NM_000256.3(MYBPC3):c.2997C>T (p.Gly999=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 5, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000618610.3
Allele description [Variation Report for NM_000256.3(MYBPC3):c.2997C>T (p.Gly999=)]
NM_000256.3(MYBPC3):c.2997C>T (p.Gly999=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Sep 1, 2024