ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.208G>T (p.Glu70Ter)

dbSNP: rs11570045
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000494482 SCV000582609 likely pathogenic not provided 2015-11-05 criteria provided, single submitter clinical testing The E70X variant in the MYBPC3 gene has not been reported as a pathogenic variant or as a benign variant to our knowledge. E70X is predicted to cause loss of normal protein function either by protein truncation or nonsense-mediated mRNA decay. Multiple other downstream nonsense variants in the MYBPC3 gene have been reported in HGMD in association with HCM (Stenson et al., 2014). Furthermore, the E70X variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations.In summary, E70X in the MYBPC3 gene is expected to be pathogenic

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