ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.231A>G (p.Leu77=)

dbSNP: rs2135266156
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001820290 SCV002064701 uncertain significance not specified 2019-07-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002077302 SCV002439038 likely benign RASopathy 2021-11-27 criteria provided, single submitter clinical testing

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