ClinVar Miner

List of variants in gene KMT2A studied for not specified

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_001197104.2(KMT2A):c.4820-45T>C rs562780 0.87322
NM_001197104.2(KMT2A):c.7254C>T (p.Asn2418=) rs2071702 0.07440
NM_001197104.2(KMT2A):c.5679A>G (p.Leu1893=) rs7107305 0.04025
NM_001197104.2(KMT2A):c.4284A>C (p.Ile1428=) rs9332801 0.04002
NM_001197104.2(KMT2A):c.8961T>A (p.Thr2987=) rs9332842 0.01910
NM_001197104.2(KMT2A):c.89C>G (p.Ala30Gly) rs9332745 0.01573
NM_001197104.2(KMT2A):c.158C>T (p.Ala53Val) rs9332747 0.00631
NM_001197104.2(KMT2A):c.1504G>A (p.Glu502Lys) rs9332772 0.00614
NM_001197104.2(KMT2A):c.6572G>A (p.Arg2191Gln) rs141727765 0.00109
NM_001197104.2(KMT2A):c.2965C>T (p.Leu989Phe) rs139989306 0.00101
NM_001197104.2(KMT2A):c.6009C>T (p.Asp2003=) rs77421119 0.00086
NM_001197104.2(KMT2A):c.10715T>G (p.Ile3572Ser) rs147014136 0.00051
NM_001197104.2(KMT2A):c.1810A>G (p.Met604Val) rs150328852 0.00046
NM_001197104.2(KMT2A):c.10113G>A (p.Arg3371=) rs369292004 0.00013
NM_001197104.2(KMT2A):c.9769T>C (p.Leu3257=) rs138046203 0.00011
NM_001197104.2(KMT2A):c.10835+1G>C rs141515578 0.00004
NM_001197104.2(KMT2A):c.10690C>T (p.Arg3564Trp) rs555310772 0.00003
NM_001197104.2(KMT2A):c.10901-5A>G rs369909433 0.00002
NM_001197104.2(KMT2A):c.5287C>T (p.Arg1763Trp) rs999060359 0.00001
NM_001197104.2(KMT2A):c.82G>T (p.Gly28Trp) rs782113710 0.00001
NM_001197104.2(KMT2A):c.10178T>C (p.Leu3393Pro) rs1555048205
NM_001197104.2(KMT2A):c.10580G>A (p.Arg3527Gln) rs147844226
NM_001197104.2(KMT2A):c.130C>A (p.Pro44Thr) rs1437526128
NM_001197104.2(KMT2A):c.134C>G (p.Pro45Arg) rs2134152876
NM_001197104.2(KMT2A):c.1877G>A (p.Arg626Lys)
NM_001197104.2(KMT2A):c.209G>A (p.Ser70Asn) rs1177309170
NM_001197104.2(KMT2A):c.2544G>C (p.Gly848=)
NM_001197104.2(KMT2A):c.2905C>G (p.Leu969Val) rs864309568
NM_001197104.2(KMT2A):c.3461G>A (p.Arg1154Gln) rs1131691799
NM_001197104.2(KMT2A):c.5961+37del rs57102960
NM_001197104.2(KMT2A):c.6446G>C (p.Arg2149Pro)
NM_001197104.2(KMT2A):c.7193A>T (p.Glu2398Val)
NM_001197104.2(KMT2A):c.7463A>G (p.Asp2488Gly)
NM_001197104.2(KMT2A):c.841C>G (p.Leu281Val)
NM_001197104.2(KMT2A):c.8766A>C (p.Glu2922Asp) rs2134400611
NM_001197104.2(KMT2A):c.9478T>C (p.Ser3160Pro) rs1555047715
NM_001197104.2(KMT2A):c.9953G>C (p.Gly3318Ala) rs1950572153

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