NM_001374353.1(GLI2):c.2136C>A (p.Phe712Leu) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002518965.10
Allele description [Variation Report for NM_001374353.1(GLI2):c.2136C>A (p.Phe712Leu)]
NM_001374353.1(GLI2):c.2136C>A (p.Phe712Leu)
Condition(s)
Assertion and evidence details
Last Updated: Nov 3, 2024