NM_001267550.2(TTN):c.46353T>C (p.Asp15451=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002413548.1
Allele description [Variation Report for NM_001267550.2(TTN):c.46353T>C (p.Asp15451=)]
NM_001267550.2(TTN):c.46353T>C (p.Asp15451=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Aug 5, 2023