SLC22A1 c.86C>T ;(p.S29L)

Variant ID: 6-160543053-C-T

NM_003057.2(SLC22A1):c.86C>T;(p.S29L)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Population pharmacogenomics: an update on ethnogeographic differences and opportunities for precision public health.

Human Genetics
Zhou, Yitian Y; Lauschke, Volker M VM
Publication Date: 2022-06

Variant appearance in text: SLC22A1: S29L; rs375175439
PubMed Link: 34652573
Variant Present in the following documents:
  • Main text
  • 439_2021_Article_2385.pdf
View BVdb publication page



Sorafenib Resistance in Hepatocellular Carcinoma: The Relevance of Genetic Heterogeneity.

Cancers
Cabral, Loraine Kay D LKD; Tiribelli, Claudio C; Sukowati, Caecilia H C CHC
Publication Date: 2020-06-15

Variant appearance in text: SLC22A1: S29L
PubMed Link: 32549224
Variant Present in the following documents:
  • Main text
  • cancers-12-01576.pdf
View BVdb publication page



Evolving neoantigen profiles in colorectal cancers with DNA repair defects.

Genome Medicine
Rospo, Giuseppe G; Lorenzato, Annalisa A; Amirouchene-Angelozzi, Nabil N; Magrì, Alessandro A; Cancelliere, Carlotta C; Corti, Giorgio G; Negrino, Carola C; Amodio, Vito V; Montone, Monica M; Bartolini, Alice A; Barault, Ludovic L; Novara, Luca L; Isella, Claudio C; Medico, Enzo E; Bertotti, Andrea A; Trusolino, Livio L; Germano, Giovanni G; Di Nicolantonio, Federica F; Bardelli, Alberto A
Publication Date: 2019-06-28

Variant appearance in text: SLC22A1: S29L
PubMed Link: 31253177
Variant Present in the following documents:
  • 13073_2019_654_MOESM2_ESM.xlsx, sheet 33
View BVdb publication page



Genetic variation in human drug-related genes.

Genome Medicine
Schärfe, Charlotta Pauline Irmgard CPI; Tremmel, Roman R; Schwab, Matthias M; Kohlbacher, Oliver O; Marks, Debora Susan DS
Publication Date: 2017-12-22

Variant appearance in text: rs375175439
PubMed Link: 29273096
Variant Present in the following documents:
  • 13073_2017_502_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page



Effects of genetic polymorphisms on the OCT1 and OCT2-mediated uptake of ranitidine.

Plos One
Meyer, Marleen Julia MJ; Seitz, Tina T; Brockmöller, Jürgen J; Tzvetkov, Mladen Vassilev MV
Publication Date: 2017

Variant appearance in text: SLC22A1: Ser29Leu
PubMed Link: 29236753
Variant Present in the following documents:
  • Main text
  • pone.0189521.pdf
View BVdb publication page



A Landscape of Pharmacogenomic Interactions in Cancer.

Cell
Iorio, Francesco F; Knijnenburg, Theo A TA; Vis, Daniel J DJ; Bignell, Graham R GR; Menden, Michael P MP; Schubert, Michael M; Aben, Nanne N; Gonçalves, Emanuel E; Barthorpe, Syd S; Lightfoot, Howard H; Cokelaer, Thomas T; Greninger, Patricia P; van Dyk, Ewald E; Chang, Han H; de Silva, Heshani H; Heyn, Holger H; Deng, Xianming X; Egan, Regina K RK; Liu, Qingsong Q; Mironenko, Tatiana T; Mitropoulos, Xeni X; Richardson, Laura L; Wang, Jinhua J; Zhang, Tinghu T; Moran, Sebastian S; Sayols, Sergi S; Soleimani, Maryam M; Tamborero, David D; Lopez-Bigas, Nuria N; Ross-Macdonald, Petra P; Esteller, Manel M; Gray, Nathanael S NS; Haber, Daniel A DA; Stratton, Michael R MR; Benes, Cyril H CH; Wessels, Lodewyk F A LFA; Saez-Rodriguez, Julio J; McDermott, Ultan U; Garnett, Mathew J MJ
Publication Date: 2016-07-28

Variant appearance in text: SLC22A1: 86C>T; S29L
PubMed Link: 27397505
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
View BVdb publication page



Global genetic analyses reveal strong inter-ethnic variability in the loss of activity of the organic cation transporter OCT1.

Genome Medicine
Seitz, Tina T; Stalmann, Robert R; Dalila, Nawar N; Chen, Jiayin J; Pojar, Sherin S; Dos Santos Pereira, Joao N JN; Krätzner, Ralph R; Brockmöller, Jürgen J; Tzvetkov, Mladen V MV
Publication Date: 2015

Variant appearance in text: SLC22A1: Ser29Leu
PubMed Link: 26157489
Variant Present in the following documents:
  • Main text
  • 13073_2015_Article_172.pdf
View BVdb publication page