PTGS1 c.763-45T>C

Variant ID: 9-125145743-T-C

NM_000962.3(PTGS1):c.763-45T>C

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11

Variant appearance in text: PTGS1: 763-45T>C; rs3842798
PubMed Link: 32046637
Variant Present in the following documents:
  • 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Next-Generation Sequencing of PTGS Genes Reveals an Increased Frequency of Non-synonymous Variants Among Patients With NSAID-Induced Liver Injury.

Frontiers In Genetics
Lucena, María Isabel MI; García-Martín, Elena E; Daly, Ann K AK; Blanca, Miguel M; Andrade, Raúl J RJ; Agúndez, José A G JAG
Publication Date: 2019

Variant appearance in text: rs3842798
PubMed Link: 30873208
Variant Present in the following documents:
  • Main text
  • fgene-10-00134.pdf
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: PTGS1: 763-45T>C; rs3842798
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.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: rs3842798
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



The IL-1B Genetic Polymorphism Is Associated with Aspirin-Induced PepticUlcers in a Korean Ethnic Group.

Gut And Liver
Cho, Jae Hee JH; Choi, Ja Sung JS; Chun, Song Wook SW; Lee, Sangheun S; Han, Ki Jun KJ; Kim, Hee Man HM
Publication Date: 2016-05-23

Variant appearance in text: rs3842798
PubMed Link: 26601827
Variant Present in the following documents:
  • Main text
  • gnl-10-362.pdf
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs3842798
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Associations between ALOX, COX, and CRP polymorphisms and breast cancer among Hispanic and non-Hispanic white women: The breast cancer health disparities study.

Molecular Carcinogenesis
Connor, Avonne E AE; Baumgartner, Richard N RN; Baumgartner, Kathy B KB; Pinkston, Christina M CM; Boone, Stephanie D SD; John, Esther M EM; Torres-Mejía, Gabriela G; Hines, Lisa M LM; Giuliano, Anna R AR; Wolff, Roger K RK; Slattery, Martha L ML
Publication Date: 2015-12

Variant appearance in text: rs3842798
PubMed Link: 25339205
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphism in glutamate cysteine ligase catalytic subunit (GCLC) is associated with sulfamethoxazole-induced hypersensitivity in HIV/AIDS patients.

Bmc Medical Genomics
Wang, Danxin D; Curtis, Amanda A; Papp, Audrey C AC; Koletar, Susan L SL; Para, Michael F MF
Publication Date: 2012-07-23

Variant appearance in text: rs3842798
PubMed Link: 22824134
Variant Present in the following documents:
  • Main text
  • 1755-8794-5-32.pdf
View BVdb publication page



Genetic variation in inflammatory pathways is related to colorectal cancer survival.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Coghill, Anna E AE; Newcomb, Polly A PA; Poole, Elizabeth M EM; Hutter, Carolyn M CM; Makar, Karen W KW; Duggan, Dave D; Potter, John D JD; Ulrich, Cornelia M CM
Publication Date: 2011-11-15

Variant appearance in text: rs3842798
PubMed Link: 21976545
Variant Present in the following documents:
  • Main text
View BVdb publication page