ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.909C>T (p.Cys303=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005033454 SCV005673247 likely benign Imerslund-Grasbeck syndrome type 1; Proteinuria, chronic benign 2024-06-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005105275 SCV005811375 likely benign Imerslund-Grasbeck syndrome 2024-11-28 criteria provided, single submitter clinical testing

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