ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1405G>A (p.Gly469Arg)

dbSNP: rs121913357
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Total submissions: 3
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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 RCV000154398 SCV000204065 likely pathogenic Non-small cell lung carcinoma 2013-10-10 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001813396 SCV002060528 pathogenic Noonan syndrome and Noonan-related syndrome 2020-07-01 criteria provided, single submitter clinical testing
Database of Curated Mutations (DoCM) RCV000433832 SCV000505605 likely pathogenic Melanoma 2015-07-14 no assertion criteria provided literature only

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