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ALK c.668-40723C>G
Variant ID: 2-29981286-G-C
NM_004304.4(
ALK
):c.668-40723C>G
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:
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: rs2631941
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
A pilot exome-wide association study of age-related cataract in Koreans.
Journal Of Biomedical Research
Eom, Sang-Yong SY; Yim, Dong-Hyuk DH; Kim, Jung-Hyun JH; Chae, Joo-Byung JB; Kim, Yong-Dae YD; Kim, Heon H
Publication Date: 2016-05
Variant appearance in text: rs2631941
PubMed Link:
27533928
Variant Present in the following documents:
Main text
jbr-30-03-186.pdf
View BVdb publication page