NM_175914.5(HNF4A):c.921C>T (p.Asp307=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000921821.8
Allele description [Variation Report for NM_175914.5(HNF4A):c.921C>T (p.Asp307=)]
NM_175914.5(HNF4A):c.921C>T (p.Asp307=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024