NM_012073.5(CCT5):c.331+14A>T AND Hereditary sensory and autonomic neuropathy with spastic paraplegia
- Germline classification:
- Conflicting interpretations of pathogenicity (3 submissions)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001154942.19
Allele description [Variation Report for NM_012073.5(CCT5):c.331+14A>T]
NM_012073.5(CCT5):c.331+14A>T
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024