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.




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