DNMT3A c.2645G>C ;(p.R882P)

Variant ID: 2-25457242-C-G

NM_022552.4(DNMT3A):c.2645G>C;(p.R882P)

This variant was identified in 81 publications

View GRCh38 version.




Publications:


Transcriptome-based molecular subtypes and differentiation hierarchies improve the classification framework of acute myeloid leukemia.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Cheng, Wen-Yan WY; Li, Jian-Feng JF; Zhu, Yong-Mei YM; Lin, Xiang-Jie XJ; Wen, Li-Jun LJ; Zhang, Fan F; Zhang, Yu-Liang YL; Zhao, Ming M; Fang, Hai H; Wang, Sheng-Yue SY; Lin, Xiao-Jing XJ; Qiao, Niu N; Yin, Wei W; Zhang, Jia-Nan JN; Dai, Yu-Ting YT; Jiang, Lu L; Sun, Xiao-Jian XJ; Xu, Yi Y; Zhang, Tong-Tong TT; Chen, Su-Ning SN; Zhu, Hong-Hu HH; Chen, Zhu Z; Jin, Jie J; Wu, De-Pei DP; Shen, Yang Y; Chen, Sai-Juan SJ
Publication Date: 2022-12-06

Variant appearance in text: DNMT3A: 2645G>C; Arg882Pro
PubMed Link: 36442087
Variant Present in the following documents:
  • pnas.2211429119.sd02.xlsx, sheet 1
View BVdb publication page



A sex-informed approach to improve the personalised decision making process in myelodysplastic syndromes: a multicentre, observational cohort study.

The Lancet. Haematology
,
Publication Date: 2022-11-24

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 36436542
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page



Recurrent missense variants in clonal hematopoiesis-related genes present in the general population.

Clinical Genetics
Ariste, Olivier O; de la Grange, Pierre P; Veitia, Reiner A RA
Publication Date: 2022-11-10

Variant appearance in text: DNMT3A: 2645G>C; Arg882Pro; rs147001633
PubMed Link: 36353970
Variant Present in the following documents:
  • CGE-103-247-s002.xlsx, sheet 1
  • CGE-103-247-s001.xlsx, sheet 1
View BVdb publication page



The antileukemic activity of decitabine upon PML/RARA-negative AML blasts is supported by all-trans retinoic acid: in vitro and in vivo evidence for cooperation.

Blood Cancer Journal
Meier, Ruth R; Greve, Gabriele G; Zimmer, Dennis D; Bresser, Helena H; Berberich, Bettina B; Langova, Ralitsa R; Stomper, Julia J; Rubarth, Anne A; Feuerbach, Lars L; Lipka, Daniel B DB; Hey, Joschka J; Grüning, Björn B; Brors, Benedikt B; Duyster, Justus J; Plass, Christoph C; Becker, Heiko H; Lübbert, Michael M
Publication Date: 2022-08-22

Variant appearance in text: DNMT3A: 2645G>C
PubMed Link: 35995769
Variant Present in the following documents:
  • 41408_2022_715_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page



Genomic landscape of patients with FLT3-mutated acute myeloid leukemia (AML) treated within the CALGB 10603/RATIFY trial.

Leukemia
Jahn, Nikolaus N; Jahn, Ekaterina E; Saadati, Maral M; Bullinger, Lars L; Larson, Richard A RA; Ottone, Tiziana T; Amadori, Sergio S; Prior, Thomas W TW; Brandwein, Joseph M JM; Appelbaum, Frederick R FR; Medeiros, Bruno C BC; Tallman, Martin S MS; Ehninger, Gerhard G; Heuser, Michael M; Ganser, Arnold A; Pallaud, Celine C; Gathmann, Insa I; Krzykalla, Julia J; Benner, Axel A; Bloomfield, Clara D CD; Thiede, Christian C; Stone, Richard M RM; Döhner, Hartmut H; Döhner, Konstanze K
Publication Date: 2022-09

Variant appearance in text: DNMT3A: R882P; rs147001633
PubMed Link: 35922444
Variant Present in the following documents:
  • 41375_2022_1650_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis.

Nature Genetics
Kar, Siddhartha P SP; Quiros, Pedro M PM; Gu, Muxin M; Jiang, Tao T; Mitchell, Jonathan J; Langdon, Ryan R; Iyer, Vivek V; Barcena, Clea C; Vijayabaskar, M S MS; Fabre, Margarete A MA; Carter, Paul P; Petrovski, Slavé S; Burgess, Stephen S; Vassiliou, George S GS
Publication Date: 2022-08

Variant appearance in text: DNMT3A: R882P
PubMed Link: 35835912
Variant Present in the following documents:
  • 41588_2022_1121_MOESM3_ESM.xlsx, sheet 2
  • 41588_2022_1121_MOESM3_ESM.xlsx, sheet 4
View BVdb publication page



Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery.

Nature Communications
Havugimana, Pierre C PC; Goel, Raghuveera Kumar RK; Phanse, Sadhna S; Youssef, Ahmed A; Padhorny, Dzmitry D; Kotelnikov, Sergei S; Kozakov, Dima D; Emili, Andrew A
Publication Date: 2022-07-13

Variant appearance in text: rs147001633
PubMed Link: 35831314
Variant Present in the following documents:
  • 41467_2022_31809_MOESM8_ESM.xlsx, sheet 3
View BVdb publication page



Clinical genomic profiling in the management of patients with soft tissue and bone sarcoma.

Nature Communications
Gounder, Mrinal M MM; Agaram, Narasimhan P NP; Trabucco, Sally E SE; Robinson, Victoria V; Ferraro, Richard A RA; Millis, Sherri Z SZ; Krishnan, Anita A; Lee, Jessica J; Attia, Steven S; Abida, Wassim W; Drilon, Alexander A; Chi, Ping P; Angelo, Sandra P D' SP; Dickson, Mark A MA; Keohan, Mary Lou ML; Kelly, Ciara M CM; Agulnik, Mark M; Chawla, Sant P SP; Choy, Edwin E; Chugh, Rashmi R; Meyer, Christian F CF; Myer, Parvathi A PA; Moore, Jessica L JL; Okimoto, Ross A RA; Pollock, Raphael E RE; Ravi, Vinod V; Singh, Arun S AS; Somaiah, Neeta N; Wagner, Andrew J AJ; Healey, John H JH; Frampton, Garrett M GM; Venstrom, Jeffrey M JM; Ross, Jeffrey S JS; Ladanyi, Marc M; Singer, Samuel S; Brennan, Murray F MF; Schwartz, Gary K GK; Lazar, Alexander J AJ; Thomas, David M DM; Maki, Robert G RG; Tap, William D WD; Ali, Siraj M SM; Jin, Dexter X DX
Publication Date: 2022-06-15

Variant appearance in text: DNMT3A: R882P
PubMed Link: 35705558
Variant Present in the following documents:
  • 41467_2022_30496_MOESM2_ESM.xls, sheet 1
View BVdb publication page



The longitudinal dynamics and natural history of clonal haematopoiesis.

Nature
Fabre, Margarete A MA; de Almeida, José Guilherme JG; Fiorillo, Edoardo E; Mitchell, Emily E; Damaskou, Aristi A; Rak, Justyna J; Orrù, Valeria V; Marongiu, Michele M; Chapman, Michael Spencer MS; Vijayabaskar, M S MS; Baxter, Joanna J; Hardy, Claire C; Abascal, Federico F; Williams, Nicholas N; Nangalia, Jyoti J; Martincorena, Iñigo I; Campbell, Peter J PJ; McKinney, Eoin F EF; Cucca, Francesco F; Gerstung, Moritz M; Vassiliou, George S GS
Publication Date: 2022-06

Variant appearance in text: DNMT3A: R882P
PubMed Link: 35650444
Variant Present in the following documents:
  • 41586_2022_4785_MOESM12_ESM.xlsx, sheet 2
  • 41586_2022_4785_MOESM13_ESM.xlsx, sheet 3
  • 41586_2022_4785_MOESM12_ESM.xlsx, sheet 1
View BVdb publication page



RUNX1 mutations contribute to the progression of MDS due to disruption of antitumor cellular defense: a study on patients with lower-risk MDS.

Leukemia
Kaisrlikova, Monika M; Vesela, Jitka J; Kundrat, David D; Votavova, Hana H; Dostalova Merkerova, Michaela M; Krejcik, Zdenek Z; Divoky, Vladimir V; Jedlicka, Marek M; Fric, Jan J; Klema, Jiri J; Mikulenkova, Dana D; Stastna Markova, Marketa M; Lauermannova, Marie M; Mertova, Jolana J; Soukupova Maaloufova, Jacqueline J; Jonasova, Anna A; Cermak, Jaroslav J; Belickova, Monika M
Publication Date: 2022-07

Variant appearance in text: DNMT3A: 2645G>C; Arg882Pro
PubMed Link: 35505182
Variant Present in the following documents:
  • 41375_2022_1584_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Probing altered enzyme activity in the biochemical characterization of cancer.

Bioscience Reports
Adam, Mowaffaq Adam Ahmed MAA; Sohl, Christal D CD
Publication Date: 2022-02-25

Variant appearance in text: DNMT3A: R882P
PubMed Link: 35048115
Variant Present in the following documents:
  • Main text
View BVdb publication page



Probing altered enzyme activity in the biochemical characterization of cancer.

Bioscience Reports
Adam, Mowaffaq Adam Ahmed MAA; Sohl, Christal D CD
Publication Date: 2022-01-20

Variant appearance in text: DNMT3A: R882P
PubMed Link: 35048115
Variant Present in the following documents:
  • Main text
View BVdb publication page



Digital-droplet PCR assays for IDH, DNMT3A and driver mutations to monitor after allogeneic stem cell transplantation minimal residual disease of myelofibrosis.

Bone Marrow Transplantation
Mannina, Daniele D; Badbaran, Anita A; Wolschke, Christine C; Klyuchnikov, Evgeny E; Christopeit, Maximilian M; Fehse, Boris B; Kröger, Nicolaus N
Publication Date: 2022-03

Variant appearance in text: DNMT3A: R882P
PubMed Link: 35046544
Variant Present in the following documents:
  • Main text
  • 41409_2022_Article_1566.pdf
View BVdb publication page



Update on recurrent mutations in angioimmunoblastic T-cell lymphoma.

International Journal Of Clinical And Experimental Pathology
Yu, Daniel Dai DD; Zhang, Jianzhong J
Publication Date: 2021

Variant appearance in text: DNMT3A: R882P
PubMed Link: 35027991
Variant Present in the following documents:
  • Main text
View BVdb publication page



Misregulation of the expression and activity of DNA methyltransferases in cancer.

Nar Cancer
Mensah, Isaiah K IK; Norvil, Allison B AB; AlAbdi, Lama L; McGovern, Sarah S; Petell, Christopher J CJ; He, Ming M; Gowher, Humaira H
Publication Date: 2021-12

Variant appearance in text: DNMT3A: Arg882Pro
PubMed Link: 34870206
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of clonal hematopoiesis with chronic obstructive pulmonary disease.

Blood
Miller, Peter G PG; Qiao, Dandi D; Rojas-Quintero, Joselyn J; Honigberg, Michael C MC; Sperling, Adam S AS; Gibson, Christopher J CJ; Bick, Alexander G AG; Niroula, Abhishek A; McConkey, Marie E ME; Sandoval, Brittany B; Miller, Brian C BC; Shi, Weiwei W; Viswanathan, Kaushik K; Leventhal, Matthew M; Werner, Lillian L; Moll, Matthew M; Cade, Brian E BE; Barr, R Graham RG; Correa, Adolfo A; Cupples, L Adrienne LA; Gharib, Sina A SA; Jain, Deepti D; Gogarten, Stephanie M SM; Lange, Leslie A LA; London, Stephanie J SJ; Manichaikul, Ani A; O'Connor, George T GT; Oelsner, Elizabeth C EC; Redline, Susan S; Rich, Stephen S SS; Rotter, Jerome I JI; Ramachandran, Vasan V; Yu, Bing B; Sholl, Lynette L; Neuberg, Donna D; Jaiswal, Siddhartha S; Levy, Bruce D BD; Owen, Caroline A CA; Natarajan, Pradeep P; Silverman, Edwin K EK; van Galen, Peter P; Tesfaigzi, Yohannes Y; Cho, Michael H MH; Ebert, Benjamin L BL; ,
Publication Date: 2022-01-20

Variant appearance in text: DNMT3A: R882P
PubMed Link: 34855941
Variant Present in the following documents:
  • 10.1182-2021013531_bloodbld2021013531-suppl1.pdf
  • bloodBLD2021013531-suppl1.pdf
View BVdb publication page



Mutational landscape of high-grade B-cell lymphoma with MYC-, BCL2 and/or BCL6 rearrangements characterized by whole-exome sequencing.

Haematologica
Künstner, Axel A; Witte, Hanno M HM; Riedl, Jörg J; Bernard, Veronica V; Stölting, Stephanie S; Merz, Hartmut H; Olschewski, Vito V; Peter, Wolfgang W; Ketzer, Julius J; Busch, Yannik Y; Trojok, Peter P; Bubnoff, Nikolas von NV; Busch, Hauke H; Feller, Alfred C AC; Gebauer, Niklas N
Publication Date: 2022-08-01

Variant appearance in text: rs147001633
PubMed Link: 34788985
Variant Present in the following documents:
  • 2021_279631_KUNSTNER_TABS5_SUPPL.xlsx, sheet 1
View BVdb publication page



Integrative Genomic Analysis of Pediatric Myeloid-Related Acute Leukemias Identifies Novel Subtypes and Prognostic Indicators.

Blood Cancer Discovery
Fornerod, Maarten M; Ma, Jing J; Noort, Sanne S; Liu, Yu Y; Walsh, Michael P MP; Shi, Lei L; Nance, Stephanie S; Liu, Yanling Y; Wang, Yuanyuan Y; Song, Guangchun G; Lamprecht, Tamara T; Easton, John J; Mulder, Heather L HL; Yergeau, Donald D; Myers, Jacquelyn J; Kamens, Jennifer L JL; Obeng, Esther A EA; Pigazzi, Martina M; Jarosova, Marie M; Kelaidi, Charikleia C; Polychronopoulou, Sophia S; Lamba, Jatinder K JK; Baker, Sharyn D SD; Rubnitz, Jeffrey E JE; Reinhardt, Dirk D; van den Heuvel-Eibrink, Marry M MM; Locatelli, Franco F; Hasle, Henrik H; Klco, Jeffery M JM; Downing, James R JR; Zhang, Jinghui J; Pounds, Stanley S; Zwaan, C Michel CM; Gruber, Tanja A TA; , ; , ; , ; , ; , ; ,
Publication Date: 2021-11

Variant appearance in text: rs147001633
PubMed Link: 34778799
Variant Present in the following documents:
  • bloodcandisc-2-586-s001.xlsx, sheet 7
View BVdb publication page



Calibration-free NGS quantitation of mutations below 0.01% VAF.

Nature Communications
Dai, Peng P; Wu, Lucia Ruojia LR; Chen, Sherry Xi SX; Wang, Michael Xiangjiang MX; Cheng, Lauren Yuxuan LY; Zhang, Jinny Xuemeng JX; Hao, Pengying P; Yao, Weijie W; Zarka, Jabra J; Issa, Ghayas C GC; Kwong, Lawrence L; Zhang, David Yu DY
Publication Date: 2021-10-21

Variant appearance in text: DNMT3A: R882P
PubMed Link: 34675197
Variant Present in the following documents:
  • 41467_2021_Article_26308.pdf
View BVdb publication page



Targeted Therapy of Papillary Thyroid Cancer: A Comprehensive Genomic Analysis.

Frontiers In Endocrinology
Hescheler, Daniel A DA; Riemann, Burkhard B; Hartmann, Milan J M MJM; Michel, Maximilian M; Faust, Michael M; Bruns, Christiane J CJ; Alakus, Hakan H; Chiapponi, Costanza C
Publication Date: 2021

Variant appearance in text: DNMT3A: R882P
PubMed Link: 34630336
Variant Present in the following documents:
  • Table_1.xlsx, sheet 2
View BVdb publication page



Mutation profile of acute myeloid leukaemia in a Chinese cohort by targeted next-generation sequencing.

Cancer Reports (Hoboken, N.J.)
Lit, Benny Man Wai BMW; Guo, Belinda B BB; Malherbe, Jacques A J JAJ; Kwong, Yok Lam YL; Erber, Wendy N WN
Publication Date: 2022-10

Variant appearance in text: DNMT3A: R882P
PubMed Link: 34617422
Variant Present in the following documents:
  • Main text
  • CNR2-5-e1573.pdf
View BVdb publication page



Mutational landscape of marginal zone B-cell lymphomas of various origin: organotypic alterations and diagnostic potential for assignment of organ origin.

Virchows Archiv : An International Journal Of Pathology
Vela, Visar V; Juskevicius, Darius D; Dirnhofer, Stefan S; Menter, Thomas T; Tzankov, Alexandar A
Publication Date: 2022-02

Variant appearance in text: rs147001633
PubMed Link: 34494161
Variant Present in the following documents:
  • 428_2021_3186_MOESM22_ESM.xlsx, sheet 1
  • 428_2021_3186_MOESM21_ESM.xlsx, sheet 1
View BVdb publication page



Transcriptional control of CBX5 by the RNA binding proteins RBMX and RBMXL1 maintains chromatin state in myeloid leukemia.

Nature Cancer
Prieto, Camila C; Nguyen, Diu T T DTT; Liu, Zhaoqi Z; Wheat, Justin J; Perez, Alexendar A; Gourkanti, Saroj S; Chou, Timothy T; Barin, Ersilia E; Velleca, Anthony A; Rohwetter, Thomas T; Chow, Arthur A; Taggart, James J; Savino, Angela M AM; Hoskova, Katerina K; Dhodapkar, Meera M; Schurer, Alexandra A; Barlowe, Trevor S TS; Vu, Ly P LP; Leslie, Christina C; Steidl, Ulrich U; Rabadan, Raul R; Kharas, Michael G MG
Publication Date: 2021-07

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 34458856
Variant Present in the following documents:
  • NIHMS1703553-supplement-Supplementary_Tables.xlsx, sheet 2
View BVdb publication page



Transcriptional control of CBX5 by the RNA binding proteins RBMX and RBMXL1 maintains chromatin state in myeloid leukemia.

Nature Cancer
Prieto, Camila C; Nguyen, Diu T T DTT; Liu, Zhaoqi Z; Wheat, Justin J; Perez, Alexendar A; Gourkanti, Saroj S; Chou, Timothy T; Barin, Ersilia E; Velleca, Anthony A; Rohwetter, Thomas T; Chow, Arthur A; Taggart, James J; Savino, Angela M AM; Hoskova, Katerina K; Dhodapkar, Meera M; Schurer, Alexandra A; Barlowe, Trevor S TS; Vu, Ly P LP; Leslie, Christina C; Steidl, Ulrich U; Rabadan, Raul R; Kharas, Michael G MG
Publication Date: 2021-07

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 34458856
Variant Present in the following documents:
  • NIHMS1703553-supplement-Supplementary_Tables.xlsx, sheet 2
View BVdb publication page



Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth Syndrome.

Nature Communications
Smith, Amanda M AM; LaValle, Taylor A TA; Shinawi, Marwan M; Ramakrishnan, Sai M SM; Abel, Haley J HJ; Hill, Cheryl A CA; Kirkland, Nicole M NM; Rettig, Michael P MP; Helton, Nichole M NM; Heath, Sharon E SE; Ferraro, Francesca F; Chen, David Y DY; Adak, Sangeeta S; Semenkovich, Clay F CF; Christian, Diana L DL; Martin, Jenna R JR; Gabel, Harrison W HW; Miller, Christopher A CA; Ley, Timothy J TJ
Publication Date: 2021-07-27

Variant appearance in text: DNMT3A: R882P
PubMed Link: 34315901
Variant Present in the following documents:
  • Main text
  • 41467_2021_Article_24800.pdf
View BVdb publication page



Effect of DNMT3A variant allele frequency and double mutation on clinicopathologic features of patients with de novo AML.

Blood Advances
Narayanan, Damodaran D; Pozdnyakova, Olga O; Hasserjian, Robert P RP; Patel, Sanjay S SS; Weinberg, Olga K OK
Publication Date: 2021-06-08

Variant appearance in text: DNMT3A: R882P
PubMed Link: 34100902
Variant Present in the following documents:
  • Main text
View BVdb publication page



A New Insight for the Identification of Oncogenic Variants in Breast and Prostate Cancers in Diverse Human Populations, With a Focus on Latinos.

Frontiers In Pharmacology
Varela, Nelson M NM; Guevara-Ramírez, Patricia P; Acevedo, Cristian C; Zambrano, Tomás T; Armendáriz-Castillo, Isaac I; Guerrero, Santiago S; Quiñones, Luis A LA; López-Cortés, Andrés A
Publication Date: 2021

Variant appearance in text: rs147001633
PubMed Link: 33912047
Variant Present in the following documents:
  • Main text
View BVdb publication page



HOXBLINC long non-coding RNA activation promotes leukemogenesis in NPM1-mutant acute myeloid leukemia.

Nature Communications
Zhu, Ganqian G; Luo, Huacheng H; Feng, Yang Y; Guryanova, Olga A OA; Xu, Jianfeng J; Chen, Shi S; Lai, Qian Q; Sharma, Arati A; Xu, Bing B; Zhao, Zhigang Z; Feng, Ru R; Ni, Hongyu H; Claxton, David D; Guo, Ying Y; Mesa, Ruben A RA; Qiu, Yi Y; Yang, Feng-Chun FC; Li, Wei W; Nimer, Stephen D SD; Huang, Suming S; Xu, Mingjiang M
Publication Date: 2021-03-29

Variant appearance in text: DNMT3A: R882P; rs147001633
PubMed Link: 33782403
Variant Present in the following documents:
  • 41467_2021_22095_MOESM1_ESM.pdf
View BVdb publication page



Full spectrum of clonal haematopoiesis-driver mutations in chronic heart failure and their associations with mortality.

Esc Heart Failure
Kiefer, Katharina C KC; Cremer, Sebastian S; Pardali, Evangelia E; Assmus, Birgit B; Abou-El-Ardat, Khalil K; Kirschbaum, Klara K; Dorsheimer, Lena L; Rasper, Tina T; Berkowitsch, Alexander A; Serve, Hubert H; Dimmeler, Stefanie S; Zeiher, Andreas M AM; Rieger, Michael A MA
Publication Date: 2021-06

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 33779075
Variant Present in the following documents:
  • EHF2-8-1873-s002.xlsx, sheet 1
View BVdb publication page



De novo mutations in folate-related genes associated with common developmental disorders.

Computational And Structural Biotechnology Journal
Luo, Tengfei T; Li, Kuokuo K; Ling, Zhengbao Z; Zhao, Guihu G; Li, Bin B; Wang, Zheng Z; Wang, Xiaomeng X; Han, Ying Y; Xia, Lu L; Zhang, Yi Y; Zhou, Qiao Q; Fang, Zhenghuan Z; Wang, Yijing Y; Chen, Qian Q; Zhou, Xun X; Pan, Hongxu H; Zhao, Yuwen Y; Wang, Yige Y; Dong, Lijie L; Huang, Yuanfeng Y; Hu, Zhengmao Z; Pan, Qian Q; Xia, Kun K; Li, Jinchen J
Publication Date: 2021

Variant appearance in text: rs147001633
PubMed Link: 33777337
Variant Present in the following documents:
  • mmc6.xlsx, sheet 1
View BVdb publication page



DNA methylation epitypes highlight underlying developmental and disease pathways in acute myeloid leukemia.

Genome Research
Giacopelli, Brian B; Wang, Min M; Cleary, Ada A; Wu, Yue-Zhong YZ; Schultz, Anna Reister AR; Schmutz, Maximilian M; Blachly, James S JS; Eisfeld, Ann-Kathrin AK; Mundy-Bosse, Bethany B; Vosberg, Sebastian S; Greif, Philipp A PA; Claus, Rainer R; Bullinger, Lars L; Garzon, Ramiro R; Coombes, Kevin R KR; Bloomfield, Clara D CD; Druker, Brian J BJ; Tyner, Jeffrey W JW; Byrd, John C JC; Oakes, Christopher C CC
Publication Date: 2021-05

Variant appearance in text: DNMT3A: R882P
PubMed Link: 33707228
Variant Present in the following documents:
  • supp_gr.269233.120_Supplemental_Tables_S1_S2_S8-11.xlsx, sheet 6
View BVdb publication page



Genomic and evolutionary portraits of disease relapse in acute myeloid leukemia.

Leukemia
Rapaport, Franck F; Neelamraju, Yaseswini Y; Baslan, Timour T; Hassane, Duane D; Gruszczynska, Agata A; Robert de Massy, Marc M; Farnoud, Noushin N; Haddox, Samuel S; Lee, Tak T; Medina-Martinez, Juan J; Sheridan, Caroline C; Thurmond, Alexis A; Becker, Michael M; Bekiranov, Stefan S; Carroll, Martin M; Moses Murdock, Heardly H; Valk, Peter J M PJM; Bullinger, Lars L; D'Andrea, Richard R; Lowe, Scott W SW; Neuberg, Donna D; Levine, Ross L RL; Melnick, Ari A; Garrett-Bakelman, Francine E FE
Publication Date: 2021-09

Variant appearance in text: DNMT3A: R882P
PubMed Link: 33580203
Variant Present in the following documents:
  • 41375_2021_1153_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Case Report: A Case With Philadelphia Chromosome Positive T-Cell Lymphoblastic Lymphoma and a Review of Literature.

Frontiers In Oncology
Li, Xuewei X; Ping, Nana N; Wang, Yong Y; Xu, Xiaoyu X; Gao, Lijuan L; Zeng, Zhao Z; Zhang, Ling L; Zhang, Zhibo Z; Xie, Yiyu Y; Ruan, Changgeng C; Wu, Depei D; Jin, Zhengming Z; Chen, Suning S
Publication Date: 2020

Variant appearance in text: DNMT3A: 2645G>C; Arg882Pro
PubMed Link: 33552960
Variant Present in the following documents:
  • Main text
  • fonc-10-584149.pdf
View BVdb publication page



Pan-cancer circulating tumor DNA detection in over 10,000 Chinese patients.

Nature Communications
Zhang, Yongliang Y; Yao, Yu Y; Xu, Yaping Y; Li, Lifeng L; Gong, Yan Y; Zhang, Kai K; Zhang, Meng M; Guan, Yanfang Y; Chang, Lianpeng L; Xia, Xuefeng X; Li, Lin L; Jia, Shuqin S; Zeng, Qiang Q
Publication Date: 2021-01-04

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 33397889
Variant Present in the following documents:
  • 41467_2020_20162_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page



Integration of intra-sample contextual error modeling for improved detection of somatic mutations from deep sequencing.

Science Advances
Abelson, Sagi S; Zeng, Andy G X AGX; Nofech-Mozes, Ido I; Wang, Ting Ting TT; Ng, Stanley W K SWK; Minden, Mark D MD; Pugh, Trevor J TJ; Awadalla, Philip P; Shlush, Liran I LI; Murphy, Tracy T; Chan, Steven M SM; Dick, John E JE; Bratman, Scott V SV
Publication Date: 2020-12

Variant appearance in text: DNMT3A: R882P
PubMed Link: 33298453
Variant Present in the following documents:
  • abe3722_Table_S3.xlsx, sheet 5
  • abe3722_Table_S3.xlsx, sheet 3
View BVdb publication page



Comprehensive next-generation profiling of clonal hematopoiesis in cancer patients using paired tumor-blood sequencing for guiding personalized therapies.

Clinical And Translational Medicine
Li, Ziyang Z; Huang, Wensou W; Yin, Jiani C JC; Na, Chenglong C; Wu, Xue X; Shao, Yang Y; Ding, Huaxin H; Li, Jinming J
Publication Date: 2020-11

Variant appearance in text: DNMT3A: R882P
PubMed Link: 33252848
Variant Present in the following documents:
  • CTM2-10-e222.pdf
  • CTM2-10-e222-s003.xlsx, sheet 1
View BVdb publication page



Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics.

Nature Communications
Morita, Kiyomi K; Wang, Feng F; Jahn, Katharina K; Hu, Tianyuan T; Tanaka, Tomoyuki T; Sasaki, Yuya Y; Kuipers, Jack J; Loghavi, Sanam S; Wang, Sa A SA; Yan, Yuanqing Y; Furudate, Ken K; Matthews, Jairo J; Little, Latasha L; Gumbs, Curtis C; Zhang, Jianhua J; Song, Xingzhi X; Thompson, Erika E; Patel, Keyur P KP; Bueso-Ramos, Carlos E CE; DiNardo, Courtney D CD; Ravandi, Farhad F; Jabbour, Elias E; Andreeff, Michael M; Cortes, Jorge J; Bhalla, Kapil K; Garcia-Manero, Guillermo G; Kantarjian, Hagop H; Konopleva, Marina M; Nakada, Daisuke D; Navin, Nicholas N; Beerenwinkel, Niko N; Futreal, P Andrew PA; Takahashi, Koichi K
Publication Date: 2020-10-21

Variant appearance in text: DNMT3A: R882P
PubMed Link: 33087716
Variant Present in the following documents:
  • 41467_2020_19119_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Inherited causes of clonal haematopoiesis in 97,691 whole genomes.

Nature
Bick, Alexander G AG; Weinstock, Joshua S JS; Nandakumar, Satish K SK; Fulco, Charles P CP; Bao, Erik L EL; Zekavat, Seyedeh M SM; Szeto, Mindy D MD; Liao, Xiaotian X; Leventhal, Matthew J MJ; Nasser, Joseph J; Chang, Kyle K; Laurie, Cecelia C; Burugula, Bala Bharathi BB; Gibson, Christopher J CJ; Lin, Amy E AE; Taub, Margaret A MA; Aguet, Francois F; Ardlie, Kristin K; Mitchell, Braxton D BD; Barnes, Kathleen C KC; Moscati, Arden A; Fornage, Myriam M; Redline, Susan S; Psaty, Bruce M BM; Silverman, Edwin K EK; Weiss, Scott T ST; Palmer, Nicholette D ND; Vasan, Ramachandran S RS; Burchard, Esteban G EG; Kardia, Sharon L R SLR; He, Jiang J; Kaplan, Robert C RC; Smith, Nicholas L NL; Arnett, Donna K DK; Schwartz, David A DA; Correa, Adolfo A; de Andrade, Mariza M; Guo, Xiuqing X; Konkle, Barbara A BA; Custer, Brian B; Peralta, Juan M JM; Gui, Hongsheng H; Meyers, Deborah A DA; McGarvey, Stephen T ST; Chen, Ida Yii-Der IY; Shoemaker, M Benjamin MB; Peyser, Patricia A PA; Broome, Jai G JG; Gogarten, Stephanie M SM; Wang, Fei Fei FF; Wong, Quenna Q; Montasser, May E ME; Daya, Michelle M; Kenny, Eimear E EE; North, Kari E KE; Launer, Lenore J LJ; Cade, Brian E BE; Bis, Joshua C JC; Cho, Michael H MH; Lasky-Su, Jessica J; Bowden, Donald W DW; Cupples, L Adrienne LA; Mak, Angel C Y ACY; Becker, Lewis C LC; Smith, Jennifer A JA; Kelly, Tanika N TN; Aslibekyan, Stella S; Heckbert, Susan R SR; Tiwari, Hemant K HK; Yang, Ivana V IV; Heit, John A JA; Lubitz, Steven A SA; Johnsen, Jill M JM; Curran, Joanne E JE; Wenzel, Sally E SE; Weeks, Daniel E DE; Rao, Dabeeru C DC; Darbar, Dawood D; Moon, Jee-Young JY; Tracy, Russell P RP; Buth, Erin J EJ; Rafaels, Nicholas N; Loos, Ruth J F RJF; Durda, Peter P; Liu, Yongmei Y; Hou, Lifang L; Lee, Jiwon J; Kachroo, Priyadarshini P; Freedman, Barry I BI; Levy, Daniel D; Bielak, Lawrence F LF; Hixson, James E JE; Floyd, James S JS; Whitsel, Eric A EA; Ellinor, Patrick T PT; Irvin, Marguerite R MR; Fingerlin, Tasha E TE; Raffield, Laura M LM; Armasu, Sebastian M SM; Wheeler, Marsha M MM; Sabino, Ester C EC; Blangero, John J; Williams, L Keoki LK; Levy, Bruce D BD; Sheu, Wayne Huey-Herng WH; Roden, Dan M DM; Boerwinkle, Eric E; Manson, JoAnn E JE; Mathias, Rasika A RA; Desai, Pinkal P; Taylor, Kent D KD; Johnson, Andrew D AD; , ; Auer, Paul L PL; Kooperberg, Charles C; Laurie, Cathy C CC; Blackwell, Thomas W TW; Smith, Albert V AV; Zhao, Hongyu H; Lange, Ethan E; Lange, Leslie L; Rich, Stephen S SS; Rotter, Jerome I JI; Wilson, James G JG; Scheet, Paul P; Kitzman, Jacob O JO; Lander, Eric S ES; Engreitz, Jesse M JM; Ebert, Benjamin L BL; Reiner, Alexander P AP; Jaiswal, Siddhartha S; Abecasis, Gonçalo G; Sankaran, Vijay G VG; Kathiresan, Sekar S; Natarajan, Pradeep P
Publication Date: 2020-10

Variant appearance in text: DNMT3A: R882P
PubMed Link: 33057201
Variant Present in the following documents:
  • NIHMS1609346-supplement-1609346_SuppTables.xlsx, sheet 4
View BVdb publication page



DNA Methyltransferases in Cancer: Biology, Paradox, Aberrations, and Targeted Therapy.

Cancers
Zhang, Jiayu J; Yang, Cheng C; Wu, Chunfu C; Cui, Wei W; Wang, Lihui L
Publication Date: 2020-07-31

Variant appearance in text: DNMT3A: R882P
PubMed Link: 32751889
Variant Present in the following documents:
  • Main text
  • cancers-12-02123.pdf
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: DNMT3A: R882P
PubMed Link: 32579932
Variant Present in the following documents:
  • mmc5.xlsx, sheet 3
View BVdb publication page



Monosomal karyotype and chromosome 17p loss or TP53 mutations in decitabine-treated patients with acute myeloid leukemia.

Annals Of Hematology
Becker, Heiko H; Pfeifer, Dietmar D; Ihorst, Gabriele G; Pantic, Milena M; Wehrle, Julius J; Rüter, Björn H BH; Bullinger, Lars L; Hackanson, Björn B; Germing, Ulrich U; Kuendgen, Andrea A; Platzbecker, Uwe U; Döhner, Konstanze K; Ganser, Arnold A; Hagemeijer, Anne A; Wijermans, Pierre W PW; Döhner, Hartmut H; Duyster, Justus J; Lübbert, Michael M
Publication Date: 2020-07

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 32504186
Variant Present in the following documents:
  • 277_2020_4082_MOESM1_ESM.pdf
View BVdb publication page



Identification of targeted therapy options for gastric adenocarcinoma by comprehensive analysis of genomic data.

Gastric Cancer : Official Journal Of The International Gastric Cancer Association And The Japanese Gastric Cancer Association
Hescheler, Daniel A DA; Plum, Patrick S PS; Zander, Thomas T; Quaas, Alexander A; Korenkov, Michael M; Gassa, Asmae A; Michel, Maximilian M; Bruns, Christiane J CJ; Alakus, Hakan H
Publication Date: 2020-07

Variant appearance in text: DNMT3A: R882P
PubMed Link: 32107691
Variant Present in the following documents:
  • 10120_2020_1045_MOESM1_ESM.xlsx, sheet 12
View BVdb publication page



AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting.

Bmc Medical Genomics
Wünsch, Christian C; Banck, Henrik H; Müller-Tidow, Carsten C; Dugas, Martin M
Publication Date: 2020-02-04

Variant appearance in text: DNMT3A: 2645G>C; R882P; rs147001633
PubMed Link: 32019565
Variant Present in the following documents:
  • 12920_2020_668_MOESM6_ESM.xls, sheet 1
  • 12920_2020_668_MOESM7_ESM.xls, sheet 1
  • 12920_2020_668_MOESM8_ESM.xls, sheet 1
View BVdb publication page



Modelling the Effects of MCM7 Variants, Somatic Mutations, and Clinical Features on Acute Myeloid Leukemia Susceptibility and Prognosis.

Journal Of Clinical Medicine
Tripon, Florin F; Iancu, Mihaela M; Trifa, Adrian A; Crauciuc, George Andrei GA; Boglis, Alina A; Dima, Delia D; Lazar, Erzsebet E; Bănescu, Claudia C
Publication Date: 2020-01-08

Variant appearance in text: rs147001633
PubMed Link: 31936215
Variant Present in the following documents:
  • Main text
  • jcm-09-00158.pdf
View BVdb publication page



Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes.

Communications Biology
Dong, Xiaobao X; Huang, Dandan D; Yi, Xianfu X; Zhang, Shijie S; Wang, Zhao Z; Yan, Bin B; Chung Sham, Pak P; Chen, Kexin K; Jun Li, Mulin M
Publication Date: 2020-01-07

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 31925297
Variant Present in the following documents:
  • 42003_2019_736_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Clinical Features and MicroRNA Expression Patterns Between AML Patients With DNMT3A R882 and Frameshift Mutations.

Frontiers In Oncology
Yang, Li L; Shen, Ke'Feng K; Zhang, Mei'Lan M; Zhang, Wei W; Cai, Hao'Dong H; Lin, Li'Man L; Long, Xiao'Lu X; Xing, Shu'Gang S; Tang, Yang Y; Xiong, Jie J; Wang, Jia'Chen J; Li, Deng'Ju D; Zhou, Jian'Feng J; Xiao, Min M
Publication Date: 2019

Variant appearance in text: DNMT3A: R882P
PubMed Link: 31709191
Variant Present in the following documents:
  • Main text
  • fonc-09-01133.pdf
View BVdb publication page



Mutations of R882 change flanking sequence preferences of the DNA methyltransferase DNMT3A and cellular methylation patterns.

Nucleic Acids Research
Emperle, Max M; Adam, Sabrina S; Kunert, Stefan S; Dukatz, Michael M; Baude, Annika A; Plass, Christoph C; Rathert, Philipp P; Bashtrykov, Pavel P; Jeltsch, Albert A
Publication Date: 2019-12-02

Variant appearance in text: DNMT3A: R882P
PubMed Link: 31620784
Variant Present in the following documents:
  • Main text
  • gkz911.pdf
View BVdb publication page



Influence of DNMT3A R882 mutations on AML prognosis determined by the allele ratio in Chinese patients.

Journal Of Translational Medicine
Yuan, Xiao-Qing XQ; Chen, Peng P; Du, Yin-Xiao YX; Zhu, Ke-Wei KW; Zhang, Dao-Yu DY; Yan, Han H; Liu, Han H; Liu, Yan-Ling YL; Cao, Shan S; Zhou, Gan G; Zeng, Hui H; Chen, Shu-Ping SP; Zhao, Xie-Lan XL; Yang, Jing J; Zeng, Wen-Jing WJ; Chen, Xiao-Ping XP
Publication Date: 2019-07-10

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 31291961
Variant Present in the following documents:
  • Main text
  • 12967_2019_Article_1959.pdf
View BVdb publication page



Clonal evolution patterns in acute myeloid leukemia with NPM1 mutation.

Nature Communications
Cocciardi, Sibylle S; Dolnik, Anna A; Kapp-Schwoerer, Silke S; Rücker, Frank G FG; Lux, Susanne S; Blätte, Tamara J TJ; Skambraks, Sabrina S; Krönke, Jan J; Heidel, Florian H FH; Schnöder, Tina M TM; Corbacioglu, Andrea A; Gaidzik, Verena I VI; Paschka, Peter P; Teleanu, Veronica V; Göhring, Gudrun G; Thol, Felicitas F; Heuser, Michael M; Ganser, Arnold A; Weber, Daniela D; Sträng, Eric E; Kestler, Hans A HA; Döhner, Hartmut H; Bullinger, Lars L; Döhner, Konstanze K
Publication Date: 2019-05-02

Variant appearance in text: N/A
PubMed Link: 31048683
Variant Present in the following documents:
View BVdb publication page



Mutational spectrum and associations with clinical features in patients with acute myeloid leukaemia based on next‑generation sequencing.

Molecular Medicine Reports
Li, Ying Y; Lv, Xiao X; Ge, Xueling X; Yuan, Dai D; Ding, Mei M; Zhen, Changqing C; Zhao, Wenbo W; Liu, Xin X; Wang, Xianghua X; Xu, Hongzhi H; Li, Ying Y; Wang, Xin X
Publication Date: 2019-05

Variant appearance in text: DNMT3A: R882P
PubMed Link: 30942411
Variant Present in the following documents:
  • Main text
  • mmr-19-05-4147.pdf
View BVdb publication page



Functional genomic landscape of acute myeloid leukaemia.

Nature
Tyner, Jeffrey W JW; Tognon, Cristina E CE; Bottomly, Daniel D; Wilmot, Beth B; Kurtz, Stephen E SE; Savage, Samantha L SL; Long, Nicola N; Schultz, Anna Reister AR; Traer, Elie E; Abel, Melissa M; Agarwal, Anupriya A; Blucher, Aurora A; Borate, Uma U; Bryant, Jade J; Burke, Russell R; Carlos, Amy A; Carpenter, Richie R; Carroll, Joseph J; Chang, Bill H BH; Coblentz, Cody C; d'Almeida, Amanda A; Cook, Rachel R; Danilov, Alexey A; Dao, Kim-Hien T KT; Degnin, Michie M; Devine, Deirdre D; Dibb, James J; Edwards, David K DK; Eide, Christopher A CA; English, Isabel I; Glover, Jason J; Henson, Rachel R; Ho, Hibery H; Jemal, Abdusebur A; Johnson, Kara K; Johnson, Ryan R; Junio, Brian B; Kaempf, Andy A; Leonard, Jessica J; Lin, Chenwei C; Liu, Selina Qiuying SQ; Lo, Pierrette P; Loriaux, Marc M MM; Luty, Samuel S; Macey, Tara T; MacManiman, Jason J; Martinez, Jacqueline J; Mori, Motomi M; Nelson, Dylan D; Nichols, Ceilidh C; Peters, Jill J; Ramsdill, Justin J; Rofelty, Angela A; Schuff, Robert R; Searles, Robert R; Segerdell, Erik E; Smith, Rebecca L RL; Spurgeon, Stephen E SE; Sweeney, Tyler T; Thapa, Aashis A; Visser, Corinne C; Wagner, Jake J; Watanabe-Smith, Kevin K; Werth, Kristen K; Wolf, Joelle J; White, Libbey L; Yates, Amy A; Zhang, Haijiao H; Cogle, Christopher R CR; Collins, Robert H RH; Connolly, Denise C DC; Deininger, Michael W MW; Drusbosky, Leylah L; Hourigan, Christopher S CS; Jordan, Craig T CT; Kropf, Patricia P; Lin, Tara L TL; Martinez, Micaela E ME; Medeiros, Bruno C BC; Pallapati, Rachel R RR; Pollyea, Daniel A DA; Swords, Ronan T RT; Watts, Justin M JM; Weir, Scott J SJ; Wiest, David L DL; Winters, Ryan M RM; McWeeney, Shannon K SK; Druker, Brian J BJ
Publication Date: 2018-10

Variant appearance in text: N/A
PubMed Link: 30333627
Variant Present in the following documents:
View BVdb publication page



An integrated genomic analysis of anaplastic meningioma identifies prognostic molecular signatures.

Scientific Reports
Collord, Grace G; Tarpey, Patrick P; Kurbatova, Natalja N; Martincorena, Inigo I; Moran, Sebastian S; Castro, Manuel M; Nagy, Tibor T; Bignell, Graham G; Maura, Francesco F; Young, Matthew D MD; Berna, Jorge J; Tubio, Jose M C JMC; McMurran, Chris E CE; Young, Adam M H AMH; Sanders, Mathijs M; Noorani, Imran I; Price, Stephen J SJ; Watts, Colin C; Leipnitz, Elke E; Kirsch, Matthias M; Schackert, Gabriele G; Pearson, Danita D; Devadass, Abel A; Ram, Zvi Z; Collins, V Peter VP; Allinson, Kieren K; Jenkinson, Michael D MD; Zakaria, Rasheed R; Syed, Khaja K; Hanemann, C Oliver CO; Dunn, Jemma J; McDermott, Michael W MW; Kirollos, Ramez W RW; Vassiliou, George S GS; Esteller, Manel M; Behjati, Sam S; Brazma, Alvis A; Santarius, Thomas T; McDermott, Ultan U
Publication Date: 2018-09-10

Variant appearance in text: DNMT3A: R882P
PubMed Link: 30202034
Variant Present in the following documents:
  • 41598_2018_31659_MOESM2_ESM.xlsx, sheet 30
View BVdb publication page



appreci8: a pipeline for precise variant calling integrating 8 tools.

Bioinformatics (Oxford, England)
Sandmann, Sarah S; Karimi, Mohsen M; de Graaf, Aniek O AO; Rohde, Christian C; Göllner, Stefanie S; Varghese, Julian J; Ernsting, Jan J; Walldin, Gunilla G; van der Reijden, Bert A BA; Müller-Tidow, Carsten C; Malcovati, Luca L; Hellström-Lindberg, Eva E; Jansen, Joop H JH; Dugas, Martin M
Publication Date: 2018-12-15

Variant appearance in text: N/A
PubMed Link: 29945233
Variant Present in the following documents:
View BVdb publication page



Distinct age-associated molecular profiles in acute myeloid leukemia defined by comprehensive clinical genomic profiling.

Oncotarget
Tarlock, Katherine K; Zhong, Shan S; He, Yuting Y; Ries, Rhonda R; Severson, Eric E; Bailey, Mark M; Morley, Samantha S; Balasubramanian, Sohail S; Erlich, Rachel R; Lipson, Doron D; Otto, Geoff A GA; Vergillo, Jo-Anne JA; Kolb, E Anders EA; Ross, Jeffrey S JS; Mughal, Tariq T; Stephens, Philip J PJ; Miller, Vincent V; Meshinchi, Soheil S; He, Jie J
Publication Date: 2018-05-29

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 29899868
Variant Present in the following documents:
  • oncotarget-09-26417-s005.xlsx, sheet 1
View BVdb publication page



Multi-omics profiling reveals a distinctive epigenome signature for high-risk acute promyelocytic leukemia.

Oncotarget
Singh, Abhishek A AA; Petraglia, Francesca F; Nebbioso, Angela A; Yi, Guoqiang G; Conte, Mariarosaria M; Valente, Sergio S; Mandoli, Amit A; Scisciola, Lucia L; Lindeboom, Rik R; Kerstens, Hinri H; Janssen-Megens, Eva M EM; Pourfarzad, Farzin F; Habibi, Ehsan E; Berentsen, Kim K; Kim, Bowon B; Logie, Colin C; Heath, Simon S; Wierenga, Albertus T J ATJ; Clarke, Laura L; Flicek, Paul P; Jansen, Joop H JH; Kuijpers, Taco T; Yaspo, Marie Laure ML; Valle, Veronique Della VD; Bernard, Olivier O; Gut, Ivo I; Vellenga, Edo E; Stunnenberg, Hendrik G HG; Mai, Antonello A; Altucci, Lucia L; Martens, Joost H A JHA
Publication Date: 2018-05-22

Variant appearance in text: DNMT3A: R882P
PubMed Link: 29876014
Variant Present in the following documents:
  • oncotarget-09-25647-s002.xlsx, sheet 1
View BVdb publication page



FLT3-ITD Compared with DNMT3A R882 Mutation Is a More Powerful Independent Inferior Prognostic Factor in Adult Acute Myeloid Leukemia Patients After Allogeneic Hematopoietic Stem Cell Transplantation: A Retrospective Cohort Study

Turkish Journal Of Haematology : Official Journal Of Turkish Society Of Haematology
Ardestani, Majid Teremmahi MT; Kazemi, Ahmad A; Chahardouli, Bahram B; Mohammadi, Saeed S; Nikbakht, Mohsen M; Rostami, Shahrbano S; Jalili, Mahdi M; Vaezi, Mohammad M; Alimoghaddam, Kamran K; Ghavamzadeh, Ardeshir A
Publication Date: 2018-08-03

Variant appearance in text: DNMT3A: 2645G>C; R882P
PubMed Link: 29786546
Variant Present in the following documents:
  • Main text
View BVdb publication page