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PPARG c.820G>C ;(p.E274Q)
Variant ID: 3-12458293-G-C
NM_138711.3(
PPARG
):c.820G>C;(p.E274Q)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
COUP-TFII in Health and Disease.
Cells
Polvani, Simone S; Pepe, Sara S; Milani, Stefano S; Galli, Andrea A
Publication Date: 2019-12-31
Variant appearance in text: PPARgamma: E276Q
PubMed Link:
31906104
Variant Present in the following documents:
Main text
cells-09-00101.pdf
View BVdb publication page
Transcriptional Factors Mediating Retinoic Acid Signals in the Control of Energy Metabolism.
International Journal Of Molecular Sciences
Zhang, Rui R; Wang, Yueqiao Y; Li, Rui R; Chen, Guoxun G
Publication Date: 2015-06-23
Variant appearance in text: NR1C3: E276Q
PubMed Link:
26110391
Variant Present in the following documents:
Main text
ijms-16-14210.pdf
View BVdb publication page
A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families.
Genetics Research International
Lee, Kwanghyuk K; Khan, Saadullah S; Ansar, Muhammad M; Santos-Cortez, Regie Lyn P RL; Ahmad, Wasim W; Leal, Suzanne M SM
Publication Date: 2011
Variant appearance in text: PPARG: E276Q
PubMed Link:
22567352
Variant Present in the following documents:
Main text
GRI2011-368915.pdf
View BVdb publication page