NM_001393392.1(AKR1C2):c.569A>C (p.Gln190Pro) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004085950.1
Allele description [Variation Report for NM_001393392.1(AKR1C2):c.569A>C (p.Gln190Pro)]
NM_001393392.1(AKR1C2):c.569A>C (p.Gln190Pro)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024