List of variants in gene MLH1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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_000249.4(MLH1):c.1732-19T>A	rs77120160	0.00923
NM_000249.4(MLH1):c.1852A>G (p.Lys618Glu)	rs35001569	0.00399
NM_000249.4(MLH1):c.-7C>T	rs104894994	0.00115
NM_000249.4(MLH1):c.-28A>G	rs56198082	0.00110
NM_000249.4(MLH1):c.1321G>A (p.Ala441Thr)	rs63750365	0.00034
NM_000249.4(MLH1):c.394G>C (p.Asp132His)	rs28930073	0.00019
NM_000249.4(MLH1):c.1820T>A (p.Leu607His)	rs41295284	0.00015
NM_000249.4(MLH1):c.955G>A (p.Glu319Lys)	rs63750796	0.00006
NM_000249.4(MLH1):c.1153C>T (p.Arg385Cys)	rs63750760	0.00005
NM_000249.4(MLH1):c.1270G>A (p.Ala424Thr)	rs377433038	0.00004
NM_000249.4(MLH1):c.1633A>G (p.Thr545Ala)	rs267607840	0.00004
NM_000249.4(MLH1):c.116+5G>A	rs267607710	0.00003
NM_000249.4(MLH1):c.1165C>T (p.Arg389Trp)	rs61751644	0.00003
NM_000249.4(MLH1):c.286A>G (p.Thr96Ala)	rs770276731	0.00003
NM_000249.4(MLH1):c.1256T>C (p.Ile419Thr)	rs377484262	0.00002
NM_000249.4(MLH1):c.925C>T (p.Pro309Ser)	rs267607808	0.00002
NM_000249.4(MLH1):c.1344G>T (p.Glu448Asp)	rs587779952	0.00001
NM_000249.4(MLH1):c.1682A>G (p.Tyr561Cys)	rs1289807424	0.00001
NM_000249.4(MLH1):c.682C>A (p.Leu228Met)	rs751628735	0.00001
NM_000249.4(MLH1):c.1039-3C>G	rs730881737
NM_000249.4(MLH1):c.1172A>G (p.Gln391Arg)	rs587782884
NM_000249.4(MLH1):c.1351A>G (p.Thr451Ala)	rs864622145
NM_000249.4(MLH1):c.1668-139dup	rs863225375
NM_000249.4(MLH1):c.1852_1853delinsGC (p.Lys618Ala)	rs35502531
NM_000249.4(MLH1):c.1853A>C (p.Lys618Thr)	rs63750449
NM_000249.4(MLH1):c.1918C>A (p.Pro640Thr)	rs63749792
NM_000249.4(MLH1):c.194G>T (p.Gly65Val)	rs63751465
NM_000249.4(MLH1):c.2041G>A (p.Ala681Thr)	rs63750217
NM_000249.4(MLH1):c.293G>A (p.Gly98Asp)	rs863225382
NM_000249.4(MLH1):c.304G>A (p.Glu102Lys)	rs63750453
NM_000249.4(MLH1):c.588+7T>C	rs1553644066
NM_000249.4(MLH1):c.589-3C>G
NM_000249.4(MLH1):c.710C>T (p.Thr237Ile)	rs771606168
NM_000249.4(MLH1):c.85G>T (p.Ala29Ser)	rs63750656

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