NM_198576.4(AGRN):c.4695G>C (p.Gln1565His) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jun 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001712390.11
Allele description [Variation Report for NM_198576.4(AGRN):c.4695G>C (p.Gln1565His)]
NM_198576.4(AGRN):c.4695G>C (p.Gln1565His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024