ClinVar Miner

Submissions for variant NM_001040142.2(SCN2A):c.607T>G (p.Tyr203Asp) (rs1553567515)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000520802 SCV000620319 uncertain significance not specified 2017-08-22 criteria provided, single submitter clinical testing A variant of uncertain significance has been identified in the SCN2A gene. The Y203D variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. The Y203D variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The Y203D 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 conserved position predicted to be within transmembrane segment S3 in the first homologous domain. In silico analysis predicts this variant is probably damaging to the protein structure/function. Additionally, the majority of missense variants in this gene are considered pathogenic (Stenson et al., 2014). Based on the currently available information, it is unclear whether this variant is a pathogenic variant or a rare benign variant.

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