ALK c.668-79853G>A

Variant ID: 2-30020416-C-T

NM_004304.4(ALK):c.668-79853G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Impact of extracellular matrix stiffness on genomic heterogeneity in MYCN-amplified neuroblastoma cell line.

Journal Of Experimental & Clinical Cancer Research : Cr
López-Carrasco, Amparo A; Martín-Vañó, Susana S; Burgos-Panadero, Rebeca R; Monferrer, Ezequiel E; Berbegall, Ana P AP; Fernández-Blanco, Beatriz B; Navarro, Samuel S; Noguera, Rosa R
Publication Date: 2020-10-28

Variant appearance in text: ALK: 668-79853G>A; rs7564486
PubMed Link: 33109237
Variant Present in the following documents:
  • 13046_2020_1729_MOESM3_ESM.xlsx, sheet 2
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: rs7564486
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page