NM_018136.5(ASPM):c.7917A>G (p.Lys2639=) AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Sep 30, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000145203.11
Allele description [Variation Report for NM_018136.5(ASPM):c.7917A>G (p.Lys2639=)]
NM_018136.5(ASPM):c.7917A>G (p.Lys2639=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jan 19, 2025