NM_016035.5(COQ4):c.357G>T (p.Pro119=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001720060.16
Allele description
NM_016035.5(COQ4):c.357G>T (p.Pro119=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024