NM_003355.3(UCP2):c.227G>A (p.Arg76Gln) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000504343.6
Allele description [Variation Report for NM_003355.3(UCP2):c.227G>A (p.Arg76Gln)]
NM_003355.3(UCP2):c.227G>A (p.Arg76Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024