NM_018319.4(TDP1):c.1317G>T (p.Leu439Phe) AND Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002493520.1
Allele description [Variation Report for NM_018319.4(TDP1):c.1317G>T (p.Leu439Phe)]
NM_018319.4(TDP1):c.1317G>T (p.Leu439Phe)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024