ClinVar Miner

Variants in gene MTOR with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 67
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HGVS dbSNP gnomAD frequency
NM_004958.4(MTOR):c.5043G>A (p.Pro1681=) rs55774271 0.01141
NM_004958.4(MTOR):c.7164+11A>G rs75573431 0.00820
NM_004958.4(MTOR):c.2779+16C>T rs28730689 0.00786
NM_004958.4(MTOR):c.3285+13C>T rs115330656 0.00644
NM_004958.4(MTOR):c.5614-16G>A rs112041289 0.00503
NM_004958.4(MTOR):c.2649+9C>T rs144243347 0.00459
NM_004958.4(MTOR):c.510G>C (p.Leu170=) rs12120294 0.00421
NM_004958.4(MTOR):c.6129C>T (p.Asn2043=) rs56096707 0.00384
NM_004958.4(MTOR):c.7455C>T (p.Asp2485=) rs41274506 0.00338
NM_004958.4(MTOR):c.985G>A (p.Ala329Thr) rs35903812 0.00262
NM_004958.4(MTOR):c.6624T>C (p.Leu2208=) rs56051835 0.00258
NM_004958.4(MTOR):c.663C>G (p.Thr221=) rs112439072 0.00198
NM_004958.4(MTOR):c.1830C>T (p.Phe610=) rs139687094 0.00140
NM_004958.4(MTOR):c.7089+9A>G rs185470535 0.00111
NM_004958.4(MTOR):c.2301C>T (p.Leu767=) rs149428637 0.00085
NM_004958.4(MTOR):c.3630T>C (p.Asp1210=) rs377751542 0.00084
NM_004958.4(MTOR):c.2070G>A (p.Ala690=) rs55752564 0.00077
NM_004958.4(MTOR):c.7158T>C (p.Ala2386=) rs143035002 0.00058
NM_004958.4(MTOR):c.2472C>T (p.Ile824=) rs138875882 0.00056
NM_004958.4(MTOR):c.4260T>C (p.Asn1420=) rs191550317 0.00056
NM_004958.4(MTOR):c.3153G>A (p.Thr1051=) rs147272284 0.00055
NM_004958.4(MTOR):c.5187G>T (p.Gln1729His) rs140288227 0.00053
NM_004958.4(MTOR):c.7593A>G (p.Gln2531=) rs149314441 0.00052
NM_004958.4(MTOR):c.2805G>A (p.Leu935=) rs137863158 0.00049
NM_004958.4(MTOR):c.7367-3T>C rs56412200 0.00048
NM_004958.4(MTOR):c.5653G>A (p.Val1885Ile) rs139043855 0.00041
NM_004958.4(MTOR):c.1145A>G (p.Asn382Ser) rs146393749 0.00039
NM_004958.4(MTOR):c.4470-3C>T rs201255391 0.00036
NM_004958.4(MTOR):c.482A>G (p.Asn161Ser) rs151205593 0.00036
NM_004958.4(MTOR):c.5501C>T (p.Thr1834Met) rs142403193 0.00036
NM_004958.4(MTOR):c.3802-4A>G rs74052909 0.00035
NM_004958.4(MTOR):c.6819G>A (p.Pro2273=) rs138151561 0.00034
NM_004958.4(MTOR):c.7401C>G (p.Ala2467=) rs151027751 0.00034
NM_004958.4(MTOR):c.5244C>A (p.Ala1748=) rs144768080 0.00030
NM_004958.4(MTOR):c.505-8T>A rs376720790 0.00029
NM_004958.4(MTOR):c.4941T>G (p.His1647Gln) rs144984370 0.00026
NM_004958.4(MTOR):c.5952G>A (p.Thr1984=) rs192740864 0.00025
NM_004958.4(MTOR):c.1821G>A (p.Ala607=) rs55881943 0.00019
NM_004958.4(MTOR):c.4841T>C (p.Ile1614Thr) rs56299586 0.00016
NM_004958.4(MTOR):c.2857G>A (p.Val953Met) rs140269225 0.00014
NM_004958.4(MTOR):c.3247A>G (p.Met1083Val) rs56164650 0.00009
NM_004958.4(MTOR):c.1566C>T (p.Tyr522=) rs369221365 0.00007
NM_004958.4(MTOR):c.5494G>A (p.Ala1832Thr) rs369088781 0.00007
NM_004958.4(MTOR):c.7314C>T (p.Gly2438=) rs142544102 0.00006
NM_004958.4(MTOR):c.889G>A (p.Asp297Asn) rs141936187 0.00006
NM_004958.4(MTOR):c.395G>A (p.Arg132His) rs201093943 0.00005
NM_004958.4(MTOR):c.5811+13G>A rs370120494 0.00005
NM_004958.4(MTOR):c.5812-19G>A rs374670621 0.00005
NM_004958.4(MTOR):c.2208+6C>T rs375405319 0.00004
NM_004958.4(MTOR):c.2412A>G (p.Glu804=) rs573881829 0.00004
NM_004958.4(MTOR):c.3352A>G (p.Ile1118Val) rs752832956 0.00004
NM_004958.4(MTOR):c.6675C>T (p.Tyr2225=) rs185523638 0.00004
NM_004958.4(MTOR):c.831G>T (p.Met277Ile) rs752049917 0.00004
NM_004958.4(MTOR):c.1942G>A (p.Ala648Thr) rs748207893 0.00002
NM_004958.4(MTOR):c.5133C>T (p.Ile1711=) rs769706061 0.00002
NM_004958.4(MTOR):c.6585T>C (p.Asp2195=) rs753584607 0.00002
NM_004958.4(MTOR):c.7496A>G (p.Gln2499Arg) rs143119651 0.00002
NM_004958.4(MTOR):c.1500T>C (p.Asp500=) rs533405069 0.00001
NM_004958.4(MTOR):c.1658G>A (p.Arg553His) rs1452329078 0.00001
NM_004958.4(MTOR):c.3801+7C>G rs558271480 0.00001
NM_004958.4(MTOR):c.5048G>A (p.Arg1683Gln) rs746116382 0.00001
NM_004958.4(MTOR):c.5473A>G (p.Ile1825Val) rs748927495 0.00001
NM_004958.4(MTOR):c.7272C>T (p.Asp2424=) rs549287479 0.00001
NM_004958.4(MTOR):c.3599T>C (p.Val1200Ala)
NM_004958.4(MTOR):c.5138C>T (p.Ala1713Val)
NM_004958.4(MTOR):c.5351G>A (p.Arg1784His)
NM_004958.4(MTOR):c.5502_5519dup (p.Ala1835_Thr1840dup) rs770515802

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