ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.4397C>A (p.Ser1466Ter)

dbSNP: rs45517341
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002513631 SCV003441713 pathogenic Tuberous sclerosis 2 2022-04-29 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 49987). This premature translational stop signal has been observed in individual(s) with tuberous sclerosis complex (PMID: 16554133, 20498439, 32211034). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Ser1466*) 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).
Tuberous sclerosis database (TSC2) RCV000043254 SCV000067055 not provided Tuberous sclerosis syndrome no assertion provided curation

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