NM_001267550.2(TTN):c.41103C>T (p.Gly13701=) AND Cardiomyopathy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 14, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000770040.10
Allele description [Variation Report for NM_001267550.2(TTN):c.41103C>T (p.Gly13701=)]
NM_001267550.2(TTN):c.41103C>T (p.Gly13701=)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
Assertion and evidence details
Last Updated: Apr 20, 2024