ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.1328A>G (p.Tyr443Cys)

gnomAD frequency: 0.00001  dbSNP: rs727503936
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000153267 SCV000202743 likely benign not specified 2014-04-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003727626 SCV004538280 benign not provided 2024-08-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV003727626 SCV005264104 likely benign not provided criteria provided, single submitter not provided

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