ClinVar Miner

Submissions for variant NM_172107.4(KCNQ2):c.341C>G (p.Thr114Ser)

dbSNP: rs1057516077
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001224717 SCV001396933 uncertain significance Early infantile epileptic encephalopathy with suppression bursts 2021-05-26 criteria provided, single submitter clinical testing 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. This variant disrupts the p.Thr114 amino acid residue in KCNQ2. Other variant(s) that disrupt this residue have been observed in individuals with KCNQ2-related conditions (PMID: 22926866, 25982755, 23271449), which suggests that this may be a clinically significant amino acid residue. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. 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 KCNQ2 protein function. This variant has not been reported in the literature in individuals with KCNQ2-related conditions. ClinVar contains an entry for this variant (Variation ID: 952581). This variant is not present in population databases (ExAC no frequency). This sequence change replaces threonine with serine at codon 114 of the KCNQ2 protein (p.Thr114Ser). The threonine residue is highly conserved and there is a small physicochemical difference between threonine and serine.

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