TRAF3 c.962G>A ;(p.R321Q)

Variant ID: 14-103369593-G-A

NM_145725.2(TRAF3):c.962G>A;(p.R321Q)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Genetic variability in COVID-19-related genes in the Brazilian population.

Human Genome Variation
Secolin, Rodrigo R; de Araujo, Tânia K TK; Gonsales, Marina C MC; Rocha, Cristiane S CS; Naslavsky, Michel M; Marco, Luiz De L; Bicalho, Maria A C MAC; Vazquez, Vinicius L VL; Zatz, Mayana M; Silva, Wilson A WA; Lopes-Cendes, Iscia I
Publication Date: 2021

Variant appearance in text: TRAF3: 962G>A; rs148461790
PubMed Link: 33824725
Variant Present in the following documents:
  • 41439_2021_146_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



mTOR Signaling and SREBP Activity Increase FADS2 Expression and Can Activate Sapienate Biosynthesis.

Cell Reports
Triki, Mouna M; Rinaldi, Gianmarco G; Planque, Melanie M; Broekaert, Dorien D; Winkelkotte, Alina M AM; Maier, Carina R CR; Janaki Raman, Sudha S; Vandekeere, Anke A; Van Elsen, Joke J; Orth, Martin F MF; Grünewald, Thomas G P TGP; Schulze, Almut A; Fendt, Sarah-Maria SM
Publication Date: 2020-06-23

Variant appearance in text: TRAF3: R321Q
PubMed Link: 32579932
Variant Present in the following documents:
  • mmc5.xlsx, sheet 3
View BVdb publication page



Clinicopathological and genetic features of limited-stage diffuse large B-cell lymphoma with late relapse: targeted sequencing analysis of gene alterations in the initial and late relapsed tumors.

Haematologica
Suzuki, Tomotaka T; Fukuhara, Suguru S; Nomoto, Junko J; Yamashita, Satoshi S; Maeshima, Akiko M AM; Ito, Yuta Y; Hatta, Shunsuke S; Yuda, Sayako S; Makita, Shinichi S; Munakata, Wataru W; Suzuki, Tatsuya T; Maruyama, Dai D; Taniguchi, Hirokazu H; Ushijima, Toshikazu T; Izutsu, Koji K; Tobinai, Kensei K; Kobayashi, Yukio Y
Publication Date: 2021-02-01

Variant appearance in text: TRAF3: 962G>A; Arg321Gln
PubMed Link: 32336683
Variant Present in the following documents:
  • 2019_235598_SUZUKI_SUPPL.pdf
View BVdb publication page



Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea.

Frontiers In Genetics
van der Spek, Ashley A; Luik, Annemarie I AI; Kocevska, Desana D; Liu, Chunyu C; Brouwer, Rutger W W RWW; van Rooij, Jeroen G J JGJ; van den Hout, Mirjam C G N MCGN; Kraaij, Robert R; Hofman, Albert A; Uitterlinden, André G AG; van IJcken, Wilfred F J WFJ; Gottlieb, Daniel J DJ; Tiemeier, Henning H; van Duijn, Cornelia M CM; Amin, Najaf N
Publication Date: 2017

Variant appearance in text: rs148461790
PubMed Link: 29093733
Variant Present in the following documents:
  • Main text
  • fgene-08-00151.pdf
View BVdb publication page