NM_175914.5(HNF4A):c.369G>A (p.Glu123=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004526759.1
Allele description [Variation Report for NM_175914.5(HNF4A):c.369G>A (p.Glu123=)]
NM_175914.5(HNF4A):c.369G>A (p.Glu123=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024