ClinVar Miner

Submissions for variant NM_001379291.1(BRD4):c.903C>T (p.Asp301=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003406884 SCV004140376 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing BRD4: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV003406884 SCV004265902 benign not provided 2024-01-30 criteria provided, single submitter clinical testing

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