NM_001267550.2(TTN):c.48783T>C (p.Asp16261=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001437796.15
Allele description [Variation Report for NM_001267550.2(TTN):c.48783T>C (p.Asp16261=)]
NM_001267550.2(TTN):c.48783T>C (p.Asp16261=)
Condition(s)
Assertion and evidence details
Last Updated: Dec 22, 2024