NM_015046.7(SETX):c.5267T>A (p.Phe1756Tyr) AND Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 28, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001169725.4
Allele description [Variation Report for NM_015046.7(SETX):c.5267T>A (p.Phe1756Tyr)]
NM_015046.7(SETX):c.5267T>A (p.Phe1756Tyr)
Condition(s)
Assertion and evidence details
Last Updated: Oct 28, 2023