NM_003321.5(TUFM):c.684+6C>T AND Combined oxidative phosphorylation defect type 4
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Aug 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001117670.5
Allele description [Variation Report for NM_003321.5(TUFM):c.684+6C>T]
NM_003321.5(TUFM):c.684+6C>T
Condition(s)
Assertion and evidence details
Last Updated: Aug 4, 2024