NM_001017989.3(OPA3):c.514C>T (p.Pro172Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001569091.12
Allele description [Variation Report for NM_001017989.3(OPA3):c.514C>T (p.Pro172Ser)]
NM_001017989.3(OPA3):c.514C>T (p.Pro172Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 9, 2024