ClinVar Miner

Submissions for variant NM_019098.5(CNGB3):c.1013A>G (p.Asn338Ser)

dbSNP: rs548817727
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001248276 SCV001421748 uncertain significance not provided 2022-09-27 criteria provided, single submitter clinical testing This sequence change replaces asparagine, which is neutral and polar, with serine, which is neutral and polar, at codon 338 of the CNGB3 protein (p.Asn338Ser). This variant is present in population databases (rs548817727, gnomAD 0.03%). This variant has not been reported in the literature in individuals affected with CNGB3-related conditions. ClinVar contains an entry for this variant (Variation ID: 972284). 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 CNGB3 protein function. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. 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.
Natera, Inc. RCV001835330 SCV002076085 uncertain significance Achromatopsia 2020-09-30 no assertion criteria provided clinical testing

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