ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.1464A>G (p.Leu488=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003756478 SCV004558949 likely benign Noonan syndrome 9 2023-04-14 criteria provided, single submitter clinical testing
Ambry Genetics RCV004992786 SCV005509532 likely benign Cardiovascular phenotype 2024-11-18 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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