CYP2C9 c.1159A>G ;(p.I387V)

Variant ID: 10-96745799-A-G

NM_000771.3(CYP2C9):c.1159A>G;(p.I387V)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Identification and in vitro functional assessment of 10 CYP2C9 variants found in Chinese Han subjects.

Frontiers In Endocrinology
Zhang, Qing Q; Qi, Yuying Y; Wang, Shuanghu S; Zhao, Fangling F; Zou, Lili L; Zhou, Quan Q; Geng, Peiwu P; Hong, Yun Y; Yang, Hang H; Luo, Qingfeng Q; Cai, Jianping J; Wu, Hualan H; Wang, Dongxu D; Chen, Hao H; Yang, Jiefu J; Dai, Dapeng D
Publication Date: 2023

Variant appearance in text: CYP2C9: I387V; rs764211126
PubMed Link: 37008923
Variant Present in the following documents:
  • Main text
  • fendo-14-1139805.pdf
View BVdb publication page



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: I387V
PubMed Link: 35181665
Variant Present in the following documents:
  • 41525_2022_283_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



CYP2C9 and CYP2C19: Deep Mutational Scanning and Functional Characterization of Genomic Missense Variants.

Clinical And Translational Science
Zhang, Lingxin L; Sarangi, Vivekananda V; Moon, Irene I; Yu, Jia J; Liu, Duan D; Devarajan, Sandhya S; Reid, Joel M JM; Kalari, Krishna R KR; Wang, Liewei L; Weinshilboum, Richard R
Publication Date: 2020-07

Variant appearance in text: CYP2C9: 1159A>G; Ile387Val; rs764211126
PubMed Link: 32004414
Variant Present in the following documents:
  • Main text
  • CTS-13-727.pdf
View BVdb publication page



Pharmacogenomics Clinical Annotation Tool (PharmCAT).

Clinical Pharmacology And Therapeutics
Sangkuhl, Katrin K; Whirl-Carrillo, Michelle M; Whaley, Ryan M RM; Woon, Mark M; Lavertu, Adam A; Altman, Russ B RB; Carter, Lester L; Verma, Anurag A; Ritchie, Marylyn D MD; Klein, Teri E TE
Publication Date: 2020-01

Variant appearance in text: rs764211126
PubMed Link: 31306493
Variant Present in the following documents:
  • CPT-107-203-s004.pdf
View BVdb publication page