ClinVar Miner

Submissions for variant NM_153026.3(PRICKLE1):c.1985_1996delinsG (p.Asn662fs)

dbSNP: rs1937772079
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001246060 SCV001419393 uncertain significance Epilepsy, progressive myoclonic, 1B 2019-07-16 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with PRICKLE1-related conditions. 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. Experimental studies and prediction algorithms are not available or were not evaluated for this variant, and the functional significance of the affected amino acid(s) is currently unknown. This variant is not present in population databases (ExAC no frequency). This sequence change results in a premature translational stop signal in the PRICKLE1 gene (p.Asn662Argfs*14). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 170 amino acids of the PRICKLE1 protein.

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