NM_175914.5(HNF4A):c.408G>A (p.Ala136=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jun 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000711957.4
Allele description [Variation Report for NM_175914.5(HNF4A):c.408G>A (p.Ala136=)]
NM_175914.5(HNF4A):c.408G>A (p.Ala136=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024