Transcript #00022339 (NM_019093.2, UGT1A3 gene)

Transcript name UDP glucuronosyltransferase 1 family, polypeptide A3
Gene name UGT1A3 (UDP glucuronosyltransferase 1 family, polypeptide A3)
Chromosome 2
Transcript - NCBI ID NM_019093.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_061966.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

106 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Haplotype     

RNA change     

Protein     
?/. - - - r.(=) p.(=)
?/. - - - r.(=) p.(=)
?/. - - - r.(=) p.(=)
?/. - - - r.(=) p.(=)
?/. - - - r.(=) p.(=)
?/. - c.-91845C>T - r.(?) p.(=)
?/. - c.-91775G>A - r.(?) p.(=)
?/. - c.-35963C>G - r.(?) p.(=)
-?/. - c.-10105C>T - r.(?) p.(=)
?/. - c.-9481A>C - r.(?) p.(=)
?/. - c.31T>C - r.(?) p.(Trp11Arg)
?/. - c.31T>C - r.(?) p.(Trp11Arg)
?/. - c.81G>A - r.(?) p.(Glu27=)
?/. - c.81G>A - r.(?) p.(Glu27=)
?/. - c.133C>T UGT1A1*4 r.(?) p.(Arg45Trp)
-?/. - c.133C>T - r.(?) p.(Arg45Trp)
?/. - c.140T>C - r.(?) p.(Val47Ala)
?/. - c.140T>C - r.(?) p.(Val47Ala)
-?/. - c.438T>C - r.(?) p.(Phe146=)
-?/. - c.473C>G - r.(?) p.(Ala158Gly)
?/. - c.477A>G - r.(?) p.(Ala159=)
?/. - c.867+51A>T - r.(=) p.(=)
+/. - c.868-6787_868-6786dup - r.(=) p.(=)
+?/. - c.868-6787_868-6786dup - r.(=) p.(=)
+/. - c.868-6703T>G - r.(=) p.(=)
+/. - c.868-6703T>G - r.(=) p.(=)
+/. - c.868-6662A>T - r.(=) p.(=)
+/. - c.868-6632C>G - r.(=) p.(=)
-?/. - c.868-6606C>T - r.(=) p.(=)
+/. - c.868-6602C>T - r.(=) p.(=)
?/. - c.868-6568T>C - r.(=) p.(=)
?/. - c.868-6565C>G - r.(=) p.(=)
-/. - c.868-6558C>T - r.(=) p.(=)
?/. - c.868-6553C>T - r.(=) p.(=)
?/. - c.868-6536G>A - r.(=) p.(=)
+/. - c.868-6536G>A - r.(=) p.(=)
+/. - c.868-6536G>A - r.(=) p.(=)
?/. - c.868-6536G>A - r.(=) p.(=)
?/. - c.868-6536G>A - r.(=) p.(=)
+/. - c.868-6525C>A - r.(=) p.(=)
+/. - c.868-6525C>A - r.(=) p.(=)
+/. - c.868-6525C>A - r.(=) p.(=)
-?/. - c.868-6462C>T - r.(=) p.(=)
?/. - c.868-6425C>T - r.(=) p.(=)
?/. - c.868-6351_868-6346del - r.(=) p.(=)
?/. - c.868-6349A>G - r.(=) p.(=)
+/. - c.868-6277del - r.(=) p.(=)
?/. - c.868-6277G>A - r.(=) p.(=)
-?/. - c.868-6270C>A - r.(=) p.(=)
-/. - c.868-6207A>G - r.(=) p.(=)
?/. - c.868-6197A>T - r.(=) p.(=)
?/. - c.868-6175C>T - r.(=) p.(=)
+/. - c.868-6171C>A - r.(=) p.(=)
+/. - c.868-6122C>T - r.(=) p.(=)
+/. - c.868-6073T>G - r.(=) p.(=)
+?/. - c.868-6073T>G - r.(=) p.(=)
-?/. - c.868-6061C>A - r.(=) p.(=)
+/. - c.868-6061C>A - r.(=) p.(=)
?/. - c.868-6061C>T - r.(=) p.(=)
?/. - c.868-5999T>C - r.(=) p.(=)
+/. - c.868-5939_868-5931del - r.(=) p.(=)
+?/. - c.868-5925del - r.(=) p.(=)
+/. - c.868-5912A>T - r.(=) p.(=)
+/. - c.868-5908del - r.(=) p.(=)
+/. - c.868-5907C>A - r.(=) p.(=)
+/. - c.880_894delinsA - r.(?) p.(Tyr294ArgfsTer27)
+/. - c.926G>A - r.(?) p.(Gly309Glu)
?/. - c.967A>G - r.(?) p.(Ile323Val)
-/. - c.999+15T>C - r.(=) p.(=)
-/. - c.999+18C>T - r.(=) p.(=)
-/. - c.1000-100_1000-99insGT - r.(=) p.(=)
+/. - c.1008G>A - r.(?) p.(Trp336Ter)
+/. - c.1009C>T - r.(?) p.(Arg337Trp)
+/. - c.1010_1013dup - r.(?) p.(Tyr338Ter)
+/. - c.1073A>G - r.(?) p.(Gln358Arg)
+?/. - c.1087G>A - r.(?) p.(Gly363Ser)
+/. - c.1087+1G>T - - p.?
+?/. - c.1094C>T - r.(?) p.(Pro365Leu)
+?/. - c.1094C>T - r.(?) p.(Pro365Leu)
+?/. - c.1094C>T - r.(?) p.(Pro365Leu)
-?/. - c.1125T>C - r.(?) p.(Gly375=)
+?/. - c.1148_1153del - r.(?) p.(Ile383_Cys384del)
?/. - c.1151G>A - r.(?) p.(Cys384Tyr)
-?/. - c.1152C>T - r.(?) p.(Cys384=)
?/. - c.1162C>T - r.(?) p.(Pro388Ser)
+/. - c.1163C>A - r.(?) p.(Pro388His)
?/. - c.1166T>C - r.(?) p.(Met389Thr)
+/. - c.1208A>C - r.(?) p.(Lys403Thr)
?/. - c.1210C>T - r.(?) p.(Arg404Cys)
+?/. - c.1210C>T - r.(?) p.(Arg404Cys)
+/. - c.1223del - r.(?) p.(Lys408ArgfsTer5)
+/. - c.1223del - r.(?) p.(Lys408ArgfsTer5)
+/. - c.1223del - r.(?) p.(Lys408ArgfsTer5)
+/. - c.1223del - r.(?) p.(Lys408ArgfsTer5)
+/. - c.1307+1G>T - r.spl? p.?
?/. - c.1325T>C - r.(?) p.(Met442Thr)
-?/. - c.1346A>G - r.(?) p.(Lys449Arg)
?/. - c.1351C>T - r.(?) p.(Arg451Cys)
?/. - c.1352G>A - r.(?) p.(Arg451His)
?/. - c.1432G>A - r.(?) p.(Ala478Thr)
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