ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.2043C>T (p.Ser681=)

gnomAD frequency: 0.00020  dbSNP: rs142854750
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000906750 SCV001051409 likely benign not provided 2024-01-22 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818796 SCV002065052 likely benign not specified 2017-12-29 criteria provided, single submitter clinical testing

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