NM_001080489.3(GLOD5):c.107G>A (p.Arg36His) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004190737.1
Allele description [Variation Report for NM_001080489.3(GLOD5):c.107G>A (p.Arg36His)]
NM_001080489.3(GLOD5):c.107G>A (p.Arg36His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024