ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.590_592del (p.Asn197_Gly198delinsSer)

gnomAD frequency: 0.00001  dbSNP: rs752918565
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001240703 SCV001413672 uncertain significance Familial focal epilepsy with variable foci 2019-10-28 criteria provided, single submitter clinical testing 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. This variant has not been reported in the literature in individuals with DEPDC5-related conditions. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the ExAC database. This variant, c.590_592del, is a complex sequence change that results in the deletion of asparagine and glycine and insertion of serine amino acid(s) in the DEPDC5 protein (p.Asn197_Gly198delinsSer). 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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