ClinVar Miner

Submissions for variant NM_198253.3(TERT):c.474C>A (p.Leu158=)

gnomAD frequency: 0.00001  dbSNP: rs752933900
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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 RCV001453382 SCV001657073 likely benign Interstitial lung disease 2; Dyskeratosis congenita, autosomal dominant 2 2021-06-17 criteria provided, single submitter clinical testing
Ambry Genetics RCV004559767 SCV002633550 likely benign Dyskeratosis congenita 2022-02-12 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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