NM_182961.4(SYNE1):c.18999G>C (p.Leu6333Phe) AND Autosomal recessive ataxia, Beauce type
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000295099.5
Allele description [Variation Report for NM_182961.4(SYNE1):c.18999G>C (p.Leu6333Phe)]
NM_182961.4(SYNE1):c.18999G>C (p.Leu6333Phe)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024