ClinVar Miner

Submissions for variant NM_014516.4(CNOT3):c.2164-7C>T

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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 RCV002745946 SCV003015116 benign not provided 2022-11-22 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002745946 SCV003918185 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing CNOT3: BP4, BS1

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