GSTP1 c.439G>T ;(p.D147Y)

Variant ID: 11-67353677-G-T

NM_000852.3(GSTP1):c.439G>T;(p.D147Y)

This variant was identified in 14 publications

View GRCh38 version.




Publications:


Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia.

Bmc Medical Genomics
Lin, Dafeng D; Wang, Dianpeng D; Li, Peimao P; Deng, Lihua L; Zhang, Zhimin Z; Zhang, Yanfang Y; Zhang, Ming M; Zhang, Naixing N
Publication Date: 2023-01-26

Variant appearance in text: GSTP1: 439G>T; Asp147Tyr; rs4986949
PubMed Link: 36703207
Variant Present in the following documents:
  • 12920_2023_1442_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Genomic characteristics of two breast malignant phyllodes tumors during pregnancy and lactation identified through whole-exome sequencing.

Orphanet Journal Of Rare Diseases
Lei, Ting T; Shen, Mengjia M; Deng, Xu X; Shi, Yongqiang Y; Peng, Yan Y; Wang, Hui H; Chen, Tongbing T
Publication Date: 2022-10-21

Variant appearance in text: GSTP1: 439G>T; D147Y
PubMed Link: 36271373
Variant Present in the following documents:
  • 13023_2022_Article_2537.pdf
View BVdb publication page



Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.

Translational And Clinical Pharmacology
Kim, Byungwook B; Yoon, Deok Yong DY; Lee, SeungHwan S; Jang, In-Jin IJ; Yu, Kyung-Sang KS; Cho, Joo-Youn JY; Oh, Jaeseong J
Publication Date: 2021-09

Variant appearance in text: GSTP1: 439G>T; D147Y; rs4986949
PubMed Link: 34621706
Variant Present in the following documents:
  • tcp-29-135-s001.xls, sheet 1
View BVdb publication page



Somatic Mutation Profiling of Papillary Thyroid Carcinomas by Whole-exome Sequencing and Its Relationship with Clinical Characteristics.

International Journal Of Medical Sciences
Qi, Tingyue T; Rong, Xin X; Feng, Qingling Q; Sun, Hongguang H; Cao, Haiyan H; Yang, Yan Y; Feng, Hao H; Zhu, Linhai L; Wang, Lei L; Du, Qiu Q
Publication Date: 2021

Variant appearance in text: GSTP1: 439G>T; Asp147Tyr; rs4986949
PubMed Link: 34104084
Variant Present in the following documents:
  • ijmsv18p2532s2.xlsx, sheet 1
View BVdb publication page



Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population.

Plos Genetics
Yu, Mullin Ho Chung MHC; Chan, Marcus Chun Yin MCY; Chung, Claudia Ching Yan CCY; Li, Andrew Wang Tat AWT; Yip, Chara Yin Wa CYW; Mak, Christopher Chun Yu CCY; Chau, Jeffrey Fong Ting JFT; Lee, Mianne M; Fung, Jasmine Lee Fong JLF; Tsang, Mandy Ho Yin MHY; Chan, Joshua Chun Ki JCK; Wong, Wilfred Hing Sang WHS; Yang, Jing J; Chui, William Chun Ming WCM; Chung, Patrick Ho Yu PHY; Yang, Wanling W; Lee, So Lun SL; Chan, Godfrey Chi Fung GCF; Tam, Paul Kwong Hang PKH; Lau, Yu Lung YL; Tang, Clara Sze Man CSM; Yeung, Kit San KS; Chung, Brian Hon Yin BHY
Publication Date: 2021-02

Variant appearance in text: rs4986949
PubMed Link: 33600428
Variant Present in the following documents:
  • pgen.1009323.s010.xlsx, sheet 1
View BVdb publication page



Population Pharmacokinetic and Pharmacogenetic Analysis of Mitotane in Patients with Adrenocortical Carcinoma: Towards Individualized Dosing.

Clinical Pharmacokinetics
Yin, Anyue A; Ettaieb, Madeleine H T MHT; Swen, Jesse J JJ; van Deun, Liselotte L; Kerkhofs, Thomas M A TMA; van der Straaten, Robert J H M RJHM; Corssmit, Eleonora P M EPM; Gelderblom, Hans H; Kerstens, Michiel N MN; Feelders, Richard A RA; Eekhoff, Marelise M; Timmers, Henri J L M HJLM; D'Avolio, Antonio A; Cusato, Jessica J; Guchelaar, Henk-Jan HJ; Haak, Harm R HR; Moes, Dirk Jan A R DJAR
Publication Date: 2021-01

Variant appearance in text: GSTP1: 439G>T; D147Y; rs4986949
PubMed Link: 32607875
Variant Present in the following documents:
  • 40262_2020_913_MOESM3_ESM.xlsx, sheet 1
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: rs4986949
PubMed Link: 29273096
Variant Present in the following documents:
  • 13073_2017_502_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page



Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes: A GeT-RM Collaborative Project.

The Journal Of Molecular Diagnostics : Jmd
Pratt, Victoria M VM; Everts, Robin E RE; Aggarwal, Praful P; Beyer, Brittany N BN; Broeckel, Ulrich U; Epstein-Baak, Ruth R; Hujsak, Paul P; Kornreich, Ruth R; Liao, Jun J; Lorier, Rachel R; Scott, Stuart A SA; Smith, Chingying Huang CH; Toji, Lorraine H LH; Turner, Amy A; Kalman, Lisa V LV
Publication Date: 2016-01

Variant appearance in text: GSTP1: D147Y
PubMed Link: 26621101
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of deleterious nsSNPs in α, μ, π and θ class of GST family and their influence on protein structure.

Genomics Data
Yadav, P P; Chatterjee, A A; Bhattacharjee, A A
Publication Date: 2014-12

Variant appearance in text: GSTP: D147Y; rs4986949
PubMed Link: 26484073
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Affymetrix DMET Plus platform reveals unique distribution of ADME-related variants in ethnic Arabs.

Disease Markers
Wakil, Salma M SM; Nguyen, Cao C; Muiya, Nzioka P NP; Andres, Editha E; Lykowska-Tarnowska, Agnieszka A; Baz, Batoul B; Tahir, Asma I AI; Meyer, Brian F BF; Morahan, Grant G; Dzimiri, Nduna N
Publication Date: 2015

Variant appearance in text: rs4986949
PubMed Link: 25802476
Variant Present in the following documents:
  • 542543.f1.xlsx, sheet 1
View BVdb publication page



The RPTEC/TERT1 cell line models key renal cell responses to the environmental toxicants, benzo[a]pyrene and cadmium.

Toxicology Reports
Simon, B R BR; Wilson, M J MJ; Wickliffe, J K JK
Publication Date: 2014

Variant appearance in text: rs4986949
PubMed Link: 25126521
Variant Present in the following documents:
  • mmc1.xls, sheet 1
View BVdb publication page



Translational medicine and reliability of single-nucleotide polymorphism studies: can we believe in SNP reports or not?

International Journal Of Medical Sciences
Valachis, Antonis A; Mauri, Davide D; Neophytou, Christodoulos C; Polyzos, Nikolaos P NP; Tsali, Lampriani L; Garras, Antonios A; Papanikolau, Evangelos G EG
Publication Date: 2011

Variant appearance in text: GSTP1: Asp147Tyr
PubMed Link: 21897762
Variant Present in the following documents:
  • Main text
  • ijmsv08p0492.pdf
View BVdb publication page



Glutathione s-transferase p1: gene sequence variation and functional genomic studies.

Cancer Research
Moyer, Ann M AM; Salavaggione, Oreste E OE; Wu, Tse-Yu TY; Moon, Irene I; Eckloff, Bruce W BW; Hildebrandt, Michelle A T MA; Schaid, Daniel J DJ; Wieben, Eric D ED; Weinshilboum, Richard M RM
Publication Date: 2008-06-15

Variant appearance in text: GSTP1: Asp147Tyr; rs4986949
PubMed Link: 18559526
Variant Present in the following documents:
  • Main text
View BVdb publication page



Structure SNP (StSNP): a web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways.

Nucleic Acids Research
Uzun, Alper A; Leslin, Chesley M CM; Abyzov, Alexej A; Ilyin, Valentin V
Publication Date: 2007-07

Variant appearance in text: GSTP1: D147Y
PubMed Link: 17537826
Variant Present in the following documents:
  • Main text
  • gkm232.pdf
View BVdb publication page