NM_001267550.2(TTN):c.25490G>A (p.Arg8497His) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001082276.16
Allele description [Variation Report for NM_001267550.2(TTN):c.25490G>A (p.Arg8497His)]
NM_001267550.2(TTN):c.25490G>A (p.Arg8497His)
Condition(s)
Assertion and evidence details
Last Updated: Dec 7, 2024