NM_001374353.1(GLI2):c.1243G>A (p.Val415Met) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000552345.11
Allele description [Variation Report for NM_001374353.1(GLI2):c.1243G>A (p.Val415Met)]
NM_001374353.1(GLI2):c.1243G>A (p.Val415Met)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024