NM_001351169.2(NT5C2):c.1467G>A (p.Thr489=) AND Hereditary spastic paraplegia 45
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000815681.6
Allele description [Variation Report for NM_001351169.2(NT5C2):c.1467G>A (p.Thr489=)]
NM_001351169.2(NT5C2):c.1467G>A (p.Thr489=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024