NM_001866.3(COX7B):c.7C>G (p.Pro3Ala) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 3, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000484569.1
Allele description [Variation Report for NM_001866.3(COX7B):c.7C>G (p.Pro3Ala)]
NM_001866.3(COX7B):c.7C>G (p.Pro3Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Oct 14, 2023