ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1743C>A (p.Cys581Ter)

dbSNP: rs1570990484
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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 RCV000798070 SCV000937666 pathogenic Familial hemiplegic migraine 2018-10-08 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Cys581*) in the ATP1A2 gene. It is expected to result in an absent or disrupted protein product. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with ATP1A2-related disease. Loss-of-function variants in ATP1A2 are known to be pathogenic (PMID: 18056581). For these reasons, this variant has been classified as Pathogenic.

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