ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.816T>C (p.Cys272=)

dbSNP: rs2536322792
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003832095 SCV004639800 likely benign RASopathy 2022-11-10 criteria provided, single submitter clinical testing

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