ClinVar Miner

Submissions for variant NM_003970.4(MYOM2):c.4211C>T (p.Thr1404Ile)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV004721769 SCV005330270 likely benign not provided 2024-02-01 criteria provided, single submitter clinical testing MYOM2: BS2
PreventionGenetics, part of Exact Sciences RCV003914141 SCV004732006 benign MYOM2-related disorder 2019-05-17 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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