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CYP2C9 c.137G>A ;(p.G46D)
Variant ID: 10-96698576-G-A
NM_000771.3(
CYP2C9
):c.137G>A;(p.G46D)
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:
Correlation of changes in subclonal architecture with progression in the MMRF CoMMpass study.
Translational Oncology
Kaur, Gurvinder G; Jena, Lingaraja L; Gupta, Ritu R; Farswan, Akanksha A; Gupta, Anubha A; Sriram, K K
Publication Date: 2022-06-28
Variant appearance in text: CYP2C9: 137G>A; Gly46Asp
PubMed Link:
35777247
Variant Present in the following documents:
mmc5.xls, sheet 3
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: 137G>A; Gly46Asp; rs777883564
PubMed Link:
35181665
Variant Present in the following documents:
41525_2022_283_MOESM4_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: 137G>A; Gly46Asp
PubMed Link:
32004414
Variant Present in the following documents:
Main text
CTS-13-727.pdf
View BVdb publication page