NM_012082.4(ZFPM2):c.2238A>G (p.Leu746=) AND Tetralogy of Fallot
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 1, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001197231.2
Allele description [Variation Report for NM_012082.4(ZFPM2):c.2238A>G (p.Leu746=)]
NM_012082.4(ZFPM2):c.2238A>G (p.Leu746=)
Condition(s)
- Name:
- Tetralogy of Fallot (TOF)
- Synonyms:
- Fallot tetralogy
- Identifiers:
- MONDO: MONDO:0008542; MedGen: C0039685; Orphanet: 3303; OMIM: 187500; Human Phenotype Ontology: HP:0001636
Assertion and evidence details
Last Updated: Mar 26, 2023