NM_001385079.1(PDE10A):c.3041C>T (p.Thr1014Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002661618.2
Allele description [Variation Report for NM_001385079.1(PDE10A):c.3041C>T (p.Thr1014Met)]
NM_001385079.1(PDE10A):c.3041C>T (p.Thr1014Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024