ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.172del (p.Ala58fs)

dbSNP: rs730880662
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000158383 SCV000208318 pathogenic not provided 2013-03-28 criteria provided, single submitter clinical testing Although the c.172delG mutation in the MYBPC3 gene has not been reported to our knowledge, this mutation causes a shift in reading frame starting at codon Alanine 58, changing it to a Proline, and creating a premature stop codon at position 9 of the new reading frame, denoted p.Ala58ProfsX9. This mutation is expected to result in either an abnormal, truncated protein product or loss of protein from this allele through nonsensemediated mRNA decay. Other frameshift mutations in the MYBPC3 gene have been reported in association with HCM.

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