NM_022489.4(INF2):c.1452T>C (p.Cys484=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 5, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000431651.11
Allele description [Variation Report for NM_022489.4(INF2):c.1452T>C (p.Cys484=)]
NM_022489.4(INF2):c.1452T>C (p.Cys484=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024