ClinVar Miner

List of variants in gene KMT2D reported as pathogenic by Ambry Genetics

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_003482.4(KMT2D):c.11547_11557dup (p.Val3853fs) rs1555188623
NM_003482.4(KMT2D):c.11938C>T (p.Gln3980Ter)
NM_003482.4(KMT2D):c.11944C>T (p.Arg3982Ter) rs1555188379
NM_003482.4(KMT2D):c.12414dup (p.Val4139fs) rs1942959186
NM_003482.4(KMT2D):c.12466del (p.Gln4156fs)
NM_003482.4(KMT2D):c.12592C>T (p.Arg4198Ter) rs587783685
NM_003482.4(KMT2D):c.13411_13412del (p.Asn4471fs) rs1555187440
NM_003482.4(KMT2D):c.13450C>T (p.Arg4484Ter) rs587783690
NM_003482.4(KMT2D):c.13986_13993dup (p.Leu4665fs) rs1555186842
NM_003482.4(KMT2D):c.14075+1G>A rs1057516039
NM_003482.4(KMT2D):c.15079C>T (p.Arg5027Ter) rs797045659
NM_003482.4(KMT2D):c.15142C>T (p.Arg5048Cys) rs398123724
NM_003482.4(KMT2D):c.15535C>T (p.Arg5179Cys) rs794727688
NM_003482.4(KMT2D):c.15858_15859del (p.Tyr5287fs)
NM_003482.4(KMT2D):c.16018C>T (p.Arg5340Ter) rs1565756115
NM_003482.4(KMT2D):c.16273G>A (p.Glu5425Lys) rs2137706560
NM_003482.4(KMT2D):c.16336dup (p.Gln5446fs) rs1555184787
NM_003482.4(KMT2D):c.16360C>T (p.Arg5454Ter) rs267607239
NM_003482.4(KMT2D):c.1967del (p.Leu656fs) rs772870804
NM_003482.4(KMT2D):c.4485C>A (p.Tyr1495Ter) rs574622908
NM_003482.4(KMT2D):c.4941del (p.Asp1648fs) rs1555194443
NM_003482.4(KMT2D):c.5124_5125del (p.Arg1709fs) rs886043506
NM_003482.4(KMT2D):c.5269C>T (p.Arg1757Ter) rs1555194045
NM_003482.4(KMT2D):c.5775del (p.Leu1926fs) rs1943599403
NM_003482.4(KMT2D):c.6295C>T (p.Arg2099Ter) rs1452715535
NM_003482.4(KMT2D):c.778del (p.Ala259_Leu260insTer) rs1938214848
NM_003482.4(KMT2D):c.9787_9791dup (p.Gln3265fs) rs1943282614

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