NM_021139.3(UGT2B4):c.587T>C (p.Val196Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004328358.1
Allele description [Variation Report for NM_021139.3(UGT2B4):c.587T>C (p.Val196Ala)]
NM_021139.3(UGT2B4):c.587T>C (p.Val196Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 19, 2024