NM_000463.3(UGT1A1):c.189C>T (p.Asp63=) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Nov 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000596864.12
Allele description [Variation Report for NM_000463.3(UGT1A1):c.189C>T (p.Asp63=)]
NM_000463.3(UGT1A1):c.189C>T (p.Asp63=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 23, 2024