ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.88898C>G (p.Thr29633Arg)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003139071 SCV003819155 uncertain significance not provided 2020-12-28 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004529250 SCV004107432 uncertain significance TTN-related disorder 2023-04-14 criteria provided, single submitter clinical testing The TTN c.88898C>G variant is predicted to result in the amino acid substitution p.Thr29633Arg. To our knowledge, this variant has not been reported in the literature or in a large population database (http://gnomad.broadinstitute.org), indicating this variant is rare. At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence.

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