NM_001267550.2(TTN):c.49038G>A (p.Val16346=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004068686.1
Allele description [Variation Report for NM_001267550.2(TTN):c.49038G>A (p.Val16346=)]
NM_001267550.2(TTN):c.49038G>A (p.Val16346=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Sep 29, 2024