NM_018263.6(ASXL2):c.4299C>G (p.Val1433=) AND ASXL2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 2, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003966644.1
Allele description [Variation Report for NM_018263.6(ASXL2):c.4299C>G (p.Val1433=)]
NM_018263.6(ASXL2):c.4299C>G (p.Val1433=)
Condition(s)
- Name:
- ASXL2-related disorder
- Synonyms:
- ASXL2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024