ClinVar Miner

List of variants in gene GATA2 reported as uncertain significance for not provided

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_032638.5(GATA2):c.481C>G (p.Pro161Ala) rs34799090 0.00854
NM_032638.5(GATA2):c.121C>G (p.Pro41Ala) rs143590990 0.00064
NM_032638.5(GATA2):c.279G>A (p.Pro93=) rs142993548 0.00051
NM_032638.5(GATA2):c.30G>T (p.Trp10Cys) rs367785289 0.00011
NM_032638.5(GATA2):c.445G>A (p.Gly149Arg) rs753645971 0.00009
NM_032638.5(GATA2):c.829A>G (p.Ser277Gly) rs141800945 0.00009
NM_032638.5(GATA2):c.1367C>T (p.Pro456Leu) rs372912472 0.00007
NM_032638.5(GATA2):c.1274C>T (p.Ser425Leu) rs146554939 0.00006
NM_032638.5(GATA2):c.1391G>T (p.Ser464Ile) rs770949428 0.00004
NM_032638.5(GATA2):c.1018-5C>T rs769196688 0.00002
NM_032638.5(GATA2):c.1370C>T (p.Thr457Met) rs139415862 0.00002
NM_032638.5(GATA2):c.142T>A (p.Phe48Ile) rs878855170 0.00002
NM_032638.5(GATA2):c.669G>A (p.Met223Ile) rs140382420 0.00002
NM_032638.5(GATA2):c.1020G>A (p.Ser340=) rs370166358 0.00001
NM_032638.5(GATA2):c.1025C>T (p.Ala342Val) rs143554523 0.00001
NM_032638.5(GATA2):c.1090G>A (p.Ala364Thr) rs766504293 0.00001
NM_032638.5(GATA2):c.1128C>T (p.Tyr376=) rs750890699 0.00001
NM_032638.5(GATA2):c.1230G>T (p.Gly410=) rs1461907039 0.00001
NM_032638.5(GATA2):c.1232C>T (p.Ala411Val) rs374457534 0.00001
NM_032638.5(GATA2):c.1348G>A (p.Gly450Arg) rs370164300 0.00001
NM_032638.5(GATA2):c.1376T>A (p.Ile459Asn) rs369407958 0.00001
NM_032638.5(GATA2):c.1402G>A (p.Gly468Ser) rs777726701 0.00001
NM_032638.5(GATA2):c.182C>T (p.Ala61Val) rs375349195 0.00001
NM_032638.5(GATA2):c.186C>G (p.Asn62Lys) rs751200779 0.00001
NM_032638.5(GATA2):c.311C>T (p.Ala104Val) rs760660470 0.00001
NM_032638.5(GATA2):c.442A>G (p.Ser148Gly) rs1161655427 0.00001
NM_032638.5(GATA2):c.515G>C (p.Gly172Ala) rs768236530 0.00001
NM_032638.5(GATA2):c.633C>G (p.Val211=) rs375773132 0.00001
NM_032638.5(GATA2):c.698T>C (p.Leu233Pro) rs1377041124 0.00001
NM_032638.5(GATA2):c.707T>C (p.Met236Thr) rs61754578 0.00001
NM_032638.5(GATA2):c.971A>G (p.Lys324Arg) rs1480450110 0.00001
NM_032638.5(GATA2):c.1016T>C (p.Leu339Pro)
NM_032638.5(GATA2):c.1017+565_1017+566del
NM_032638.5(GATA2):c.1036_1056dup (p.Gly346_Cys352dup) rs1576745241
NM_032638.5(GATA2):c.1052A>G (p.Asn351Ser) rs1576745252
NM_032638.5(GATA2):c.1154C>T (p.Pro385Leu) rs2107668121
NM_032638.5(GATA2):c.1160_1165del (p.Thr387_Met388del) rs2107668101
NM_032638.5(GATA2):c.1161_1172del (p.Met388_Glu391del) rs2107668082
NM_032638.5(GATA2):c.1165AAG[1] (p.Lys390del) rs1576744556
NM_032638.5(GATA2):c.1165_1170del (p.Lys389_Lys390del) rs1576744556
NM_032638.5(GATA2):c.1178T>C (p.Ile393Thr) rs2068625277
NM_032638.5(GATA2):c.1322_1325dup (p.His442fs) rs2107667819
NM_032638.5(GATA2):c.1333C>G (p.Pro445Ala)
NM_032638.5(GATA2):c.1339A>C (p.Ser447Arg) rs1576744275
NM_032638.5(GATA2):c.1385C>A (p.Ser462Tyr) rs1559984575
NM_032638.5(GATA2):c.1429A>G (p.Thr477Ala) rs2107667621
NM_032638.5(GATA2):c.14_15inv (p.Pro5Arg)
NM_032638.5(GATA2):c.171C>G (p.Asn57Lys) rs2068708105
NM_032638.5(GATA2):c.175T>A (p.Tyr59Asn)
NM_032638.5(GATA2):c.319G>A (p.Ala107Thr) rs2107672841
NM_032638.5(GATA2):c.35C>A (p.Ala12Glu) rs1263269900
NM_032638.5(GATA2):c.393TGGAGGCCC[1] (p.132GGP[1]) rs2068696512
NM_032638.5(GATA2):c.484A>G (p.Thr162Ala) rs770215567
NM_032638.5(GATA2):c.494A>G (p.His165Arg) rs1559987389
NM_032638.5(GATA2):c.495C>T (p.His165=) rs887833751
NM_032638.5(GATA2):c.524C>G (p.Pro175Arg) rs755939655
NM_032638.5(GATA2):c.596G>T (p.Gly199Val) rs780930549
NM_032638.5(GATA2):c.61C>T (p.His21Tyr)
NM_032638.5(GATA2):c.64C>A (p.Pro22Thr) rs1172590651
NM_032638.5(GATA2):c.657G>T (p.Glu219Asp) rs138688940
NM_032638.5(GATA2):c.682C>T (p.Pro228Ser) rs375298899
NM_032638.5(GATA2):c.695G>C (p.Gly232Ala) rs2068689323
NM_032638.5(GATA2):c.697C>G (p.Leu233Val) rs745497331
NM_032638.5(GATA2):c.706A>G (p.Met236Val) rs746737860
NM_032638.5(GATA2):c.778_780del (p.Tyr260del) rs747128645
NM_032638.5(GATA2):c.785G>A (p.Ser262Asn) rs1305082777
NM_032638.5(GATA2):c.852C>T (p.Ser284=) rs1282036381
NM_032638.5(GATA2):c.857C>T (p.Ala286Val) rs797045592
NM_032638.5(GATA2):c.872-13T>A
NM_032638.5(GATA2):c.962_963insAGT (p.Leu321_Tyr322insVal) rs2107670384
NM_032638.5(GATA2):c.989G>T (p.Arg330Leu) rs2107670339

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