CYP2C19 c.1213G>C ;(p.E405Q)

Variant ID: 10-96609737-G-C

NM_000769.1(CYP2C19):c.1213G>C;(p.E405Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: CYP2C19: 1213G>C; E405Q
PubMed Link: 32004414
Variant Present in the following documents:
  • Main text
  • CTS-13-727.pdf
View BVdb publication page