ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.67348C>G (p.Gln22450Glu)

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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 RCV004531629 SCV004110267 uncertain significance TTN-related disorder 2023-03-20 criteria provided, single submitter clinical testing The TTN c.67348C>G variant is predicted to result in the amino acid substitution p.Gln22450Glu. 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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