ClinVar Miner

Submissions for variant NM_001040142.2(SCN2A):c.1027G>T (p.Asp343Tyr) (rs796053175)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000189200 SCV000242832 pathogenic not provided 2017-02-24 criteria provided, single submitter clinical testing The D343Y variant in the SCN2A gene has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. However, different pathogenic variants at the same position (D343H, D343V) have been identified at GeneDx in individuals with seizures. The D343Y variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The D343Y variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is conserved in mammals and is predicted to be within the pore forming loop between the S5 and S6 transmembrane segments of the first homologous domain. In silico analysis predicts this variant is probably damaging to the protein structure/function. Additionally, targeted parental testing indicates this variant is apparently de novo in an individual tested at GeneDx.

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