ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4326C>T (p.Pro1442=)

dbSNP: rs76633938
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000887218 SCV001030766 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV000887218 SCV001784917 likely benign not provided 2021-04-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000887218 SCV005206639 likely benign not provided criteria provided, single submitter not provided

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