ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1205C>G (p.Pro402Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospital RCV000678901 SCV000805098 uncertain significance Noonan syndrome 2015-06-25 no assertion criteria provided clinical testing

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