HTR2A c.*402A>C

Variant ID: 13-47408570-T-G

NM_000621.4(HTR2A):c.*402A>C

This variant was identified in 9 publications

View GRCh38 version.




Publications:


The Role of Pharmacogenetics in Personalizing the Antidepressant and Anxiolytic Therapy.

Genes
Radosavljevic, Milica M; Svob Strac, Dubravka D; Jancic, Jasna J; Samardzic, Janko J
Publication Date: 2023-05-16

Variant appearance in text: rs3803189
PubMed Link: 37239455
Variant Present in the following documents:
  • Main text
  • genes-14-01095.pdf
View BVdb publication page



Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer
Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC
Publication Date: 2021-05-29

Variant appearance in text: rs3803189
PubMed Link: 34051734
Variant Present in the following documents:
  • 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page



Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients.

Frontiers In Pharmacology
Kao, Chung-Feng CF; Kuo, Po-Hsiu PH; Yu, Younger W-Y YW; Yang, Albert C AC; Lin, Eugene E; Liu, Yu-Li YL; Tsai, Shih-Jen SJ
Publication Date: 2020

Variant appearance in text: rs3803189
PubMed Link: 33519430
Variant Present in the following documents:
  • Main text
  • fphar-11-559601.pdf
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: rs3803189
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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: rs3803189
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
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: rs3803189
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



An efficient weighted tag SNP-set analytical method in genome-wide association studies.

Bmc Genetics
Yan, Bin B; Wang, Shudong S; Jia, Huaqian H; Liu, Xing X; Wang, Xinzeng X
Publication Date: 2015-03-13

Variant appearance in text: rs3803189
PubMed Link: 25879733
Variant Present in the following documents:
  • Main text
  • 12863_2015_Article_182.pdf
View BVdb publication page



Multiple regulatory variants modulate expression of 5-hydroxytryptamine 2A receptors in human cortex.

Biological Psychiatry
Smith, Ryan M RM; Papp, Audrey C AC; Webb, Amy A; Ruble, Cara L CL; Munsie, Leanne M LM; Nisenbaum, Laura K LK; Kleinman, Joel E JE; Lipska, Barbara K BK; Sadee, Wolfgang W
Publication Date: 2013-03-15

Variant appearance in text: rs3803189
PubMed Link: 23158458
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.

Bmc Genetics
Harris, Sarah E SE; Fox, Helen H; Wright, Alan F AF; Hayward, Caroline C; Starr, John M JM; Whalley, Lawrence J LJ; Deary, Ian J IJ
Publication Date: 2007-07-02

Variant appearance in text: rs3803189
PubMed Link: 17601350
Variant Present in the following documents:
  • Main text
  • 1471-2156-8-43.pdf
View BVdb publication page