ClinVar Miner

Submissions for variant NM_153026.3(PRICKLE1):c.1443C>T (p.Gly481=)

gnomAD frequency: 0.00006  dbSNP: rs376123082
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001299774 SCV001488885 likely benign Epilepsy, progressive myoclonic, 1B 2025-01-30 criteria provided, single submitter clinical testing
Ambry Genetics RCV004036151 SCV002699371 likely benign not specified 2018-07-11 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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