ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.55324del (p.Ser18442fs)

dbSNP: rs794729326
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000184314 SCV000236939 pathogenic not provided 2013-07-29 criteria provided, single submitter clinical testing c.50401delT: p.Ser16801GlnfsX2 (S16801QfsX2) in exon 236 of the TTN gene (NM_001256850.1). The normal sequence with the base that is deleted in braces is: CTCC{T}CAGT. The c.50401delT mutation in the TTN gene has not been reported previously as a disease-causing mutation or as a benign polymorphism to our knowledge. c.50401delT causes a shift in reading frame starting at codon Serine 16801, changing it to a Glutamine, and creating a premature stop codon at position 2 of the new reading frame, denoted p.Ser16801GlnfsX2. This mutation is expected to result in either an abnormal, truncated protein product or loss of protein from this allele through nonsense-mediated mRNA decay. Other truncating TTN variants have been reported in approximately 3% of control alleles (Herman D et al., 2012). However, c.50401delT is located in the A-band region of titin, where the majority of truncating mutations associated with DCM have been reported (Herman D et al., 2012). In summary, c.50401delT in the TTN gene is interpreted as a disease-causing mutation. The variant is found in DCM panel(s).

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