ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.88562C>A (p.Ser29521Ter)

dbSNP: rs1436663696
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001377726 SCV001575126 likely pathogenic Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2017-04-29 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Likely Pathogenic. This variant is found in the A-band of this gene. While this particular variant has not been reported in the literature, truncating variants in the A-band of TTN are significantly overrepresented in patients with dilated cardiomyopathy and are considered to be likely pathogenic for the disease (PMID: 25589632). This sequence change creates a premature translational stop signal at codon 29521 (p.Ser29521*) of the TTN gene. It is expected to result in a disrupted protein product.

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