ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.105del (p.Phe36fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003511298 SCV004285565 pathogenic Brugada syndrome 5 2023-12-19 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Phe36Serfs*111) in the SCN1B gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 233 amino acid(s) of the SCN1B protein. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with SCN1B-related conditions. This variant disrupts a region of the SCN1B protein in which other variant(s) (p.Cys121Trp) have been determined to be pathogenic (PMID: 9697698, 12011299, 17020904, 20628201, 27277800, 28331474). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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