Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.114677989A=CA1190276620AMPD1c.1133T= (p.Val378=)
c.1145T= (p.Val382=)
c.928T= (n.928T=)
n.810T=
c.1232T= (p.Val411=)
c.1244T= (p.Val415=)
1g.114677989A>CCA1020207AMPD1c.1133T>G (p.Val378Gly)
c.1145T>G (p.Val382Gly)
c.928T>G (n.928T>G)
n.810T>G
c.1232T>G (p.Val411Gly)
c.1244T>G (p.Val415Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.114677989A>GCA341749114AMPD1c.1133T>C (p.Val378Ala)
c.1145T>C (p.Val382Ala)
c.928T>C (n.928T>C)
n.810T>C
c.1232T>C (p.Val411Ala)
c.1244T>C (p.Val415Ala)
dbSNP
1g.114677989A>TCA341749113AMPD1c.1133T>A (p.Val378Glu)
c.1145T>A (p.Val382Glu)
c.928T>A (n.928T>A)
n.810T>A
c.1232T>A (p.Val411Glu)
c.1244T>A (p.Val415Glu)
1g.114677990C>ACA341749115AMPD1c.1132G>T (p.Val378Leu)
c.1144G>T (p.Val382Leu)
c.927G>T (n.927G>T)
n.809G>T
c.1231G>T (p.Val411Leu)
c.1243G>T (p.Val415Leu)
1g.114677990C>GCA341749116AMPD1c.1132G>C (p.Val378Leu)
c.1144G>C (p.Val382Leu)
c.927G>C (n.927G>C)
n.809G>C
c.1231G>C (p.Val411Leu)
c.1243G>C (p.Val415Leu)
1g.114677990C>TCA341749117AMPD1c.1132G>A (p.Val378Ile)
c.1144G>A (p.Val382Ile)
c.927G>A (n.927G>A)
n.809G>A
c.1231G>A (p.Val411Ile)
c.1243G>A (p.Val415Ile)
gnomAD v4
1g.114677991A=CA1190276621AMPD1c.1131T= (p.Pro377=)
c.1143T= (p.Pro381=)
c.926T= (n.926T=)
n.808T=
c.1230T= (p.Pro410=)
c.1242T= (p.Pro414=)
1g.114677991A>CCA419883120AMPD1c.1131T>G (p.Pro377=)
c.1143T>G (p.Pro381=)
c.926T>G (n.926T>G)
n.808T>G
c.1230T>G (p.Pro410=)
c.1242T>G (p.Pro414=)
dbSNP gnomAD v4
1g.114677991A>GCA419883119AMPD1c.1131T>C (p.Pro377=)
c.1143T>C (p.Pro381=)
c.926T>C (n.926T>C)
n.808T>C
c.1230T>C (p.Pro410=)
c.1242T>C (p.Pro414=)
1g.114677991A>TCA419883118AMPD1c.1131T>A (p.Pro377=)
c.1143T>A (p.Pro381=)
c.926T>A (n.926T>A)
n.808T>A
c.1230T>A (p.Pro410=)
c.1242T>A (p.Pro414=)
1g.114677992G>ACA29055384AMPD1c.1130C>T (p.Pro377Leu)
c.1142C>T (p.Pro381Leu)
c.925C>T (n.925C>T)
n.807C>T
c.1229C>T (p.Pro410Leu)
c.1241C>T (p.Pro414Leu)
dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
1g.114677992G>CCA341749118AMPD1c.1130C>G (p.Pro377Arg)
c.1142C>G (p.Pro381Arg)
c.925C>G (n.925C>G)
n.807C>G
c.1229C>G (p.Pro410Arg)
c.1241C>G (p.Pro414Arg)
1g.114677992G=CA1146335914AMPD1c.1130C= (p.Pro377=)
c.1142C= (p.Pro381=)
c.925C= (n.925C=)
n.807C=
c.1229C= (p.Pro410=)
c.1241C= (p.Pro414=)
1g.114677992G>TCA341749119AMPD1c.1130C>A (p.Pro377His)
c.1142C>A (p.Pro381His)
c.925C>A (n.925C>A)
n.807C>A
c.1229C>A (p.Pro410His)
c.1241C>A (p.Pro414His)
1g.114677993G>ACA341749120AMPD1c.1129C>T (p.Pro377Ser)
c.1141C>T (p.Pro381Ser)
c.924C>T (n.924C>T)
n.806C>T
c.1228C>T (p.Pro410Ser)
c.1240C>T (p.Pro414Ser)
dbSNP gnomAD v4
1g.114677993G>CCA341749121AMPD1c.1129C>G (p.Pro377Ala)
c.1141C>G (p.Pro381Ala)
c.924C>G (n.924C>G)
n.806C>G
c.1228C>G (p.Pro410Ala)
c.1240C>G (p.Pro414Ala)
1g.114677993G=CA1190276622AMPD1c.1129C= (p.Pro377=)
c.1141C= (p.Pro381=)
c.924C= (n.924C=)
n.806C=
c.1228C= (p.Pro410=)
c.1240C= (p.Pro414=)
1g.114677993G>TCA341749122AMPD1c.1129C>A (p.Pro377Thr)
c.1141C>A (p.Pro381Thr)
c.924C>A (n.924C>A)
n.806C>A
c.1228C>A (p.Pro410Thr)
c.1240C>A (p.Pro414Thr)
1g.114677994A=CA1143581691AMPD1c.1128T= (p.Asn376=)
c.1140T= (p.Asn380=)
c.923T= (n.923T=)
n.805T=
c.1227T= (p.Asn409=)
c.1239T= (p.Asn413=)
1g.114677994A>CCA341749123AMPD1c.1128T>G (p.Asn376Lys)
c.1140T>G (p.Asn380Lys)
c.923T>G (n.923T>G)
n.805T>G
c.1227T>G (p.Asn409Lys)
c.1239T>G (p.Asn413Lys)
1g.114677994A>GCA29055386AMPD1c.1128T>C (p.Asn376=)
c.1140T>C (p.Asn380=)
c.923T>C (n.923T>C)
n.805T>C
c.1227T>C (p.Asn409=)
c.1239T>C (p.Asn413=)
dbSNP gnomAD v4
1g.114677994A>TCA341749124AMPD1c.1128T>A (p.Asn376Lys)
c.1140T>A (p.Asn380Lys)
c.923T>A (n.923T>A)
n.805T>A
c.1227T>A (p.Asn409Lys)
c.1239T>A (p.Asn413Lys)
gnomAD v4
1g.114677995T>ACA341749127AMPD1c.1127A>T (p.Asn376Ile)
c.1139A>T (p.Asn380Ile)
c.922A>T (n.922A>T)
n.804A>T
c.1226A>T (p.Asn409Ile)
c.1238A>T (p.Asn413Ile)
1g.114677995T>CCA341749126AMPD1c.1127A>G (p.Asn376Ser)
c.1139A>G (p.Asn380Ser)
c.922A>G (n.922A>G)
n.804A>G
c.1226A>G (p.Asn409Ser)
c.1238A>G (p.Asn413Ser)
1g.114677995T>GCA341749125AMPD1c.1127A>C (p.Asn376Thr)
c.1139A>C (p.Asn380Thr)
c.922A>C (n.922A>C)
n.804A>C
c.1226A>C (p.Asn409Thr)
c.1238A>C (p.Asn413Thr)
1g.114677996T>ACA341749129AMPD1c.1126A>T (p.Asn376Tyr)
c.1138A>T (p.Asn380Tyr)
c.921A>T (n.921A>T)
n.803A>T
c.1225A>T (p.Asn409Tyr)
c.1237A>T (p.Asn413Tyr)
1g.114677996T>CCA341749128AMPD1c.1126A>G (p.Asn376Asp)
c.1138A>G (p.Asn380Asp)
c.921A>G (n.921A>G)
n.803A>G
c.1225A>G (p.Asn409Asp)
c.1237A>G (p.Asn413Asp)
1g.114677996T>GCA341749130AMPD1c.1126A>C (p.Asn376His)
c.1138A>C (p.Asn380His)
c.921A>C (n.921A>C)
n.803A>C
c.1225A>C (p.Asn409His)
c.1237A>C (p.Asn413His)
1g.114677997A>CCA341749131AMPD1c.1125T>G (p.Tyr375Ter)
c.1137T>G (p.Tyr379Ter)
c.920T>G (n.920T>G)
n.802T>G
c.1224T>G (p.Tyr408Ter)
c.1236T>G (p.Tyr412Ter)
1g.114677997A>GCA419883121AMPD1c.1125T>C (p.Tyr375=)
c.1137T>C (p.Tyr379=)
c.920T>C (n.920T>C)
n.802T>C
c.1224T>C (p.Tyr408=)
c.1236T>C (p.Tyr412=)
1g.114677997A>TCA341749132AMPD1c.1125T>A (p.Tyr375Ter)
c.1137T>A (p.Tyr379Ter)
c.920T>A (n.920T>A)
n.802T>A
c.1224T>A (p.Tyr408Ter)
c.1236T>A (p.Tyr412Ter)
1g.114677998T>ACA341749133AMPD1c.1124A>T (p.Tyr375Phe)
c.1136A>T (p.Tyr379Phe)
c.919A>T (n.919A>T)
n.801A>T
c.1223A>T (p.Tyr408Phe)
c.1235A>T (p.Tyr412Phe)
1g.114677998T>CCA341749134AMPD1c.1124A>G (p.Tyr375Cys)
c.1136A>G (p.Tyr379Cys)
c.919A>G (n.919A>G)
n.801A>G
c.1223A>G (p.Tyr408Cys)
c.1235A>G (p.Tyr412Cys)
1g.114677998T>GCA341749135AMPD1c.1124A>C (p.Tyr375Ser)
c.1136A>C (p.Tyr379Ser)
c.919A>C (n.919A>C)
n.801A>C
c.1223A>C (p.Tyr408Ser)
c.1235A>C (p.Tyr412Ser)
1g.114677999A>CCA341749136AMPD1c.1123T>G (p.Tyr375Asp)
c.1135T>G (p.Tyr379Asp)
c.918T>G (n.918T>G)
n.800T>G
c.1222T>G (p.Tyr408Asp)
c.1234T>G (p.Tyr412Asp)
1g.114677999A>GCA341749137AMPD1c.1123T>C (p.Tyr375His)
c.1135T>C (p.Tyr379His)
c.918T>C (n.918T>C)
n.800T>C
c.1222T>C (p.Tyr408His)
c.1234T>C (p.Tyr412His)
gnomAD v4
1g.114677999A>TCA341749138AMPD1c.1123T>A (p.Tyr375Asn)
c.1135T>A (p.Tyr379Asn)
c.918T>A (n.918T>A)
n.800T>A
c.1222T>A (p.Tyr408Asn)
c.1234T>A (p.Tyr412Asn)
1g.114677999_114678001delinsATTCA1190276623AMPD1c.1121_1123delinsAAT (p.Lys374=)
c.1133_1135delinsAAT (p.Lys378=)
c.916_918delinsAAT (n.916_918delinsAAT)
n.798_800delinsAAT
c.1220_1222delinsAAT (p.Lys407=)
c.1232_1234delinsAAT (p.Lys411=)
1g.114678000T>ACA341749139AMPD1c.1122A>T (p.Lys374Asn)
c.1134A>T (p.Lys378Asn)
c.917A>T (n.917A>T)
n.799A>T
c.1221A>T (p.Lys407Asn)
c.1233A>T (p.Lys411Asn)
1g.114678000T>CCA419883122AMPD1c.1122A>G (p.Lys374=)
c.1134A>G (p.Lys378=)
c.917A>G (n.917A>G)
n.799A>G
c.1221A>G (p.Lys407=)
c.1233A>G (p.Lys411=)
1g.114678000T>GCA341749140AMPD1c.1122A>C (p.Lys374Asn)
c.1134A>C (p.Lys378Asn)
c.917A>C (n.917A>C)
n.799A>C
c.1221A>C (p.Lys407Asn)
c.1233A>C (p.Lys411Asn)
1g.114678001_114678002delCA525418509AMPD1c.1121_1122del (p.Lys374IlefsTer2)
c.1133_1134del (p.Lys378IlefsTer2)
c.916_917del (n.916_917del)
n.798_799del
c.1220_1221del (p.Lys407IlefsTer2)
c.1232_1233del (p.Lys411IlefsTer2)
dbSNP gnomAD v2 gnomAD v4
1g.114678001T>ACA341749141AMPD1c.1121A>T (p.Lys374Ile)
c.1133A>T (p.Lys378Ile)
c.916A>T (n.916A>T)
n.798A>T
c.1220A>T (p.Lys407Ile)
c.1232A>T (p.Lys411Ile)
1g.114678001T>CCA341749142AMPD1c.1121A>G (p.Lys374Arg)
c.1133A>G (p.Lys378Arg)
c.916A>G (n.916A>G)
n.798A>G
c.1220A>G (p.Lys407Arg)
c.1232A>G (p.Lys411Arg)
dbSNP
1g.114678001T>GCA341749143AMPD1c.1121A>C (p.Lys374Thr)
c.1133A>C (p.Lys378Thr)
c.916A>C (n.916A>C)
n.798A>C
c.1220A>C (p.Lys407Thr)
c.1232A>C (p.Lys411Thr)
1g.114678001T=CA1190276624AMPD1c.1121A= (p.Lys374=)
c.1133A= (p.Lys378=)
c.916A= (n.916A=)
n.798A=
c.1220A= (p.Lys407=)
c.1232A= (p.Lys411=)
1g.114678002T>ACA341749144AMPD1c.1120A>T (p.Lys374Ter)
c.1132A>T (p.Lys378Ter)
c.915A>T (n.915A>T)
n.797A>T
c.1219A>T (p.Lys407Ter)
c.1231A>T (p.Lys411Ter)
1g.114678002T>CCA341749145AMPD1c.1120A>G (p.Lys374Glu)
c.1132A>G (p.Lys378Glu)
c.915A>G (n.915A>G)
n.797A>G
c.1219A>G (p.Lys407Glu)
c.1231A>G (p.Lys411Glu)
1g.114678002T>GCA29055391AMPD1c.1120A>C (p.Lys374Gln)
c.1132A>C (p.Lys378Gln)
c.915A>C (n.915A>C)
n.797A>C
c.1219A>C (p.Lys407Gln)
c.1231A>C (p.Lys411Gln)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched