NM_015338.6(ASXL1):c.3933T>C (p.Ala1311=) AND ASXL1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004551831.1
Allele description [Variation Report for NM_015338.6(ASXL1):c.3933T>C (p.Ala1311=)]
NM_015338.6(ASXL1):c.3933T>C (p.Ala1311=)
Condition(s)
- Name:
- ASXL1-related disorder
- Synonyms:
- ASXL1-Related Disorders; ASXL1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 1, 2024