ClinVar Miner

Submissions for variant NM_031443.4(CCM2):c.228dup (p.Pro77fs)

dbSNP: rs2128747319
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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 RCV001383102 SCV001582125 pathogenic Cerebral cavernous malformation 2 2021-04-01 criteria provided, single submitter clinical testing This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Pro77Thrfs*9) in the CCM2 gene. It is expected to result in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with CCM2-related conditions. For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in CCM2 are known to be pathogenic (PMID: 18300272, 24689081).

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