NM_001286611.2(REPS1):c.1722A>G (p.Gly574=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 11, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002933372.2
Allele description [Variation Report for NM_001286611.2(REPS1):c.1722A>G (p.Gly574=)]
NM_001286611.2(REPS1):c.1722A>G (p.Gly574=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024