ClinVar Miner

Submissions for variant NM_000329.3(RPE65):c.406G>C (p.Val136Leu)

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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 RCV003783954 SCV004571649 uncertain significance Leber congenital amaurosis 2; Retinitis pigmentosa 20 2023-03-08 criteria provided, single submitter clinical testing This sequence change replaces valine, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 136 of the RPE65 protein (p.Val136Leu). 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 not expected to disrupt RPE65 protein function. This variant has not been reported in the literature in individuals affected with RPE65-related conditions. This variant is present in population databases (rs544763671, gnomAD 0.02%).

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