NM_018263.6(ASXL2):c.3816G>T (p.Gln1272His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003050599.2
Allele description [Variation Report for NM_018263.6(ASXL2):c.3816G>T (p.Gln1272His)]
NM_018263.6(ASXL2):c.3816G>T (p.Gln1272His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024