RARA c.865G>A ;(p.G289R)

Variant ID: 17-38510611-G-A

NM_000964.3(RARA):c.865G>A;(p.G289R)

This variant was identified in 6 publications

View GRCh38 version.




Publications:


CTCF DNA-binding domain undergoes dynamic and selective protein-protein interactions.

Iscience
Zhou, Rong R; Tian, Kai K; Huang, Jie J; Duan, Wenjia W; Fu, Hongye H; Feng, Ying Y; Wang, Hui H; Jiang, Yongpeng Y; Li, Yuanjun Y; Wang, Rui R; Hu, Jiazhi J; Ma, Hanhui H; Qi, Zhi Z; Ji, Xiong X
Publication Date: 2022-09-16

Variant appearance in text: RARA: 865G>A; G289R
PubMed Link: 36117989
Variant Present in the following documents:
  • mmc4.xlsx, sheet 1
View BVdb publication page



Genomic characterization of lymphomas in patients with inborn errors of immunity.

Blood Advances
Ye, Xiaofei X; Maglione, Paul J PJ; Wehr, Claudia C; Li, Xiaobo X; Wang, Yating Y; Abolhassani, Hassan H; Deripapa, Elena E; Liu, Dongbing D; Borte, Stephan S; Du, Likun L; Wan, Hui H; Plötner, Andreas A; Giannoula, Yvonne Y; Ko, Huai-Bin HB; Hou, Yong Y; Zhu, Shida S; Grossman, Jennifer K JK; Sander, Birgitta B; Grimbacher, Bodo B; Hammarström, Lennart L; Fedorova, Alina A; Rosenzweig, Sergio D SD; Shcherbina, Anna A; Wu, Kui K; Warnatz, Klaus K; Cunningham-Rundles, Charlotte C; Pan-Hammarström, Qiang Q
Publication Date: 2022-09-27

Variant appearance in text: RARA: G289R
PubMed Link: 35687490
Variant Present in the following documents:
  • advancesADV2021006654-suppl12.xlsx, sheet 1
  • advancesADV2021006654-suppl4.xlsx, sheet 25
View BVdb publication page



Genomic Abnormalities as Biomarkers and Therapeutic Targets in Acute Myeloid Leukemia.

Cancers
Ribeiro, Sara S; Eiring, Anna M AM; Khorashad, Jamshid S JS
Publication Date: 2021-10-09

Variant appearance in text: RARA: G289R
PubMed Link: 34680203
Variant Present in the following documents:
  • Main text
  • cancers-13-05055.pdf
View BVdb publication page



NOTCH and DNA repair pathways are more frequently targeted by genomic alterations in inflammatory than in non-inflammatory breast cancers.

Molecular Oncology
Bertucci, François F; Rypens, Charlotte C; Finetti, Pascal P; Guille, Arnaud A; Adélaïde, José J; Monneur, Audrey A; Carbuccia, Nadine N; Garnier, Séverine S; Dirix, Piet P; Gonçalves, Anthony A; Vermeulen, Peter P; Debeb, Bisrat G BG; Wang, Xiaoping X; Dirix, Luc L; Ueno, Naoto T NT; Viens, Patrice P; Cristofanilli, Massimo M; Chaffanet, Max M; Birnbaum, Daniel D; Van Laere, Steven S
Publication Date: 2020-03

Variant appearance in text: RARA: G289R
PubMed Link: 31854063
Variant Present in the following documents:
  • MOL2-14-504-s010.xlsx, sheet 1
View BVdb publication page



Analysis on GENIE reveals novel recurrent variants that affect molecular diagnosis of sizable number of cancer patients.

Bmc Cancer
Koyama, Takahiko T; Rhrissorrakrai, Kahn K; Parida, Laxmi L
Publication Date: 2019-02-01

Variant appearance in text: RARA: 865G>A; G289R
PubMed Link: 30709382
Variant Present in the following documents:
  • 12885_2019_5313_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Dual origin of relapses in retinoic-acid resistant acute promyelocytic leukemia.

Nature Communications
Lehmann-Che, Jacqueline J; Bally, Cécile C; Letouzé, Eric E; Berthier, Caroline C; Yuan, Hao H; Jollivet, Florence F; Ades, Lionel L; Cassinat, Bruno B; Hirsch, Pierre P; Pigneux, Arnaud A; Mozziconacci, Marie-Joelle MJ; Kogan, Scott S; Fenaux, Pierre P; de Thé, Hugues H
Publication Date: 2018-05-24

Variant appearance in text: RARA: Gly289Arg
PubMed Link: 29795382
Variant Present in the following documents:
  • 41467_2018_4384_MOESM5_ESM.xlsx, sheet 1
  • 41467_2018_4384_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page