NM_018127.7(ELAC2):c.333A>G (p.Thr111=) AND Combined oxidative phosphorylation defect type 17
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 6, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003851427.1
Allele description [Variation Report for NM_018127.7(ELAC2):c.333A>G (p.Thr111=)]
NM_018127.7(ELAC2):c.333A>G (p.Thr111=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024