NM_003366.4(UQCRC2):c.761G>A (p.Arg254His) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 10, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000432664.1
Allele description [Variation Report for NM_003366.4(UQCRC2):c.761G>A (p.Arg254His)]
NM_003366.4(UQCRC2):c.761G>A (p.Arg254His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024