ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.1090_1099del (p.Ile364fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology RCV003985968 SCV004801782 likely pathogenic Tuberous sclerosis 2 criteria provided, single submitter clinical testing A previously undescribed nucleotide variant creates a frameshift p.Ile364GlyfsTer22 in the TSC2 gene. The variant was observed in heterozygous state in an individual affected with tuberous sclerosis. Loss-of-function variants are reported in patients with Tuberous sclerosis-2, 613254. The variant is not present in population database (gnomAD no frequency). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as likely pathogenic.

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