Annotation Detail
Information
- Associated Genes
- CYP2C9
- Associated Variants
-
NM_000771.3(CYP2C9):c.[430C=;1075A=] AND Warfarin response
NM_000771.3(CYP2C9):c.[430C=;1075A=] AND Warfarin response
CYP2C9 p.Ile359Leu (p.I359L) ( ENST00000260682.8 )
CYP2C9 p.Ile359Leu (p.I359L) ( ENST00000260682.8 ) - Source Database
- ClinVar
- Description
- NM_000771.3(CYP2C9):c.[430C=;1075A>C] AND Warfarin response
- ClinVar Allele ID
- 175331
- ClinVar Allele ID
- 23447
- ClinVar RefSeq Alternation Syntax
- NM_000771.4:c.1075A>C
- ClinVar RefSeq Alternation Syntax
- NM_000771.4:c.430=
- Clinical Significance Description
- drug response
- Clinical Significance Last Update
- 2006-11-20
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000150378
- Observed Origin Sample
- germline
Drugs