CYP2B6 c.*1072G>T

Variant ID: 19-41523804-G-T

NM_000767.4(CYP2B6):c.*1072G>T

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs28969420
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs28969420
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Variants in the CYP2B6 3'UTR Alter In Vitro and In Vivo CYP2B6 Activity: Potential Role of MicroRNAs.

Clinical Pharmacology And Therapeutics
Burgess, Kimberly S KS; Ipe, Joseph J; Swart, Marelize M; Metzger, Ingrid F IF; Lu, Jessica J; Gufford, Brandon T BT; Thong, Nancy N; Desta, Zeruesenay Z; Gaedigk, Roger R; Pearce, Robin E RE; Gaedigk, Andrea A; Liu, Yunlong Y; Skaar, Todd C TC
Publication Date: 2018-07

Variant appearance in text: rs28969420
PubMed Link: 28960269
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variation in the 3'-UTR of CYP1A2, CYP2B6, CYP2D6, CYP3A4, NR1I2, and UGT2B7: potential effects on regulation by microRNA and pharmacogenomics relevance.

Frontiers In Genetics
Swart, Marelize M; Dandara, Collet C
Publication Date: 2014

Variant appearance in text: rs28969420
PubMed Link: 24926315
Variant Present in the following documents:
  • Main text
  • fgene-05-00167.pdf
View BVdb publication page