NM_001371279.1(REEP1):c.*658C>G AND Hereditary spastic paraplegia 31
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001142430.4
Allele description [Variation Report for NM_001371279.1(REEP1):c.*658C>G]
NM_001371279.1(REEP1):c.*658C>G
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023