NM_000260.4(MYO7A):c.5589C>T (p.His1863=) AND MYO7A-related condition
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 9, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003945821.1
Allele description [Variation Report for NM_000260.4(MYO7A):c.5589C>T (p.His1863=)]
NM_000260.4(MYO7A):c.5589C>T (p.His1863=)
Condition(s)
- Name:
- MYO7A-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Mar 16, 2024