TF c.1204-156G>A

Variant ID: 3-133482870-G-A

NM_001063.3(TF):c.1204-156G>A

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs8177272
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Association between serum iron status and primary liver cancer risk: a Mendelian randomization analysis.

Annals Of Translational Medicine
Tian, Tao T; Xiao, Feng F; Li, Hongdong H; Ding, Dongyang D; Dong, Wei W; Hou, Guojun G; Zhao, Linghao L; Yang, Yun Y; Yang, Yuan Y; Zhou, Weiping W
Publication Date: 2021-10

Variant appearance in text: rs8177272
PubMed Link: 34790739
Variant Present in the following documents:
  • Main text
  • atm-09-20-1533.pdf
View BVdb publication page



Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.

Nature Communications
Benyamin, Beben B; Esko, Tonu T; Ried, Janina S JS; Radhakrishnan, Aparna A; Vermeulen, Sita H SH; Traglia, Michela M; Gögele, Martin M; Anderson, Denise D; Broer, Linda L; Podmore, Clara C; Luan, Jian'an J; Kutalik, Zoltan Z; Sanna, Serena S; van der Meer, Peter P; Tanaka, Toshiko T; Wang, Fudi F; Westra, Harm-Jan HJ; Franke, Lude L; Mihailov, Evelin E; Milani, Lili L; Hälldin, Jonas J; Häldin, Jonas J; Winkelmann, Juliane J; Meitinger, Thomas T; Thiery, Joachim J; Peters, Annette A; Waldenberger, Melanie M; Rendon, Augusto A; Jolley, Jennifer J; Sambrook, Jennifer J; Kiemeney, Lambertus A LA; Sweep, Fred C FC; Sala, Cinzia F CF; Schwienbacher, Christine C; Pichler, Irene I; Hui, Jennie J; Demirkan, Ayse A; Isaacs, Aaron A; Amin, Najaf N; Steri, Maristella M; Waeber, Gérard G; Verweij, Niek N; Powell, Joseph E JE; Nyholt, Dale R DR; Heath, Andrew C AC; Madden, Pamela A F PA; Visscher, Peter M PM; Wright, Margaret J MJ; Montgomery, Grant W GW; Martin, Nicholas G NG; Hernandez, Dena D; Bandinelli, Stefania S; van der Harst, Pim P; Uda, Manuela M; Vollenweider, Peter P; Scott, Robert A RA; Langenberg, Claudia C; Wareham, Nicholas J NJ; , ; van Duijn, Cornelia C; Beilby, John J; Pramstaller, Peter P PP; Hicks, Andrew A AA; Ouwehand, Willem H WH; Oexle, Konrad K; Gieger, Christian C; Metspalu, Andres A; Camaschella, Clara C; Toniolo, Daniela D; Swinkels, Dorine W DW; Whitfield, John B JB
Publication Date: 2014-10-29

Variant appearance in text: rs8177272
PubMed Link: 25352340
Variant Present in the following documents:
  • NIHMS619770-supplement-1.pdf
View BVdb publication page



Genome-wide association study identifies genetic loci associated with iron deficiency.

Plos One
McLaren, Christine E CE; Garner, Chad P CP; Constantine, Clare C CC; McLachlan, Stela S; Vulpe, Chris D CD; Snively, Beverly M BM; Gordeuk, Victor R VR; Nickerson, Debbie A DA; Cook, James D JD; Leiendecker-Foster, Catherine C; Beckman, Kenneth B KB; Eckfeldt, John H JH; Barcellos, Lisa F LF; Murray, Joseph A JA; Adams, Paul C PC; Acton, Ronald T RT; Killeen, Anthony A AA; McLaren, Gordon D GD
Publication Date: 2011-03-31

Variant appearance in text: rs8177272
PubMed Link: 21483845
Variant Present in the following documents:
  • Main text
  • pone.0017390.pdf
View BVdb publication page