Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.8073781_8073947delCA645553620GATA3c.1090_1256del (p.Arg364HisfsTer?)
c.1093_1259del (p.Arg365HisfsTer?)
n.612_778del
 COSMIC
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
10g.8073941C>ACA375975871GATA3c.1250C>A (p.Thr417Asn)
c.1253C>A (p.Thr418Asn)
n.772C>A
 dbSNP gnomAD v3 gnomAD v4
10g.8073941C=CA1888996168GATA3c.1250C= (p.Thr417=)
c.1253C= (p.Thr418=)
n.772C=
10g.8073941C>GCA375975872GATA3c.1250C>G (p.Thr417Ser)
c.1253C>G (p.Thr418Ser)
n.772C>G
 dbSNP
10g.8073941C>TCA375975873GATA3c.1250C>T (p.Thr417Ile)
c.1253C>T (p.Thr418Ile)
n.772C>T
 dbSNP
10g.8073942dupCA645553639GATA3c.1251dup (p.Thr418HisfsTer?)
c.1254dup (p.Thr419HisfsTer?)
n.773dup
 COSMIC
10g.8073942C>ACA468401065GATA3c.1251C>A (p.Thr417=)
c.1254C>A (p.Thr418=)
n.773C>A
10g.8073942C>GCA468401066GATA3c.1251C>G (p.Thr417=)
c.1254C>G (p.Thr418=)
n.773C>G
 dbSNP
10g.8073942C>TCA468401067GATA3c.1251C>T (p.Thr417=)
c.1254C>T (p.Thr418=)
n.773C>T
 dbSNP COSMIC
10g.8073943A>CCA375975874GATA3c.1252A>C (p.Thr418Pro)
c.1255A>C (p.Thr419Pro)
n.774A>C
 dbSNP
10g.8073943A>GCA375975875GATA3c.1252A>G (p.Thr418Ala)
c.1255A>G (p.Thr419Ala)
n.774A>G
10g.8073943A>TCA375975876GATA3c.1252A>T (p.Thr418Ser)
c.1255A>T (p.Thr419Ser)
n.774A>T
 dbSNP
10g.8073944C>ACA375975878GATA3c.1253C>A (p.Thr418Lys)
c.1256C>A (p.Thr419Lys)
n.775C>A
10g.8073944C=CA1888996173GATA3c.1253C= (p.Thr418=)
c.1256C= (p.Thr419=)
n.775C=
10g.8073944C>GCA375975877GATA3c.1253C>G (p.Thr418Arg)
c.1256C>G (p.Thr419Arg)
n.775C>G
 dbSNP
10g.8073944C>TCA5404575GATA3c.1253C>T (p.Thr418Met)
c.1256C>T (p.Thr419Met)
n.775C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073944dupCA468401070GATA3c.1253dup (p.Pro419AlafsTer?)
c.1256dup (p.Pro420AlafsTer?)
n.775dup
10g.8073945G>ACA5404576GATA3c.1254G>A (p.Thr418=)
c.1257G>A (p.Thr419=)
n.776G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073945G>CCA468401074GATA3c.1254G>C (p.Thr418=)
c.1257G>C (p.Thr419=)
n.776G>C
 dbSNP
10g.8073945G=CA1888996179GATA3c.1254G= (p.Thr418=)
c.1257G= (p.Thr419=)
n.776G=
10g.8073945G>TCA468401075GATA3c.1254G>T (p.Thr418=)
c.1257G>T (p.Thr419=)
n.776G>T
10g.8073946C>ACA375975879GATA3c.1255C>A (p.Pro419Thr)
c.1258C>A (p.Pro420Thr)
n.777C>A
 dbSNP gnomAD v2 gnomAD v4
10g.8073946C=CA1888996183GATA3c.1255C= (p.Pro419=)
c.1258C= (p.Pro420=)
n.777C=
10g.8073946C>GCA375975880GATA3c.1255C>G (p.Pro419Ala)
c.1258C>G (p.Pro420Ala)
n.777C>G
 dbSNP
10g.8073946C>TCA5404577GATA3c.1255C>T (p.Pro419Ser)
c.1258C>T (p.Pro420Ser)
n.777C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073949_8073962delCA645553640GATA3c.1258_1271del (p.Thr420AlafsTer?)
c.1261_1274del (p.Thr421AlafsTer?)
n.780_793del
 COSMIC
10g.8073947C>ACA375975881GATA3c.1256C>A (p.Pro419His)
c.1259C>A (p.Pro420His)
n.778C>A
10g.8073947C>GCA375975882GATA3c.1256C>G (p.Pro419Arg)
c.1259C>G (p.Pro420Arg)
n.778C>G
10g.8073947C>TCA375975883GATA3c.1256C>T (p.Pro419Leu)
c.1259C>T (p.Pro420Leu)
n.778C>T
10g.8073948C>ACA5404578GATA3c.1257C>A (p.Pro419=)
c.1260C>A (p.Pro420=)
n.779C>A
 dbSNP ExAC gnomAD v2
10g.8073948C=CA1888996187GATA3c.1257C= (p.Pro419=)
c.1260C= (p.Pro420=)
n.779C=
10g.8073948C>GCA468401079GATA3c.1257C>G (p.Pro419=)
c.1260C>G (p.Pro420=)
n.779C>G
10g.8073948C>TCA468401080GATA3c.1257C>T (p.Pro419=)
c.1260C>T (p.Pro420=)
n.779C>T
 dbSNP
10g.8073949A>CCA375975884GATA3c.1258A>C (p.Thr420Pro)
c.1261A>C (p.Thr421Pro)
n.780A>C
 dbSNP
10g.8073949A>GCA375975885GATA3c.1258A>G (p.Thr420Ala)
c.1261A>G (p.Thr421Ala)
n.780A>G
 gnomAD v4
10g.8073949A>TCA375975886GATA3c.1258A>T (p.Thr420Ser)
c.1261A>T (p.Thr421Ser)
n.780A>T
 dbSNP
10g.8073949dupCA645553641GATA3c.1258dup (p.Thr420AsnfsTer?)
c.1261dup (p.Thr421AsnfsTer?)
n.780dup
 COSMIC COSMIC
10g.8073950C>ACA375975887GATA3c.1259C>A (p.Thr420Lys)
c.1262C>A (p.Thr421Lys)
n.781C>A
10g.8073950C=CA1888996192GATA3c.1259C= (p.Thr420=)
c.1262C= (p.Thr421=)
n.781C=
10g.8073950C>GCA375975888GATA3c.1259C>G (p.Thr420Arg)
c.1262C>G (p.Thr421Arg)
n.781C>G
 dbSNP gnomAD v3 gnomAD v4
10g.8073950C>TCA5404579GATA3c.1259C>T (p.Thr420Met)
c.1262C>T (p.Thr421Met)
n.781C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.8073951G>ACA5404580GATA3c.1260G>A (p.Thr420=)
c.1263G>A (p.Thr421=)
n.782G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073951G>CCA468401085GATA3c.1260G>C (p.Thr420=)
c.1263G>C (p.Thr421=)
n.782G>C
 dbSNP
10g.8073951G=CA1888996195GATA3c.1260G= (p.Thr420=)
c.1263G= (p.Thr421=)
n.782G=
10g.8073951G>TCA468401084GATA3c.1260G>T (p.Thr420=)
c.1263G>T (p.Thr421=)
n.782G>T
10g.8073952C>ACA375975889GATA3c.1261C>A (p.Pro421Thr)
c.1264C>A (p.Pro422Thr)
n.783C>A
 dbSNP
10g.8073952C=CA1888996198GATA3c.1261C= (p.Pro421=)
c.1264C= (p.Pro422=)
n.783C=
10g.8073952C>GCA375975890GATA3c.1261C>G (p.Pro421Ala)
c.1264C>G (p.Pro422Ala)
n.783C>G
 dbSNP
10g.8073952C>TCA375975891GATA3c.1261C>T (p.Pro421Ser)
c.1264C>T (p.Pro422Ser)
n.783C>T
 dbSNP gnomAD v3 gnomAD v4
10g.8073953C>ACA375975892GATA3c.1262C>A (p.Pro421Gln)
c.1265C>A (p.Pro422Gln)
n.784C>A
10g.8073953C=CA1888996202GATA3c.1262C= (p.Pro421=)
c.1265C= (p.Pro422=)
n.784C=
10g.8073953C>GCA375975893GATA3c.1262C>G (p.Pro421Arg)
c.1265C>G (p.Pro422Arg)
n.784C>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.8073953C>TCA5404581GATA3c.1262C>T (p.Pro421Leu)
c.1265C>T (p.Pro422Leu)
n.784C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073954G>ACA5404582GATA3c.1263G>A (p.Pro421=)
c.1266G>A (p.Pro422=)
n.785G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.8073954G>CCA468401090GATA3c.1263G>C (p.Pro421=)
c.1266G>C (p.Pro422=)
n.785G>C
 dbSNP
10g.8073954G=CA1888996206GATA3c.1263G= (p.Pro421=)
c.1266G= (p.Pro422=)
n.785G=
10g.8073954G>TCA468401091GATA3c.1263G>T (p.Pro421=)
c.1266G>T (p.Pro422=)
n.785G>T
 COSMIC
10g.8073955A>CCA375975894GATA3c.1264A>C (p.Met422Leu)
c.1267A>C (p.Met423Leu)
n.786A>C
 dbSNP
10g.8073955A>GCA375975895GATA3c.1264A>G (p.Met422Val)
c.1267A>G (p.Met423Val)
n.786A>G
 dbSNP
10g.8073955A>TCA375975896GATA3c.1264A>T (p.Met422Leu)
c.1267A>T (p.Met423Leu)
n.786A>T
 dbSNP
10g.8073956T>ACA375975897GATA3c.1265T>A (p.Met422Lys)
c.1268T>A (p.Met423Lys)
n.787T>A
 dbSNP
10g.8073956T>CCA375975898GATA3c.1265T>C (p.Met422Thr)
c.1268T>C (p.Met423Thr)
n.787T>C
 gnomAD v4
10g.8073956T>GCA375975899GATA3c.1265T>G (p.Met422Arg)
c.1268T>G (p.Met423Arg)
n.787T>G
 dbSNP
10g.8073957G>ACA375975900GATA3c.1266G>A (p.Met422Ile)
c.1269G>A (p.Met423Ile)
n.788G>A
 dbSNP
10g.8073957G>CCA375975902GATA3c.1266G>C (p.Met422Ile)
c.1269G>C (p.Met423Ile)
n.788G>C
 dbSNP
10g.8073957G>TCA375975901GATA3c.1266G>T (p.Met422Ile)
c.1269G>T (p.Met423Ile)
n.788G>T
10g.8073957dupCA645553643GATA3c.1266dup (p.His423AlafsTer?)
c.1269dup (p.His424AlafsTer?)
n.788dup
 COSMIC COSMIC
10g.8073957_8073963delCA645553642GATA3c.1266_1272del (p.Met422IlefsTer?)
c.1269_1275del (p.Met423IlefsTer?)
n.788_794del
 COSMIC
10g.8073958C>ACA375975903GATA3c.1267C>A (p.His423Asn)
c.1270C>A (p.His424Asn)
n.789C>A
 dbSNP
10g.8073958C>GCA375975905GATA3c.1267C>G (p.His423Asp)
c.1270C>G (p.His424Asp)
n.789C>G
 dbSNP
10g.8073958C>TCA375975904GATA3c.1267C>T (p.His423Tyr)
c.1270C>T (p.His424Tyr)
n.789C>T
 dbSNP
10g.8073959_8073962dupCA645553644GATA3c.1268_1271dup (p.Ser426AlafsTer?)
c.1271_1274dup (p.Ser427AlafsTer?)
n.790_793dup
 COSMIC
10g.8073959A=CA1888996210GATA3c.1268A= (p.His423=)
c.1271A= (p.His424=)
n.790A=
10g.8073959A>CCA375975906GATA3c.1268A>C (p.His423Pro)
c.1271A>C (p.His424Pro)
n.790A>C
 dbSNP
10g.8073959A>GCA375975908GATA3c.1268A>G (p.His423Arg)
c.1271A>G (p.His424Arg)
n.790A>G
 dbSNP
10g.8073959A>TCA375975907GATA3c.1268A>T (p.His423Leu)
c.1271A>T (p.His424Leu)
n.790A>T
 dbSNP
10g.8073960C>ACA375975909GATA3c.1269C>A (p.His423Gln)
c.1272C>A (p.His424Gln)
n.791C>A
 dbSNP
10g.8073960C=CA1888996214GATA3c.1269C= (p.His423=)
c.1272C= (p.His424=)
n.791C=
10g.8073960C>GCA375975910GATA3c.1269C>G (p.His423Gln)
c.1272C>G (p.His424Gln)
n.791C>G
 dbSNP
10g.8073960C>TCA5404583GATA3c.1269C>T (p.His423=)
c.1272C>T (p.His424=)
n.791C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073962dupCA468401099GATA3c.1271dup (p.Pro425AlafsTer?)
c.1274dup (p.Pro426AlafsTer?)
n.793dup
10g.8073962_8073965dupCA645553645GATA3c.1271_1274dup (p.Ser426AlafsTer?)
c.1274_1277dup (p.Ser427AlafsTer?)
n.793_796dup
 COSMIC
10g.8073961C>ACA375975911GATA3c.1270C>A (p.Pro424Thr)
c.1273C>A (p.Pro425Thr)
n.792C>A
10g.8073961C>GCA375975912GATA3c.1270C>G (p.Pro424Ala)
c.1273C>G (p.Pro425Ala)
n.792C>G
10g.8073961C>TCA375975913GATA3c.1270C>T (p.Pro424Ser)
c.1273C>T (p.Pro425Ser)
n.792C>T
 gnomAD v4
10g.8073962C>ACA375975914GATA3c.1271C>A (p.Pro424Gln)
c.1274C>A (p.Pro425Gln)
n.793C>A
 dbSNP
10g.8073962C=CA1888996220GATA3c.1271C= (p.Pro424=)
c.1274C= (p.Pro425=)
n.793C=
10g.8073962C>GCA375975915GATA3c.1271C>G (p.Pro424Arg)
c.1274C>G (p.Pro425Arg)
n.793C>G
 dbSNP
10g.8073962C>TCA375975916GATA3c.1271C>T (p.Pro424Leu)
c.1274C>T (p.Pro425Leu)
n.793C>T
 dbSNP gnomAD v3 gnomAD v4
10g.8073963G>ACA5404584GATA3c.1272G>A (p.Pro424=)
c.1275G>A (p.Pro425=)
n.794G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073963G>CCA468401102GATA3c.1272G>C (p.Pro424=)
c.1275G>C (p.Pro425=)
n.794G>C
 dbSNP
10g.8073963G=CA1888996223GATA3c.1272G= (p.Pro424=)
c.1275G= (p.Pro425=)
n.794G=
10g.8073963G>TCA468401105GATA3c.1272G>T (p.Pro424=)
c.1275G>T (p.Pro425=)
n.794G>T
10g.8073964C>ACA375975919GATA3c.1273C>A (p.Pro425Thr)
c.1276C>A (p.Pro426Thr)
n.795C>A
 dbSNP gnomAD v4
10g.8073964C=CA1888996225GATA3c.1273C= (p.Pro425=)
c.1276C= (p.Pro426=)
n.795C=
10g.8073964C>GCA375975917GATA3c.1273C>G (p.Pro425Ala)
c.1276C>G (p.Pro426Ala)
n.795C>G
 dbSNP
10g.8073964C>TCA375975918GATA3c.1273C>T (p.Pro425Ser)
c.1276C>T (p.Pro426Ser)
n.795C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.8073965dupCA468401107GATA3c.1274dup (p.Ser426IlefsTer?)
c.1277dup (p.Ser427IlefsTer?)
n.796dup
10g.8073965C>ACA375975920GATA3c.1274C>A (p.Pro425Gln)
c.1277C>A (p.Pro426Gln)
n.796C>A
10g.8073965C>GCA375975921GATA3c.1274C>G (p.Pro425Arg)
c.1277C>G (p.Pro426Arg)
n.796C>G
 dbSNP
10g.8073965C>TCA375975922GATA3c.1274C>T (p.Pro425Leu)
c.1277C>T (p.Pro426Leu)
n.796C>T
 dbSNP
10g.8073966A>CCA468401112GATA3c.1275A>C (p.Pro425=)
c.1278A>C (p.Pro426=)
n.797A>C
 dbSNP
10g.8073966A>GCA468401115GATA3c.1275A>G (p.Pro425=)
c.1278A>G (p.Pro426=)
n.797A>G
 dbSNP
10g.8073966A>TCA468401110GATA3c.1275A>T (p.Pro425=)
c.1278A>T (p.Pro426=)
n.797A>T
 dbSNP
10g.8073966dupCA645553646GATA3c.1275dup (p.Ser426IlefsTer?)
c.1278dup (p.Ser427IlefsTer?)
n.797dup
 COSMIC COSMIC
10g.8073966_8073967dupCA645553647GATA3c.1275_1276dup (p.Ser426TyrfsTer?)
c.1278_1279dup (p.Ser427TyrfsTer?)
n.797_798dup
 COSMIC
10g.8073967T>ACA375975923GATA3c.1276T>A (p.Ser426Thr)
c.1279T>A (p.Ser427Thr)
n.798T>A
10g.8073967T>CCA375975924GATA3c.1276T>C (p.Ser426Pro)
c.1279T>C (p.Ser427Pro)
n.798T>C
10g.8073967T>GCA375975925GATA3c.1276T>G (p.Ser426Ala)
c.1279T>G (p.Ser427Ala)
n.798T>G
10g.8073967_8073977delCA645553648GATA3c.1276_1286del (p.Ser426LeufsTer?)
c.1279_1289del (p.Ser427LeufsTer?)
n.798_808del
 COSMIC
10g.8073968C>ACA375975926GATA3c.1277C>A (p.Ser426Tyr)
c.1280C>A (p.Ser427Tyr)
n.799C>A
 dbSNP
10g.8073968C>GCA375975927GATA3c.1277C>G (p.Ser426Cys)
c.1280C>G (p.Ser427Cys)
n.799C>G
 dbSNP gnomAD v4
10g.8073968C>TCA375975928GATA3c.1277C>T (p.Ser426Phe)
c.1280C>T (p.Ser427Phe)
n.799C>T
 dbSNP COSMIC
10g.8073969dupCA468401119GATA3c.1278dup (p.Ser427GlnfsTer?)
c.1281dup (p.Ser428GlnfsTer?)
n.800dup
10g.8073969C>ACA468401120GATA3c.1278C>A (p.Ser426=)
c.1281C>A (p.Ser427=)
n.800C>A
 dbSNP
10g.8073969C=CA1888996231GATA3c.1278C= (p.Ser426=)
c.1281C= (p.Ser427=)
n.800C=
10g.8073969C>GCA468401121GATA3c.1278C>G (p.Ser426=)
c.1281C>G (p.Ser427=)
n.800C>G
 dbSNP
10g.8073969C>TCA5404585GATA3c.1278C>T (p.Ser426=)
c.1281C>T (p.Ser427=)
n.800C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.8073970A>CCA375975930GATA3c.1279A>C (p.Ser427Arg)
c.1282A>C (p.Ser428Arg)
n.801A>C
10g.8073970A>GCA375975931GATA3c.1279A>G (p.Ser427Gly)
c.1282A>G (p.Ser428Gly)
n.801A>G
 dbSNP
10g.8073970A>TCA375975929GATA3c.1279A>T (p.Ser427Cys)
c.1282A>T (p.Ser428Cys)
n.801A>T
 dbSNP
10g.8073971G>ACA375975932GATA3c.1280G>A (p.Ser427Asn)
c.1283G>A (p.Ser428Asn)
n.802G>A
 dbSNP
10g.8073971G>CCA375975933GATA3c.1280G>C (p.Ser427Thr)
c.1283G>C (p.Ser428Thr)
n.802G>C
 dbSNP
10g.8073971G>TCA375975934GATA3c.1280G>T (p.Ser427Ile)
c.1283G>T (p.Ser428Ile)
n.802G>T
 dbSNP COSMIC
10g.8073972C>ACA375975935GATA3c.1281C>A (p.Ser427Arg)
c.1284C>A (p.Ser428Arg)
n.803C>A
 dbSNP
10g.8073972C=CA1888996234GATA3c.1281C= (p.Ser427=)
c.1284C= (p.Ser428=)
n.803C=
10g.8073972C>GCA375975936GATA3c.1281C>G (p.Ser427Arg)
c.1284C>G (p.Ser428Arg)
n.803C>G
 dbSNP
10g.8073972C>TCA468401123GATA3c.1281C>T (p.Ser427=)
c.1284C>T (p.Ser428=)
n.803C>T
 dbSNP
10g.8073973C>ACA375975937GATA3c.1282C>A (p.Leu428Met)
c.1285C>A (p.Leu429Met)
n.804C>A
 dbSNP
10g.8073973C=CA1888996238GATA3c.1282C= (p.Leu428=)
c.1285C= (p.Leu429=)
n.804C=
10g.8073973C>GCA375975938GATA3c.1282C>G (p.Leu428Val)
c.1285C>G (p.Leu429Val)
n.804C>G
 dbSNP
10g.8073973C>TCA5404586GATA3c.1282C>T (p.Leu428=)
c.1285C>T (p.Leu429=)
n.804C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.8073974T>ACA375975939GATA3c.1283T>A (p.Leu428Gln)
c.1286T>A (p.Leu429Gln)
n.805T>A
 dbSNP
10g.8073974T>CCA375975940GATA3c.1283T>C (p.Leu428Pro)
c.1286T>C (p.Leu429Pro)
n.805T>C
 dbSNP
10g.8073974T>GCA375975941GATA3c.1283T>G (p.Leu428Arg)
c.1286T>G (p.Leu429Arg)
n.805T>G
 dbSNP
10g.8073975G>ACA468401124GATA3c.1284G>A (p.Leu428=)
c.1287G>A (p.Leu429=)
n.806G>A
 dbSNP
10g.8073975G>CCA468401125GATA3c.1284G>C (p.Leu428=)
c.1287G>C (p.Leu429=)
n.806G>C
 dbSNP
10g.8073975G>TCA468401126GATA3c.1284G>T (p.Leu428=)
c.1287G>T (p.Leu429=)
n.806G>T
 COSMIC
10g.8073976T>ACA375975943GATA3c.1285T>A (p.Ser429Thr)
c.1288T>A (p.Ser430Thr)
n.807T>A
 dbSNP
10g.8073976T>CCA375975944GATA3c.1285T>C (p.Ser429Pro)
c.1288T>C (p.Ser430Pro)
n.807T>C
 dbSNP
10g.8073976T>GCA375975942GATA3c.1285T>G (p.Ser429Ala)
c.1288T>G (p.Ser430Ala)
n.807T>G
 dbSNP
10g.8073977C>ACA375975945GATA3c.1286C>A (p.Ser429Tyr)
c.1289C>A (p.Ser430Tyr)
n.808C>A
 dbSNP
10g.8073977C>GCA375975946GATA3c.1286C>G (p.Ser429Cys)
c.1289C>G (p.Ser430Cys)
n.808C>G
 dbSNP gnomAD v4
10g.8073977C>TCA375975947GATA3c.1286C>T (p.Ser429Phe)
c.1289C>T (p.Ser430Phe)
n.808C>T
 dbSNP
10g.8073978C>ACA468401130GATA3c.1287C>A (p.Ser429=)
c.1290C>A (p.Ser430=)
n.809C>A
 dbSNP gnomAD v4
10g.8073978C>GCA468401131GATA3c.1287C>G (p.Ser429=)
c.1290C>G (p.Ser430=)
n.809C>G
 dbSNP
10g.8073978C>TCA468401132GATA3c.1287C>T (p.Ser429=)
c.1290C>T (p.Ser430=)
n.809C>T
 dbSNP
10g.8073979T>ACA375975948GATA3c.1288T>A (p.Phe430Ile)
c.1291T>A (p.Phe431Ile)
n.810T>A
 dbSNP
10g.8073979T>CCA375975949GATA3c.1288T>C (p.Phe430Leu)
c.1291T>C (p.Phe431Leu)
n.810T>C
 dbSNP gnomAD v4
10g.8073979T>GCA375975950GATA3c.1288T>G (p.Phe430Val)
c.1291T>G (p.Phe431Val)
n.810T>G
10g.8073981dupCA468401136GATA3c.1290dup (p.Gly431TrpfsTer?)
c.1293dup (p.Gly432TrpfsTer?)
n.812dup
10g.8073980_8073981delCA645553649GATA3c.1289_1290del (p.Phe430TrpfsTer?)
c.1292_1293del (p.Phe431TrpfsTer?)
n.811_812del
 COSMIC
10g.8073980T>ACA375975951GATA3c.1289T>A (p.Phe430Tyr)
c.1292T>A (p.Phe431Tyr)
n.811T>A
 dbSNP
10g.8073980T>CCA375975953GATA3c.1289T>C (p.Phe430Ser)
c.1292T>C (p.Phe431Ser)
n.811T>C
 dbSNP
10g.8073980T>GCA375975952GATA3c.1289T>G (p.Phe430Cys)
c.1292T>G (p.Phe431Cys)
n.811T>G
10g.8073981T>ACA375975954GATA3c.1290T>A (p.Phe430Leu)
c.1293T>A (p.Phe431Leu)
n.812T>A
10g.8073981T>CCA468401138GATA3c.1290T>C (p.Phe430=)
c.1293T>C (p.Phe431=)
n.812T>C
10g.8073981T>GCA375975955GATA3c.1290T>G (p.Phe430Leu)
c.1293T>G (p.Phe431Leu)
n.812T>G
10g.8073982G>ACA202464399GATA3c.1291G>A (p.Gly431Arg)
c.1294G>A (p.Gly432Arg)
n.813G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.8073982G>CCA375975956GATA3c.1291G>C (p.Gly431Arg)
c.1294G>C (p.Gly432Arg)
n.813G>C
 dbSNP
10g.8073982G=CA1888996253GATA3c.1291G= (p.Gly431=)
c.1294G= (p.Gly432=)
n.813G=
10g.8073982G>TCA375975957GATA3c.1291G>T (p.Gly431Ter)
c.1294G>T (p.Gly432Ter)
n.813G>T
 dbSNP gnomAD v4
10g.8073983dupCA645553650GATA3c.1292dup (p.Pro432ThrfsTer?)
c.1295dup (p.Pro433ThrfsTer?)
n.814dup
 COSMIC COSMIC
10g.8073983G>ACA202464403GATA3c.1292G>A (p.Gly431Glu)
c.1295G>A (p.Gly432Glu)
n.814G>A
 dbSNP gnomAD v3 gnomAD v4
10g.8073983G>CCA375975959GATA3c.1292G>C (p.Gly431Ala)
c.1295G>C (p.Gly432Ala)
n.814G>C
 dbSNP
10g.8073983G=CA1888996254GATA3c.1292G= (p.Gly431=)
c.1295G= (p.Gly432=)
n.814G=
10g.8073983G>TCA375975958GATA3c.1292G>T (p.Gly431Val)
c.1295G>T (p.Gly432Val)
n.814G>T
 dbSNP
10g.8073984A>CCA468401141GATA3c.1293A>C (p.Gly431=)
c.1296A>C (p.Gly432=)
n.815A>C
10g.8073984A>GCA468401143GATA3c.1293A>G (p.Gly431=)
c.1296A>G (p.Gly432=)
n.815A>G
10g.8073984A>TCA468401142GATA3c.1293A>T (p.Gly431=)
c.1296A>T (p.Gly432=)
n.815A>T
10g.8073984_8073985insGCA468401144GATA3c.1293_1294insG (p.Pro432AlafsTer?)
c.1296_1297insG (p.Pro433AlafsTer?)
n.815_816insG
10g.8073985C>ACA375975962GATA3c.1294C>A (p.Pro432Thr)
c.1297C>A (p.Pro433Thr)
n.816C>A
10g.8073985C=CA1888996255GATA3c.1294C= (p.Pro432=)
c.1297C= (p.Pro433=)
n.816C=
10g.8073985C>GCA375975960GATA3c.1294C>G (p.Pro432Ala)
c.1297C>G (p.Pro433Ala)
n.816C>G
10g.8073985C>TCA375975961GATA3c.1294C>T (p.Pro432Ser)
c.1297C>T (p.Pro433Ser)
n.816C>T
 dbSNP gnomAD v4
10g.8073986C>ACA375975963GATA3c.1295C>A (p.Pro432Gln)
c.1298C>A (p.Pro433Gln)
n.817C>A
10g.8073986C>GCA375975964GATA3c.1295C>G (p.Pro432Arg)
c.1298C>G (p.Pro433Arg)
n.817C>G
10g.8073986C>TCA375975965GATA3c.1295C>T (p.Pro432Leu)
c.1298C>T (p.Pro433Leu)
n.817C>T
 dbSNP
10g.8073987A>CCA468401146GATA3c.1296A>C (p.Pro432=)
c.1299A>C (p.Pro433=)
n.818A>C
 dbSNP
10g.8073987A>GCA468401147GATA3c.1296A>G (p.Pro432=)
c.1299A>G (p.Pro433=)
n.818A>G
 dbSNP
10g.8073987A>TCA468401148GATA3c.1296A>T (p.Pro432=)
c.1299A>T (p.Pro433=)
n.818A>T
 dbSNP
10g.8073988C>ACA375975966GATA3c.1297C>A (p.His433Asn)
c.1300C>A (p.His434Asn)
n.819C>A
 dbSNP
10g.8073988C>GCA375975967GATA3c.1297C>G (p.His433Asp)
c.1300C>G (p.His434Asp)
n.819C>G
 dbSNP
10g.8073988C>TCA375975968GATA3c.1297C>T (p.His433Tyr)
c.1300C>T (p.His434Tyr)
n.819C>T
 dbSNP gnomAD v4
10g.8073992_8074011delCA645553651GATA3c.1301_1320del (p.His434ArgfsTer?)
c.1304_1323del (p.His435ArgfsTer?)
n.823_842del
 COSMIC
10g.8073989A>CCA375975969GATA3c.1298A>C (p.His433Pro)
c.1301A>C (p.His434Pro)
n.820A>C
10g.8073989A>GCA375975970GATA3c.1298A>G (p.His433Arg)
c.1301A>G (p.His434Arg)
n.820A>G
10g.8073989A>TCA375975971GATA3c.1298A>T (p.His433Leu)
c.1301A>T (p.His434Leu)
n.820A>T
10g.8073990C>ACA375975972GATA3c.1299C>A (p.His433Gln)
c.1302C>A (p.His434Gln)
n.821C>A
10g.8073990C>GCA375975973GATA3c.1299C>G (p.His433Gln)
c.1302C>G (p.His434Gln)
n.821C>G
10g.8073990C>TCA468401149GATA3c.1299C>T (p.His433=)
c.1302C>T (p.His434=)
n.821C>T
 gnomAD v4
10g.8073991dupCA468401151GATA3c.1300dup (p.His434ProfsTer?)
c.1303dup (p.His435ProfsTer?)
n.822dup
 COSMIC
10g.8073990_8073991dupCA645553652GATA3c.1299_1300dup (p.His434ProfsTer?)
c.1302_1303dup (p.His435ProfsTer?)
n.821_822dup
 COSMIC
10g.8073991C>ACA375975974GATA3c.1300C>A (p.His434Asn)
c.1303C>A (p.His435Asn)
n.822C>A
 dbSNP
10g.8073991C>GCA375975976GATA3c.1300C>G (p.His434Asp)
c.1303C>G (p.His435Asp)
n.822C>G
 dbSNP
10g.8073991C>TCA375975975GATA3c.1300C>T (p.His434Tyr)
c.1303C>T (p.His435Tyr)
n.822C>T
 dbSNP
10g.8073992delCA645553653GATA3c.1301del (p.His434ProfsTer?)
c.1304del (p.His435ProfsTer?)
n.823del
 COSMIC
10g.8073992A>CCA375975977GATA3c.1301A>C (p.His434Pro)
c.1304A>C (p.His435Pro)
n.823A>C
10g.8073992A>GCA375975978GATA3c.1301A>G (p.His434Arg)
c.1304A>G (p.His435Arg)
n.823A>G
10g.8073992A>TCA375975979GATA3c.1301A>T (p.His434Leu)
c.1304A>T (p.His435Leu)
n.823A>T
 dbSNP gnomAD v4
10g.8073993C>ACA375975980GATA3c.1302C>A (p.His434Gln)
c.1305C>A (p.His435Gln)
n.824C>A
 gnomAD v4
10g.8073993C>GCA375975981GATA3c.1302C>G (p.His434Gln)
c.1305C>G (p.His435Gln)
n.824C>G
 dbSNP gnomAD v4
10g.8073993C>TCA468401155GATA3c.1302C>T (p.His434=)
c.1305C>T (p.His435=)
n.824C>T
10g.8073996dupCA468401156GATA3c.1305dup (p.Ser436LeufsTer?)
c.1308dup (p.Ser437LeufsTer?)
n.827dup
 COSMIC COSMIC
10g.8073995_8073996dupCA645553654GATA3c.1304_1305dup (p.Ser436ProfsTer?)
c.1307_1308dup (p.Ser437ProfsTer?)
n.826_827dup
 COSMIC COSMIC
10g.8073994_8073996dupCA645553655GATA3c.1303_1305dup (p.Pro435_Ser436insPro)
c.1306_1308dup (p.Pro436_Ser437insPro)
n.825_827dup
 COSMIC
10g.8073996delCA2721006322GATA3c.1305del (p.Ser436ProfsTer?)
c.1308del (p.Ser437ProfsTer?)
n.827del
 dbSNP
10g.8073994C>ACA375975982GATA3c.1303C>A (p.Pro435Thr)
c.1306C>A (p.Pro436Thr)
n.825C>A
 dbSNP gnomAD v4
10g.8073994C=CA1888996256GATA3c.1303C= (p.Pro435=)
c.1306C= (p.Pro436=)
n.825C=
10g.8073994C>GCA375975983GATA3c.1303C>G (p.Pro435Ala)
c.1306C>G (p.Pro436Ala)
n.825C>G
 ClinVar dbSNP gnomAD v4
10g.8073994C>TCA375975984GATA3c.1303C>T (p.Pro435Ser)
c.1306C>T (p.Pro436Ser)
n.825C>T
 dbSNP gnomAD v4 COSMIC
10g.8073995C>ACA375975985GATA3c.1304C>A (p.Pro435His)
c.1307C>A (p.Pro436His)
n.826C>A
 dbSNP
10g.8073995C>GCA375975986GATA3c.1304C>G (p.Pro435Arg)
c.1307C>G (p.Pro436Arg)
n.826C>G
 dbSNP COSMIC
10g.8073995C>TCA375975987GATA3c.1304C>T (p.Pro435Leu)
c.1307C>T (p.Pro436Leu)
n.826C>T
 dbSNP
10g.8073996C>ACA468401161GATA3c.1305C>A (p.Pro435=)
c.1308C>A (p.Pro436=)
n.827C>A
 dbSNP
10g.8073996C>GCA468401162GATA3c.1305C>G (p.Pro435=)
c.1308C>G (p.Pro436=)
n.827C>G
 dbSNP
10g.8073996C>TCA468401159GATA3c.1305C>T (p.Pro435=)
c.1308C>T (p.Pro436=)
n.827C>T
10g.8073997T>ACA375975989GATA3c.1306T>A (p.Ser436Thr)
c.1309T>A (p.Ser437Thr)
n.828T>A
10g.8073997T>CCA375975990GATA3c.1306T>C (p.Ser436Pro)
c.1309T>C (p.Ser437Pro)
n.828T>C
10g.8073997T>GCA375975988GATA3c.1306T>G (p.Ser436Ala)
c.1309T>G (p.Ser437Ala)
n.828T>G
10g.8073998C>ACA375975991GATA3c.1307C>A (p.Ser436Tyr)
c.1310C>A (p.Ser437Tyr)
n.829C>A
 dbSNP
10g.8073998C>GCA375975992GATA3c.1307C>G (p.Ser436Cys)
c.1310C>G (p.Ser437Cys)
n.829C>G
 dbSNP
10g.8073998C>TCA375975993GATA3c.1307C>T (p.Ser436Phe)
c.1310C>T (p.Ser437Phe)
n.829C>T
 dbSNP gnomAD v4
10g.8073999dupCA645553656GATA3c.1308dup (p.Ser437GlnfsTer?)
c.1311dup (p.Ser438GlnfsTer?)
n.830dup
 COSMIC
10g.8073999C>ACA468401163GATA3c.1308C>A (p.Ser436=)
c.1311C>A (p.Ser437=)
n.830C>A
10g.8073999C>GCA468401165GATA3c.1308C>G (p.Ser436=)
c.1311C>G (p.Ser437=)
n.830C>G
 dbSNP
10g.8073999C>TCA468401164GATA3c.1308C>T (p.Ser436=)
c.1311C>T (p.Ser437=)
n.830C>T
 dbSNP gnomAD v4
10g.8074000A>CCA375975994GATA3c.1309A>C (p.Ser437Arg)
c.1312A>C (p.Ser438Arg)
n.831A>C
10g.8074000A>GCA375975995GATA3c.1309A>G (p.Ser437Gly)
c.1312A>G (p.Ser438Gly)
n.831A>G
10g.8074000A>TCA375975996GATA3c.1309A>T (p.Ser437Cys)
c.1312A>T (p.Ser438Cys)
n.831A>T
10g.8074000_8074004dupCA645553657GATA3c.1309_1313dup (p.Met438IlefsTer?)
c.1312_1316dup (p.Met439IlefsTer?)
n.831_835dup
 COSMIC COSMIC
10g.8074000_8074001insAGCATCA645553658GATA3c.1309_1310insAGCAT (p.Ser437LysfsTer?)
c.1312_1313insAGCAT (p.Ser438LysfsTer?)
n.831_832insAGCAT
 COSMIC
10g.8074001G>ACA375976002GATA3c.1310G>A (p.Ser437Asn)
c.1313G>A (p.Ser438Asn)
n.832G>A
 dbSNP
10g.8074001G>CCA375975997GATA3c.1310G>C (p.Ser437Thr)
c.1313G>C (p.Ser438Thr)
n.832G>C
 dbSNP
10g.8074001G>TCA375976000GATA3c.1310G>T (p.Ser437Ile)
c.1313G>T (p.Ser438Ile)
n.832G>T
10g.8074002C>ACA375976003GATA3c.1311C>A (p.Ser437Arg)
c.1314C>A (p.Ser438Arg)
n.833C>A
10g.8074002C>GCA375976005GATA3c.1311C>G (p.Ser437Arg)
c.1314C>G (p.Ser438Arg)
n.833C>G
 dbSNP
10g.8074002C>TCA468401167GATA3c.1311C>T (p.Ser437=)
c.1314C>T (p.Ser438=)
n.833C>T
 dbSNP
10g.8074003A>CCA375976016GATA3c.1312A>C (p.Met438Leu)
c.1315A>C (p.Met439Leu)
n.834A>C
 dbSNP
10g.8074003A>GCA375976018GATA3c.1312A>G (p.Met438Val)
c.1315A>G (p.Met439Val)
n.834A>G
 dbSNP
10g.8074003A>TCA375976020GATA3c.1312A>T (p.Met438Leu)
c.1315A>T (p.Met439Leu)
n.834A>T
 dbSNP
10g.8074003dupCA468401170GATA3c.1312dup (p.Met438AsnfsTer?)
c.1315dup (p.Met439AsnfsTer?)
n.834dup
10g.8074004T>ACA375976023GATA3c.1313T>A (p.Met438Lys)
c.1316T>A (p.Met439Lys)
n.835T>A
10g.8074004T>CCA375976027GATA3c.1313T>C (p.Met438Thr)
c.1316T>C (p.Met439Thr)
n.835T>C
10g.8074004T>GCA375976025GATA3c.1313T>G (p.Met438Arg)
c.1316T>G (p.Met439Arg)
n.835T>G
10g.8074005G>ACA375976029GATA3c.1314G>A (p.Met438Ile)
c.1317G>A (p.Met439Ile)
n.836G>A
 dbSNP
10g.8074005G>CCA375976031GATA3c.1314G>C (p.Met438Ile)
c.1317G>C (p.Met439Ile)
n.836G>C
 dbSNP
10g.8074005G>TCA375976033GATA3c.1314G>T (p.Met438Ile)
c.1317G>T (p.Met439Ile)
n.836G>T
10g.8074006G>ACA375976035GATA3c.1315G>A (p.Val439Ile)
c.1318G>A (p.Val440Ile)
n.837G>A
 dbSNP gnomAD v4
10g.8074006G>CCA375976036GATA3c.1315G>C (p.Val439Leu)
c.1318G>C (p.Val440Leu)
n.837G>C
 dbSNP
10g.8074006G>TCA375976037GATA3c.1315G>T (p.Val439Phe)
c.1318G>T (p.Val440Phe)
n.837G>T
 dbSNP
10g.8074007T>ACA375976040GATA3c.1316T>A (p.Val439Asp)
c.1319T>A (p.Val440Asp)
n.838T>A
 dbSNP
10g.8074007T>CCA375976042GATA3c.1316T>C (p.Val439Ala)
c.1319T>C (p.Val440Ala)
n.838T>C
 dbSNP
10g.8074007T>GCA375976043GATA3c.1316T>G (p.Val439Gly)
c.1319T>G (p.Val440Gly)
n.838T>G
10g.8074008C>ACA468200796GATA3c.1317C>A (p.Val439=)
c.1320C>A (p.Val440=)
n.839C>A
 dbSNP
10g.8074008C>GCA468200798GATA3c.1317C>G (p.Val439=)
c.1320C>G (p.Val440=)
n.839C>G
 dbSNP
10g.8074008C>TCA468200800GATA3c.1317C>T (p.Val439=)
c.1320C>T (p.Val440=)
n.839C>T
 dbSNP
10g.8074008_8074022delCA645553659GATA3c.1317_1331del (p.Thr440_Ter444del)
c.1320_1334del (p.Thr441_Ter445del)
n.839_853del
 COSMIC
10g.8074009A>CCA375976046GATA3c.1318A>C (p.Thr440Pro)
c.1321A>C (p.Thr441Pro)
n.840A>C
 dbSNP
10g.8074009A>GCA375976048GATA3c.1318A>G (p.Thr440Ala)
c.1321A>G (p.Thr441Ala)
n.840A>G
 dbSNP
10g.8074009A>TCA375976049GATA3c.1318A>T (p.Thr440Ser)
c.1321A>T (p.Thr441Ser)
n.840A>T
 dbSNP
10g.8074010C>ACA375976052GATA3c.1319C>A (p.Thr440Asn)
c.1322C>A (p.Thr441Asn)
n.841C>A
 dbSNP
10g.8074010C>GCA375976055GATA3c.1319C>G (p.Thr440Ser)
c.1322C>G (p.Thr441Ser)
n.841C>G
 dbSNP
10g.8074010C>TCA375976053GATA3c.1319C>T (p.Thr440Ile)
c.1322C>T (p.Thr441Ile)
n.841C>T
 dbSNP
10g.8074011_8074014delCA645553660GATA3c.1320_1323del (p.Ala441TrpfsTer?)
c.1323_1326del (p.Ala442TrpfsTer?)
n.842_845del
 COSMIC
10g.8074011C>ACA468200810GATA3c.1320C>A (p.Thr440=)
c.1323C>A (p.Thr441=)
n.842C>A
 dbSNP
10g.8074011C=CA1888996257GATA3c.1320C= (p.Thr440=)
c.1323C= (p.Thr441=)
n.842C=
10g.8074011C>GCA468200812GATA3c.1320C>G (p.Thr440=)
c.1323C>G (p.Thr441=)
n.842C>G
 dbSNP
10g.8074011C>TCA5404587GATA3c.1320C>T (p.Thr440=)
c.1323C>T (p.Thr441=)
n.842C>T
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
10g.8074012_8074013dupCA645553661GATA3c.1321_1322dup (p.Met442ProfsTer?)
c.1324_1325dup (p.Met443ProfsTer?)
n.843_844dup
 COSMIC
10g.8074012G>ACA375976059GATA3c.1321G>A (p.Ala441Thr)
c.1324G>A (p.Ala442Thr)
n.843G>A
 gnomAD v4 COSMIC
10g.8074012G>CCA375976058GATA3c.1321G>C (p.Ala441Pro)
c.1324G>C (p.Ala442Pro)
n.843G>C
10g.8074012G>TCA375976061GATA3c.1321G>T (p.Ala441Ser)
c.1324G>T (p.Ala442Ser)
n.843G>T
10g.8074013C>ACA375976064GATA3c.1322C>A (p.Ala441Asp)
c.1325C>A (p.Ala442Asp)
n.844C>A
 dbSNP
10g.8074013C>GCA375976067GATA3c.1322C>G (p.Ala441Gly)
c.1325C>G (p.Ala442Gly)
n.844C>G
 dbSNP
10g.8074013C>TCA375976065GATA3c.1322C>T (p.Ala441Val)
c.1325C>T (p.Ala442Val)
n.844C>T
 dbSNP
10g.8074014C>ACA5404588GATA3c.1323C>A (p.Ala441=)
c.1326C>A (p.Ala442=)
n.845C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.8074014C=CA1888996258GATA3c.1323C= (p.Ala441=)
c.1326C= (p.Ala442=)
n.845C=
10g.8074014C>GCA468200818GATA3c.1323C>G (p.Ala441=)
c.1326C>G (p.Ala442=)
n.845C>G
 dbSNP COSMIC
10g.8074014C>TCA468200816GATA3c.1323C>T (p.Ala441=)
c.1326C>T (p.Ala442=)
n.845C>T
 dbSNP
10g.8074015A>CCA375976070GATA3c.1324A>C (p.Met442Leu)
c.1327A>C (p.Met443Leu)
n.846A>C
 dbSNP
10g.8074015A>GCA375976071GATA3c.1324A>G (p.Met442Val)
c.1327A>G (p.Met443Val)
n.846A>G
10g.8074015A>TCA375976073GATA3c.1324A>T (p.Met442Leu)
c.1327A>T (p.Met443Leu)
n.846A>T
 dbSNP gnomAD v4
10g.8074016T>ACA375976075GATA3c.1325T>A (p.Met442Lys)
c.1328T>A (p.Met443Lys)
n.847T>A
10g.8074016T>CCA375976077GATA3c.1325T>C (p.Met442Thr)
c.1328T>C (p.Met443Thr)
n.847T>C
10g.8074016T>GCA375976079GATA3c.1325T>G (p.Met442Arg)
c.1328T>G (p.Met443Arg)
n.847T>G
10g.8074016dupCA468200829GATA3c.1325dup (p.Met442IlefsTer?)
c.1328dup (p.Met443IlefsTer?)
n.847dup
10g.8074017G>ACA375976082GATA3c.1326G>A (p.Met442Ile)
c.1329G>A (p.Met443Ile)
n.848G>A
 dbSNP
10g.8074017G>CCA375976083GATA3c.1326G>C (p.Met442Ile)
c.1329G>C (p.Met443Ile)
n.848G>C
 dbSNP
10g.8074017G>TCA375976084GATA3c.1326G>T (p.Met442Ile)
c.1329G>T (p.Met443Ile)
n.848G>T
 dbSNP COSMIC
10g.8074019dupCA645553662GATA3c.1328dup (p.Ter444LeuextTer?)
c.1331dup (p.Ter445LeuextTer?)
n.850dup
 COSMIC
10g.8074018G>ACA375976087GATA3c.1327G>A (p.Gly443Ser)
c.1330G>A (p.Gly444Ser)
n.849G>A
 dbSNP
10g.8074018G>CCA375976088GATA3c.1327G>C (p.Gly443Arg)
c.1330G>C (p.Gly444Arg)
n.849G>C
10g.8074018G>TCA375976090GATA3c.1327G>T (p.Gly443Cys)
c.1330G>T (p.Gly444Cys)
n.849G>T
 dbSNP
10g.8074019G>ACA375976092GATA3c.1328G>A (p.Gly443Asp)
c.1331G>A (p.Gly444Asp)
n.850G>A
 gnomAD v4
10g.8074019G>CCA375976096GATA3c.1328G>C (p.Gly443Ala)
c.1331G>C (p.Gly444Ala)
n.850G>C
10g.8074019G>TCA375976094GATA3c.1328G>T (p.Gly443Val)
c.1331G>T (p.Gly444Val)
n.850G>T
10g.8074020T>ACA468200841GATA3c.1329T>A (p.Gly443=)
c.1332T>A (p.Gly444=)
n.851T>A
 dbSNP gnomAD v4 COSMIC
10g.8074020T>CCA468200843GATA3c.1329T>C (p.Gly443=)
c.1332T>C (p.Gly444=)
n.851T>C
 dbSNP
10g.8074020T>GCA468200844GATA3c.1329T>G (p.Gly443=)
c.1332T>G (p.Gly444=)
n.851T>G
 dbSNP
10g.8074020T=CA1888996260GATA3c.1329T= (p.Gly443=)
c.1332T= (p.Gly444=)
n.851T=
10g.8074021dupCA468200845GATA3c.1330dup (p.Ter444LeuextTer?)
c.1333dup (p.Ter445LeuextTer?)
n.852dup
 COSMIC
10g.8074021delCA645553663GATA3c.1330del (p.Ter444ArgextTer?)
c.1333del (p.Ter445ArgextTer?)
n.852del
 COSMIC

Number of alleles fetched