NM_000463.3(UGT1A1):c.1155C>T (p.Gly385=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002001719.5
Allele description [Variation Report for NM_000463.3(UGT1A1):c.1155C>T (p.Gly385=)]
NM_000463.3(UGT1A1):c.1155C>T (p.Gly385=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 16, 2024