ClinVar Miner

List of variants in gene MLH1 reported as uncertain significance by Counsyl

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Total variants: 79
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HGVS dbSNP
NM_000249.3(MLH1):c.*3A>G rs587778880
NM_000249.3(MLH1):c.-42C>T rs41285097
NM_000249.3(MLH1):c.1007G>A (p.Gly336Asp) rs587781750
NM_000249.3(MLH1):c.1010C>G (p.Ser337Cys) rs763847201
NM_000249.3(MLH1):c.1088_1090CAA[1] (p.Thr364del) rs876660192
NM_000249.3(MLH1):c.1117G>A (p.Gly373Arg) rs766904735
NM_000249.3(MLH1):c.1122T>G (p.Ser374Arg) rs759868546
NM_000249.3(MLH1):c.1136A>G (p.Tyr379Cys) rs143009528
NM_000249.3(MLH1):c.1148T>C (p.Met383Thr) rs141344760
NM_000249.3(MLH1):c.1154G>A (p.Arg385His) rs63750430
NM_000249.3(MLH1):c.116+5G>A rs267607710
NM_000249.3(MLH1):c.1166G>A (p.Arg389Gln) rs63750361
NM_000249.3(MLH1):c.1202G>A (p.Ser401Asn) rs587779951
NM_000249.3(MLH1):c.125C>T (p.Ala42Val) rs587778901
NM_000249.3(MLH1):c.1261A>G (p.Ser421Gly) rs755898663
NM_000249.3(MLH1):c.1268G>A (p.Arg423Lys) rs370687064
NM_000249.3(MLH1):c.1344G>T (p.Glu448Asp) rs587779952
NM_000249.3(MLH1):c.1360G>C (p.Gly454Arg) rs63750527
NM_000249.3(MLH1):c.1410-8C>T rs1057521668
NM_000249.3(MLH1):c.1420C>G (p.Arg474Gly) rs147939838
NM_000249.3(MLH1):c.1421G>A (p.Arg474Gln) rs63751083
NM_000249.3(MLH1):c.144A>C (p.Gln48His) rs147342421
NM_000249.3(MLH1):c.1487C>G (p.Pro496Arg) rs63750226
NM_000249.3(MLH1):c.1487C>T (p.Pro496Leu) rs63750226
NM_000249.3(MLH1):c.1502T>G (p.Ile501Ser) rs587780679
NM_000249.3(MLH1):c.1514G>A (p.Ser505Asn) rs771044689
NM_000249.3(MLH1):c.1558+5G>A rs199935667
NM_000249.3(MLH1):c.1559-11T>C rs730881750
NM_000249.3(MLH1):c.1564C>T (p.Arg522Trp) rs63751703
NM_000249.3(MLH1):c.1565G>A (p.Arg522Gln) rs63751630
NM_000249.3(MLH1):c.1572G>T (p.Met524Ile) rs587779953
NM_000249.3(MLH1):c.1591G>A (p.Val531Met) rs764663152
NM_000249.3(MLH1):c.1628A>G (p.His543Arg) rs730881742
NM_000249.3(MLH1):c.1637A>G (p.Lys546Arg) rs587779954
NM_000249.3(MLH1):c.1682A>G (p.Tyr561Cys) rs1289807424
NM_000249.3(MLH1):c.1690C>T (p.Leu564Phe) rs786202693
NM_000249.3(MLH1):c.1709A>G (p.Asn570Ser) rs375853155
NM_000249.3(MLH1):c.1730C>T (p.Ser577Leu) rs56185292
NM_000249.3(MLH1):c.1775G>C (p.Ser592Thr) rs587782621
NM_000249.3(MLH1):c.1853A>T (p.Lys618Met) rs63750449
NM_000249.3(MLH1):c.191A>G (p.Asn64Ser) rs63750952
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.1990-6G>A rs117221851
NM_000249.3(MLH1):c.2038T>G (p.Cys680Gly) rs63750809
NM_000249.3(MLH1):c.2051A>G (p.Tyr684Cys) rs267607886
NM_000249.3(MLH1):c.2162A>G (p.Tyr721Cys) rs587778986
NM_000249.3(MLH1):c.2173C>G (p.Arg725Gly) rs138584384
NM_000249.3(MLH1):c.2213G>A (p.Gly738Glu) rs148317871
NM_000249.3(MLH1):c.277A>G (p.Ser93Gly) rs41295282
NM_000249.3(MLH1):c.283T>G (p.Ser95Ala) rs63751070
NM_000249.3(MLH1):c.290A>G (p.Tyr97Cys) rs773647920
NM_000249.3(MLH1):c.299G>A (p.Arg100Gln) rs63750266
NM_000249.3(MLH1):c.347C>A (p.Thr116Lys) rs63750465
NM_000249.3(MLH1):c.376T>A (p.Tyr126Asn) rs200076893
NM_000249.3(MLH1):c.37G>A (p.Glu13Lys) rs587779008
NM_000249.3(MLH1):c.415C>G (p.Pro139Ala) rs779562531
NM_000249.3(MLH1):c.438A>G (p.Gln146=) rs377279035
NM_000249.3(MLH1):c.52C>T (p.Arg18Cys) rs367654552
NM_000249.3(MLH1):c.539T>G (p.Val180Gly) rs63750102
NM_000249.3(MLH1):c.589-6T>G rs781244266
NM_000249.3(MLH1):c.595G>C (p.Glu199Gln) rs63749887
NM_000249.3(MLH1):c.601G>C (p.Val201Leu) rs534184145
NM_000249.3(MLH1):c.626A>G (p.Asn209Ser) rs150478207
NM_000249.3(MLH1):c.65G>C (p.Gly22Ala) rs41295280
NM_000249.3(MLH1):c.682C>A (p.Leu228Met) rs751628735
NM_000249.3(MLH1):c.69A>T (p.Glu23Asp) rs63750555
NM_000249.3(MLH1):c.721A>G (p.Lys241Glu) rs587778447
NM_000249.3(MLH1):c.776T>C (p.Leu259Ser) rs56250509
NM_000249.3(MLH1):c.779T>A (p.Leu260His) rs63751283
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.85G>T (p.Ala29Ser) rs63750656
NM_000249.3(MLH1):c.887T>C (p.Leu296Ser) rs63750547
NM_000249.3(MLH1):c.91_92delinsTG (p.Ala31Cys) rs63749994
NM_000249.3(MLH1):c.955G>A (p.Glu319Lys) rs63750796
NM_000249.3(MLH1):c.979C>G (p.Gln327Glu) rs587782087

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