ClinVar Miner

Submissions for variant NM_003319.4(TTN):c.50226dup (p.Ser16743fs)

dbSNP: rs730880343
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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 RCV000154660 SCV000204337 likely pathogenic Primary dilated cardiomyopathy 2015-05-20 criteria provided, single submitter clinical testing The p.Ser23240fs variant in TTN has been identified by our laboratory in 1 Cauca sian individual with DCM as well as in 1 affected relative. It was absent from l arge population studies. This variant is predicted to cause a frameshift, which alters the protein?s amino acid sequence beginning at position 23240 and leads t o a premature termination codon 19 amino acids downstream. This alteration is th en predicted to lead to a truncated or absent protein. Frameshift and other trun cating variants in TTN are strongly associated with DCM if they are located in t he exons encoding for the A-band (Herman 2012, Pugh 2014) and/or are located in an exon that is highly expressed in the heart (Roberts 2015). The p.Ser23240fs v ariant is located in A-band in the highly expressed exon 275. In summary, althou gh additional studies are required to fully establish its clinical significance, the p.Ser23240fs variant is likely pathogenic.

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