ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2744del (p.Glu915fs)

dbSNP: rs730880661
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000158378 SCV000208313 pathogenic not provided 2014-01-19 criteria provided, single submitter clinical testing Although the c.2744delA mutation in the MYBPC3 gene has not been reported to our knowledge, this mutation causes a shift in reading frame starting at codon Glutamic acid915, changing it to a Glycine, and creating a premature stop codon at position nine of the new reading frame, denoted p.Glu915GlyfsX9. 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 frameshift mutations in the MYBPC3 gene have been reported in association with cardiomyopathy. In summary, c.2744delA in the MYBPC3 gene is interpreted as a disease-causing mutation.

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