ClinVar Miner

Submissions for variant NM_001077350.3(NPRL3):c.1205T>C (p.Leu402Pro)

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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 RCV003591339 SCV004310136 uncertain significance Epilepsy, familial focal, with variable foci 3 2023-07-25 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with NPRL3-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt NPRL3 protein function. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces leucine, which is neutral and non-polar, with proline, which is neutral and non-polar, at codon 402 of the NPRL3 protein (p.Leu402Pro).

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