ClinVar Miner

Submissions for variant NM_012281.3(KCND2):c.1411G>A (p.Gly471Ser)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV003263262 SCV003976981 likely benign Inborn genetic diseases 2023-05-18 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV003497989 SCV004277526 likely benign Early myoclonic encephalopathy 2024-07-05 criteria provided, single submitter clinical testing

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