ClinVar Miner

Submissions for variant NM_001069.3(TUBB2A):c.882C>T (p.Phe294=)

gnomAD frequency: 0.00014  dbSNP: rs1445909923
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001794579 SCV002032398 likely benign not provided 2021-06-10 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 27535533)
Labcorp Genetics (formerly Invitae), Labcorp RCV001794579 SCV002349663 likely benign not provided 2024-10-23 criteria provided, single submitter clinical testing

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