ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.95885A>T (p.Asn31962Ile)

gnomAD frequency: 0.00008  dbSNP: rs535943753
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000731624 SCV000859468 uncertain significance not provided 2018-01-31 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000731624 SCV003820257 uncertain significance not provided 2020-10-07 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000731624 SCV001918539 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000731624 SCV001967777 uncertain significance not provided no assertion criteria provided clinical testing

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