ClinVar Miner

Submissions for variant NM_006009.4(TUBA1A):c.786T>C (p.Tyr262=)

gnomAD frequency: 0.00096  dbSNP: rs762008241
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000193654 SCV000249301 likely benign not specified 2015-12-28 criteria provided, single submitter clinical testing
Invitae RCV000879998 SCV001023057 likely benign not provided 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000879998 SCV001855324 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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