ClinVar Miner

List of variants in gene RUNX1 reported as likely benign for Familial platelet disorder with associated myeloid malignancy

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Gene type:
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Total variants: 81
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HGVS dbSNP
NM_001754.4(RUNX1):c.*1683_*1684del rs55761346
NM_001754.4(RUNX1):c.*2193del rs201977305
NM_001754.4(RUNX1):c.*2201dup rs201214658
NM_001754.4(RUNX1):c.*2467dup rs200050352
NM_001754.4(RUNX1):c.*3527T>G rs548011352
NM_001754.4(RUNX1):c.*3977G>A rs189557277
NM_001754.4(RUNX1):c.*4188G>C rs761390141
NM_001754.4(RUNX1):c.*582del rs201200981
NM_001754.4(RUNX1):c.*667del rs200576340
NM_001754.4(RUNX1):c.*700dup rs11424731
NM_001754.4(RUNX1):c.*730dup rs11424730
NM_001754.4(RUNX1):c.1005G>T (p.Gln335His) rs80314254
NM_001754.4(RUNX1):c.1029C>T (p.Ser343=) rs767579059
NM_001754.4(RUNX1):c.1032C>T (p.Asp344=) rs1601333645
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.1272G>C (p.Ser424=) rs1459260782
NM_001754.4(RUNX1):c.1275G>A (p.Pro425=) rs886038488
NM_001754.4(RUNX1):c.1290G>A (p.Pro430=) rs1336841746
NM_001754.4(RUNX1):c.1311C>G (p.Thr437=) rs1555884827
NM_001754.4(RUNX1):c.1338C>T (p.Leu446=) rs769628054
NM_001754.4(RUNX1):c.1355T>G (p.Val452Gly) rs751710767
NM_001754.4(RUNX1):c.1396A>T (p.Met466Leu) rs762213305
NM_001754.4(RUNX1):c.1401G>A (p.Ala467=) rs754338287
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.165G>A (p.Ala55=) rs766206710
NM_001754.4(RUNX1):c.180C>T (p.Ala60=) rs375562861
NM_001754.4(RUNX1):c.18A>G (p.Ile6Met) rs199929612
NM_001754.4(RUNX1):c.204C>G (p.Ala68=) rs746342521
NM_001754.4(RUNX1):c.219C>T (p.Ser73=) rs1157495777
NM_001754.4(RUNX1):c.253C>A (p.His85Asn) rs121912500
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.300C>T (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.336G>T (p.Leu112=) rs977880516
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.509-8C>G rs1601470889
NM_001754.4(RUNX1):c.552G>A (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+9A>G rs553468449
NM_001754.4(RUNX1):c.59-10G>T rs1569090482
NM_001754.4(RUNX1):c.613+7G>A rs1375122279
NM_001754.4(RUNX1):c.614-9C>T rs999210074
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.651G>C (p.Gly217=) rs1569037346
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.666C>T (p.Ser222=) rs747906151
NM_001754.4(RUNX1):c.668A>G (p.Glu223Gly) rs780999703
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.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.812G>A (p.Arg271Lys) rs750826029
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.924C>T (p.Ser308=) rs1060504666
NM_001754.4(RUNX1):c.936C>T (p.Thr312=) rs368294941
NM_001754.4(RUNX1):c.939_950del (p.Ala315_Ser318del) rs748122795
NM_001754.4(RUNX1):c.967+8A>T rs113054726
NM_001754.4(RUNX1):c.968-7C>T rs1601334068
NM_001754.4(RUNX1):c.96C>T (p.His32=) rs748758482
NM_001754.4(RUNX1):c.979C>T (p.Leu327=) rs1157267880
NM_001754.4(RUNX1):c.981G>C (p.Leu327=) rs376269814
NM_001754.4(RUNX1):c.984A>G (p.Thr328=) rs377305704
NM_001754.4(RUNX1):c.994G>A (p.Asp332Asn) rs757030094
NM_001754.5(RUNX1):c.*263C>G

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