NM_205861.3(DHDDS):c.292C>T (p.Arg98Trp) AND Retinitis pigmentosa 59
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001862719.4
Allele description [Variation Report for NM_205861.3(DHDDS):c.292C>T (p.Arg98Trp)]
NM_205861.3(DHDDS):c.292C>T (p.Arg98Trp)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024