ClinVar Miner

Submissions for variant NM_000180.4(GUCY2D):c.1120T>G (p.Ser374Ala)

dbSNP: rs749607771
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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 RCV001993409 SCV002255477 uncertain significance Cone-rod dystrophy 6; Leber congenital amaurosis 1 2023-08-30 criteria provided, single submitter clinical testing 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 GUCY2D protein function. ClinVar contains an entry for this variant (Variation ID: 1467413). This variant has not been reported in the literature in individuals affected with GUCY2D-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces serine, which is neutral and polar, with alanine, which is neutral and non-polar, at codon 374 of the GUCY2D protein (p.Ser374Ala).

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