NM_000895.3(LTA4H):c.796T>G (p.Phe266Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004118943.1
Allele description [Variation Report for NM_000895.3(LTA4H):c.796T>G (p.Phe266Val)]
NM_000895.3(LTA4H):c.796T>G (p.Phe266Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024