WTAP c.309G>T ;(p.P103=)

Variant ID: 6-160169258-G-T

NM_001270531.1(WTAP):c.309G>T;(p.P103=)

This variant was identified in 23 publications

View GRCh38 version.




Publications:


Association of RNA m7G Modification Gene Polymorphisms with Pediatric Glioma Risk.

Biomed Research International
Zhu, Jinhong J; Liu, Xiaoping X; Chen, Wei W; Liao, Yuxiang Y; Liu, Jiabin J; Yuan, Li L; Ruan, Jichen J; He, Jing J
Publication Date: 2023

Variant appearance in text: rs7766006
PubMed Link: 36733406
Variant Present in the following documents:
  • BMRI2023-3678327.pdf
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: WTAP: P103P
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
View BVdb publication page



The RNA m6A writer WTAP in diseases: structure, roles, and mechanisms.

Cell Death & Disease
Huang, Qibo Q; Mo, Jie J; Liao, Zhibin Z; Chen, Xiaoping X; Zhang, Bixiang B
Publication Date: 2022-10-07

Variant appearance in text: rs7766006
PubMed Link: 36207306
Variant Present in the following documents:
  • Main text
  • 41419_2022_Article_5268.pdf
View BVdb publication page



Role of WTAP in Cancer: From Mechanisms to the Therapeutic Potential.

Biomolecules
Fan, Yongfei Y; Li, Xinwei X; Sun, Huihui H; Gao, Zhaojia Z; Zhu, Zheng Z; Yuan, Kai K
Publication Date: 2022-09-02

Variant appearance in text: rs7766006
PubMed Link: 36139062
Variant Present in the following documents:
  • Main text
  • biomolecules-12-01224.pdf
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METTL1 gene polymorphisms synergistically confer hepatoblastoma susceptibility.

Discover. Oncology
Ge, Lili L; Zhu, Jinhong J; Liu, Jiabin J; Li, Li L; Zhang, Jiao J; Cheng, Jiwen J; Li, Yong Y; Yang, Zhonghua Z; Li, Suhong S; He, Jing J; Zhang, Xianwei X
Publication Date: 2022-08-20

Variant appearance in text: rs7766006
PubMed Link: 35986847
Variant Present in the following documents:
  • Main text
  • 12672_2022_Article_545.pdf
View BVdb publication page



The Genetic Changes of Hepatoblastoma.

Frontiers In Oncology
Chen, Huitong H; Guan, Qian Q; Guo, Huiqin H; Miao, Lei L; Zhuo, Zhenjian Z
Publication Date: 2021

Variant appearance in text: rs7766006
PubMed Link: 34367972
Variant Present in the following documents:
  • Main text
  • fonc-11-690641.pdf
View BVdb publication page



IGF2BP2 promotes the progression of colorectal cancer through a YAP-dependent mechanism.

Cancer Science
Cui, Jie J; Tian, Jiale J; Wang, Weiwei W; He, Tao T; Li, Xin X; Gu, Chenzheng C; Wang, Lixin L; Wu, Jian J; Shang, Anquan A
Publication Date: 2021-10

Variant appearance in text: rs7766006
PubMed Link: 34309973
Variant Present in the following documents:
  • Main text
  • CAS-112-4087.pdf
View BVdb publication page



Integrative genomic analysis of N6-methyladenosine-single nucleotide polymorphisms (m6A-SNPs) associated with breast cancer.

Bioengineered
Xuan, Zixue Z; Zhang, Yiwen Y; Jiang, Jinying J; Zheng, Xiaowei X; Hu, Xiaoping X; Yang, Xiuli X; Shao, Yanfei Y; Zhang, Guobing G; Huang, Ping P
Publication Date: 2021-12

Variant appearance in text: rs7766006
PubMed Link: 34151731
Variant Present in the following documents:
  • Main text
  • KBIE_12_1935406.pdf
View BVdb publication page



Integrative genomic analysis of N6-methyladenosine-single nucleotide polymorphisms (m6A-SNPs) associated with breast cancer.

Bioengineered
Xuan, Zixue Z; Zhang, Yiwen Y; Jiang, Jinying J; Zheng, Xiaowei X; Hu, Xiaoping X; Yang, Xiuli X; Shao, Yanfei Y; Zhang, Guobing G; Huang, Ping P
Publication Date: 2021-12

Variant appearance in text: rs7766006
PubMed Link: 34151731
Variant Present in the following documents:
  • Main text
  • KBIE_12_1935406.pdf
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: N/A
PubMed Link: 33791233
Variant Present in the following documents:
View BVdb publication page



Genetic variants in m6A modification core genes are associated with glioma risk in Chinese children.

Molecular Therapy Oncolytics
He, Jing J; Yuan, Li L; Lin, Huiran H; Lin, Ao A; Chen, Huitong H; Luo, Ailing A; Zhuo, Zhenjian Z; Liu, Xiaoping X
Publication Date: 2021-03-26

Variant appearance in text: rs7766006
PubMed Link: 33665358
Variant Present in the following documents:
  • Main text
  • main.pdf
  • mmc2.pdf
View BVdb publication page



Associations between WTAP gene polymorphisms and neuroblastoma susceptibility in Chinese children.

Translational Pediatrics
Tang, Jue J; Lu, Hongting H; Yang, Zhonghua Z; Li, Le L; Li, Li L; Zhang, Jiao J; Cheng, Jiwen J; Li, Yong Y; Li, Suhong S; Zhou, Haixia H; He, Jing J; Liu, Wei W
Publication Date: 2021-01

Variant appearance in text: rs7766006
PubMed Link: 33633946
Variant Present in the following documents:
  • Main text
  • tp-10-01-146.pdf
View BVdb publication page



WTAP Gene Variants Confer Hepatoblastoma Susceptibility: A Seven-Center Case-Control Study.

Molecular Therapy Oncolytics
Zhuo, Zhen-Jian ZJ; Hua, Rui-Xi RX; Chen, Zhen Z; Zhu, Jinhong J; Wang, Mi M; Yang, Zhonghua Z; Zhang, Jiao J; Li, Yong Y; Li, Li L; Li, Suhong S; Xin, Yijuan Y; Xia, Huimin H; He, Jing J
Publication Date: 2020-09-25

Variant appearance in text: rs7766006
PubMed Link: 32671187
Variant Present in the following documents:
  • Main text
  • main.pdf
  • mmc2.pdf
View BVdb publication page



Loss of heterozygosity of essential genes represents a widespread class of potential cancer vulnerabilities.

Nature Communications
Nichols, Caitlin A CA; Gibson, William J WJ; Brown, Meredith S MS; Kosmicki, Jack A JA; Busanovich, John P JP; Wei, Hope H; Urbanski, Laura M LM; Curimjee, Naomi N; Berger, Ashton C AC; Gao, Galen F GF; Cherniack, Andrew D AD; Dhe-Paganon, Sirano S; Paolella, Brenton R BR; Beroukhim, Rameen R
Publication Date: 2020-05-20

Variant appearance in text: WTAP: 309G>T; rs7766006
PubMed Link: 32433464
Variant Present in the following documents:
  • 41467_2020_16399_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: N/A
PubMed Link: 31597922
Variant Present in the following documents:
View BVdb publication page



Multiple genetic mutations caused by NKX6.3 depletion contribute to gastric tumorigenesis.

Scientific Reports
Yoon, Jung Hwan JH; Kim, Olga O; Eun, Jung Woo JW; Choi, Sung Sook SS; Ashktorab, Hassan H; Smoot, Duane T DT; Nam, Suk Woo SW; Park, Won Sang WS
Publication Date: 2018-12-04

Variant appearance in text: rs7766006
PubMed Link: 30514953
Variant Present in the following documents:
  • 41598_2018_35733_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: WTAP: 309G>T; rs7766006
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_5.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs7766006
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.

Nature Communications
Dadaev, Tokhir T; Saunders, Edward J EJ; Newcombe, Paul J PJ; Anokian, Ezequiel E; Leongamornlert, Daniel A DA; Brook, Mark N MN; Cieza-Borrella, Clara C; Mijuskovic, Martina M; Wakerell, Sarah S; Olama, Ali Amin Al AAA; Schumacher, Fredrick R FR; Berndt, Sonja I SI; Benlloch, Sara S; Ahmed, Mahbubl M; Goh, Chee C; Sheng, Xin X; Zhang, Zhuo Z; Muir, Kenneth K; Govindasami, Koveela K; Lophatananon, Artitaya A; Stevens, Victoria L VL; Gapstur, Susan M SM; Carter, Brian D BD; Tangen, Catherine M CM; Goodman, Phyllis P; Thompson, Ian M IM; Batra, Jyotsna J; Chambers, Suzanne S; Moya, Leire L; Clements, Judith J; Horvath, Lisa L; Tilley, Wayne W; Risbridger, Gail G; Gronberg, Henrik H; Aly, Markus M; Nordström, Tobias T; Pharoah, Paul P; Pashayan, Nora N; Schleutker, Johanna J; Tammela, Teuvo L J TLJ; Sipeky, Csilla C; Auvinen, Anssi A; Albanes, Demetrius D; Weinstein, Stephanie S; Wolk, Alicja A; Hakansson, Niclas N; West, Catharine C; Dunning, Alison M AM; Burnet, Neil N; Mucci, Lorelei L; Giovannucci, Edward E; Andriole, Gerald G; Cussenot, Olivier O; Cancel-Tassin, Géraldine G; Koutros, Stella S; Freeman, Laura E Beane LEB; Sorensen, Karina Dalsgaard KD; Orntoft, Torben Falck TF; Borre, Michael M; Maehle, Lovise L; Grindedal, Eli Marie EM; Neal, David E DE; Donovan, Jenny L JL; Hamdy, Freddie C FC; Martin, Richard M RM; Travis, Ruth C RC; Key, Tim J TJ; Hamilton, Robert J RJ; Fleshner, Neil E NE; Finelli, Antonio A; Ingles, Sue Ann SA; Stern, Mariana C MC; Rosenstein, Barry B; Kerns, Sarah S; Ostrer, Harry H; Lu, Yong-Jie YJ; Zhang, Hong-Wei HW; Feng, Ninghan N; Mao, Xueying X; Guo, Xin X; Wang, Guomin G; Sun, Zan Z; Giles, Graham G GG; Southey, Melissa C MC; MacInnis, Robert J RJ; FitzGerald, Liesel M LM; Kibel, Adam S AS; Drake, Bettina F BF; Vega, Ana A; Gómez-Caamaño, Antonio A; Fachal, Laura L; Szulkin, Robert R; Eklund, Martin M; Kogevinas, Manolis M; Llorca, Javier J; Castaño-Vinyals, Gemma G; Penney, Kathryn L KL; Stampfer, Meir M; Park, Jong Y JY; Sellers, Thomas A TA; Lin, Hui-Yi HY; Stanford, Janet L JL; Cybulski, Cezary C; Wokolorczyk, Dominika D; Lubinski, Jan J; Ostrander, Elaine A EA; Geybels, Milan S MS; Nordestgaard, Børge G BG; Nielsen, Sune F SF; Weisher, Maren M; Bisbjerg, Rasmus R; Røder, Martin Andreas MA; Iversen, Peter P; Brenner, Hermann H; Cuk, Katarina K; Holleczek, Bernd B; Maier, Christiane C; Luedeke, Manuel M; Schnoeller, Thomas T; Kim, Jeri J; Logothetis, Christopher J CJ; John, Esther M EM; Teixeira, Manuel R MR; Paulo, Paula P; Cardoso, Marta M; Neuhausen, Susan L SL; Steele, Linda L; Ding, Yuan Chun YC; De Ruyck, Kim K; De Meerleer, Gert G; Ost, Piet P; Razack, Azad A; Lim, Jasmine J; Teo, Soo-Hwang SH; Lin, Daniel W DW; Newcomb, Lisa F LF; Lessel, Davor D; Gamulin, Marija M; Kulis, Tomislav T; Kaneva, Radka R; Usmani, Nawaid N; Slavov, Chavdar C; Mitev, Vanio V; Parliament, Matthew M; Singhal, Sandeep S; Claessens, Frank F; Joniau, Steven S; Van den Broeck, Thomas T; Larkin, Samantha S; Townsend, Paul A PA; Aukim-Hastie, Claire C; Gago-Dominguez, Manuela M; Castelao, Jose Esteban JE; Martinez, Maria Elena ME; Roobol, Monique J MJ; Jenster, Guido G; van Schaik, Ron H N RHN; Menegaux, Florence F; Truong, Thérèse T; Koudou, Yves Akoli YA; Xu, Jianfeng J; Khaw, Kay-Tee KT; Cannon-Albright, Lisa L; Pandha, Hardev H; Michael, Agnieszka A; Kierzek, Andrzej A; Thibodeau, Stephen N SN; McDonnell, Shannon K SK; Schaid, Daniel J DJ; Lindstrom, Sara S; Turman, Constance C; Ma, Jing J; Hunter, David J DJ; Riboli, Elio E; Siddiq, Afshan A; Canzian, Federico F; Kolonel, Laurence N LN; Le Marchand, Loic L; Hoover, Robert N RN; Machiela, Mitchell J MJ; Kraft, Peter P; , ; Freedman, Matthew M; Wiklund, Fredrik F; Chanock, Stephen S; Henderson, Brian E BE; Easton, Douglas F DF; Haiman, Christopher A CA; Eeles, Rosalind A RA; Conti, David V DV; Kote-Jarai, Zsofia Z
Publication Date: 2018-06-11

Variant appearance in text: N/A
PubMed Link: 29892050
Variant Present in the following documents:
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs7766006
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Principles Governing A-to-I RNA Editing in the Breast Cancer Transcriptome.

Cell Reports
Fumagalli, Debora D; Gacquer, David D; Rothé, Françoise F; Lefort, Anne A; Libert, Frederick F; Brown, David D; Kheddoumi, Naima N; Shlien, Adam A; Konopka, Tomasz T; Salgado, Roberto R; Larsimont, Denis D; Polyak, Kornelia K; Willard-Gallo, Karen K; Desmedt, Christine C; Piccart, Martine M; Abramowicz, Marc M; Campbell, Peter J PJ; Sotiriou, Christos C; Detours, Vincent V
Publication Date: 2015-10-13

Variant appearance in text: rs7766006
PubMed Link: 26440892
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: N/A
PubMed Link: 25390934
Variant Present in the following documents:
View BVdb publication page



Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Publication Date: 2014

Variant appearance in text: WTAP: P103P; rs7766006
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Effect of a poly(ADP-ribose) polymerase-1 inhibitor against esophageal squamous cell carcinoma cell lines.

Cancer Science
Nasuno, Tomomitsu T; Mimaki, Sachiyo S; Okamoto, Makito M; Esumi, Hiroyasu H; Tsuchihara, Katsuya K
Publication Date: 2014-02

Variant appearance in text: N/A
PubMed Link: 24219164
Variant Present in the following documents:
View BVdb publication page