ADAR c.*1016C>T

Variant ID: 1-154556266-G-A

NM_001111.4(ADAR):c.*1016C>T

This variant was identified in 14 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: rs1127314
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs1127314
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs1127314
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Genome-wide analysis of consistently RNA edited sites in human blood reveals interactions with mRNA processing genes and suggests correlations with cell types and biological variables.

Bmc Genomics
Giacopuzzi, Edoardo E; Gennarelli, Massimo M; Sacco, Chiara C; Filippini, Alice A; Mingardi, Jessica J; Magri, Chiara C; Barbon, Alessandro A
Publication Date: 2018-12-27

Variant appearance in text: rs1127314
PubMed Link: 30587120
Variant Present in the following documents:
  • 12864_2018_5364_MOESM1_ESM.pdf
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs1127314
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page



ADAR1 polymorphisms are related to severity of liver fibrosis in HIV/HCV-coinfected patients.

Scientific Reports
Medrano, Luz M LM; Berenguer, Juan J; Jiménez-Sousa, María A MA; Aldámiz-Echevarria, Teresa T; Tejerina, Francisco F; Diez, Cristina C; Vigón, Lorena L; Fernández-Rodríguez, Amanda A; Resino, Salvador S
Publication Date: 2017-10-10

Variant appearance in text: rs1127314
PubMed Link: 29018269
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_12885.pdf
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs1127314
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Impact of polymorphisms in microRNA biogenesis genes on colon cancer risk and microRNA expression levels: a population-based, case-control study.

Bmc Medical Genomics
Mullany, Lila E LE; Herrick, Jennifer S JS; Wolff, Roger K RK; Buas, Matthew F MF; Slattery, Martha L ML
Publication Date: 2016-04-23

Variant appearance in text: rs1127314
PubMed Link: 27107574
Variant Present in the following documents:
  • Main text
  • 12920_2016_Article_181.pdf
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs1127314
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
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: rs1127314
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Nominal association with CHRNA4 variants and nicotine dependence.

Genes, Brain, And Behavior
Kamens, H M HM; Corley, R P RP; McQueen, M B MB; Stallings, M C MC; Hopfer, C J CJ; Crowley, T J TJ; Brown, S A SA; Hewitt, J K JK; Ehringer, M A MA
Publication Date: 2013-04

Variant appearance in text: rs1127314
PubMed Link: 23350800
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal
Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV
Publication Date: 2012-12

Variant appearance in text: rs1127314
PubMed Link: 21808284
Variant Present in the following documents:
  • Main text
  • nihms305090.pdf
  • NIHMS305090-supplement-3.pdf
View BVdb publication page



Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation.

Human Molecular Genetics
Conti, David V DV; Lee, Won W; Li, Dalin D; Liu, Jinghua J; Van Den Berg, David D; Thomas, Paul D PD; Bergen, Andrew W AW; Swan, Gary E GE; Tyndale, Rachel F RF; Benowitz, Neal L NL; Lerman, Caryn C; ,
Publication Date: 2008-09-15

Variant appearance in text: rs1127314
PubMed Link: 18593715
Variant Present in the following documents:
  • Main text
  • ddn181.pdf
View BVdb publication page



Association of alpha4beta2 nicotinic receptor and heavy smoking in schizophrenia.

Journal Of Psychiatry & Neuroscience : Jpn
Voineskos, Sophocles S; De Luca, Vincenzo V; Mensah, Albert A; Vincent, John B JB; Potapova, Natalia N; Kennedy, James L JL
Publication Date: 2007-11

Variant appearance in text: rs1127314
PubMed Link: 18043764
Variant Present in the following documents:
  • Main text
View BVdb publication page