NM_018136.5(ASPM):c.1688C>A (p.Thr563Lys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004067784.1
Allele description [Variation Report for NM_018136.5(ASPM):c.1688C>A (p.Thr563Lys)]
NM_018136.5(ASPM):c.1688C>A (p.Thr563Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024