NM_001267550.2(TTN):c.35678C>G (p.Thr11893Ser) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000532364.4
Allele description [Variation Report for NM_001267550.2(TTN):c.35678C>G (p.Thr11893Ser)]
NM_001267550.2(TTN):c.35678C>G (p.Thr11893Ser)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024