Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.128479422_128481318dupCA1139532682
3g.128481175A=CA1400714074GATA2c.1287T= (p.Ser429=)
c.1569T= (p.Ser523=)
c.262T= (p.Cys88=)
c.1245T= (p.Ser415=)
n.404T=
3g.128481175A>CCA354412851GATA2c.1287T>G (p.Ser429Arg)
c.1569T>G (p.Ser523Arg)
c.262T>G (p.Cys88Gly)
c.1245T>G (p.Ser415Arg)
n.404T>G
3g.128481175A>GCA435524863GATA2c.1287T>C (p.Ser429=)
c.1569T>C (p.Ser523=)
c.262T>C (p.Cys88Arg)
c.1245T>C (p.Ser415=)
n.404T>C
ClinVar
3g.128481175A>TCA2599807GATA2c.1287T>A (p.Ser429Arg)
c.1569T>A (p.Ser523Arg)
c.262T>A (p.Cys88Ser)
c.1245T>A (p.Ser415Arg)
n.404T>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128481176C>ACA354412853GATA2c.1286G>T (p.Ser429Ile)
c.1568G>T (p.Ser523Ile)
c.261G>T (p.Gln87His)
c.1244G>T (p.Ser415Ile)
n.403G>T
3g.128481176C=CA1400714083GATA2c.1286G= (p.Ser429=)
c.1568G= (p.Ser523=)
c.261G= (p.Gln87=)
c.1244G= (p.Ser415=)
n.403G=
3g.128481176C>GCA2599808GATA2c.1286G>C (p.Ser429Thr)
c.1568G>C (p.Ser523Thr)
c.261G>C (p.Gln87His)
c.1244G>C (p.Ser415Thr)
n.403G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481176C>TCA354412856GATA2c.1286G>A (p.Ser429Asn)
c.1568G>A (p.Ser523Asn)
c.261G>A (p.Gln87=)
c.1244G>A (p.Ser415Asn)
n.403G>A
ClinVar dbSNP gnomAD v4
3g.128481177T>ACA354412859GATA2c.1285A>T (p.Ser429Cys)
c.1567A>T (p.Ser523Cys)
c.260A>T (p.Gln87Leu)
c.1243A>T (p.Ser415Cys)
n.402A>T
3g.128481177T>CCA354412861GATA2c.1285A>G (p.Ser429Gly)
c.1567A>G (p.Ser523Gly)
c.260A>G (p.Gln87Arg)
c.1243A>G (p.Ser415Gly)
n.402A>G
gnomAD v4
3g.128481177T>GCA354412858GATA2c.1285A>C (p.Ser429Arg)
c.1567A>C (p.Ser523Arg)
c.260A>C (p.Gln87Pro)
c.1243A>C (p.Ser415Arg)
n.402A>C
3g.128481178G>ACA435524870GATA2c.1284C>T (p.Phe428=)
c.1566C>T (p.Phe522=)
c.259C>T (p.Gln87Ter)
c.1242C>T (p.Phe414=)
n.401C>T
3g.128481178G>CCA354412862GATA2c.1284C>G (p.Phe428Leu)
c.1566C>G (p.Phe522Leu)
c.259C>G (p.Gln87Glu)
c.1242C>G (p.Phe414Leu)
n.401C>G
3g.128481178G>TCA354412864GATA2c.1284C>A (p.Phe428Leu)
c.1566C>A (p.Phe522Leu)
c.259C>A (p.Gln87Lys)
c.1242C>A (p.Phe414Leu)
n.401C>A
3g.128481179A>CCA354412865GATA2c.1283T>G (p.Phe428Cys)
c.1565T>G (p.Phe522Cys)
c.258T>G (p.Leu86=)
c.1241T>G (p.Phe414Cys)
n.400T>G
3g.128481179A>GCA354412866GATA2c.1283T>C (p.Phe428Ser)
c.1565T>C (p.Phe522Ser)
c.258T>C (p.Leu86=)
c.1241T>C (p.Phe414Ser)
n.400T>C
3g.128481179A>TCA354412867GATA2c.1283T>A (p.Phe428Tyr)
c.1565T>A (p.Phe522Tyr)
c.258T>A (p.Leu86=)
c.1241T>A (p.Phe414Tyr)
n.400T>A
ClinVar
3g.128481180A=CA1400714094GATA2c.1282T= (p.Phe428=)
c.1564T= (p.Phe522=)
c.257T= (p.Leu86=)
c.1240T= (p.Phe414=)
n.399T=
3g.128481180A>CCA354412869GATA2c.1282T>G (p.Phe428Val)
c.1564T>G (p.Phe522Val)
c.257T>G (p.Leu86Arg)
c.1240T>G (p.Phe414Val)
n.399T>G
3g.128481180A>GCA354412871GATA2c.1282T>C (p.Phe428Leu)
c.1564T>C (p.Phe522Leu)
c.257T>C (p.Leu86Pro)
c.1240T>C (p.Phe414Leu)
n.399T>C
3g.128481180A>TCA16611345GATA2c.1282T>A (p.Phe428Ile)
c.1564T>A (p.Phe522Ile)
c.257T>A (p.Leu86His)
c.1240T>A (p.Phe414Ile)
n.399T>A
ClinVar dbSNP gnomAD v4
3g.128481181G>ACA435524876GATA2c.1281C>T (p.Pro427=)
c.1563C>T (p.Pro521=)
c.256C>T (p.Leu86Phe)
c.1239C>T (p.Pro413=)
n.398C>T
ClinVar gnomAD v4
3g.128481181G>CCA435524879GATA2c.1281C>G (p.Pro427=)
c.1563C>G (p.Pro521=)
c.256C>G (p.Leu86Val)
c.1239C>G (p.Pro413=)
n.398C>G
ClinVar dbSNP
3g.128481181G>TCA435524881GATA2c.1281C>A (p.Pro427=)
c.1563C>A (p.Pro521=)
c.256C>A (p.Leu86Ile)
c.1239C>A (p.Pro413=)
n.398C>A
3g.128481185dupCA2499216425GATA2c.1281dup (p.Phe428LeufsTer?)
c.1563dup (p.Phe522LeufsTer?)
c.256dup (p.Leu86ProfsTer?)
c.1239dup (p.Phe414LeufsTer?)
n.398dup
ClinVar dbSNP
3g.128481185delCA435524882GATA2c.1281del (p.Phe428SerfsTer?)
c.1563del (p.Phe522SerfsTer?)
c.256del (p.Leu86PhefsTer?)
c.1239del (p.Phe414SerfsTer?)
n.398del
COSMIC
3g.128481182G>ACA354412873GATA2c.1280C>T (p.Pro427Leu)
c.1562C>T (p.Pro521Leu)
c.255C>T (p.Pro85=)
c.1238C>T (p.Pro413Leu)
n.397C>T
ClinVar
3g.128481182G>CCA354412874GATA2c.1280C>G (p.Pro427Arg)
c.1562C>G (p.Pro521Arg)
c.255C>G (p.Pro85=)
c.1238C>G (p.Pro413Arg)
n.397C>G
ClinVar dbSNP
3g.128481182G=CA1400714098GATA2c.1280C= (p.Pro427=)
c.1562C= (p.Pro521=)
c.255C= (p.Pro85=)
c.1238C= (p.Pro413=)
n.397C=
3g.128481182G>TCA354412876GATA2c.1280C>A (p.Pro427His)
c.1562C>A (p.Pro521His)
c.255C>A (p.Pro85=)
c.1238C>A (p.Pro413His)
n.397C>A
3g.128481183G>ACA354412879GATA2c.1279C>T (p.Pro427Ser)
c.1561C>T (p.Pro521Ser)
c.254C>T (p.Pro85Leu)
c.1237C>T (p.Pro413Ser)
n.396C>T
3g.128481183G>CCA354412881GATA2c.1279C>G (p.Pro427Ala)
c.1561C>G (p.Pro521Ala)
c.254C>G (p.Pro85Arg)
c.1237C>G (p.Pro413Ala)
n.396C>G
ClinVar dbSNP gnomAD v4
3g.128481183G>TCA354412878GATA2c.1279C>A (p.Pro427Thr)
c.1561C>A (p.Pro521Thr)
c.254C>A (p.Pro85His)
c.1237C>A (p.Pro413Thr)
n.396C>A
3g.128481184G>ACA435524889GATA2c.1278C>T (p.Ser426=)
c.1560C>T (p.Ser520=)
c.253C>T (p.Pro85Ser)
c.1236C>T (p.Ser412=)
n.395C>T
dbSNP gnomAD v2
3g.128481184G>CCA435524891GATA2c.1278C>G (p.Ser426=)
c.1560C>G (p.Ser520=)
c.253C>G (p.Pro85Ala)
c.1236C>G (p.Ser412=)
n.395C>G
3g.128481184G=CA1400714103GATA2c.1278C= (p.Ser426=)
c.1560C= (p.Ser520=)
c.253C= (p.Pro85=)
c.1236C= (p.Ser412=)
n.395C=
3g.128481184G>TCA435524893GATA2c.1278C>A (p.Ser426=)
c.1560C>A (p.Ser520=)
c.253C>A (p.Pro85Thr)
c.1236C>A (p.Ser412=)
n.395C>A
3g.128481185G>ACA354412883GATA2c.1277C>T (p.Ser426Phe)
c.1559C>T (p.Ser520Phe)
c.252C>T (p.Ile84=)
c.1235C>T (p.Ser412Phe)
n.394C>T
3g.128481185G>CCA354412884GATA2c.1277C>G (p.Ser426Cys)
c.1559C>G (p.Ser520Cys)
c.252C>G (p.Ile84Met)
c.1235C>G (p.Ser412Cys)
n.394C>G
3g.128481185G=CA1400714105GATA2c.1277C= (p.Ser426=)
c.1559C= (p.Ser520=)
c.252C= (p.Ile84=)
c.1235C= (p.Ser412=)
n.394C=
3g.128481185G>TCA354412886GATA2c.1277C>A (p.Ser426Tyr)
c.1559C>A (p.Ser520Tyr)
c.252C>A (p.Ile84=)
c.1235C>A (p.Ser412Tyr)
n.394C>A
ClinVar dbSNP gnomAD v4
3g.128481186A=CA1400714108GATA2c.1276T= (p.Ser426=)
c.1558T= (p.Ser520=)
c.251T= (p.Ile84=)
c.1234T= (p.Ser412=)
n.393T=
3g.128481186A>CCA354412887GATA2c.1276T>G (p.Ser426Ala)
c.1558T>G (p.Ser520Ala)
c.251T>G (p.Ile84Ser)
c.1234T>G (p.Ser412Ala)
n.393T>G
3g.128481186A>GCA354412889GATA2c.1276T>C (p.Ser426Pro)
c.1558T>C (p.Ser520Pro)
c.251T>C (p.Ile84Thr)
c.1234T>C (p.Ser412Pro)
n.393T>C
ClinVar dbSNP
3g.128481186A>TCA354412890GATA2c.1276T>A (p.Ser426Thr)
c.1558T>A (p.Ser520Thr)
c.251T>A (p.Ile84Asn)
c.1234T>A (p.Ser412Thr)
n.393T>A
gnomAD v4
3g.128481187T>ACA435524899GATA2c.1275A>T (p.Ser425=)
c.1557A>T (p.Ser519=)
c.250A>T (p.Ile84Phe)
c.1233A>T (p.Ser411=)
n.392A>T
3g.128481187T>CCA435524901GATA2c.1275A>G (p.Ser425=)
c.1557A>G (p.Ser519=)
c.250A>G (p.Ile84Val)
c.1233A>G (p.Ser411=)
n.392A>G
dbSNP gnomAD v2 gnomAD v4
3g.128481187T>GCA435524902GATA2c.1275A>C (p.Ser425=)
c.1557A>C (p.Ser519=)
c.250A>C (p.Ile84Leu)
c.1233A>C (p.Ser411=)
n.392A>C
gnomAD v4
3g.128481187T=CA1400714113GATA2c.1275A= (p.Ser425=)
c.1557A= (p.Ser519=)
c.250A= (p.Ile84=)
c.1233A= (p.Ser411=)
n.392A=
3g.128481188G>ACA2599809GATA2c.1274C>T (p.Ser425Leu)
c.1556C>T (p.Ser519Leu)
c.249C>T (p.Val83=)
c.1232C>T (p.Ser411Leu)
n.391C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481188G>CCA354412893GATA2c.1274C>G (p.Ser425Ter)
c.1556C>G (p.Ser519Ter)
c.249C>G (p.Val83=)
c.1232C>G (p.Ser411Ter)
n.391C>G
3g.128481188G=CA1400714117GATA2c.1274C= (p.Ser425=)
c.1556C= (p.Ser519=)
c.249C= (p.Val83=)
c.1232C= (p.Ser411=)
n.391C=
3g.128481188G>TCA354412892GATA2c.1274C>A (p.Ser425Ter)
c.1556C>A (p.Ser519Ter)
c.249C>A (p.Val83=)
c.1232C>A (p.Ser411Ter)
n.391C>A
3g.128481189A=CA1400714125GATA2c.1273T= (p.Ser425=)
c.1555T= (p.Ser519=)
c.248T= (p.Val83=)
c.1231T= (p.Ser411=)
n.390T=
3g.128481189A>CCA2599810GATA2c.1273T>G (p.Ser425Ala)
c.1555T>G (p.Ser519Ala)
c.248T>G (p.Val83Gly)
c.1231T>G (p.Ser411Ala)
n.390T>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481189A>GCA354412896GATA2c.1273T>C (p.Ser425Pro)
c.1555T>C (p.Ser519Pro)
c.248T>C (p.Val83Ala)
c.1231T>C (p.Ser411Pro)
n.390T>C
ClinVar dbSNP
3g.128481189A>TCA354412897GATA2c.1273T>A (p.Ser425Thr)
c.1555T>A (p.Ser519Thr)
c.248T>A (p.Val83Asp)
c.1231T>A (p.Ser411Thr)
n.390T>A
3g.128481190C>ACA354412899GATA2c.1272G>T (p.Lys424Asn)
c.1554G>T (p.Lys518Asn)
c.247G>T (p.Val83Phe)
c.1230G>T (p.Lys410Asn)
n.389G>T
3g.128481190C>GCA354412900GATA2c.1272G>C (p.Lys424Asn)
c.1554G>C (p.Lys518Asn)
c.247G>C (p.Val83Leu)
c.1230G>C (p.Lys410Asn)
n.389G>C
3g.128481190C>TCA435524908GATA2c.1272G>A (p.Lys424=)
c.1554G>A (p.Lys518=)
c.247G>A (p.Val83Ile)
c.1230G>A (p.Lys410=)
n.389G>A
ClinVar dbSNP gnomAD v4
3g.128481191T>ACA354412904GATA2c.1271A>T (p.Lys424Met)
c.1553A>T (p.Lys518Met)
c.246A>T (p.Glu82Asp)
c.1229A>T (p.Lys410Met)
n.388A>T
3g.128481191T>CCA354412905GATA2c.1271A>G (p.Lys424Arg)
c.1553A>G (p.Lys518Arg)
c.246A>G (p.Glu82=)
c.1229A>G (p.Lys410Arg)
n.388A>G
3g.128481191T>GCA354412902GATA2c.1271A>C (p.Lys424Thr)
c.1553A>C (p.Lys518Thr)
c.246A>C (p.Glu82Asp)
c.1229A>C (p.Lys410Thr)
n.388A>C
3g.128481192T>ACA354412906GATA2c.1270A>T (p.Lys424Ter)
c.1552A>T (p.Lys518Ter)
c.245A>T (p.Glu82Val)
c.1228A>T (p.Lys410Ter)
n.387A>T
3g.128481192T>CCA354412908GATA2c.1270A>G (p.Lys424Glu)
c.1552A>G (p.Lys518Glu)
c.245A>G (p.Glu82Gly)
c.1228A>G (p.Lys410Glu)
n.387A>G
3g.128481192T>GCA354412909GATA2c.1270A>C (p.Lys424Gln)
c.1552A>C (p.Lys518Gln)
c.245A>C (p.Glu82Ala)
c.1228A>C (p.Lys410Gln)
n.387A>C
3g.128481192_128481195delinsTCTCCA1400714130GATA2c.1267_1270delinsGAGA (p.Glu423=)
c.1549_1552delinsGAGA (p.Glu517=)
c.242_245delinsGAGA (p.Gly81=)
c.1225_1228delinsGAGA (p.Glu409=)
n.384_387delinsGAGA
3g.128481193C>ACA354412911GATA2c.1269G>T (p.Glu423Asp)
c.1551G>T (p.Glu517Asp)
c.244G>T (p.Glu82Ter)
c.1227G>T (p.Glu409Asp)
n.386G>T
gnomAD v4
3g.128481193C=CA1400714132GATA2c.1269G= (p.Glu423=)
c.1551G= (p.Glu517=)
c.244G= (p.Glu82=)
c.1227G= (p.Glu409=)
n.386G=
3g.128481193C>GCA354412913GATA2c.1269G>C (p.Glu423Asp)
c.1551G>C (p.Glu517Asp)
c.244G>C (p.Glu82Gln)
c.1227G>C (p.Glu409Asp)
n.386G>C
ClinVar
3g.128481193C>TCA435524915GATA2c.1269G>A (p.Glu423=)
c.1551G>A (p.Glu517=)
c.244G>A (p.Glu82Lys)
c.1227G>A (p.Glu409=)
n.386G>A
dbSNP
3g.128481195_128481197delCA546415757GATA2c.1267_1269del (p.Glu423del)
c.1549_1551del (p.Glu517del)
c.242_244del (p.Gly81del)
c.1225_1227del (p.Glu409del)
n.384_386del
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128481194T>ACA354412914GATA2c.1268A>T (p.Glu423Val)
c.1550A>T (p.Glu517Val)
c.243A>T (p.Gly81=)
c.1226A>T (p.Glu409Val)
n.385A>T
3g.128481194T>CCA354412915GATA2c.1268A>G (p.Glu423Gly)
c.1550A>G (p.Glu517Gly)
c.243A>G (p.Gly81=)
c.1226A>G (p.Glu409Gly)
n.385A>G
3g.128481194T>GCA354412917GATA2c.1268A>C (p.Glu423Ala)
c.1550A>C (p.Glu517Ala)
c.243A>C (p.Gly81=)
c.1226A>C (p.Glu409Ala)
n.385A>C
3g.128481195C>ACA354412919GATA2c.1267G>T (p.Glu423Ter)
c.1549G>T (p.Glu517Ter)
c.242G>T (p.Gly81Val)
c.1225G>T (p.Glu409Ter)
n.384G>T
3g.128481195C=CA1400714136GATA2c.1267G= (p.Glu423=)
c.1549G= (p.Glu517=)
c.242G= (p.Gly81=)
c.1225G= (p.Glu409=)
n.384G=
3g.128481195C>GCA354412921GATA2c.1267G>C (p.Glu423Gln)
c.1549G>C (p.Glu517Gln)
c.242G>C (p.Gly81Ala)
c.1225G>C (p.Glu409Gln)
n.384G>C
3g.128481195C>TCA2599811GATA2c.1267G>A (p.Glu423Lys)
c.1549G>A (p.Glu517Lys)
c.242G>A (p.Gly81Glu)
c.1225G>A (p.Glu409Lys)
n.384G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128481196delCA2580068693GATA2c.1267del (p.Glu423ArgfsTer?)
c.1549del (p.Glu517ArgfsTer?)
c.242del (p.Gly81GlufsTer?)
c.1225del (p.Glu409ArgfsTer?)
n.384del
ClinVar
3g.128481196C>ACA354412923GATA2c.1266G>T (p.Gln422His)
c.1548G>T (p.Gln516His)
c.241G>T (p.Gly81Ter)
c.1224G>T (p.Gln408His)
n.383G>T
3g.128481196C=CA1400714140GATA2c.1266G= (p.Gln422=)
c.1548G= (p.Gln516=)
c.241G= (p.Gly81=)
c.1224G= (p.Gln408=)
n.383G=
3g.128481196C>GCA354412925GATA2c.1266G>C (p.Gln422His)
c.1548G>C (p.Gln516His)
c.241G>C (p.Gly81Arg)
c.1224G>C (p.Gln408His)
n.383G>C
3g.128481196C>TCA83376267GATA2c.1266G>A (p.Gln422=)
c.1548G>A (p.Gln516=)
c.241G>A (p.Gly81Arg)
c.1224G>A (p.Gln408=)
n.383G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.128481197T>ACA354412929GATA2c.1265A>T (p.Gln422Leu)
c.1547A>T (p.Gln516Leu)
c.240A>T (p.Ala80=)
c.1223A>T (p.Gln408Leu)
n.382A>T
gnomAD v4
3g.128481197T>CCA354412927GATA2c.1265A>G (p.Gln422Arg)
c.1547A>G (p.Gln516Arg)
c.240A>G (p.Ala80=)
c.1223A>G (p.Gln408Arg)
n.382A>G
3g.128481197T>GCA354412926GATA2c.1265A>C (p.Gln422Pro)
c.1547A>C (p.Gln516Pro)
c.240A>C (p.Ala80=)
c.1223A>C (p.Gln408Pro)
n.382A>C
3g.128481198G>ACA354412930GATA2c.1264C>T (p.Gln422Ter)
c.1546C>T (p.Gln516Ter)
c.239C>T (p.Ala80Val)
c.1222C>T (p.Gln408Ter)
n.381C>T
3g.128481198G>CCA354412931GATA2c.1264C>G (p.Gln422Glu)
c.1546C>G (p.Gln516Glu)
c.239C>G (p.Ala80Gly)
c.1222C>G (p.Gln408Glu)
n.381C>G
3g.128481198G>TCA354412932GATA2c.1264C>A (p.Gln422Lys)
c.1546C>A (p.Gln516Lys)
c.239C>A (p.Ala80Glu)
c.1222C>A (p.Gln408Lys)
n.381C>A
3g.128481199C>ACA354412934GATA2c.1263G>T (p.Met421Ile)
c.1545G>T (p.Met515Ile)
c.238G>T (p.Ala80Ser)
c.1221G>T (p.Met407Ile)
n.380G>T
3g.128481199C=CA1400714146GATA2c.1263G= (p.Met421=)
c.1545G= (p.Met515=)
c.238G= (p.Ala80=)
c.1221G= (p.Met407=)
n.380G=
3g.128481199C>GCA354412935GATA2c.1263G>C (p.Met421Ile)
c.1545G>C (p.Met515Ile)
c.238G>C (p.Ala80Pro)
c.1221G>C (p.Met407Ile)
n.380G>C
3g.128481199C>TCA354412936GATA2c.1263G>A (p.Met421Ile)
c.1545G>A (p.Met515Ile)
c.238G>A (p.Ala80Thr)
c.1221G>A (p.Met407Ile)
n.380G>A
ClinVar dbSNP
3g.128481200A=CA1400714149GATA2c.1262T= (p.Met421=)
c.1544T= (p.Met515=)
c.237T= (p.His79=)
c.1220T= (p.Met407=)
n.379T=
3g.128481200A>CCA354412938GATA2c.1262T>G (p.Met421Arg)
c.1544T>G (p.Met515Arg)
c.237T>G (p.His79Gln)
c.1220T>G (p.Met407Arg)
n.379T>G
3g.128481200A>GCA354412940GATA2c.1262T>C (p.Met421Thr)
c.1544T>C (p.Met515Thr)
c.237T>C (p.His79=)
c.1220T>C (p.Met407Thr)
n.379T>C
dbSNP COSMIC
3g.128481200A>TCA354412942GATA2c.1262T>A (p.Met421Lys)
c.1544T>A (p.Met515Lys)
c.237T>A (p.His79Gln)
c.1220T>A (p.Met407Lys)
n.379T>A
3g.128481201T>ACA354412943GATA2c.1261A>T (p.Met421Leu)
c.1543A>T (p.Met515Leu)
c.236A>T (p.His79Leu)
c.1219A>T (p.Met407Leu)
n.378A>T
ClinVar dbSNP
3g.128481201T>CCA2599812GATA2c.1261A>G (p.Met421Val)
c.1543A>G (p.Met515Val)
c.236A>G (p.His79Arg)
c.1219A>G (p.Met407Val)
n.378A>G
dbSNP ExAC gnomAD v2 gnomAD v4
3g.128481201T>GCA354412945GATA2c.1261A>C (p.Met421Leu)
c.1543A>C (p.Met515Leu)
c.236A>C (p.His79Pro)
c.1219A>C (p.Met407Leu)
n.378A>C
3g.128481201T=CA1400714153GATA2c.1261A= (p.Met421=)
c.1543A= (p.Met515=)
c.236A= (p.His79=)
c.1219A= (p.Met407=)
n.378A=
3g.128481202G>ACA435524935GATA2c.1260C>T (p.Cys420=)
c.1542C>T (p.Cys514=)
c.235C>T (p.His79Tyr)
c.1218C>T (p.Cys406=)
n.377C>T
3g.128481202G>CCA354412947GATA2c.1260C>G (p.Cys420Trp)
c.1542C>G (p.Cys514Trp)
c.235C>G (p.His79Asp)
c.1218C>G (p.Cys406Trp)
n.377C>G
3g.128481202G>TCA354412949GATA2c.1260C>A (p.Cys420Ter)
c.1542C>A (p.Cys514Ter)
c.235C>A (p.His79Asn)
c.1218C>A (p.Cys406Ter)
n.377C>A
3g.128481203C>ACA354412950GATA2c.1259G>T (p.Cys420Phe)
c.1541G>T (p.Cys514Phe)
c.234G>T (p.Val78=)
c.1217G>T (p.Cys406Phe)
n.376G>T
3g.128481203C=CA1400714157GATA2c.1259G= (p.Cys420=)
c.1541G= (p.Cys514=)
c.234G= (p.Val78=)
c.1217G= (p.Cys406=)
n.376G=
3g.128481203C>GCA354412952GATA2c.1259G>C (p.Cys420Ser)
c.1541G>C (p.Cys514Ser)
c.234G>C (p.Val78=)
c.1217G>C (p.Cys406Ser)
n.376G>C
3g.128481203C>TCA83376272GATA2c.1259G>A (p.Cys420Tyr)
c.1541G>A (p.Cys514Tyr)
c.234G>A (p.Val78=)
c.1217G>A (p.Cys406Tyr)
n.376G>A
dbSNP gnomAD v3 gnomAD v4
3g.128481204A>CCA354412954GATA2c.1258T>G (p.Cys420Gly)
c.1540T>G (p.Cys514Gly)
c.233T>G (p.Val78Gly)
c.1216T>G (p.Cys406Gly)
n.375T>G
ClinVar
3g.128481204A>GCA354412955GATA2c.1258T>C (p.Cys420Arg)
c.1540T>C (p.Cys514Arg)
c.233T>C (p.Val78Ala)
c.1216T>C (p.Cys406Arg)
n.375T>C
3g.128481204A>TCA354412956GATA2c.1258T>A (p.Cys420Ser)
c.1540T>A (p.Cys514Ser)
c.233T>A (p.Val78Glu)
c.1216T>A (p.Cys406Ser)
n.375T>A
3g.128481205C>ACA354412958GATA2c.1257G>T (p.Lys419Asn)
c.1539G>T (p.Lys513Asn)
c.232G>T (p.Val78Leu)
c.1215G>T (p.Lys405Asn)
n.374G>T
3g.128481205C>GCA354412960GATA2c.1257G>C (p.Lys419Asn)
c.1539G>C (p.Lys513Asn)
c.232G>C (p.Val78Leu)
c.1215G>C (p.Lys405Asn)
n.374G>C
3g.128481205C>TCA435524943GATA2c.1257G>A (p.Lys419=)
c.1539G>A (p.Lys513=)
c.232G>A (p.Val78Met)
c.1215G>A (p.Lys405=)
n.374G>A
3g.128481206T>ACA354412964GATA2c.1256A>T (p.Lys419Met)
c.1538A>T (p.Lys513Met)
c.231A>T (p.Lys77Asn)
c.1214A>T (p.Lys405Met)
n.373A>T
3g.128481206T>CCA354412963GATA2c.1256A>G (p.Lys419Arg)
c.1538A>G (p.Lys513Arg)
c.231A>G (p.Lys77=)
c.1214A>G (p.Lys405Arg)
n.373A>G
3g.128481206T>GCA354412962GATA2c.1256A>C (p.Lys419Thr)
c.1538A>C (p.Lys513Thr)
c.231A>C (p.Lys77Asn)
c.1214A>C (p.Lys405Thr)
n.373A>C
3g.128481208dupCA2667540267GATA2c.1256dup (p.Cys420ValfsTer?)
c.1538dup (p.Cys514ValfsTer?)
c.231dup (p.Val78SerfsTer?)
c.1214dup (p.Cys406ValfsTer?)
n.373dup
gnomAD v4
3g.128481207T>ACA354412966GATA2c.1255A>T (p.Lys419Ter)
c.1537A>T (p.Lys513Ter)
c.230A>T (p.Lys77Ile)
c.1213A>T (p.Lys405Ter)
n.372A>T
3g.128481207T>CCA354412968GATA2c.1255A>G (p.Lys419Glu)
c.1537A>G (p.Lys513Glu)
c.230A>G (p.Lys77Arg)
c.1213A>G (p.Lys405Glu)
n.372A>G
gnomAD v4
3g.128481207T>GCA354412969GATA2c.1255A>C (p.Lys419Gln)
c.1537A>C (p.Lys513Gln)
c.230A>C (p.Lys77Thr)
c.1213A>C (p.Lys405Gln)
n.372A>C
3g.128481208T>ACA435524948GATA2c.1254A>T (p.Ser418=)
c.1536A>T (p.Ser512=)
c.229A>T (p.Lys77Ter)
c.1212A>T (p.Ser404=)
n.371A>T
3g.128481208T>CCA435524950GATA2c.1254A>G (p.Ser418=)
c.1536A>G (p.Ser512=)
c.229A>G (p.Lys77Glu)
c.1212A>G (p.Ser404=)
n.371A>G
ClinVar dbSNP
3g.128481208T>GCA435524951GATA2c.1254A>C (p.Ser418=)
c.1536A>C (p.Ser512=)
c.229A>C (p.Lys77Gln)
c.1212A>C (p.Ser404=)
n.371A>C
3g.128481209G>ACA354412971GATA2c.1253C>T (p.Ser418Leu)
c.1535C>T (p.Ser512Leu)
c.228C>T (p.Val76=)
c.1211C>T (p.Ser404Leu)
n.370C>T
3g.128481209G>CCA354412972GATA2c.1253C>G (p.Ser418Ter)
c.1535C>G (p.Ser512Ter)
c.228C>G (p.Val76=)
c.1211C>G (p.Ser404Ter)
n.370C>G
3g.128481209G>TCA354412974GATA2c.1253C>A (p.Ser418Ter)
c.1535C>A (p.Ser512Ter)
c.228C>A (p.Val76=)
c.1211C>A (p.Ser404Ter)
n.370C>A
3g.128481210A>CCA354412976GATA2c.1252T>G (p.Ser418Ala)
c.1534T>G (p.Ser512Ala)
c.227T>G (p.Val76Gly)
c.1210T>G (p.Ser404Ala)
n.369T>G
3g.128481210A>GCA354412978GATA2c.1252T>C (p.Ser418Pro)
c.1534T>C (p.Ser512Pro)
c.227T>C (p.Val76Ala)
c.1210T>C (p.Ser404Pro)
n.369T>C
3g.128481210A>TCA354412977GATA2c.1252T>A (p.Ser418Thr)
c.1534T>A (p.Ser512Thr)
c.227T>A (p.Val76Asp)
c.1210T>A (p.Ser404Thr)
n.369T>A
ClinVar gnomAD v4
3g.128481211C>ACA435524956GATA2c.1251G>T (p.Leu417=)
c.1533G>T (p.Leu511=)
c.226G>T (p.Val76Phe)
c.1209G>T (p.Leu403=)
n.368G>T
3g.128481211C>GCA435524957GATA2c.1251G>C (p.Leu417=)
c.1533G>C (p.Leu511=)
c.226G>C (p.Val76Leu)
c.1209G>C (p.Leu403=)
n.368G>C
3g.128481211C>TCA435524959GATA2c.1251G>A (p.Leu417=)
c.1533G>A (p.Leu511=)
c.226G>A (p.Val76Ile)
c.1209G>A (p.Leu403=)
n.368G>A
gnomAD v4
3g.128481212A>CCA354412980GATA2c.1250T>G (p.Leu417Arg)
c.1532T>G (p.Leu511Arg)
c.225T>G (p.Ala75=)
c.1208T>G (p.Leu403Arg)
n.367T>G
3g.128481212A>GCA354412981GATA2c.1250T>C (p.Leu417Pro)
c.1532T>C (p.Leu511Pro)
c.225T>C (p.Ala75=)
c.1208T>C (p.Leu403Pro)
n.367T>C
ClinVar dbSNP
3g.128481212A>TCA354412983GATA2c.1250T>A (p.Leu417Gln)
c.1532T>A (p.Leu511Gln)
c.225T>A (p.Ala75=)
c.1208T>A (p.Leu403Gln)
n.367T>A
3g.128481213G>ACA435524962GATA2c.1249C>T (p.Leu417=)
c.1531C>T (p.Leu511=)
c.224C>T (p.Ala75Val)
c.1207C>T (p.Leu403=)
n.366C>T
3g.128481213G>CCA354412985GATA2c.1249C>G (p.Leu417Val)
c.1531C>G (p.Leu511Val)
c.224C>G (p.Ala75Gly)
c.1207C>G (p.Leu403Val)
n.366C>G
gnomAD v4
3g.128481213G>TCA354412986GATA2c.1249C>A (p.Leu417Met)
c.1531C>A (p.Leu511Met)
c.224C>A (p.Ala75Asp)
c.1207C>A (p.Leu403Met)
n.366C>A
3g.128481214C>ACA354412987GATA2c.1248G>T (p.Glu416Asp)
c.1530G>T (p.Glu510Asp)
c.223G>T (p.Ala75Ser)
c.1206G>T (p.Glu402Asp)
n.365G>T
3g.128481214C=CA1400714162GATA2c.1248G= (p.Glu416=)
c.1530G= (p.Glu510=)
c.223G= (p.Ala75=)
c.1206G= (p.Glu402=)
n.365G=
3g.128481214C>GCA354412989GATA2c.1248G>C (p.Glu416Asp)
c.1530G>C (p.Glu510Asp)
c.223G>C (p.Ala75Pro)
c.1206G>C (p.Glu402Asp)
n.365G>C
ClinVar dbSNP gnomAD v4
3g.128481214C>TCA435524966GATA2c.1248G>A (p.Glu416=)
c.1530G>A (p.Glu510=)
c.223G>A (p.Ala75Thr)
c.1206G>A (p.Glu402=)
n.365G>A
ClinVar
3g.128481215T>ACA354412991GATA2c.1247A>T (p.Glu416Val)
c.1529A>T (p.Glu510Val)
c.222A>T (p.Gly74=)
c.1205A>T (p.Glu402Val)
n.364A>T
3g.128481215T>CCA354412993GATA2c.1247A>G (p.Glu416Gly)
c.1529A>G (p.Glu510Gly)
c.222A>G (p.Gly74=)
c.1205A>G (p.Glu402Gly)
n.364A>G
3g.128481215T>GCA354412994GATA2c.1247A>C (p.Glu416Ala)
c.1529A>C (p.Glu510Ala)
c.222A>C (p.Gly74=)
c.1205A>C (p.Glu402Ala)
n.364A>C
3g.128481215_128481216delinsAACA2580068695GATA2c.1246_1247delinsTT (p.Glu416Leu)
c.1528_1529delinsTT (p.Glu510Leu)
c.221_222delinsTT (p.Gly74Val)
c.1204_1205delinsTT (p.Glu402Leu)
n.363_364delinsTT
ClinVar
3g.128481216C>ACA354412996GATA2c.1246G>T (p.Glu416Ter)
c.1528G>T (p.Glu510Ter)
c.221G>T (p.Gly74Val)
c.1204G>T (p.Glu402Ter)
n.363G>T
3g.128481216C>GCA354412999GATA2c.1246G>C (p.Glu416Gln)
c.1528G>C (p.Glu510Gln)
c.221G>C (p.Gly74Ala)
c.1204G>C (p.Glu402Gln)
n.363G>C
3g.128481216C>TCA354412997GATA2c.1246G>A (p.Glu416Lys)
c.1528G>A (p.Glu510Lys)
c.221G>A (p.Gly74Glu)
c.1204G>A (p.Glu402Lys)
n.363G>A
ClinVar dbSNP gnomAD v4
3g.128481217C>ACA354413001GATA2c.1245G>T (p.Glu415Asp)
c.1527G>T (p.Glu509Asp)
c.220G>T (p.Gly74Ter)
c.1203G>T (p.Glu401Asp)
n.362G>T
3g.128481217C>GCA354413002GATA2c.1245G>C (p.Glu415Asp)
c.1527G>C (p.Glu509Asp)
c.220G>C (p.Gly74Arg)
c.1203G>C (p.Glu401Asp)
n.362G>C
3g.128481217C>TCA435524972GATA2c.1245G>A (p.Glu415=)
c.1527G>A (p.Glu509=)
c.220G>A (p.Gly74Arg)
c.1203G>A (p.Glu401=)
n.362G>A
3g.128481218T>ACA354413003GATA2c.1244A>T (p.Glu415Val)
c.1526A>T (p.Glu509Val)
c.219A>T (p.Arg73=)
c.1202A>T (p.Glu401Val)
n.361A>T
3g.128481218T>CCA354413006GATA2c.1244A>G (p.Glu415Gly)
c.1526A>G (p.Glu509Gly)
c.219A>G (p.Arg73=)
c.1202A>G (p.Glu401Gly)
n.361A>G
3g.128481218T>GCA354413004GATA2c.1244A>C (p.Glu415Ala)
c.1526A>C (p.Glu509Ala)
c.219A>C (p.Arg73=)
c.1202A>C (p.Glu401Ala)
n.361A>C
3g.128481219C>ACA354413008GATA2c.1243G>T (p.Glu415Ter)
c.1525G>T (p.Glu509Ter)
c.218G>T (p.Arg73Leu)
c.1201G>T (p.Glu401Ter)
n.360G>T
3g.128481219C=CA1400714166GATA2c.1243G= (p.Glu415=)
c.1525G= (p.Glu509=)
c.218G= (p.Arg73=)
c.1201G= (p.Glu401=)
n.360G=
3g.128481219C>GCA354413011GATA2c.1243G>C (p.Glu415Gln)
c.1525G>C (p.Glu509Gln)
c.218G>C (p.Arg73Pro)
c.1201G>C (p.Glu401Gln)
n.360G>C
3g.128481219C>TCA354413009GATA2c.1243G>A (p.Glu415Lys)
c.1525G>A (p.Glu509Lys)
c.218G>A (p.Arg73Gln)
c.1201G>A (p.Glu401Lys)
n.360G>A
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
3g.128481220G>ACA2599813GATA2c.1242C>T (p.Phe414=)
c.1524C>T (p.Phe508=)
c.217C>T (p.Arg73Ter)
c.1200C>T (p.Phe400=)
n.359C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481220G>CCA2599814GATA2c.1242C>G (p.Phe414Leu)
c.1524C>G (p.Phe508Leu)
c.217C>G (p.Arg73Gly)
c.1200C>G (p.Phe400Leu)
n.359C>G
ClinVar dbSNP ExAC gnomAD v2
3g.128481220G=CA1400714172GATA2c.1242C= (p.Phe414=)
c.1524C= (p.Phe508=)
c.217C= (p.Arg73=)
c.1200C= (p.Phe400=)
n.359C=
3g.128481220G>TCA354413013GATA2c.1242C>A (p.Phe414Leu)
c.1524C>A (p.Phe508Leu)
c.217C>A (p.Arg73=)
c.1200C>A (p.Phe400Leu)
n.359C>A
3g.128481221A>CCA354413015GATA2c.1241T>G (p.Phe414Cys)
c.1523T>G (p.Phe508Cys)
c.216T>G (p.Leu72=)
c.1199T>G (p.Phe400Cys)
n.358T>G
3g.128481221A>GCA354413018GATA2c.1241T>C (p.Phe414Ser)
c.1523T>C (p.Phe508Ser)
c.216T>C (p.Leu72=)
c.1199T>C (p.Phe400Ser)
n.358T>C
ClinVar
3g.128481221A>TCA354413017GATA2c.1241T>A (p.Phe414Tyr)
c.1523T>A (p.Phe508Tyr)
c.216T>A (p.Leu72=)
c.1199T>A (p.Phe400Tyr)
n.358T>A
3g.128481222A>CCA354413020GATA2c.1240T>G (p.Phe414Val)
c.1522T>G (p.Phe508Val)
c.215T>G (p.Leu72Arg)
c.1198T>G (p.Phe400Val)
n.357T>G
3g.128481222A>GCA354413023GATA2c.1240T>C (p.Phe414Leu)
c.1522T>C (p.Phe508Leu)
c.215T>C (p.Leu72Pro)
c.1198T>C (p.Phe400Leu)
n.357T>C
3g.128481222A>TCA354413022GATA2c.1240T>A (p.Phe414Ile)
c.1522T>A (p.Phe508Ile)
c.215T>A (p.Leu72His)
c.1198T>A (p.Phe400Ile)
n.357T>A
3g.128481223G>ACA435524985GATA2c.1239C>T (p.Cys413=)
c.1521C>T (p.Cys507=)
c.214C>T (p.Leu72Phe)
c.1197C>T (p.Cys399=)
n.356C>T
3g.128481223G>CCA354413025GATA2c.1239C>G (p.Cys413Trp)
c.1521C>G (p.Cys507Trp)
c.214C>G (p.Leu72Val)
c.1197C>G (p.Cys399Trp)
n.356C>G
3g.128481223G>TCA354413026GATA2c.1239C>A (p.Cys413Ter)
c.1521C>A (p.Cys507Ter)
c.214C>A (p.Leu72Ile)
c.1197C>A (p.Cys399Ter)
n.356C>A
3g.128481224C>ACA354413028GATA2c.1238G>T (p.Cys413Phe)
c.1520G>T (p.Cys507Phe)
c.213G>T (p.Val71=)
c.1196G>T (p.Cys399Phe)
n.355G>T
dbSNP gnomAD v2 gnomAD v4
3g.128481224C=CA1400714177GATA2c.1238G= (p.Cys413=)
c.1520G= (p.Cys507=)
c.213G= (p.Val71=)
c.1196G= (p.Cys399=)
n.355G=
3g.128481224C>GCA354413032GATA2c.1238G>C (p.Cys413Ser)
c.1520G>C (p.Cys507Ser)
c.213G>C (p.Val71=)
c.1196G>C (p.Cys399Ser)
n.355G>C
3g.128481224C>TCA354413030GATA2c.1238G>A (p.Cys413Tyr)
c.1520G>A (p.Cys507Tyr)
c.213G>A (p.Val71=)
c.1196G>A (p.Cys399Tyr)
n.355G>A
ClinVar dbSNP gnomAD v4
3g.128481225A>CCA354413033GATA2c.1237T>G (p.Cys413Gly)
c.1519T>G (p.Cys507Gly)
c.212T>G (p.Val71Gly)
c.1195T>G (p.Cys399Gly)
n.354T>G
3g.128481225A>GCA354413036GATA2c.1237T>C (p.Cys413Arg)
c.1519T>C (p.Cys507Arg)
c.212T>C (p.Val71Ala)
c.1195T>C (p.Cys399Arg)
n.354T>C
3g.128481225A>TCA354413034GATA2c.1237T>A (p.Cys413Ser)
c.1519T>A (p.Cys507Ser)
c.212T>A (p.Val71Glu)
c.1195T>A (p.Cys399Ser)
n.354T>A
3g.128481226C>ACA354413038GATA2c.1236G>T (p.Glu412Asp)
c.1518G>T (p.Glu506Asp)
c.211G>T (p.Val71Leu)
c.1194G>T (p.Glu398Asp)
n.353G>T
ClinVar dbSNP
3g.128481226C=CA1400714180GATA2c.1236G= (p.Glu412=)
c.1518G= (p.Glu506=)
c.211G= (p.Val71=)
c.1194G= (p.Glu398=)
n.353G=
3g.128481226C>GCA354413040GATA2c.1236G>C (p.Glu412Asp)
c.1518G>C (p.Glu506Asp)
c.211G>C (p.Val71Leu)
c.1194G>C (p.Glu398Asp)
n.353G>C
3g.128481226C>TCA435524992GATA2c.1236G>A (p.Glu412=)
c.1518G>A (p.Glu506=)
c.211G>A (p.Val71Met)
c.1194G>A (p.Glu398=)
n.353G>A
ClinVar dbSNP gnomAD v4
3g.128481227T>ACA354413041GATA2c.1235A>T (p.Glu412Val)
c.1517A>T (p.Glu506Val)
c.210A>T (p.Gly70=)
c.1193A>T (p.Glu398Val)
n.352A>T
3g.128481227T>CCA354413043GATA2c.1235A>G (p.Glu412Gly)
c.1517A>G (p.Glu506Gly)
c.210A>G (p.Gly70=)
c.1193A>G (p.Glu398Gly)
n.352A>G
3g.128481227T>GCA354413045GATA2c.1235A>C (p.Glu412Ala)
c.1517A>C (p.Glu506Ala)
c.210A>C (p.Gly70=)
c.1193A>C (p.Glu398Ala)
n.352A>C
3g.128481228C>ACA354413046GATA2c.1234G>T (p.Glu412Ter)
c.1516G>T (p.Glu506Ter)
c.209G>T (p.Gly70Val)
c.1192G>T (p.Glu398Ter)
n.351G>T
3g.128481228C>GCA354413047GATA2c.1234G>C (p.Glu412Gln)
c.1516G>C (p.Glu506Gln)
c.209G>C (p.Gly70Ala)
c.1192G>C (p.Glu398Gln)
n.351G>C
3g.128481228C>TCA354413048GATA2c.1234G>A (p.Glu412Lys)
c.1516G>A (p.Glu506Lys)
c.209G>A (p.Gly70Glu)
c.1192G>A (p.Glu398Lys)
n.351G>A
gnomAD v4
3g.128481229C>ACA435524997GATA2c.1233G>T (p.Ala411=)
c.1515G>T (p.Ala505=)
c.208G>T (p.Gly70Ter)
c.1191G>T (p.Ala397=)
n.350G>T
3g.128481229C=CA1400714184GATA2c.1233G= (p.Ala411=)
c.1515G= (p.Ala505=)
c.208G= (p.Gly70=)
c.1191G= (p.Ala397=)
n.350G=
3g.128481229C>GCA435524999GATA2c.1233G>C (p.Ala411=)
c.1515G>C (p.Ala505=)
c.208G>C (p.Gly70Arg)
c.1191G>C (p.Ala397=)
n.350G>C
3g.128481229C>TCA2599815GATA2c.1233G>A (p.Ala411=)
c.1515G>A (p.Ala505=)
c.208G>A (p.Gly70Arg)
c.1191G>A (p.Ala397=)
n.350G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481230G>ACA2599816GATA2c.1232C>T (p.Ala411Val)
c.1514C>T (p.Ala505Val)
c.207C>T (p.Gly69=)
c.1190C>T (p.Ala397Val)
n.349C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481230G>CCA354413051GATA2c.1232C>G (p.Ala411Gly)
c.1514C>G (p.Ala505Gly)
c.207C>G (p.Gly69=)
c.1190C>G (p.Ala397Gly)
n.349C>G
3g.128481230G=CA1400714193GATA2c.1232C= (p.Ala411=)
c.1514C= (p.Ala505=)
c.207C= (p.Gly69=)
c.1190C= (p.Ala397=)
n.349C=
3g.128481230G>TCA354413053GATA2c.1232C>A (p.Ala411Glu)
c.1514C>A (p.Ala505Glu)
c.207C>A (p.Gly69=)
c.1190C>A (p.Ala397Glu)
n.349C>A
ClinVar dbSNP
3g.128481231C>ACA354413058GATA2c.1231G>T (p.Ala411Ser)
c.1513G>T (p.Ala505Ser)
c.206G>T (p.Gly69Val)
c.1189G>T (p.Ala397Ser)
n.348G>T
3g.128481231C=CA1400714198GATA2c.1231G= (p.Ala411=)
c.1513G= (p.Ala505=)
c.206G= (p.Gly69=)
c.1189G= (p.Ala397=)
n.348G=
3g.128481231C>GCA354413056GATA2c.1231G>C (p.Ala411Pro)
c.1513G>C (p.Ala505Pro)
c.206G>C (p.Gly69Ala)
c.1189G>C (p.Ala397Pro)
n.348G>C
ClinVar dbSNP gnomAD v4
3g.128481231C>TCA354413054GATA2c.1231G>A (p.Ala411Thr)
c.1513G>A (p.Ala505Thr)
c.206G>A (p.Gly69Asp)
c.1189G>A (p.Ala397Thr)
n.348G>A
gnomAD v4
3g.128481232C>ACA435525004GATA2c.1230G>T (p.Gly410=)
c.1512G>T (p.Gly504=)
c.205G>T (p.Gly69Cys)
c.1188G>T (p.Gly396=)
n.347G>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128481232C=CA1400714201GATA2c.1230G= (p.Gly410=)
c.1512G= (p.Gly504=)
c.205G= (p.Gly69=)
c.1188G= (p.Gly396=)
n.347G=
3g.128481232C>GCA435525005GATA2c.1230G>C (p.Gly410=)
c.1512G>C (p.Gly504=)
c.205G>C (p.Gly69Arg)
c.1188G>C (p.Gly396=)
n.347G>C
3g.128481232C>TCA435525007GATA2c.1230G>A (p.Gly410=)
c.1512G>A (p.Gly504=)
c.205G>A (p.Gly69Ser)
c.1188G>A (p.Gly396=)
n.347G>A
ClinVar dbSNP
3g.128481233C>ACA354413059GATA2c.1229G>T (p.Gly410Val)
c.1511G>T (p.Gly504Val)
c.204G>T (p.Arg68Ser)
c.1187G>T (p.Gly396Val)
n.346G>T
3g.128481233C>GCA354413061GATA2c.1229G>C (p.Gly410Ala)
c.1511G>C (p.Gly504Ala)
c.204G>C (p.Arg68Ser)
c.1187G>C (p.Gly396Ala)
n.346G>C
3g.128481233C>TCA354413063GATA2c.1229G>A (p.Gly410Glu)
c.1511G>A (p.Gly504Glu)
c.204G>A (p.Arg68=)
c.1187G>A (p.Gly396Glu)
n.346G>A
gnomAD v4
3g.128481234C>ACA354413064GATA2c.1228G>T (p.Gly410Trp)
c.1510G>T (p.Gly504Trp)
c.203G>T (p.Arg68Met)
c.1186G>T (p.Gly396Trp)
n.345G>T
3g.128481234C=CA1400714204GATA2c.1228G= (p.Gly410=)
c.1510G= (p.Gly504=)
c.203G= (p.Arg68=)
c.1186G= (p.Gly396=)
n.345G=
3g.128481234C>GCA354413066GATA2c.1228G>C (p.Gly410Arg)
c.1510G>C (p.Gly504Arg)
c.203G>C (p.Arg68Thr)
c.1186G>C (p.Gly396Arg)
n.345G>C
3g.128481234C>TCA354413067GATA2c.1228G>A (p.Gly410Arg)
c.1510G>A (p.Gly504Arg)
c.203G>A (p.Arg68Lys)
c.1186G>A (p.Gly396Arg)
n.345G>A
dbSNP gnomAD v2
3g.128481235T>ACA354413069GATA2c.1227A>T (p.Lys409Asn)
c.1509A>T (p.Lys503Asn)
c.202A>T (p.Arg68Trp)
c.1185A>T (p.Lys395Asn)
n.344A>T
3g.128481235T>CCA435525012GATA2c.1227A>G (p.Lys409=)
c.1509A>G (p.Lys503=)
c.202A>G (p.Arg68Gly)
c.1185A>G (p.Lys395=)
n.344A>G
3g.128481235T>GCA354413070GATA2c.1227A>C (p.Lys409Asn)
c.1509A>C (p.Lys503Asn)
c.202A>C (p.Arg68=)
c.1185A>C (p.Lys395Asn)
n.344A>C
3g.128481236T>ACA354413072GATA2c.1226A>T (p.Lys409Ile)
c.1508A>T (p.Lys503Ile)
c.201A>T (p.Glu67Asp)
c.1184A>T (p.Lys395Ile)
n.343A>T
3g.128481236T>CCA354413074GATA2c.1226A>G (p.Lys409Arg)
c.1508A>G (p.Lys503Arg)
c.201A>G (p.Glu67=)
c.1184A>G (p.Lys395Arg)
n.343A>G
dbSNP
3g.128481236T>GCA354413075GATA2c.1226A>C (p.Lys409Thr)
c.1508A>C (p.Lys503Thr)
c.201A>C (p.Glu67Asp)
c.1184A>C (p.Lys395Thr)
n.343A>C
3g.128481236T=CA1400714206GATA2c.1226A= (p.Lys409=)
c.1508A= (p.Lys503=)
c.201A= (p.Glu67=)
c.1184A= (p.Lys395=)
n.343A=
3g.128481237T>ACA354413083GATA2c.1225A>T (p.Lys409Ter)
c.1507A>T (p.Lys503Ter)
c.200A>T (p.Glu67Val)
c.1183A>T (p.Lys395Ter)
n.342A>T
3g.128481237T>CCA354413081GATA2c.1225A>G (p.Lys409Glu)
c.1507A>G (p.Lys503Glu)
c.200A>G (p.Glu67Gly)
c.1183A>G (p.Lys395Glu)
n.342A>G
3g.128481237T>GCA354413077GATA2c.1225A>C (p.Lys409Gln)
c.1507A>C (p.Lys503Gln)
c.200A>C (p.Glu67Ala)
c.1183A>C (p.Lys395Gln)
n.342A>C
3g.128481238C>ACA354413084GATA2c.1224G>T (p.Lys408Asn)
c.1506G>T (p.Lys502Asn)
c.199G>T (p.Glu67Ter)
c.1182G>T (p.Lys394Asn)
n.341G>T
3g.128481238C>GCA354413085GATA2c.1224G>C (p.Lys408Asn)
c.1506G>C (p.Lys502Asn)
c.199G>C (p.Glu67Gln)
c.1182G>C (p.Lys394Asn)
n.341G>C
3g.128481238C>TCA435525019GATA2c.1224G>A (p.Lys408=)
c.1506G>A (p.Lys502=)
c.199G>A (p.Glu67Lys)
c.1182G>A (p.Lys394=)
n.341G>A
3g.128481239T>ACA354413087GATA2c.1223A>T (p.Lys408Met)
c.1505A>T (p.Lys502Met)
c.198A>T (p.Gln66His)
c.1181A>T (p.Lys394Met)
n.340A>T
3g.128481239T>CCA354413089GATA2c.1223A>G (p.Lys408Arg)
c.1505A>G (p.Lys502Arg)
c.198A>G (p.Gln66=)
c.1181A>G (p.Lys394Arg)
n.340A>G
ClinVar dbSNP gnomAD v4
3g.128481239T>GCA354413091GATA2c.1223A>C (p.Lys408Thr)
c.1505A>C (p.Lys502Thr)
c.198A>C (p.Gln66His)
c.1181A>C (p.Lys394Thr)
n.340A>C
3g.128481240T>ACA354413092GATA2c.1222A>T (p.Lys408Ter)
c.1504A>T (p.Lys502Ter)
c.197A>T (p.Gln66Leu)
c.1180A>T (p.Lys394Ter)
n.339A>T
3g.128481240T>CCA354413093GATA2c.1222A>G (p.Lys408Glu)
c.1504A>G (p.Lys502Glu)
c.197A>G (p.Gln66Arg)
c.1180A>G (p.Lys394Glu)
n.339A>G
ClinVar dbSNP gnomAD v4
3g.128481240T>GCA354413095GATA2c.1222A>C (p.Lys408Gln)
c.1504A>C (p.Lys502Gln)
c.197A>C (p.Gln66Pro)
c.1180A>C (p.Lys394Gln)
n.339A>C
3g.128481240T=CA1400714210GATA2c.1222A= (p.Lys408=)
c.1504A= (p.Lys502=)
c.197A= (p.Gln66=)
c.1180A= (p.Lys394=)
n.339A=
3g.128481241G>ACA435525025GATA2c.1221C>T (p.Ser407=)
c.1503C>T (p.Ser501=)
c.196C>T (p.Gln66Ter)
c.1179C>T (p.Ser393=)
n.338C>T
3g.128481241G>CCA354413097GATA2c.1221C>G (p.Ser407Arg)
c.1503C>G (p.Ser501Arg)
c.196C>G (p.Gln66Glu)
c.1179C>G (p.Ser393Arg)
n.338C>G
3g.128481241G=CA1400714213GATA2c.1221C= (p.Ser407=)
c.1503C= (p.Ser501=)
c.196C= (p.Gln66=)
c.1179C= (p.Ser393=)
n.338C=
3g.128481241G>TCA354413098GATA2c.1221C>A (p.Ser407Arg)
c.1503C>A (p.Ser501Arg)
c.196C>A (p.Gln66Lys)
c.1179C>A (p.Ser393Arg)
n.338C>A
ClinVar dbSNP
3g.128481242C>ACA354413100GATA2c.1220G>T (p.Ser407Ile)
c.1502G>T (p.Ser501Ile)
c.195G>T (p.Glu65Asp)
c.1178G>T (p.Ser393Ile)
n.337G>T
3g.128481242C=CA1400714215GATA2c.1220G= (p.Ser407=)
c.1502G= (p.Ser501=)
c.195G= (p.Glu65=)
c.1178G= (p.Ser393=)
n.337G=
3g.128481242C>GCA354413102GATA2c.1220G>C (p.Ser407Thr)
c.1502G>C (p.Ser501Thr)
c.195G>C (p.Glu65Asp)
c.1178G>C (p.Ser393Thr)
n.337G>C
3g.128481242C>TCA354413103GATA2c.1220G>A (p.Ser407Asn)
c.1502G>A (p.Ser501Asn)
c.195G>A (p.Glu65=)
c.1178G>A (p.Ser393Asn)
n.337G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128481243T>ACA354413105GATA2c.1219A>T (p.Ser407Cys)
c.1501A>T (p.Ser501Cys)
c.194A>T (p.Glu65Val)
c.1177A>T (p.Ser393Cys)
n.336A>T
3g.128481243T>CCA354413108GATA2c.1219A>G (p.Ser407Gly)
c.1501A>G (p.Ser501Gly)
c.194A>G (p.Glu65Gly)
c.1177A>G (p.Ser393Gly)
n.336A>G
3g.128481243T>GCA354413106GATA2c.1219A>C (p.Ser407Arg)
c.1501A>C (p.Ser501Arg)
c.194A>C (p.Glu65Ala)
c.1177A>C (p.Ser393Arg)
n.336A>C
3g.128481244C>ACA354413113GATA2c.1218G>T (p.Lys406Asn)
c.1500G>T (p.Lys500Asn)
c.193G>T (p.Glu65Ter)
c.1176G>T (p.Lys392Asn)
n.335G>T
3g.128481244C>GCA354413115GATA2c.1218G>C (p.Lys406Asn)
c.1500G>C (p.Lys500Asn)
c.193G>C (p.Glu65Gln)
c.1176G>C (p.Lys392Asn)
n.335G>C
3g.128481244C>TCA435525033GATA2c.1218G>A (p.Lys406=)
c.1500G>A (p.Lys500=)
c.193G>A (p.Glu65Lys)
c.1176G>A (p.Lys392=)
n.335G>A
3g.128481245T>ACA2599817GATA2c.1217A>T (p.Lys406Met)
c.1499A>T (p.Lys500Met)
c.192A>T (p.Glu64Asp)
c.1175A>T (p.Lys392Met)
n.334A>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481245T>CCA354413118GATA2c.1217A>G (p.Lys406Arg)
c.1499A>G (p.Lys500Arg)
c.192A>G (p.Glu64=)
c.1175A>G (p.Lys392Arg)
n.334A>G
ClinVar dbSNP gnomAD v4
3g.128481245T>GCA354413119GATA2c.1217A>C (p.Lys406Thr)
c.1499A>C (p.Lys500Thr)
c.192A>C (p.Glu64Asp)
c.1175A>C (p.Lys392Thr)
n.334A>C
3g.128481245T=CA1400714222GATA2c.1217A= (p.Lys406=)
c.1499A= (p.Lys500=)
c.192A= (p.Glu64=)
c.1175A= (p.Lys392=)
n.334A=
3g.128481246delCA2580068696GATA2c.1217del (p.Lys406ArgfsTer?)
c.1499del (p.Lys500ArgfsTer?)
c.192del (p.Glu65SerfsTer?)
c.1175del (p.Lys392ArgfsTer?)
n.334del
ClinVar
3g.128481246T>ACA354413121GATA2c.1216A>T (p.Lys406Ter)
c.1498A>T (p.Lys500Ter)
c.191A>T (p.Glu64Val)
c.1174A>T (p.Lys392Ter)
n.333A>T
3g.128481246T>CCA354413122GATA2c.1216A>G (p.Lys406Glu)
c.1498A>G (p.Lys500Glu)
c.191A>G (p.Glu64Gly)
c.1174A>G (p.Lys392Glu)
n.333A>G
3g.128481246T>GCA354413123GATA2c.1216A>C (p.Lys406Gln)
c.1498A>C (p.Lys500Gln)
c.191A>C (p.Glu64Ala)
c.1174A>C (p.Lys392Gln)
n.333A>C
ClinVar dbSNP
3g.128481246T=CA1400714226GATA2c.1216A= (p.Lys406=)
c.1498A= (p.Lys500=)
c.191A= (p.Glu64=)
c.1174A= (p.Lys392=)
n.333A=
3g.128481246_128481262dupCA2499216426GATA2c.1200_1216dup (p.Lys406SerfsTer?)
c.1482_1498dup (p.Lys500SerfsTer?)
c.175_191dup (p.Glu65SerfsTer?)
c.1158_1174dup (p.Lys392SerfsTer?)
n.317_333dup
ClinVar dbSNP
3g.128481247C>ACA2599819GATA2c.1215G>T (p.Lys405Asn)
c.1497G>T (p.Lys499Asn)
c.190G>T (p.Glu64Ter)
c.1173G>T (p.Lys391Asn)
n.332G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128481247C=CA1400714229GATA2c.1215G= (p.Lys405=)
c.1497G= (p.Lys499=)
c.190G= (p.Glu64=)
c.1173G= (p.Lys391=)
n.332G=
3g.128481247C>GCA2599818GATA2c.1215G>C (p.Lys405Asn)
c.1497G>C (p.Lys499Asn)
c.190G>C (p.Glu64Gln)
c.1173G>C (p.Lys391Asn)
n.332G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481247C>TCA435525039GATA2c.1215G>A (p.Lys405=)
c.1497G>A (p.Lys499=)
c.190G>A (p.Glu64Lys)
c.1173G>A (p.Lys391=)
n.332G>A
dbSNP
3g.128481248T>ACA354413128GATA2c.1214A>T (p.Lys405Met)
c.1496A>T (p.Lys499Met)
c.189A>T (p.Gln63His)
c.1172A>T (p.Lys391Met)
n.331A>T
3g.128481248T>CCA2599820GATA2c.1214A>G (p.Lys405Arg)
c.1496A>G (p.Lys499Arg)
c.189A>G (p.Gln63=)
c.1172A>G (p.Lys391Arg)
n.331A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128481248T>GCA354413126GATA2c.1214A>C (p.Lys405Thr)
c.1496A>C (p.Lys499Thr)
c.189A>C (p.Gln63His)
c.1172A>C (p.Lys391Thr)
n.331A>C
3g.128481248T=CA1400714232GATA2c.1214A= (p.Lys405=)
c.1496A= (p.Lys499=)
c.189A= (p.Gln63=)
c.1172A= (p.Lys391=)
n.331A=
3g.128481249T>ACA354413130GATA2c.1213A>T (p.Lys405Ter)
c.1495A>T (p.Lys499Ter)
c.188A>T (p.Gln63Leu)
c.1171A>T (p.Lys391Ter)
n.330A>T
3g.128481249T>CCA354413132GATA2c.1213A>G (p.Lys405Glu)
c.1495A>G (p.Lys499Glu)
c.188A>G (p.Gln63Arg)
c.1171A>G (p.Lys391Glu)
n.330A>G
gnomAD v4
3g.128481249T>GCA354413133GATA2c.1213A>C (p.Lys405Gln)
c.1495A>C (p.Lys499Gln)
c.188A>C (p.Gln63Pro)
c.1171A>C (p.Lys391Gln)
n.330A>C
3g.128481250G>ACA435525045GATA2c.1212C>T (p.Ser404=)
c.1494C>T (p.Ser498=)
c.187C>T (p.Gln63Ter)
c.1170C>T (p.Ser390=)
n.329C>T
ClinVar dbSNP
3g.128481250G>CCA435525047GATA2c.1212C>G (p.Ser404=)
c.1494C>G (p.Ser498=)
c.187C>G (p.Gln63Glu)
c.1170C>G (p.Ser390=)
n.329C>G
3g.128481250G>TCA435525048GATA2c.1212C>A (p.Ser404=)
c.1494C>A (p.Ser498=)
c.187C>A (p.Gln63Lys)
c.1170C>A (p.Ser390=)
n.329C>A
3g.128481251G>ACA354413135GATA2c.1211C>T (p.Ser404Phe)
c.1493C>T (p.Ser498Phe)
c.186C>T (p.Val62=)
c.1169C>T (p.Ser390Phe)
n.328C>T
3g.128481251G>CCA354413137GATA2c.1211C>G (p.Ser404Cys)
c.1493C>G (p.Ser498Cys)
c.186C>G (p.Val62=)
c.1169C>G (p.Ser390Cys)
n.328C>G
3g.128481251G>TCA354413139GATA2c.1211C>A (p.Ser404Tyr)
c.1493C>A (p.Ser498Tyr)
c.186C>A (p.Val62=)
c.1169C>A (p.Ser390Tyr)
n.328C>A
dbSNP gnomAD v3 gnomAD v4
3g.128481252A>CCA354413145GATA2c.1210T>G (p.Ser404Ala)
c.1492T>G (p.Ser498Ala)
c.185T>G (p.Val62Gly)
c.1168T>G (p.Ser390Ala)
n.327T>G
3g.128481252A>GCA354413142GATA2c.1210T>C (p.Ser404Pro)
c.1492T>C (p.Ser498Pro)
c.185T>C (p.Val62Ala)
c.1168T>C (p.Ser390Pro)
n.327T>C
ClinVar dbSNP
3g.128481252A>TCA354413143GATA2c.1210T>A (p.Ser404Thr)
c.1492T>A (p.Ser498Thr)
c.185T>A (p.Val62Asp)
c.1168T>A (p.Ser390Thr)
n.327T>A
3g.128481253C>ACA354413146GATA2c.1209G>T (p.Lys403Asn)
c.1491G>T (p.Lys497Asn)
c.184G>T (p.Val62Phe)
c.1167G>T (p.Lys389Asn)
n.326G>T
3g.128481253C=CA1400714235GATA2c.1209G= (p.Lys403=)
c.1491G= (p.Lys497=)
c.184G= (p.Val62=)
c.1167G= (p.Lys389=)
n.326G=
3g.128481253C>GCA354413147GATA2c.1209G>C (p.Lys403Asn)
c.1491G>C (p.Lys497Asn)
c.184G>C (p.Val62Leu)
c.1167G>C (p.Lys389Asn)
n.326G>C
3g.128481253C>TCA435525054GATA2c.1209G>A (p.Lys403=)
c.1491G>A (p.Lys497=)
c.184G>A (p.Val62Ile)
c.1167G>A (p.Lys389=)
n.326G>A
dbSNP gnomAD v4
3g.128481254T>ACA354413150GATA2c.1208A>T (p.Lys403Met)
c.1490A>T (p.Lys497Met)
c.183A>T (p.Gln61His)
c.1166A>T (p.Lys389Met)
n.325A>T
3g.128481254T>CCA354413151GATA2c.1208A>G (p.Lys403Arg)
c.1490A>G (p.Lys497Arg)
c.183A>G (p.Gln61=)
c.1166A>G (p.Lys389Arg)
n.325A>G
3g.128481254T>GCA354413152GATA2c.1208A>C (p.Lys403Thr)
c.1490A>C (p.Lys497Thr)
c.183A>C (p.Gln61His)
c.1166A>C (p.Lys389Thr)
n.325A>C
3g.128481255T>ACA354413154GATA2c.1207A>T (p.Lys403Ter)
c.1489A>T (p.Lys497Ter)
c.182A>T (p.Gln61Leu)
c.1165A>T (p.Lys389Ter)
n.324A>T
3g.128481255T>CCA354413157GATA2c.1207A>G (p.Lys403Glu)
c.1489A>G (p.Lys497Glu)
c.182A>G (p.Gln61Arg)
c.1165A>G (p.Lys389Glu)
n.324A>G
dbSNP
3g.128481255T>GCA354413155GATA2c.1207A>C (p.Lys403Gln)
c.1489A>C (p.Lys497Gln)
c.182A>C (p.Gln61Pro)
c.1165A>C (p.Lys389Gln)
n.324A>C
3g.128481255T=CA1400714237GATA2c.1207A= (p.Lys403=)
c.1489A= (p.Lys497=)
c.182A= (p.Gln61=)
c.1165A= (p.Lys389=)
n.324A=
3g.128481256G>ACA2599821GATA2c.1206C>T (p.Asn402=)
c.1488C>T (p.Asn496=)
c.181C>T (p.Gln61Ter)
c.1164C>T (p.Asn388=)
n.323C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128481256G>CCA354413160GATA2c.1206C>G (p.Asn402Lys)
c.1488C>G (p.Asn496Lys)
c.181C>G (p.Gln61Glu)
c.1164C>G (p.Asn388Lys)
n.323C>G
3g.128481256G=CA1400714240GATA2c.1206C= (p.Asn402=)
c.1488C= (p.Asn496=)
c.181C= (p.Gln61=)
c.1164C= (p.Asn388=)
n.323C=
3g.128481256G>TCA354413161GATA2c.1206C>A (p.Asn402Lys)
c.1488C>A (p.Asn496Lys)
c.181C>A (p.Gln61Lys)
c.1164C>A (p.Asn388Lys)
n.323C>A
3g.128481257T>ACA354413162GATA2c.1205A>T (p.Asn402Ile)
c.1487A>T (p.Asn496Ile)
c.180A>T (p.Gln60His)
c.1163A>T (p.Asn388Ile)
n.322A>T
3g.128481257T>CCA2599822GATA2c.1205A>G (p.Asn402Ser)
c.1487A>G (p.Asn496Ser)
c.180A>G (p.Gln60=)
c.1163A>G (p.Asn388Ser)
n.322A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128481257T>GCA354413163GATA2c.1205A>C (p.Asn402Thr)
c.1487A>C (p.Asn496Thr)
c.180A>C (p.Gln60His)
c.1163A>C (p.Asn388Thr)
n.322A>C
3g.128481257T=CA1400714249GATA2c.1205A= (p.Asn402=)
c.1487A= (p.Asn496=)
c.180A= (p.Gln60=)
c.1163A= (p.Asn388=)
n.322A=
3g.128481258T>ACA354413165GATA2c.1204A>T (p.Asn402Tyr)
c.1486A>T (p.Asn496Tyr)
c.179A>T (p.Gln60Leu)
c.1162A>T (p.Asn388Tyr)
n.321A>T
3g.128481258T>CCA354413166GATA2c.1204A>G (p.Asn402Asp)
c.1486A>G (p.Asn496Asp)
c.179A>G (p.Gln60Arg)
c.1162A>G (p.Asn388Asp)
n.321A>G
3g.128481258T>GCA354413168GATA2c.1204A>C (p.Asn402His)
c.1486A>C (p.Asn496His)
c.179A>C (p.Gln60Pro)
c.1162A>C (p.Asn388His)
n.321A>C
COSMIC
3g.128481259G>ACA435525066GATA2c.1203C>T (p.Ser401=)
c.1485C>T (p.Ser495=)
c.178C>T (p.Gln60Ter)
c.1161C>T (p.Ser387=)
n.320C>T
dbSNP gnomAD v3 gnomAD v4
3g.128481259G>CCA435525067GATA2c.1203C>G (p.Ser401=)
c.1485C>G (p.Ser495=)
c.178C>G (p.Gln60Glu)
c.1161C>G (p.Ser387=)
n.320C>G
3g.128481259G=CA1400714254GATA2c.1203C= (p.Ser401=)
c.1485C= (p.Ser495=)
c.178C= (p.Gln60=)
c.1161C= (p.Ser387=)
n.320C=
3g.128481259G>TCA435525068GATA2c.1203C>A (p.Ser401=)
c.1485C>A (p.Ser495=)
c.178C>A (p.Gln60Lys)
c.1161C>A (p.Ser387=)
n.320C>A
3g.128481260G>ACA354413170GATA2c.1202C>T (p.Ser401Phe)
c.1484C>T (p.Ser495Phe)
c.177C>T (p.Val59=)
c.1160C>T (p.Ser387Phe)
n.319C>T
3g.128481260G>CCA354413174GATA2c.1202C>G (p.Ser401Cys)
c.1484C>G (p.Ser495Cys)
c.177C>G (p.Val59=)
c.1160C>G (p.Ser387Cys)
n.319C>G
ClinVar
3g.128481260G>TCA354413176GATA2c.1202C>A (p.Ser401Tyr)
c.1484C>A (p.Ser495Tyr)
c.177C>A (p.Val59=)
c.1160C>A (p.Ser387Tyr)
n.319C>A
3g.128481261A>CCA354413178GATA2c.1201T>G (p.Ser401Ala)
c.1483T>G (p.Ser495Ala)
c.176T>G (p.Val59Gly)
c.1159T>G (p.Ser387Ala)
n.318T>G
3g.128481261A>GCA354413181GATA2c.1201T>C (p.Ser401Pro)
c.1483T>C (p.Ser495Pro)
c.176T>C (p.Val59Ala)
c.1159T>C (p.Ser387Pro)
n.318T>C
3g.128481261A>TCA354413180GATA2c.1201T>A (p.Ser401Thr)
c.1483T>A (p.Ser495Thr)
c.176T>A (p.Val59Asp)
c.1159T>A (p.Ser387Thr)
n.318T>A
3g.128481262C>ACA354413183GATA2c.1200G>T (p.Met400Ile)
c.1482G>T (p.Met494Ile)
c.175G>T (p.Val59Phe)
c.1158G>T (p.Met386Ile)
n.317G>T
3g.128481262C=CA1400714257GATA2c.1200G= (p.Met400=)
c.1482G= (p.Met494=)
c.175G= (p.Val59=)
c.1158G= (p.Met386=)
n.317G=
3g.128481262C>GCA354413185GATA2c.1200G>C (p.Met400Ile)
c.1482G>C (p.Met494Ile)
c.175G>C (p.Val59Leu)
c.1158G>C (p.Met386Ile)
n.317G>C
3g.128481262C>TCA16611352GATA2c.1200G>A (p.Met400Ile)
c.1482G>A (p.Met494Ile)
c.175G>A (p.Val59Ile)
c.1158G>A (p.Met386Ile)
n.317G>A
ClinVar dbSNP gnomAD v4
3g.128481263A>CCA354413187GATA2c.1199T>G (p.Met400Arg)
c.1481T>G (p.Met494Arg)
c.174T>G (p.Asp58Glu)
c.1157T>G (p.Met386Arg)
n.316T>G
3g.128481263A>GCA354413188GATA2c.1199T>C (p.Met400Thr)
c.1481T>C (p.Met494Thr)
c.174T>C (p.Asp58=)
c.1157T>C (p.Met386Thr)
n.316T>C
ClinVar dbSNP
3g.128481263A>TCA354413189GATA2c.1199T>A (p.Met400Lys)
c.1481T>A (p.Met494Lys)
c.174T>A (p.Asp58Glu)
c.1157T>A (p.Met386Lys)
n.316T>A
3g.128481264T>ACA354413192GATA2c.1198A>T (p.Met400Leu)
c.1480A>T (p.Met494Leu)
c.173A>T (p.Asp58Val)
c.1156A>T (p.Met386Leu)
n.315A>T
ClinVar dbSNP gnomAD v4 COSMIC
3g.128481264T>CCA354413194GATA2c.1198A>G (p.Met400Val)
c.1480A>G (p.Met494Val)
c.173A>G (p.Asp58Gly)
c.1156A>G (p.Met386Val)
n.315A>G
gnomAD v4
3g.128481264T>GCA354413195GATA2c.1198A>C (p.Met400Leu)
c.1480A>C (p.Met494Leu)
c.173A>C (p.Asp58Ala)
c.1156A>C (p.Met386Leu)
n.315A>C
dbSNP
3g.128481264T=CA1400714265GATA2c.1198A= (p.Met400=)
c.1480A= (p.Met494=)
c.173A= (p.Asp58=)
c.1156A= (p.Met386=)
n.315A=
3g.128481264_128481619delCA2499216427GATA2c.1143+200_1198del
c.1425+200_1480del
c.126+200_173del
c.1101+200_1156del
n.260+200_315del
ClinVar dbSNP
3g.128481265C>ACA83376298GATA2c.1197G>T (p.Lys399Asn)
c.1479G>T (p.Lys493Asn)
c.172G>T (p.Asp58Tyr)
c.1155G>T (p.Lys385Asn)
n.314G>T
ClinVar dbSNP
3g.128481265C=CA1400714271GATA2c.1197G= (p.Lys399=)
c.1479G= (p.Lys493=)
c.172G= (p.Asp58=)
c.1155G= (p.Lys385=)
n.314G=
3g.128481265C>GCA354413197GATA2c.1197G>C (p.Lys399Asn)
c.1479G>C (p.Lys493Asn)
c.172G>C (p.Asp58His)
c.1155G>C (p.Lys385Asn)
n.314G>C
3g.128481265C>TCA435525079GATA2c.1197G>A (p.Lys399=)
c.1479G>A (p.Lys493=)
c.172G>A (p.Asp58Asn)
c.1155G>A (p.Lys385=)
n.314G>A
COSMIC
3g.128481265_128481266insCTCA2740090988GATA2c.1196_1197insAG (p.Met400GlyfsTer?)
c.1478_1479insAG (p.Met494GlyfsTer?)
c.171_172insAG (p.Asp58ArgfsTer?)
c.1154_1155insAG (p.Met386GlyfsTer?)
n.313_314insAG
ClinVar
3g.128481266T>ACA354413203GATA2c.1196A>T (p.Lys399Met)
c.1478A>T (p.Lys493Met)
c.171A>T (p.Glu57Asp)
c.1154A>T (p.Lys385Met)
n.313A>T
3g.128481266T>CCA354413201GATA2c.1196A>G (p.Lys399Arg)
c.1478A>G (p.Lys493Arg)
c.171A>G (p.Glu57=)
c.1154A>G (p.Lys385Arg)
n.313A>G
dbSNP gnomAD v2 gnomAD v4
3g.128481266T>GCA354413200GATA2c.1196A>C (p.Lys399Thr)
c.1478A>C (p.Lys493Thr)
c.171A>C (p.Glu57Asp)
c.1154A>C (p.Lys385Thr)
n.313A>C
3g.128481266T=CA1400714274GATA2c.1196A= (p.Lys399=)
c.1478A= (p.Lys493=)
c.171A= (p.Glu57=)
c.1154A= (p.Lys385=)
n.313A=
3g.128481267T>ACA354413205GATA2c.1195A>T (p.Lys399Ter)
c.1477A>T (p.Lys493Ter)
c.170A>T (p.Glu57Val)
c.1153A>T (p.Lys385Ter)
n.312A>T
3g.128481267T>CCA354413206GATA2c.1195A>G (p.Lys399Glu)
c.1477A>G (p.Lys493Glu)
c.170A>G (p.Glu57Gly)
c.1153A>G (p.Lys385Glu)
n.312A>G
3g.128481267T>GCA354413208GATA2c.1195A>C (p.Lys399Gln)
c.1477A>C (p.Lys493Gln)
c.170A>C (p.Glu57Ala)
c.1153A>C (p.Lys385Gln)
n.312A>C
3g.128481268C>ACA435525084GATA2c.1194G>T (p.Arg398=)
c.1476G>T (p.Arg492=)
c.169G>T (p.Glu57Ter)
c.1152G>T (p.Arg384=)
n.311G>T
3g.128481268C=CA1400714278GATA2c.1194G= (p.Arg398=)
c.1476G= (p.Arg492=)
c.169G= (p.Glu57=)
c.1152G= (p.Arg384=)
n.311G=
3g.128481268C>GCA435525086GATA2c.1194G>C (p.Arg398=)
c.1476G>C (p.Arg492=)
c.169G>C (p.Glu57Gln)
c.1152G>C (p.Arg384=)
n.311G>C
ClinVar dbSNP gnomAD v4
3g.128481268C>TCA435525088GATA2c.1194G>A (p.Arg398=)
c.1476G>A (p.Arg492=)
c.169G>A (p.Glu57Lys)
c.1152G>A (p.Arg384=)
n.311G>A
ClinVar
3g.128481269C>ACA354413209GATA2c.1193G>T (p.Arg398Leu)
c.1475G>T (p.Arg492Leu)
c.168G>T (p.Pro56=)
c.1151G>T (p.Arg384Leu)
n.310G>T
3g.128481269C=CA1400714284GATA2c.1193G= (p.Arg398=)
c.1475G= (p.Arg492=)
c.168G= (p.Pro56=)
c.1151G= (p.Arg384=)
n.310G=
3g.128481269C>GCA354413211GATA2c.1193G>C (p.Arg398Pro)
c.1475G>C (p.Arg492Pro)
c.168G>C (p.Pro56=)
c.1151G>C (p.Arg384Pro)
n.310G>C
3g.128481269C>TCA354413213GATA2c.1193G>A (p.Arg398Gln)
c.1475G>A (p.Arg492Gln)
c.168G>A (p.Pro56=)
c.1151G>A (p.Arg384Gln)
n.310G>A
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
3g.128481270G>ACA128572GATA2c.1192C>T (p.Arg398Trp)
c.1474C>T (p.Arg492Trp)
c.167C>T (p.Pro56Leu)
c.1150C>T (p.Arg384Trp)
n.309C>T
ClinVar dbSNP gnomAD v4 COSMIC
3g.128481270G>CCA354413214GATA2c.1192C>G (p.Arg398Gly)
c.1474C>G (p.Arg492Gly)
c.167C>G (p.Pro56Arg)
c.1150C>G (p.Arg384Gly)
n.309C>G
ClinVar
3g.128481270G=CA1400714294GATA2c.1192C= (p.Arg398=)
c.1474C= (p.Arg492=)
c.167C= (p.Pro56=)
c.1150C= (p.Arg384=)
n.309C=
3g.128481270G>TCA435525093GATA2c.1192C>A (p.Arg398=)
c.1474C>A (p.Arg492=)
c.167C>A (p.Pro56Gln)
c.1150C>A (p.Arg384=)
n.309C>A
3g.128481271G>ACA435525094GATA2c.1191C>T (p.Asn397=)
c.1473C>T (p.Asn491=)
c.166C>T (p.Pro56Ser)
c.1149C>T (p.Asn383=)
n.308C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128481271G>CCA354413217GATA2c.1191C>G (p.Asn397Lys)
c.1473C>G (p.Asn491Lys)
c.166C>G (p.Pro56Ala)
c.1149C>G (p.Asn383Lys)
n.308C>G
3g.128481271G=CA1400714298GATA2c.1191C= (p.Asn397=)
c.1473C= (p.Asn491=)
c.166C= (p.Pro56=)
c.1149C= (p.Asn383=)
n.308C=
3g.128481271G>TCA354413219GATA2c.1191C>A (p.Asn397Lys)
c.1473C>A (p.Asn491Lys)
c.166C>A (p.Pro56Thr)
c.1149C>A (p.Asn383Lys)
n.308C>A
3g.128481272T>ACA354413220GATA2c.1190A>T (p.Asn397Ile)
c.1472A>T (p.Asn491Ile)
c.165A>T (p.Glu55Asp)
c.1148A>T (p.Asn383Ile)
n.307A>T
3g.128481272T>CCA354413222GATA2c.1190A>G (p.Asn397Ser)
c.1472A>G (p.Asn491Ser)
c.165A>G (p.Glu55=)
c.1148A>G (p.Asn383Ser)
n.307A>G
3g.128481272T>GCA354413223GATA2c.1190A>C (p.Asn397Thr)
c.1472A>C (p.Asn491Thr)
c.165A>C (p.Glu55Asp)
c.1148A>C (p.Asn383Thr)
n.307A>C
3g.128481273T>ACA354413225GATA2c.1189A>T (p.Asn397Tyr)
c.1471A>T (p.Asn491Tyr)
c.164A>T (p.Glu55Val)
c.1147A>T (p.Asn383Tyr)
n.306A>T
3g.128481273T>CCA354413227GATA2c.1189A>G (p.Asn397Asp)
c.1471A>G (p.Asn491Asp)
c.164A>G (p.Glu55Gly)
c.1147A>G (p.Asn383Asp)
n.306A>G
3g.128481273T>GCA354413224GATA2c.1189A>C (p.Asn397His)
c.1471A>C (p.Asn491His)
c.164A>C (p.Glu55Ala)
c.1147A>C (p.Asn383His)
n.306A>C
3g.128481274C>ACA435525101GATA2c.1188G>T (p.Arg396=)
c.1470G>T (p.Arg490=)
c.163G>T (p.Glu55Ter)
c.1146G>T (p.Arg382=)
n.305G>T
gnomAD v4
3g.128481274C>GCA435525102GATA2c.1188G>C (p.Arg396=)
c.1470G>C (p.Arg490=)
c.163G>C (p.Glu55Gln)
c.1146G>C (p.Arg382=)
n.305G>C
3g.128481274C>TCA435525104GATA2c.1188G>A (p.Arg396=)
c.1470G>A (p.Arg490=)
c.163G>A (p.Glu55Lys)
c.1146G>A (p.Arg382=)
n.305G>A
ClinVar gnomAD v4
3g.128481275C>ACA354413235GATA2c.1187G>T (p.Arg396Leu)
c.1469G>T (p.Arg490Leu)
c.162G>T (p.Ser54=)
c.1145G>T (p.Arg382Leu)
n.304G>T
ClinVar dbSNP COSMIC
3g.128481275C=CA1400714302GATA2c.1187G= (p.Arg396=)
c.1469G= (p.Arg490=)
c.162G= (p.Ser54=)
c.1145G= (p.Arg382=)
n.304G=
3g.128481275C>GCA354413232GATA2c.1187G>C (p.Arg396Pro)
c.1469G>C (p.Arg490Pro)
c.162G>C (p.Ser54=)
c.1145G>C (p.Arg382Pro)
n.304G>C
3g.128481275C>TCA354413234GATA2c.1187G>A (p.Arg396Gln)
c.1469G>A (p.Arg490Gln)
c.162G>A (p.Ser54=)
c.1145G>A (p.Arg382Gln)
n.304G>A
ClinVar dbSNP COSMIC

Number of alleles fetched