NM_001080421.3(UNC13A):c.591T>C (p.Arg197=) AND UNC13A-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003944250.2
Allele description [Variation Report for NM_001080421.3(UNC13A):c.591T>C (p.Arg197=)]
NM_001080421.3(UNC13A):c.591T>C (p.Arg197=)
Condition(s)
- Name:
- UNC13A-related disorder
- Synonyms:
- UNC13A-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 13, 2024