| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.128485200_128487231del | CA358451 | GATA2 | c.-45-155_871+527del c.238-155_1153+527del | ClinVar |
| 3 | g.128485206_128487871del | CA916081440 | GATA2 | c.-200_871+527del c.83_1153+527del c.-45-789_871+527del | |
| 3 | g.128485794T>A | CA435763804 | GATA2 | c.804A>T (p.Gly268=) c.1086A>T (p.Gly362=) | |
| 3 | g.128485794T>C | CA435763805 | GATA2 | c.804A>G (p.Gly268=) c.1086A>G (p.Gly362=) | gnomAD v4 |
| 3 | g.128485794T>G | CA435763807 | GATA2 | c.804A>C (p.Gly268=) c.1086A>C (p.Gly362=) | |
| 3 | g.128485794T= | CA1400719030 | GATA2 | c.804A= (p.Gly268=) c.1086A= (p.Gly362=) | |
| 3 | g.128485795C>A | CA354405861 | GATA2 | c.803G>T (p.Gly268Val) c.1085G>T (p.Gly362Val) | ClinVar dbSNP |
| 3 | g.128485795C= | CA1400719035 | GATA2 | c.803G= (p.Gly268=) c.1085G= (p.Gly362=) | |
| 3 | g.128485795C>G | CA354405862 | GATA2 | c.803G>C (p.Gly268Ala) c.1085G>C (p.Gly362Ala) | |
| 3 | g.128485795C>T | CA354405863 | GATA2 | c.803G>A (p.Gly268Glu) c.1085G>A (p.Gly362Glu) | ClinVar dbSNP |
| 3 | g.128485796del | CA2586965892 | GATA2 | c.803del (p.Gly268GlufsTer?) c.1085del (p.Gly362GlufsTer?) | |
| 3 | g.128485803_128485804insCCCCCGGGGTGG | CA1400719033 | GATA2 | c.803_804insGGGCCACCCCGG (p.Gly268_Gly269insGlyHisProGly) c.1085_1086insGGGCCACCCCGG (p.Gly362_Gly363insGlyHisProGly) | ClinVar dbSNP |
| 3 | g.128485796C>A | CA354405865 | GATA2 | c.802G>T (p.Gly268Ter) c.1084G>T (p.Gly362Ter) | ClinVar dbSNP |
| 3 | g.128485796C= | CA1400719038 | GATA2 | c.802G= (p.Gly268=) c.1084G= (p.Gly362=) | |
| 3 | g.128485796C>G | CA354405867 | GATA2 | c.802G>C (p.Gly268Arg) c.1084G>C (p.Gly362Arg) | ClinVar dbSNP |
| 3 | g.128485796C>T | CA2599960 | GATA2 | c.802G>A (p.Gly268Arg) c.1084G>A (p.Gly362Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.128485796_128485805del | CA1139532795 | GATA2 | c.793_802del (p.Phe265GlufsTer?) c.1075_1084del (p.Phe359GlufsTer?) | ClinVar dbSNP |
| 3 | g.128485797G>A | CA2599961 | GATA2 | c.801C>T (p.Pro267=) c.1083C>T (p.Pro361=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485797G>C | CA435763816 | GATA2 | c.801C>G (p.Pro267=) c.1083C>G (p.Pro361=) | gnomAD v4 |
| 3 | g.128485797G= | CA1400719043 | GATA2 | c.801C= (p.Pro267=) c.1083C= (p.Pro361=) | |
| 3 | g.128485797G>T | CA435763817 | GATA2 | c.801C>A (p.Pro267=) c.1083C>A (p.Pro361=) | dbSNP |
| 3 | g.128485829_128485830insGGGGGTGGAAGAGTCCGCTGCTGTAGTCGTGGGC | CA2740090989 | GATA2 | c.801_802insCGCCCACGACTACAGCAGCGGACTCTTCCACCCC (p.Gly268ArgfsTer25) c.1083_1084insCGCCCACGACTACAGCAGCGGACTCTTCCACCCC (p.Gly362ArgfsTer25) | |
| 3 | g.128485798G>A | CA10615220 | GATA2 | c.800C>T (p.Pro267Leu) c.1082C>T (p.Pro361Leu) | ClinVar dbSNP COSMIC |
| 3 | g.128485798G>C | CA354405874 | GATA2 | c.800C>G (p.Pro267Arg) c.1082C>G (p.Pro361Arg) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485798G= | CA1400719051 | GATA2 | c.800C= (p.Pro267=) c.1082C= (p.Pro361=) | |
| 3 | g.128485798G>T | CA354405870 | GATA2 | c.800C>A (p.Pro267His) c.1082C>A (p.Pro361His) | ClinVar |
| 3 | g.128485799G>A | CA354405875 | GATA2 | c.799C>T (p.Pro267Ser) c.1081C>T (p.Pro361Ser) | |
| 3 | g.128485799G>C | CA354405878 | GATA2 | c.799C>G (p.Pro267Ala) c.1081C>G (p.Pro361Ala) | |
| 3 | g.128485799G>T | CA354405876 | GATA2 | c.799C>A (p.Pro267Thr) c.1081C>A (p.Pro361Thr) | |
| 3 | g.128485800G>A | CA435763825 | GATA2 | c.798C>T (p.His266=) c.1080C>T (p.His360=) | ClinVar gnomAD v4 |
| 3 | g.128485800G>C | CA354405879 | GATA2 | c.798C>G (p.His266Gln) c.1080C>G (p.His360Gln) | |
| 3 | g.128485800G= | CA1400719061 | GATA2 | c.798C= (p.His266=) c.1080C= (p.His360=) | |
| 3 | g.128485800G>T | CA83371757 | GATA2 | c.798C>A (p.His266Gln) c.1080C>A (p.His360Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.128485801T>A | CA354405881 | GATA2 | c.797A>T (p.His266Leu) c.1079A>T (p.His360Leu) | |
| 3 | g.128485801T>C | CA2599962 | GATA2 | c.797A>G (p.His266Arg) c.1079A>G (p.His360Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.128485801T>G | CA354405883 | GATA2 | c.797A>C (p.His266Pro) c.1079A>C (p.His360Pro) | |
| 3 | g.128485801T= | CA1400719064 | GATA2 | c.797A= (p.His266=) c.1079A= (p.His360=) | |
| 3 | g.128485802G>A | CA83371764 | GATA2 | c.796C>T (p.His266Tyr) c.1078C>T (p.His360Tyr) | ClinVar dbSNP |
| 3 | g.128485802G>C | CA354405885 | GATA2 | c.796C>G (p.His266Asp) c.1078C>G (p.His360Asp) | |
| 3 | g.128485802G= | CA1400719067 | GATA2 | c.796C= (p.His266=) c.1078C= (p.His360=) | |
| 3 | g.128485802G>T | CA354405887 | GATA2 | c.796C>A (p.His266Asn) c.1078C>A (p.His360Asn) | |
| 3 | g.128485803G>A | CA435763832 | GATA2 | c.795C>T (p.Phe265=) c.1077C>T (p.Phe359=) | ClinVar |
| 3 | g.128485803G>C | CA354405889 | GATA2 | c.795C>G (p.Phe265Leu) c.1077C>G (p.Phe359Leu) | |
| 3 | g.128485803G>T | CA354405891 | GATA2 | c.795C>A (p.Phe265Leu) c.1077C>A (p.Phe359Leu) | |
| 3 | g.128485804A>C | CA354405892 | GATA2 | c.794T>G (p.Phe265Cys) c.1076T>G (p.Phe359Cys) | |
| 3 | g.128485804A>G | CA354405893 | GATA2 | c.794T>C (p.Phe265Ser) c.1076T>C (p.Phe359Ser) | |
| 3 | g.128485804A>T | CA354405894 | GATA2 | c.794T>A (p.Phe265Tyr) c.1076T>A (p.Phe359Tyr) | |
| 3 | g.128485805dup | CA2830782392 | GATA2 | c.794dup (p.His266ProfsTer16) c.1076dup (p.His360ProfsTer16) | |
| 3 | g.128485805A>C | CA354405899 | GATA2 | c.793T>G (p.Phe265Val) c.1075T>G (p.Phe359Val) | |
| 3 | g.128485805A>G | CA354405897 | GATA2 | c.793T>C (p.Phe265Leu) c.1075T>C (p.Phe359Leu) | |
| 3 | g.128485805A>T | CA354405895 | GATA2 | c.793T>A (p.Phe265Ile) c.1075T>A (p.Phe359Ile) | |
| 3 | g.128485806G>A | CA16611356 | GATA2 | c.792C>T (p.Leu264=) c.1074C>T (p.Leu358=) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485806G>C | CA435763840 | GATA2 | c.792C>G (p.Leu264=) c.1074C>G (p.Leu358=) | |
| 3 | g.128485806G= | CA1400719069 | GATA2 | c.792C= (p.Leu264=) c.1074C= (p.Leu358=) | |
| 3 | g.128485806G>T | CA435763841 | GATA2 | c.792C>A (p.Leu264=) c.1074C>A (p.Leu358=) | |
| 3 | g.128485807A>C | CA354405901 | GATA2 | c.791T>G (p.Leu264Arg) c.1073T>G (p.Leu358Arg) | |
| 3 | g.128485807A>G | CA354405902 | GATA2 | c.791T>C (p.Leu264Pro) c.1073T>C (p.Leu358Pro) | |
| 3 | g.128485807A>T | CA354405904 | GATA2 | c.791T>A (p.Leu264His) c.1073T>A (p.Leu358His) | |
| 3 | g.128485808G>A | CA354405905 | GATA2 | c.790C>T (p.Leu264Phe) c.1072C>T (p.Leu358Phe) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485808G>C | CA354405907 | GATA2 | c.790C>G (p.Leu264Val) c.1072C>G (p.Leu358Val) | |
| 3 | g.128485808G= | CA1400719071 | GATA2 | c.790C= (p.Leu264=) c.1072C= (p.Leu358=) | |
| 3 | g.128485808G>T | CA354405908 | GATA2 | c.790C>A (p.Leu264Ile) c.1072C>A (p.Leu358Ile) | |
| 3 | g.128485809T>A | CA435763849 | GATA2 | c.789A>T (p.Gly263=) c.1071A>T (p.Gly357=) | gnomAD v4 |
| 3 | g.128485809T>C | CA435763850 | GATA2 | c.789A>G (p.Gly263=) c.1071A>G (p.Gly357=) | |
| 3 | g.128485809T>G | CA435763851 | GATA2 | c.789A>C (p.Gly263=) c.1071A>C (p.Gly357=) | ClinVar |
| 3 | g.128485810C>A | CA354405910 | GATA2 | c.788G>T (p.Gly263Val) c.1070G>T (p.Gly357Val) | dbSNP gnomAD v2 |
| 3 | g.128485810C= | CA1400719075 | GATA2 | c.788G= (p.Gly263=) c.1070G= (p.Gly357=) | |
| 3 | g.128485810C>G | CA354405911 | GATA2 | c.788G>C (p.Gly263Ala) c.1070G>C (p.Gly357Ala) | ClinVar dbSNP |
| 3 | g.128485810C>T | CA354405912 | GATA2 | c.788G>A (p.Gly263Glu) c.1070G>A (p.Gly357Glu) | gnomAD v4 COSMIC |
| 3 | g.128485811C>A | CA354405914 | GATA2 | c.787G>T (p.Gly263Ter) c.1069G>T (p.Gly357Ter) | |
| 3 | g.128485811C= | CA1400719079 | GATA2 | c.787G= (p.Gly263=) c.1069G= (p.Gly357=) | |
| 3 | g.128485811C>G | CA354405915 | GATA2 | c.787G>C (p.Gly263Arg) c.1069G>C (p.Gly357Arg) | |
| 3 | g.128485811C>T | CA159909 | GATA2 | c.787G>A (p.Gly263Arg) c.1069G>A (p.Gly357Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485812_128485816dup | CA2740090990 | GATA2 | c.783_787dup (p.Gly263AlafsTer?) c.1065_1069dup (p.Gly357AlafsTer?) | ClinVar |
| 3 | g.128485812G>A | CA435763856 | GATA2 | c.786C>T (p.Ser262=) c.1068C>T (p.Ser356=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485812G>C | CA354405917 | GATA2 | c.786C>G (p.Ser262Arg) c.1068C>G (p.Ser356Arg) | ClinVar gnomAD v4 |
| 3 | g.128485812G= | CA1400719082 | GATA2 | c.786C= (p.Ser262=) c.1068C= (p.Ser356=) | |
| 3 | g.128485812G>T | CA354405916 | GATA2 | c.786C>A (p.Ser262Arg) c.1068C>A (p.Ser356Arg) | |
| 3 | g.128485813C>A | CA354405919 | GATA2 | c.785G>T (p.Ser262Ile) c.1067G>T (p.Ser356Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.128485813C= | CA1400719084 | GATA2 | c.785G= (p.Ser262=) c.1067G= (p.Ser356=) | |
| 3 | g.128485813C>G | CA354405920 | GATA2 | c.785G>C (p.Ser262Thr) c.1067G>C (p.Ser356Thr) | |
| 3 | g.128485813C>T | CA354405922 | GATA2 | c.785G>A (p.Ser262Asn) c.1067G>A (p.Ser356Asn) | ClinVar dbSNP |
| 3 | g.128485814T>A | CA354405924 | GATA2 | c.784A>T (p.Ser262Cys) c.1066A>T (p.Ser356Cys) | |
| 3 | g.128485814T>C | CA354405926 | GATA2 | c.784A>G (p.Ser262Gly) c.1066A>G (p.Ser356Gly) | ClinVar gnomAD v4 |
| 3 | g.128485814T>G | CA354405927 | GATA2 | c.784A>C (p.Ser262Arg) c.1066A>C (p.Ser356Arg) | |
| 3 | g.128485815G>A | CA435763861 | GATA2 | c.783C>T (p.Ser261=) c.1065C>T (p.Ser355=) | |
| 3 | g.128485815G>C | CA354405930 | GATA2 | c.783C>G (p.Ser261Arg) c.1065C>G (p.Ser355Arg) | |
| 3 | g.128485815G>T | CA354405928 | GATA2 | c.783C>A (p.Ser261Arg) c.1065C>A (p.Ser355Arg) | |
| 3 | g.128485815_128485816delinsAG | CA2573136525 | GATA2 | c.782_783delinsCT (p.Ser261Thr) c.1064_1065delinsCT (p.Ser355Thr) | ClinVar dbSNP |
| 3 | g.128485816C>A | CA354405931 | GATA2 | c.782G>T (p.Ser261Ile) c.1064G>T (p.Ser355Ile) | |
| 3 | g.128485816C= | CA1400719088 | GATA2 | c.782G= (p.Ser261=) c.1064G= (p.Ser355=) | |
| 3 | g.128485816C>G | CA354405933 | GATA2 | c.782G>C (p.Ser261Thr) c.1064G>C (p.Ser355Thr) | |
| 3 | g.128485816C>T | CA354405935 | GATA2 | c.782G>A (p.Ser261Asn) c.1064G>A (p.Ser355Asn) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485817T>A | CA354405936 | GATA2 | c.781A>T (p.Ser261Cys) c.1063A>T (p.Ser355Cys) | |
| 3 | g.128485817T>C | CA354405937 | GATA2 | c.781A>G (p.Ser261Gly) c.1063A>G (p.Ser355Gly) | dbSNP gnomAD v4 |
| 3 | g.128485817T>G | CA354405939 | GATA2 | c.781A>C (p.Ser261Arg) c.1063A>C (p.Ser355Arg) | |
| 3 | g.128485817T= | CA1400719092 | GATA2 | c.781A= (p.Ser261=) c.1063A= (p.Ser355=) | |
| 3 | g.128485817_128485820delinsTGTA | CA1400719091 | GATA2 | c.778_781delinsTACA (p.Tyr260=) c.1060_1063delinsTACA (p.Tyr354=) | |
| 3 | g.128485818G>A | CA435763871 | GATA2 | c.780C>T (p.Tyr260=) c.1062C>T (p.Tyr354=) | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.128485818G>C | CA354405941 | GATA2 | c.780C>G (p.Tyr260Ter) c.1062C>G (p.Tyr354Ter) | |
| 3 | g.128485818G= | CA1400719095 | GATA2 | c.780C= (p.Tyr260=) c.1062C= (p.Tyr354=) | |
| 3 | g.128485818G>T | CA354405943 | GATA2 | c.780C>A (p.Tyr260Ter) c.1062C>A (p.Tyr354Ter) | |
| 3 | g.128485820_128485822del | CA2599963 | GATA2 | c.778_780del (p.Tyr260del) c.1060_1062del (p.Tyr354del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.128485819T>A | CA354405945 | GATA2 | c.779A>T (p.Tyr260Phe) c.1061A>T (p.Tyr354Phe) | |
| 3 | g.128485819T>C | CA354405946 | GATA2 | c.779A>G (p.Tyr260Cys) c.1061A>G (p.Tyr354Cys) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485819T>G | CA354405947 | GATA2 | c.779A>C (p.Tyr260Ser) c.1061A>C (p.Tyr354Ser) | |
| 3 | g.128485819T= | CA1400719100 | GATA2 | c.779A= (p.Tyr260=) c.1061A= (p.Tyr354=) | |
| 3 | g.128485820A>C | CA354405949 | GATA2 | c.778T>G (p.Tyr260Asp) c.1060T>G (p.Tyr354Asp) | |
| 3 | g.128485820A>G | CA354405951 | GATA2 | c.778T>C (p.Tyr260His) c.1060T>C (p.Tyr354His) | ClinVar dbSNP |
| 3 | g.128485820A>T | CA354405952 | GATA2 | c.778T>A (p.Tyr260Asn) c.1060T>A (p.Tyr354Asn) | |
| 3 | g.128485822_128485831dup | CA1139532794 | GATA2 | c.769_778dup (p.Tyr260CysfsTer25) c.1051_1060dup (p.Tyr354CysfsTer25) | ClinVar dbSNP |
| 3 | g.128485821G>A | CA435763879 | GATA2 | c.777C>T (p.Asp259=) c.1059C>T (p.Asp353=) | |
| 3 | g.128485821G>C | CA354405954 | GATA2 | c.777C>G (p.Asp259Glu) c.1059C>G (p.Asp353Glu) | dbSNP |
| 3 | g.128485821G= | CA1400719102 | GATA2 | c.777C= (p.Asp259=) c.1059C= (p.Asp353=) | |
| 3 | g.128485821G>T | CA354405956 | GATA2 | c.777C>A (p.Asp259Glu) c.1059C>A (p.Asp353Glu) | |
| 3 | g.128485822T>A | CA354405957 | GATA2 | c.776A>T (p.Asp259Val) c.1058A>T (p.Asp353Val) | |
| 3 | g.128485822T>C | CA354405959 | GATA2 | c.776A>G (p.Asp259Gly) c.1058A>G (p.Asp353Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.128485822T>G | CA354405960 | GATA2 | c.776A>C (p.Asp259Ala) c.1058A>C (p.Asp353Ala) | |
| 3 | g.128485822T= | CA1400719105 | GATA2 | c.776A= (p.Asp259=) c.1058A= (p.Asp353=) | |
| 3 | g.128485823C>A | CA354405963 | GATA2 | c.775G>T (p.Asp259Tyr) c.1057G>T (p.Asp353Tyr) | |
| 3 | g.128485823C= | CA1400719108 | GATA2 | c.775G= (p.Asp259=) c.1057G= (p.Asp353=) | |
| 3 | g.128485823C>G | CA2599964 | GATA2 | c.775G>C (p.Asp259His) c.1057G>C (p.Asp353His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.128485823C>T | CA354405962 | GATA2 | c.775G>A (p.Asp259Asn) c.1057G>A (p.Asp353Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.128485824G>A | CA435763884 | GATA2 | c.774C>T (p.His258=) c.1056C>T (p.His352=) | |
| 3 | g.128485824G>C | CA354405965 | GATA2 | c.774C>G (p.His258Gln) c.1056C>G (p.His352Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.128485824G= | CA1400719111 | GATA2 | c.774C= (p.His258=) c.1056C= (p.His352=) | |
| 3 | g.128485824G>T | CA354405966 | GATA2 | c.774C>A (p.His258Gln) c.1056C>A (p.His352Gln) | ClinVar dbSNP |
| 3 | g.128485825T>A | CA354405968 | GATA2 | c.773A>T (p.His258Leu) c.1055A>T (p.His352Leu) | |
| 3 | g.128485825T>C | CA354405970 | GATA2 | c.773A>G (p.His258Arg) c.1055A>G (p.His352Arg) | |
| 3 | g.128485825T>G | CA354405971 | GATA2 | c.773A>C (p.His258Pro) c.1055A>C (p.His352Pro) | |
| 3 | g.128485826G>A | CA354405976 | GATA2 | c.772C>T (p.His258Tyr) c.1054C>T (p.His352Tyr) | |
| 3 | g.128485826G>C | CA354405974 | GATA2 | c.772C>G (p.His258Asp) c.1054C>G (p.His352Asp) | |
| 3 | g.128485826G>T | CA354405973 | GATA2 | c.772C>A (p.His258Asn) c.1054C>A (p.His352Asn) | |
| 3 | g.128485827G>A | CA435763887 | GATA2 | c.771C>T (p.Ala257=) c.1053C>T (p.Ala351=) | |
| 3 | g.128485827G>C | CA435763888 | GATA2 | c.771C>G (p.Ala257=) c.1053C>G (p.Ala351=) | |
| 3 | g.128485827G>T | CA435763889 | GATA2 | c.771C>A (p.Ala257=) c.1053C>A (p.Ala351=) | |
| 3 | g.128485828G>A | CA354405977 | GATA2 | c.770C>T (p.Ala257Val) c.1052C>T (p.Ala351Val) | |
| 3 | g.128485828G>C | CA354405979 | GATA2 | c.770C>G (p.Ala257Gly) c.1052C>G (p.Ala351Gly) | |
| 3 | g.128485828G>T | CA354405980 | GATA2 | c.770C>A (p.Ala257Asp) c.1052C>A (p.Ala351Asp) | |
| 3 | g.128485829C>A | CA354405982 | GATA2 | c.769G>T (p.Ala257Ser) c.1051G>T (p.Ala351Ser) | |
| 3 | g.128485829C= | CA1400719114 | GATA2 | c.769G= (p.Ala257=) c.1051G= (p.Ala351=) | |
| 3 | g.128485829C>G | CA354405984 | GATA2 | c.769G>C (p.Ala257Pro) c.1051G>C (p.Ala351Pro) | |
| 3 | g.128485829C>T | CA354405986 | GATA2 | c.769G>A (p.Ala257Thr) c.1051G>A (p.Ala351Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.128485830A>C | CA435763893 | GATA2 | c.768T>G (p.Ala256=) c.1050T>G (p.Ala350=) | |
| 3 | g.128485830A>G | CA435763894 | GATA2 | c.768T>C (p.Ala256=) c.1050T>C (p.Ala350=) | gnomAD v4 |
| 3 | g.128485830A>T | CA435763895 | GATA2 | c.768T>A (p.Ala256=) c.1050T>A (p.Ala350=) | |
| 3 | g.128485831G>A | CA354405989 | GATA2 | c.767C>T (p.Ala256Val) c.1049C>T (p.Ala350Val) | dbSNP |
| 3 | g.128485831G>C | CA354405987 | GATA2 | c.767C>G (p.Ala256Gly) c.1049C>G (p.Ala350Gly) | dbSNP |
| 3 | g.128485831G>T | CA354405988 | GATA2 | c.767C>A (p.Ala256Asp) c.1049C>A (p.Ala350Asp) | |
| 3 | g.128485832C>A | CA354405991 | GATA2 | c.766G>T (p.Ala256Ser) c.1048G>T (p.Ala350Ser) | |
| 3 | g.128485832C= | CA1400719116 | GATA2 | c.766G= (p.Ala256=) c.1048G= (p.Ala350=) | |
| 3 | g.128485832C>G | CA354405992 | GATA2 | c.766G>C (p.Ala256Pro) c.1048G>C (p.Ala350Pro) | |
| 3 | g.128485832C>T | CA354405994 | GATA2 | c.766G>A (p.Ala256Thr) c.1048G>A (p.Ala350Thr) | dbSNP |
| 3 | g.128485833C>A | CA435763897 | GATA2 | c.765G>T (p.Ala255=) c.1047G>T (p.Ala349=) | |
| 3 | g.128485833C>G | CA435763898 | GATA2 | c.765G>C (p.Ala255=) c.1047G>C (p.Ala349=) | |
| 3 | g.128485833C>T | CA435763899 | GATA2 | c.765G>A (p.Ala255=) c.1047G>A (p.Ala349=) | ClinVar |
| 3 | g.128485834G>A | CA354405996 | GATA2 | c.764C>T (p.Ala255Val) c.1046C>T (p.Ala349Val) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485834G>C | CA354405997 | GATA2 | c.764C>G (p.Ala255Gly) c.1046C>G (p.Ala349Gly) | ClinVar dbSNP |
| 3 | g.128485834G= | CA1400719118 | GATA2 | c.764C= (p.Ala255=) c.1046C= (p.Ala349=) | |
| 3 | g.128485834G>T | CA354405999 | GATA2 | c.764C>A (p.Ala255Glu) c.1046C>A (p.Ala349Glu) | |
| 3 | g.128485834_128485835delinsAA | CA2499216465 | GATA2 | c.763_764delinsTT (p.Ala255Leu) c.1045_1046delinsTT (p.Ala349Leu) | ClinVar dbSNP |
| 3 | g.128485835C>A | CA354406000 | GATA2 | c.763G>T (p.Ala255Ser) c.1045G>T (p.Ala349Ser) | dbSNP |
| 3 | g.128485835C= | CA1400719121 | GATA2 | c.763G= (p.Ala255=) c.1045G= (p.Ala349=) | |
| 3 | g.128485835C>G | CA354406002 | GATA2 | c.763G>C (p.Ala255Pro) c.1045G>C (p.Ala349Pro) | |
| 3 | g.128485835C>T | CA354406003 | GATA2 | c.763G>A (p.Ala255Thr) c.1045G>A (p.Ala349Thr) | |
| 3 | g.128485836C>A | CA83371775 | GATA2 | c.762G>T (p.Pro254=) c.1044G>T (p.Pro348=) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485836C= | CA1400719123 | GATA2 | c.762G= (p.Pro254=) c.1044G= (p.Pro348=) | |
| 3 | g.128485836C>G | CA435763903 | GATA2 | c.762G>C (p.Pro254=) c.1044G>C (p.Pro348=) | gnomAD v4 |
| 3 | g.128485836C>T | CA435763904 | GATA2 | c.762G>A (p.Pro254=) c.1044G>A (p.Pro348=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.128485837G>A | CA128576 | GATA2 | c.761C>T (p.Pro254Leu) c.1043C>T (p.Pro348Leu) | ClinVar dbSNP |
| 3 | g.128485837G>C | CA354406006 | GATA2 | c.761C>G (p.Pro254Arg) c.1043C>G (p.Pro348Arg) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485837G= | CA1400719127 | GATA2 | c.761C= (p.Pro254=) c.1043C= (p.Pro348=) | |
| 3 | g.128485837G>T | CA354406008 | GATA2 | c.761C>A (p.Pro254Gln) c.1043C>A (p.Pro348Gln) | |
| 3 | g.128485838G>A | CA354406009 | GATA2 | c.760C>T (p.Pro254Ser) c.1042C>T (p.Pro348Ser) | dbSNP |
| 3 | g.128485838G>C | CA354406011 | GATA2 | c.760C>G (p.Pro254Ala) c.1042C>G (p.Pro348Ala) | |
| 3 | g.128485838G= | CA1400719131 | GATA2 | c.760C= (p.Pro254=) c.1042C= (p.Pro348=) | |
| 3 | g.128485838G>T | CA354406010 | GATA2 | c.760C>A (p.Pro254Thr) c.1042C>A (p.Pro348Thr) | |
| 3 | g.128485839C>A | CA435763908 | GATA2 | c.759G>T (p.Val253=) c.1041G>T (p.Val347=) | |
| 3 | g.128485839C>G | CA435763909 | GATA2 | c.759G>C (p.Val253=) c.1041G>C (p.Val347=) | ClinVar |
| 3 | g.128485839C>T | CA435763910 | GATA2 | c.759G>A (p.Val253=) c.1041G>A (p.Val347=) | gnomAD v4 |
| 3 | g.128485840A>C | CA354406012 | GATA2 | c.758T>G (p.Val253Gly) c.1040T>G (p.Val347Gly) | |
| 3 | g.128485840A>G | CA354406014 | GATA2 | c.758T>C (p.Val253Ala) c.1040T>C (p.Val347Ala) | |
| 3 | g.128485840A>T | CA354406016 | GATA2 | c.758T>A (p.Val253Glu) c.1040T>A (p.Val347Glu) | |
| 3 | g.128485841C>A | CA354406018 | GATA2 | c.757G>T (p.Val253Leu) c.1039G>T (p.Val347Leu) | |
| 3 | g.128485841C>G | CA354406020 | GATA2 | c.757G>C (p.Val253Leu) c.1039G>C (p.Val347Leu) | |
| 3 | g.128485841C>T | CA354406022 | GATA2 | c.757G>A (p.Val253Met) c.1039G>A (p.Val347Met) | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.128485842A= | CA1400719136 | GATA2 | c.756T= (p.Tyr252=) c.1038T= (p.Tyr346=) | |
| 3 | g.128485842A>C | CA354406024 | GATA2 | c.756T>G (p.Tyr252Ter) c.1038T>G (p.Tyr346Ter) | |
| 3 | g.128485842A>G | CA2599965 | GATA2 | c.756T>C (p.Tyr252=) c.1038T>C (p.Tyr346=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485842A>T | CA354406027 | GATA2 | c.756T>A (p.Tyr252Ter) c.1038T>A (p.Tyr346Ter) | |
| 3 | g.128485843T>A | CA354406028 | GATA2 | c.755A>T (p.Tyr252Phe) c.1037A>T (p.Tyr346Phe) | dbSNP COSMIC |
| 3 | g.128485843T>C | CA16611142 | GATA2 | c.755A>G (p.Tyr252Cys) c.1037A>G (p.Tyr346Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485843T>G | CA354406031 | GATA2 | c.755A>C (p.Tyr252Ser) c.1037A>C (p.Tyr346Ser) | |
| 3 | g.128485843T= | CA1400719145 | GATA2 | c.755A= (p.Tyr252=) c.1037A= (p.Tyr346=) | |
| 3 | g.128485844A>C | CA354406036 | GATA2 | c.754T>G (p.Tyr252Asp) c.1036T>G (p.Tyr346Asp) | |
| 3 | g.128485844A>G | CA354406032 | GATA2 | c.754T>C (p.Tyr252His) c.1036T>C (p.Tyr346His) | |
| 3 | g.128485844A>T | CA354406034 | GATA2 | c.754T>A (p.Tyr252Asn) c.1036T>A (p.Tyr346Asn) | gnomAD v4 |
| 3 | g.128485845G>A | CA435763917 | GATA2 | c.753C>T (p.Ser251=) c.1035C>T (p.Ser345=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.128485845G>C | CA435763918 | GATA2 | c.753C>G (p.Ser251=) c.1035C>G (p.Ser345=) | ClinVar |
| 3 | g.128485845G= | CA1400719153 | GATA2 | c.753C= (p.Ser251=) c.1035C= (p.Ser345=) | |
| 3 | g.128485845G>T | CA435763919 | GATA2 | c.753C>A (p.Ser251=) c.1035C>A (p.Ser345=) | |
| 3 | g.128485846G>A | CA354406038 | GATA2 | c.752C>T (p.Ser251Phe) c.1034C>T (p.Ser345Phe) | |
| 3 | g.128485846G>C | CA354406040 | GATA2 | c.752C>G (p.Ser251Cys) c.1034C>G (p.Ser345Cys) | dbSNP |
| 3 | g.128485846G>T | CA354406042 | GATA2 | c.752C>A (p.Ser251Tyr) c.1034C>A (p.Ser345Tyr) | |
| 3 | g.128485847_128485848dup | CA2573136503 | GATA2 | c.751_752dup (p.Tyr252ProfsTer?) c.1033_1034dup (p.Tyr346ProfsTer?) | ClinVar dbSNP |
| 3 | g.128485847A>C | CA354406044 | GATA2 | c.751T>G (p.Ser251Ala) c.1033T>G (p.Ser345Ala) | |
| 3 | g.128485847A>G | CA354406045 | GATA2 | c.751T>C (p.Ser251Pro) c.1033T>C (p.Ser345Pro) | |
| 3 | g.128485847A>T | CA354406047 | GATA2 | c.751T>A (p.Ser251Thr) c.1033T>A (p.Ser345Thr) | gnomAD v4 |
| 3 | g.128485848G>A | CA435763922 | GATA2 | c.750C>T (p.Pro250=) c.1032C>T (p.Pro344=) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485848G>C | CA435763924 | GATA2 | c.750C>G (p.Pro250=) c.1032C>G (p.Pro344=) | ClinVar |
| 3 | g.128485848G= | CA1400719156 | GATA2 | c.750C= (p.Pro250=) c.1032C= (p.Pro344=) | |
| 3 | g.128485848G>T | CA435763925 | GATA2 | c.750C>A (p.Pro250=) c.1032C>A (p.Pro344=) | |
| 3 | g.128485851del | CA2580068744 | GATA2 | c.750del (p.Ser251ProfsTer?) c.1032del (p.Ser345ProfsTer?) | ClinVar |
| 3 | g.128485850_128485851del | CA2504403872 | GATA2 | c.749_750del (p.Pro250LeufsTer?) c.1031_1032del (p.Pro344LeufsTer?) | |
| 3 | g.128485849G>A | CA2599966 | GATA2 | c.749C>T (p.Pro250Leu) c.1031C>T (p.Pro344Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.128485849G>C | CA354406049 | GATA2 | c.749C>G (p.Pro250Arg) c.1031C>G (p.Pro344Arg) | |
| 3 | g.128485849G= | CA1400719158 | GATA2 | c.749C= (p.Pro250=) c.1031C= (p.Pro344=) | |
| 3 | g.128485849G>T | CA354406051 | GATA2 | c.749C>A (p.Pro250His) c.1031C>A (p.Pro344His) | |
| 3 | g.128485850G>A | CA2599967 | GATA2 | c.748C>T (p.Pro250Ser) c.1030C>T (p.Pro344Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485850G>C | CA159899 | GATA2 | c.748C>G (p.Pro250Ala) c.1030C>G (p.Pro344Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485850G= | CA1400719163 | GATA2 | c.748C= (p.Pro250=) c.1030C= (p.Pro344=) | |
| 3 | g.128485850G>T | CA354406054 | GATA2 | c.748C>A (p.Pro250Thr) c.1030C>A (p.Pro344Thr) | |
| 3 | g.128485851G>A | CA2599968 | GATA2 | c.747C>T (p.Tyr249=) c.1029C>T (p.Tyr343=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.128485851G>C | CA354406057 | GATA2 | c.747C>G (p.Tyr249Ter) c.1029C>G (p.Tyr343Ter) | |
| 3 | g.128485851G= | CA1400719168 | GATA2 | c.747C= (p.Tyr249=) c.1029C= (p.Tyr343=) | |
| 3 | g.128485851G>T | CA354406056 | GATA2 | c.747C>A (p.Tyr249Ter) c.1029C>A (p.Tyr343Ter) | |
| 3 | g.128485852T>A | CA354406061 | GATA2 | c.746A>T (p.Tyr249Phe) c.1028A>T (p.Tyr343Phe) | dbSNP |
| 3 | g.128485852T>C | CA354406059 | GATA2 | c.746A>G (p.Tyr249Cys) c.1028A>G (p.Tyr343Cys) | |
| 3 | g.128485852T>G | CA354406062 | GATA2 | c.746A>C (p.Tyr249Ser) c.1028A>C (p.Tyr343Ser) | dbSNP |
| 3 | g.128485853A>C | CA354406064 | GATA2 | c.745T>G (p.Tyr249Asp) c.1027T>G (p.Tyr343Asp) | |
| 3 | g.128485853A>G | CA354406067 | GATA2 | c.745T>C (p.Tyr249His) c.1027T>C (p.Tyr343His) | |
| 3 | g.128485853A>T | CA354406065 | GATA2 | c.745T>A (p.Tyr249Asn) c.1027T>A (p.Tyr343Asn) | gnomAD v4 |
| 3 | g.128485854G>A | CA435763929 | GATA2 | c.744C>T (p.Thr248=) c.1026C>T (p.Thr342=) | ClinVar dbSNP COSMIC |
| 3 | g.128485854G>C | CA435763930 | GATA2 | c.744C>G (p.Thr248=) c.1026C>G (p.Thr342=) | ClinVar |
| 3 | g.128485854G>T | CA435763931 | GATA2 | c.744C>A (p.Thr248=) c.1026C>A (p.Thr342=) | |
| 3 | g.128485855G>A | CA354406068 | GATA2 | c.743C>T (p.Thr248Ile) c.1025C>T (p.Thr342Ile) | ClinVar dbSNP |
| 3 | g.128485855G>C | CA354406069 | GATA2 | c.743C>G (p.Thr248Ser) c.1025C>G (p.Thr342Ser) | |
| 3 | g.128485855G= | CA1400719173 | GATA2 | c.743C= (p.Thr248=) c.1025C= (p.Thr342=) | |
| 3 | g.128485855G>T | CA354406071 | GATA2 | c.743C>A (p.Thr248Asn) c.1025C>A (p.Thr342Asn) | |
| 3 | g.128485856T>A | CA354406073 | GATA2 | c.742A>T (p.Thr248Ser) c.1024A>T (p.Thr342Ser) | ClinVar dbSNP |
| 3 | g.128485856T>C | CA354406075 | GATA2 | c.742A>G (p.Thr248Ala) c.1024A>G (p.Thr342Ala) | |
| 3 | g.128485856T>G | CA354406076 | GATA2 | c.742A>C (p.Thr248Pro) c.1024A>C (p.Thr342Pro) | dbSNP |
| 3 | g.128485856T= | CA1400719180 | GATA2 | c.742A= (p.Thr248=) c.1024A= (p.Thr342=) | |
| 3 | g.128485857G>A | CA435763932 | GATA2 | c.741C>T (p.Pro247=) c.1023C>T (p.Pro341=) | ClinVar |
| 3 | g.128485857G>C | CA435763934 | GATA2 | c.741C>G (p.Pro247=) c.1023C>G (p.Pro341=) | |
| 3 | g.128485857G>T | CA435763936 | GATA2 | c.741C>A (p.Pro247=) c.1023C>A (p.Pro341=) | |
| 3 | g.128485858G>A | CA354406078 | GATA2 | c.740C>T (p.Pro247Leu) c.1022C>T (p.Pro341Leu) | ClinVar dbSNP |
| 3 | g.128485858G>C | CA354406079 | GATA2 | c.740C>G (p.Pro247Arg) c.1022C>G (p.Pro341Arg) | ClinVar |
| 3 | g.128485858G= | CA1400719186 | GATA2 | c.740C= (p.Pro247=) c.1022C= (p.Pro341=) | |
| 3 | g.128485858G>T | CA354406081 | GATA2 | c.740C>A (p.Pro247His) c.1022C>A (p.Pro341His) | |
| 3 | g.128485859G>A | CA354406082 | GATA2 | c.739C>T (p.Pro247Ser) c.1021C>T (p.Pro341Ser) | ClinVar dbSNP |
| 3 | g.128485859G>C | CA354406083 | GATA2 | c.739C>G (p.Pro247Ala) c.1021C>G (p.Pro341Ala) | COSMIC |
| 3 | g.128485859G>T | CA354406085 | GATA2 | c.739C>A (p.Pro247Thr) c.1021C>A (p.Pro341Thr) | gnomAD v4 |
| 3 | g.128485860G>A | CA435763938 | GATA2 | c.738C>T (p.Ile246=) c.1020C>T (p.Ile340=) | dbSNP |
| 3 | g.128485860G>C | CA354406087 | GATA2 | c.738C>G (p.Ile246Met) c.1020C>G (p.Ile340Met) | |
| 3 | g.128485860G= | CA1400719191 | GATA2 | c.738C= (p.Ile246=) c.1020C= (p.Ile340=) | |
| 3 | g.128485860G>T | CA435763941 | GATA2 | c.738C>A (p.Ile246=) c.1020C>A (p.Ile340=) | |
| 3 | g.128485861A>C | CA354406089 | GATA2 | c.737T>G (p.Ile246Ser) c.1019T>G (p.Ile340Ser) | |
| 3 | g.128485861A>G | CA354406090 | GATA2 | c.737T>C (p.Ile246Thr) c.1019T>C (p.Ile340Thr) | |
| 3 | g.128485861A>T | CA354406092 | GATA2 | c.737T>A (p.Ile246Asn) c.1019T>A (p.Ile340Asn) | gnomAD v4 |
| 3 | g.128485862T>A | CA354406093 | GATA2 | c.736A>T (p.Ile246Phe) c.1018A>T (p.Ile340Phe) | |
| 3 | g.128485862T>C | CA354406095 | GATA2 | c.736A>G (p.Ile246Val) c.1018A>G (p.Ile340Val) | gnomAD v4 |
| 3 | g.128485862T>G | CA354406096 | GATA2 | c.736A>C (p.Ile246Leu) c.1018A>C (p.Ile340Leu) | dbSNP |
| 3 | g.128485863G>A | CA435763943 | GATA2 | c.735C>T (p.Pro245=) c.1017C>T (p.Pro339=) | ClinVar dbSNP |
| 3 | g.128485863G>C | CA435763944 | GATA2 | c.735C>G (p.Pro245=) c.1017C>G (p.Pro339=) | |
| 3 | g.128485863G>T | CA435763946 | GATA2 | c.735C>A (p.Pro245=) c.1017C>A (p.Pro339=) | |
| 3 | g.128485866dup | CA1139532793 | GATA2 | c.735dup (p.Ile246HisfsTer?) c.1017dup (p.Ile340HisfsTer?) | ClinVar dbSNP |
| 3 | g.128485864G>A | CA354406098 | GATA2 | c.734C>T (p.Pro245Leu) c.1016C>T (p.Pro339Leu) | |
| 3 | g.128485864G>C | CA354406099 | GATA2 | c.734C>G (p.Pro245Arg) c.1016C>G (p.Pro339Arg) | ClinVar dbSNP |
| 3 | g.128485864G>T | CA354406101 | GATA2 | c.734C>A (p.Pro245His) c.1016C>A (p.Pro339His) | |
| 3 | g.128485865G>A | CA354406103 | GATA2 | c.733C>T (p.Pro245Ser) c.1015C>T (p.Pro339Ser) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485865G>C | CA354406104 | GATA2 | c.733C>G (p.Pro245Ala) c.1015C>G (p.Pro339Ala) | gnomAD v4 |
| 3 | g.128485865G= | CA1400719194 | GATA2 | c.733C= (p.Pro245=) c.1015C= (p.Pro339=) | |
| 3 | g.128485865G>T | CA354406106 | GATA2 | c.733C>A (p.Pro245Thr) c.1015C>A (p.Pro339Thr) | ClinVar |
| 3 | g.128485866G>A | CA16611243 | GATA2 | c.732C>T (p.His244=) c.1014C>T (p.His338=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.128485866G>C | CA83371792 | GATA2 | c.732C>G (p.His244Gln) c.1014C>G (p.His338Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485866G= | CA1400719200 | GATA2 | c.732C= (p.His244=) c.1014C= (p.His338=) | |
| 3 | g.128485866G>T | CA354406108 | GATA2 | c.732C>A (p.His244Gln) c.1014C>A (p.His338Gln) | ClinVar dbSNP |
| 3 | g.128485867T>A | CA354406111 | GATA2 | c.731A>T (p.His244Leu) c.1013A>T (p.His338Leu) | |
| 3 | g.128485867T>C | CA354406112 | GATA2 | c.731A>G (p.His244Arg) c.1013A>G (p.His338Arg) | |
| 3 | g.128485867T>G | CA354406114 | GATA2 | c.731A>C (p.His244Pro) c.1013A>C (p.His338Pro) | dbSNP |
| 3 | g.128485867T= | CA1400719211 | GATA2 | c.731A= (p.His244=) c.1013A= (p.His338=) | |
| 3 | g.128485868G>A | CA354406115 | GATA2 | c.730C>T (p.His244Tyr) c.1012C>T (p.His338Tyr) | |
| 3 | g.128485868G>C | CA354406117 | GATA2 | c.730C>G (p.His244Asp) c.1012C>G (p.His338Asp) | |
| 3 | g.128485868G>T | CA354406119 | GATA2 | c.730C>A (p.His244Asn) c.1012C>A (p.His338Asn) | ClinVar |
| 3 | g.128485869G>A | CA2599969 | GATA2 | c.729C>T (p.His243=) c.1011C>T (p.His337=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485869G>C | CA354406121 | GATA2 | c.729C>G (p.His243Gln) c.1011C>G (p.His337Gln) | ClinVar dbSNP |
| 3 | g.128485869G= | CA1400719219 | GATA2 | c.729C= (p.His243=) c.1011C= (p.His337=) | |
| 3 | g.128485869G>T | CA354406122 | GATA2 | c.729C>A (p.His243Gln) c.1011C>A (p.His337Gln) | |
| 3 | g.128485870T>A | CA354406125 | GATA2 | c.728A>T (p.His243Leu) c.1010A>T (p.His337Leu) | |
| 3 | g.128485870T>C | CA354406126 | GATA2 | c.728A>G (p.His243Arg) c.1010A>G (p.His337Arg) | |
| 3 | g.128485870T>G | CA354406129 | GATA2 | c.728A>C (p.His243Pro) c.1010A>C (p.His337Pro) | |
| 3 | g.128485871G>A | CA354406133 | GATA2 | c.727C>T (p.His243Tyr) c.1009C>T (p.His337Tyr) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485871G>C | CA354406132 | GATA2 | c.727C>G (p.His243Asp) c.1009C>G (p.His337Asp) | |
| 3 | g.128485871G= | CA1400719232 | GATA2 | c.727C= (p.His243=) c.1009C= (p.His337=) | |
| 3 | g.128485871G>T | CA354406131 | GATA2 | c.727C>A (p.His243Asn) c.1009C>A (p.His337Asn) | |
| 3 | g.128485872T>A | CA2599970 | GATA2 | c.726A>T (p.Thr242=) c.1008A>T (p.Thr336=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.128485872T>C | CA435763955 | GATA2 | c.726A>G (p.Thr242=) c.1008A>G (p.Thr336=) | |
| 3 | g.128485872T>G | CA435763956 | GATA2 | c.726A>C (p.Thr242=) c.1008A>C (p.Thr336=) | |
| 3 | g.128485872T= | CA1400719237 | GATA2 | c.726A= (p.Thr242=) c.1008A= (p.Thr336=) | |
| 3 | g.128485873G>A | CA354406137 | GATA2 | c.725C>T (p.Thr242Ile) c.1007C>T (p.Thr336Ile) | dbSNP |
| 3 | g.128485873G>C | CA354406139 | GATA2 | c.725C>G (p.Thr242Arg) c.1007C>G (p.Thr336Arg) | |
| 3 | g.128485873G= | CA1400719239 | GATA2 | c.725C= (p.Thr242=) c.1007C= (p.Thr336=) | |
| 3 | g.128485873G>T | CA354406140 | GATA2 | c.725C>A (p.Thr242Lys) c.1007C>A (p.Thr336Lys) | |
| 3 | g.128485874T>A | CA354406143 | GATA2 | c.724A>T (p.Thr242Ser) c.1006A>T (p.Thr336Ser) | |
| 3 | g.128485874T>C | CA10614773 | GATA2 | c.724A>G (p.Thr242Ala) c.1006A>G (p.Thr336Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.128485874T>G | CA354406145 | GATA2 | c.724A>C (p.Thr242Pro) c.1006A>C (p.Thr336Pro) | dbSNP |
| 3 | g.128485874T= | CA1400719244 | GATA2 | c.724A= (p.Thr242=) c.1006A= (p.Thr336=) | |
| 3 | g.128485875A= | CA1400719246 | GATA2 | c.723T= (p.Ala241=) c.1005T= (p.Ala335=) | |
| 3 | g.128485875A>C | CA435763960 | GATA2 | c.723T>G (p.Ala241=) c.1005T>G (p.Ala335=) | ClinVar dbSNP |
| 3 | g.128485875A>G | CA435763961 | GATA2 | c.723T>C (p.Ala241=) c.1005T>C (p.Ala335=) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 3 | g.128485875A>T | CA435763962 | GATA2 | c.723T>A (p.Ala241=) c.1005T>A (p.Ala335=) | |
| 3 | g.128485876G>A | CA354406146 | GATA2 | c.722C>T (p.Ala241Val) c.1004C>T (p.Ala335Val) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485876G>C | CA354406148 | GATA2 | c.722C>G (p.Ala241Gly) c.1004C>G (p.Ala335Gly) | |
| 3 | g.128485876G= | CA1400719251 | GATA2 | c.722C= (p.Ala241=) c.1004C= (p.Ala335=) | |
| 3 | g.128485876G>T | CA354406149 | GATA2 | c.722C>A (p.Ala241Asp) c.1004C>A (p.Ala335Asp) | |
| 3 | g.128485877C>A | CA354406150 | GATA2 | c.721G>T (p.Ala241Ser) c.1003G>T (p.Ala335Ser) | |
| 3 | g.128485877C>G | CA354406151 | GATA2 | c.721G>C (p.Ala241Pro) c.1003G>C (p.Ala335Pro) | |
| 3 | g.128485877C>T | CA354406153 | GATA2 | c.721G>A (p.Ala241Thr) c.1003G>A (p.Ala335Thr) | gnomAD v4 |
| 3 | g.128485878A>C | CA435763966 | GATA2 | c.720T>G (p.Pro240=) c.1002T>G (p.Pro334=) | |
| 3 | g.128485878A>G | CA435763967 | GATA2 | c.720T>C (p.Pro240=) c.1002T>C (p.Pro334=) | |
| 3 | g.128485878A>T | CA435763968 | GATA2 | c.720T>A (p.Pro240=) c.1002T>A (p.Pro334=) | |
| 3 | g.128485879G>A | CA354406156 | GATA2 | c.719C>T (p.Pro240Leu) c.1001C>T (p.Pro334Leu) | ClinVar dbSNP gnomAD v4 |
| 3 | g.128485879G>C | CA354406158 | GATA2 | c.719C>G (p.Pro240Arg) c.1001C>G (p.Pro334Arg) | |
| 3 | g.128485879G= | CA1400719254 | GATA2 | c.719C= (p.Pro240=) c.1001C= (p.Pro334=) | |
| 3 | g.128485879G>T | CA354406155 | GATA2 | c.719C>A (p.Pro240His) c.1001C>A (p.Pro334His) | |
| 3 | g.128485880G>A | CA354406163 | GATA2 | c.718C>T (p.Pro240Ser) c.1000C>T (p.Pro334Ser) | dbSNP |
| 3 | g.128485880G>C | CA354406160 | GATA2 | c.718C>G (p.Pro240Ala) c.1000C>G (p.Pro334Ala) | |
| 3 | g.128485880G>T | CA354406161 | GATA2 | c.718C>A (p.Pro240Thr) c.1000C>A (p.Pro334Thr) | |
| 3 | g.128485881C>A | CA354406165 | GATA2 | c.717G>T (p.Gln239His) c.999G>T (p.Gln333His) | |
| 3 | g.128485881C= | CA1400719257 | GATA2 | c.717G= (p.Gln239=) c.999G= (p.Gln333=) | |
| 3 | g.128485881C>G | CA354406166 | GATA2 | c.717G>C (p.Gln239His) c.999G>C (p.Gln333His) | |
| 3 | g.128485881C>T | CA435763972 | GATA2 | c.717G>A (p.Gln239=) c.999G>A (p.Gln333=) | dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.128485882T>A | CA354406168 | GATA2 | c.716A>T (p.Gln239Leu) c.998A>T (p.Gln333Leu) | |
| 3 | g.128485882T>C | CA354406170 | GATA2 | c.716A>G (p.Gln239Arg) c.998A>G (p.Gln333Arg) | |
| 3 | g.128485882T>G | CA354406171 | GATA2 | c.716A>C (p.Gln239Pro) c.998A>C (p.Gln333Pro) | |
| 3 | g.128485883G>A | CA354406173 | GATA2 | c.715C>T (p.Gln239Ter) c.997C>T (p.Gln333Ter) | dbSNP |
| 3 | g.128485883G>C | CA354406174 | GATA2 | c.715C>G (p.Gln239Glu) c.997C>G (p.Gln333Glu) | |
| 3 | g.128485883G>T | CA354406176 | GATA2 | c.715C>A (p.Gln239Lys) c.997C>A (p.Gln333Lys) | |
| 3 | g.128485884G>A | CA435763976 | GATA2 | c.714C>T (p.Thr238=) c.996C>T (p.Thr332=) | gnomAD v4 |
| 3 | g.128485884G>C | CA83371801 | GATA2 | c.714C>G (p.Thr238=) c.996C>G (p.Thr332=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485884G= | CA1400719259 | GATA2 | c.714C= (p.Thr238=) c.996C= (p.Thr332=) | |
| 3 | g.128485884G>T | CA435763977 | GATA2 | c.714C>A (p.Thr238=) c.996C>A (p.Thr332=) | |
| 3 | g.128485885G>A | CA354406178 | GATA2 | c.713C>T (p.Thr238Ile) c.995C>T (p.Thr332Ile) | dbSNP gnomAD v4 COSMIC |
| 3 | g.128485885G>C | CA354406180 | GATA2 | c.713C>G (p.Thr238Ser) c.995C>G (p.Thr332Ser) | |
| 3 | g.128485885G= | CA1400719262 | GATA2 | c.713C= (p.Thr238=) c.995C= (p.Thr332=) | |
| 3 | g.128485885G>T | CA354406181 | GATA2 | c.713C>A (p.Thr238Asn) c.995C>A (p.Thr332Asn) | ClinVar |
| 3 | g.128485886T>A | CA354406186 | GATA2 | c.712A>T (p.Thr238Ser) c.994A>T (p.Thr332Ser) | |
| 3 | g.128485886T>C | CA354406183 | GATA2 | c.712A>G (p.Thr238Ala) c.994A>G (p.Thr332Ala) | |
| 3 | g.128485886T>G | CA354406185 | GATA2 | c.712A>C (p.Thr238Pro) c.994A>C (p.Thr332Pro) | dbSNP |
| 3 | g.128485887G>A | CA435763981 | GATA2 | c.711C>T (p.Gly237=) c.993C>T (p.Gly331=) | ClinVar |
| 3 | g.128485887G>C | CA435763982 | GATA2 | c.711C>G (p.Gly237=) c.993C>G (p.Gly331=) | gnomAD v4 |
| 3 | g.128485887G>T | CA435763983 | GATA2 | c.711C>A (p.Gly237=) c.993C>A (p.Gly331=) | |
| 3 | g.128485888C>A | CA354406187 | GATA2 | c.710G>T (p.Gly237Val) c.992G>T (p.Gly331Val) | |
| 3 | g.128485888C= | CA1400719265 | GATA2 | c.710G= (p.Gly237=) c.992G= (p.Gly331=) | |
| 3 | g.128485888C>G | CA354406188 | GATA2 | c.710G>C (p.Gly237Ala) c.992G>C (p.Gly331Ala) | |
| 3 | g.128485888C>T | CA2599971 | GATA2 | c.710G>A (p.Gly237Asp) c.992G>A (p.Gly331Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485890del | CA1139532792 | GATA2 | c.710del (p.Gly237AlafsTer?) c.992del (p.Gly331AlafsTer?) | ClinVar dbSNP |
| 3 | g.128485889C>A | CA354406191 | GATA2 | c.709G>T (p.Gly237Cys) c.991G>T (p.Gly331Cys) | |
| 3 | g.128485889C>G | CA354406192 | GATA2 | c.709G>C (p.Gly237Arg) c.991G>C (p.Gly331Arg) | |
| 3 | g.128485889C>T | CA354406194 | GATA2 | c.709G>A (p.Gly237Ser) c.991G>A (p.Gly331Ser) | ClinVar dbSNP |
| 3 | g.128485890C>A | CA354406195 | GATA2 | c.708G>T (p.Met236Ile) c.990G>T (p.Met330Ile) | |
| 3 | g.128485890C>G | CA354406197 | GATA2 | c.708G>C (p.Met236Ile) c.990G>C (p.Met330Ile) | |
| 3 | g.128485890C>T | CA354406199 | GATA2 | c.708G>A (p.Met236Ile) c.990G>A (p.Met330Ile) | |
| 3 | g.128485891A= | CA1400719271 | GATA2 | c.707T= (p.Met236=) c.989T= (p.Met330=) | |
| 3 | g.128485891A>C | CA354406200 | GATA2 | c.707T>G (p.Met236Arg) c.989T>G (p.Met330Arg) | |
| 3 | g.128485891A>G | CA2599972 | GATA2 | c.707T>C (p.Met236Thr) c.989T>C (p.Met330Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485891A>T | CA354406202 | GATA2 | c.707T>A (p.Met236Lys) c.989T>A (p.Met330Lys) | |
| 3 | g.128485892T>A | CA354406205 | GATA2 | c.706A>T (p.Met236Leu) c.988A>T (p.Met330Leu) | ClinVar dbSNP |
| 3 | g.128485892T>C | CA2599973 | GATA2 | c.706A>G (p.Met236Val) c.988A>G (p.Met330Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485892T>G | CA2599974 | GATA2 | c.706A>C (p.Met236Leu) c.988A>C (p.Met330Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.128485892T= | CA1400719275 | GATA2 | c.706A= (p.Met236=) c.988A= (p.Met330=) | |
| 3 | g.128485893A>C | CA435763990 | GATA2 | c.705T>G (p.Thr235=) c.987T>G (p.Thr329=) | |
| 3 | g.128485893A>G | CA435763991 | GATA2 | c.705T>C (p.Thr235=) c.987T>C (p.Thr329=) | |
| 3 | g.128485893A>T | CA435763992 | GATA2 | c.705T>A (p.Thr235=) c.987T>A (p.Thr329=) | |
| 3 | g.128485894G>A | CA354406206 | GATA2 | c.704C>T (p.Thr235Ile) c.986C>T (p.Thr329Ile) | |
| 3 | g.128485894G>C | CA354406207 | GATA2 | c.704C>G (p.Thr235Ser) c.986C>G (p.Thr329Ser) | |
| 3 | g.128485894G= | CA1400719279 | GATA2 | c.704C= (p.Thr235=) c.986C= (p.Thr329=) | |
| 3 | g.128485894G>T | CA83371814 | GATA2 | c.704C>A (p.Thr235Asn) c.986C>A (p.Thr329Asn) | dbSNP |