ClinVar Miner

List of variants in gene RUNX1 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 103
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HGVS dbSNP
NM_001754.4(RUNX1):c.*1012C>T rs55767668
NM_001754.4(RUNX1):c.*1096A>C rs528969148
NM_001754.4(RUNX1):c.*1138C>A rs55744508
NM_001754.4(RUNX1):c.*113C>T rs187995123
NM_001754.4(RUNX1):c.*121G>C rs549844608
NM_001754.4(RUNX1):c.*1466G>A rs144796880
NM_001754.4(RUNX1):c.*1683_*1684delAT rs55761346
NM_001754.4(RUNX1):c.*1720C>T rs568766039
NM_001754.4(RUNX1):c.*1823A>C rs369678325
NM_001754.4(RUNX1):c.*2005A>G rs115087797
NM_001754.4(RUNX1):c.*2193delG rs201977305
NM_001754.4(RUNX1):c.*2201dupT rs201214658
NM_001754.4(RUNX1):c.*2329A>G rs529363958
NM_001754.4(RUNX1):c.*2467dupA rs200050352
NM_001754.4(RUNX1):c.*2626A>G rs77550657
NM_001754.4(RUNX1):c.*2642A>G rs112327235
NM_001754.4(RUNX1):c.*264C>T rs560356828
NM_001754.4(RUNX1):c.*2770C>G rs75192893
NM_001754.4(RUNX1):c.*2840A>T rs188812411
NM_001754.4(RUNX1):c.*2886T>C rs140071395
NM_001754.4(RUNX1):c.*3060T>C rs76478380
NM_001754.4(RUNX1):c.*3277G>T rs187846118
NM_001754.4(RUNX1):c.*3297T>C rs144175289
NM_001754.4(RUNX1):c.*3444A>G rs183666715
NM_001754.4(RUNX1):c.*3527T>G rs548011352
NM_001754.4(RUNX1):c.*3619A>G rs139372063
NM_001754.4(RUNX1):c.*3721A>T rs188246960
NM_001754.4(RUNX1):c.*3977G>A rs189557277
NM_001754.4(RUNX1):c.*4140C>T rs141693054
NM_001754.4(RUNX1):c.*4238G>T rs138870671
NM_001754.4(RUNX1):c.*4250C>T rs186103543
NM_001754.4(RUNX1):c.*429T>C rs533151594
NM_001754.4(RUNX1):c.*44C>G rs535532916
NM_001754.4(RUNX1):c.*484T>C rs147934675
NM_001754.4(RUNX1):c.*582delC rs201200981
NM_001754.4(RUNX1):c.*613A>T rs191743993
NM_001754.4(RUNX1):c.*667delG rs200576340
NM_001754.4(RUNX1):c.*683G>T rs575769251
NM_001754.4(RUNX1):c.*700dupT rs11424731
NM_001754.4(RUNX1):c.*730dupT rs11424730
NM_001754.4(RUNX1):c.*919A>G rs8131520
NM_001754.4(RUNX1):c.-135G>T rs140075488
NM_001754.4(RUNX1):c.-19G>A
NM_001754.4(RUNX1):c.-59-10C>T rs578080277
NM_001754.4(RUNX1):c.-89T>C rs77393863
NM_001754.4(RUNX1):c.1005G>T (p.Gln335His) rs80314254
NM_001754.4(RUNX1):c.1044C>T (p.His348=) rs773671764
NM_001754.4(RUNX1):c.1119G>C (p.Ser373=) rs766678402
NM_001754.4(RUNX1):c.111C>T (p.Ser37=) rs1555899908
NM_001754.4(RUNX1):c.1190A>G (p.Gln397Arg) rs762292084
NM_001754.4(RUNX1):c.1215G>A (p.Leu405=) rs1488763689
NM_001754.4(RUNX1):c.1269C>T (p.Arg423=) rs544247912
NM_001754.4(RUNX1):c.1275G>A (p.Pro425=) rs886038488
NM_001754.4(RUNX1):c.1311C>G (p.Thr437=) rs1555884827
NM_001754.4(RUNX1):c.1317C>T (p.Ser439=) rs1060504667
NM_001754.4(RUNX1):c.1355T>G (p.Val452Gly) rs751710767
NM_001754.4(RUNX1):c.1415T>C (p.Leu472Pro) rs764689239
NM_001754.4(RUNX1):c.1440C>T (p.Tyr480=) rs1555884783
NM_001754.4(RUNX1):c.144C>T (p.Ser48=) rs147889692
NM_001754.4(RUNX1):c.165G>A (p.Ala55=) rs766206710
NM_001754.4(RUNX1):c.167T>C (p.Leu56Ser) rs111527738
NM_001754.4(RUNX1):c.180C>T (p.Ala60=) rs375562861
NM_001754.4(RUNX1):c.183G>A (p.Pro61=) rs76558016
NM_001754.4(RUNX1):c.219C>T (p.Ser73=) rs1157495777
NM_001754.4(RUNX1):c.265C>T (p.Leu89=) rs1060504665
NM_001754.4(RUNX1):c.294C>G (p.Leu98=) rs1368531129
NM_001754.4(RUNX1):c.300C>G (p.Ser100=) rs764387069
NM_001754.4(RUNX1):c.303G>A (p.Val101=) rs142472642
NM_001754.4(RUNX1):c.303G>T (p.Val101=) rs142472642
NM_001754.4(RUNX1):c.351+15A>G rs199881885
NM_001754.4(RUNX1):c.36G>A (p.Ser12=) rs201490575
NM_001754.4(RUNX1):c.402T>C (p.Ala134=) rs1555898635
NM_001754.4(RUNX1):c.423G>A (p.Ser141=) rs745649956
NM_001754.4(RUNX1):c.444C>T (p.Thr148=) rs773689002
NM_001754.4(RUNX1):c.492C>T (p.Val164=) rs200907577
NM_001754.4(RUNX1):c.508+18A>G
NM_001754.4(RUNX1):c.552G>T (p.Pro184=) rs752586117
NM_001754.4(RUNX1):c.558C>T (p.Val186=) rs938065676
NM_001754.4(RUNX1):c.579C>T (p.Ile193=) rs762702957
NM_001754.4(RUNX1):c.58+23A>G
NM_001754.4(RUNX1):c.613+7G>A rs1375122279
NM_001754.4(RUNX1):c.613+8C>T rs186585782
NM_001754.4(RUNX1):c.630A>G (p.Leu210=) rs367978995
NM_001754.4(RUNX1):c.645G>A (p.Lys215=) rs1312588693
NM_001754.4(RUNX1):c.648C>T (p.Pro216=) rs199759556
NM_001754.4(RUNX1):c.654C>T (p.Ser218=) rs145230602
NM_001754.4(RUNX1):c.65T>A (p.Ile22Lys) rs749430925
NM_001754.4(RUNX1):c.698G>A (p.Arg233His) rs150042294
NM_001754.4(RUNX1):c.705C>T (p.Ala235=) rs772770088
NM_001754.4(RUNX1):c.714C>T (p.Val238=) rs776056802
NM_001754.4(RUNX1):c.729A>C (p.Pro243=) rs999807714
NM_001754.4(RUNX1):c.741C>T (p.Pro247=) rs1060504668
NM_001754.4(RUNX1):c.744C>T (p.Asn248=) rs1555889947
NM_001754.4(RUNX1):c.768C>T (p.Ser256=) rs780019726
NM_001754.4(RUNX1):c.824C>T (p.Pro275Leu) rs201164283
NM_001754.4(RUNX1):c.843C>T (p.Tyr281=) rs377142186
NM_001754.4(RUNX1):c.882T>C (p.Pro294=) rs376963970
NM_001754.4(RUNX1):c.900G>A (p.Thr300=)
NM_001754.4(RUNX1):c.924C>T (p.Ser308=) rs1060504666
NM_001754.4(RUNX1):c.927C>T (p.Gly309=) rs59802347
NM_001754.4(RUNX1):c.967+8A>T rs113054726
NM_001754.4(RUNX1):c.96C>T (p.His32=) rs748758482
NM_001754.4(RUNX1):c.984A>G (p.Thr328=) rs377305704

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