NM_000168.6(GLI3):c.1800G>A (p.Thr600=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 16, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000975287.3
Allele description [Variation Report for NM_000168.6(GLI3):c.1800G>A (p.Thr600=)]
NM_000168.6(GLI3):c.1800G>A (p.Thr600=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jul 29, 2023