NM_001267550.2(TTN):c.60086C>A (p.Thr20029Asn) AND Cardiovascular phenotype
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 4, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002445808.2
Allele description [Variation Report for NM_001267550.2(TTN):c.60086C>A (p.Thr20029Asn)]
NM_001267550.2(TTN):c.60086C>A (p.Thr20029Asn)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: May 1, 2024