List of variants in gene KMT2D reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_003482.4(KMT2D):c.7479G>T (p.Gly2493=)	rs10747559	0.42978
NM_003482.4(KMT2D):c.10836G>A (p.Gln3612=)	rs3782357	0.42594
NM_003482.4(KMT2D):c.2826C>T (p.Ile942=)	rs2241726	0.39054
NM_003482.4(KMT2D):c.12510A>G (p.Pro4170=)	rs3741622	0.25778
NM_003482.4(KMT2D):c.1426G>A (p.Ala476Thr)	rs1064210	0.09584
NM_003482.4(KMT2D):c.13689C>T (p.Pro4563=)	rs11168830	0.06301
NM_003482.4(KMT2D):c.10671A>G (p.Pro3557=)	rs61942218	0.04331
NM_003482.4(KMT2D):c.2438C>T (p.Pro813Leu)	rs75226229	0.04312
NM_003482.4(KMT2D):c.14251+18T>C	rs74830946	0.04121
NM_003482.4(KMT2D):c.14238G>A (p.Arg4746=)	rs75340924	0.04096
NM_003482.4(KMT2D):c.15978T>G (p.Leu5326=)	rs55776396	0.02513
NM_003482.4(KMT2D):c.12028T>C (p.Ser4010Pro)	rs80132640	0.02449
NM_003482.4(KMT2D):c.5467+19A>C	rs78764337	0.02428
NM_003482.4(KMT2D):c.248G>A (p.Arg83Gln)	rs55865069	0.02422
NM_003482.4(KMT2D):c.5217C>T (p.Gly1739=)	rs111924728	0.01973
NM_003482.4(KMT2D):c.8091C>T (p.Arg2697=)	rs116686402	0.01940
NM_003482.4(KMT2D):c.7188T>C (p.Cys2396=)	rs111305262	0.01710
NM_003482.4(KMT2D):c.7670C>T (p.Pro2557Leu)	rs189888707	0.01025
NM_003482.4(KMT2D):c.10192A>G (p.Met3398Val)	rs75937132	0.00847
NM_003482.4(KMT2D):c.6180C>T (p.Tyr2060=)	rs186577948	0.00315
NM_003482.4(KMT2D):c.13102A>G (p.Thr4368Ala)	rs189357192	0.00243
NM_003482.4(KMT2D):c.8774C>T (p.Ala2925Val)	rs199547661	0.00223
NM_003482.4(KMT2D):c.6752C>T (p.Ser2251Leu)	rs189199944	0.00200
NM_003482.4(KMT2D):c.8149C>T (p.Pro2717Ser)	rs201336660	0.00165
NM_003482.4(KMT2D):c.7046C>T (p.Pro2349Leu)	rs201581582	0.00061
NM_003482.4(KMT2D):c.6354C>T (p.Pro2118=)	rs377392943	0.00053
NM_003482.4(KMT2D):c.4143G>A (p.Val1381=)	rs398123745	0.00011
NM_003482.4(KMT2D):c.6704G>A (p.Arg2235Lys)	rs551403860	0.00001
NM_003482.4(KMT2D):c.10441-9T>A	rs572158148
NM_003482.4(KMT2D):c.15555C>T (p.Phe5185=)	rs575965702
NM_003482.4(KMT2D):c.16412+16del	rs34546217
NM_003482.4(KMT2D):c.3408G>A (p.Glu1136=)	rs372234918
NM_003482.4(KMT2D):c.4021-15CT[2]	rs55776244
NM_003482.4(KMT2D):c.8148T>C (p.Pro2716=)	rs369429157

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