NM_000322.5(PRPH2):c.708C>T (p.Tyr236=) 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:
- RCV001159969.5
Allele description [Variation Report for NM_000322.5(PRPH2):c.708C>T (p.Tyr236=)]
NM_000322.5(PRPH2):c.708C>T (p.Tyr236=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 24, 2024