ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1204C>T (p.Pro402Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005047870 SCV005674176 uncertain significance Cardiofaciocutaneous syndrome 1; LEOPARD syndrome 3; Noonan syndrome 7; Melanoma, cutaneous malignant, susceptibility to, 1; Colorectal cancer; Lung cancer 2024-01-01 criteria provided, single submitter clinical testing

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