ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.3783C>T (p.Ala1261=)

gnomAD frequency: 0.00001  dbSNP: rs2090170500
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001419121 SCV001621366 likely benign Tuberous sclerosis 2 2023-10-23 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004804168 SCV005427199 likely benign Tuberous sclerosis syndrome 2024-03-14 criteria provided, single submitter clinical testing
Ambry Genetics RCV004951715 SCV005523408 likely benign Hereditary cancer-predisposing syndrome 2024-07-05 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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