ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.102846T>A (p.Thr34282=)

dbSNP: rs876657618
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000215260 SCV000271122 likely benign not specified 2015-06-09 criteria provided, single submitter clinical testing p.Thr31714Thr in exon 307 of TTN: This variant is not expected to have clinical significance because it does not alter an amino acid residue and is not located within the splice consensus sequence.

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