NM_025137.4(SPG11):c.5796T>C (p.His1932=) AND SPG11-related condition
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003965694.1
Allele description [Variation Report for NM_025137.4(SPG11):c.5796T>C (p.His1932=)]
NM_025137.4(SPG11):c.5796T>C (p.His1932=)
Condition(s)
- Name:
- SPG11-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Apr 15, 2024