ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.783G>T (p.Thr261=)

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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 RCV002751312 SCV003019942 likely benign Imerslund-Grasbeck syndrome 2024-07-02 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV004725372 SCV005329959 likely benign not provided 2024-08-01 criteria provided, single submitter clinical testing CUBN: BP4, BP7

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