NM_018319.4(TDP1):c.1705A>G (p.Thr569Ala) AND Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
- Germline classification:
- 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:
- RCV000364956.6
Allele description [Variation Report for NM_018319.4(TDP1):c.1705A>G (p.Thr569Ala)]
NM_018319.4(TDP1):c.1705A>G (p.Thr569Ala)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024