ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.6710_6719del (p.Arg2237fs)

dbSNP: rs1042488847
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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 RCV000653330 SCV000775209 uncertain significance Episodic ataxia type 2; Developmental and epileptic encephalopathy, 42 2022-12-14 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. ClinVar contains an entry for this variant (Variation ID: 542826). This variant has not been reported in the literature in individuals affected with CACNA1A-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change results in a frameshift in the CACNA1A gene (p.Arg2238Leufs*266). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 24 amino acid(s) of the CACNA1A protein and extend the protein by 241 additional amino acid residues.

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