ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1314+12T>C

gnomAD frequency: 0.00001  dbSNP: rs765090629
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000421554 SCV000521610 likely benign not specified 2015-11-30 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002062449 SCV002466409 likely benign RASopathy 2023-03-30 criteria provided, single submitter clinical testing

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