NM_001267550.2(TTN):c.48849C>T (p.Thr16283=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001487485.15
Allele description [Variation Report for NM_001267550.2(TTN):c.48849C>T (p.Thr16283=)]
NM_001267550.2(TTN):c.48849C>T (p.Thr16283=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 24, 2024