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CYP2B6 c.866A>T ;(p.N289I)
Variant ID: 19-41515942-A-T
NM_000767.4(
CYP2B6
):c.866A>T;(p.N289I)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: CYP2B6: 866A>T; Asn289Ile; rs1400093417
PubMed Link:
35181665
Variant Present in the following documents:
41525_2022_283_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page
Multi-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation.
The Pharmacogenomics Journal
Martis, S S; Mei, H H; Vijzelaar, R R; Edelmann, L L; Desnick, R J RJ; Scott, S A SA
Publication Date: 2013-12
Variant appearance in text: CYP2B6: N289I
PubMed Link:
23164804
Variant Present in the following documents:
Main text
nihms414574.pdf
View BVdb publication page