Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.67240275G>ACA116015IL23Rc.1142G>A (p.Arg381Gln)
c.533G>A (p.Arg178Gln)
c.-58-15562G>A (p.=)
c.377G>A (p.Arg126Gln)
c.191-15562G>A (p.=)
c.380G>A (p.Arg127Gln)
c.1232G>A (p.Arg411Gln)
n.1228+3473G>A
ClinVar dbSNP ExAC gnomAD
1g.67240275G>CCA340725938IL23Rc.1142G>C (p.Arg381Pro)
c.533G>C (p.Arg178Pro)
c.-58-15562G>C (p.=)
c.377G>C (p.Arg126Pro)
c.191-15562G>C (p.=)
c.380G>C (p.Arg127Pro)
c.1232G>C (p.Arg411Pro)
n.1228+3473G>C
1g.67240275G=CA1140248460IL23Rc.1142G= (p.Arg381=)
c.533G= (p.Arg178=)
c.-58-15562G= (p.=)
c.377G= (p.Arg126=)
c.191-15562G= (p.=)
c.380G= (p.Arg127=)
c.1232G= (p.Arg411=)
n.1228+3473G=
1g.67240275G>TCA340725939IL23Rc.1142G>T (p.Arg381Leu)
c.533G>T (p.Arg178Leu)
c.-58-15562G>T (p.=)
c.377G>T (p.Arg126Leu)
c.191-15562G>T (p.=)
c.380G>T (p.Arg127Leu)
c.1232G>T (p.Arg411Leu)
n.1228+3473G>T
1g.67240276A>CCA418269034IL23Rc.1143A>C (p.Arg381=)
c.534A>C (p.Arg178=)
c.-58-15561A>C (p.=)
c.378A>C (p.Arg126=)
c.191-15561A>C (p.=)
c.381A>C (p.Arg127=)
c.1233A>C (p.Arg411=)
n.1228+3474A>C
1g.67240276A>GCA418269035IL23Rc.1143A>G (p.Arg381=)
c.534A>G (p.Arg178=)
c.-58-15561A>G (p.=)
c.378A>G (p.Arg126=)
c.191-15561A>G (p.=)
c.381A>G (p.Arg127=)
c.1233A>G (p.Arg411=)
n.1228+3474A>G
1g.67240276A>TCA418269036IL23Rc.1143A>T (p.Arg381=)
c.534A>T (p.Arg178=)
c.-58-15561A>T (p.=)
c.378A>T (p.Arg126=)
c.191-15561A>T (p.=)
c.381A>T (p.Arg127=)
c.1233A>T (p.Arg411=)
n.1228+3474A>T
1g.67240277A>CCA340725940IL23Rc.1144A>C (p.Thr382Pro)
c.535A>C (p.Thr179Pro)
c.-58-15560A>C (p.=)
c.379A>C (p.Thr127Pro)
c.191-15560A>C (p.=)
c.382A>C (p.Thr128Pro)
c.1234A>C (p.Thr412Pro)
n.1228+3475A>C
1g.67240277A>GCA340725941IL23Rc.1144A>G (p.Thr382Ala)
c.535A>G (p.Thr179Ala)
c.-58-15560A>G (p.=)
c.379A>G (p.Thr127Ala)
c.191-15560A>G (p.=)
c.382A>G (p.Thr128Ala)
c.1234A>G (p.Thr412Ala)
n.1228+3475A>G
1g.67240277A>TCA340725942IL23Rc.1144A>T (p.Thr382Ser)
c.535A>T (p.Thr179Ser)
c.-58-15560A>T (p.=)
c.379A>T (p.Thr127Ser)
c.191-15560A>T (p.=)
c.382A>T (p.Thr128Ser)
c.1234A>T (p.Thr412Ser)
n.1228+3475A>T
1g.67240278C>ACA340725943IL23Rc.1145C>A (p.Thr382Asn)
c.536C>A (p.Thr179Asn)
c.-58-15559C>A (p.=)
c.380C>A (p.Thr127Asn)
c.191-15559C>A (p.=)
c.383C>A (p.Thr128Asn)
c.1235C>A (p.Thr412Asn)
n.1228+3476C>A
1g.67240278C>GCA340725944IL23Rc.1145C>G (p.Thr382Ser)
c.536C>G (p.Thr179Ser)
c.-58-15559C>G (p.=)
c.380C>G (p.Thr127Ser)
c.191-15559C>G (p.=)
c.383C>G (p.Thr128Ser)
c.1235C>G (p.Thr412Ser)
n.1228+3476C>G
1g.67240278C>TCA340725945IL23Rc.1145C>T (p.Thr382Ile)
c.536C>T (p.Thr179Ile)
c.-58-15559C>T (p.=)
c.380C>T (p.Thr127Ile)
c.191-15559C>T (p.=)
c.383C>T (p.Thr128Ile)
c.1235C>T (p.Thr412Ile)
n.1228+3476C>T
1g.67240279T>ACA418269037IL23Rc.1146T>A (p.Thr382=)
c.537T>A (p.Thr179=)
c.-58-15558T>A (p.=)
c.381T>A (p.Thr127=)
c.191-15558T>A (p.=)
c.384T>A (p.Thr128=)
c.1236T>A (p.Thr412=)
n.1228+3477T>A
1g.67240279T>CCA418269038IL23Rc.1146T>C (p.Thr382=)
c.537T>C (p.Thr179=)
c.-58-15558T>C (p.=)
c.381T>C (p.Thr127=)
c.191-15558T>C (p.=)
c.384T>C (p.Thr128=)
c.1236T>C (p.Thr412=)
n.1228+3477T>C
1g.67240279T>GCA418269039IL23Rc.1146T>G (p.Thr382=)
c.537T>G (p.Thr179=)
c.-58-15558T>G (p.=)
c.381T>G (p.Thr127=)
c.191-15558T>G (p.=)
c.384T>G (p.Thr128=)
c.1236T>G (p.Thr412=)
n.1228+3477T>G
1g.67240280G>ACA340725948IL23Rc.1147G>A (p.Gly383Arg)
c.538G>A (p.Gly180Arg)
c.-58-15557G>A (p.=)
c.382G>A (p.Gly128Arg)
c.191-15557G>A (p.=)
c.385G>A (p.Gly129Arg)
c.1237G>A (p.Gly413Arg)
n.1228+3478G>A
gnomAD
1g.67240280G>CCA340725947IL23Rc.1147G>C (p.Gly383Arg)
c.538G>C (p.Gly180Arg)
c.-58-15557G>C (p.=)
c.382G>C (p.Gly128Arg)
c.191-15557G>C (p.=)
c.385G>C (p.Gly129Arg)
c.1237G>C (p.Gly413Arg)
n.1228+3478G>C
1g.67240280G=CA1173056559IL23Rc.1147G= (p.Gly383=)
c.538G= (p.Gly180=)
c.-58-15557G= (p.=)
c.382G= (p.Gly128=)
c.191-15557G= (p.=)
c.385G= (p.Gly129=)
c.1237G= (p.Gly413=)
n.1228+3478G=
1g.67240280G>TCA340725946IL23Rc.1147G>T (p.Gly383Trp)
c.538G>T (p.Gly180Trp)
c.-58-15557G>T (p.=)
c.382G>T (p.Gly128Trp)
c.191-15557G>T (p.=)
c.385G>T (p.Gly129Trp)
c.1237G>T (p.Gly413Trp)
n.1228+3478G>T
1g.67240281G>ACA340725949IL23Rc.1148G>A (p.Gly383Glu)
c.539G>A (p.Gly180Glu)
c.-58-15556G>A (p.=)
c.383G>A (p.Gly128Glu)
c.191-15556G>A (p.=)
c.386G>A (p.Gly129Glu)
c.1238G>A (p.Gly413Glu)
n.1228+3479G>A
1g.67240281G>CCA340725950IL23Rc.1148G>C (p.Gly383Ala)
c.539G>C (p.Gly180Ala)
c.-58-15556G>C (p.=)
c.383G>C (p.Gly128Ala)
c.191-15556G>C (p.=)
c.386G>C (p.Gly129Ala)
c.1238G>C (p.Gly413Ala)
n.1228+3479G>C
1g.67240281G>TCA340725951IL23Rc.1148G>T (p.Gly383Val)
c.539G>T (p.Gly180Val)
c.-58-15556G>T (p.=)
c.383G>T (p.Gly128Val)
c.191-15556G>T (p.=)
c.386G>T (p.Gly129Val)
c.1238G>T (p.Gly413Val)
n.1228+3479G>T
1g.67240282G>ACA340725952IL23Rc.1148+1G>A (p.=)
c.539+1G>A (p.=)
c.-58-15555G>A (p.=)
c.383+1G>A (p.=)
c.191-15555G>A (p.=)
c.386+1G>A (p.=)
c.1238+1G>A (p.=)
n.1228+3480G>A
COSMIC
1g.67240282G>CCA340725953IL23Rc.1148+1G>C (p.=)
c.539+1G>C (p.=)
c.-58-15555G>C (p.=)
c.383+1G>C (p.=)
c.191-15555G>C (p.=)
c.386+1G>C (p.=)
c.1238+1G>C (p.=)
n.1228+3480G>C
1g.67240282G>TCA340725954IL23Rc.1148+1G>T (p.=)
c.539+1G>T (p.=)
c.-58-15555G>T (p.=)
c.383+1G>T (p.=)
c.191-15555G>T (p.=)
c.386+1G>T (p.=)
c.1238+1G>T (p.=)
n.1228+3480G>T
1g.67240283T>ACA340725955IL23Rc.1148+2T>A (p.=)
c.539+2T>A (p.=)
c.-58-15554T>A (p.=)
c.383+2T>A (p.=)
c.191-15554T>A (p.=)
c.386+2T>A (p.=)
c.1238+2T>A (p.=)
n.1228+3481T>A
1g.67240283T>CCA340725956IL23Rc.1148+2T>C (p.=)
c.539+2T>C (p.=)
c.-58-15554T>C (p.=)
c.383+2T>C (p.=)
c.191-15554T>C (p.=)
c.386+2T>C (p.=)
c.1238+2T>C (p.=)
n.1228+3481T>C
1g.67240283T>GCA340725957IL23Rc.1148+2T>G (p.=)
c.539+2T>G (p.=)
c.-58-15554T>G (p.=)
c.383+2T>G (p.=)
c.191-15554T>G (p.=)
c.386+2T>G (p.=)
c.1238+2T>G (p.=)
n.1228+3481T>G
1g.67240286G>ACA738070493IL23Rc.1148+5G>A (p.=)
c.539+5G>A (p.=)
c.-58-15551G>A (p.=)
c.383+5G>A (p.=)
c.191-15551G>A (p.=)
c.386+5G>A (p.=)
c.1238+5G>A (p.=)
n.1228+3484G>A
1g.67240286G=CA1173056561IL23Rc.1148+5G= (p.=)
c.539+5G= (p.=)
c.-58-15551G= (p.=)
c.383+5G= (p.=)
c.191-15551G= (p.=)
c.386+5G= (p.=)
c.1238+5G= (p.=)
n.1228+3484G=
1g.67240286_67240287delinsGTCA1173056560IL23Rc.1148+5_1148+6delinsGT (p.=)
c.539+5_539+6delinsGT (p.=)
c.-58-15551_-58-15550delinsGT (p.=)
c.383+5_383+6delinsGT (p.=)
c.191-15551_191-15550delinsGT (p.=)
c.386+5_386+6delinsGT (p.=)
c.1238+5_1238+6delinsGT (p.=)
n.1228+3484_1228+3485delinsGT
1g.67240291delCA523279869IL23Rc.1148+10del (p.=)
c.539+10del (p.=)
c.-58-15546del (p.=)
c.383+10del (p.=)
c.191-15546del (p.=)
c.386+10del (p.=)
c.1238+10del (p.=)
n.1228+3489del
dbSNP gnomAD
1g.67240300T>CCA1173056564IL23Rc.1148+19T>C (p.=)
c.539+19T>C (p.=)
c.-58-15537T>C (p.=)
c.383+19T>C (p.=)
c.191-15537T>C (p.=)
c.386+19T>C (p.=)
c.1238+19T>C (p.=)
n.1228+3498T>C
1g.67240300T=CA1173056563IL23Rc.1148+19T= (p.=)
c.539+19T= (p.=)
c.-58-15537T= (p.=)
c.383+19T= (p.=)
c.191-15537T= (p.=)
c.386+19T= (p.=)
c.1238+19T= (p.=)
n.1228+3498T=
1g.67240300_67240301delinsTCCA1173056562IL23Rc.1148+19_1148+20delinsTC (p.=)
c.539+19_539+20delinsTC (p.=)
c.-58-15537_-58-15536delinsTC (p.=)
c.383+19_383+20delinsTC (p.=)
c.191-15537_191-15536delinsTC (p.=)
c.386+19_386+20delinsTC (p.=)
c.1238+19_1238+20delinsTC (p.=)
n.1228+3498_1228+3499delinsTC
1g.67240301delCA899941IL23Rc.1148+20del (p.=)
c.539+20del (p.=)
c.-58-15536del (p.=)
c.383+20del (p.=)
c.191-15536del (p.=)
c.386+20del (p.=)
c.1238+20del (p.=)
n.1228+3499del
dbSNP ExAC gnomAD
1g.67240301C=CA1140262061IL23Rc.1148+20C= (p.=)
c.539+20C= (p.=)
c.-58-15536C= (p.=)
c.383+20C= (p.=)
c.191-15536C= (p.=)
c.386+20C= (p.=)
c.1238+20C= (p.=)
n.1228+3499C=
1g.67240301C>TCA899942IL23Rc.1148+20C>T (p.=)
c.539+20C>T (p.=)
c.-58-15536C>T (p.=)
c.383+20C>T (p.=)
c.191-15536C>T (p.=)
c.386+20C>T (p.=)
c.1238+20C>T (p.=)
n.1228+3499C>T
ClinVar dbSNP ExAC gnomAD
1g.67240303G>ACA523279872IL23Rc.1148+22G>A (p.=)
c.539+22G>A (p.=)
c.-58-15534G>A (p.=)
c.383+22G>A (p.=)
c.191-15534G>A (p.=)
c.386+22G>A (p.=)
c.1238+22G>A (p.=)
n.1228+3501G>A
gnomAD
1g.67240303G>CCA899943IL23Rc.1148+22G>C (p.=)
c.539+22G>C (p.=)
c.-58-15534G>C (p.=)
c.383+22G>C (p.=)
c.191-15534G>C (p.=)
c.386+22G>C (p.=)
c.1238+22G>C (p.=)
n.1228+3501G>C
dbSNP ExAC gnomAD
1g.67240303G=CA1173056565IL23Rc.1148+22G= (p.=)
c.539+22G= (p.=)
c.-58-15534G= (p.=)
c.383+22G= (p.=)
c.191-15534G= (p.=)
c.386+22G= (p.=)
c.1238+22G= (p.=)
n.1228+3501G=
1g.67240308C=CA1173056566IL23Rc.1148+27C= (p.=)
c.539+27C= (p.=)
c.-58-15529C= (p.=)
c.383+27C= (p.=)
c.191-15529C= (p.=)
c.386+27C= (p.=)
c.1238+27C= (p.=)
n.1228+3506C=
1g.67240308C>TCA23490148IL23Rc.1148+27C>T (p.=)
c.539+27C>T (p.=)
c.-58-15529C>T (p.=)
c.383+27C>T (p.=)
c.191-15529C>T (p.=)
c.386+27C>T (p.=)
c.1238+27C>T (p.=)
n.1228+3506C>T
dbSNP
1g.67240310G>ACA523279874IL23Rc.1148+29G>A (p.=)
c.539+29G>A (p.=)
c.-58-15527G>A (p.=)
c.383+29G>A (p.=)
c.191-15527G>A (p.=)
c.386+29G>A (p.=)
c.1238+29G>A (p.=)
n.1228+3508G>A
gnomAD
1g.67240310G=CA1173056567IL23Rc.1148+29G= (p.=)
c.539+29G= (p.=)
c.-58-15527G= (p.=)
c.383+29G= (p.=)
c.191-15527G= (p.=)
c.386+29G= (p.=)
c.1238+29G= (p.=)
n.1228+3508G=
1g.67240312T>CCA899944IL23Rc.1148+31T>C (p.=)
c.539+31T>C (p.=)
c.-58-15525T>C (p.=)
c.383+31T>C (p.=)
c.191-15525T>C (p.=)
c.386+31T>C (p.=)
c.1238+31T>C (p.=)
n.1228+3510T>C
dbSNP ExAC gnomAD
1g.67240312T=CA1144974452IL23Rc.1148+31T= (p.=)
c.539+31T= (p.=)
c.-58-15525T= (p.=)
c.383+31T= (p.=)
c.191-15525T= (p.=)
c.386+31T= (p.=)
c.1238+31T= (p.=)
n.1228+3510T=
1g.67240317A=CA1173056568IL23Rc.1148+36A= (p.=)
c.539+36A= (p.=)
c.-58-15520A= (p.=)
c.383+36A= (p.=)
c.191-15520A= (p.=)
c.386+36A= (p.=)
c.1238+36A= (p.=)
n.1228+3515A=
1g.67240317A>CCA523279875IL23Rc.1148+36A>C (p.=)
c.539+36A>C (p.=)
c.-58-15520A>C (p.=)
c.383+36A>C (p.=)
c.191-15520A>C (p.=)
c.386+36A>C (p.=)
c.1238+36A>C (p.=)
n.1228+3515A>C
gnomAD

Number of alleles fetched