NM_000554.6(CRX):c.533G>C (p.Gly178Ala) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001930438.3
Allele description [Variation Report for NM_000554.6(CRX):c.533G>C (p.Gly178Ala)]
NM_000554.6(CRX):c.533G>C (p.Gly178Ala)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024