ClinVar Miner

Submissions for variant NM_007363.5(NONO):c.447C>T (p.Ser149=)

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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 RCV002581604 SCV003489113 benign not provided 2024-01-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002581604 SCV004165751 likely benign not provided 2023-09-01 criteria provided, single submitter clinical testing NONO: BP4, BP7, BS2

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