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CYP2C8 c.642+151G>T
Variant ID: 10-96824406-C-A
NM_000770.3(
CYP2C8
):c.642+151G>T
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:
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: rs11572093
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Global variation in CYP2C8-CYP2C9 functional haplotypes.
The Pharmacogenomics Journal
Speed, William C WC; Kang, Soonmo Peter SP; Tuck, David P DP; Harris, Lyndsay N LN; Kidd, Kenneth K KK
Publication Date: 2009-08
Variant appearance in text: rs11572093
PubMed Link:
19381162
Variant Present in the following documents:
tpj200910a.pdf
View BVdb publication page