NM_000463.3(UGT1A1):c.611T>C (p.Met204Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003491828.2
Allele description [Variation Report for NM_000463.3(UGT1A1):c.611T>C (p.Met204Thr)]
NM_000463.3(UGT1A1):c.611T>C (p.Met204Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens nucleobindin 2 (NUCB2), transcript variant 12, mRNA
Homo sapiens nucleobindin 2 (NUCB2), transcript variant 12, mRNAgi|1890341946|ref|NM_001352670.2|Nucleotide
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Last Updated: Sep 1, 2024