NM_001378969.1(KCND3):c.693G>C (p.Thr231=) AND Spinocerebellar ataxia type 19/22
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001411213.15
Allele description [Variation Report for NM_001378969.1(KCND3):c.693G>C (p.Thr231=)]
NM_001378969.1(KCND3):c.693G>C (p.Thr231=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 3, 2024