ClinVar Miner

List of variants in gene MLH1 reported as likely benign by Counsyl

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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_000249.3(MLH1):c.-107C>G rs587778886
NM_000249.3(MLH1):c.-28A>G rs56198082
NM_000249.3(MLH1):c.1039-4A>G rs368618417
NM_000249.3(MLH1):c.1039-5T>C rs587782626
NM_000249.3(MLH1):c.1104G>A (p.Ser368=) rs769364808
NM_000249.3(MLH1):c.1128T>C (p.Asp376=) rs267607824
NM_000249.3(MLH1):c.117-39G>A rs1057517605
NM_000249.3(MLH1):c.117-48A>G rs377111182
NM_000249.3(MLH1):c.1210C>T (p.Leu404=) rs1057517538
NM_000249.3(MLH1):c.1266C>T (p.Gly422=) rs63750791
NM_000249.3(MLH1):c.1269G>A (p.Arg423=) rs373076967
NM_000249.3(MLH1):c.1284T>C (p.Asp428=) rs772555970
NM_000249.3(MLH1):c.1321G>A (p.Ala441Thr) rs63750365
NM_000249.3(MLH1):c.1379A>C (p.Glu460Ala) rs202038499
NM_000249.3(MLH1):c.1731+14C>G rs745643356
NM_000249.3(MLH1):c.1731+8T>C rs370108219
NM_000249.3(MLH1):c.1743G>A (p.Pro581=) rs567838745
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.1896+7C>T rs863224339
NM_000249.3(MLH1):c.18G>A (p.Gly6=) rs786202312
NM_000249.3(MLH1):c.2040C>T (p.Cys680=) rs63749867
NM_000249.3(MLH1):c.207+26del rs1057517621
NM_000249.3(MLH1):c.2088C>G (p.Thr696=) rs1060504015
NM_000249.3(MLH1):c.2104-22T>C rs267607890
NM_000249.3(MLH1):c.2172G>A (p.Leu724=) rs780045031
NM_000249.3(MLH1):c.2252A>G (p.Lys751Arg) rs140195825
NM_000249.3(MLH1):c.307-10T>C rs572853043
NM_000249.3(MLH1):c.375A>G (p.Ala125=) rs1800144
NM_000249.3(MLH1):c.381-43C>G rs368847278
NM_000249.3(MLH1):c.545+19G>T rs41285099
NM_000249.3(MLH1):c.546-18T>C rs1057517622
NM_000249.3(MLH1):c.579A>G (p.Ser193=) rs587781038
NM_000249.3(MLH1):c.589-24T>C rs1057517607
NM_000249.3(MLH1):c.589-25G>A rs188146618
NM_000249.3(MLH1):c.636C>T (p.Thr212=) rs138735345
NM_000249.3(MLH1):c.677+7C>T rs556224377
NM_000249.3(MLH1):c.69A>G (p.Glu23=) rs63750555
NM_000249.3(MLH1):c.705T>C (p.Asp235=) rs876658869
NM_000249.3(MLH1):c.790+17dup rs757064565
NM_000249.3(MLH1):c.791-14T>C rs751254837
NM_000249.3(MLH1):c.884+10C>T rs864622424
NM_000249.3(MLH1):c.884+10del rs878853793
NM_000249.3(MLH1):c.884+15A>G rs372817491
NM_000249.3(MLH1):c.884+16A>G rs377598055
NM_000249.3(MLH1):c.885-8C>T rs762836160
NM_000249.3(MLH1):c.927C>T (p.Pro309=) rs63749896
NM_000249.3(MLH1):c.954C>T (p.His318=) rs146777069
NM_000249.3(MLH1):c.974G>A (p.Arg325Gln) rs63750268

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