ClinVar Miner

List of variants in gene KMT2D reported as likely benign by PreventionGenetics

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Total variants: 21
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HGVS dbSNP
NM_003482.3(KMT2D):c.10233C>T (p.Asp3411=) rs148688181
NM_003482.3(KMT2D):c.10508-11T>G rs374068805
NM_003482.3(KMT2D):c.11037A>G (p.Gln3679=) rs374418866
NM_003482.3(KMT2D):c.12913G>A (p.Val4305Ile) rs199895011
NM_003482.3(KMT2D):c.13644C>T (p.Ser4548=) rs201119371
NM_003482.3(KMT2D):c.15540G>C (p.Val5180=) rs149393179
NM_003482.3(KMT2D):c.16599G>A (p.Arg5533=) rs199798179
NM_003482.3(KMT2D):c.1725A>T (p.Pro575=) rs371243627
NM_003482.3(KMT2D):c.2074C>A (p.Pro692Thr) rs202076833
NM_003482.3(KMT2D):c.2156C>T (p.Pro719Leu) rs185660524
NM_003482.3(KMT2D):c.2785C>T (p.Leu929=) rs745396055
NM_003482.3(KMT2D):c.3819C>T (p.Cys1273=) rs373373098
NM_003482.3(KMT2D):c.4089C>T (p.Thr1363=) rs369601017
NM_003482.3(KMT2D):c.4518C>A (p.Thr1506=) rs150988159
NM_003482.3(KMT2D):c.5220C>T (p.Ala1740=) rs200369026
NM_003482.3(KMT2D):c.6629C>T (p.Pro2210Leu) rs201190869
NM_003482.3(KMT2D):c.6733C>G (p.Leu2245Val) rs201931833
NM_003482.3(KMT2D):c.8211C>T (p.Thr2737=) rs370558457
NM_003482.3(KMT2D):c.8547C>T (p.Ala2849=) rs368381758
NM_003482.3(KMT2D):c.9034C>T (p.Leu3012=) rs752355105
NM_003482.3(KMT2D):c.9343C>T (p.Leu3115Phe) rs587778471

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