NM_000533.5(PLP1):c.282C>T (p.Thr94=) AND Hereditary spastic paraplegia 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003827761.2
Allele description [Variation Report for NM_000533.5(PLP1):c.282C>T (p.Thr94=)]
NM_000533.5(PLP1):c.282C>T (p.Thr94=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024