Transcript #00020535

Transcript name UDP glucuronosyltransferase 1 family, polypeptide A9
Gene name UGT1A9 (UDP glucuronosyltransferase 1 family, polypeptide A9)
Chromosome 2
Transcript - NCBI ID NM_021027.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_066307.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

457 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-33T>G r.(=) p.(=)
?/? c.-22T>C r.(=) p.(=)
?/? c.-16C>T r.(=) p.(=)
?/? c.7T>C r.(?) p.(Cys3Arg)
?/? c.8G>A r.(?) p.(Cys3Tyr)
?/? c.42G>A r.(=) p.(=)
?/? c.69C>T r.(=) p.(=)
?/? c.98T>C r.(?) p.(Met33Thr)
?/? c.101A>G r.(?) p.(Asp34Gly)
?/? c.128C>T r.(?) p.(Ser43Leu)
?/? c.156G>A r.(=) p.(=)
?/? c.175A>C r.(?) p.(Met59Leu)
?/? c.196C>T r.(=) p.(=)
?/? c.262C>T r.(?) p.(Arg88Trp)
?/? c.331G>A r.(?) p.(Gly111Ser)
?/? c.337T>C r.(?) p.(Tyr113His)
?/? c.369del r.(?) p.(Cys124Alafs*10)
?/? c.369T>C r.(=) p.(=)
?/? c.388G>C r.(?) p.(Asp130His)
?/? c.404A>T r.(?) p.(Glu135Val)
?/? c.406T>A r.(?) p.(Tyr136Asn)
?/? c.423T>G r.(=) p.(=)
?/? c.432A>G r.(=) p.(=)
?/? c.462C>T r.(=) p.(=)
?/? c.484T>C r.(?) p.(Ser162Pro)
?/? c.500T>C r.(?) p.(Val167Ala)
?/? c.503T>C r.(?) p.(Phe168Ser)
?/? c.505G>T r.(?) p.(Ala169Ser)
?/? c.526T>C r.(?) p.(Tyr176His)
?/? c.547T>G r.(?) p.(Cys183Gly)
?/? c.567T>C r.(=) p.(=)
?/? c.583T>A r.(?) p.(Leu195Ile)
?/? c.588G>T r.(=) p.(=)
?/? c.615G>A r.(=) p.(=)
?/? c.616A>G r.(?) p.(Arg206Gly)
?/? c.641T>G r.(?) p.(Leu214Trp)
?/? c.684A>G r.(=) p.(=)
?/? c.716T>A r.(?) p.(Val239Asp)
?/? c.761G>A r.(?) p.(Arg254Gln)
?/? c.764C>T r.(?) p.(Thr255Met)
?/? c.780C>G r.(?) p.(Asp260Glu)
?/? c.781T>C r.(?) p.(Tyr261His)
?/? c.793G>A r.(?) p.(Val265Met)
?/? c.802A>G r.(?) p.(Asn268Asp)
?/? c.805A>T r.(?) p.(Met269Leu)
?/? c.835C>T r.(?) p.(Gln279*)
?/? c.838G>A r.(?) p.(Gly280Arg)
?/? c.851C>G r.(?) p.(Pro284Arg)
?/? c.855del r.(?) p.(Glu286Asnfs*77)
?/? c.855+37C>T r.(=) p.(=)
?/? c.855+9103T>C r.(=) p.(=)
?/? c.855+9181C>A r.(=) p.(=)
?/? c.855+9242C>T r.(?) p.(Pro32Ser)
?/? c.855+9256C>T r.(=) p.(=)
?/? c.855+9262G>A r.(?) p.(Trp38*)
?/? c.855+9271G>A r.(?) p.(Met41Ile)
?/? c.855+9292C>T r.(=) p.(=)
?/? c.855+9302G>A r.(?) p.(Gly52Arg)
?/? c.855+9343A>G r.(=) p.(=)
?/? c.855+9375C>T r.(?) p.(Thr76Ile)
?/? c.855+9386T>G r.(?) p.(Ser80Ala)
?/? c.855+9387C>G r.(?) p.(Ser80*)
?/? c.855+9391C>A r.(?) p.(Tyr81*)
?/? c.855+9410C>T r.(?) p.(Arg88Trp)
?/? c.855+9414del r.(?) p.(Glu89Glyfs*21)
?/? c.855+9422G>A r.(?) p.(Val92Ile)
?/? c.855+9430C>T r.(=) p.(=)
?/? c.855+9487C>T r.(=) p.(=)
?/? c.855+9491G>A r.(?) p.(Gly115Ser)
?/? c.855+9500G>T r.(?) p.(Asp118Tyr)
?/? c.855+9534A>G r.(?) p.(Asn129Ser)
?/? c.855+9565G>C r.(?) p.(Glu139Asp)
?/? c.855+9570G>C r.(?) p.(Cys141Ser)
?/? c.855+9583G>A r.(=) p.(=)
?/? c.855+9594C>T r.(?) p.(Pro149Leu)
?/? c.855+9615T>C r.(?) p.(Ile156Thr)
?/? c.855+9650del r.(?) p.(Phe168Serfs*28)
?/? c.855+9725C>A r.(?) p.(Leu193Ile)
?/? c.855+9750T>C r.(?) p.(Met201Thr)
?/? c.855+9760G>A r.(=) p.(=)
?/? c.855+9770T>C r.(?) p.(Trp208Arg)
?/? c.855+9791G>A r.(?) p.(Glu215Lys)
?/? c.855+9808C>T r.(=) p.(=)
?/? c.855+9820C>A r.(?) p.(Phe224Leu)
?/? c.855+9838del r.(?) p.(Ile230Metfs*36)
?/? c.855+9860C>T r.(?) p.(Pro238Ser)
?/? c.855+9867C>T r.(?) p.(Thr240Met)
?/? c.855+9877T>C r.(=) p.(=)
?/? c.855+9901G>A r.(?) p.(Trp251*)
?/? c.855+9904G>A r.(=) p.(=)
?/? c.855+9909G>A r.(?) p.(Arg254Gln)
?/? c.855+9930A>G r.(?) p.(Tyr261Cys)
?/? c.855+9951A>G r.(?) p.(Asn268Ser)
?/? c.855+9960T>C r.(?) p.(Phe271Ser)
?/? c.855+9963T>C r.(?) p.(Ile272Thr)
?/? c.855+9976C>A r.(?) p.(Asn276Lys)
?/? c.855+10002T>C r.(?) p.(Met285Thr)
?/? c.855+10008G>C r.(=) p.(=)
?/? c.855+10027A>T r.(=) p.(=)
?/? c.855+20170A>G r.(=) p.(=)
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