NM_001079802.2(FKTN):c.1102T>C (p.Phe368Leu) AND Cardiovascular phenotype
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002429730.3
Allele description [Variation Report for NM_001079802.2(FKTN):c.1102T>C (p.Phe368Leu)]
NM_001079802.2(FKTN):c.1102T>C (p.Phe368Leu)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Oct 8, 2024