NM_018136.5(ASPM):c.933C>G (p.Ser311Arg) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 5, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000192474.11
Allele description [Variation Report for NM_018136.5(ASPM):c.933C>G (p.Ser311Arg)]
NM_018136.5(ASPM):c.933C>G (p.Ser311Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 4, 2024