NM_001378969.1(KCND3):c.789C>T (p.Asp263=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 2, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002409014.9
Allele description [Variation Report for NM_001378969.1(KCND3):c.789C>T (p.Asp263=)]
NM_001378969.1(KCND3):c.789C>T (p.Asp263=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Nov 10, 2024