NM_170606.3(KMT2C):c.7258C>G (p.Leu2420Val) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004364887.1
Allele description [Variation Report for NM_170606.3(KMT2C):c.7258C>G (p.Leu2420Val)]
NM_170606.3(KMT2C):c.7258C>G (p.Leu2420Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 7, 2024