Transcript #00025937 (NM_138711.3, PPARG gene)

Transcript name transcript variant 3
Gene name PPARG (peroxisome proliferator-activated receptor gamma)
Chromosome 3
Transcript - NCBI ID NM_138711.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_619725.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks RefSeq select
Date created 2024-07-12 11:31:57 +02:00 (CEST)
Date last edited N/A


Variants

63 entries on 1 page. Showing entries 1 - 63.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-2-28069G>A r.(=) p.(=)
-?/. - c.-2-14A>G r.(=) p.(=)
-?/. - c.27A>G r.(?) p.(Pro9=)
-?/. - c.39C>G r.(?) p.(Thr13=)
-?/. - c.69C>T r.(?) p.(Ser23=)
-?/. - c.112A>G r.(?) p.(Thr38Ala)
?/. - c.151G>A r.(?) p.(Glu51Lys)
-?/. - c.156C>T r.(?) p.(Asp52=)
-?/. - c.187G>A r.(?) p.(Ala63Thr)
-?/. - c.226+18A>G r.(=) p.(=)
?/. - c.257C>T r.(?) p.(Pro86Leu)
?/. - c.347A>G r.(?) p.(Asp116Gly)
?/. - c.347A>G r.(?) p.(Asp116Gly)
-?/. - c.354T>C r.(?) p.(Ala118=)
+?/. - c.368A>G r.(?) p.(Tyr123Cys)
-?/. - c.396+7A>T r.(=) p.(=)
-?/. - c.397-3C>T r.spl? p.?
-?/. - c.408G>T r.(?) p.(=)
?/. - c.409A>G r.(?) p.(Arg137Gly)
?/. - c.410G>C r.(?) p.(Arg137Thr)
-?/. - c.423G>A r.(?) p.(Leu141=)
?/. - c.426G>C r.(?) p.(Lys142Asn)
+?/. - c.449T>C r.(?) p.(Leu150Pro)
?/. - c.489G>C r.(?) p.(Gln163His)
?/. - c.530A>G r.(?) p.(His177Arg)
+?/. - c.557C>T r.(?) p.(Pro186Leu)
+/. - c.557C>T r.(?) p.(Pro186Leu)
?/. - c.565G>A r.(?) p.(Glu189Lys)
-?/. - c.584C>T r.(?) p.(Ala195Val)
?/. - c.698C>T r.(?) p.(Ala233Val)
-?/. - c.705G>A r.(?) p.(Ala235=)
-?/. - c.735+31dup r.(=) p.(=)
-?/. - c.742G>A r.(?) p.(Val248Ile)
+?/. - c.750T>G r.(?) p.(Tyr250*)
?/. - c.758A>G r.(?) p.(Asn253Ser)
-?/. - c.807C>G r.(?) p.(Pro269=)
-?/. - c.807C>T r.(?) p.(Pro269=)
+/. - c.809del r.(?) p.(Leu270ArgfsTer38)
-?/. - c.867C>T r.(?) p.(=)
+/. - c.868G>A r.(?) p.(Val290Met)
+/. - c.868G>A r.(?) p.(Val290Met)
?/. - c.895T>G r.(?) p.(Tyr299Asp)
?/. - c.895T>G r.(?) p.(Tyr299Asp)
?/. - c.907A>G r.(?) p.(Ile303Val)
-?/. - c.919G>C r.(?) p.(Val307Leu)
?/. - c.965T>G r.(?) p.(Val322Gly)
-?/. - c.969C>T r.(?) p.(His323=)
?/. - c.970G>C r.(?) p.(Glu324Gln)
?/. - c.970G>C r.(?) p.(Glu324Gln)
?/. - c.1039T>G r.(?) p.(Phe347Val)
?/. - c.1052A>G r.(?) p.(Glu351Gly)
+/. - c.1069C>T r.(?) p.(Arg357Ter)
?/. - c.1111G>T r.(?) p.(Ala371Ser)
-?/. - c.1147G>A r.(?) p.(Asp383Asn)
?/. - c.1151T>G r.(?) p.(Leu384Trp)
?/. - c.1163T>C r.(?) p.(Ile388Thr)
+?/. - c.1228C>T r.(?) p.(Gln410*)
?/. - c.1244A>G r.(?) p.(Gln415Arg)
-/. - c.1287A>G r.(?) p.(Ser429=)
?/. - c.1340C>A r.(?) p.(Thr447Lys)
-?/. - c.1368C>T r.(?) p.(Ile456=)
-?/. - c.1368C>T r.(?) p.(Ile456=)
?/. - c.1378G>A r.(?) p.(Glu460Lys)
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