NM_001378969.1(KCND3):c.1587A>G (p.Pro529=) AND Spinocerebellar ataxia type 19/22
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002913540.3
Allele description [Variation Report for NM_001378969.1(KCND3):c.1587A>G (p.Pro529=)]
NM_001378969.1(KCND3):c.1587A>G (p.Pro529=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024