NM_031448.6(C19orf12):c.72T>C (p.Ala24=) AND Hereditary spastic paraplegia 43
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003743215.1
Allele description [Variation Report for NM_031448.6(C19orf12):c.72T>C (p.Ala24=)]
NM_031448.6(C19orf12):c.72T>C (p.Ala24=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024