NM_000257.4(MYH7):c.2967T>C (p.Ile989=) AND Hypertrophic cardiomyopathy 1
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001094091.12
Allele description [Variation Report for NM_000257.4(MYH7):c.2967T>C (p.Ile989=)]
NM_000257.4(MYH7):c.2967T>C (p.Ile989=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 26, 2024