NM_001098.3(ACO2):c.231C>T (p.Pro77=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Apr 13, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000429948.3
Allele description [Variation Report for NM_001098.3(ACO2):c.231C>T (p.Pro77=)]
NM_001098.3(ACO2):c.231C>T (p.Pro77=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024