NM_015560.2(OPA1):c.2471G>A (p.Arg824Gln) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 29, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000199363.2
Allele description
NM_015560.2(OPA1):c.2471G>A (p.Arg824Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 7, 2019