NM_000283.4(PDE6B):c.682C>A (p.Leu228Ile) AND Congenital stationary night blindness autosomal dominant 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000379626.5
Allele description [Variation Report for NM_000283.4(PDE6B):c.682C>A (p.Leu228Ile)]
NM_000283.4(PDE6B):c.682C>A (p.Leu228Ile)
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024