NM_003482.4(KMT2D):c.8310C>T (p.Asp2770=) AND KMT2D-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004536866.2
Allele description [Variation Report for NM_003482.4(KMT2D):c.8310C>T (p.Asp2770=)]
NM_003482.4(KMT2D):c.8310C>T (p.Asp2770=)
Condition(s)
- Name:
- KMT2D-related disorder
- Identifiers:
Assertion and evidence details
Last Updated: Oct 13, 2024