NM_001267550.2(TTN):c.28099C>T (p.Leu9367Phe) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 15, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000465094.3
Allele description [Variation Report for NM_001267550.2(TTN):c.28099C>T (p.Leu9367Phe)]
NM_001267550.2(TTN):c.28099C>T (p.Leu9367Phe)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023