NM_024876.4(COQ8B):c.1035+7_1035+8inv AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 24, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000486871.1
Allele description [Variation Report for NM_024876.4(COQ8B):c.1035+7_1035+8inv]
NM_024876.4(COQ8B):c.1035+7_1035+8inv
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024