ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.258C>A (p.Thr86=)

gnomAD frequency: 0.00001  dbSNP: rs760454617
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 RCV002112521 SCV002384763 likely benign RASopathy 2022-08-15 criteria provided, single submitter clinical testing

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