ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.741T>A (p.Phe247Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics, Centre for Human Genetics RCV003454374 SCV004190083 pathogenic Noonan syndrome 1 no assertion criteria provided clinical testing

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