ClinVar Miner

Submissions for variant NM_001061.7(TBXAS1):c.1284C>T (p.Gly428=)

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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 RCV002615095 SCV003495580 likely benign not provided 2023-03-03 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004765679 SCV005381331 likely benign not specified 2024-08-06 criteria provided, single submitter clinical testing

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