NM_001098.3(ACO2):c.2302G>C (p.Ala768Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002838819.2
Allele description [Variation Report for NM_001098.3(ACO2):c.2302G>C (p.Ala768Pro)]
NM_001098.3(ACO2):c.2302G>C (p.Ala768Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024