NM_001122769.3(LCA5):c.1746C>T (p.Asn582=) AND Leber congenital amaurosis 5
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000260046.5
Allele description [Variation Report for NM_001122769.3(LCA5):c.1746C>T (p.Asn582=)]
NM_001122769.3(LCA5):c.1746C>T (p.Asn582=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024