Varaico: Literature-Extracted Genetic Variants

Gene:SLC28A1
Variant:p.V189I
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SLC28A1

NM_004213.5:p.V189I

Associated Papers

Pathogenic germline variants in small cell lung cancer: A systematic review and meta-analysis.

Ul Haq S et al.

Hgg Advances, 2025

40308030 (PubMed )
Supplement: mmc2.xlsx › Table_S3

Single-cell exome sequencing reveals polyclonal seeding and TRPS1 mutations in colon cancer metastasis.

Cai J et al.

Signal Transduction and Targeted Therapy, 2024

39307879 (PubMed )
Supplement: 41392_2024_1960_MOESM6_ESM.xlsx › Table_S5

Effect of donor GSTM3 rs7483 genetic variant on tacrolimus elimination in the early period after liver transplantation.

Zhang T et al.

Peerj, 2024

39465171 (PubMed )
Supplement: peerj-12-18360-s002.7z › drug-metabolizing_enzymes_and_transporter__DMET__microarray › markerlist.xlsx › markerlist.TXT

Custom multi‑tumor next‑generation sequencing panel for routine molecular diagnosis of solid tumors: Validation and results from three‑year clinical use.

Chevrier S et al.

International Journal of Molecular Medicine, 2022

Genetic and clinical determinants of mizoribine pharmacokinetics in renal transplant recipients.

Dai R et al.

European Journal of Clinical Pharmacology, 2021

Discovering novel SNPs that are correlated with patient outcome in a Singaporean cancer patient cohort treated with gemcitabine-based chemotherapy.

Limviphuvadh V et al.

Bmc Cancer, 2018

29751792 (PubMed )
Supplement: 12885_2018_4471_MOESM1_ESM.zip › TableS2R2.xlsx › Table_S2

Codon-level co-occurrences of germline variants and somatic mutations in cancer are rare but often lead to incorrect variant annotation and underestimated impact prediction.

Koire A et al.

Plos One, 2017

28350864 (PubMed )
Supplement: pone.0174766.s004.xlsx › Sheet1

Use of dedicated gene panel sequencing using next generation sequencing to improve the personalized care of lung cancer.

Kaderbhai CG et al.

Oncotarget, 2016

27027238 (PubMed )
Supplement: oncotarget-07-24860-s001.pdf

Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations.

Cocca M et al.

Journal of Translational Medicine, 2016

26801900 (PubMed )
Supplement: 12967_2016_778_MOESM3_ESM.xls › Sheet1

Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.

Molnár J et al.

Plos One, 2016

26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism

Development of a novel, fully-automated genotyping system: principle and applications.

Suzuki S et al.

Sensors (basel, Switzerland), 2012

Equilibrative nucleoside transporter 1 genotype, cytidine deaminase activity and age predict gemcitabine plasma clearance in patients with solid tumours.

Gusella M et al.

British Journal of Clinical Pharmacology, 2011

Effect of genetic polymorphisms of SLC28A1, ABCG2, and ABCC4 on bioavailability of mizoribine in healthy Japanese males.

Fukao M et al.

Drug Metabolism and Pharmacokinetics, 2011

Polymorphisms in ABCG2, ABCC3 and CNT1 genes and their possible impact on chemotherapy outcome of lung cancer patients.

Müller PJ et al.

International Journal of Cancer, 2009

Polymorphisms in transporter and phase II metabolism genes as potential modifiers of the predisposition to and treatment outcome of de novo acute myeloid leukemia in Israeli ethnic groups.

Müller P et al.

Leukemia Research, 2008

Pharmacogenetics of cancer chemotherapy.

Abraham J et al.

Biochimica Et Biophysica Acta, 2006

Pharmacogenetics for individualized cancer chemotherapy.

Efferth T et al.

Pharmacology & Therapeutics, 2005

Functional and genetic diversity in the concentrative nucleoside transporter, CNT1, in human populations.

Gray JH et al.

Molecular Pharmacology, 2004

Gemcitabine and platinum pathway pharmacogenetics in Asian breast cancer patients.

Wong AL et al.

Cancer Genomics & Proteomics, 0

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