ClinVar Miner

Submissions for variant NM_021222.3(PRUNE1):c.763A>G (p.Met255Val)

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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 RCV003005012 SCV003300899 benign not provided 2022-06-02 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003005012 SCV005051406 likely benign not provided 2024-04-01 criteria provided, single submitter clinical testing PRUNE1: BP4, BS2

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