ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.69448A>T (p.Asn23150Tyr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV004536927 SCV004722179 uncertain significance TTN-related disorder 2023-11-27 no assertion criteria provided clinical testing The TTN c.69448A>T variant is predicted to result in the amino acid substitution p.Asn23150Tyr. 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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