NM_182961.4(SYNE1):c.22137C>T (p.Asp7379=) AND Autosomal recessive ataxia, Beauce type
- Germline classification:
- Likely benign (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:
- RCV000329165.5
Allele description [Variation Report for NM_182961.4(SYNE1):c.22137C>T (p.Asp7379=)]
NM_182961.4(SYNE1):c.22137C>T (p.Asp7379=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024