ClinVar Miner

List of variants in gene MLH1 reported as likely benign for Lynch syndrome

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Total variants: 90
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HGVS dbSNP
NM_000249.3(MLH1):c.*162_*165delGATT rs796807655
NM_000249.3(MLH1):c.*35_*37delCTT rs193922366
NM_000249.3(MLH1):c.-107C>G rs587778886
NM_000249.3(MLH1):c.-269C>G rs35032294
NM_000249.3(MLH1):c.-93G>A rs1800734
NM_000249.3(MLH1):c.1003C>T (p.Leu335=) rs267607812
NM_000249.3(MLH1):c.1005G>A (p.Leu335=) rs1060504008
NM_000249.3(MLH1):c.1008C>A (p.Gly336=) rs863224338
NM_000249.3(MLH1):c.1035C>T (p.Thr345=) rs758668630
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-9T>G rs1060504009
NM_000249.3(MLH1):c.1136A>G (p.Tyr379Cys) rs143009528
NM_000249.3(MLH1):c.1151T>A (p.Val384Asp) rs63750447
NM_000249.3(MLH1):c.116+10_116+12delGAG rs1060504007
NM_000249.3(MLH1):c.116+8G>A rs904872305
NM_000249.3(MLH1):c.1164C>T (p.Ser388=) rs1060504014
NM_000249.3(MLH1):c.117-43_117-39del rs587778895
NM_000249.3(MLH1):c.117-9A>G rs1060504004
NM_000249.3(MLH1):c.1185A>G (p.Ala395=) rs878853774
NM_000249.3(MLH1):c.1267A>G (p.Arg423Gly)
NM_000249.3(MLH1):c.1407C>G (p.Pro469=) rs1060504002
NM_000249.3(MLH1):c.1407C>T (p.Pro469=) rs1060504002
NM_000249.3(MLH1):c.144A>G (p.Gln48=) rs147342421
NM_000249.3(MLH1):c.1474G>A (p.Ala492Thr) rs63751145
NM_000249.3(MLH1):c.1554T>C (p.His518=) rs1060504010
NM_000249.3(MLH1):c.1558+14G>A rs41562513
NM_000249.3(MLH1):c.1558+3232_1558+3692delins2
NM_000249.3(MLH1):c.1559-8T>C rs753196249
NM_000249.3(MLH1):c.159G>A (p.Glu53=) rs1060504012
NM_000249.3(MLH1):c.1653C>T (p.Asn551=) rs587778936
NM_000249.3(MLH1):c.1732-5C>T rs587778941
NM_000249.3(MLH1):c.1732-6T>C rs878853782
NM_000249.3(MLH1):c.1732-9T>C rs267607857
NM_000249.3(MLH1):c.1742C>T (p.Pro581Leu) rs63751684
NM_000249.3(MLH1):c.1808C>G (p.Pro603Arg) rs63750876
NM_000249.3(MLH1):c.1818A>G (p.Gly606=) rs1057522427
NM_000249.3(MLH1):c.1820T>A (p.Leu607His) rs41295284
NM_000249.3(MLH1):c.1824T>A (p.Ala608=) rs876659019
NM_000249.3(MLH1):c.1852A>G (p.Lys618Glu) rs35001569
NM_000249.3(MLH1):c.1853A>G (p.Lys618Arg) rs63750449
NM_000249.3(MLH1):c.1872C>T (p.Asp624=) rs145535636
NM_000249.3(MLH1):c.1897-17C>G rs2308316
NM_000249.3(MLH1):c.1960C>T (p.Pro654Ser)
NM_000249.3(MLH1):c.1963A>G (p.Ile655Val) rs55907433
NM_000249.3(MLH1):c.1983C>T (p.Ala661=) rs1060504001
NM_000249.3(MLH1):c.198C>T (p.Thr66=) rs61751642
NM_000249.3(MLH1):c.1990-9T>C rs756846181
NM_000249.3(MLH1):c.1995T>C (p.Asn665=) rs1060504011
NM_000249.3(MLH1):c.2010G>A (p.Lys670=) rs1060504013
NM_000249.3(MLH1):c.208-9A>G rs1057523558
NM_000249.3(MLH1):c.2082G>A (p.Glu694=) rs1057521441
NM_000249.3(MLH1):c.2101C>A (p.Gln701Lys) rs63750114
NM_000249.3(MLH1):c.2103+10_2103+14delTGATG rs864622755
NM_000249.3(MLH1):c.2152C>T (p.His718Tyr) rs2020873
NM_000249.3(MLH1):c.2252A>G (p.Lys751Arg) rs140195825
NM_000249.3(MLH1):c.261C>T (p.Ser87=) rs63750923
NM_000249.3(MLH1):c.303T>G (p.Gly101=) rs4647220
NM_000249.3(MLH1):c.306+8A>G rs587779002
NM_000249.3(MLH1):c.307-10T>C rs572853043
NM_000249.3(MLH1):c.307-19A>G rs121909451
NM_000249.3(MLH1):c.330G>A (p.Val110=) rs863224340
NM_000249.3(MLH1):c.375A>G (p.Ala125=) rs1800144
NM_000249.3(MLH1):c.381-5A>C rs1060504016
NM_000249.3(MLH1):c.42A>G (p.Thr14=) rs369737664
NM_000249.3(MLH1):c.438A>G (p.Gln146=) rs377279035
NM_000249.3(MLH1):c.474C>T (p.Asn158=) rs4647256
NM_000249.3(MLH1):c.545+43C>G rs267607761
NM_000249.3(MLH1):c.546-9C>G rs878853789
NM_000249.3(MLH1):c.588+11G>C rs4647258
NM_000249.3(MLH1):c.588+8C>A rs1060504005
NM_000249.3(MLH1):c.589-15C>T rs55658850
NM_000249.3(MLH1):c.589-7T>C rs371767464
NM_000249.3(MLH1):c.589-9G>A rs566497442
NM_000249.3(MLH1):c.621A>G (p.Leu207=) rs770554901
NM_000249.3(MLH1):c.637G>A (p.Val213Met) rs2308317
NM_000249.3(MLH1):c.655A>G (p.Ile219Val) rs1799977
NM_000249.3(MLH1):c.702G>A (p.Glu234=) rs35908749
NM_000249.3(MLH1):c.716C>T (p.Ala239Val)
NM_000249.3(MLH1):c.756A>C (p.Ser252=) rs864622458
NM_000249.3(MLH1):c.791-23delG rs267607797
NM_000249.3(MLH1):c.81G>A (p.Arg27=) rs878853791
NM_000249.3(MLH1):c.836T>G (p.Val279Gly) rs1553646683
NM_000249.3(MLH1):c.845C>G (p.Ala282Gly) rs63750360
NM_000249.3(MLH1):c.884+10delC rs878853793
NM_000249.3(MLH1):c.885-16_885-15delCT rs267607804
NM_000249.3(MLH1):c.885-24T>A rs201594027
NM_000249.3(MLH1):c.885-5G>T rs267607802
NM_000249.3(MLH1):c.906T>C (p.Asn302=) rs1060504006
NM_000249.3(MLH1):c.939A>G (p.Glu313=) rs864622432
NM_000249.3(MLH1):c.974G>A (p.Arg325Gln) rs63750268

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