GSTP1 c.262G>A ;(p.A88T)

Variant ID: 11-67352638-G-A

NM_000852.3(GSTP1):c.262G>A;(p.A88T)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Early diagnostic potential of APC hypermethylation in esophageal cancer.

Cancer Management And Research
Wang, Bujiang B; Song, Haojun H; Jiang, Haizhong H; Fu, Yangbo Y; Ding, Xiaoyun X; Zhou, Chongchang C
Publication Date: 2018

Variant appearance in text: GSTP1: A88T
PubMed Link: 29440928
Variant Present in the following documents:
  • Main text
View BVdb publication page



Functional polymorphisms in antioxidant genes in Hurthle cell thyroid neoplasm - an association of GPX1 polymorphism and recurrent Hurthle cell thyroid carcinoma.

Radiology And Oncology
Krhin, Blaz B; Goricar, Katja K; Gazic, Barbara B; Dolzan, Vita V; Besic, Nikola N
Publication Date: 2016-09-01

Variant appearance in text: GSTP1: 262G>A
PubMed Link: 27679545
Variant Present in the following documents:
  • raon-2016-0031.pdf
View BVdb publication page