ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.81C>T (p.Cys27=)

gnomAD frequency: 0.00003  dbSNP: rs774401401
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001457695 SCV001661500 likely benign RASopathy 2023-05-04 criteria provided, single submitter clinical testing
GeneDx RCV001692383 SCV001909292 benign not provided 2016-04-12 criteria provided, single submitter clinical testing

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