NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) AND MYH7-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004541080.1
Allele description [Variation Report for NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr)]
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr)
Condition(s)
- Name:
- MYH7-related disorder
- Synonyms:
- MYH7-related condition; MYH7-Related Disorders; MYH7-related disease
- Identifiers:
Assertion and evidence details
Last Updated: Aug 18, 2024