NM_014946.4(SPAST):c.828T>C (p.Ser276=) AND Hereditary spastic paraplegia 4
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000379470.7
Allele description [Variation Report for NM_014946.4(SPAST):c.828T>C (p.Ser276=)]
NM_014946.4(SPAST):c.828T>C (p.Ser276=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024