NM_001199753.2(CPT1C):c.2105_2106del (p.Tyr702fs) AND Hereditary spastic paraplegia 73
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001809031.1
Allele description [Variation Report for NM_001199753.2(CPT1C):c.2105_2106del (p.Tyr702fs)]
NM_001199753.2(CPT1C):c.2105_2106del (p.Tyr702fs)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023