Annotation Detail
Information
- Associated Genes
- CYP2C9
- Associated Variants
-
CYP2C9 p.Arg144Cys (p.R144C)
(
ENST00000461906.1,
ENST00000260682.8 )
CYP2C9 p.Arg144Cys (p.R144C) ( ENST00000260682.8, ENST00000461906.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- CYP2C9*2 AND not specified
- Observed Origin Sample
- germline
- ClinVar Allele ID
- 23448
- ClinVar RefSeq Alternation Syntax
- NM_000771.4:c.430C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2018-03-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000309101
- ClinVar Disease
- not specified
Drugs