ClinVar Miner

Submissions for variant NM_000350.3(ABCA4):c.5923G>C (p.Gly1975Arg)

dbSNP: rs61753036
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000085777 SCV001532725 pathogenic not provided 2023-02-01 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 1975 of the ABCA4 protein (p.Gly1975Arg). For these reasons, this variant has been classified as Pathogenic. 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 ABCA4 protein function. ClinVar contains an entry for this variant (Variation ID: 99420). This missense change has been observed in individual(s) with clinical features of Stargardt disease (PMID: 10958763, 30204727; Invitae). In at least one individual the data is consistent with being in trans (on the opposite chromosome) from a pathogenic variant. This variant is not present in population databases (gnomAD no frequency).
Retina International RCV000085777 SCV000117919 not provided not provided no assertion provided not provided

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