NM_173561.3(UNC5CL):c.1485C>G (p.His495Gln) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004084353.1
Allele description [Variation Report for NM_173561.3(UNC5CL):c.1485C>G (p.His495Gln)]
NM_173561.3(UNC5CL):c.1485C>G (p.His495Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024