NM_000283.4(PDE6B):c.2150G>A (p.Cys717Tyr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001208664.7
Allele description [Variation Report for NM_000283.4(PDE6B):c.2150G>A (p.Cys717Tyr)]
NM_000283.4(PDE6B):c.2150G>A (p.Cys717Tyr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024