Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.8073781_8073947delCA645553620GATA3c.1090_1256del (p.Arg364HisfsTer?)
c.1093_1259del (p.Arg365HisfsTer?)
n.612_778del
 COSMIC
10g.8073840G>ACA468400792GATA3c.1149G>A (p.Glu383=)
c.1152G>A (p.Glu384=)
n.671G>A
 dbSNP
10g.8073840G>CCA375975644GATA3c.1149G>C (p.Glu383Asp)
c.1152G>C (p.Glu384Asp)
n.671G>C
 dbSNP gnomAD v4
10g.8073840G>TCA375975645GATA3c.1149G>T (p.Glu383Asp)
c.1152G>T (p.Glu384Asp)
n.671G>T
 dbSNP
10g.8073841G>ACA375975646GATA3c.1150G>A (p.Asp384Asn)
c.1153G>A (p.Asp385Asn)
n.672G>A
 dbSNP gnomAD v3 gnomAD v4
10g.8073841G>CCA375975647GATA3c.1150G>C (p.Asp384His)
c.1153G>C (p.Asp385His)
n.672G>C
 dbSNP
10g.8073841G>TCA375975648GATA3c.1150G>T (p.Asp384Tyr)
c.1153G>T (p.Asp385Tyr)
n.672G>T
 dbSNP
10g.8073842A>CCA375975649GATA3c.1151A>C (p.Asp384Ala)
c.1154A>C (p.Asp385Ala)
n.673A>C
 dbSNP
10g.8073842A>GCA375975650GATA3c.1151A>G (p.Asp384Gly)
c.1154A>G (p.Asp385Gly)
n.673A>G
 dbSNP
10g.8073842A>TCA375975651GATA3c.1151A>T (p.Asp384Val)
c.1154A>T (p.Asp385Val)
n.673A>T
 dbSNP
10g.8073843C>ACA375975652GATA3c.1152C>A (p.Asp384Glu)
c.1155C>A (p.Asp385Glu)
n.674C>A
10g.8073843C>GCA375975653GATA3c.1152C>G (p.Asp384Glu)
c.1155C>G (p.Asp385Glu)
n.674C>G
 dbSNP gnomAD v4
10g.8073843C>TCA468400798GATA3c.1152C>T (p.Asp384=)
c.1155C>T (p.Asp385=)
n.674C>T
 dbSNP
10g.8073844T>ACA375975656GATA3c.1153T>A (p.Phe385Ile)
c.1156T>A (p.Phe386Ile)
n.675T>A
 dbSNP
10g.8073844T>CCA375975654GATA3c.1153T>C (p.Phe385Leu)
c.1156T>C (p.Phe386Leu)
n.675T>C
 dbSNP
10g.8073844T>GCA375975655GATA3c.1153T>G (p.Phe385Val)
c.1156T>G (p.Phe386Val)
n.675T>G
 COSMIC
10g.8073845T>ACA375975657GATA3c.1154T>A (p.Phe385Tyr)
c.1157T>A (p.Phe386Tyr)
n.676T>A
10g.8073845T>CCA375975658GATA3c.1154T>C (p.Phe385Ser)
c.1157T>C (p.Phe386Ser)
n.676T>C
10g.8073845T>GCA375975659GATA3c.1154T>G (p.Phe385Cys)
c.1157T>G (p.Phe386Cys)
n.676T>G
10g.8073846C>ACA375975660GATA3c.1155C>A (p.Phe385Leu)
c.1158C>A (p.Phe386Leu)
n.677C>A
10g.8073846C>GCA375975661GATA3c.1155C>G (p.Phe385Leu)
c.1158C>G (p.Phe386Leu)
n.677C>G
 dbSNP
10g.8073846C>TCA468400804GATA3c.1155C>T (p.Phe385=)
c.1158C>T (p.Phe386=)
n.677C>T
 dbSNP
10g.8073848_8073849delCA645553622GATA3c.1157_1158del (p.Pro386GlnfsTer6)
c.1160_1161del (p.Pro387GlnfsTer6)
n.679_680del
 COSMIC
10g.8073847C>ACA375975662GATA3c.1156C>A (p.Pro386Thr)
c.1159C>A (p.Pro387Thr)
n.678C>A
10g.8073847C>GCA375975663GATA3c.1156C>G (p.Pro386Ala)
c.1159C>G (p.Pro387Ala)
n.678C>G
10g.8073847C>TCA375975664GATA3c.1156C>T (p.Pro386Ser)
c.1159C>T (p.Pro387Ser)
n.678C>T
10g.8073847_8073848insTTCTTCATAGTCAGGGGTCA2565926680GATA3c.1156_1157insTTCTTCATAGTCAGGGGT (p.Pro386delinsLeuLeuHisSerGlnGlySer)
c.1159_1160insTTCTTCATAGTCAGGGGT (p.Pro387delinsLeuLeuHisSerGlnGlySer)
n.678_679insTTCTTCATAGTCAGGGGT
10g.8073848C>ACA375975665GATA3c.1157C>A (p.Pro386His)
c.1160C>A (p.Pro387His)
n.679C>A
 dbSNP
10g.8073848C>GCA375975666GATA3c.1157C>G (p.Pro386Arg)
c.1160C>G (p.Pro387Arg)
n.679C>G
 dbSNP
10g.8073848C>TCA375975667GATA3c.1157C>T (p.Pro386Leu)
c.1160C>T (p.Pro387Leu)
n.679C>T
 dbSNP
10g.8073849C>ACA468400806GATA3c.1158C>A (p.Pro386=)
c.1161C>A (p.Pro387=)
n.680C>A
 dbSNP
10g.8073849C=CA1888996011GATA3c.1158C= (p.Pro386=)
c.1161C= (p.Pro387=)
n.680C=
10g.8073849C>GCA468400807GATA3c.1158C>G (p.Pro386=)
c.1161C>G (p.Pro387=)
n.680C>G
 dbSNP
10g.8073849C>TCA5404557GATA3c.1158C>T (p.Pro386=)
c.1161C>T (p.Pro387=)
n.680C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073850A>CCA375975669GATA3c.1159A>C (p.Lys387Gln)
c.1162A>C (p.Lys388Gln)
n.681A>C
10g.8073850A>GCA375975670GATA3c.1159A>G (p.Lys387Glu)
c.1162A>G (p.Lys388Glu)
n.681A>G
 dbSNP
10g.8073850A>TCA375975668GATA3c.1159A>T (p.Lys387Ter)
c.1162A>T (p.Lys388Ter)
n.681A>T
 dbSNP
10g.8073851A>CCA375975672GATA3c.1160A>C (p.Lys387Thr)
c.1163A>C (p.Lys388Thr)
n.682A>C
10g.8073851A>GCA375975671GATA3c.1160A>G (p.Lys387Arg)
c.1163A>G (p.Lys388Arg)
n.682A>G
 dbSNP
10g.8073851A>TCA375975673GATA3c.1160A>T (p.Lys387Met)
c.1163A>T (p.Lys388Met)
n.682A>T
 dbSNP
10g.8073852G>ACA468400812GATA3c.1161G>A (p.Lys387=)
c.1164G>A (p.Lys388=)
n.683G>A
 dbSNP
10g.8073852G>CCA375975674GATA3c.1161G>C (p.Lys387Asn)
c.1164G>C (p.Lys388Asn)
n.683G>C
 dbSNP
10g.8073852G>TCA375975675GATA3c.1161G>T (p.Lys387Asn)
c.1164G>T (p.Lys388Asn)
n.683G>T
 dbSNP gnomAD v4
10g.8073852_8073874delCA645553623GATA3c.1161_1183del (p.Lys387AsnfsTer?)
c.1164_1186del (p.Lys388AsnfsTer?)
n.683_705del
 COSMIC
10g.8073853A>CCA375975676GATA3c.1162A>C (p.Asn388His)
c.1165A>C (p.Asn389His)
n.684A>C
 dbSNP
10g.8073853A>GCA375975677GATA3c.1162A>G (p.Asn388Asp)
c.1165A>G (p.Asn389Asp)
n.684A>G
 dbSNP
10g.8073853A>TCA375975678GATA3c.1162A>T (p.Asn388Tyr)
c.1165A>T (p.Asn389Tyr)
n.684A>T
 dbSNP
10g.8073854A=CA1888996017GATA3c.1163A= (p.Asn388=)
c.1166A= (p.Asn389=)
n.685A=
10g.8073854A>CCA5404559GATA3c.1163A>C (p.Asn388Thr)
c.1166A>C (p.Asn389Thr)
n.685A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073854A>GCA5404558GATA3c.1163A>G (p.Asn388Ser)
c.1166A>G (p.Asn389Ser)
n.685A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073854A>TCA375975679GATA3c.1163A>T (p.Asn388Ile)
c.1166A>T (p.Asn389Ile)
n.685A>T
 dbSNP
10g.8073855C>ACA375975680GATA3c.1164C>A (p.Asn388Lys)
c.1167C>A (p.Asn389Lys)
n.686C>A
 dbSNP
10g.8073855C=CA1888996020GATA3c.1164C= (p.Asn388=)
c.1167C= (p.Asn389=)
n.686C=
10g.8073855C>GCA375975681GATA3c.1164C>G (p.Asn388Lys)
c.1167C>G (p.Asn389Lys)
n.686C>G
 dbSNP
10g.8073855C>TCA202464289GATA3c.1164C>T (p.Asn388=)
c.1167C>T (p.Asn389=)
n.686C>T
 dbSNP
10g.8073856A>CCA375975684GATA3c.1165A>C (p.Ser389Arg)
c.1168A>C (p.Ser390Arg)
n.687A>C
10g.8073856A>GCA375975683GATA3c.1165A>G (p.Ser389Gly)
c.1168A>G (p.Ser390Gly)
n.687A>G
 gnomAD v4
10g.8073856A>TCA375975682GATA3c.1165A>T (p.Ser389Cys)
c.1168A>T (p.Ser390Cys)
n.687A>T
 dbSNP gnomAD v4
10g.8073857G>ACA202464292GATA3c.1166G>A (p.Ser389Asn)
c.1169G>A (p.Ser390Asn)
n.688G>A
 dbSNP
10g.8073857G>CCA375975685GATA3c.1166G>C (p.Ser389Thr)
c.1169G>C (p.Ser390Thr)
n.688G>C
 dbSNP
10g.8073857G=CA1888996023GATA3c.1166G= (p.Ser389=)
c.1169G= (p.Ser390=)
n.688G=
10g.8073857G>TCA375975686GATA3c.1166G>T (p.Ser389Ile)
c.1169G>T (p.Ser390Ile)
n.688G>T
 dbSNP
10g.8073858C>ACA375975687GATA3c.1167C>A (p.Ser389Arg)
c.1170C>A (p.Ser390Arg)
n.689C>A
 dbSNP
10g.8073858C>GCA375975688GATA3c.1167C>G (p.Ser389Arg)
c.1170C>G (p.Ser390Arg)
n.689C>G
 dbSNP
10g.8073858C>TCA468400819GATA3c.1167C>T (p.Ser389=)
c.1170C>T (p.Ser390=)
n.689C>T
 dbSNP
10g.8073859T>ACA375975689GATA3c.1168T>A (p.Ser390Thr)
c.1171T>A (p.Ser391Thr)
n.690T>A
 dbSNP
10g.8073859T>CCA375975690GATA3c.1168T>C (p.Ser390Pro)
c.1171T>C (p.Ser391Pro)
n.690T>C
 dbSNP
10g.8073859T>GCA375975691GATA3c.1168T>G (p.Ser390Ala)
c.1171T>G (p.Ser391Ala)
n.690T>G
 dbSNP
10g.8073860C>ACA375975692GATA3c.1169C>A (p.Ser390Ter)
c.1172C>A (p.Ser391Ter)
n.691C>A
 dbSNP
10g.8073860C=CA1888996025GATA3c.1169C= (p.Ser390=)
c.1172C= (p.Ser391=)
n.691C=
10g.8073860C>GCA375975693GATA3c.1169C>G (p.Ser390Trp)
c.1172C>G (p.Ser391Trp)
n.691C>G
 dbSNP
10g.8073860C>TCA375975694GATA3c.1169C>T (p.Ser390Leu)
c.1172C>T (p.Ser391Leu)
n.691C>T
 dbSNP gnomAD v2 gnomAD v4
10g.8073861G>ACA5404560GATA3c.1170G>A (p.Ser390=)
c.1173G>A (p.Ser391=)
n.692G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.8073861G>CCA468400822GATA3c.1170G>C (p.Ser390=)
c.1173G>C (p.Ser391=)
n.692G>C
 dbSNP gnomAD v2 gnomAD v4
10g.8073861G=CA1888996028GATA3c.1170G= (p.Ser390=)
c.1173G= (p.Ser391=)
n.692G=
10g.8073861G>TCA468400820GATA3c.1170G>T (p.Ser390=)
c.1173G>T (p.Ser391=)
n.692G>T
10g.8073862T>ACA375975697GATA3c.1171T>A (p.Phe391Ile)
c.1174T>A (p.Phe392Ile)
n.693T>A
 dbSNP
10g.8073862T>CCA375975696GATA3c.1171T>C (p.Phe391Leu)
c.1174T>C (p.Phe392Leu)
n.693T>C
 dbSNP
10g.8073862T>GCA375975695GATA3c.1171T>G (p.Phe391Val)
c.1174T>G (p.Phe392Val)
n.693T>G
 dbSNP
10g.8073863T>ACA375975698GATA3c.1172T>A (p.Phe391Tyr)
c.1175T>A (p.Phe392Tyr)
n.694T>A
 dbSNP
10g.8073863T>CCA375975699GATA3c.1172T>C (p.Phe391Ser)
c.1175T>C (p.Phe392Ser)
n.694T>C
10g.8073863T>GCA375975700GATA3c.1172T>G (p.Phe391Cys)
c.1175T>G (p.Phe392Cys)
n.694T>G
 dbSNP
10g.8073864T>ACA375975701GATA3c.1173T>A (p.Phe391Leu)
c.1176T>A (p.Phe392Leu)
n.695T>A
 dbSNP
10g.8073864T>CCA468400825GATA3c.1173T>C (p.Phe391=)
c.1176T>C (p.Phe392=)
n.695T>C
10g.8073864T>GCA375975702GATA3c.1173T>G (p.Phe391Leu)
c.1176T>G (p.Phe392Leu)
n.695T>G
 dbSNP
10g.8073864T=CA1888996034GATA3c.1173T= (p.Phe391=)
c.1176T= (p.Phe392=)
n.695T=
10g.8073865A>CCA375975705GATA3c.1174A>C (p.Asn392His)
c.1177A>C (p.Asn393His)
n.696A>C
 dbSNP
10g.8073865A>GCA375975704GATA3c.1174A>G (p.Asn392Asp)
c.1177A>G (p.Asn393Asp)
n.696A>G
10g.8073865A>TCA375975703GATA3c.1174A>T (p.Asn392Tyr)
c.1177A>T (p.Asn393Tyr)
n.696A>T
 dbSNP
10g.8073869_8073870insTCAACCCCA645553624GATA3c.1178_1179insTCAACCC (p.Ala394GlnfsTer?)
c.1181_1182insTCAACCC (p.Ala395GlnfsTer?)
n.700_701insTCAACCC
 COSMIC
10g.8073866A>CCA375975706GATA3c.1175A>C (p.Asn392Thr)
c.1178A>C (p.Asn393Thr)
n.697A>C
 dbSNP
10g.8073866A>GCA375975707GATA3c.1175A>G (p.Asn392Ser)
c.1178A>G (p.Asn393Ser)
n.697A>G
 dbSNP
10g.8073866A>TCA375975708GATA3c.1175A>T (p.Asn392Ile)
c.1178A>T (p.Asn393Ile)
n.697A>T
 dbSNP COSMIC
10g.8073867C>ACA375975709GATA3c.1176C>A (p.Asn392Lys)
c.1179C>A (p.Asn393Lys)
n.698C>A
 dbSNP
10g.8073867C=CA1888996042GATA3c.1176C= (p.Asn392=)
c.1179C= (p.Asn393=)
n.698C=
10g.8073867C>GCA375975710GATA3c.1176C>G (p.Asn392Lys)
c.1179C>G (p.Asn393Lys)
n.698C>G
 dbSNP gnomAD v4
10g.8073867C>TCA5404561GATA3c.1176C>T (p.Asn392=)
c.1179C>T (p.Asn393=)
n.698C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073868C>ACA375975711GATA3c.1177C>A (p.Pro393Thr)
c.1180C>A (p.Pro394Thr)
n.699C>A
 dbSNP
10g.8073868C>GCA375975713GATA3c.1177C>G (p.Pro393Ala)
c.1180C>G (p.Pro394Ala)
n.699C>G
 dbSNP
10g.8073868C>TCA375975712GATA3c.1177C>T (p.Pro393Ser)
c.1180C>T (p.Pro394Ser)
n.699C>T
 dbSNP gnomAD v4
10g.8073869C>ACA375975714GATA3c.1178C>A (p.Pro393Gln)
c.1181C>A (p.Pro394Gln)
n.700C>A
 dbSNP
10g.8073869C=CA1888996046GATA3c.1178C= (p.Pro393=)
c.1181C= (p.Pro394=)
n.700C=
10g.8073869C>GCA375975715GATA3c.1178C>G (p.Pro393Arg)
c.1181C>G (p.Pro394Arg)
n.700C>G
 dbSNP
10g.8073869C>TCA375975716GATA3c.1178C>T (p.Pro393Leu)
c.1181C>T (p.Pro394Leu)
n.700C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.8073870G>ACA5404562GATA3c.1179G>A (p.Pro393=)
c.1182G>A (p.Pro394=)
n.701G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073870G>CCA468400834GATA3c.1179G>C (p.Pro393=)
c.1182G>C (p.Pro394=)
n.701G>C
 dbSNP
10g.8073870G=CA1888996050GATA3c.1179G= (p.Pro393=)
c.1182G= (p.Pro394=)
n.701G=
10g.8073870G>TCA468400836GATA3c.1179G>T (p.Pro393=)
c.1182G>T (p.Pro394=)
n.701G>T
 dbSNP gnomAD v4
10g.8073871dupCA468400835GATA3c.1180dup (p.Ala394GlyfsTer?)
c.1183dup (p.Ala395GlyfsTer?)
n.702dup
10g.8073871G>ACA375975717GATA3c.1180G>A (p.Ala394Thr)
c.1183G>A (p.Ala395Thr)
n.702G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.8073871G>CCA375975718GATA3c.1180G>C (p.Ala394Pro)
c.1183G>C (p.Ala395Pro)
n.702G>C
 dbSNP
10g.8073871G=CA1888996053GATA3c.1180G= (p.Ala394=)
c.1183G= (p.Ala395=)
n.702G=
10g.8073871G>TCA375975719GATA3c.1180G>T (p.Ala394Ser)
c.1183G>T (p.Ala395Ser)
n.702G>T
 dbSNP
10g.8073872C>ACA375975720GATA3c.1181C>A (p.Ala394Asp)
c.1184C>A (p.Ala395Asp)
n.703C>A
 dbSNP
10g.8073872C=CA1888996057GATA3c.1181C= (p.Ala394=)
c.1184C= (p.Ala395=)
n.703C=
10g.8073872C>GCA375975721GATA3c.1181C>G (p.Ala394Gly)
c.1184C>G (p.Ala395Gly)
n.703C>G
 dbSNP
10g.8073872C>TCA5404563GATA3c.1181C>T (p.Ala394Val)
c.1184C>T (p.Ala395Val)
n.703C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073873C>ACA468400844GATA3c.1182C>A (p.Ala394=)
c.1185C>A (p.Ala395=)
n.704C>A
 dbSNP
10g.8073873C=CA1888996059GATA3c.1182C= (p.Ala394=)
c.1185C= (p.Ala395=)
n.704C=
10g.8073873C>GCA468400845GATA3c.1182C>G (p.Ala394=)
c.1185C>G (p.Ala395=)
n.704C>G
 dbSNP
10g.8073873C>TCA5404564GATA3c.1182C>T (p.Ala394=)
c.1185C>T (p.Ala395=)
n.704C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073874G>ACA159918GATA3c.1183G>A (p.Ala395Thr)
c.1186G>A (p.Ala396Thr)
n.705G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.8073874G>CCA375975723GATA3c.1183G>C (p.Ala395Pro)
c.1186G>C (p.Ala396Pro)
n.705G>C
10g.8073874G=CA1888996062GATA3c.1183G= (p.Ala395=)
c.1186G= (p.Ala396=)
n.705G=
10g.8073874G>TCA375975722GATA3c.1183G>T (p.Ala395Ser)
c.1186G>T (p.Ala396Ser)
n.705G>T
 dbSNP
10g.8073875C>ACA375975726GATA3c.1184C>A (p.Ala395Asp)
c.1187C>A (p.Ala396Asp)
n.706C>A
 dbSNP
10g.8073875C>GCA375975724GATA3c.1184C>G (p.Ala395Gly)
c.1187C>G (p.Ala396Gly)
n.706C>G
 dbSNP
10g.8073875C>TCA375975725GATA3c.1184C>T (p.Ala395Val)
c.1187C>T (p.Ala396Val)
n.706C>T
 dbSNP gnomAD v4
10g.8073876C>ACA468400850GATA3c.1185C>A (p.Ala395=)
c.1188C>A (p.Ala396=)
n.707C>A
 dbSNP
10g.8073876C>GCA468400849GATA3c.1185C>G (p.Ala395=)
c.1188C>G (p.Ala396=)
n.707C>G
 dbSNP
10g.8073876C>TCA468400852GATA3c.1185C>T (p.Ala395=)
c.1188C>T (p.Ala396=)
n.707C>T
 dbSNP gnomAD v4
10g.8073877C>ACA375975727GATA3c.1186C>A (p.Leu396Ile)
c.1189C>A (p.Leu397Ile)
n.708C>A
 dbSNP gnomAD v4 COSMIC
10g.8073877C>GCA375975728GATA3c.1186C>G (p.Leu396Val)
c.1189C>G (p.Leu397Val)
n.708C>G
10g.8073877C>TCA375975729GATA3c.1186C>T (p.Leu396Phe)
c.1189C>T (p.Leu397Phe)
n.708C>T
 dbSNP
10g.8073878T>ACA375975730GATA3c.1187T>A (p.Leu396His)
c.1190T>A (p.Leu397His)
n.709T>A
 dbSNP
10g.8073878T>CCA375975731GATA3c.1187T>C (p.Leu396Pro)
c.1190T>C (p.Leu397Pro)
n.709T>C
 dbSNP
10g.8073878T>GCA375975732GATA3c.1187T>G (p.Leu396Arg)
c.1190T>G (p.Leu397Arg)
n.709T>G
10g.8073879C>ACA468400855GATA3c.1188C>A (p.Leu396=)
c.1191C>A (p.Leu397=)
n.710C>A
10g.8073879C=CA1888996070GATA3c.1188C= (p.Leu396=)
c.1191C= (p.Leu397=)
n.710C=
10g.8073879C>GCA468400856GATA3c.1188C>G (p.Leu396=)
c.1191C>G (p.Leu397=)
n.710C>G
 dbSNP
10g.8073879C>TCA468400857GATA3c.1188C>T (p.Leu396=)
c.1191C>T (p.Leu397=)
n.710C>T
 dbSNP gnomAD v2 gnomAD v4
10g.8073880T>ACA375975733GATA3c.1189T>A (p.Ser397Thr)
c.1192T>A (p.Ser398Thr)
n.711T>A
 gnomAD v4
10g.8073880T>CCA375975734GATA3c.1189T>C (p.Ser397Pro)
c.1192T>C (p.Ser398Pro)
n.711T>C
10g.8073880T>GCA375975735GATA3c.1189T>G (p.Ser397Ala)
c.1192T>G (p.Ser398Ala)
n.711T>G
 gnomAD v4
10g.8073881C>ACA375975736GATA3c.1190C>A (p.Ser397Tyr)
c.1193C>A (p.Ser398Tyr)
n.712C>A
 gnomAD v4
10g.8073881C>GCA375975737GATA3c.1190C>G (p.Ser397Cys)
c.1193C>G (p.Ser398Cys)
n.712C>G
 dbSNP
10g.8073881C>TCA375975738GATA3c.1190C>T (p.Ser397Phe)
c.1193C>T (p.Ser398Phe)
n.712C>T
 dbSNP COSMIC
10g.8073882dupCA468400952GATA3c.1191dup (p.Arg398GlnfsTer?)
c.1194dup (p.Arg399GlnfsTer?)
n.713dup
 COSMIC
10g.8073882C>ACA468400955GATA3c.1191C>A (p.Ser397=)
c.1194C>A (p.Ser398=)
n.713C>A
 dbSNP
10g.8073882C=CA1888996074GATA3c.1191C= (p.Ser397=)
c.1194C= (p.Ser398=)
n.713C=
10g.8073882C>GCA468400958GATA3c.1191C>G (p.Ser397=)
c.1194C>G (p.Ser398=)
n.713C>G
 dbSNP
10g.8073882C>TCA5404565GATA3c.1191C>T (p.Ser397=)
c.1194C>T (p.Ser398=)
n.713C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073882_8073883delCA645553625GATA3c.1191_1192del (p.Arg398ThrfsTer?)
c.1194_1195del (p.Arg399ThrfsTer?)
n.713_714del
 COSMIC
10g.8073883A=CA1888996077GATA3c.1192A= (p.Arg398=)
c.1195A= (p.Arg399=)
n.714A=
10g.8073883A>CCA468400960GATA3c.1192A>C (p.Arg398=)
c.1195A>C (p.Arg399=)
n.714A>C
10g.8073883A>GCA5404566GATA3c.1192A>G (p.Arg398Gly)
c.1195A>G (p.Arg399Gly)
n.714A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073883A>TCA375975739GATA3c.1192A>T (p.Arg398Ter)
c.1195A>T (p.Arg399Ter)
n.714A>T
 dbSNP
10g.8073884_8073885delCA645553626GATA3c.1193_1194del (p.Arg398ThrfsTer?)
c.1196_1197del (p.Arg399ThrfsTer?)
n.715_716del
 COSMIC
10g.8073883_8073904delinsGGCA2580650497GATA3c.1192_1213delinsGG (p.Arg398GlyfsTer?)
c.1195_1216delinsGG (p.Arg399GlyfsTer?)
n.714_735delinsGG
10g.8073883_8073884insAACACACCCCA2786559741GATA3c.1192_1193insAACACACCC (p.Ser397_Arg398insLysHisThr)
c.1195_1196insAACACACCC (p.Ser398_Arg399insLysHisThr)
n.714_715insAACACACCC
10g.8073884G>ACA375975740GATA3c.1193G>A (p.Arg398Lys)
c.1196G>A (p.Arg399Lys)
n.715G>A
10g.8073884G>CCA375975741GATA3c.1193G>C (p.Arg398Thr)
c.1196G>C (p.Arg399Thr)
n.715G>C
10g.8073884G>TCA375975742GATA3c.1193G>T (p.Arg398Ile)
c.1196G>T (p.Arg399Ile)
n.715G>T
10g.8073885A>CCA375975743GATA3c.1194A>C (p.Arg398Ser)
c.1197A>C (p.Arg399Ser)
n.716A>C
 dbSNP
10g.8073885A>GCA468400961GATA3c.1194A>G (p.Arg398=)
c.1197A>G (p.Arg399=)
n.716A>G
 gnomAD v4
10g.8073885A>TCA375975744GATA3c.1194A>T (p.Arg398Ser)
c.1197A>T (p.Arg399Ser)
n.716A>T
 dbSNP
10g.8073888_8073889delCA2695211824GATA3c.1197_1198del (p.Met400ValfsTer?)
c.1200_1201del (p.Met401ValfsTer?)
n.719_720del
10g.8073886C>ACA375975745GATA3c.1195C>A (p.His399Asn)
c.1198C>A (p.His400Asn)
n.717C>A
 dbSNP gnomAD v4
10g.8073886C>GCA375975746GATA3c.1195C>G (p.His399Asp)
c.1198C>G (p.His400Asp)
n.717C>G
 dbSNP
10g.8073886C>TCA375975747GATA3c.1195C>T (p.His399Tyr)
c.1198C>T (p.His400Tyr)
n.717C>T
10g.8073887A=CA1888996081GATA3c.1196A= (p.His399=)
c.1199A= (p.His400=)
n.718A=
10g.8073887A>CCA375975748GATA3c.1196A>C (p.His399Pro)
c.1199A>C (p.His400Pro)
n.718A>C
 dbSNP gnomAD v2 gnomAD v4
10g.8073887A>GCA375975749GATA3c.1196A>G (p.His399Arg)
c.1199A>G (p.His400Arg)
n.718A>G
 ClinVar dbSNP gnomAD v4
10g.8073887A>TCA375975750GATA3c.1196A>T (p.His399Leu)
c.1199A>T (p.His400Leu)
n.718A>T
 dbSNP
10g.8073888C>ACA375975752GATA3c.1197C>A (p.His399Gln)
c.1200C>A (p.His400Gln)
n.719C>A
 dbSNP
10g.8073888C=CA1888996087GATA3c.1197C= (p.His399=)
c.1200C= (p.His400=)
n.719C=
10g.8073888C>GCA375975751GATA3c.1197C>G (p.His399Gln)
c.1200C>G (p.His400Gln)
n.719C>G
 dbSNP
10g.8073888C>TCA202464304GATA3c.1197C>T (p.His399=)
c.1200C>T (p.His400=)
n.719C>T
 dbSNP gnomAD v2 gnomAD v4
10g.8073888_8073889insCATGTCCTCCCTGAGCCA645553628GATA3c.1197_1198insCATGTCCTCCCTGAGC (p.Met400HisfsTer?)
c.1200_1201insCATGTCCTCCCTGAGC (p.Met401HisfsTer?)
n.719_720insCATGTCCTCCCTGAGC
 COSMIC
10g.8073888_8073890delinsCATCA1888996085GATA3c.1197_1199delinsCAT (p.His399=)
c.1200_1202delinsCAT (p.His400=)
n.719_721delinsCAT
10g.8073890_8073905dupCA645553627GATA3c.1199_1214dup (p.Ile406ValfsTer?)
c.1202_1217dup (p.Ile407ValfsTer?)
n.721_736dup
 COSMIC
10g.8073889A=CA1888996098GATA3c.1198A= (p.Met400=)
c.1201A= (p.Met401=)
n.720A=
10g.8073889A>CCA375975753GATA3c.1198A>C (p.Met400Leu)
c.1201A>C (p.Met401Leu)
n.720A>C
 dbSNP gnomAD v4
10g.8073889A>GCA375975755GATA3c.1198A>G (p.Met400Val)
c.1201A>G (p.Met401Val)
n.720A>G
 dbSNP gnomAD v3 gnomAD v4
10g.8073889A>TCA375975754GATA3c.1198A>T (p.Met400Leu)
c.1201A>T (p.Met401Leu)
n.720A>T
 dbSNP gnomAD v4
10g.8073889dupCA468400969GATA3c.1198dup (p.Met400AsnfsTer?)
c.1201dup (p.Met401AsnfsTer?)
n.720dup
 COSMIC
10g.8073889_8073890delCA645294058GATA3c.1198_1199del (p.Met400ValfsTer?)
c.1201_1202del (p.Met401ValfsTer?)
n.720_721del
 ClinVar dbSNP COSMIC
10g.8073890T>ACA375975756GATA3c.1199T>A (p.Met400Lys)
c.1202T>A (p.Met401Lys)
n.721T>A
 dbSNP
10g.8073890T>CCA375975757GATA3c.1199T>C (p.Met400Thr)
c.1202T>C (p.Met401Thr)
n.721T>C
 dbSNP gnomAD v3 gnomAD v4
10g.8073890T>GCA375975758GATA3c.1199T>G (p.Met400Arg)
c.1202T>G (p.Met401Arg)
n.721T>G
10g.8073890T=CA1888996102GATA3c.1199T= (p.Met400=)
c.1202T= (p.Met401=)
n.721T=
10g.8073890_8073892delCA2786559742GATA3c.1199_1201del (p.Met400_Ser401delinsThr)
c.1202_1204del (p.Met401_Ser402delinsThr)
n.721_723del
10g.8073890_8073891insACA468400971GATA3c.1199_1200insA (p.Met400IlefsTer?)
c.1202_1203insA (p.Met401IlefsTer?)
n.721_722insA
10g.8073891G>ACA375975759GATA3c.1200G>A (p.Met400Ile)
c.1203G>A (p.Met401Ile)
n.722G>A
 ClinVar
10g.8073891G>CCA375975760GATA3c.1200G>C (p.Met400Ile)
c.1203G>C (p.Met401Ile)
n.722G>C
 dbSNP
10g.8073891G>TCA375975761GATA3c.1200G>T (p.Met400Ile)
c.1203G>T (p.Met401Ile)
n.722G>T
 dbSNP
10g.8073891dupCA468400972GATA3c.1200dup (p.Ser401ValfsTer?)
c.1203dup (p.Ser402ValfsTer?)
n.722dup
 COSMIC
10g.8073892T>ACA375975762GATA3c.1201T>A (p.Ser401Thr)
c.1204T>A (p.Ser402Thr)
n.723T>A
10g.8073892T>CCA375975763GATA3c.1201T>C (p.Ser401Pro)
c.1204T>C (p.Ser402Pro)
n.723T>C
10g.8073892T>GCA375975764GATA3c.1201T>G (p.Ser401Ala)
c.1204T>G (p.Ser402Ala)
n.723T>G
 gnomAD v4
10g.8073892_8073895dupCA645553629GATA3c.1201_1204dup (p.Ser402PhefsTer?)
c.1204_1207dup (p.Ser403PhefsTer?)
n.723_726dup
 COSMIC COSMIC
10g.8073893C>ACA375975765GATA3c.1202C>A (p.Ser401Tyr)
c.1205C>A (p.Ser402Tyr)
n.724C>A
10g.8073893C>GCA375975766GATA3c.1202C>G (p.Ser401Cys)
c.1205C>G (p.Ser402Cys)
n.724C>G
 dbSNP
10g.8073893C>TCA375975767GATA3c.1202C>T (p.Ser401Phe)
c.1205C>T (p.Ser402Phe)
n.724C>T
 dbSNP
10g.8073894dupCA645553630GATA3c.1203dup (p.Ser402LeufsTer?)
c.1206dup (p.Ser403LeufsTer?)
n.725dup
 COSMIC
10g.8073894C>ACA468400976GATA3c.1203C>A (p.Ser401=)
c.1206C>A (p.Ser402=)
n.725C>A
 dbSNP
10g.8073894C=CA1888996105GATA3c.1203C= (p.Ser401=)
c.1206C= (p.Ser402=)
n.725C=
10g.8073894C>GCA5404567GATA3c.1203C>G (p.Ser401=)
c.1206C>G (p.Ser402=)
n.725C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073894C>TCA468400977GATA3c.1203C>T (p.Ser401=)
c.1206C>T (p.Ser402=)
n.725C>T
 dbSNP
10g.8073895T>ACA375975768GATA3c.1204T>A (p.Ser402Thr)
c.1207T>A (p.Ser403Thr)
n.726T>A
10g.8073895T>CCA375975769GATA3c.1204T>C (p.Ser402Pro)
c.1207T>C (p.Ser403Pro)
n.726T>C
10g.8073895T>GCA375975770GATA3c.1204T>G (p.Ser402Ala)
c.1207T>G (p.Ser403Ala)
n.726T>G
10g.8073896C>ACA375975771GATA3c.1205C>A (p.Ser402Tyr)
c.1208C>A (p.Ser403Tyr)
n.727C>A
 dbSNP
10g.8073896C>GCA375975772GATA3c.1205C>G (p.Ser402Cys)
c.1208C>G (p.Ser403Cys)
n.727C>G
 dbSNP
10g.8073896C>TCA375975773GATA3c.1205C>T (p.Ser402Phe)
c.1208C>T (p.Ser403Phe)
n.727C>T
 dbSNP
10g.8073898dupCA468400981GATA3c.1207dup (p.Leu403ProfsTer?)
c.1210dup (p.Leu404ProfsTer?)
n.729dup
10g.8073897C>ACA468400983GATA3c.1206C>A (p.Ser402=)
c.1209C>A (p.Ser403=)
n.728C>A
 dbSNP
10g.8073897C>GCA468400985GATA3c.1206C>G (p.Ser402=)
c.1209C>G (p.Ser403=)
n.728C>G
 dbSNP
10g.8073897C>TCA468400986GATA3c.1206C>T (p.Ser402=)
c.1209C>T (p.Ser403=)
n.728C>T
 dbSNP COSMIC
10g.8073898C>ACA375975774GATA3c.1207C>A (p.Leu403Met)
c.1210C>A (p.Leu404Met)
n.729C>A
10g.8073898C=CA1888996108GATA3c.1207C= (p.Leu403=)
c.1210C= (p.Leu404=)
n.729C=
10g.8073898C>GCA375975775GATA3c.1207C>G (p.Leu403Val)
c.1210C>G (p.Leu404Val)
n.729C>G
 dbSNP
10g.8073898C>TCA468400988GATA3c.1207C>T (p.Leu403=)
c.1210C>T (p.Leu404=)
n.729C>T
 dbSNP gnomAD v2 gnomAD v4
10g.8073898_8073899delCA645553631GATA3c.1207_1208del (p.Leu403GlufsTer?)
c.1210_1211del (p.Leu404GlufsTer?)
n.729_730del
 COSMIC
10g.8073899T>ACA375975776GATA3c.1208T>A (p.Leu403Gln)
c.1211T>A (p.Leu404Gln)
n.730T>A
10g.8073899T>CCA375975777GATA3c.1208T>C (p.Leu403Pro)
c.1211T>C (p.Leu404Pro)
n.730T>C
 gnomAD v4
10g.8073899T>GCA375975778GATA3c.1208T>G (p.Leu403Arg)
c.1211T>G (p.Leu404Arg)
n.730T>G
10g.8073899dupCA645553632GATA3c.1208dup (p.Ser404GlufsTer?)
c.1211dup (p.Ser405GlufsTer?)
n.730dup
 COSMIC
10g.8073899_8073900insCCA645553633GATA3c.1208_1209insC (p.Ser404GlufsTer?)
c.1211_1212insC (p.Ser405GlufsTer?)
n.730_731insC
 COSMIC
10g.8073900G>ACA468400992GATA3c.1209G>A (p.Leu403=)
c.1212G>A (p.Leu404=)
n.731G>A
 dbSNP
10g.8073900G>CCA468400989GATA3c.1209G>C (p.Leu403=)
c.1212G>C (p.Leu404=)
n.731G>C
10g.8073900G>TCA468400991GATA3c.1209G>T (p.Leu403=)
c.1212G>T (p.Leu404=)
n.731G>T
 COSMIC
10g.8073901A>CCA375975779GATA3c.1210A>C (p.Ser404Arg)
c.1213A>C (p.Ser405Arg)
n.732A>C
 dbSNP
10g.8073901A>GCA375975780GATA3c.1210A>G (p.Ser404Gly)
c.1213A>G (p.Ser405Gly)
n.732A>G
 dbSNP
10g.8073901A>TCA375975781GATA3c.1210A>T (p.Ser404Cys)
c.1213A>T (p.Ser405Cys)
n.732A>T
 dbSNP
10g.8073902G>ACA375975784GATA3c.1211G>A (p.Ser404Asn)
c.1214G>A (p.Ser405Asn)
n.733G>A
10g.8073902G>CCA375975783GATA3c.1211G>C (p.Ser404Thr)
c.1214G>C (p.Ser405Thr)
n.733G>C
10g.8073902G>TCA375975782GATA3c.1211G>T (p.Ser404Ile)
c.1214G>T (p.Ser405Ile)
n.733G>T
10g.8073903C>ACA375975785GATA3c.1212C>A (p.Ser404Arg)
c.1215C>A (p.Ser405Arg)
n.734C>A
 dbSNP
10g.8073903C>GCA375975786GATA3c.1212C>G (p.Ser404Arg)
c.1215C>G (p.Ser405Arg)
n.734C>G
 dbSNP
10g.8073903C>TCA468400998GATA3c.1212C>T (p.Ser404=)
c.1215C>T (p.Ser405=)
n.734C>T
 dbSNP gnomAD v4
10g.8073904C>ACA375975787GATA3c.1213C>A (p.His405Asn)
c.1216C>A (p.His406Asn)
n.735C>A
 dbSNP
10g.8073904C>GCA375975789GATA3c.1213C>G (p.His405Asp)
c.1216C>G (p.His406Asp)
n.735C>G
 dbSNP
10g.8073904C>TCA375975788GATA3c.1213C>T (p.His405Tyr)
c.1216C>T (p.His406Tyr)
n.735C>T
 dbSNP
10g.8073905A>CCA375975790GATA3c.1214A>C (p.His405Pro)
c.1217A>C (p.His406Pro)
n.736A>C
 dbSNP
10g.8073905A>GCA375975792GATA3c.1214A>G (p.His405Arg)
c.1217A>G (p.His406Arg)
n.736A>G
 dbSNP
10g.8073905A>TCA375975791GATA3c.1214A>T (p.His405Leu)
c.1217A>T (p.His406Leu)
n.736A>T
 dbSNP
10g.8073906C>ACA375975793GATA3c.1215C>A (p.His405Gln)
c.1218C>A (p.His406Gln)
n.737C>A
10g.8073906C=CA1888996111GATA3c.1215C= (p.His405=)
c.1218C= (p.His406=)
n.737C=
10g.8073906C>GCA375975794GATA3c.1215C>G (p.His405Gln)
c.1218C>G (p.His406Gln)
n.737C>G
 dbSNP
10g.8073906C>TCA468401003GATA3c.1215C>T (p.His405=)
c.1218C>T (p.His406=)
n.737C>T
 dbSNP gnomAD v2 gnomAD v4
10g.8073907A=CA1888996115GATA3c.1216A= (p.Ile406=)
c.1219A= (p.Ile407=)
n.738A=
10g.8073907A>CCA375975795GATA3c.1216A>C (p.Ile406Leu)
c.1219A>C (p.Ile407Leu)
n.738A>C
 dbSNP
10g.8073907A>GCA202464305GATA3c.1216A>G (p.Ile406Val)
c.1219A>G (p.Ile407Val)
n.738A>G
 dbSNP gnomAD v3 gnomAD v4
10g.8073907A>TCA375975796GATA3c.1216A>T (p.Ile406Phe)
c.1219A>T (p.Ile407Phe)
n.738A>T
 dbSNP
10g.8073908T>ACA375975797GATA3c.1217T>A (p.Ile406Asn)
c.1220T>A (p.Ile407Asn)
n.739T>A
 dbSNP
10g.8073908T>CCA375975798GATA3c.1217T>C (p.Ile406Thr)
c.1220T>C (p.Ile407Thr)
n.739T>C
 dbSNP
10g.8073908T>GCA375975799GATA3c.1217T>G (p.Ile406Ser)
c.1220T>G (p.Ile407Ser)
n.739T>G
10g.8073910_8073911delCA645553634GATA3c.1219_1220del (p.Ser407AlafsTer?)
c.1222_1223del (p.Ser408AlafsTer?)
n.741_742del
 COSMIC
10g.8073909delCA468401012GATA3c.1218del (p.Ser407ArgfsTer10)
c.1221del (p.Ser408ArgfsTer10)
n.740del
 COSMIC
10g.8073909C>ACA468401007GATA3c.1218C>A (p.Ile406=)
c.1221C>A (p.Ile407=)
n.740C>A
10g.8073909C>GCA375975800GATA3c.1218C>G (p.Ile406Met)
c.1221C>G (p.Ile407Met)
n.740C>G
 dbSNP gnomAD v4
10g.8073909C>TCA468401010GATA3c.1218C>T (p.Ile406=)
c.1221C>T (p.Ile407=)
n.740C>T
 dbSNP
10g.8073909dupCA2695211826GATA3c.1218dup (p.Ser407LeufsTer?)
c.1221dup (p.Ser408LeufsTer?)
n.740dup
10g.8073910T>ACA375975801GATA3c.1219T>A (p.Ser407Thr)
c.1222T>A (p.Ser408Thr)
n.741T>A
10g.8073910T>CCA375975802GATA3c.1219T>C (p.Ser407Pro)
c.1222T>C (p.Ser408Pro)
n.741T>C
 dbSNP
10g.8073910T>GCA375975803GATA3c.1219T>G (p.Ser407Ala)
c.1222T>G (p.Ser408Ala)
n.741T>G
10g.8073911delCA468401015GATA3c.1220del (p.Ser407CysfsTer10)
c.1223del (p.Ser408CysfsTer10)
n.742del
 COSMIC
10g.8073911C>ACA375975805GATA3c.1220C>A (p.Ser407Ter)
c.1223C>A (p.Ser408Ter)
n.742C>A
10g.8073911C=CA1888996124GATA3c.1220C= (p.Ser407=)
c.1223C= (p.Ser408=)
n.742C=
10g.8073911C>GCA375975804GATA3c.1220C>G (p.Ser407Trp)
c.1223C>G (p.Ser408Trp)
n.742C>G
 dbSNP gnomAD v4
10g.8073911C>TCA5404568GATA3c.1220C>T (p.Ser407Leu)
c.1223C>T (p.Ser408Leu)
n.742C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.8073911dupCA468401014GATA3c.1220dup (p.Pro408AlafsTer?)
c.1223dup (p.Pro409AlafsTer?)
n.742dup
 COSMIC
10g.8073912_8073913delCA645553635GATA3c.1221_1222del (p.Pro408LeufsTer?)
c.1224_1225del (p.Pro409LeufsTer?)
n.743_744del
 COSMIC
10g.8073911_8073912insACA645553636GATA3c.1220_1221insA (p.Pro408AlafsTer?)
c.1223_1224insA (p.Pro409AlafsTer?)
n.742_743insA
 COSMIC
10g.8073912G>ACA5404569GATA3c.1221G>A (p.Ser407=)
c.1224G>A (p.Ser408=)
n.743G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073912G>CCA468401017GATA3c.1221G>C (p.Ser407=)
c.1224G>C (p.Ser408=)
n.743G>C
 dbSNP gnomAD v4
10g.8073912G=CA1888996132GATA3c.1221G= (p.Ser407=)
c.1224G= (p.Ser408=)
n.743G=
10g.8073912G>TCA468401020GATA3c.1221G>T (p.Ser407=)
c.1224G>T (p.Ser408=)
n.743G>T
 dbSNP
10g.8073912dupCA468401022GATA3c.1221dup (p.Pro408AlafsTer?)
c.1224dup (p.Pro409AlafsTer?)
n.743dup
 COSMIC
10g.8073912_8073913insACA468401023GATA3c.1221_1222insA (p.Pro408ThrfsTer?)
c.1224_1225insA (p.Pro409ThrfsTer?)
n.743_744insA
 COSMIC
10g.8073912_8073913insTCA468401024GATA3c.1221_1222insT (p.Pro408SerfsTer?)
c.1224_1225insT (p.Pro409SerfsTer?)
n.743_744insT
 COSMIC
10g.8073913C>ACA375975806GATA3c.1222C>A (p.Pro408Thr)
c.1225C>A (p.Pro409Thr)
n.744C>A
 dbSNP
10g.8073913C>GCA375975807GATA3c.1222C>G (p.Pro408Ala)
c.1225C>G (p.Pro409Ala)
n.744C>G
 dbSNP
10g.8073913C>TCA375975808GATA3c.1222C>T (p.Pro408Ser)
c.1225C>T (p.Pro409Ser)
n.744C>T
 dbSNP
10g.8073915delCA2608207648GATA3c.1224del (p.Phe409SerfsTer8)
c.1227del (p.Phe410SerfsTer8)
n.746del
 gnomAD v4
10g.8073913_8073914insACA468401027GATA3c.1222_1223insA (p.Pro408HisfsTer?)
c.1225_1226insA (p.Pro409HisfsTer?)
n.744_745insA
10g.8073913_8073914insGCA468401029GATA3c.1222_1223insG (p.Pro408ArgfsTer?)
c.1225_1226insG (p.Pro409ArgfsTer?)
n.744_745insG
10g.8073914C>ACA375975809GATA3c.1223C>A (p.Pro408His)
c.1226C>A (p.Pro409His)
n.745C>A
 dbSNP COSMIC
10g.8073914C>GCA375975810GATA3c.1223C>G (p.Pro408Arg)
c.1226C>G (p.Pro409Arg)
n.745C>G
 dbSNP
10g.8073914C>TCA375975811GATA3c.1223C>T (p.Pro408Leu)
c.1226C>T (p.Pro409Leu)
n.745C>T
 dbSNP
10g.8073914_8073915insGCA468401030GATA3c.1223_1224insG (p.Phe409LeufsTer?)
c.1226_1227insG (p.Phe410LeufsTer?)
n.745_746insG
10g.8073915C>ACA468401034GATA3c.1224C>A (p.Pro408=)
c.1227C>A (p.Pro409=)
n.746C>A
 dbSNP
10g.8073915C>GCA468401036GATA3c.1224C>G (p.Pro408=)
c.1227C>G (p.Pro409=)
n.746C>G
10g.8073915C>TCA468401033GATA3c.1224C>T (p.Pro408=)
c.1227C>T (p.Pro409=)
n.746C>T
 dbSNP
10g.8073916T>ACA375975812GATA3c.1225T>A (p.Phe409Ile)
c.1228T>A (p.Phe410Ile)
n.747T>A
 dbSNP
10g.8073916T>CCA375975813GATA3c.1225T>C (p.Phe409Leu)
c.1228T>C (p.Phe410Leu)
n.747T>C
 dbSNP
10g.8073916T>GCA375975814GATA3c.1225T>G (p.Phe409Val)
c.1228T>G (p.Phe410Val)
n.747T>G
10g.8073917dupCA468401039GATA3c.1226dup (p.Ser410GlnfsTer?)
c.1229dup (p.Ser411GlnfsTer?)
n.748dup
10g.8073917T>ACA375975815GATA3c.1226T>A (p.Phe409Tyr)
c.1229T>A (p.Phe410Tyr)
n.748T>A
10g.8073917T>CCA375975816GATA3c.1226T>C (p.Phe409Ser)
c.1229T>C (p.Phe410Ser)
n.748T>C
10g.8073917T>GCA375975817GATA3c.1226T>G (p.Phe409Cys)
c.1229T>G (p.Phe410Cys)
n.748T>G
10g.8073918C>ACA375975819GATA3c.1227C>A (p.Phe409Leu)
c.1230C>A (p.Phe410Leu)
n.749C>A
 dbSNP
10g.8073918C>GCA375975818GATA3c.1227C>G (p.Phe409Leu)
c.1230C>G (p.Phe410Leu)
n.749C>G
 dbSNP
10g.8073918C>TCA468401040GATA3c.1227C>T (p.Phe409=)
c.1230C>T (p.Phe410=)
n.749C>T
 dbSNP
10g.8073919A>CCA375975820GATA3c.1228A>C (p.Ser410Arg)
c.1231A>C (p.Ser411Arg)
n.750A>C
10g.8073919A>GCA375975821GATA3c.1228A>G (p.Ser410Gly)
c.1231A>G (p.Ser411Gly)
n.750A>G
 dbSNP gnomAD v4
10g.8073919A>TCA375975822GATA3c.1228A>T (p.Ser410Cys)
c.1231A>T (p.Ser411Cys)
n.750A>T
 dbSNP
10g.8073920G>ACA375975823GATA3c.1229G>A (p.Ser410Asn)
c.1232G>A (p.Ser411Asn)
n.751G>A
10g.8073920G>CCA375975824GATA3c.1229G>C (p.Ser410Thr)
c.1232G>C (p.Ser411Thr)
n.751G>C
10g.8073920G>TCA375975825GATA3c.1229G>T (p.Ser410Ile)
c.1232G>T (p.Ser411Ile)
n.751G>T
10g.8073921C>ACA375975826GATA3c.1230C>A (p.Ser410Arg)
c.1233C>A (p.Ser411Arg)
n.752C>A
 dbSNP
10g.8073921C>GCA375975827GATA3c.1230C>G (p.Ser410Arg)
c.1233C>G (p.Ser411Arg)
n.752C>G
 dbSNP
10g.8073921C>TCA468401045GATA3c.1230C>T (p.Ser410=)
c.1233C>T (p.Ser411=)
n.752C>T
 dbSNP
10g.8073922C>ACA375975828GATA3c.1231C>A (p.His411Asn)
c.1234C>A (p.His412Asn)
n.753C>A
 dbSNP
10g.8073922C>GCA375975830GATA3c.1231C>G (p.His411Asp)
c.1234C>G (p.His412Asp)
n.753C>G
10g.8073922C>TCA375975829GATA3c.1231C>T (p.His411Tyr)
c.1234C>T (p.His412Tyr)
n.753C>T
 dbSNP
10g.8073923A>CCA375975831GATA3c.1232A>C (p.His411Pro)
c.1235A>C (p.His412Pro)
n.754A>C
 dbSNP
10g.8073923A>GCA375975832GATA3c.1232A>G (p.His411Arg)
c.1235A>G (p.His412Arg)
n.754A>G
10g.8073923A>TCA375975833GATA3c.1232A>T (p.His411Leu)
c.1235A>T (p.His412Leu)
n.754A>T
 dbSNP
10g.8073924C>ACA375975834GATA3c.1233C>A (p.His411Gln)
c.1236C>A (p.His412Gln)
n.755C>A
 dbSNP
10g.8073924C>GCA375975835GATA3c.1233C>G (p.His411Gln)
c.1236C>G (p.His412Gln)
n.755C>G
 dbSNP
10g.8073924C>TCA468401047GATA3c.1233C>T (p.His411=)
c.1236C>T (p.His412=)
n.755C>T
 dbSNP gnomAD v4
10g.8073925T>ACA375975836GATA3c.1234T>A (p.Ser412Thr)
c.1237T>A (p.Ser413Thr)
n.756T>A
10g.8073925T>CCA5404570GATA3c.1234T>C (p.Ser412Pro)
c.1237T>C (p.Ser413Pro)
n.756T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073925T>GCA375975837GATA3c.1234T>G (p.Ser412Ala)
c.1237T>G (p.Ser413Ala)
n.756T>G
10g.8073925T=CA1888996137GATA3c.1234T= (p.Ser412=)
c.1237T= (p.Ser413=)
n.756T=
10g.8073926C>ACA375975838GATA3c.1235C>A (p.Ser412Tyr)
c.1238C>A (p.Ser413Tyr)
n.757C>A
 dbSNP
10g.8073926C>GCA375975839GATA3c.1235C>G (p.Ser412Cys)
c.1238C>G (p.Ser413Cys)
n.757C>G
 dbSNP
10g.8073926C>TCA375975840GATA3c.1235C>T (p.Ser412Phe)
c.1238C>T (p.Ser413Phe)
n.757C>T
 dbSNP
10g.8073927dupCA645553637GATA3c.1236dup (p.Ser413GlnfsTer?)
c.1239dup (p.Ser414GlnfsTer?)
n.758dup
 COSMIC COSMIC
10g.8073927C>ACA468401051GATA3c.1236C>A (p.Ser412=)
c.1239C>A (p.Ser413=)
n.758C>A
 dbSNP
10g.8073927C=CA1888996142GATA3c.1236C= (p.Ser412=)
c.1239C= (p.Ser413=)
n.758C=
10g.8073927C>GCA468401050GATA3c.1236C>G (p.Ser412=)
c.1239C>G (p.Ser413=)
n.758C>G
10g.8073927C>TCA468401049GATA3c.1236C>T (p.Ser412=)
c.1239C>T (p.Ser413=)
n.758C>T
 dbSNP gnomAD v4
10g.8073928A=CA1888996144GATA3c.1237A= (p.Ser413=)
c.1240A= (p.Ser414=)
n.759A=
10g.8073928A>CCA375975841GATA3c.1237A>C (p.Ser413Arg)
c.1240A>C (p.Ser414Arg)
n.759A>C
10g.8073928A>GCA5404571GATA3c.1237A>G (p.Ser413Gly)
c.1240A>G (p.Ser414Gly)
n.759A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073928A>TCA375975842GATA3c.1237A>T (p.Ser413Cys)
c.1240A>T (p.Ser414Cys)
n.759A>T
 dbSNP gnomAD v4
10g.8073929G>ACA375975843GATA3c.1238G>A (p.Ser413Asn)
c.1241G>A (p.Ser414Asn)
n.760G>A
 dbSNP gnomAD v4
10g.8073929G>CCA375975844GATA3c.1238G>C (p.Ser413Thr)
c.1241G>C (p.Ser414Thr)
n.760G>C
 dbSNP
10g.8073929G>TCA375975845GATA3c.1238G>T (p.Ser413Ile)
c.1241G>T (p.Ser414Ile)
n.760G>T
10g.8073930C>ACA375975846GATA3c.1239C>A (p.Ser413Arg)
c.1242C>A (p.Ser414Arg)
n.761C>A
 dbSNP
10g.8073930C=CA1888996147GATA3c.1239C= (p.Ser413=)
c.1242C= (p.Ser414=)
n.761C=
10g.8073930C>GCA375975847GATA3c.1239C>G (p.Ser413Arg)
c.1242C>G (p.Ser414Arg)
n.761C>G
 dbSNP
10g.8073930C>TCA5404572GATA3c.1239C>T (p.Ser413=)
c.1242C>T (p.Ser414=)
n.761C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073931dupCA645553638GATA3c.1240dup (p.His414ProfsTer?)
c.1243dup (p.His415ProfsTer?)
n.762dup
 COSMIC COSMIC
10g.8073931C>ACA375975848GATA3c.1240C>A (p.His414Asn)
c.1243C>A (p.His415Asn)
n.762C>A
 dbSNP
10g.8073931C>GCA375975850GATA3c.1240C>G (p.His414Asp)
c.1243C>G (p.His415Asp)
n.762C>G
10g.8073931C>TCA375975849GATA3c.1240C>T (p.His414Tyr)
c.1243C>T (p.His415Tyr)
n.762C>T
 dbSNP gnomAD v4
10g.8073932A>CCA375975851GATA3c.1241A>C (p.His414Pro)
c.1244A>C (p.His415Pro)
n.763A>C
 dbSNP
10g.8073932A>GCA375975853GATA3c.1241A>G (p.His414Arg)
c.1244A>G (p.His415Arg)
n.763A>G
10g.8073932A>TCA375975852GATA3c.1241A>T (p.His414Leu)
c.1244A>T (p.His415Leu)
n.763A>T
 dbSNP
10g.8073933C>ACA375975854GATA3c.1242C>A (p.His414Gln)
c.1245C>A (p.His415Gln)
n.764C>A
10g.8073933C=CA1888996149GATA3c.1242C= (p.His414=)
c.1245C= (p.His415=)
n.764C=
10g.8073933C>GCA375975855GATA3c.1242C>G (p.His414Gln)
c.1245C>G (p.His415Gln)
n.764C>G
 dbSNP
10g.8073933C>TCA5404573GATA3c.1242C>T (p.His414=)
c.1245C>T (p.His415=)
n.764C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073934A=CA1888996151GATA3c.1243A= (p.Met415=)
c.1246A= (p.Met416=)
n.765A=
10g.8073934A>CCA375975856GATA3c.1243A>C (p.Met415Leu)
c.1246A>C (p.Met416Leu)
n.765A>C
10g.8073934A>GCA375975857GATA3c.1243A>G (p.Met415Val)
c.1246A>G (p.Met416Val)
n.765A>G
 dbSNP gnomAD v4
10g.8073934A>TCA375975858GATA3c.1243A>T (p.Met415Leu)
c.1246A>T (p.Met416Leu)
n.765A>T
 dbSNP
10g.8073935T>ACA375975859GATA3c.1244T>A (p.Met415Lys)
c.1247T>A (p.Met416Lys)
n.766T>A
 dbSNP
10g.8073935T>CCA375975860GATA3c.1244T>C (p.Met415Thr)
c.1247T>C (p.Met416Thr)
n.766T>C
 dbSNP gnomAD v4
10g.8073935T>GCA375975861GATA3c.1244T>G (p.Met415Arg)
c.1247T>G (p.Met416Arg)
n.766T>G
 dbSNP
10g.8073935T=CA1888996154GATA3c.1244T= (p.Met415=)
c.1247T= (p.Met416=)
n.766T=
10g.8073936G>ACA375975862GATA3c.1245G>A (p.Met415Ile)
c.1248G>A (p.Met416Ile)
n.767G>A
 dbSNP gnomAD v4
10g.8073936G>CCA375975863GATA3c.1245G>C (p.Met415Ile)
c.1248G>C (p.Met416Ile)
n.767G>C
 dbSNP
10g.8073936G>TCA375975864GATA3c.1245G>T (p.Met415Ile)
c.1248G>T (p.Met416Ile)
n.767G>T
 dbSNP COSMIC
10g.8073937C>ACA375975865GATA3c.1246C>A (p.Leu416Met)
c.1249C>A (p.Leu417Met)
n.768C>A
 dbSNP
10g.8073937C=CA1888996157GATA3c.1246C= (p.Leu416=)
c.1249C= (p.Leu417=)
n.768C=
10g.8073937C>GCA202464327GATA3c.1246C>G (p.Leu416Val)
c.1249C>G (p.Leu417Val)
n.768C>G
 dbSNP
10g.8073937C>TCA468401057GATA3c.1246C>T (p.Leu416=)
c.1249C>T (p.Leu417=)
n.768C>T
 dbSNP
10g.8073938T>ACA375975866GATA3c.1247T>A (p.Leu416Gln)
c.1250T>A (p.Leu417Gln)
n.769T>A
 dbSNP COSMIC
10g.8073938T>CCA375975867GATA3c.1247T>C (p.Leu416Pro)
c.1250T>C (p.Leu417Pro)
n.769T>C
10g.8073938T>GCA375975868GATA3c.1247T>G (p.Leu416Arg)
c.1250T>G (p.Leu417Arg)
n.769T>G
10g.8073939G>ACA468401059GATA3c.1248G>A (p.Leu416=)
c.1251G>A (p.Leu417=)
n.770G>A
 dbSNP
10g.8073939G>CCA468401060GATA3c.1248G>C (p.Leu416=)
c.1251G>C (p.Leu417=)
n.770G>C
 dbSNP
10g.8073939G=CA1888996159GATA3c.1248G= (p.Leu416=)
c.1251G= (p.Leu417=)
n.770G=
10g.8073939G>TCA468401061GATA3c.1248G>T (p.Leu416=)
c.1251G>T (p.Leu417=)
n.770G>T
 dbSNP
10g.8073940A=CA1888996163GATA3c.1249A= (p.Thr417=)
c.1252A= (p.Thr418=)
n.771A=
10g.8073940A>CCA5404574GATA3c.1249A>C (p.Thr417Pro)
c.1252A>C (p.Thr418Pro)
n.771A>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073940A>GCA375975869GATA3c.1249A>G (p.Thr417Ala)
c.1252A>G (p.Thr418Ala)
n.771A>G
 gnomAD v4
10g.8073940A>TCA375975870GATA3c.1249A>T (p.Thr417Ser)
c.1252A>T (p.Thr418Ser)
n.771A>T

Number of alleles fetched