NM_000545.8(HNF1A):c.1383C>T (p.Pro461=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000501197.6
Allele description [Variation Report for NM_000545.8(HNF1A):c.1383C>T (p.Pro461=)]
NM_000545.8(HNF1A):c.1383C>T (p.Pro461=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024