ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.2037G>C (p.Gly679=)

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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 RCV003585621 SCV004279065 likely benign Tatton-Brown-Rahman overgrowth syndrome 2023-12-28 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004747312 SCV005356990 likely benign DNMT3A-related disorder 2022-12-08 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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