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CYP2C9 c.818A>G ;(p.K273R)
Variant ID: 10-96709040-A-G
NM_000771.3(
CYP2C9
):c.818A>G;(p.K273R)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Clinical pharmacogenetic analysis in 5,001 individuals with diagnostic Exome Sequencing data.
Npj Genomic Medicine
Lanillos, Javier J; Carcajona, Marta M; Maietta, Paolo P; Alvarez, Sara S; Rodriguez-Antona, Cristina C
Publication Date: 2022-02-18
Variant appearance in text: CYP2C9: K273R
PubMed Link:
35181665
Variant Present in the following documents:
41525_2022_283_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
Pharmacogenomics of CYP2C9: Functional and Clinical Considerations.
Journal Of Personalized Medicine
Daly, Ann K AK; Rettie, Allan E AE; Fowler, Douglas M DM; Miners, John O JO
Publication Date: 2017-12-28
Variant appearance in text: CYP2C9: Lys273Arg
PubMed Link:
29283396
Variant Present in the following documents:
Main text
jpm-08-00001.pdf
View BVdb publication page