NM_130837.3(OPA1):c.321G>A (p.Ser107=) AND Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001787890.2
Allele description [Variation Report for NM_130837.3(OPA1):c.321G>A (p.Ser107=)]
NM_130837.3(OPA1):c.321G>A (p.Ser107=)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024