ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.84504dup (p.Ser28169fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV003315113 SCV004014685 likely pathogenic Dilated cardiomyopathy 1G 2023-01-09 criteria provided, single submitter clinical testing The TTN c.84504dup (p.Ser28169IlefsTer12) variant results in the duplication of a nucleotide at position c.84504, causing a shift in the protein reading frame that is predicted to result in premature termination of the protein. Loss of normal protein function through either protein truncation or nonsense-mediated mRNA decay is expected. This variant is located in exon 327 of the meta transcript of titin within the A-band, which is highly expressed cardiac tissue (PMID: 25589632). In a meta-analysis of TTN truncating variants in patients with dilated cardiomyopathy (DCM) and controls, variants in this region were associated with a significantly increased risk of developing DCM (odds ratio 49.8) (PMID: 27869827). This variant has been identified in one individual with DCM as well as in two family members (PMID: 35054181). This variant is not found in version 2.1.1 or version 3.1.2 of the Genome Aggregation Database. Based on the available evidence, the c.84504dup (p.Ser28169IlefsTer12) variant is classified as likely pathogenic for dilated cardiomyopathy.

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