NM_001393392.1(AKR1C2):c.666T>C (p.His222=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002249600.1
Allele description [Variation Report for NM_001393392.1(AKR1C2):c.666T>C (p.His222=)]
NM_001393392.1(AKR1C2):c.666T>C (p.His222=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 19, 2024