NM_000283.4(PDE6B):c.145G>T (p.Asp49Tyr) AND Retinitis pigmentosa
- Germline classification:
- Likely benign (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:
- RCV000358857.5
Allele description [Variation Report for NM_000283.4(PDE6B):c.145G>T (p.Asp49Tyr)]
NM_000283.4(PDE6B):c.145G>T (p.Asp49Tyr)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024