ClinVar Miner

Submissions for variant NM_000335.4(SCN5A):c.3944G>A (p.Arg1315Gln)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000802412 SCV000942243 uncertain significance Brugada syndrome 2018-08-31 criteria provided, single submitter clinical testing This sequence change replaces arginine with glutamine at codon 1316 of the SCN5A protein (p.Arg1316Gln). The arginine residue is highly conserved and there is a small physicochemical difference between arginine and glutamine. This variant is present in population databases (rs765907469, ExAC 0.004%). This variant has not been reported in the literature in individuals with SCN5A-related disease. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. 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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