IRF1 c.*1012C>A

Variant ID: 5-131818631-G-T

NM_002198.2(IRF1):c.*1012C>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs6873426
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs6873426
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
  • oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page



Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).

Blood
Wassel, Christina L CL; Lange, Leslie A LA; Keating, Brendan J BJ; Taylor, Kira C KC; Johnson, Andrew D AD; Palmer, Cameron C; Ho, Lindsey A LA; Smith, Nicholas L NL; Lange, Ethan M EM; Li, Yun Y; Yang, Qiong Q; Delaney, Joseph A JA; Tang, Weihong W; Tofler, Geoffrey G; Redline, Susan S; Taylor, Herman A HA; Wilson, James G JG; Tracy, Russell P RP; Jacobs, David R DR; Folsom, Aaron R AR; Green, David D; O'Donnell, Christopher J CJ; Reiner, Alexander P AP
Publication Date: 2011-01-06

Variant appearance in text: rs6873426
PubMed Link: 20978265
Variant Present in the following documents:
  • Main text
View BVdb publication page