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CYP2C9 c.226G>A ;(p.V76M)
Variant ID: 10-96701672-G-A
NM_000771.3(
CYP2C9
):c.226G>A;(p.V76M)
This variant was identified in 3 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: V76M
PubMed Link:
35181665
Variant Present in the following documents:
41525_2022_283_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
An optimized prediction framework to assess the functional impact of pharmacogenetic variants.
The Pharmacogenomics Journal
Zhou, Yitian Y; Mkrtchian, Souren S; Kumondai, Masaki M; Hiratsuka, Masahiro M; Lauschke, Volker M VM
Publication Date: 2019-04
Variant appearance in text: CYP2C9: V76M
PubMed Link:
30206299
Variant Present in the following documents:
41397_2018_44_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page
Effects of polymorphic variation on the thermostability of heterogenous populations of CYP3A4 and CYP2C9 enzymes in solution.
Scientific Reports
Arendse, Lauren B LB; Blackburn, Jonathan M JM
Publication Date: 2018-08-08
Variant appearance in text: CYP2C9: V76M
PubMed Link:
30089838
Variant Present in the following documents:
Main text
41598_2018_Article_30195.pdf
41598_2018_30195_MOESM1_ESM.pdf
View BVdb publication page