ATM c.5497-292T>C

Variant ID: 11-108175110-T-C

NM_000051.3(ATM):c.5497-292T>C

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: rs4988044
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Use a survival model to correlate single-nucleotide polymorphisms of DNA repair genes with radiation dose-response in patients with non-small cell lung cancer.

Radiotherapy And Oncology : Journal Of The European Society For Therapeutic Radiology And Oncology
Jin, Jian-Yue JY; Wang, Weili W; Ten Haken, Randall K RK; Chen, Jie J; Bi, Nan N; Sadek, Ramses R; Zhang, Hong H; Lawrence, Theodore S TS; Kong, Feng-Ming Spring FM
Publication Date: 2015-10

Variant appearance in text: rs4988044
PubMed Link: 26253951
Variant Present in the following documents:
  • Main text
View BVdb publication page