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.Arg144Cys (p.R144C) ( ENST00000461906.1, ENST00000260682.8 )
CYP2C9 p.Arg144Cys (p.R144C) ( ENST00000260682.8, ENST00000461906.1 ) - Source Database
- ClinVar
- Description
- NM_000771.3(CYP2C9):c.[430C>T;1075A=] AND Warfarin response
- ClinVar Allele ID
- 175053
- ClinVar Allele ID
- 23448
- ClinVar RefSeq Alternation Syntax
- NM_000771.4:c.430C>T
- ClinVar RefSeq Alternation Syntax
- NM_000771.4:c.1075=
- 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/RCV000154312
- Observed Origin Sample
- germline
Drugs