ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1443A>C (p.Ala481=)

dbSNP: rs2129019701
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002187489 SCV002349069 likely benign RASopathy 2021-08-20 criteria provided, single submitter clinical testing

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