NM_014946.4(SPAST):c.1119T>C (p.Ala373=) AND Hereditary spastic paraplegia 4
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002607853.3
Allele description [Variation Report for NM_014946.4(SPAST):c.1119T>C (p.Ala373=)]
NM_014946.4(SPAST):c.1119T>C (p.Ala373=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024