Variants in MYBPC3 in Three Patients with Hypertrophic Cardiomyopathy
AuthorsWood, Katherine A.; orcid: 0000-0002-6459-2127; email: email@example.com
Ellingford, Jamie M.; email: firstname.lastname@example.org
Eden, James; email: email@example.com
Thomas, Huw B.; orcid: 0000-0001-9626-9706; email: firstname.lastname@example.org
O’Keefe, Raymond T.; email: email@example.com
Hopton, Claire; email: firstname.lastname@example.org
Newman, William G.; email: email@example.com
MetadataShow full item record
AbstractGenetic variants in MYBPC3 are one of the most common causes of hypertrophic cardiomyopathy (HCM). While variants in MYBPC3 affecting canonical splice site dinucleotides are a well-characterised cause of HCM, only recently has work begun to investigate the pathogenicity of more deeply intronic variants. Here, we present three patients with HCM and intronic splice-affecting MYBPC3 variants and analyse the impact of variants on splicing using in vitro minigene assays. We show that the three variants, a novel c.927-8G>A variant and the previously reported c.1624+4A>T and c.3815-10T>G variants, result in MYBPC3 splicing errors. Analysis of blood-derived patient RNA for the c.3815-10T>G variant revealed only wild type spliced product, indicating that mis-spliced transcripts from the mutant allele are degraded. These data indicate that the c.927-8G>A variant of uncertain significance and likely benign c.3815-10T>G should be reclassified as likely pathogenic. Furthermore, we find shortcomings in commonly applied bioinformatics strategies to prioritise variants impacting MYBPC3 splicing and re-emphasise the need for functional assessment of variants of uncertain significance in diagnostic testing.
CitationCardiogenetics, volume 11, issue 2, page 73-83
DescriptionFrom MDPI via Jisc Publications Router
History: accepted 2021-05-25, pub-electronic 2021-06-02
Publication status: Published
Funder: Medical Research Council; Grant(s): 1916606, IS-BRC-1215-20007, BB/N000258/1
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