NM_001378969.1(KCND3):c.1784T>G (p.Leu595Trp) AND Spinocerebellar ataxia type 19/22
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000811749.7
Allele description [Variation Report for NM_001378969.1(KCND3):c.1784T>G (p.Leu595Trp)]
NM_001378969.1(KCND3):c.1784T>G (p.Leu595Trp)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024