ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.51129dup (p.Val17044fs)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV003358159 SCV004053260 likely pathogenic Cardiovascular phenotype 2023-08-01 criteria provided, single submitter clinical testing The c.23934dupA variant, located in coding exon 97 of the TTN gene, results from a duplication of A at nucleotide position 23934, causing a translational frameshift with a predicted alternate stop codon (p.V7979Sfs*12). This exon is located in the A-band region of the N2-B isoform of the titin protein and is constitutively expressed in TTN transcripts (percent spliced in or PSI 100%). This variant is considered to be rare based on population cohorts in the Genome Aggregation Database (gnomAD). This alteration is expected to result in loss of function by premature protein truncation or nonsense-mediated mRNA decay. While truncating variants in TTN are present in 1-3% of the general population, truncating variants in the A-band are the most common cause of dilated cardiomyopathy (DCM) (Herman DS et al. N. Engl. J. Med., 2012 Feb;366:619-28; Roberts AM et al. Sci Transl Med, 2015 Jan;7:270ra6). TTN truncating variants encoded in constitutive exons (PSI >90%) have been found to be significantly associated with DCM regardless of their position in titin (Schafer S et al. Nat. Genet., 2017 01;49:46-53). Based on the majority of available evidence to date, this variant is likely to be pathogenic.
Research Unit of Cardiovascular and Metabolic Disease, Inserm RCV003233320 SCV003932098 likely pathogenic Primary dilated cardiomyopathy 2022-07-21 no assertion criteria provided research

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