ClinVar Miner

List of variants in gene RUNX1 reported as benign by Invitae

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001754.5(RUNX1):c.58+103A>G rs8133634 0.59069
NM_001754.5(RUNX1):c.1389C>G (p.Pro463=) rs61750222 0.04709
NM_001754.5(RUNX1):c.167T>C (p.Leu56Ser) rs111527738 0.01206
NM_001754.5(RUNX1):c.927C>T (p.Gly309=) rs59802347 0.01119
NM_001754.5(RUNX1):c.183G>A (p.Pro61=) rs76558016 0.00454
NM_001754.5(RUNX1):c.351+15A>G rs199881885 0.00396
NM_001754.5(RUNX1):c.144C>T (p.Ser48=) rs147889692 0.00344
NM_001754.5(RUNX1):c.613+8C>T rs186585782 0.00300
NM_001754.5(RUNX1):c.303G>T (p.Val101=) rs142472642 0.00200
NM_001754.5(RUNX1):c.1086G>C (p.Ser362=) rs143947839 0.00072
NM_001754.5(RUNX1):c.654C>T (p.Ser218=) rs145230602 0.00063
NM_001754.5(RUNX1):c.1269C>T (p.Arg423=) rs544247912 0.00040
NM_001754.5(RUNX1):c.952T>G (p.Ser318Ala) rs545554349 0.00013
NM_001754.5(RUNX1):c.1005G>T (p.Gln335His) rs80314254 0.00011
NM_001754.5(RUNX1):c.1062C>G (p.Thr354=) rs748629722 0.00010
NM_001754.5(RUNX1):c.613+18G>C rs374732985 0.00009
NM_001754.5(RUNX1):c.492C>T (p.Val164=) rs200907577 0.00008
NM_001754.5(RUNX1):c.552G>T (p.Pro184=) rs752586117 0.00006
NM_001754.5(RUNX1):c.18A>G (p.Ile6Met) rs199929612 0.00005
NM_001754.5(RUNX1):c.342C>A (p.Ile114=) rs201747706 0.00001
NM_001754.5(RUNX1):c.165G>T (p.Ala55=)
NM_001754.5(RUNX1):c.170C>G (p.Pro57Arg) rs1266842690
NM_001754.5(RUNX1):c.170C>T (p.Pro57Leu) rs1266842690
NM_001754.5(RUNX1):c.393T>C (p.Thr131=) rs746650216

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