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ALK c.953-74778T>C
Variant ID: 2-29829760-A-G
NM_004304.4(
ALK
):c.953-74778T>C
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:
Ensemble learning for detecting gene-gene interactions in colorectal cancer.
Peerj
Dorani, Faramarz F; Hu, Ting T; Woods, Michael O MO; Zhai, Guangju G
Publication Date: 2018
Variant appearance in text: rs7594717
PubMed Link:
30397551
Variant Present in the following documents:
Main text
peerj-06-5854.pdf
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: rs7594717
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page