ClinVar Miner

Submissions for variant NM_001130987.2(DYSF):c.5000G>T (p.Gly1667Val)

dbSNP: rs1573020369
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000815299 SCV000955748 pathogenic Qualitative or quantitative defects of dysferlin 2022-09-03 criteria provided, single submitter clinical testing 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 DYSF protein function. ClinVar contains an entry for this variant (Variation ID: 658470). This missense change has been observed in individual(s) with DYSF-related conditions (PMID: 19528035, 33610434; Invitae). This variant is not present in population databases (gnomAD no frequency). This sequence change replaces glycine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 1628 of the DYSF protein (p.Gly1628Val). This variant disrupts the p.Gly1628 amino acid residue in DYSF. Other variant(s) that disrupt this residue have been observed in individuals with DYSF-related conditions (PMID: 22194990), which suggests that this may be a clinically significant amino acid residue. For these reasons, this variant has been classified as Pathogenic.

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