NM_001351169.2(NT5C2):c.1139A>G (p.His380Arg) AND Hereditary spastic paraplegia 45
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000797354.5
Allele description [Variation Report for NM_001351169.2(NT5C2):c.1139A>G (p.His380Arg)]
NM_001351169.2(NT5C2):c.1139A>G (p.His380Arg)
Condition(s)
Assertion and evidence details
Last Updated: Feb 7, 2023