ClinVar Miner

Submissions for variant NM_002074.5(GNB1):c.814G>A (p.Gly272Arg)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Lab, CHRU Brest RCV003883378 SCV004697794 likely pathogenic Acute lymphoid leukemia; Myelodysplastic syndrome; Intellectual disability, autosomal dominant 42 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005101447 SCV005818856 uncertain significance not provided 2024-11-03 criteria provided, single submitter clinical testing This sequence change replaces glycine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 272 of the GNB1 protein (p.Gly272Arg). This variant is present in population databases (no rsID available, gnomAD 0.007%). This variant has not been reported in the literature in individuals affected with GNB1-related conditions. ClinVar contains an entry for this variant (Variation ID: 3024332). Invitae Evidence Modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) indicates that this missense variant is expected to disrupt GNB1 protein function with a positive predictive value of 80%. 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.

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