NM_015338.6(ASXL1):c.4115C>G (p.Thr1372Ser) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002166990.13
Allele description [Variation Report for NM_015338.6(ASXL1):c.4115C>G (p.Thr1372Ser)]
NM_015338.6(ASXL1):c.4115C>G (p.Thr1372Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024