NM_018136.5(ASPM):c.9773A>G (p.His3258Arg) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 8, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000145240.9
Allele description [Variation Report for NM_018136.5(ASPM):c.9773A>G (p.His3258Arg)]
NM_018136.5(ASPM):c.9773A>G (p.His3258Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024