ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.3156del (p.Ala1053fs)

dbSNP: rs2151437486
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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 RCV001884601 SCV002158023 pathogenic Tuberous sclerosis 2 2021-07-31 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Ala1053Argfs*17) in the TSC2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in TSC2 are known to be pathogenic (PMID: 10205261, 17304050). This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with TSC2-related conditions. For these reasons, this variant has been classified as Pathogenic.

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