NM_001385079.1(PDE10A):c.2595T>C (p.Thr865=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002716809.2
Allele description [Variation Report for NM_001385079.1(PDE10A):c.2595T>C (p.Thr865=)]
NM_001385079.1(PDE10A):c.2595T>C (p.Thr865=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024