ClinVar Miner

Submissions for variant NM_001012338.3(NTRK3):c.278C>T (p.Thr93Met)

gnomAD frequency: 0.00004  dbSNP: rs147992979
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002250159 SCV002517820 benign not specified 2022-05-04 criteria provided, single submitter clinical testing
Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust RCV003326013 SCV003853441 uncertain significance Neonatal cardiomyopathy 2023-03-23 criteria provided, single submitter clinical testing

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