PTEN c.209+329T>C

Variant ID: 10-89685643-T-C

NM_000314.4(PTEN):c.209+329T>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Roles of genetic variants in the PI3K/PTEN pathways in susceptibility to colorectal carcinoma and clinical outcomes treated with FOLFOX regimen.

International Journal Of Clinical And Experimental Pathology
Lin, Lin L; Zhang, Zhaoxu Z; Zhang, Wen W; Wang, Lin L; Wang, Jinwan J
Publication Date: 2015

Variant appearance in text: rs10490920
PubMed Link: 26722535
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cellular adhesion gene SELP is associated with rheumatoid arthritis and displays differential allelic expression.

Plos One
Burkhardt, Jana J; Blume, Mechthild M; Petit-Teixeira, Elisabeth E; Hugo Teixeira, Vitor V; Steiner, Anke A; Quente, Elfi E; Wolfram, Grit G; Scholz, Markus M; Pierlot, Céline C; Migliorini, Paola P; Bombardieri, Stefano S; Balsa, Alejandro A; Westhovens, René R; Barrera, Pilar P; Radstake, Timothy R D J TR; Alves, Helena H; Bardin, Thomas T; Prum, Bernard B; Emmrich, Frank F; Cornelis, François F; Ahnert, Peter P; Kirsten, Holger H
Publication Date: 2014

Variant appearance in text: rs10490920
PubMed Link: 25147926
Variant Present in the following documents:
  • Main text
  • pone.0103872.pdf
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Loss of PTEN expression is associated with poor prognosis in patients with intraductal papillary mucinous neoplasms of the pancreas.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Garcia-Carracedo, Dario D; Turk, Andrew T AT; Fine, Stuart A SA; Akhavan, Nathan N; Tweel, Benjamin C BC; Parsons, Ramon R; Chabot, John A JA; Allendorf, John D JD; Genkinger, Jeanine M JM; Remotti, Helen E HE; Su, Gloria H GH
Publication Date: 2013-12-15

Variant appearance in text: rs10490920
PubMed Link: 24132918
Variant Present in the following documents:
  • Main text
View BVdb publication page



Germ-line sequence variants of PTEN do not have an important role in hereditary and non-hereditary prostate cancer susceptibility.

Journal Of Human Genetics
Xie, Chunmei C CC; Lu, Lingyi L; Sun, Jielin J; Zheng, S Lilly SL; Isaacs, William B WB; Gronberg, Henrik H; Xu, Jianfeng J
Publication Date: 2011-07

Variant appearance in text: rs10490920
PubMed Link: 21633361
Variant Present in the following documents:
  • Main text
View BVdb publication page



Persons with age-related maculopathy risk genotypes and clinically normal eyes have reduced mesopic vision.

Investigative Ophthalmology & Visual Science
Feigl, Beatrix B; Cao, Dingcai D; Morris, Charles P CP; Zele, Andrew J AJ
Publication Date: 2011-02

Variant appearance in text: rs10490920
PubMed Link: 20881291
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.

American Journal Of Human Genetics
Pezzolesi, Marcus G MG; Li, Yan Y; Zhou, Xiao-Ping XP; Pilarski, Robert R; Shen, Lei L; Eng, Charis C
Publication Date: 2006-11

Variant appearance in text: rs10490920
PubMed Link: 17033968
Variant Present in the following documents:
  • Main text
View BVdb publication page