PPARG c.706A>T ;(p.T236S)

Variant ID: 3-12447557-A-T

NM_138711.3(PPARG):c.706A>T;(p.T236S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Systematic dissection of coding exons at single nucleotide resolution supports an additional role in cell-specific transcriptional regulation.

Plos Genetics
Birnbaum, Ramon Y RY; Patwardhan, Rupali P RP; Kim, Mee J MJ; Findlay, Gregory M GM; Martin, Beth B; Zhao, Jingjing J; Bell, Robert J A RJ; Smith, Robin P RP; Ku, Angel A AA; Shendure, Jay J; Ahituv, Nadav N
Publication Date: 2014-10

Variant appearance in text: PPARG: T238S
PubMed Link: 25340400
Variant Present in the following documents:
  • pgen.1004592.s009.xlsx, sheet 3
View BVdb publication page



Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.

Human Reproduction Update
Tempfer, C B CB; Simoni, M M; Destenaves, B B; Fauser, B C J M BC
Publication Date: 2009

Variant appearance in text: PPARG: T238S
PubMed Link: 18805939
Variant Present in the following documents:
  • Main text
View BVdb publication page