Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.49253165_49253173delCA2514943595FOXP3c.892_900del (p.Phe298_Asn300del)
c.997_1005del (p.Phe333_Asn335del)
c.1066_1074del (p.Phe356_Asn358del)
c.916_924del (p.Phe306_Asn308del)
c.967+744_967+752del (n.967+744_967+752del)
c.847_855del (p.Phe283_Asn285del)
c.1216_1224del (p.Phe406_Asn408del)
c.1015_1023del (p.Phe339_Asn341del)
c.1252_1260del (p.Phe418_Asn420del)
c.943_951del (p.Phe315_Asn317del)
Xg.49253171delCA2579609006FOXP3c.895del (p.His299ThrfsTer?)
c.1000del (p.His334ThrfsTer?)
c.1069del (p.His357ThrfsTer?)
c.919del (p.His307ThrfsTer?)
c.967+747del (n.967+747del)
c.850del (p.His284ThrfsTer?)
c.1219del (p.His407ThrfsTer?)
c.1018del (p.His340ThrfsTer?)
c.1255del (p.His419ThrfsTer?)
c.946del (p.His316ThrfsTer?)
Xg.49253171G>ACA516395817FOXP3c.894C>T (p.Phe298=)
c.999C>T (p.Phe333=)
c.1068C>T (p.Phe356=)
c.918C>T (p.Phe306=)
c.967+746C>T (n.967+746C>T)
c.849C>T (p.Phe283=)
c.1218C>T (p.Phe406=)
c.1017C>T (p.Phe339=)
c.1254C>T (p.Phe418=)
c.945C>T (p.Phe315=)
Xg.49253171G>CCA412950266FOXP3c.894C>G (p.Phe298Leu)
c.999C>G (p.Phe333Leu)
c.1068C>G (p.Phe356Leu)
c.918C>G (p.Phe306Leu)
c.967+746C>G (n.967+746C>G)
c.849C>G (p.Phe283Leu)
c.1218C>G (p.Phe406Leu)
c.1017C>G (p.Phe339Leu)
c.1254C>G (p.Phe418Leu)
c.945C>G (p.Phe315Leu)
Xg.49253171G>TCA412950268FOXP3c.894C>A (p.Phe298Leu)
c.999C>A (p.Phe333Leu)
c.1068C>A (p.Phe356Leu)
c.918C>A (p.Phe306Leu)
c.967+746C>A (n.967+746C>A)
c.849C>A (p.Phe283Leu)
c.1218C>A (p.Phe406Leu)
c.1017C>A (p.Phe339Leu)
c.1254C>A (p.Phe418Leu)
c.945C>A (p.Phe315Leu)
Xg.49253172A>CCA412950270FOXP3c.893T>G (p.Phe298Cys)
c.998T>G (p.Phe333Cys)
c.1067T>G (p.Phe356Cys)
c.917T>G (p.Phe306Cys)
c.967+745T>G (n.967+745T>G)
c.848T>G (p.Phe283Cys)
c.1217T>G (p.Phe406Cys)
c.1016T>G (p.Phe339Cys)
c.1253T>G (p.Phe418Cys)
c.944T>G (p.Phe315Cys)
Xg.49253172A>GCA412950272FOXP3c.893T>C (p.Phe298Ser)
c.998T>C (p.Phe333Ser)
c.1067T>C (p.Phe356Ser)
c.917T>C (p.Phe306Ser)
c.967+745T>C (n.967+745T>C)
c.848T>C (p.Phe283Ser)
c.1217T>C (p.Phe406Ser)
c.1016T>C (p.Phe339Ser)
c.1253T>C (p.Phe418Ser)
c.944T>C (p.Phe315Ser)
Xg.49253172A>TCA412950274FOXP3c.893T>A (p.Phe298Tyr)
c.998T>A (p.Phe333Tyr)
c.1067T>A (p.Phe356Tyr)
c.917T>A (p.Phe306Tyr)
c.967+745T>A (n.967+745T>A)
c.848T>A (p.Phe283Tyr)
c.1217T>A (p.Phe406Tyr)
c.1016T>A (p.Phe339Tyr)
c.1253T>A (p.Phe418Tyr)
c.944T>A (p.Phe315Tyr)
 ClinVar dbSNP gnomAD v4
Xg.49253173A>CCA412950276FOXP3c.892T>G (p.Phe298Val)
c.997T>G (p.Phe333Val)
c.1066T>G (p.Phe356Val)
c.916T>G (p.Phe306Val)
c.967+744T>G (n.967+744T>G)
c.847T>G (p.Phe283Val)
c.1216T>G (p.Phe406Val)
c.1015T>G (p.Phe339Val)
c.1252T>G (p.Phe418Val)
c.943T>G (p.Phe315Val)
Xg.49253173A>GCA412950278FOXP3c.892T>C (p.Phe298Leu)
c.997T>C (p.Phe333Leu)
c.1066T>C (p.Phe356Leu)
c.916T>C (p.Phe306Leu)
c.967+744T>C (n.967+744T>C)
c.847T>C (p.Phe283Leu)
c.1216T>C (p.Phe406Leu)
c.1015T>C (p.Phe339Leu)
c.1252T>C (p.Phe418Leu)
c.943T>C (p.Phe315Leu)
Xg.49253173A>TCA412950280FOXP3c.892T>A (p.Phe298Ile)
c.997T>A (p.Phe333Ile)
c.1066T>A (p.Phe356Ile)
c.916T>A (p.Phe306Ile)
c.967+744T>A (n.967+744T>A)
c.847T>A (p.Phe283Ile)
c.1216T>A (p.Phe406Ile)
c.1015T>A (p.Phe339Ile)
c.1252T>A (p.Phe418Ile)
c.943T>A (p.Phe315Ile)
Xg.49253174C>ACA412950284FOXP3c.891G>T (p.Lys297Asn)
c.996G>T (p.Lys332Asn)
c.1065G>T (p.Lys355Asn)
c.915G>T (p.Lys305Asn)
c.967+743G>T (n.967+743G>T)
c.846G>T (p.Lys282Asn)
c.1215G>T (p.Lys405Asn)
c.1014G>T (p.Lys338Asn)
c.1251G>T (p.Lys417Asn)
c.942G>T (p.Lys314Asn)
Xg.49253174C>GCA412950282FOXP3c.891G>C (p.Lys297Asn)
c.996G>C (p.Lys332Asn)
c.1065G>C (p.Lys355Asn)
c.915G>C (p.Lys305Asn)
c.967+743G>C (n.967+743G>C)
c.846G>C (p.Lys282Asn)
c.1215G>C (p.Lys405Asn)
c.1014G>C (p.Lys338Asn)
c.1251G>C (p.Lys417Asn)
c.942G>C (p.Lys314Asn)
Xg.49253174C>TCA516395827FOXP3c.891G>A (p.Lys297=)
c.996G>A (p.Lys332=)
c.1065G>A (p.Lys355=)
c.915G>A (p.Lys305=)
c.967+743G>A (n.967+743G>A)
c.846G>A (p.Lys282=)
c.1215G>A (p.Lys405=)
c.1014G>A (p.Lys338=)
c.1251G>A (p.Lys417=)
c.942G>A (p.Lys314=)
Xg.49253174_49253175insACA2515603302FOXP3c.890_891insT (p.Lys297AsnfsTer31)
c.995_996insT (p.Lys332AsnfsTer31)
c.1064_1065insT (p.Lys355AsnfsTer31)
c.914_915insT (p.Lys305AsnfsTer31)
c.967+742_967+743insT (n.967+742_967+743insT)
c.845_846insT (p.Lys282AsnfsTer31)
c.1214_1215insT (p.Lys405AsnfsTer31)
c.1013_1014insT (p.Lys338AsnfsTer31)
c.1250_1251insT (p.Lys417AsnfsTer31)
c.941_942insT (p.Lys314AsnfsTer31)
Xg.49253175T>ACA412950286FOXP3c.890A>T (p.Lys297Met)
c.995A>T (p.Lys332Met)
c.1064A>T (p.Lys355Met)
c.914A>T (p.Lys305Met)
c.967+742A>T (n.967+742A>T)
c.845A>T (p.Lys282Met)
c.1214A>T (p.Lys405Met)
c.1013A>T (p.Lys338Met)
c.1250A>T (p.Lys417Met)
c.941A>T (p.Lys314Met)
Xg.49253175T>CCA10411687FOXP3c.890A>G (p.Lys297Arg)
c.995A>G (p.Lys332Arg)
c.1064A>G (p.Lys355Arg)
c.914A>G (p.Lys305Arg)
c.967+742A>G (n.967+742A>G)
c.845A>G (p.Lys282Arg)
c.1214A>G (p.Lys405Arg)
c.1013A>G (p.Lys338Arg)
c.1250A>G (p.Lys417Arg)
c.941A>G (p.Lys314Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.49253175T>GCA412950288FOXP3c.890A>C (p.Lys297Thr)
c.995A>C (p.Lys332Thr)
c.1064A>C (p.Lys355Thr)
c.914A>C (p.Lys305Thr)
c.967+742A>C (n.967+742A>C)
c.845A>C (p.Lys282Thr)
c.1214A>C (p.Lys405Thr)
c.1013A>C (p.Lys338Thr)
c.1250A>C (p.Lys417Thr)
c.941A>C (p.Lys314Thr)
Xg.49253175T=CA2428551810FOXP3c.890A= (p.Lys297=)
c.995A= (p.Lys332=)
c.1064A= (p.Lys355=)
c.914A= (p.Lys305=)
c.967+742A= (n.967+742A=)
c.845A= (p.Lys282=)
c.1214A= (p.Lys405=)
c.1013A= (p.Lys338=)
c.1250A= (p.Lys417=)
c.941A= (p.Lys314=)
Xg.49253176T>ACA412950291FOXP3c.889A>T (p.Lys297Ter)
c.994A>T (p.Lys332Ter)
c.1063A>T (p.Lys355Ter)
c.913A>T (p.Lys305Ter)
c.967+741A>T (n.967+741A>T)
c.844A>T (p.Lys282Ter)
c.1213A>T (p.Lys405Ter)
c.1012A>T (p.Lys338Ter)
c.1249A>T (p.Lys417Ter)
c.940A>T (p.Lys314Ter)
Xg.49253176T>CCA412950293FOXP3c.889A>G (p.Lys297Glu)
c.994A>G (p.Lys332Glu)
c.1063A>G (p.Lys355Glu)
c.913A>G (p.Lys305Glu)
c.967+741A>G (n.967+741A>G)
c.844A>G (p.Lys282Glu)
c.1213A>G (p.Lys405Glu)
c.1012A>G (p.Lys338Glu)
c.1249A>G (p.Lys417Glu)
c.940A>G (p.Lys314Glu)
Xg.49253176T>GCA412950294FOXP3c.889A>C (p.Lys297Gln)
c.994A>C (p.Lys332Gln)
c.1063A>C (p.Lys355Gln)
c.913A>C (p.Lys305Gln)
c.967+741A>C (n.967+741A>C)
c.844A>C (p.Lys282Gln)
c.1213A>C (p.Lys405Gln)
c.1012A>C (p.Lys338Gln)
c.1249A>C (p.Lys417Gln)
c.940A>C (p.Lys314Gln)
Xg.49253176_49253177insAAAAAACA2510287106FOXP3c.888_889insTTTTTT (p.Phe296_Lys297insPhePhe)
c.993_994insTTTTTT (p.Phe331_Lys332insPhePhe)
c.1062_1063insTTTTTT (p.Phe354_Lys355insPhePhe)
c.912_913insTTTTTT (p.Phe304_Lys305insPhePhe)
c.967+740_967+741insTTTTTT (n.967+740_967+741insTTTTTT)
c.843_844insTTTTTT (p.Phe281_Lys282insPhePhe)
c.1212_1213insTTTTTT (p.Phe404_Lys405insPhePhe)
c.1011_1012insTTTTTT (p.Phe337_Lys338insPhePhe)
c.1248_1249insTTTTTT (p.Phe416_Lys417insPhePhe)
c.939_940insTTTTTT (p.Phe313_Lys314insPhePhe)
Xg.49253177delCA2579609007FOXP3c.888del (p.Phe296LeufsTer?)
c.993del (p.Phe331LeufsTer?)
c.1062del (p.Phe354LeufsTer?)
c.912del (p.Phe304LeufsTer?)
c.967+740del (n.967+740del)
c.843del (p.Phe281LeufsTer?)
c.1212del (p.Phe404LeufsTer?)
c.1011del (p.Phe337LeufsTer?)
c.1248del (p.Phe416LeufsTer?)
c.939del (p.Phe313LeufsTer?)
Xg.49253177G>ACA516395837FOXP3c.888C>T (p.Phe296=)
c.993C>T (p.Phe331=)
c.1062C>T (p.Phe354=)
c.912C>T (p.Phe304=)
c.967+740C>T (n.967+740C>T)
c.843C>T (p.Phe281=)
c.1212C>T (p.Phe404=)
c.1011C>T (p.Phe337=)
c.1248C>T (p.Phe416=)
c.939C>T (p.Phe313=)
Xg.49253177G>CCA412950296FOXP3c.888C>G (p.Phe296Leu)
c.993C>G (p.Phe331Leu)
c.1062C>G (p.Phe354Leu)
c.912C>G (p.Phe304Leu)
c.967+740C>G (n.967+740C>G)
c.843C>G (p.Phe281Leu)
c.1212C>G (p.Phe404Leu)
c.1011C>G (p.Phe337Leu)
c.1248C>G (p.Phe416Leu)
c.939C>G (p.Phe313Leu)
Xg.49253177G>TCA412950298FOXP3c.888C>A (p.Phe296Leu)
c.993C>A (p.Phe331Leu)
c.1062C>A (p.Phe354Leu)
c.912C>A (p.Phe304Leu)
c.967+740C>A (n.967+740C>A)
c.843C>A (p.Phe281Leu)
c.1212C>A (p.Phe404Leu)
c.1011C>A (p.Phe337Leu)
c.1248C>A (p.Phe416Leu)
c.939C>A (p.Phe313Leu)
Xg.49253178A>CCA412950300FOXP3c.887T>G (p.Phe296Cys)
c.992T>G (p.Phe331Cys)
c.1061T>G (p.Phe354Cys)
c.911T>G (p.Phe304Cys)
c.967+739T>G (n.967+739T>G)
c.842T>G (p.Phe281Cys)
c.1211T>G (p.Phe404Cys)
c.1010T>G (p.Phe337Cys)
c.1247T>G (p.Phe416Cys)
c.938T>G (p.Phe313Cys)
Xg.49253178A>GCA412950302FOXP3c.887T>C (p.Phe296Ser)
c.992T>C (p.Phe331Ser)
c.1061T>C (p.Phe354Ser)
c.911T>C (p.Phe304Ser)
c.967+739T>C (n.967+739T>C)
c.842T>C (p.Phe281Ser)
c.1211T>C (p.Phe404Ser)
c.1010T>C (p.Phe337Ser)
c.1247T>C (p.Phe416Ser)
c.938T>C (p.Phe313Ser)
 ClinVar
Xg.49253178A>TCA412950304FOXP3c.887T>A (p.Phe296Tyr)
c.992T>A (p.Phe331Tyr)
c.1061T>A (p.Phe354Tyr)
c.911T>A (p.Phe304Tyr)
c.967+739T>A (n.967+739T>A)
c.842T>A (p.Phe281Tyr)
c.1211T>A (p.Phe404Tyr)
c.1010T>A (p.Phe337Tyr)
c.1247T>A (p.Phe416Tyr)
c.938T>A (p.Phe313Tyr)
Xg.49253179A>CCA412950306FOXP3c.886T>G (p.Phe296Val)
c.991T>G (p.Phe331Val)
c.1060T>G (p.Phe354Val)
c.910T>G (p.Phe304Val)
c.967+738T>G (n.967+738T>G)
c.841T>G (p.Phe281Val)
c.1210T>G (p.Phe404Val)
c.1009T>G (p.Phe337Val)
c.1246T>G (p.Phe416Val)
c.937T>G (p.Phe313Val)
Xg.49253179A>GCA412950308FOXP3c.886T>C (p.Phe296Leu)
c.991T>C (p.Phe331Leu)
c.1060T>C (p.Phe354Leu)
c.910T>C (p.Phe304Leu)
c.967+738T>C (n.967+738T>C)
c.841T>C (p.Phe281Leu)
c.1210T>C (p.Phe404Leu)
c.1009T>C (p.Phe337Leu)
c.1246T>C (p.Phe416Leu)
c.937T>C (p.Phe313Leu)
Xg.49253179A>TCA412950309FOXP3c.886T>A (p.Phe296Ile)
c.991T>A (p.Phe331Ile)
c.1060T>A (p.Phe354Ile)
c.910T>A (p.Phe304Ile)
c.967+738T>A (n.967+738T>A)
c.841T>A (p.Phe281Ile)
c.1210T>A (p.Phe404Ile)
c.1009T>A (p.Phe337Ile)
c.1246T>A (p.Phe416Ile)
c.937T>A (p.Phe313Ile)
Xg.49253180G>ACA516395842FOXP3c.885C>T (p.Tyr295=)
c.990C>T (p.Tyr330=)
c.1059C>T (p.Tyr353=)
c.909C>T (p.Tyr303=)
c.967+737C>T (n.967+737C>T)
c.840C>T (p.Tyr280=)
c.1209C>T (p.Tyr403=)
c.1008C>T (p.Tyr336=)
c.1245C>T (p.Tyr415=)
c.936C>T (p.Tyr312=)
Xg.49253180G>CCA412950313FOXP3c.885C>G (p.Tyr295Ter)
c.990C>G (p.Tyr330Ter)
c.1059C>G (p.Tyr353Ter)
c.909C>G (p.Tyr303Ter)
c.967+737C>G (n.967+737C>G)
c.840C>G (p.Tyr280Ter)
c.1209C>G (p.Tyr403Ter)
c.1008C>G (p.Tyr336Ter)
c.1245C>G (p.Tyr415Ter)
c.936C>G (p.Tyr312Ter)
Xg.49253180G>TCA412950311FOXP3c.885C>A (p.Tyr295Ter)
c.990C>A (p.Tyr330Ter)
c.1059C>A (p.Tyr353Ter)
c.909C>A (p.Tyr303Ter)
c.967+737C>A (n.967+737C>A)
c.840C>A (p.Tyr280Ter)
c.1209C>A (p.Tyr403Ter)
c.1008C>A (p.Tyr336Ter)
c.1245C>A (p.Tyr415Ter)
c.936C>A (p.Tyr312Ter)
Xg.49253181T>ACA412950316FOXP3c.884A>T (p.Tyr295Phe)
c.989A>T (p.Tyr330Phe)
c.1058A>T (p.Tyr353Phe)
c.908A>T (p.Tyr303Phe)
c.967+736A>T (n.967+736A>T)
c.839A>T (p.Tyr280Phe)
c.1208A>T (p.Tyr403Phe)
c.1007A>T (p.Tyr336Phe)
c.1244A>T (p.Tyr415Phe)
c.935A>T (p.Tyr312Phe)
Xg.49253181T>CCA412950319FOXP3c.884A>G (p.Tyr295Cys)
c.989A>G (p.Tyr330Cys)
c.1058A>G (p.Tyr353Cys)
c.908A>G (p.Tyr303Cys)
c.967+736A>G (n.967+736A>G)
c.839A>G (p.Tyr280Cys)
c.1208A>G (p.Tyr403Cys)
c.1007A>G (p.Tyr336Cys)
c.1244A>G (p.Tyr415Cys)
c.935A>G (p.Tyr312Cys)
Xg.49253181T>GCA412950317FOXP3c.884A>C (p.Tyr295Ser)
c.989A>C (p.Tyr330Ser)
c.1058A>C (p.Tyr353Ser)
c.908A>C (p.Tyr303Ser)
c.967+736A>C (n.967+736A>C)
c.839A>C (p.Tyr280Ser)
c.1208A>C (p.Tyr403Ser)
c.1007A>C (p.Tyr336Ser)
c.1244A>C (p.Tyr415Ser)
c.935A>C (p.Tyr312Ser)
Xg.49253182A>CCA412950321FOXP3c.883T>G (p.Tyr295Asp)
c.988T>G (p.Tyr330Asp)
c.1057T>G (p.Tyr353Asp)
c.907T>G (p.Tyr303Asp)
c.967+735T>G (n.967+735T>G)
c.838T>G (p.Tyr280Asp)
c.1207T>G (p.Tyr403Asp)
c.1006T>G (p.Tyr336Asp)
c.1243T>G (p.Tyr415Asp)
c.934T>G (p.Tyr312Asp)
Xg.49253182A>GCA412950323FOXP3c.883T>C (p.Tyr295His)
c.988T>C (p.Tyr330His)
c.1057T>C (p.Tyr353His)
c.907T>C (p.Tyr303His)
c.967+735T>C (n.967+735T>C)
c.838T>C (p.Tyr280His)
c.1207T>C (p.Tyr403His)
c.1006T>C (p.Tyr336His)
c.1243T>C (p.Tyr415His)
c.934T>C (p.Tyr312His)
Xg.49253182A>TCA412950325FOXP3c.883T>A (p.Tyr295Asn)
c.988T>A (p.Tyr330Asn)
c.1057T>A (p.Tyr353Asn)
c.907T>A (p.Tyr303Asn)
c.967+735T>A (n.967+735T>A)
c.838T>A (p.Tyr280Asn)
c.1207T>A (p.Tyr403Asn)
c.1006T>A (p.Tyr336Asn)
c.1243T>A (p.Tyr415Asn)
c.934T>A (p.Tyr312Asn)
Xg.49253183G>ACA516395849FOXP3c.882C>T (p.Asp294=)
c.987C>T (p.Asp329=)
c.1056C>T (p.Asp352=)
c.906C>T (p.Asp302=)
c.967+734C>T (n.967+734C>T)
c.837C>T (p.Asp279=)
c.1206C>T (p.Asp402=)
c.1005C>T (p.Asp335=)
c.1242C>T (p.Asp414=)
c.933C>T (p.Asp311=)
Xg.49253183G>CCA412950327FOXP3c.882C>G (p.Asp294Glu)
c.987C>G (p.Asp329Glu)
c.1056C>G (p.Asp352Glu)
c.906C>G (p.Asp302Glu)
c.967+734C>G (n.967+734C>G)
c.837C>G (p.Asp279Glu)
c.1206C>G (p.Asp402Glu)
c.1005C>G (p.Asp335Glu)
c.1242C>G (p.Asp414Glu)
c.933C>G (p.Asp311Glu)
Xg.49253183G>TCA412950329FOXP3c.882C>A (p.Asp294Glu)
c.987C>A (p.Asp329Glu)
c.1056C>A (p.Asp352Glu)
c.906C>A (p.Asp302Glu)
c.967+734C>A (n.967+734C>A)
c.837C>A (p.Asp279Glu)
c.1206C>A (p.Asp402Glu)
c.1005C>A (p.Asp335Glu)
c.1242C>A (p.Asp414Glu)
c.933C>A (p.Asp311Glu)
Xg.49253184T>ACA412950334FOXP3c.881A>T (p.Asp294Val)
c.986A>T (p.Asp329Val)
c.1055A>T (p.Asp352Val)
c.905A>T (p.Asp302Val)
c.967+733A>T (n.967+733A>T)
c.836A>T (p.Asp279Val)
c.1205A>T (p.Asp402Val)
c.1004A>T (p.Asp335Val)
c.1241A>T (p.Asp414Val)
c.932A>T (p.Asp311Val)
Xg.49253184T>CCA412950333FOXP3c.881A>G (p.Asp294Gly)
c.986A>G (p.Asp329Gly)
c.1055A>G (p.Asp352Gly)
c.905A>G (p.Asp302Gly)
c.967+733A>G (n.967+733A>G)
c.836A>G (p.Asp279Gly)
c.1205A>G (p.Asp402Gly)
c.1004A>G (p.Asp335Gly)
c.1241A>G (p.Asp414Gly)
c.932A>G (p.Asp311Gly)
Xg.49253184T>GCA412950331FOXP3c.881A>C (p.Asp294Ala)
c.986A>C (p.Asp329Ala)
c.1055A>C (p.Asp352Ala)
c.905A>C (p.Asp302Ala)
c.967+733A>C (n.967+733A>C)
c.836A>C (p.Asp279Ala)
c.1205A>C (p.Asp402Ala)
c.1004A>C (p.Asp335Ala)
c.1241A>C (p.Asp414Ala)
c.932A>C (p.Asp311Ala)
Xg.49253185C>ACA412950336FOXP3c.880G>T (p.Asp294Tyr)
c.985G>T (p.Asp329Tyr)
c.1054G>T (p.Asp352Tyr)
c.904G>T (p.Asp302Tyr)
c.967+732G>T (n.967+732G>T)
c.835G>T (p.Asp279Tyr)
c.1204G>T (p.Asp402Tyr)
c.1003G>T (p.Asp335Tyr)
c.1240G>T (p.Asp414Tyr)
c.931G>T (p.Asp311Tyr)
Xg.49253185C>GCA412950338FOXP3c.880G>C (p.Asp294His)
c.985G>C (p.Asp329His)
c.1054G>C (p.Asp352His)
c.904G>C (p.Asp302His)
c.967+732G>C (n.967+732G>C)
c.835G>C (p.Asp279His)
c.1204G>C (p.Asp402His)
c.1003G>C (p.Asp335His)
c.1240G>C (p.Asp414His)
c.931G>C (p.Asp311His)

Number of alleles fetched