ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2737del (p.Cys913fs)

dbSNP: rs730880658
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000158375 SCV000208310 pathogenic not provided 2016-05-11 criteria provided, single submitter clinical testing Although the c.2737delT pathogenic variant in the MYBPC3 gene has not been reported to our knowledge, this pathogenic variant causes a shift in reading frame starting at codon Cysteine 913, changing it to an Alanine, and creating a premature stop codon at position 11 of the new reading frame, denoted p.C913AfsX11. This pathogenic variant 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 pathogenic variants in the MYBPC3 gene have been reported in association with HCM. In summary, c.2737delT in the MYBPC3 gene is interpreted as a disease-causing pathogenic variant.

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