NM_001079802.2(FKTN):c.357A>G (p.Leu119=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 22, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002460093.2
Allele description [Variation Report for NM_001079802.2(FKTN):c.357A>G (p.Leu119=)]
NM_001079802.2(FKTN):c.357A>G (p.Leu119=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Jun 9, 2024