NM_002474.3(MYH11):c.3866T>C (p.Val1289Ala) AND Lissencephaly, Recessive
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000274667.13
Allele description [Variation Report for NM_002474.3(MYH11):c.3866T>C (p.Val1289Ala)]
NM_002474.3(MYH11):c.3866T>C (p.Val1289Ala)
Condition(s)
- Name:
- Lissencephaly, Recessive
- Identifiers:
- MedGen: CN239458
Assertion and evidence details
Last Updated: Jun 9, 2024