ClinVar Miner

List of variants in gene MLH1 reported as benign by International Society for Gastrointestinal Hereditary Tumours (InSiGHT)

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Gene type:
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Total variants: 53
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HGVS dbSNP
NM_000249.3(MLH1):c.*32_*34CTT[1] rs193922366
NM_000249.3(MLH1):c.-93G>A rs1800734
NM_000249.3(MLH1):c.1038+1005G>T rs3774338
NM_000249.3(MLH1):c.1038+86T>C rs2286939
NM_000249.3(MLH1):c.1039-33_1039-29del rs148615368
NM_000249.3(MLH1):c.1039-78A>G rs11129748
NM_000249.3(MLH1):c.1039-8T>A rs193922367
NM_000249.3(MLH1):c.1040C>A (p.Thr347Asn) rs201541505
NM_000249.3(MLH1):c.1128T>C (p.Asp376=) rs267607824
NM_000249.3(MLH1):c.1151T>A (p.Val384Asp) rs63750447
NM_000249.3(MLH1):c.1217G>A (p.Ser406Asn) rs41294980
NM_000249.3(MLH1):c.1321G>A (p.Ala441Thr) rs63750365
NM_000249.3(MLH1):c.1410-54C>T rs7633154
NM_000249.3(MLH1):c.1558+14G>A rs41562513
NM_000249.3(MLH1):c.1558+2204A>C rs3774335
NM_000249.3(MLH1):c.1558+4245A>G rs3774332
NM_000249.3(MLH1):c.1559-3171A>G rs4678925
NM_000249.3(MLH1):c.1652A>G (p.Asn551Ser) rs63750271
NM_000249.3(MLH1):c.1668-19A>G rs9876116
NM_000249.3(MLH1):c.1668-254C>T rs41552415
NM_000249.3(MLH1):c.1668-885T>C rs748766
NM_000249.3(MLH1):c.1733A>G (p.Glu578Gly) rs63751612
NM_000249.3(MLH1):c.1799A>G (p.Glu600Gly) rs267607861
NM_000249.3(MLH1):c.1852_1853delinsGC (p.Lys618Ala) rs35502531
NM_000249.3(MLH1):c.1853A>C (p.Lys618Thr) rs63750449
NM_000249.3(MLH1):c.1959G>T (p.Leu653=) rs1800146
NM_000249.3(MLH1):c.1990-121C>T rs2241031
NM_000249.3(MLH1):c.2066A>G (p.Gln689Arg) rs63750702
NM_000249.3(MLH1):c.207+571C>T rs9852378
NM_000249.3(MLH1):c.2074T>C (p.Ser692Pro) rs587779957
NM_000249.3(MLH1):c.2146G>A (p.Val716Met) rs35831931
NM_000249.3(MLH1):c.2152C>T (p.His718Tyr) rs2020873
NM_000249.3(MLH1):c.306+416A>C rs4647222
NM_000249.3(MLH1):c.307-1403A>T rs1540354
NM_000249.3(MLH1):c.307-29C>A rs139620056
NM_000249.3(MLH1):c.381-41A>G rs4647245
NM_000249.3(MLH1):c.394G>C (p.Asp132His) rs28930073
NM_000249.3(MLH1):c.453+25A>G rs4647246
NM_000249.3(MLH1):c.453+554C>T rs267607748
NM_000249.3(MLH1):c.453+79A>G rs4234259
NM_000249.3(MLH1):c.454-51T>C rs4647255
NM_000249.3(MLH1):c.474C>T (p.Asn158=) rs4647256
NM_000249.3(MLH1):c.588+11G>C rs4647258
NM_000249.3(MLH1):c.637G>A (p.Val213Met) rs2308317
NM_000249.3(MLH1):c.655A>C (p.Ile219Leu) rs1799977
NM_000249.3(MLH1):c.655A>G (p.Ile219Val) rs1799977
NM_000249.3(MLH1):c.65G>C (p.Gly22Ala) rs41295280
NM_000249.3(MLH1):c.790+10A>G rs182733777
NM_000249.3(MLH1):c.790+955C>A rs1558528
NM_000249.3(MLH1):c.791-1406C>T rs4647269
NM_000249.3(MLH1):c.803A>G (p.Glu268Gly) rs63750650
NM_000249.3(MLH1):c.885-81G>C rs104894999
NM_000249.3(MLH1):c.977T>C (p.Val326Ala) rs63751049

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