NM_001351169.2(NT5C2):c.1662A>G (p.Glu554=) AND Hereditary spastic paraplegia 45
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 30, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001478584.12
Allele description [Variation Report for NM_001351169.2(NT5C2):c.1662A>G (p.Glu554=)]
NM_001351169.2(NT5C2):c.1662A>G (p.Glu554=)
Condition(s)
Assertion and evidence details
Last Updated: Jun 2, 2024