NM_001378969.1(KCND3):c.1865C>T (p.Ala622Val) AND Spinocerebellar ataxia type 19/22
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 17, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001478107.7
Allele description [Variation Report for NM_001378969.1(KCND3):c.1865C>T (p.Ala622Val)]
NM_001378969.1(KCND3):c.1865C>T (p.Ala622Val)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024