ALK c.1155-53129T>G

Variant ID: 2-29659854-A-C

NM_004304.4(ALK):c.1155-53129T>G

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: rs4128317
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Prediction of Colorectal Cancer Risk Using a Genetic Risk Score: The Korean Cancer Prevention Study-II (KCPS-II).

Genomics & Informatics
Jo, Jaeseong J; Nam, Chung Mo CM; Sull, Jae Woong JW; Yun, Ji Eun JE; Kim, Sang Yeun SY; Lee, Sun Ju SJ; Kim, Yoon Nam YN; Park, Eun Jung EJ; Kimm, Heejin H; Jee, Sun Ha SH
Publication Date: 2012-09

Variant appearance in text: rs4128317
PubMed Link: 23166528
Variant Present in the following documents:
  • Main text
  • gni-10-175.pdf
View BVdb publication page