NM_000168.6(GLI3):c.2373G>A (p.Pro791=) 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:
- RCV000538308.9
Allele description [Variation Report for NM_000168.6(GLI3):c.2373G>A (p.Pro791=)]
NM_000168.6(GLI3):c.2373G>A (p.Pro791=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 10, 2024