NM_014363.6(SACS):c.7742C>T (p.Ala2581Val) AND Spastic paraplegia
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002550670.3
Allele description [Variation Report for NM_014363.6(SACS):c.7742C>T (p.Ala2581Val)]
NM_014363.6(SACS):c.7742C>T (p.Ala2581Val)
Condition(s)
- Name:
- Spastic paraplegia
- Identifiers:
- MedGen: C0037772; Human Phenotype Ontology: HP:0001258
Assertion and evidence details
Last Updated: Oct 20, 2024