NM_022552.5(DNMT3A):c.1833T>A (p.Asn611Lys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 18, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002759529.2
Allele description [Variation Report for NM_022552.5(DNMT3A):c.1833T>A (p.Asn611Lys)]
NM_022552.5(DNMT3A):c.1833T>A (p.Asn611Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024