ClinVar Miner

List of variants reported as benign for Acute myeloid leukemia

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_001754.5(RUNX1):c.614-34C>T rs11702841 0.99999
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522 0.62654
NM_198253.3(TERT):c.915G>A (p.Ala305=) rs2736098 0.21206
NM_004364.5(CEBPA):c.690G>T (p.Thr230=) rs34529039 0.16355
NM_198253.3(TERT):c.3039C>T (p.His1013=) rs33954691 0.08834
NM_001754.5(RUNX1):c.1389C>G (p.Pro463=) rs61750222 0.04709
NM_198253.3(TERT):c.2031C>T (p.Gly677=) rs33956095 0.02136
NM_004364.5(CEBPA):c.573C>T (p.His191=) rs192240793 0.02004
NM_198253.3(TERT):c.1950+10C>T rs33948291 0.01758
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_198253.3(TERT):c.1659C>T (p.Val553=) rs35809415 0.00838
NM_004364.5(CEBPA):c.693C>G (p.Pro231=) rs550308123 0.00808
NM_004364.5(CEBPA):c.756G>T (p.Ala252=) rs571969199 0.00778
NM_004364.5(CEBPA):c.1041G>A (p.Glu347=) rs141430731 0.00752
NM_198253.3(TERT):c.2097C>T (p.Ala699=) rs33963617 0.00739
NM_001754.5(RUNX1):c.183G>A (p.Pro61=) rs76558016 0.00454
NM_001754.5(RUNX1):c.351+15A>G rs199881885 0.00396
NM_004364.5(CEBPA):c.402G>A (p.Ala134=) rs752254340 0.00295
NM_198253.3(TERT):c.969G>A (p.Pro323=) rs148549782 0.00224
NM_198253.3(TERT):c.1574-7G>A rs34846301 0.00220
NM_004364.5(CEBPA):c.612G>C (p.Pro204=) rs552634598 0.00214
NM_001754.5(RUNX1):c.303G>T (p.Val101=) rs142472642 0.00200
NM_198253.3(TERT):c.2517G>A (p.Thr839=) rs140124989 0.00178
NM_198253.3(TERT):c.2769G>A (p.Pro923=) rs200174990 0.00118
NM_198253.3(TERT):c.1884C>T (p.Asp628=) rs143992655 0.00088
NM_198253.3(TERT):c.1849C>T (p.Leu617=) rs140951453 0.00083
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_004364.5(CEBPA):c.561G>C (p.Pro187=) rs538441046 0.00022
NM_004364.5(CEBPA):c.811G>C (p.Ala271Pro) rs756632245 0.00015
NM_198253.3(TERT):c.1392C>T (p.Phe464=) rs186596886 0.00008
NM_004364.5(CEBPA):c.459G>A (p.Pro153=) rs779373951 0.00001
NM_000546.6(TP53):c.805A>T (p.Ser269Cys)
NM_000546.6(TP53):c.952C>T (p.Pro318Ser)
NM_000546.6(TP53):c.954A>T (p.Pro318=)
NM_000546.6(TP53):c.969G>C (p.Leu323=)
NM_000546.6(TP53):c.970G>A (p.Asp324Asn)
NM_000546.6(TP53):c.978A>G (p.Glu326=)
NM_003025.4(SH3GL1):c.771C>G (p.Pro257=) rs243261
NM_004364.5(CEBPA):c.296GCG[7] (p.Gly104dup) rs780345232
NM_004364.5(CEBPA):c.296GCG[8] (p.Gly103_Gly104dup) rs780345232
NM_004364.5(CEBPA):c.572ACCCGC[4] (p.191HP[4]) rs762459325

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