ClinVar Miner

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

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Total variants: 32
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HGVS dbSNP
NM_001754.4(RUNX1):c.*2285A>C rs75749444
NM_001754.4(RUNX1):c.*2474T>C rs56202419
NM_001754.4(RUNX1):c.*2549_*2550dupTG rs371955155
NM_001754.4(RUNX1):c.*2768A>C rs74950917
NM_001754.4(RUNX1):c.*27C>A rs13051066
NM_001754.4(RUNX1):c.*3345A>T rs56151547
NM_001754.4(RUNX1):c.*3380A>G rs79122814
NM_001754.4(RUNX1):c.*3574A>G rs113375138
NM_001754.4(RUNX1):c.*4032T>C rs78335539
NM_001754.4(RUNX1):c.*559T>C rs73362827
NM_001754.4(RUNX1):c.*70T>C rs150481777
NM_001754.4(RUNX1):c.*88G>T rs539980908
NM_001754.4(RUNX1):c.1005G>T (p.Gln335His) rs80314254
NM_001754.4(RUNX1):c.1086G>C (p.Ser362=) rs143947839
NM_001754.4(RUNX1):c.1269C>T (p.Arg423=) rs544247912
NM_001754.4(RUNX1):c.1355T>G (p.Val452Gly) rs751710767
NM_001754.4(RUNX1):c.1389C>G (p.Pro463=) rs61750222
NM_001754.4(RUNX1):c.144C>T (p.Ser48=) rs147889692
NM_001754.4(RUNX1):c.167T>C (p.Leu56Ser) rs111527738
NM_001754.4(RUNX1):c.183G>A (p.Pro61=) rs76558016
NM_001754.4(RUNX1):c.18A>G (p.Ile6Met) rs199929612
NM_001754.4(RUNX1):c.303G>T (p.Val101=) rs142472642
NM_001754.4(RUNX1):c.342C>A (p.Ile114=) rs201747706
NM_001754.4(RUNX1):c.351+15A>G rs199881885
NM_001754.4(RUNX1):c.552G>T (p.Pro184=) rs752586117
NM_001754.4(RUNX1):c.613+8C>T rs186585782
NM_001754.4(RUNX1):c.614-34C>T rs11702841
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.824C>T (p.Pro275Leu) rs201164283
NM_001754.4(RUNX1):c.927C>T (p.Gly309=) rs59802347
NM_001754.4(RUNX1):c.952T>G (p.Ser318Ala) rs545554349

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