NM_001267550.2(TTN):c.52847G>A (p.Trp17616Ter) AND multiple conditions
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Nov 28, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002036047.5
Allele description [Variation Report for NM_001267550.2(TTN):c.52847G>A (p.Trp17616Ter)]
NM_001267550.2(TTN):c.52847G>A (p.Trp17616Ter)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024