NM_005920.4(MEF2D):c.676G>C (p.Val226Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004324858.1
Allele description [Variation Report for NM_005920.4(MEF2D):c.676G>C (p.Val226Leu)]
NM_005920.4(MEF2D):c.676G>C (p.Val226Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024