ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.500T>C (p.Leu167Pro)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Health, Inc RCV001182342 SCV001347775 uncertain significance Cardiomyopathy 2018-11-14 criteria provided, single submitter clinical testing
Agnes Ginges Centre for Molecular Cardiology,Centenary Institute RCV001254762 SCV001430855 uncertain significance Sudden cardiac arrest 2019-04-09 no assertion criteria provided research This variant has been identified as part of our research program. Refer to the 'condition' field for the phenotype of the proband identified with this variant. For further information please feel free to contact us.

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