ClinVar Miner

List of variants in gene MLH1 reported as uncertain significance by Integrated Genetics/Laboratory Corporation of America

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Gene type:
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Total variants: 93
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HGVS dbSNP
NM_000249.3(MLH1):c.-11C>T rs776898290
NM_000249.3(MLH1):c.1039-10T>A rs1353365805
NM_000249.3(MLH1):c.1104G>A (p.Ser368=) rs769364808
NM_000249.3(MLH1):c.1136A>G (p.Tyr379Cys) rs143009528
NM_000249.3(MLH1):c.1153C>T (p.Arg385Cys) rs63750760
NM_000249.3(MLH1):c.1154G>A (p.Arg385His) rs63750430
NM_000249.3(MLH1):c.116+8G>A rs904872305
NM_000249.3(MLH1):c.1164C>T (p.Ser388=) rs1060504014
NM_000249.3(MLH1):c.1166G>A (p.Arg389Gln) rs63750361
NM_000249.3(MLH1):c.117-10G>A rs576724240
NM_000249.3(MLH1):c.1172A>G (p.Gln391Arg) rs587782884
NM_000249.3(MLH1):c.1184C>T (p.Ala395Val) rs1064794142
NM_000249.3(MLH1):c.1268G>A (p.Arg423Lys) rs370687064
NM_000249.3(MLH1):c.1309C>G (p.Pro437Ala) rs587782273
NM_000249.3(MLH1):c.1359G>C (p.Lys453Asn) rs756099600
NM_000249.3(MLH1):c.1360G>C (p.Gly454Arg) rs63750527
NM_000249.3(MLH1):c.1415G>A (p.Arg472Lys) rs63750498
NM_000249.3(MLH1):c.1489C>T (p.Arg497Trp) rs200830026
NM_000249.3(MLH1):c.1501A>G (p.Ile501Val) rs748613173
NM_000249.3(MLH1):c.1558+5G>A rs199935667
NM_000249.3(MLH1):c.1559T>C (p.Val520Ala) rs1200485334
NM_000249.3(MLH1):c.1564C>T (p.Arg522Trp) rs63751703
NM_000249.3(MLH1):c.1569G>T (p.Glu523Asp) rs63751680
NM_000249.3(MLH1):c.1618T>C (p.Leu540=) rs1448439825
NM_000249.3(MLH1):c.1633A>G (p.Thr545Ala) rs267607840
NM_000249.3(MLH1):c.1657A>G (p.Thr553Ala) rs1559575796
NM_000249.3(MLH1):c.1665T>C (p.Leu555=) rs749204990
NM_000249.3(MLH1):c.1706C>T (p.Ala569Val) rs1559578814
NM_000249.3(MLH1):c.1709A>G (p.Asn570Ser) rs375853155
NM_000249.3(MLH1):c.1731+8T>C rs370108219
NM_000249.3(MLH1):c.1732-4C>G rs876658984
NM_000249.3(MLH1):c.1734G>C (p.Glu578Asp) rs1553662589
NM_000249.3(MLH1):c.1744C>T (p.Leu582Phe) rs63751713
NM_000249.3(MLH1):c.1780G>A (p.Glu594Lys) rs1553662786
NM_000249.3(MLH1):c.1834G>A (p.Val612Ile) rs587779956
NM_000249.3(MLH1):c.1850A>C (p.Lys617Thr) rs780199021
NM_000249.3(MLH1):c.1853A>T (p.Lys618Met) rs63750449
NM_000249.3(MLH1):c.1890T>G (p.Ile630Met) rs774878438
NM_000249.3(MLH1):c.1896+17T>C rs193922368
NM_000249.3(MLH1):c.1897-10C>T rs1553663687
NM_000249.3(MLH1):c.1908G>A (p.Leu636=) rs1800145
NM_000249.3(MLH1):c.1937A>G (p.Tyr646Cys) rs35045067
NM_000249.3(MLH1):c.1964T>C (p.Ile655Thr) rs63751225
NM_000249.3(MLH1):c.1984A>C (p.Thr662Pro) rs587778964
NM_000249.3(MLH1):c.2048T>C (p.Phe683Ser) rs587778972
NM_000249.3(MLH1):c.2080_2081inv (p.Glu694Ser)
NM_000249.3(MLH1):c.2094A>G (p.Ser698=) rs786202433
NM_000249.3(MLH1):c.2135G>C (p.Trp712Ser) rs63750561
NM_000249.3(MLH1):c.2161T>C (p.Tyr721His) rs1453792999
NM_000249.3(MLH1):c.2162A>G (p.Tyr721Cys) rs587778986
NM_000249.3(MLH1):c.2174G>A (p.Arg725His) rs566928243
NM_000249.3(MLH1):c.2194A>C (p.Lys732Gln) rs267607906
NM_000249.3(MLH1):c.2213G>A (p.Gly738Glu) rs148317871
NM_000249.3(MLH1):c.2239C>T (p.Pro747Ser) rs587779958
NM_000249.3(MLH1):c.2266T>G (p.Cys756Gly) rs765480781
NM_000249.3(MLH1):c.261C>T (p.Ser87=) rs63750923
NM_000249.3(MLH1):c.27G>T (p.Arg9=) rs759680369
NM_000249.3(MLH1):c.299G>A (p.Arg100Gln) rs63750266
NM_000249.3(MLH1):c.30G>T (p.Arg10=) rs876660759
NM_000249.3(MLH1):c.317G>A (p.Ser106Asn) rs368208495
NM_000249.3(MLH1):c.319A>G (p.Ile107Val) rs572906317
NM_000249.3(MLH1):c.347C>A (p.Thr116Lys) rs63750465
NM_000249.3(MLH1):c.380+10T>C rs1553641403
NM_000249.3(MLH1):c.453+10G>T rs1553642170
NM_000249.3(MLH1):c.453G>A (p.Thr151=) rs369521379
NM_000249.3(MLH1):c.539T>C (p.Val180Ala) rs63750102
NM_000249.3(MLH1):c.545+19G>T rs41285099
NM_000249.3(MLH1):c.552A>T (p.Ser184=) rs35225190
NM_000249.3(MLH1):c.589-8T>C rs1017112753
NM_000249.3(MLH1):c.589-9_589-6delGTTT rs587779026
NM_000249.3(MLH1):c.621A>G (p.Leu207=) rs770554901
NM_000249.3(MLH1):c.682C>A (p.Leu228Met) rs751628735
NM_000249.3(MLH1):c.69A>G (p.Glu23=) rs63750555
NM_000249.3(MLH1):c.729T>C (p.Asn243=) rs876660573
NM_000249.3(MLH1):c.743A>G (p.Asn248Ser) rs587782800
NM_000249.3(MLH1):c.762G>A (p.Lys254=) rs863224341
NM_000249.3(MLH1):c.776T>C (p.Leu259Ser) rs56250509
NM_000249.3(MLH1):c.791-49_791-45delTCACC rs1559538882
NM_000249.3(MLH1):c.794G>A (p.Arg265His) rs63751448
NM_000249.3(MLH1):c.808A>G (p.Thr270Ala) rs371302926
NM_000249.3(MLH1):c.80G>A (p.Arg27Gln) rs138705565
NM_000249.3(MLH1):c.80G>C (p.Arg27Pro) rs138705565
NM_000249.3(MLH1):c.848A>G (p.Tyr283Cys) rs201931669
NM_000249.3(MLH1):c.884+16A>G rs377598055
NM_000249.3(MLH1):c.887T>C (p.Leu296Ser) rs63750547
NM_000249.3(MLH1):c.927C>T (p.Pro309=) rs63749896
NM_000249.3(MLH1):c.928A>G (p.Thr310Ala) rs779581111
NM_000249.3(MLH1):c.92C>T (p.Ala31Val) rs730882127
NM_000249.3(MLH1):c.931A>G (p.Lys311Glu) rs876658657
NM_000249.3(MLH1):c.94A>G (p.Ile32Val) rs2020872
NM_000249.3(MLH1):c.954C>T (p.His318=) rs146777069
NM_000249.3(MLH1):c.969G>C (p.Leu323=) rs1553648063
NM_000249.3(MLH1):c.974G>A (p.Arg325Gln) rs63750268

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