NM_182961.4(SYNE1):c.10022T>C (p.Val3341Ala) AND Autosomal recessive ataxia, Beauce type
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000296988.6
Allele description [Variation Report for NM_182961.4(SYNE1):c.10022T>C (p.Val3341Ala)]
NM_182961.4(SYNE1):c.10022T>C (p.Val3341Ala)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024