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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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