ClinVar Miner

List of variants in gene MLH1 reported as benign by Invitae

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Gene type:
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Total variants: 66
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HGVS dbSNP
NM_000249.3(MLH1):c.-269C>G rs35032294
NM_000249.3(MLH1):c.-28A>G rs56198082
NM_000249.3(MLH1):c.-7C>T rs104894994
NM_000249.3(MLH1):c.1038+51C>T rs55986674
NM_000249.3(MLH1):c.1039-10_1039-8dupTTT rs57509953
NM_000249.3(MLH1):c.1039-13_1039-8dupTTTTTT rs57509953
NM_000249.3(MLH1):c.1039-6dup rs1553650466
NM_000249.3(MLH1):c.1039-8T>A rs193922367
NM_000249.3(MLH1):c.1039-8_1039-7insTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-8_1039-7insTTTTTTTTTTTTTTTTTTTTTTTTTTA rs535965616
NM_000249.3(MLH1):c.1039-9_1039-8dupTT rs57509953
NM_000249.3(MLH1):c.1050A>G (p.Pro350=) rs137937003
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.1166G>A (p.Arg389Gln) rs63750361
NM_000249.3(MLH1):c.1217G>A (p.Ser406Asn) rs41294980
NM_000249.3(MLH1):c.1266C>T (p.Gly422=) rs63750791
NM_000249.3(MLH1):c.1321G>A (p.Ala441Thr) rs63750365
NM_000249.3(MLH1):c.1410-10T>G rs372053184
NM_000249.3(MLH1):c.1732-19T>A rs77120160
NM_000249.3(MLH1):c.1808C>G (p.Pro603Arg) rs63750876
NM_000249.3(MLH1):c.1852A>G (p.Lys618Glu) rs35001569
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.1853A>G (p.Lys618Arg) rs63750449
NM_000249.3(MLH1):c.1959G>T (p.Leu653=) rs1800146
NM_000249.3(MLH1):c.1963A>G (p.Ile655Val) rs55907433
NM_000249.3(MLH1):c.198C>T (p.Thr66=) rs61751642
NM_000249.3(MLH1):c.2066A>G (p.Gln689Arg) rs63750702
NM_000249.3(MLH1):c.2101C>A (p.Gln701Lys) rs63750114
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.2174G>A (p.Arg725His) rs566928243
NM_000249.3(MLH1):c.2252A>G (p.Lys751Arg) rs140195825
NM_000249.3(MLH1):c.277A>G (p.Ser93Gly) rs41295282
NM_000249.3(MLH1):c.303T>G (p.Gly101=) rs4647220
NM_000249.3(MLH1):c.375A>G (p.Ala125=) rs1800144
NM_000249.3(MLH1):c.394G>C (p.Asp132His) rs28930073
NM_000249.3(MLH1):c.42A>C (p.Thr14=) rs369737664
NM_000249.3(MLH1):c.474C>T (p.Asn158=) rs4647256
NM_000249.3(MLH1):c.479C>T (p.Ala160Val) rs63749924
NM_000249.3(MLH1):c.579A>G (p.Ser193=) rs587781038
NM_000249.3(MLH1):c.637G>A (p.Val213Met) rs2308317
NM_000249.3(MLH1):c.65G>C (p.Gly22Ala) rs41295280
NM_000249.3(MLH1):c.702G>A (p.Glu234=) rs35908749
NM_000249.3(MLH1):c.790+10A>G rs182733777
NM_000249.3(MLH1):c.803A>G (p.Glu268Gly) rs63750650
NM_000249.3(MLH1):c.977T>C (p.Val326Ala) rs63751049

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