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.




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