PPARG c.620C>T ;(p.A207V)

Variant ID: 3-12447471-C-T

NM_138711.3(PPARG):c.620C>T;(p.A207V)

This variant was identified in 1 publication

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: A209V
PubMed Link: 25340400
Variant Present in the following documents:
  • pgen.1004592.s009.xlsx, sheet 3
View BVdb publication page