ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.6128G>T (p.Gly2043Val)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV003985137 SCV004801420 uncertain significance Episodic ataxia type 2 criteria provided, single submitter clinical testing The missense c.6128G>T(p.Gly2043Val) variant in CACNA1A gene has not been reported previously as a pathogenic variant nor a benign variant, to our knowledge. The p.Gly2043Val variant is novel (not in any individuals) in gnomAD Exomes and 1000 Genomes. This variant has not been reported to the ClinVar database. The amino acid change p.Gly2043Val in CACNA1A is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Gly at position 2043 is changed to a Val changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as a Uncertain significance (VUS).

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