ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.698T>C (p.Leu233Pro)

dbSNP: rs2059190252
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001348493 SCV001542797 uncertain significance Episodic ataxia type 2; Developmental and epileptic encephalopathy, 42 2020-05-07 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with CACNA1A-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces leucine with proline at codon 233 of the CACNA1A protein (p.Leu233Pro). The leucine residue is highly conserved and there is a moderate physicochemical difference between leucine and proline.

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