ClinVar Miner

Submissions for variant NM_000350.3(ABCA4):c.1908G>T (p.Gln636His)

dbSNP: rs61752400
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000085441 SCV002232688 pathogenic not provided 2022-09-06 criteria provided, single submitter clinical testing 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: 99097). This missense change has been observed in individuals with clinical features of Stargardt disease (PMID: 9781034, 19217903, 24677105, 28327576). This variant is not present in population databases (gnomAD no frequency). This sequence change replaces glutamine, which is neutral and polar, with histidine, which is basic and polar, at codon 636 of the ABCA4 protein (p.Gln636His).
Retina International RCV000085441 SCV000117578 not provided not provided no assertion provided not provided

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