ClinVar Miner

Submissions for variant NM_153026.3(PRICKLE1):c.531T>A (p.Ile177=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV004052396 SCV002646805 likely benign not specified 2019-09-03 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV005096768 SCV005756387 likely benign Epilepsy, progressive myoclonic, 1B 2024-05-27 criteria provided, single submitter clinical testing

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