ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.28204C>T (p.Arg9402Cys)

gnomAD frequency: 0.00003  dbSNP: rs369553799
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001699714 SCV004237123 uncertain significance not provided 2023-08-03 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699714 SCV001926225 uncertain significance not provided no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001699714 SCV001963272 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001699714 SCV001967094 uncertain significance not provided no assertion criteria provided clinical testing

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