ClinVar Miner

Submissions for variant NM_207037.2(TCF12):c.1465A>G (p.Met489Val)

gnomAD frequency: 0.00114  dbSNP: rs149621019
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 RCV000889742 SCV001033445 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000889742 SCV003827100 uncertain significance not provided 2019-03-28 criteria provided, single submitter clinical testing

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