NM_014363.6(SACS):c.9969T>C (p.Ala3323=) AND Spastic paraplegia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003818646.1
Allele description [Variation Report for NM_014363.6(SACS):c.9969T>C (p.Ala3323=)]
NM_014363.6(SACS):c.9969T>C (p.Ala3323=)
Condition(s)
- Name:
- Spastic paraplegia
- Identifiers:
- MedGen: C0037772; Human Phenotype Ontology: HP:0001258
Assertion and evidence details
Last Updated: Mar 5, 2024