ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1501G>C (p.Glu501Gln)

dbSNP: rs180177038
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000037923 SCV000061586 likely pathogenic Cardio-facio-cutaneous syndrome 2010-04-23 criteria provided, single submitter clinical testing

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