ClinVar Miner

List of variants in gene GATA2 reported as likely benign for not provided

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Gene type:
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Total variants: 39
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HGVS dbSNP
NM_001145661.2(GATA2):c.-5C>G rs374415484
NM_001145661.2(GATA2):c.1029A>G (p.Arg343=) rs1415762927
NM_001145661.2(GATA2):c.1035C>G (p.Ala345=) rs371599112
NM_001145661.2(GATA2):c.1143+9G>A rs533617078
NM_001145661.2(GATA2):c.1144-10T>C rs1060503830
NM_001145661.2(GATA2):c.1144-6C>T rs878855167
NM_001145661.2(GATA2):c.1386C>T (p.Ser462=) rs1060503833
NM_001145661.2(GATA2):c.1410C>T (p.Pro470=) rs878855169
NM_001145661.2(GATA2):c.333C>T (p.His111=) rs148554346
NM_001145661.2(GATA2):c.480C>T (p.Thr160=) rs199640729
NM_001145661.2(GATA2):c.481C>G (p.Pro161Ala) rs34799090
NM_001145661.2(GATA2):c.492C>A (p.Ala164=) rs1363204381
NM_001145661.2(GATA2):c.573G>A (p.Ala191=) rs1060503832
NM_001145661.2(GATA2):c.66C>G (p.Pro22=) rs113384352
NM_001145661.2(GATA2):c.732C>T (p.His244=) rs954005309
NM_001145661.2(GATA2):c.872-5T>C rs886038417
NM_032638.5(GATA2):c.1017+9G>C rs753634658
NM_032638.5(GATA2):c.1143+13C>T rs112111696
NM_032638.5(GATA2):c.1194G>C (p.Arg398=) rs1576744514
NM_032638.5(GATA2):c.1371G>C (p.Thr457=) rs763539605
NM_032638.5(GATA2):c.1434C>T (p.Ala478=) rs1180428559
NM_032638.5(GATA2):c.147C>T (p.Phe49=) rs1474218678
NM_032638.5(GATA2):c.162G>T (p.Ser54=) rs758797691
NM_032638.5(GATA2):c.174C>A (p.Pro58=) rs112460453
NM_032638.5(GATA2):c.189C>T (p.Pro63=) rs763735447
NM_032638.5(GATA2):c.222C>T (p.Pro74=) rs1190822571
NM_032638.5(GATA2):c.315C>G (p.Leu105=) rs750545562
NM_032638.5(GATA2):c.372G>A (p.Thr124=) rs1462031219
NM_032638.5(GATA2):c.399C>T (p.Gly133=) rs1231963924
NM_032638.5(GATA2):c.417T>C (p.Ser139=) rs1576749006
NM_032638.5(GATA2):c.42G>A (p.Pro14=) rs372722885
NM_032638.5(GATA2):c.468G>A (p.Val156=) rs1576748915
NM_032638.5(GATA2):c.477C>T (p.Leu159=) rs761892289
NM_032638.5(GATA2):c.48G>T (p.Val16=) rs757404617
NM_032638.5(GATA2):c.504C>T (p.Ser168=) rs1436261988
NM_032638.5(GATA2):c.66C>T (p.Pro22=) rs113384352
NM_032638.5(GATA2):c.822G>A (p.Pro274=) rs772881173
NM_032638.5(GATA2):c.903A>G (p.Thr301=) rs1420799186
NM_032638.5(GATA2):c.966C>T (p.Tyr322=) rs775516037

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