ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.1172G>T (p.Arg391Met)

dbSNP: rs587782972
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000143944 SCV000188824 likely pathogenic Noonan syndrome 2013-11-14 no assertion criteria provided clinical testing
Service de Génétique Moléculaire, Hôpital Robert Debré RCV000143944 SCV001438542 likely benign Noonan syndrome no assertion criteria provided clinical testing

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