NM_001080421.3(UNC13A):c.2220G>A (p.Val740=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000889938.8
Allele description [Variation Report for NM_001080421.3(UNC13A):c.2220G>A (p.Val740=)]
NM_001080421.3(UNC13A):c.2220G>A (p.Val740=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024