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TG c.4002+1242G>T
Variant ID: 8-133921827-G-T
NM_003235.4(
TG
):c.4002+1242G>T
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: rs2687834
PubMed Link:
32879140
Variant Present in the following documents:
jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page
An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.
Plos One
Landa, Iñigo I; Boullosa, Cesar C; Inglada-Pérez, Lucía L; Sastre-Perona, Ana A; Pastor, Susana S; Velázquez, Antonia A; Mancikova, Veronika V; Ruiz-Llorente, Sergio S; Schiavi, Francesca F; Marcos, Ricard R; Malats, Nuria N; Opocher, Giuseppe G; Diaz-Uriarte, Ramon R; Santisteban, Pilar P; Valencia, Alfonso A; Robledo, Mercedes M
Publication Date: 2013
Variant appearance in text: rs2687834
PubMed Link:
24086368
Variant Present in the following documents:
Main text
pone.0074765.pdf
View BVdb publication page