Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.128485200_128487231delCA358451GATA2c.-45-155_871+527del
c.238-155_1153+527del
ClinVar
3g.128485206_128487871delCA916081440GATA2c.-200_871+527del
c.83_1153+527del
c.-45-789_871+527del
3g.128486300delCA1139532778GATA2c.302del (p.Gly101AlafsTer18)
c.584del (p.Gly195AlafsTer18)
ClinVar dbSNP
3g.128486301_128486302insAGGCCCGCA645523652GATA2c.300_301insCCTCGGG (p.Gly101ProfsTer?)
c.582_583insCCTCGGG (p.Gly195ProfsTer?)
COSMIC
3g.128486300C>ACA354407505GATA2c.298G>T (p.Gly100Trp)
c.580G>T (p.Gly194Trp)
3g.128486300C=CA1400719506GATA2c.298G= (p.Gly100=)
c.580G= (p.Gly194=)
3g.128486300C>GCA354407506GATA2c.298G>C (p.Gly100Arg)
c.580G>C (p.Gly194Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.128486300C>TCA354407508GATA2c.298G>A (p.Gly100Arg)
c.580G>A (p.Gly194Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.128486301G>ACA435510348GATA2c.297C>T (p.Asp99=)
c.579C>T (p.Asp193=)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.128486301G>CCA354407510GATA2c.297C>G (p.Asp99Glu)
c.579C>G (p.Asp193Glu)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.128486301G=CA1400719507GATA2c.297C= (p.Asp99=)
c.579C= (p.Asp193=)
3g.128486301G>TCA354407512GATA2c.297C>A (p.Asp99Glu)
c.579C>A (p.Asp193Glu)
ClinVar gnomAD v4
3g.128486302T>ACA354407514GATA2c.296A>T (p.Asp99Val)
c.578A>T (p.Asp193Val)
gnomAD v4
3g.128486302T>CCA2600044GATA2c.296A>G (p.Asp99Gly)
c.578A>G (p.Asp193Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128486302T>GCA354407517GATA2c.296A>C (p.Asp99Ala)
c.578A>C (p.Asp193Ala)
3g.128486302T=CA1400719508GATA2c.296A= (p.Asp99=)
c.578A= (p.Asp193=)
3g.128486303C>ACA2600045GATA2c.295G>T (p.Asp99Tyr)
c.577G>T (p.Asp193Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486303C=CA1400719509GATA2c.295G= (p.Asp99=)
c.577G= (p.Asp193=)
3g.128486303C>GCA354407522GATA2c.295G>C (p.Asp99His)
c.577G>C (p.Asp193His)
3g.128486303C>TCA354407518GATA2c.295G>A (p.Asp99Asn)
c.577G>A (p.Asp193Asn)
3g.128486304C>ACA435510349GATA2c.294G>T (p.Leu98=)
c.576G>T (p.Leu192=)
gnomAD v4
3g.128486304C>GCA435510350GATA2c.294G>C (p.Leu98=)
c.576G>C (p.Leu192=)
3g.128486304C>TCA435510351GATA2c.294G>A (p.Leu98=)
c.576G>A (p.Leu192=)
gnomAD v4
3g.128486305A>CCA354407525GATA2c.293T>G (p.Leu98Arg)
c.575T>G (p.Leu192Arg)
3g.128486305A>GCA354407529GATA2c.293T>C (p.Leu98Pro)
c.575T>C (p.Leu192Pro)
3g.128486305A>TCA354407526GATA2c.293T>A (p.Leu98Gln)
c.575T>A (p.Leu192Gln)
3g.128486306G>ACA435510352GATA2c.292C>T (p.Leu98=)
c.574C>T (p.Leu192=)
gnomAD v4
3g.128486306G>CCA354407531GATA2c.292C>G (p.Leu98Val)
c.574C>G (p.Leu192Val)
3g.128486306G>TCA354407534GATA2c.292C>A (p.Leu98Met)
c.574C>A (p.Leu192Met)
gnomAD v4
3g.128486307C>ACA354407535GATA2c.291G>T (p.Trp97Cys)
c.573G>T (p.Trp191Cys)
gnomAD v4
3g.128486307C>GCA354407539GATA2c.291G>C (p.Trp97Cys)
c.573G>C (p.Trp191Cys)
3g.128486307C>TCA354407537GATA2c.291G>A (p.Trp97Ter)
c.573G>A (p.Trp191Ter)
3g.128486308C>ACA354407541GATA2c.290G>T (p.Trp97Leu)
c.572G>T (p.Trp191Leu)
3g.128486308C>GCA354407543GATA2c.290G>C (p.Trp97Ser)
c.572G>C (p.Trp191Ser)
3g.128486308C>TCA354407544GATA2c.290G>A (p.Trp97Ter)
c.572G>A (p.Trp191Ter)
3g.128486309A=CA1400719510GATA2c.289T= (p.Trp97=)
c.571T= (p.Trp191=)
3g.128486309A>CCA354407546GATA2c.289T>G (p.Trp97Gly)
c.571T>G (p.Trp191Gly)
3g.128486309A>GCA354407548GATA2c.289T>C (p.Trp97Arg)
c.571T>C (p.Trp191Arg)
dbSNP gnomAD v2 gnomAD v4
3g.128486309A>TCA354407551GATA2c.289T>A (p.Trp97Arg)
c.571T>A (p.Trp191Arg)
dbSNP gnomAD v2 gnomAD v4
3g.128486309_128486310delCA2580068754GATA2c.288_289del (p.Trp97AlafsTer?)
c.570_571del (p.Trp191AlafsTer?)
ClinVar
3g.128486310G>ACA435510353GATA2c.288C>T (p.Pro96=)
c.570C>T (p.Pro190=)
ClinVar dbSNP gnomAD v2
3g.128486310G>CCA435510354GATA2c.288C>G (p.Pro96=)
c.570C>G (p.Pro190=)
3g.128486310G=CA1400719511GATA2c.288C= (p.Pro96=)
c.570C= (p.Pro190=)
3g.128486310G>TCA435510355GATA2c.288C>A (p.Pro96=)
c.570C>A (p.Pro190=)
gnomAD v4
3g.128486311G>ACA354407557GATA2c.287C>T (p.Pro96Leu)
c.569C>T (p.Pro190Leu)
gnomAD v4
3g.128486311G>CCA354407553GATA2c.287C>G (p.Pro96Arg)
c.569C>G (p.Pro190Arg)
3g.128486311G>TCA354407554GATA2c.287C>A (p.Pro96His)
c.569C>A (p.Pro190His)
gnomAD v4
3g.128486312G>ACA83372083GATA2c.286C>T (p.Pro96Ser)
c.568C>T (p.Pro190Ser)
ClinVar dbSNP gnomAD v4
3g.128486312G>CCA354407560GATA2c.286C>G (p.Pro96Ala)
c.568C>G (p.Pro190Ala)
3g.128486312G=CA1400719512GATA2c.286C= (p.Pro96=)
c.568C= (p.Pro190=)
3g.128486312G>TCA354407571GATA2c.286C>A (p.Pro96Thr)
c.568C>A (p.Pro190Thr)
gnomAD v4
3g.128486313C>ACA354407576GATA2c.285G>T (p.Leu95Phe)
c.567G>T (p.Leu189Phe)
gnomAD v4
3g.128486313C>GCA354407578GATA2c.285G>C (p.Leu95Phe)
c.567G>C (p.Leu189Phe)
3g.128486313C>TCA435510356GATA2c.285G>A (p.Leu95=)
c.567G>A (p.Leu189=)
gnomAD v4
3g.128486314A>CCA354407581GATA2c.284T>G (p.Leu95Trp)
c.566T>G (p.Leu189Trp)
3g.128486314A>GCA354407583GATA2c.284T>C (p.Leu95Ser)
c.566T>C (p.Leu189Ser)
3g.128486314A>TCA354407582GATA2c.284T>A (p.Leu95Ter)
c.566T>A (p.Leu189Ter)
3g.128486315A>CCA354407584GATA2c.283T>G (p.Leu95Val)
c.565T>G (p.Leu189Val)
ClinVar
3g.128486315A>GCA435510357GATA2c.283T>C (p.Leu95=)
c.565T>C (p.Leu189=)
3g.128486315A>TCA354407585GATA2c.283T>A (p.Leu95Met)
c.565T>A (p.Leu189Met)
3g.128486316A>CCA435510358GATA2c.282T>G (p.Gly94=)
c.564T>G (p.Gly188=)
3g.128486316A>GCA435510359GATA2c.282T>C (p.Gly94=)
c.564T>C (p.Gly188=)
3g.128486316A>TCA435510360GATA2c.282T>A (p.Gly94=)
c.564T>A (p.Gly188=)
3g.128486317C>ACA354407593GATA2c.281G>T (p.Gly94Val)
c.563G>T (p.Gly188Val)
ClinVar dbSNP gnomAD v4
3g.128486317C=CA1400719513GATA2c.281G= (p.Gly94=)
c.563G= (p.Gly188=)
3g.128486317C>GCA354407597GATA2c.281G>C (p.Gly94Ala)
c.563G>C (p.Gly188Ala)
3g.128486317C>TCA354407600GATA2c.281G>A (p.Gly94Asp)
c.563G>A (p.Gly188Asp)
3g.128486319delCA1139768889GATA2c.281del (p.Gly94ValfsTer25)
c.563del (p.Gly188ValfsTer25)
3g.128486318C>ACA354407609GATA2c.280G>T (p.Gly94Cys)
c.562G>T (p.Gly188Cys)
gnomAD v4
3g.128486318C=CA1400719514GATA2c.280G= (p.Gly94=)
c.562G= (p.Gly188=)
3g.128486318C>GCA354407611GATA2c.280G>C (p.Gly94Arg)
c.562G>C (p.Gly188Arg)
3g.128486318C>TCA354407614GATA2c.280G>A (p.Gly94Ser)
c.562G>A (p.Gly188Ser)
dbSNP gnomAD v2 gnomAD v4
3g.128486319C>ACA2600048GATA2c.279G>T (p.Pro93=)
c.561G>T (p.Pro187=)
ClinVar dbSNP ExAC gnomAD v4
3g.128486319C=CA1400719515GATA2c.279G= (p.Pro93=)
c.561G= (p.Pro187=)
3g.128486319C>GCA2600047GATA2c.279G>C (p.Pro93=)
c.561G>C (p.Pro187=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486319C>TCA2600046GATA2c.279G>A (p.Pro93=)
c.561G>A (p.Pro187=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128486320G>ACA354407620GATA2c.278C>T (p.Pro93Leu)
c.560C>T (p.Pro187Leu)
dbSNP gnomAD v2 gnomAD v4
3g.128486320G>CCA354407624GATA2c.278C>G (p.Pro93Arg)
c.560C>G (p.Pro187Arg)
gnomAD v4
3g.128486320G=CA1400719516GATA2c.278C= (p.Pro93=)
c.560C= (p.Pro187=)
3g.128486320G>TCA354407621GATA2c.278C>A (p.Pro93Gln)
c.560C>A (p.Pro187Gln)
ClinVar dbSNP gnomAD v4
3g.128486321G>ACA354407628GATA2c.277C>T (p.Pro93Ser)
c.559C>T (p.Pro187Ser)
ClinVar
3g.128486321G>CCA354407629GATA2c.277C>G (p.Pro93Ala)
c.559C>G (p.Pro187Ala)
3g.128486321G>TCA354407630GATA2c.277C>A (p.Pro93Thr)
c.559C>A (p.Pro187Thr)
3g.128486322G>ACA435510361GATA2c.276C>T (p.Ser92=)
c.558C>T (p.Ser186=)
3g.128486322G>CCA354407631GATA2c.276C>G (p.Ser92Arg)
c.558C>G (p.Ser186Arg)
3g.128486322G>TCA354407632GATA2c.276C>A (p.Ser92Arg)
c.558C>A (p.Ser186Arg)
gnomAD v4 COSMIC
3g.128486323C>ACA354407633GATA2c.275G>T (p.Ser92Ile)
c.557G>T (p.Ser186Ile)
gnomAD v4
3g.128486323C=CA1400719517GATA2c.275G= (p.Ser92=)
c.557G= (p.Ser186=)
3g.128486323C>GCA354407636GATA2c.275G>C (p.Ser92Thr)
c.557G>C (p.Ser186Thr)
gnomAD v4
3g.128486323C>TCA2600049GATA2c.275G>A (p.Ser92Asn)
c.557G>A (p.Ser186Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486324T>ACA354407643GATA2c.274A>T (p.Ser92Cys)
c.556A>T (p.Ser186Cys)
3g.128486324T>CCA354407646GATA2c.274A>G (p.Ser92Gly)
c.556A>G (p.Ser186Gly)
3g.128486324T>GCA354407648GATA2c.274A>C (p.Ser92Arg)
c.556A>C (p.Ser186Arg)
3g.128486325G>ACA435510362GATA2c.273C>T (p.His91=)
c.555C>T (p.His185=)
ClinVar gnomAD v4
3g.128486325G>CCA354407652GATA2c.273C>G (p.His91Gln)
c.555C>G (p.His185Gln)
gnomAD v4
3g.128486325G>TCA354407659GATA2c.273C>A (p.His91Gln)
c.555C>A (p.His185Gln)
3g.128486326T>ACA354407673GATA2c.272A>T (p.His91Leu)
c.554A>T (p.His185Leu)
3g.128486326T>CCA354407678GATA2c.272A>G (p.His91Arg)
c.554A>G (p.His185Arg)
gnomAD v4
3g.128486326T>GCA354407675GATA2c.272A>C (p.His91Pro)
c.554A>C (p.His185Pro)
3g.128486327G>ACA354407690GATA2c.271C>T (p.His91Tyr)
c.553C>T (p.His185Tyr)
gnomAD v4
3g.128486327G>CCA354407693GATA2c.271C>G (p.His91Asp)
c.553C>G (p.His185Asp)
3g.128486327G>TCA354407695GATA2c.271C>A (p.His91Asn)
c.553C>A (p.His185Asn)
gnomAD v4
3g.128486328C>ACA354407698GATA2c.270G>T (p.Leu90Phe)
c.552G>T (p.Leu184Phe)
gnomAD v4
3g.128486328C>GCA354407705GATA2c.270G>C (p.Leu90Phe)
c.552G>C (p.Leu184Phe)
3g.128486328C>TCA435510364GATA2c.270G>A (p.Leu90=)
c.552G>A (p.Leu184=)
gnomAD v4
3g.128486329A>CCA354407708GATA2c.269T>G (p.Leu90Trp)
c.551T>G (p.Leu184Trp)
3g.128486329A>GCA354407709GATA2c.269T>C (p.Leu90Ser)
c.551T>C (p.Leu184Ser)
gnomAD v4
3g.128486329A>TCA354407711GATA2c.269T>A (p.Leu90Ter)
c.551T>A (p.Leu184Ter)
3g.128486330A=CA1400719518GATA2c.268T= (p.Leu90=)
c.550T= (p.Leu184=)
3g.128486330A>CCA354407716GATA2c.268T>G (p.Leu90Val)
c.550T>G (p.Leu184Val)
ClinVar
3g.128486330A>GCA435510365GATA2c.268T>C (p.Leu90=)
c.550T>C (p.Leu184=)
ClinVar dbSNP gnomAD v4
3g.128486330A>TCA354407720GATA2c.268T>A (p.Leu90Met)
c.550T>A (p.Leu184Met)
gnomAD v4
3g.128486331C>ACA354407726GATA2c.267G>T (p.Leu89Phe)
c.549G>T (p.Leu183Phe)
3g.128486331C=CA1400719519GATA2c.267G= (p.Leu89=)
c.549G= (p.Leu183=)
3g.128486331C>GCA354407731GATA2c.267G>C (p.Leu89Phe)
c.549G>C (p.Leu183Phe)
3g.128486331C>TCA435510366GATA2c.267G>A (p.Leu89=)
c.549G>A (p.Leu183=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128486332A>CCA354407733GATA2c.266T>G (p.Leu89Trp)
c.548T>G (p.Leu183Trp)
3g.128486332A>GCA354407753GATA2c.266T>C (p.Leu89Ser)
c.548T>C (p.Leu183Ser)
3g.128486332A>TCA354407746GATA2c.266T>A (p.Leu89Ter)
c.548T>A (p.Leu183Ter)
3g.128486333A=CA1400719520GATA2c.265T= (p.Leu89=)
c.547T= (p.Leu183=)
3g.128486333A>CCA354407757GATA2c.265T>G (p.Leu89Val)
c.547T>G (p.Leu183Val)
3g.128486333A>GCA2600050GATA2c.265T>C (p.Leu89=)
c.547T>C (p.Leu183=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486333A>TCA354407768GATA2c.265T>A (p.Leu89Met)
c.547T>A (p.Leu183Met)
3g.128486334G>ACA435510367GATA2c.264C>T (p.His88=)
c.546C>T (p.His182=)
dbSNP gnomAD v2 gnomAD v4
3g.128486334G>CCA354407770GATA2c.264C>G (p.His88Gln)
c.546C>G (p.His182Gln)
3g.128486334G=CA1400719521GATA2c.264C= (p.His88=)
c.546C= (p.His182=)
3g.128486334G>TCA354407771GATA2c.264C>A (p.His88Gln)
c.546C>A (p.His182Gln)
gnomAD v4
3g.128486335T>ACA354407772GATA2c.263A>T (p.His88Leu)
c.545A>T (p.His182Leu)
3g.128486335T>CCA354407773GATA2c.263A>G (p.His88Arg)
c.545A>G (p.His182Arg)
gnomAD v4
3g.128486335T>GCA354407777GATA2c.263A>C (p.His88Pro)
c.545A>C (p.His182Pro)
3g.128486336G>ACA354407779GATA2c.262C>T (p.His88Tyr)
c.544C>T (p.His182Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.128486336G>CCA354407784GATA2c.262C>G (p.His88Asp)
c.544C>G (p.His182Asp)
3g.128486336G=CA1400719522GATA2c.262C= (p.His88=)
c.544C= (p.His182=)
3g.128486336G>TCA354407785GATA2c.262C>A (p.His88Asn)
c.544C>A (p.His182Asn)
gnomAD v4
3g.128486337T>ACA435510368GATA2c.261A>T (p.Pro87=)
c.543A>T (p.Pro181=)
3g.128486337T>CCA435510369GATA2c.261A>G (p.Pro87=)
c.543A>G (p.Pro181=)
3g.128486337T>GCA435510370GATA2c.261A>C (p.Pro87=)
c.543A>C (p.Pro181=)
3g.128486338G>ACA354407789GATA2c.260C>T (p.Pro87Leu)
c.542C>T (p.Pro181Leu)
gnomAD v4
3g.128486338G>CCA354407787GATA2c.260C>G (p.Pro87Arg)
c.542C>G (p.Pro181Arg)
COSMIC
3g.128486338G>TCA354407786GATA2c.260C>A (p.Pro87Gln)
c.542C>A (p.Pro181Gln)
gnomAD v4
3g.128486339G>ACA354407792GATA2c.259C>T (p.Pro87Ser)
c.541C>T (p.Pro181Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.128486339G>CCA354407795GATA2c.259C>G (p.Pro87Ala)
c.541C>G (p.Pro181Ala)
3g.128486339G=CA1400719523GATA2c.259C= (p.Pro87=)
c.541C= (p.Pro181=)
3g.128486339G>TCA354407797GATA2c.259C>A (p.Pro87Thr)
c.541C>A (p.Pro181Thr)
gnomAD v4
3g.128486340G>ACA435510371GATA2c.258C>T (p.Arg86=)
c.540C>T (p.Arg180=)
ClinVar dbSNP gnomAD v4
3g.128486340G>CCA435510372GATA2c.258C>G (p.Arg86=)
c.540C>G (p.Arg180=)
gnomAD v4
3g.128486340G=CA1400719524GATA2c.258C= (p.Arg86=)
c.540C= (p.Arg180=)
3g.128486340G>TCA435510373GATA2c.258C>A (p.Arg86=)
c.540C>A (p.Arg180=)
dbSNP gnomAD v4
3g.128486341_128486342delCA1139532776GATA2c.257_258del (p.Arg86ProfsTer?)
c.539_540del (p.Arg180ProfsTer?)
ClinVar dbSNP
3g.128486341C>ACA354407801GATA2c.257G>T (p.Arg86Leu)
c.539G>T (p.Arg180Leu)
gnomAD v4
3g.128486341C=CA1400719525GATA2c.257G= (p.Arg86=)
c.539G= (p.Arg180=)
3g.128486341C>GCA354407803GATA2c.257G>C (p.Arg86Pro)
c.539G>C (p.Arg180Pro)
3g.128486341C>TCA354407806GATA2c.257G>A (p.Arg86His)
c.539G>A (p.Arg180His)
ClinVar dbSNP gnomAD v4
3g.128486342G>ACA83372090GATA2c.256C>T (p.Arg86Cys)
c.538C>T (p.Arg180Cys)
dbSNP gnomAD v4
3g.128486342G>CCA354407807GATA2c.256C>G (p.Arg86Gly)
c.538C>G (p.Arg180Gly)
3g.128486342G=CA1400719526GATA2c.256C= (p.Arg86=)
c.538C= (p.Arg180=)
3g.128486342G>TCA354407808GATA2c.256C>A (p.Arg86Ser)
c.538C>A (p.Arg180Ser)
gnomAD v4
3g.128486343delCA1139532777GATA2c.256del (p.Arg86AlafsTer?)
c.538del (p.Arg180AlafsTer?)
ClinVar dbSNP
3g.128486343G>ACA435510375GATA2c.255C>T (p.Cys85=)
c.537C>T (p.Cys179=)
ClinVar dbSNP gnomAD v4
3g.128486343G>CCA354407809GATA2c.255C>G (p.Cys85Trp)
c.537C>G (p.Cys179Trp)
3g.128486343G=CA1400719527GATA2c.255C= (p.Cys85=)
c.537C= (p.Cys179=)
3g.128486343G>TCA354407810GATA2c.255C>A (p.Cys85Ter)
c.537C>A (p.Cys179Ter)
gnomAD v4
3g.128486344C>ACA354407818GATA2c.254G>T (p.Cys85Phe)
c.536G>T (p.Cys179Phe)
3g.128486344C>GCA354407816GATA2c.254G>C (p.Cys85Ser)
c.536G>C (p.Cys179Ser)
3g.128486344C>TCA354407813GATA2c.254G>A (p.Cys85Tyr)
c.536G>A (p.Cys179Tyr)
ClinVar
3g.128486345A>CCA354407821GATA2c.253T>G (p.Cys85Gly)
c.535T>G (p.Cys179Gly)
3g.128486345A>GCA354407828GATA2c.253T>C (p.Cys85Arg)
c.535T>C (p.Cys179Arg)
ClinVar
3g.128486345A>TCA354407829GATA2c.253T>A (p.Cys85Ser)
c.535T>A (p.Cys179Ser)
3g.128486346C>ACA354407834GATA2c.252G>T (p.Met84Ile)
c.534G>T (p.Met178Ile)
gnomAD v4
3g.128486346C>GCA354407835GATA2c.252G>C (p.Met84Ile)
c.534G>C (p.Met178Ile)
3g.128486346C>TCA354407839GATA2c.252G>A (p.Met84Ile)
c.534G>A (p.Met178Ile)
gnomAD v4
3g.128486347A>CCA354407843GATA2c.251T>G (p.Met84Arg)
c.533T>G (p.Met178Arg)
3g.128486347A>GCA354407844GATA2c.251T>C (p.Met84Thr)
c.533T>C (p.Met178Thr)
3g.128486347A>TCA354407846GATA2c.251T>A (p.Met84Lys)
c.533T>A (p.Met178Lys)
3g.128486348T>ACA354407848GATA2c.250A>T (p.Met84Leu)
c.532A>T (p.Met178Leu)
gnomAD v4
3g.128486348T>CCA354407854GATA2c.250A>G (p.Met84Val)
c.532A>G (p.Met178Val)
gnomAD v4
3g.128486348T>GCA354407857GATA2c.250A>C (p.Met84Leu)
c.532A>C (p.Met178Leu)
3g.128486349C>ACA354407860GATA2c.249G>T (p.Gln83His)
c.531G>T (p.Gln177His)
dbSNP gnomAD v4
3g.128486349C=CA1400719528GATA2c.249G= (p.Gln83=)
c.531G= (p.Gln177=)
3g.128486349C>GCA354407859GATA2c.249G>C (p.Gln83His)
c.531G>C (p.Gln177His)
gnomAD v4
3g.128486349C>TCA435510376GATA2c.249G>A (p.Gln83=)
c.531G>A (p.Gln177=)
3g.128486350delCA2586972847GATA2c.248del (p.Gln83ArgfsTer?)
c.530del (p.Gln177ArgfsTer?)
3g.128486350T>ACA354407868GATA2c.248A>T (p.Gln83Leu)
c.530A>T (p.Gln177Leu)
gnomAD v4
3g.128486350T>CCA354407870GATA2c.248A>G (p.Gln83Arg)
c.530A>G (p.Gln177Arg)
ClinVar dbSNP gnomAD v4
3g.128486350T>GCA354407872GATA2c.248A>C (p.Gln83Pro)
c.530A>C (p.Gln177Pro)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.128486350T=CA1400719529GATA2c.248A= (p.Gln83=)
c.530A= (p.Gln177=)
3g.128486351G>ACA354407875GATA2c.247C>T (p.Gln83Ter)
c.529C>T (p.Gln177Ter)
gnomAD v4
3g.128486351G>CCA354407878GATA2c.247C>G (p.Gln83Glu)
c.529C>G (p.Gln177Glu)
3g.128486351G>TCA354407880GATA2c.247C>A (p.Gln83Lys)
c.529C>A (p.Gln177Lys)
gnomAD v4
3g.128486352G>ACA435510377GATA2c.246C>T (p.Gly82=)
c.528C>T (p.Gly176=)
ClinVar gnomAD v4
3g.128486352G>CCA435510378GATA2c.246C>G (p.Gly82=)
c.528C>G (p.Gly176=)
3g.128486352G>TCA435510379GATA2c.246C>A (p.Gly82=)
c.528C>A (p.Gly176=)
gnomAD v4
3g.128486352_128486354delCA2586972848GATA2c.244_246del (p.Gly82del)
c.526_528del (p.Gly176del)
3g.128486353C>ACA354407883GATA2c.245G>T (p.Gly82Val)
c.527G>T (p.Gly176Val)
ClinVar gnomAD v4
3g.128486353C=CA1400719530GATA2c.245G= (p.Gly82=)
c.527G= (p.Gly176=)
3g.128486353C>GCA354407886GATA2c.245G>C (p.Gly82Ala)
c.527G>C (p.Gly176Ala)
3g.128486353C>TCA354407888GATA2c.245G>A (p.Gly82Asp)
c.527G>A (p.Gly176Asp)
dbSNP gnomAD v4
3g.128486354C>ACA354407891GATA2c.244G>T (p.Gly82Cys)
c.526G>T (p.Gly176Cys)
gnomAD v4
3g.128486354C=CA1400719531GATA2c.244G= (p.Gly82=)
c.526G= (p.Gly176=)
3g.128486354C>GCA354407894GATA2c.244G>C (p.Gly82Arg)
c.526G>C (p.Gly176Arg)
3g.128486354C>TCA354407897GATA2c.244G>A (p.Gly82Ser)
c.526G>A (p.Gly176Ser)
dbSNP gnomAD v3 gnomAD v4
3g.128486354_128486355delinsCTCA1400719532GATA2c.243_244delinsAG (p.Gly81=)
c.525_526delinsAG (p.Gly175=)
3g.128486355T>ACA435510381GATA2c.243A>T (p.Gly81=)
c.525A>T (p.Gly175=)
3g.128486355T>CCA435510382GATA2c.243A>G (p.Gly81=)
c.525A>G (p.Gly175=)
gnomAD v4
3g.128486355T>GCA435510383GATA2c.243A>C (p.Gly81=)
c.525A>C (p.Gly175=)
3g.128486355delinsGCCA358694GATA2c.243delinsGC (p.Gly82ArgfsTer?)
c.525delinsGC (p.Gly176ArgfsTer?)
ClinVar dbSNP
3g.128486356C>ACA354407909GATA2c.242G>T (p.Gly81Val)
c.524G>T (p.Gly175Val)
gnomAD v4
3g.128486356C=CA1400719533GATA2c.242G= (p.Gly81=)
c.524G= (p.Gly175=)
3g.128486356C>GCA16611184GATA2c.242G>C (p.Gly81Ala)
c.524G>C (p.Gly175Ala)
ClinVar dbSNP gnomAD v4
3g.128486356C>TCA354407906GATA2c.242G>A (p.Gly81Glu)
c.524G>A (p.Gly175Glu)
gnomAD v4
3g.128486357C>ACA354407918GATA2c.241G>T (p.Gly81Ter)
c.523G>T (p.Gly175Ter)
gnomAD v4
3g.128486357C=CA1400719534GATA2c.241G= (p.Gly81=)
c.523G= (p.Gly175=)
3g.128486357C>GCA354407915GATA2c.241G>C (p.Gly81Arg)
c.523G>C (p.Gly175Arg)
dbSNP gnomAD v4
3g.128486357C>TCA83372097GATA2c.241G>A (p.Gly81Arg)
c.523G>A (p.Gly175Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.128486358G>ACA83372100GATA2c.240C>T (p.Thr80=)
c.522C>T (p.Thr174=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.128486358G>CCA435510384GATA2c.240C>G (p.Thr80=)
c.522C>G (p.Thr174=)
dbSNP
3g.128486358G=CA1400719535GATA2c.240C= (p.Thr80=)
c.522C= (p.Thr174=)
3g.128486358G>TCA435510385GATA2c.240C>A (p.Thr80=)
c.522C>A (p.Thr174=)
gnomAD v4
3g.128486359dupCA645523653GATA2c.240dup (p.Gly81ArgfsTer?)
c.522dup (p.Gly175ArgfsTer?)
COSMIC
3g.128486359G>ACA354407925GATA2c.239C>T (p.Thr80Ile)
c.521C>T (p.Thr174Ile)
dbSNP gnomAD v2 gnomAD v4
3g.128486359G>CCA354407932GATA2c.239C>G (p.Thr80Ser)
c.521C>G (p.Thr174Ser)
gnomAD v4
3g.128486359G=CA1400719536GATA2c.239C= (p.Thr80=)
c.521C= (p.Thr174=)
3g.128486359G>TCA354407934GATA2c.239C>A (p.Thr80Asn)
c.521C>A (p.Thr174Asn)
ClinVar dbSNP gnomAD v4
3g.128486360T>ACA354407939GATA2c.238A>T (p.Thr80Ser)
c.520A>T (p.Thr174Ser)
3g.128486360T>CCA354407940GATA2c.238A>G (p.Thr80Ala)
c.520A>G (p.Thr174Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.128486360T>GCA354407946GATA2c.238A>C (p.Thr80Pro)
c.520A>C (p.Thr174Pro)
gnomAD v4
3g.128486360T=CA1400719537GATA2c.238A= (p.Thr80=)
c.520A= (p.Thr174=)
3g.128486361C>ACA435510386GATA2c.237G>T (p.Leu79=)
c.519G>T (p.Leu173=)
gnomAD v4
3g.128486361C>GCA435510387GATA2c.237G>C (p.Leu79=)
c.519G>C (p.Leu173=)
dbSNP
3g.128486361C>TCA435510388GATA2c.237G>A (p.Leu79=)
c.519G>A (p.Leu173=)
gnomAD v4 COSMIC
3g.128486362A>CCA354407953GATA2c.236T>G (p.Leu79Arg)
c.518T>G (p.Leu173Arg)
3g.128486362A>GCA354407956GATA2c.236T>C (p.Leu79Pro)
c.518T>C (p.Leu173Pro)
ClinVar gnomAD v4
3g.128486362A>TCA354407958GATA2c.236T>A (p.Leu79Gln)
c.518T>A (p.Leu173Gln)
gnomAD v4
3g.128486363G>ACA435510389GATA2c.235C>T (p.Leu79=)
c.517C>T (p.Leu173=)
3g.128486363G>CCA354407960GATA2c.235C>G (p.Leu79Val)
c.517C>G (p.Leu173Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.128486363G=CA1400719538GATA2c.235C= (p.Leu79=)
c.517C= (p.Leu173=)
3g.128486363G>TCA354407967GATA2c.235C>A (p.Leu79Met)
c.517C>A (p.Leu173Met)
dbSNP gnomAD v2 gnomAD v4
3g.128486364G>ACA435510390GATA2c.234C>T (p.Arg78=)
c.516C>T (p.Arg172=)
gnomAD v4
3g.128486364G>CCA435510391GATA2c.234C>G (p.Arg78=)
c.516C>G (p.Arg172=)
3g.128486364G>TCA435510392GATA2c.234C>A (p.Arg78=)
c.516C>A (p.Arg172=)
gnomAD v4
3g.128486365C>ACA354407978GATA2c.233G>T (p.Arg78Leu)
c.515G>T (p.Arg172Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.128486365C=CA1400719539GATA2c.233G= (p.Arg78=)
c.515G= (p.Arg172=)
3g.128486365C>GCA354407972GATA2c.233G>C (p.Arg78Pro)
c.515G>C (p.Arg172Pro)
3g.128486365C>TCA83372109GATA2c.233G>A (p.Arg78His)
c.515G>A (p.Arg172His)
dbSNP gnomAD v3 gnomAD v4
3g.128486366G>ACA354407986GATA2c.232C>T (p.Arg78Cys)
c.514C>T (p.Arg172Cys)
gnomAD v4
3g.128486366G>CCA354407988GATA2c.232C>G (p.Arg78Gly)
c.514C>G (p.Arg172Gly)
3g.128486366G>TCA354407989GATA2c.232C>A (p.Arg78Ser)
c.514C>A (p.Arg172Ser)
ClinVar gnomAD v4
3g.128486368dupCA658820608GATA2c.232dup (p.Arg78ProfsTer?)
c.514dup (p.Arg172ProfsTer?)
ClinVar dbSNP
3g.128486368delCA2667541077GATA2c.232del (p.Arg78AlafsTer2)
c.514del (p.Arg172AlafsTer2)
gnomAD v4
3g.128486367G>ACA435510393GATA2c.231C>T (p.Ala77=)
c.513C>T (p.Ala171=)
ClinVar dbSNP gnomAD v4
3g.128486367G>CCA435510394GATA2c.231C>G (p.Ala77=)
c.513C>G (p.Ala171=)
3g.128486367G>TCA435510395GATA2c.231C>A (p.Ala77=)
c.513C>A (p.Ala171=)
gnomAD v4
3g.128486367_128486368insCCATCACCTACCA2552406085GATA2c.230_231insGTAGGTGATGG (p.Arg78Ter)
c.512_513insGTAGGTGATGG (p.Arg172Ter)
3g.128486368G>ACA354407992GATA2c.230C>T (p.Ala77Val)
c.512C>T (p.Ala171Val)
dbSNP gnomAD v4
3g.128486368G>CCA354407998GATA2c.230C>G (p.Ala77Gly)
c.512C>G (p.Ala171Gly)
3g.128486368G=CA1400719540GATA2c.230C= (p.Ala77=)
c.512C= (p.Ala171=)
3g.128486368G>TCA354408000GATA2c.230C>A (p.Ala77Asp)
c.512C>A (p.Ala171Asp)
gnomAD v4
3g.128486369C>ACA354408003GATA2c.230-1G>T (n.230-1G>T)
c.512-1G>T (n.512-1G>T)
gnomAD v4
3g.128486369C>GCA354408005GATA2c.230-1G>C (n.230-1G>C)
c.512-1G>C (n.512-1G>C)
3g.128486369C>TCA354408007GATA2c.230-1G>A (n.230-1G>A)
c.512-1G>A (n.512-1G>A)
gnomAD v4 COSMIC
3g.128486369_128486370insAATTCTGAACATTGCCGGTGCCGGTGACCACGTGGTCGCTTCGCCCTCCGTGTACGGCGGTACCTATAACCTGCTCAAGTACACCCTCGCCGATCTCGGCATCGAAACCACCTTCGTCA2518105356GATA2c.230-2_230-1insACGAAGGTGGTTTCGATGCCGAGATCGGCGAGGGTGTACTTGAGCAGGTTATAGGTACCGCCGTACACGGAGGGCGAAGCGACCACGTGGTCACCGGCACCGGCAATGTTCAGAATT (n.230-2_230-1insACGAAGGTGGTTTCGATGCCGAGATCGGCGAGGGTGTACTTGAGCAGGTTATAGGTACCGCCGTACACGGAGGGCGAAGCGACCACGTGGTCACCGGCACCGGCAATGTTCAGAATT)
c.512-2_512-1insACGAAGGTGGTTTCGATGCCGAGATCGGCGAGGGTGTACTTGAGCAGGTTATAGGTACCGCCGTACACGGAGGGCGAAGCGACCACGTGGTCACCGGCACCGGCAATGTTCAGAATT (n.512-2_512-1insACGAAGGTGGTTTCGATGCCGAGATCGGCGAGGGTGTACTTGAGCAGGTTATAGGTACCGCCGTACACGGAGGGCGAAGCGACCACGTGGTCACCGGCACCGGCAATGTTCAGAATT)
3g.128486370T>ACA354408016GATA2c.230-2A>T (n.230-2A>T)
c.512-2A>T (n.512-2A>T)
3g.128486370T>CCA354408018GATA2c.230-2A>G (n.230-2A>G)
c.512-2A>G (n.512-2A>G)
gnomAD v4
3g.128486370T>GCA354408022GATA2c.230-2A>C (n.230-2A>C)
c.512-2A>C (n.512-2A>C)
3g.128486371G>ACA2667541079GATA2c.230-3C>T (n.230-3C>T)
c.512-3C>T (n.512-3C>T)
gnomAD v4
3g.128486371G>TCA2667541078GATA2c.230-3C>A (n.230-3C>A)
c.512-3C>A (n.512-3C>A)
gnomAD v4
3g.128486372C=CA1400719541GATA2c.230-4G= (n.230-4G=)
c.512-4G= (n.512-4G=)
3g.128486372C>TCA2600051GATA2c.230-4G>A (n.230-4G>A)
c.512-4G>A (n.512-4G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128486373G>ACA546098525GATA2c.230-5C>T (n.230-5C>T)
c.512-5C>T (n.512-5C>T)
ClinVar gnomAD v2 gnomAD v4
3g.128486373G=CA1400719542GATA2c.230-5C= (n.230-5C=)
c.512-5C= (n.512-5C=)
3g.128486373G>TCA2667541081GATA2c.230-5C>A (n.230-5C>A)
c.512-5C>A (n.512-5C>A)
gnomAD v4
3g.128486375delCA2667541080GATA2c.230-5del (n.230-5del)
c.512-5del (n.512-5del)
gnomAD v4
3g.128486374G>ACA2573136508GATA2c.230-6C>T (n.230-6C>T)
c.512-6C>T (n.512-6C>T)
ClinVar dbSNP gnomAD v4
3g.128486374G>CCA2667541082GATA2c.230-6C>G (n.230-6C>G)
c.512-6C>G (n.512-6C>G)
ClinVar gnomAD v4
3g.128486374G>TCA2667541083GATA2c.230-6C>A (n.230-6C>A)
c.512-6C>A (n.512-6C>A)
gnomAD v4
3g.128486385_128486386insAAGGCAAAGAGAGACA546098526GATA2c.230-6_230-5insTTTCTCTCTTTGCC (n.230-6_230-5insTTTCTCTCTTTGCC)
c.512-6_512-5insTTTCTCTCTTTGCC (n.512-6_512-5insTTTCTCTCTTTGCC)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128486375G>ACA1053363328GATA2c.230-7C>T (n.230-7C>T)
c.512-7C>T (n.512-7C>T)
dbSNP gnomAD v3 gnomAD v4
3g.128486375G=CA1400719543GATA2c.230-7C= (n.230-7C=)
c.512-7C= (n.512-7C=)
3g.128486375G>TCA2600052GATA2c.230-7C>A (n.230-7C>A)
c.512-7C>A (n.512-7C>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128486375_128486376insTCACAGCTCCCCACCACAAAAACGCAAATGCTCCCCTCTTCCA2667541084GATA2c.230-8_230-7insGAAGAGGGGAGCATTTGCGTTTTTGTGGTGGGGAGCTGTGA (n.230-8_230-7insGAAGAGGGGAGCATTTGCGTTTTTGTGGTGGGGAGCTGTGA)
c.512-8_512-7insGAAGAGGGGAGCATTTGCGTTTTTGTGGTGGGGAGCTGTGA (n.512-8_512-7insGAAGAGGGGAGCATTTGCGTTTTTGTGGTGGGGAGCTGTGA)
gnomAD v4
3g.128486376C>ACA2600054GATA2c.230-8G>T (n.230-8G>T)
c.512-8G>T (n.512-8G>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486376C=CA1400719545GATA2c.230-8G= (n.230-8G=)
c.512-8G= (n.512-8G=)
3g.128486376C>GCA2667541085GATA2c.230-8G>C (n.230-8G>C)
c.512-8G>C (n.512-8G>C)
gnomAD v4
3g.128486376_128486378delinsCAACA1400719544GATA2c.230-10_230-8delinsTTG (n.230-10_230-8delinsTTG)
c.512-10_512-8delinsTTG (n.512-10_512-8delinsTTG)
3g.128486376_128486380delinsCAAAGCA1400719546GATA2c.230-12_230-8delinsCTTTG (n.230-12_230-8delinsCTTTG)
c.512-12_512-8delinsCTTTG (n.512-12_512-8delinsCTTTG)
3g.128486377A>GCA2667541086GATA2c.230-9T>C (n.230-9T>C)
c.512-9T>C (n.512-9T>C)
gnomAD v4
3g.128486379delCA2667541087GATA2c.230-9del (n.230-9del)
c.512-9del (n.512-9del)
gnomAD v4
3g.128486378_128486379delCA1400719547GATA2c.230-10_230-9del (n.230-10_230-9del)
c.512-10_512-9del (n.512-10_512-9del)
dbSNP gnomAD v4
3g.128486378_128486381delCA2600053GATA2c.230-12_230-9del (n.230-12_230-9del)
c.512-12_512-9del (n.512-12_512-9del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128486378A=CA1400719549GATA2c.230-10T= (n.230-10T=)
c.512-10T= (n.512-10T=)
3g.128486378A>CCA546098527GATA2c.230-10T>G (n.230-10T>G)
c.512-10T>G (n.512-10T>G)
dbSNP gnomAD v2 gnomAD v4
3g.128486378A>GCA1400719550GATA2c.230-10T>C (n.230-10T>C)
c.512-10T>C (n.512-10T>C)
dbSNP
3g.128486378_128486382delinsAAGAGCA1400719548GATA2c.230-14_230-10delinsCTCTT (n.230-14_230-10delinsCTCTT)
c.512-14_512-10delinsCTCTT (n.512-14_512-10delinsCTCTT)
3g.128486379A>GCA2667541088GATA2c.230-11T>C (n.230-11T>C)
c.512-11T>C (n.512-11T>C)
gnomAD v4
3g.128486387_128486388delCA435510397GATA2c.230-12_230-11del (n.230-12_230-11del)
c.512-12_512-11del (n.512-12_512-11del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128486385_128486388delCA546098528GATA2c.230-14_230-11del (n.230-14_230-11del)
c.512-14_512-11del (n.512-14_512-11del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128486380G>ACA2573136509GATA2c.230-12C>T (n.230-12C>T)
c.512-12C>T (n.512-12C>T)
ClinVar dbSNP gnomAD v4
3g.128486380G>TCA2667541089GATA2c.230-12C>A (n.230-12C>A)
c.512-12C>A (n.512-12C>A)
gnomAD v4
3g.128486381A>GCA2667541090GATA2c.230-13T>C (n.230-13T>C)
c.512-13T>C (n.512-13T>C)
gnomAD v4
3g.128486382G>ACA83372119GATA2c.230-14C>T (n.230-14C>T)
c.512-14C>T (n.512-14C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128486382G=CA1400719551GATA2c.230-14C= (n.230-14C=)
c.512-14C= (n.512-14C=)
3g.128486382G>TCA2667541091GATA2c.230-14C>A (n.230-14C>A)
c.512-14C>A (n.512-14C>A)
gnomAD v4
3g.128486383A>GCA2667541092GATA2c.230-15T>C (n.230-15T>C)
c.512-15T>C (n.512-15T>C)
gnomAD v4
3g.128486384G>CCA2573136510GATA2c.230-16C>G (n.230-16C>G)
c.512-16C>G (n.512-16C>G)
ClinVar dbSNP
3g.128486384G>TCA2667541093GATA2c.230-16C>A (n.230-16C>A)
c.512-16C>A (n.512-16C>A)
gnomAD v4
3g.128486385A=CA1400719552GATA2c.230-17T= (n.230-17T=)
c.512-17T= (n.512-17T=)
3g.128486385A>GCA2600055GATA2c.230-17T>C (n.230-17T>C)
c.512-17T>C (n.512-17T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.128486385A>TCA2667541094GATA2c.230-17T>A (n.230-17T>A)
c.512-17T>A (n.512-17T>A)
gnomAD v4
3g.128486386G>ACA83372123GATA2c.230-18C>T (n.230-18C>T)
c.512-18C>T (n.512-18C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128486386G>CCA546098529GATA2c.230-18C>G (n.230-18C>G)
c.512-18C>G (n.512-18C>G)
dbSNP gnomAD v2 gnomAD v4
3g.128486386G=CA1400719553GATA2c.230-18C= (n.230-18C=)
c.512-18C= (n.512-18C=)
3g.128486386G>TCA2667541095GATA2c.230-18C>A (n.230-18C>A)
c.512-18C>A (n.512-18C>A)
gnomAD v4
3g.128486387A>GCA2667541096GATA2c.230-19T>C (n.230-19T>C)
c.512-19T>C (n.512-19T>C)
gnomAD v4
3g.128486388G>ACA2577890769GATA2c.230-20C>T (n.230-20C>T)
c.512-20C>T (n.512-20C>T)
ClinVar gnomAD v4
3g.128486388G>TCA2667541097GATA2c.230-20C>A (n.230-20C>A)
c.512-20C>A (n.512-20C>A)
gnomAD v4
3g.128486388_128486406delinsGGATCAGGGTGGGCAGAAACA1400719554GATA2c.230-38_230-20delinsTTTCTGCCCACCCTGATCC (n.230-38_230-20delinsTTTCTGCCCACCCTGATCC)
c.512-38_512-20delinsTTTCTGCCCACCCTGATCC (n.512-38_512-20delinsTTTCTGCCCACCCTGATCC)
3g.128486389G>ACA546098531GATA2c.230-21C>T (n.230-21C>T)
c.512-21C>T (n.512-21C>T)
dbSNP gnomAD v2 gnomAD v4
3g.128486389G=CA1400719555GATA2c.230-21C= (n.230-21C=)
c.512-21C= (n.512-21C=)
3g.128486389G>TCA546098532GATA2c.230-21C>A (n.230-21C>A)
c.512-21C>A (n.512-21C>A)
dbSNP gnomAD v2 gnomAD v4
3g.128486398_128486415dupCA546098533GATA2c.230-38_230-21dup (n.230-38_230-21dup)
c.512-38_512-21dup (n.512-38_512-21dup)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128486398_128486415delCA546098530GATA2c.230-38_230-21del (n.230-38_230-21del)
c.512-38_512-21del (n.512-38_512-21del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.128486390A=CA1400719557GATA2c.230-22T= (n.230-22T=)
c.512-22T= (n.512-22T=)
3g.128486390A>GCA1400719556GATA2c.230-22T>C (n.230-22T>C)
c.512-22T>C (n.512-22T>C)
dbSNP
3g.128486390A>TCA2667541098GATA2c.230-22T>A (n.230-22T>A)
c.512-22T>A (n.512-22T>A)
gnomAD v4
3g.128486391T>ACA2758339483GATA2c.230-23A>T (n.230-23A>T)
c.512-23A>T (n.512-23A>T)
3g.128486392C>ACA2667541099GATA2c.230-24G>T (n.230-24G>T)
c.512-24G>T (n.512-24G>T)
gnomAD v4
3g.128486392C=CA1400719558GATA2c.230-24G= (n.230-24G=)
c.512-24G= (n.512-24G=)
3g.128486392C>GCA2667541100GATA2c.230-24G>C (n.230-24G>C)
c.512-24G>C (n.512-24G>C)
gnomAD v4
3g.128486392C>TCA2600056GATA2c.230-24G>A (n.230-24G>A)
c.512-24G>A (n.512-24G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486393A>GCA2577890770GATA2c.230-25T>C (n.230-25T>C)
c.512-25T>C (n.512-25T>C)
gnomAD v4
3g.128486393A>TCA2667541101GATA2c.230-25T>A (n.230-25T>A)
c.512-25T>A (n.512-25T>A)
gnomAD v4
3g.128486393_128486394delinsAGCA1400719559GATA2c.230-26_230-25delinsCT (n.230-26_230-25delinsCT)
c.512-26_512-25delinsCT (n.512-26_512-25delinsCT)
3g.128486394G>ACA2667541102GATA2c.230-26C>T (n.230-26C>T)
c.512-26C>T (n.512-26C>T)
gnomAD v4
3g.128486394G>CCA2600058GATA2c.230-26C>G (n.230-26C>G)
c.512-26C>G (n.512-26C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486394G=CA1400719560GATA2c.230-26C= (n.230-26C=)
c.512-26C= (n.512-26C=)
3g.128486394G>TCA2667541103GATA2c.230-26C>A (n.230-26C>A)
c.512-26C>A (n.512-26C>A)
gnomAD v4
3g.128486396delCA2600057GATA2c.230-26del (n.230-26del)
c.512-26del (n.512-26del)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486395G>ACA546098534GATA2c.230-27C>T (n.230-27C>T)
c.512-27C>T (n.512-27C>T)
dbSNP gnomAD v2 gnomAD v4
3g.128486395G=CA1400719561GATA2c.230-27C= (n.230-27C=)
c.512-27C= (n.512-27C=)
3g.128486395G>TCA2667541104GATA2c.230-27C>A (n.230-27C>A)
c.512-27C>A (n.512-27C>A)
gnomAD v4
3g.128486396G>ACA2667541105GATA2c.230-28C>T (n.230-28C>T)
c.512-28C>T (n.512-28C>T)
gnomAD v4
3g.128486396G>CCA2600059GATA2c.230-28C>G (n.230-28C>G)
c.512-28C>G (n.512-28C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486396G=CA1400719562GATA2c.230-28C= (n.230-28C=)
c.512-28C= (n.512-28C=)
3g.128486396G>TCA2667541106GATA2c.230-28C>A (n.230-28C>A)
c.512-28C>A (n.512-28C>A)
gnomAD v4
3g.128486397T>CCA1400719563GATA2c.230-29A>G (n.230-29A>G)
c.512-29A>G (n.512-29A>G)
dbSNP gnomAD v4
3g.128486397T>GCA1400719564GATA2c.230-29A>C (n.230-29A>C)
c.512-29A>C (n.512-29A>C)
dbSNP
3g.128486397T=CA1400719565GATA2c.230-29A= (n.230-29A=)
c.512-29A= (n.512-29A=)
3g.128486398G>ACA2667541107GATA2c.230-30C>T (n.230-30C>T)
c.512-30C>T (n.512-30C>T)
gnomAD v4
3g.128486398G=CA1400719566GATA2c.230-30C= (n.230-30C=)
c.512-30C= (n.512-30C=)
3g.128486398G>TCA1053363346GATA2c.230-30C>A (n.230-30C>A)
c.512-30C>A (n.512-30C>A)
dbSNP gnomAD v3 gnomAD v4
3g.128486399G>ACA2577890771GATA2c.230-31C>T (n.230-31C>T)
c.512-31C>T (n.512-31C>T)
gnomAD v4
3g.128486399G>TCA2667541109GATA2c.230-31C>A (n.230-31C>A)
c.512-31C>A (n.512-31C>A)
gnomAD v4
3g.128486405_128486422delCA2667541108GATA2c.230-48_230-31del (n.230-48_230-31del)
c.512-48_512-31del (n.512-48_512-31del)
gnomAD v4
3g.128486400G>ACA2600060GATA2c.230-32C>T (n.230-32C>T)
c.512-32C>T (n.512-32C>T)
dbSNP ExAC gnomAD v3 gnomAD v4
3g.128486400G>CCA2600061GATA2c.230-32C>G (n.230-32C>G)
c.512-32C>G (n.512-32C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.128486400G=CA1400719567GATA2c.230-32C= (n.230-32C=)
c.512-32C= (n.512-32C=)
3g.128486400G>TCA2667541110GATA2c.230-32C>A (n.230-32C>A)
c.512-32C>A (n.512-32C>A)
gnomAD v4

Number of alleles fetched