NM_000545.8(HNF1A):c.1015G>A (p.Gly339Ser) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000866953.12
Allele description [Variation Report for NM_000545.8(HNF1A):c.1015G>A (p.Gly339Ser)]
NM_000545.8(HNF1A):c.1015G>A (p.Gly339Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024