ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.6474C>T (p.Arg2158=)

gnomAD frequency: 0.00017  dbSNP: rs368016666
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001463532 SCV001667478 likely benign Episodic ataxia type 2; Developmental and epileptic encephalopathy, 42 2024-01-22 criteria provided, single submitter clinical testing
GeneDx RCV001581145 SCV001814111 likely benign not provided 2019-04-11 criteria provided, single submitter clinical testing
Ambry Genetics RCV002359032 SCV002654764 likely benign Inborn genetic diseases 2018-12-18 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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