ClinVar Miner

Submissions for variant NM_003235.5(TG):c.7893C>T (p.Ala2631=)

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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 RCV003850991 SCV004656636 likely benign not provided 2024-02-22 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004555684 SCV004798255 likely benign TG-related disorder 2022-11-14 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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