ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1799_1810delinsATG (p.Val600_Trp604delinsAspGly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital RCV003445403 SCV004174084 pathogenic Lymphatic malformation no assertion criteria provided clinical testing

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