NM_018319.4(TDP1):c.716A>G (p.His239Arg) AND Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
- 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:
- RCV000321653.5
Allele description [Variation Report for NM_018319.4(TDP1):c.716A>G (p.His239Arg)]
NM_018319.4(TDP1):c.716A>G (p.His239Arg)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024