ALK c.667+99301G>A

Variant ID: 2-30043558-C-T

NM_004304.4(ALK):c.667+99301G>A

This variant was identified in 2 publications

View GRCh38 version.




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: rs11890191
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



A Sparse Regression Method for Group-Wise Feature Selection with False Discovery Rate Control.

Ieee/Acm Transactions On Computational Biology And Bioinformatics
Gossmann, Alexej A; Cao, Shaolong S; Brzyski, Damian D; Zhao, Lan-Juan LJ; Deng, Hong-Wen HW; Wang, Yu-Ping YP
Publication Date: 2018

Variant appearance in text: rs11890191
PubMed Link: 29990279
Variant Present in the following documents:
  • Main text
View BVdb publication page