Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.54814638G>ACA2430312946MAGED2c.1272-23G>A (n.1272-23G>A)
c.1218-23G>A (n.1218-23G>A)
c.1017-23G>A (n.1017-23G>A)
 dbSNP gnomAD v4
Xg.54814638G=CA2430312945MAGED2c.1272-23G= (n.1272-23G=)
c.1218-23G= (n.1218-23G=)
c.1017-23G= (n.1017-23G=)
Xg.54814640C>ACA2693856144MAGED2c.1272-21C>A (n.1272-21C>A)
c.1218-21C>A (n.1218-21C>A)
c.1017-21C>A (n.1017-21C>A)
 gnomAD v4
Xg.54814642T>CCA2430312948MAGED2c.1272-19T>C (n.1272-19T>C)
c.1218-19T>C (n.1218-19T>C)
c.1017-19T>C (n.1017-19T>C)
 dbSNP gnomAD v4
Xg.54814642T=CA2430312947MAGED2c.1272-19T= (n.1272-19T=)
c.1218-19T= (n.1218-19T=)
c.1017-19T= (n.1017-19T=)
Xg.54814644G>ACA2693856147MAGED2c.1272-17G>A (n.1272-17G>A)
c.1218-17G>A (n.1218-17G>A)
c.1017-17G>A (n.1017-17G>A)
 gnomAD v4
Xg.54814646A=CA2430312949MAGED2c.1272-15A= (n.1272-15A=)
c.1218-15A= (n.1218-15A=)
c.1017-15A= (n.1017-15A=)
Xg.54814646A>CCA10426867MAGED2c.1272-15A>C (n.1272-15A>C)
c.1218-15A>C (n.1218-15A>C)
c.1017-15A>C (n.1017-15A>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814647C>ACA2579623079MAGED2c.1272-14C>A (n.1272-14C>A)
c.1218-14C>A (n.1218-14C>A)
c.1017-14C>A (n.1017-14C>A)
 gnomAD v4
Xg.54814648C>ACA2693856156MAGED2c.1272-13C>A (n.1272-13C>A)
c.1218-13C>A (n.1218-13C>A)
c.1017-13C>A (n.1017-13C>A)
 gnomAD v4
Xg.54814648C=CA2430312950MAGED2c.1272-13C= (n.1272-13C=)
c.1218-13C= (n.1218-13C=)
c.1017-13C= (n.1017-13C=)
Xg.54814648C>TCA876410806MAGED2c.1272-13C>T (n.1272-13C>T)
c.1218-13C>T (n.1218-13C>T)
c.1017-13C>T (n.1017-13C>T)
 dbSNP gnomAD v4
Xg.54814649T>CCA2693856160MAGED2c.1272-12T>C (n.1272-12T>C)
c.1218-12T>C (n.1218-12T>C)
c.1017-12T>C (n.1017-12T>C)
 gnomAD v4
Xg.54814650C>ACA10426869MAGED2c.1272-11C>A (n.1272-11C>A)
c.1218-11C>A (n.1218-11C>A)
c.1017-11C>A (n.1017-11C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814650C=CA2430312951MAGED2c.1272-11C= (n.1272-11C=)
c.1218-11C= (n.1218-11C=)
c.1017-11C= (n.1017-11C=)
Xg.54814650C>GCA10426868MAGED2c.1272-11C>G (n.1272-11C>G)
c.1218-11C>G (n.1218-11C>G)
c.1017-11C>G (n.1017-11C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814650C>TCA876410808MAGED2c.1272-11C>T (n.1272-11C>T)
c.1218-11C>T (n.1218-11C>T)
c.1017-11C>T (n.1017-11C>T)
 dbSNP gnomAD v4
Xg.54814651T>CCA2693856172MAGED2c.1272-10T>C (n.1272-10T>C)
c.1218-10T>C (n.1218-10T>C)
c.1017-10T>C (n.1017-10T>C)
 gnomAD v4
Xg.54814652C>ACA2693856177MAGED2c.1272-9C>A (n.1272-9C>A)
c.1218-9C>A (n.1218-9C>A)
c.1017-9C>A (n.1017-9C>A)
 gnomAD v4
Xg.54814652C=CA2430312952MAGED2c.1272-9C= (n.1272-9C=)
c.1218-9C= (n.1218-9C=)
c.1017-9C= (n.1017-9C=)
Xg.54814652C>GCA10426870MAGED2c.1272-9C>G (n.1272-9C>G)
c.1218-9C>G (n.1218-9C>G)
c.1017-9C>G (n.1017-9C>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814652C>TCA2430312953MAGED2c.1272-9C>T (n.1272-9C>T)
c.1218-9C>T (n.1218-9C>T)
c.1017-9C>T (n.1017-9C>T)
 dbSNP gnomAD v4
Xg.54814655delCA2579623080MAGED2c.1272-6del (n.1272-6del)
c.1218-6del (n.1218-6del)
c.1017-6del (n.1017-6del)
Xg.54814656C>ACA2693856182MAGED2c.1272-5C>A (n.1272-5C>A)
c.1218-5C>A (n.1218-5C>A)
c.1017-5C>A (n.1017-5C>A)
 gnomAD v4
Xg.54814656C>TCA2579623081MAGED2c.1272-5C>T (n.1272-5C>T)
c.1218-5C>T (n.1218-5C>T)
c.1017-5C>T (n.1017-5C>T)
Xg.54814657C>ACA2693856185MAGED2c.1272-4C>A (n.1272-4C>A)
c.1218-4C>A (n.1218-4C>A)
c.1017-4C>A (n.1017-4C>A)
 gnomAD v4
Xg.54814657C=CA2430312954MAGED2c.1272-4C= (n.1272-4C=)
c.1218-4C= (n.1218-4C=)
c.1017-4C= (n.1017-4C=)
Xg.54814657C>TCA1133261318MAGED2c.1272-4C>T (n.1272-4C>T)
c.1218-4C>T (n.1218-4C>T)
c.1017-4C>T (n.1017-4C>T)
 dbSNP gnomAD v3 gnomAD v4
Xg.54814658A=CA2430312955MAGED2c.1272-3A= (n.1272-3A=)
c.1218-3A= (n.1218-3A=)
c.1017-3A= (n.1017-3A=)
Xg.54814658A>CCA641373715MAGED2c.1272-3A>C (n.1272-3A>C)
c.1218-3A>C (n.1218-3A>C)
c.1017-3A>C (n.1017-3A>C)
 dbSNP gnomAD v2 gnomAD v4
Xg.54814658A>GCA10426871MAGED2c.1272-3A>G (n.1272-3A>G)
c.1218-3A>G (n.1218-3A>G)
c.1017-3A>G (n.1017-3A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.54814658A>TCA2693856193MAGED2c.1272-3A>T (n.1272-3A>T)
c.1218-3A>T (n.1218-3A>T)
c.1017-3A>T (n.1017-3A>T)
 gnomAD v4
Xg.54814659A>CCA413273770MAGED2c.1272-2A>C (n.1272-2A>C)
c.1218-2A>C (n.1218-2A>C)
c.1017-2A>C (n.1017-2A>C)
Xg.54814659A>GCA413273772MAGED2c.1272-2A>G (n.1272-2A>G)
c.1218-2A>G (n.1218-2A>G)
c.1017-2A>G (n.1017-2A>G)
 gnomAD v4
Xg.54814659A>TCA413273775MAGED2c.1272-2A>T (n.1272-2A>T)
c.1218-2A>T (n.1218-2A>T)
c.1017-2A>T (n.1017-2A>T)
Xg.54814660G>ACA413273777MAGED2c.1272-1G>A (n.1272-1G>A)
c.1218-1G>A (n.1218-1G>A)
c.1017-1G>A (n.1017-1G>A)
Xg.54814660G>CCA413273780MAGED2c.1272-1G>C (n.1272-1G>C)
c.1218-1G>C (n.1218-1G>C)
c.1017-1G>C (n.1017-1G>C)
Xg.54814660G>TCA413273783MAGED2c.1272-1G>T (n.1272-1G>T)
c.1218-1G>T (n.1218-1G>T)
c.1017-1G>T (n.1017-1G>T)
Xg.54814661G>ACA516582411MAGED2c.1272G>A (p.Lys424=)
c.1218G>A (p.Lys406=)
c.1017G>A (p.Lys339=)
 gnomAD v4
Xg.54814661G>CCA413273785MAGED2c.1272G>C (p.Lys424Asn)
c.1218G>C (p.Lys406Asn)
c.1017G>C (p.Lys339Asn)
Xg.54814661G>TCA413273788MAGED2c.1272G>T (p.Lys424Asn)
c.1218G>T (p.Lys406Asn)
c.1017G>T (p.Lys339Asn)
Xg.54814662T>ACA413273794MAGED2c.1273T>A (p.Tyr425Asn)
c.1219T>A (p.Tyr407Asn)
c.1018T>A (p.Tyr340Asn)
Xg.54814662T>CCA413273796MAGED2c.1273T>C (p.Tyr425His)
c.1219T>C (p.Tyr407His)
c.1018T>C (p.Tyr340His)
 gnomAD v4
Xg.54814662T>GCA413273791MAGED2c.1273T>G (p.Tyr425Asp)
c.1219T>G (p.Tyr407Asp)
c.1018T>G (p.Tyr340Asp)
Xg.54814663A>CCA413273801MAGED2c.1274A>C (p.Tyr425Ser)
c.1220A>C (p.Tyr407Ser)
c.1019A>C (p.Tyr340Ser)
Xg.54814663A>GCA413273804MAGED2c.1274A>G (p.Tyr425Cys)
c.1220A>G (p.Tyr407Cys)
c.1019A>G (p.Tyr340Cys)
Xg.54814663A>TCA413273805MAGED2c.1274A>T (p.Tyr425Phe)
c.1220A>T (p.Tyr407Phe)
c.1019A>T (p.Tyr340Phe)
Xg.54814664C>ACA413273809MAGED2c.1275C>A (p.Tyr425Ter)
c.1221C>A (p.Tyr407Ter)
c.1020C>A (p.Tyr340Ter)
 gnomAD v4
Xg.54814664C>GCA413273811MAGED2c.1275C>G (p.Tyr425Ter)
c.1221C>G (p.Tyr407Ter)
c.1020C>G (p.Tyr340Ter)
Xg.54814664C>TCA516582417MAGED2c.1275C>T (p.Tyr425=)
c.1221C>T (p.Tyr407=)
c.1020C>T (p.Tyr340=)
 gnomAD v4
Xg.54814665C>ACA413273814MAGED2c.1276C>A (p.Leu426Met)
c.1222C>A (p.Leu408Met)
c.1021C>A (p.Leu341Met)
 gnomAD v4
Xg.54814665C>GCA413273817MAGED2c.1276C>G (p.Leu426Val)
c.1222C>G (p.Leu408Val)
c.1021C>G (p.Leu341Val)
Xg.54814665C>TCA516582418MAGED2c.1276C>T (p.Leu426=)
c.1222C>T (p.Leu408=)
c.1021C>T (p.Leu341=)
 gnomAD v4
Xg.54814666T>ACA413273818MAGED2c.1277T>A (p.Leu426Gln)
c.1223T>A (p.Leu408Gln)
c.1022T>A (p.Leu341Gln)
Xg.54814666T>CCA413273821MAGED2c.1277T>C (p.Leu426Pro)
c.1223T>C (p.Leu408Pro)
c.1022T>C (p.Leu341Pro)
Xg.54814666T>GCA413273824MAGED2c.1277T>G (p.Leu426Arg)
c.1223T>G (p.Leu408Arg)
c.1022T>G (p.Leu341Arg)
Xg.54814667G>ACA516582423MAGED2c.1278G>A (p.Leu426=)
c.1224G>A (p.Leu408=)
c.1023G>A (p.Leu341=)
Xg.54814667G>CCA516582425MAGED2c.1278G>C (p.Leu426=)
c.1224G>C (p.Leu408=)
c.1023G>C (p.Leu341=)
 COSMIC
Xg.54814667G>TCA516582426MAGED2c.1278G>T (p.Leu426=)
c.1224G>T (p.Leu408=)
c.1023G>T (p.Leu341=)
Xg.54814668delCA2579623082MAGED2c.1279del (p.Asp427ThrfsTer28)
c.1225del (p.Asp409ThrfsTer28)
c.1024del (p.Asp342ThrfsTer28)
Xg.54814668G>ACA413273827MAGED2c.1279G>A (p.Asp427Asn)
c.1225G>A (p.Asp409Asn)
c.1024G>A (p.Asp342Asn)
Xg.54814668G>CCA413273830MAGED2c.1279G>C (p.Asp427His)
c.1225G>C (p.Asp409His)
c.1024G>C (p.Asp342His)
 dbSNP gnomAD v4
Xg.54814668G=CA2430312956MAGED2c.1279G= (p.Asp427=)
c.1225G= (p.Asp409=)
c.1024G= (p.Asp342=)
Xg.54814668G>TCA413273833MAGED2c.1279G>T (p.Asp427Tyr)
c.1225G>T (p.Asp409Tyr)
c.1024G>T (p.Asp342Tyr)
 gnomAD v4
Xg.54814669A>CCA413273840MAGED2c.1280A>C (p.Asp427Ala)
c.1226A>C (p.Asp409Ala)
c.1025A>C (p.Asp342Ala)
Xg.54814669A>GCA413273837MAGED2c.1280A>G (p.Asp427Gly)
c.1226A>G (p.Asp409Gly)
c.1025A>G (p.Asp342Gly)
 gnomAD v4
Xg.54814669A>TCA413273835MAGED2c.1280A>T (p.Asp427Val)
c.1226A>T (p.Asp409Val)
c.1025A>T (p.Asp342Val)
 gnomAD v4
Xg.54814670C>ACA413273843MAGED2c.1281C>A (p.Asp427Glu)
c.1227C>A (p.Asp409Glu)
c.1026C>A (p.Asp342Glu)
Xg.54814670C>GCA413273845MAGED2c.1281C>G (p.Asp427Glu)
c.1227C>G (p.Asp409Glu)
c.1026C>G (p.Asp342Glu)
Xg.54814670C>TCA516582433MAGED2c.1281C>T (p.Asp427=)
c.1227C>T (p.Asp409=)
c.1026C>T (p.Asp342=)
Xg.54814671T>ACA413273849MAGED2c.1282T>A (p.Tyr428Asn)
c.1228T>A (p.Tyr410Asn)
c.1027T>A (p.Tyr343Asn)
Xg.54814671T>CCA413273851MAGED2c.1282T>C (p.Tyr428His)
c.1228T>C (p.Tyr410His)
c.1027T>C (p.Tyr343His)
Xg.54814671T>GCA413273855MAGED2c.1282T>G (p.Tyr428Asp)
c.1228T>G (p.Tyr410Asp)
c.1027T>G (p.Tyr343Asp)
Xg.54814672A>CCA413273858MAGED2c.1283A>C (p.Tyr428Ser)
c.1229A>C (p.Tyr410Ser)
c.1028A>C (p.Tyr343Ser)
Xg.54814672A>GCA413273860MAGED2c.1283A>G (p.Tyr428Cys)
c.1229A>G (p.Tyr410Cys)
c.1028A>G (p.Tyr343Cys)
 gnomAD v4
Xg.54814672A>TCA413273863MAGED2c.1283A>T (p.Tyr428Phe)
c.1229A>T (p.Tyr410Phe)
c.1028A>T (p.Tyr343Phe)
Xg.54814673T>ACA413273865MAGED2c.1284T>A (p.Tyr428Ter)
c.1230T>A (p.Tyr410Ter)
c.1029T>A (p.Tyr343Ter)
Xg.54814673T>CCA516582434MAGED2c.1284T>C (p.Tyr428=)
c.1230T>C (p.Tyr410=)
c.1029T>C (p.Tyr343=)
 gnomAD v4
Xg.54814673T>GCA413273868MAGED2c.1284T>G (p.Tyr428Ter)
c.1230T>G (p.Tyr410Ter)
c.1029T>G (p.Tyr343Ter)
Xg.54814674G>ACA413273872MAGED2c.1285G>A (p.Ala429Thr)
c.1231G>A (p.Ala411Thr)
c.1030G>A (p.Ala344Thr)
Xg.54814674G>CCA413273874MAGED2c.1285G>C (p.Ala429Pro)
c.1231G>C (p.Ala411Pro)
c.1030G>C (p.Ala344Pro)
Xg.54814674G>TCA413273877MAGED2c.1285G>T (p.Ala429Ser)
c.1231G>T (p.Ala411Ser)
c.1030G>T (p.Ala344Ser)
Xg.54814675C>ACA413273880MAGED2c.1286C>A (p.Ala429Asp)
c.1232C>A (p.Ala411Asp)
c.1031C>A (p.Ala344Asp)
 gnomAD v4
Xg.54814675C=CA2430312957MAGED2c.1286C= (p.Ala429=)
c.1232C= (p.Ala411=)
c.1031C= (p.Ala344=)
Xg.54814675C>GCA413273884MAGED2c.1286C>G (p.Ala429Gly)
c.1232C>G (p.Ala411Gly)
c.1031C>G (p.Ala344Gly)
Xg.54814675C>TCA413273882MAGED2c.1286C>T (p.Ala429Val)
c.1232C>T (p.Ala411Val)
c.1031C>T (p.Ala344Val)
 dbSNP gnomAD v2 gnomAD v4
Xg.54814676C>ACA516582438MAGED2c.1287C>A (p.Ala429=)
c.1233C>A (p.Ala411=)
c.1032C>A (p.Ala344=)
 gnomAD v4
Xg.54814676C=CA2430312958MAGED2c.1287C= (p.Ala429=)
c.1233C= (p.Ala411=)
c.1032C= (p.Ala344=)
Xg.54814676C>GCA516582439MAGED2c.1287C>G (p.Ala429=)
c.1233C>G (p.Ala411=)
c.1032C>G (p.Ala344=)
Xg.54814676C>TCA328940303MAGED2c.1287C>T (p.Ala429=)
c.1233C>T (p.Ala411=)
c.1032C>T (p.Ala344=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814677A>CCA516582443MAGED2c.1288A>C (p.Arg430=)
c.1234A>C (p.Arg412=)
c.1033A>C (p.Arg345=)
Xg.54814677A>GCA413273886MAGED2c.1288A>G (p.Arg430Gly)
c.1234A>G (p.Arg412Gly)
c.1033A>G (p.Arg345Gly)
 gnomAD v4
Xg.54814677A>TCA413273889MAGED2c.1288A>T (p.Arg430Ter)
c.1234A>T (p.Arg412Ter)
c.1033A>T (p.Arg345Ter)
Xg.54814678G>ACA413273893MAGED2c.1289G>A (p.Arg430Lys)
c.1235G>A (p.Arg412Lys)
c.1034G>A (p.Arg345Lys)
Xg.54814678G>CCA413273896MAGED2c.1289G>C (p.Arg430Thr)
c.1235G>C (p.Arg412Thr)
c.1034G>C (p.Arg345Thr)
Xg.54814678G>TCA413273894MAGED2c.1289G>T (p.Arg430Ile)
c.1235G>T (p.Arg412Ile)
c.1034G>T (p.Arg345Ile)
Xg.54814679A>CCA413273900MAGED2c.1290A>C (p.Arg430Ser)
c.1236A>C (p.Arg412Ser)
c.1035A>C (p.Arg345Ser)
Xg.54814679A>GCA516582445MAGED2c.1290A>G (p.Arg430=)
c.1236A>G (p.Arg412=)
c.1035A>G (p.Arg345=)
Xg.54814679A>TCA413273902MAGED2c.1290A>T (p.Arg430Ser)
c.1236A>T (p.Arg412Ser)
c.1035A>T (p.Arg345Ser)
Xg.54814680G>ACA413273905MAGED2c.1291G>A (p.Val431Ile)
c.1237G>A (p.Val413Ile)
c.1036G>A (p.Val346Ile)
 dbSNP gnomAD v4
Xg.54814680G>CCA413273909MAGED2c.1291G>C (p.Val431Leu)
c.1237G>C (p.Val413Leu)
c.1036G>C (p.Val346Leu)
Xg.54814680G=CA2430312959MAGED2c.1291G= (p.Val431=)
c.1237G= (p.Val413=)
c.1036G= (p.Val346=)
Xg.54814680G>TCA413273907MAGED2c.1291G>T (p.Val431Phe)
c.1237G>T (p.Val413Phe)
c.1036G>T (p.Val346Phe)
Xg.54814681T>ACA413273913MAGED2c.1292T>A (p.Val431Asp)
c.1238T>A (p.Val413Asp)
c.1037T>A (p.Val346Asp)
Xg.54814681T>CCA413273914MAGED2c.1292T>C (p.Val431Ala)
c.1238T>C (p.Val413Ala)
c.1037T>C (p.Val346Ala)
Xg.54814681T>GCA413273916MAGED2c.1292T>G (p.Val431Gly)
c.1238T>G (p.Val413Gly)
c.1037T>G (p.Val346Gly)
 gnomAD v4
Xg.54814682C>ACA516582451MAGED2c.1293C>A (p.Val431=)
c.1239C>A (p.Val413=)
c.1038C>A (p.Val346=)
 dbSNP
Xg.54814682C=CA2430312960MAGED2c.1293C= (p.Val431=)
c.1239C= (p.Val413=)
c.1038C= (p.Val346=)
Xg.54814682C>GCA516582452MAGED2c.1293C>G (p.Val431=)
c.1239C>G (p.Val413=)
c.1038C>G (p.Val346=)
Xg.54814682C>TCA10426872MAGED2c.1293C>T (p.Val431=)
c.1239C>T (p.Val413=)
c.1038C>T (p.Val346=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.54814684_54814685delCA2579623083MAGED2c.1295_1296del (p.Pro432GlnfsTer2)
c.1241_1242del (p.Pro414GlnfsTer2)
c.1040_1041del (p.Pro347GlnfsTer2)
Xg.54814683C>ACA413273922MAGED2c.1294C>A (p.Pro432Thr)
c.1240C>A (p.Pro414Thr)
c.1039C>A (p.Pro347Thr)
Xg.54814683C>GCA413273925MAGED2c.1294C>G (p.Pro432Ala)
c.1240C>G (p.Pro414Ala)
c.1039C>G (p.Pro347Ala)
Xg.54814683C>TCA413273928MAGED2c.1294C>T (p.Pro432Ser)
c.1240C>T (p.Pro414Ser)
c.1039C>T (p.Pro347Ser)
Xg.54814684C>ACA413273931MAGED2c.1295C>A (p.Pro432His)
c.1241C>A (p.Pro414His)
c.1040C>A (p.Pro347His)
 gnomAD v4
Xg.54814684C>GCA413273934MAGED2c.1295C>G (p.Pro432Arg)
c.1241C>G (p.Pro414Arg)
c.1040C>G (p.Pro347Arg)
Xg.54814684C>TCA413273936MAGED2c.1295C>T (p.Pro432Leu)
c.1241C>T (p.Pro414Leu)
c.1040C>T (p.Pro347Leu)
Xg.54814685C>ACA516582453MAGED2c.1296C>A (p.Pro432=)
c.1242C>A (p.Pro414=)
c.1041C>A (p.Pro347=)
Xg.54814685C>GCA516582454MAGED2c.1296C>G (p.Pro432=)
c.1242C>G (p.Pro414=)
c.1041C>G (p.Pro347=)
Xg.54814685C>TCA516582456MAGED2c.1296C>T (p.Pro432=)
c.1242C>T (p.Pro414=)
c.1041C>T (p.Pro347=)
Xg.54814686A>CCA413273939MAGED2c.1297A>C (p.Asn433His)
c.1243A>C (p.Asn415His)
c.1042A>C (p.Asn348His)
Xg.54814686A>GCA413273942MAGED2c.1297A>G (p.Asn433Asp)
c.1243A>G (p.Asn415Asp)
c.1042A>G (p.Asn348Asp)
Xg.54814686A>TCA413273945MAGED2c.1297A>T (p.Asn433Tyr)
c.1243A>T (p.Asn415Tyr)
c.1042A>T (p.Asn348Tyr)
Xg.54814687A=CA2430312961MAGED2c.1298A= (p.Asn433=)
c.1244A= (p.Asn415=)
c.1043A= (p.Asn348=)
Xg.54814687A>CCA413273948MAGED2c.1298A>C (p.Asn433Thr)
c.1244A>C (p.Asn415Thr)
c.1043A>C (p.Asn348Thr)
Xg.54814687A>GCA10426873MAGED2c.1298A>G (p.Asn433Ser)
c.1244A>G (p.Asn415Ser)
c.1043A>G (p.Asn348Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814687A>TCA413273951MAGED2c.1298A>T (p.Asn433Ile)
c.1244A>T (p.Asn415Ile)
c.1043A>T (p.Asn348Ile)
Xg.54814688T>ACA413273957MAGED2c.1299T>A (p.Asn433Lys)
c.1245T>A (p.Asn415Lys)
c.1044T>A (p.Asn348Lys)
Xg.54814688T>CCA516582459MAGED2c.1299T>C (p.Asn433=)
c.1245T>C (p.Asn415=)
c.1044T>C (p.Asn348=)
 gnomAD v4
Xg.54814688T>GCA413273959MAGED2c.1299T>G (p.Asn433Lys)
c.1245T>G (p.Asn415Lys)
c.1044T>G (p.Asn348Lys)
Xg.54814689A>CCA413273963MAGED2c.1300A>C (p.Ser434Arg)
c.1246A>C (p.Ser416Arg)
c.1045A>C (p.Ser349Arg)
Xg.54814689A>GCA413273965MAGED2c.1300A>G (p.Ser434Gly)
c.1246A>G (p.Ser416Gly)
c.1045A>G (p.Ser349Gly)
Xg.54814689A>TCA413273967MAGED2c.1300A>T (p.Ser434Cys)
c.1246A>T (p.Ser416Cys)
c.1045A>T (p.Ser349Cys)
Xg.54814690G>ACA413273971MAGED2c.1301G>A (p.Ser434Asn)
c.1247G>A (p.Ser416Asn)
c.1046G>A (p.Ser349Asn)
Xg.54814690G>CCA413273974MAGED2c.1301G>C (p.Ser434Thr)
c.1247G>C (p.Ser416Thr)
c.1046G>C (p.Ser349Thr)
Xg.54814690G>TCA413273976MAGED2c.1301G>T (p.Ser434Ile)
c.1247G>T (p.Ser416Ile)
c.1046G>T (p.Ser349Ile)
Xg.54814691C>ACA413273978MAGED2c.1302C>A (p.Ser434Arg)
c.1248C>A (p.Ser416Arg)
c.1047C>A (p.Ser349Arg)
 dbSNP gnomAD v2 gnomAD v4
Xg.54814691C=CA2430312962MAGED2c.1302C= (p.Ser434=)
c.1248C= (p.Ser416=)
c.1047C= (p.Ser349=)
Xg.54814691C>GCA413273980MAGED2c.1302C>G (p.Ser434Arg)
c.1248C>G (p.Ser416Arg)
c.1047C>G (p.Ser349Arg)
Xg.54814691C>TCA516582462MAGED2c.1302C>T (p.Ser434=)
c.1248C>T (p.Ser416=)
c.1047C>T (p.Ser349=)
 dbSNP gnomAD v2 gnomAD v4
Xg.54814692A>CCA413273986MAGED2c.1303A>C (p.Asn435His)
c.1249A>C (p.Asn417His)
c.1048A>C (p.Asn350His)
Xg.54814692A>GCA413273985MAGED2c.1303A>G (p.Asn435Asp)
c.1249A>G (p.Asn417Asp)
c.1048A>G (p.Asn350Asp)
Xg.54814692A>TCA413273983MAGED2c.1303A>T (p.Asn435Tyr)
c.1249A>T (p.Asn417Tyr)
c.1048A>T (p.Asn350Tyr)
Xg.54814693A=CA2430312963MAGED2c.1304A= (p.Asn435=)
c.1250A= (p.Asn417=)
c.1049A= (p.Asn350=)
Xg.54814693A>CCA413273992MAGED2c.1304A>C (p.Asn435Thr)
c.1250A>C (p.Asn417Thr)
c.1049A>C (p.Asn350Thr)
Xg.54814693A>GCA10426874MAGED2c.1304A>G (p.Asn435Ser)
c.1250A>G (p.Asn417Ser)
c.1049A>G (p.Asn350Ser)
 dbSNP ExAC
Xg.54814693A>TCA413273990MAGED2c.1304A>T (p.Asn435Ile)
c.1250A>T (p.Asn417Ile)
c.1049A>T (p.Asn350Ile)
Xg.54814694T>ACA413273994MAGED2c.1305T>A (p.Asn435Lys)
c.1251T>A (p.Asn417Lys)
c.1050T>A (p.Asn350Lys)
Xg.54814694T>CCA516582467MAGED2c.1305T>C (p.Asn435=)
c.1251T>C (p.Asn417=)
c.1050T>C (p.Asn350=)
Xg.54814694T>GCA413273996MAGED2c.1305T>G (p.Asn435Lys)
c.1251T>G (p.Asn417Lys)
c.1050T>G (p.Asn350Lys)
Xg.54814695C>ACA413273998MAGED2c.1306C>A (p.Pro436Thr)
c.1252C>A (p.Pro418Thr)
c.1051C>A (p.Pro351Thr)
 gnomAD v4
Xg.54814695C=CA2430312964MAGED2c.1306C= (p.Pro436=)
c.1252C= (p.Pro418=)
c.1051C= (p.Pro351=)
Xg.54814695C>GCA413274000MAGED2c.1306C>G (p.Pro436Ala)
c.1252C>G (p.Pro418Ala)
c.1051C>G (p.Pro351Ala)
Xg.54814695C>TCA10426875MAGED2c.1306C>T (p.Pro436Ser)
c.1252C>T (p.Pro418Ser)
c.1051C>T (p.Pro351Ser)
 ClinVar dbSNP ExAC gnomAD v2
Xg.54814699delCA2693856256MAGED2c.1310del (p.Pro437LeufsTer18)
c.1256del (p.Pro419LeufsTer18)
c.1055del (p.Pro352LeufsTer18)
 gnomAD v4
Xg.54814696C>ACA413274003MAGED2c.1307C>A (p.Pro436His)
c.1253C>A (p.Pro418His)
c.1052C>A (p.Pro351His)
 gnomAD v4
Xg.54814696C>GCA413274007MAGED2c.1307C>G (p.Pro436Arg)
c.1253C>G (p.Pro418Arg)
c.1052C>G (p.Pro351Arg)
Xg.54814696C>TCA413274005MAGED2c.1307C>T (p.Pro436Leu)
c.1253C>T (p.Pro418Leu)
c.1052C>T (p.Pro351Leu)
Xg.54814697C>ACA10426876MAGED2c.1308C>A (p.Pro436=)
c.1254C>A (p.Pro418=)
c.1053C>A (p.Pro351=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814697C=CA2430312965MAGED2c.1308C= (p.Pro436=)
c.1254C= (p.Pro418=)
c.1053C= (p.Pro351=)
Xg.54814697C>GCA516582473MAGED2c.1308C>G (p.Pro436=)
c.1254C>G (p.Pro418=)
c.1053C>G (p.Pro351=)
Xg.54814697C>TCA516582471MAGED2c.1308C>T (p.Pro436=)
c.1254C>T (p.Pro418=)
c.1053C>T (p.Pro351=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814698C>ACA413274008MAGED2c.1309C>A (p.Pro437Thr)
c.1255C>A (p.Pro419Thr)
c.1054C>A (p.Pro352Thr)
Xg.54814698C>GCA413274009MAGED2c.1309C>G (p.Pro437Ala)
c.1255C>G (p.Pro419Ala)
c.1054C>G (p.Pro352Ala)
Xg.54814698C>TCA413274011MAGED2c.1309C>T (p.Pro437Ser)
c.1255C>T (p.Pro419Ser)
c.1054C>T (p.Pro352Ser)
 COSMIC
Xg.54814699C>ACA413274013MAGED2c.1310C>A (p.Pro437His)
c.1256C>A (p.Pro419His)
c.1055C>A (p.Pro352His)
 gnomAD v4
Xg.54814699C>GCA413274017MAGED2c.1310C>G (p.Pro437Arg)
c.1256C>G (p.Pro419Arg)
c.1055C>G (p.Pro352Arg)
Xg.54814699C>TCA413274015MAGED2c.1310C>T (p.Pro437Leu)
c.1256C>T (p.Pro419Leu)
c.1055C>T (p.Pro352Leu)
Xg.54814700T>ACA516582479MAGED2c.1311T>A (p.Pro437=)
c.1257T>A (p.Pro419=)
c.1056T>A (p.Pro352=)
Xg.54814700T>CCA516582480MAGED2c.1311T>C (p.Pro437=)
c.1257T>C (p.Pro419=)
c.1056T>C (p.Pro352=)
Xg.54814700T>GCA516582481MAGED2c.1311T>G (p.Pro437=)
c.1257T>G (p.Pro419=)
c.1056T>G (p.Pro352=)
Xg.54814701G>ACA413274019MAGED2c.1312G>A (p.Glu438Lys)
c.1258G>A (p.Glu420Lys)
c.1057G>A (p.Glu353Lys)
Xg.54814701G>CCA413274021MAGED2c.1312G>C (p.Glu438Gln)
c.1258G>C (p.Glu420Gln)
c.1057G>C (p.Glu353Gln)
Xg.54814701G>TCA413274023MAGED2c.1312G>T (p.Glu438Ter)
c.1258G>T (p.Glu420Ter)
c.1057G>T (p.Glu353Ter)
Xg.54814702A>CCA413274025MAGED2c.1313A>C (p.Glu438Ala)
c.1259A>C (p.Glu420Ala)
c.1058A>C (p.Glu353Ala)
Xg.54814702A>GCA413274027MAGED2c.1313A>G (p.Glu438Gly)
c.1259A>G (p.Glu420Gly)
c.1058A>G (p.Glu353Gly)
Xg.54814702A>TCA413274028MAGED2c.1313A>T (p.Glu438Val)
c.1259A>T (p.Glu420Val)
c.1058A>T (p.Glu353Val)
Xg.54814703A>CCA413274030MAGED2c.1314A>C (p.Glu438Asp)
c.1260A>C (p.Glu420Asp)
c.1059A>C (p.Glu353Asp)
Xg.54814703A>GCA516582485MAGED2c.1314A>G (p.Glu438=)
c.1260A>G (p.Glu420=)
c.1059A>G (p.Glu353=)
Xg.54814703A>TCA413274032MAGED2c.1314A>T (p.Glu438Asp)
c.1260A>T (p.Glu420Asp)
c.1059A>T (p.Glu353Asp)
Xg.54814704T>ACA413274033MAGED2c.1315T>A (p.Tyr439Asn)
c.1261T>A (p.Tyr421Asn)
c.1060T>A (p.Tyr354Asn)
Xg.54814704T>CCA413274035MAGED2c.1315T>C (p.Tyr439His)
c.1261T>C (p.Tyr421His)
c.1060T>C (p.Tyr354His)
Xg.54814704T>GCA413274037MAGED2c.1315T>G (p.Tyr439Asp)
c.1261T>G (p.Tyr421Asp)
c.1060T>G (p.Tyr354Asp)
Xg.54814705A=CA2430312966MAGED2c.1316A= (p.Tyr439=)
c.1262A= (p.Tyr421=)
c.1061A= (p.Tyr354=)
Xg.54814705A>CCA413274041MAGED2c.1316A>C (p.Tyr439Ser)
c.1262A>C (p.Tyr421Ser)
c.1061A>C (p.Tyr354Ser)
Xg.54814705A>GCA413274043MAGED2c.1316A>G (p.Tyr439Cys)
c.1262A>G (p.Tyr421Cys)
c.1061A>G (p.Tyr354Cys)
 dbSNP gnomAD v3 gnomAD v4
Xg.54814705A>TCA413274039MAGED2c.1316A>T (p.Tyr439Phe)
c.1262A>T (p.Tyr421Phe)
c.1061A>T (p.Tyr354Phe)
Xg.54814706T>ACA413274045MAGED2c.1317T>A (p.Tyr439Ter)
c.1263T>A (p.Tyr421Ter)
c.1062T>A (p.Tyr354Ter)
Xg.54814706T>CCA516582487MAGED2c.1317T>C (p.Tyr439=)
c.1263T>C (p.Tyr421=)
c.1062T>C (p.Tyr354=)
 dbSNP gnomAD v4
Xg.54814706T>GCA413274047MAGED2c.1317T>G (p.Tyr439Ter)
c.1263T>G (p.Tyr421Ter)
c.1062T>G (p.Tyr354Ter)
Xg.54814706T=CA2430312967MAGED2c.1317T= (p.Tyr439=)
c.1263T= (p.Tyr421=)
c.1062T= (p.Tyr354=)
Xg.54814707G>ACA413274050MAGED2c.1318G>A (p.Glu440Lys)
c.1264G>A (p.Glu422Lys)
c.1063G>A (p.Glu355Lys)
Xg.54814707G>CCA413274051MAGED2c.1318G>C (p.Glu440Gln)
c.1264G>C (p.Glu422Gln)
c.1063G>C (p.Glu355Gln)
Xg.54814707G>TCA413274053MAGED2c.1318G>T (p.Glu440Ter)
c.1264G>T (p.Glu422Ter)
c.1063G>T (p.Glu355Ter)
Xg.54814708A>CCA413274056MAGED2c.1319A>C (p.Glu440Ala)
c.1265A>C (p.Glu422Ala)
c.1064A>C (p.Glu355Ala)
Xg.54814708A>GCA413274057MAGED2c.1319A>G (p.Glu440Gly)
c.1265A>G (p.Glu422Gly)
c.1064A>G (p.Glu355Gly)
Xg.54814708A>TCA413274059MAGED2c.1319A>T (p.Glu440Val)
c.1265A>T (p.Glu422Val)
c.1064A>T (p.Glu355Val)
Xg.54814709G>ACA516582489MAGED2c.1320G>A (p.Glu440=)
c.1266G>A (p.Glu422=)
c.1065G>A (p.Glu355=)
Xg.54814709G>CCA413274060MAGED2c.1320G>C (p.Glu440Asp)
c.1266G>C (p.Glu422Asp)
c.1065G>C (p.Glu355Asp)
 dbSNP
Xg.54814709G=CA2430312968MAGED2c.1320G= (p.Glu440=)
c.1266G= (p.Glu422=)
c.1065G= (p.Glu355=)
Xg.54814709G>TCA413274061MAGED2c.1320G>T (p.Glu440Asp)
c.1266G>T (p.Glu422Asp)
c.1065G>T (p.Glu355Asp)
Xg.54814710T>ACA413274064MAGED2c.1321T>A (p.Phe441Ile)
c.1267T>A (p.Phe423Ile)
c.1066T>A (p.Phe356Ile)
Xg.54814710T>CCA413274065MAGED2c.1321T>C (p.Phe441Leu)
c.1267T>C (p.Phe423Leu)
c.1066T>C (p.Phe356Leu)
Xg.54814710T>GCA413274067MAGED2c.1321T>G (p.Phe441Val)
c.1267T>G (p.Phe423Val)
c.1066T>G (p.Phe356Val)
 gnomAD v4
Xg.54814711T>ACA413274071MAGED2c.1322T>A (p.Phe441Tyr)
c.1268T>A (p.Phe423Tyr)
c.1067T>A (p.Phe356Tyr)
Xg.54814711T>CCA413274070MAGED2c.1322T>C (p.Phe441Ser)
c.1268T>C (p.Phe423Ser)
c.1067T>C (p.Phe356Ser)
Xg.54814711T>GCA413274069MAGED2c.1322T>G (p.Phe441Cys)
c.1268T>G (p.Phe423Cys)
c.1067T>G (p.Phe356Cys)
Xg.54814712C>ACA413274074MAGED2c.1323C>A (p.Phe441Leu)
c.1269C>A (p.Phe423Leu)
c.1068C>A (p.Phe356Leu)
Xg.54814712C>GCA413274076MAGED2c.1323C>G (p.Phe441Leu)
c.1269C>G (p.Phe423Leu)
c.1068C>G (p.Phe356Leu)
Xg.54814712C>TCA516582496MAGED2c.1323C>T (p.Phe441=)
c.1269C>T (p.Phe423=)
c.1068C>T (p.Phe356=)
 gnomAD v4
Xg.54814713T>ACA413274077MAGED2c.1324T>A (p.Phe442Ile)
c.1270T>A (p.Phe424Ile)
c.1069T>A (p.Phe357Ile)
Xg.54814713T>CCA413274079MAGED2c.1324T>C (p.Phe442Leu)
c.1270T>C (p.Phe424Leu)
c.1069T>C (p.Phe357Leu)
Xg.54814713T>GCA413274081MAGED2c.1324T>G (p.Phe442Val)
c.1270T>G (p.Phe424Val)
c.1069T>G (p.Phe357Val)
Xg.54814714T>ACA413274083MAGED2c.1325T>A (p.Phe442Tyr)
c.1271T>A (p.Phe424Tyr)
c.1070T>A (p.Phe357Tyr)
Xg.54814714T>CCA413274085MAGED2c.1325T>C (p.Phe442Ser)
c.1271T>C (p.Phe424Ser)
c.1070T>C (p.Phe357Ser)
Xg.54814714T>GCA413274087MAGED2c.1325T>G (p.Phe442Cys)
c.1271T>G (p.Phe424Cys)
c.1070T>G (p.Phe357Cys)
Xg.54814715C>ACA413274089MAGED2c.1326C>A (p.Phe442Leu)
c.1272C>A (p.Phe424Leu)
c.1071C>A (p.Phe357Leu)
Xg.54814715C>GCA413274091MAGED2c.1326C>G (p.Phe442Leu)
c.1272C>G (p.Phe424Leu)
c.1071C>G (p.Phe357Leu)
Xg.54814715C>TCA516582499MAGED2c.1326C>T (p.Phe442=)
c.1272C>T (p.Phe424=)
c.1071C>T (p.Phe357=)
Xg.54814716T>ACA413274093MAGED2c.1327T>A (p.Trp443Arg)
c.1273T>A (p.Trp425Arg)
c.1072T>A (p.Trp358Arg)
Xg.54814716T>CCA413274094MAGED2c.1327T>C (p.Trp443Arg)
c.1273T>C (p.Trp425Arg)
c.1072T>C (p.Trp358Arg)
Xg.54814716T>GCA413274096MAGED2c.1327T>G (p.Trp443Gly)
c.1273T>G (p.Trp425Gly)
c.1072T>G (p.Trp358Gly)
Xg.54814717G>ACA413274100MAGED2c.1328G>A (p.Trp443Ter)
c.1274G>A (p.Trp425Ter)
c.1073G>A (p.Trp358Ter)
 dbSNP gnomAD v2 gnomAD v4
Xg.54814717G>CCA413274101MAGED2c.1328G>C (p.Trp443Ser)
c.1274G>C (p.Trp425Ser)
c.1073G>C (p.Trp358Ser)
Xg.54814717G=CA2430312969MAGED2c.1328G= (p.Trp443=)
c.1274G= (p.Trp425=)
c.1073G= (p.Trp358=)
Xg.54814717G>TCA413274099MAGED2c.1328G>T (p.Trp443Leu)
c.1274G>T (p.Trp425Leu)
c.1073G>T (p.Trp358Leu)
Xg.54814718G>ACA413274104MAGED2c.1329G>A (p.Trp443Ter)
c.1275G>A (p.Trp425Ter)
c.1074G>A (p.Trp358Ter)
Xg.54814718G>CCA413274106MAGED2c.1329G>C (p.Trp443Cys)
c.1275G>C (p.Trp425Cys)
c.1074G>C (p.Trp358Cys)
Xg.54814718G>TCA413274107MAGED2c.1329G>T (p.Trp443Cys)
c.1275G>T (p.Trp425Cys)
c.1074G>T (p.Trp358Cys)
Xg.54814719G>ACA413274109MAGED2c.1330G>A (p.Gly444Ser)
c.1276G>A (p.Gly426Ser)
c.1075G>A (p.Gly359Ser)
Xg.54814719G>CCA413274114MAGED2c.1330G>C (p.Gly444Arg)
c.1276G>C (p.Gly426Arg)
c.1075G>C (p.Gly359Arg)
Xg.54814719G>TCA413274116MAGED2c.1330G>T (p.Gly444Cys)
c.1276G>T (p.Gly426Cys)
c.1075G>T (p.Gly359Cys)
Xg.54814720G>ACA413274118MAGED2c.1331G>A (p.Gly444Asp)
c.1277G>A (p.Gly426Asp)
c.1076G>A (p.Gly359Asp)
Xg.54814720G>CCA413274120MAGED2c.1331G>C (p.Gly444Ala)
c.1277G>C (p.Gly426Ala)
c.1076G>C (p.Gly359Ala)
Xg.54814720G>TCA413274122MAGED2c.1331G>T (p.Gly444Val)
c.1277G>T (p.Gly426Val)
c.1076G>T (p.Gly359Val)
Xg.54814721C>ACA516582503MAGED2c.1332C>A (p.Gly444=)
c.1278C>A (p.Gly426=)
c.1077C>A (p.Gly359=)
Xg.54814721C>GCA516582504MAGED2c.1332C>G (p.Gly444=)
c.1278C>G (p.Gly426=)
c.1077C>G (p.Gly359=)
Xg.54814721C>TCA516582505MAGED2c.1332C>T (p.Gly444=)
c.1278C>T (p.Gly426=)
c.1077C>T (p.Gly359=)
Xg.54814722C>ACA413274123MAGED2c.1333C>A (p.Leu445Met)
c.1279C>A (p.Leu427Met)
c.1078C>A (p.Leu360Met)
Xg.54814722C>GCA413274125MAGED2c.1333C>G (p.Leu445Val)
c.1279C>G (p.Leu427Val)
c.1078C>G (p.Leu360Val)
Xg.54814722C>TCA516582507MAGED2c.1333C>T (p.Leu445=)
c.1279C>T (p.Leu427=)
c.1078C>T (p.Leu360=)
Xg.54814723T>ACA413274131MAGED2c.1334T>A (p.Leu445Gln)
c.1280T>A (p.Leu427Gln)
c.1079T>A (p.Leu360Gln)
Xg.54814723T>CCA413274129MAGED2c.1334T>C (p.Leu445Pro)
c.1280T>C (p.Leu427Pro)
c.1079T>C (p.Leu360Pro)
Xg.54814723T>GCA413274127MAGED2c.1334T>G (p.Leu445Arg)
c.1280T>G (p.Leu427Arg)
c.1079T>G (p.Leu360Arg)
Xg.54814724G>ACA516582509MAGED2c.1335G>A (p.Leu445=)
c.1281G>A (p.Leu427=)
c.1080G>A (p.Leu360=)
Xg.54814724G>CCA516582510MAGED2c.1335G>C (p.Leu445=)
c.1281G>C (p.Leu427=)
c.1080G>C (p.Leu360=)
Xg.54814724G>TCA516582512MAGED2c.1335G>T (p.Leu445=)
c.1281G>T (p.Leu427=)
c.1080G>T (p.Leu360=)
Xg.54814725C>ACA413274132MAGED2c.1336C>A (p.Arg446Ser)
c.1282C>A (p.Arg428Ser)
c.1081C>A (p.Arg361Ser)
Xg.54814725C=CA2430312970MAGED2c.1336C= (p.Arg446=)
c.1282C= (p.Arg428=)
c.1081C= (p.Arg361=)
Xg.54814725C>GCA413274134MAGED2c.1336C>G (p.Arg446Gly)
c.1282C>G (p.Arg428Gly)
c.1081C>G (p.Arg361Gly)
Xg.54814725C>TCA10576212MAGED2c.1336C>T (p.Arg446Cys)
c.1282C>T (p.Arg428Cys)
c.1081C>T (p.Arg361Cys)
 ClinVar dbSNP gnomAD v4
Xg.54814726G>ACA413274137MAGED2c.1337G>A (p.Arg446His)
c.1283G>A (p.Arg428His)
c.1082G>A (p.Arg361His)
 gnomAD v4
Xg.54814726G>CCA413274138MAGED2c.1337G>C (p.Arg446Pro)
c.1283G>C (p.Arg428Pro)
c.1082G>C (p.Arg361Pro)
Xg.54814726G>TCA413274140MAGED2c.1337G>T (p.Arg446Leu)
c.1283G>T (p.Arg428Leu)
c.1082G>T (p.Arg361Leu)
Xg.54814727C>ACA516582516MAGED2c.1338C>A (p.Arg446=)
c.1284C>A (p.Arg428=)
c.1083C>A (p.Arg361=)
Xg.54814727C=CA2430312971MAGED2c.1338C= (p.Arg446=)
c.1284C= (p.Arg428=)
c.1083C= (p.Arg361=)
Xg.54814727C>GCA516582517MAGED2c.1338C>G (p.Arg446=)
c.1284C>G (p.Arg428=)
c.1083C>G (p.Arg361=)
Xg.54814727C>TCA516582518MAGED2c.1338C>T (p.Arg446=)
c.1284C>T (p.Arg428=)
c.1083C>T (p.Arg361=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814728T>ACA413274142MAGED2c.1339T>A (p.Ser447Thr)
c.1285T>A (p.Ser429Thr)
c.1084T>A (p.Ser362Thr)
Xg.54814728T>CCA413274144MAGED2c.1339T>C (p.Ser447Pro)
c.1285T>C (p.Ser429Pro)
c.1084T>C (p.Ser362Pro)
Xg.54814728T>GCA413274146MAGED2c.1339T>G (p.Ser447Ala)
c.1285T>G (p.Ser429Ala)
c.1084T>G (p.Ser362Ala)
Xg.54814729C>ACA413274148MAGED2c.1340C>A (p.Ser447Tyr)
c.1286C>A (p.Ser429Tyr)
c.1085C>A (p.Ser362Tyr)
Xg.54814729C>GCA413274150MAGED2c.1340C>G (p.Ser447Cys)
c.1286C>G (p.Ser429Cys)
c.1085C>G (p.Ser362Cys)
Xg.54814729C>TCA413274151MAGED2c.1340C>T (p.Ser447Phe)
c.1286C>T (p.Ser429Phe)
c.1085C>T (p.Ser362Phe)
 gnomAD v4
Xg.54814730T>ACA516582524MAGED2c.1341T>A (p.Ser447=)
c.1287T>A (p.Ser429=)
c.1086T>A (p.Ser362=)
Xg.54814730T>CCA516582523MAGED2c.1341T>C (p.Ser447=)
c.1287T>C (p.Ser429=)
c.1086T>C (p.Ser362=)
Xg.54814730T>GCA516582522MAGED2c.1341T>G (p.Ser447=)
c.1287T>G (p.Ser429=)
c.1086T>G (p.Ser362=)
Xg.54814731T>ACA413274157MAGED2c.1342T>A (p.Tyr448Asn)
c.1288T>A (p.Tyr430Asn)
c.1087T>A (p.Tyr363Asn)
Xg.54814731T>CCA413274156MAGED2c.1342T>C (p.Tyr448His)
c.1288T>C (p.Tyr430His)
c.1087T>C (p.Tyr363His)
Xg.54814731T>GCA413274154MAGED2c.1342T>G (p.Tyr448Asp)
c.1288T>G (p.Tyr430Asp)
c.1087T>G (p.Tyr363Asp)
Xg.54814732A=CA2430312972MAGED2c.1343A= (p.Tyr448=)
c.1289A= (p.Tyr430=)
c.1088A= (p.Tyr363=)
Xg.54814732A>CCA413274159MAGED2c.1343A>C (p.Tyr448Ser)
c.1289A>C (p.Tyr430Ser)
c.1088A>C (p.Tyr363Ser)
 dbSNP gnomAD v2 gnomAD v4
Xg.54814732A>GCA413274161MAGED2c.1343A>G (p.Tyr448Cys)
c.1289A>G (p.Tyr430Cys)
c.1088A>G (p.Tyr363Cys)
Xg.54814732A>TCA413274160MAGED2c.1343A>T (p.Tyr448Phe)
c.1289A>T (p.Tyr430Phe)
c.1088A>T (p.Tyr363Phe)
Xg.54814733C>ACA413274162MAGED2c.1344C>A (p.Tyr448Ter)
c.1290C>A (p.Tyr430Ter)
c.1089C>A (p.Tyr363Ter)
 COSMIC
Xg.54814733C>GCA413274164MAGED2c.1344C>G (p.Tyr448Ter)
c.1290C>G (p.Tyr430Ter)
c.1089C>G (p.Tyr363Ter)
Xg.54814733C>TCA516582529MAGED2c.1344C>T (p.Tyr448=)
c.1290C>T (p.Tyr430=)
c.1089C>T (p.Tyr363=)
Xg.54814734T>ACA413274167MAGED2c.1345T>A (p.Tyr449Asn)
c.1291T>A (p.Tyr431Asn)
c.1090T>A (p.Tyr364Asn)
Xg.54814734T>CCA413274168MAGED2c.1345T>C (p.Tyr449His)
c.1291T>C (p.Tyr431His)
c.1090T>C (p.Tyr364His)
Xg.54814734T>GCA413274170MAGED2c.1345T>G (p.Tyr449Asp)
c.1291T>G (p.Tyr431Asp)
c.1090T>G (p.Tyr364Asp)
Xg.54814735A=CA2430312973MAGED2c.1346A= (p.Tyr449=)
c.1292A= (p.Tyr431=)
c.1091A= (p.Tyr364=)
Xg.54814735A>CCA413274172MAGED2c.1346A>C (p.Tyr449Ser)
c.1292A>C (p.Tyr431Ser)
c.1091A>C (p.Tyr364Ser)
Xg.54814735A>GCA10426877MAGED2c.1346A>G (p.Tyr449Cys)
c.1292A>G (p.Tyr431Cys)
c.1091A>G (p.Tyr364Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.54814735A>TCA413274174MAGED2c.1346A>T (p.Tyr449Phe)
c.1292A>T (p.Tyr431Phe)
c.1091A>T (p.Tyr364Phe)
Xg.54814736T>ACA413274176MAGED2c.1347T>A (p.Tyr449Ter)
c.1293T>A (p.Tyr431Ter)
c.1092T>A (p.Tyr364Ter)
Xg.54814736T>CCA516582533MAGED2c.1347T>C (p.Tyr449=)
c.1293T>C (p.Tyr431=)
c.1092T>C (p.Tyr364=)
Xg.54814736T>GCA413274178MAGED2c.1347T>G (p.Tyr449Ter)
c.1293T>G (p.Tyr431Ter)
c.1092T>G (p.Tyr364Ter)

Number of alleles fetched