NM_002397.5(MEF2C):c.1207A>G (p.Thr403Ala) AND Intellectual disability, autosomal dominant 20
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002056996.7
Allele description [Variation Report for NM_002397.5(MEF2C):c.1207A>G (p.Thr403Ala)]
NM_002397.5(MEF2C):c.1207A>G (p.Thr403Ala)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024