ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP
NM_006231.3(POLE):c.1106+7C>A rs369889926
NM_006231.3(POLE):c.1226+13G>A rs577646338
NM_006231.3(POLE):c.1359+18C>T rs5744775
NM_006231.3(POLE):c.1360-20C>G rs781212006
NM_006231.3(POLE):c.1473+19G>A rs1057517628
NM_006231.3(POLE):c.1474-13G>A rs1555228383
NM_006231.3(POLE):c.1641C>A (p.Leu547=) rs267603387
NM_006231.3(POLE):c.1687-13A>G rs527311638
NM_006231.3(POLE):c.1687-16C>G rs530732187
NM_006231.3(POLE):c.16G>C (p.Gly6Arg) rs202220778
NM_006231.3(POLE):c.1795-14C>T rs369023182
NM_006231.3(POLE):c.1924-6T>C rs755311168
NM_006231.3(POLE):c.2026+14G>T rs751509566
NM_006231.3(POLE):c.2026+9C>T rs373790607
NM_006231.3(POLE):c.2027-16A>G rs1057517614
NM_006231.3(POLE):c.2174-15C>T rs750771177
NM_006231.3(POLE):c.2320-9G>T rs769834031
NM_006231.3(POLE):c.2468+10C>T rs5744823
NM_006231.3(POLE):c.2468+19G>A rs768950827
NM_006231.3(POLE):c.2561+6T>C rs116231808
NM_006231.3(POLE):c.2707-9G>A rs1057521516
NM_006231.3(POLE):c.3061-12G>C rs779496994
NM_006231.3(POLE):c.3265_3275+15dup rs1555225627
NM_006231.3(POLE):c.3275+12_3275+37dup rs1057517627
NM_006231.3(POLE):c.3275+14C>G rs368185422
NM_006231.3(POLE):c.3378+10A>G rs193075152
NM_006231.3(POLE):c.3378+15C>T rs574954983
NM_006231.3(POLE):c.3378+7G>T rs755370377
NM_006231.3(POLE):c.3379-17G>A rs907214942
NM_006231.3(POLE):c.3379-18C>T rs1057517632
NM_006231.3(POLE):c.4005+20G>A rs775205537
NM_006231.3(POLE):c.4149+12C>G rs566422403
NM_006231.3(POLE):c.4150-12T>C rs551697046
NM_006231.3(POLE):c.4150-13G>A rs780409701
NM_006231.3(POLE):c.4150-6C>T rs756837862
NM_006231.3(POLE):c.423+20T>C rs201628896
NM_006231.3(POLE):c.424-10C>T rs748433747
NM_006231.3(POLE):c.4259C>T (p.Ala1420Val) rs41561818
NM_006231.3(POLE):c.4291-11G>A rs369564167
NM_006231.3(POLE):c.4728+14_4728+21del rs1311664292
NM_006231.3(POLE):c.4729-13dup rs1057517615
NM_006231.3(POLE):c.4952+11T>A rs779889181
NM_006231.3(POLE):c.4952+13C>T rs1057517612
NM_006231.3(POLE):c.4952+17C>T rs750268044
NM_006231.3(POLE):c.4952+17_4952+19dupCGT rs571641918
NM_006231.3(POLE):c.4952+20_4952+22del rs752389775
NM_006231.3(POLE):c.5173+10C>T rs371098994
NM_006231.3(POLE):c.5173+17A>G rs368209692
NM_006231.3(POLE):c.5174-17G>A rs201254290
NM_006231.3(POLE):c.5174-6G>C rs770466844
NM_006231.3(POLE):c.5379-19C>T rs376722984
NM_006231.3(POLE):c.5379-5T>C rs761910924
NM_006231.3(POLE):c.5679-14T>C rs1555221517
NM_006231.3(POLE):c.5811+13C>T rs150195182
NM_006231.3(POLE):c.5811+16T>C rs115381003
NM_006231.3(POLE):c.6004+11A>G rs201591857
NM_006231.3(POLE):c.63-14C>T rs373998767
NM_006231.3(POLE):c.6331-8C>T rs769766403
NM_006231.3(POLE):c.6418G>A (p.Glu2140Lys) rs5745066
NM_006231.3(POLE):c.6494G>A (p.Arg2165His) rs5745068
NM_006231.3(POLE):c.6532-11G>C rs372829291
NM_006231.3(POLE):c.6532-19G>T rs201114228
NM_006231.3(POLE):c.6532-21_6532-20del rs1555301127
NM_006231.3(POLE):c.6658-12G>C rs1555300850
NM_006231.3(POLE):c.6658-19C>G rs5745081
NM_006231.3(POLE):c.6658-7C>A rs531482240
NM_006231.3(POLE):c.6763A>T (p.Ile2255Phe) rs73155056
NM_006231.3(POLE):c.720+16T>C rs200320553
NM_006231.3(POLE):c.721-9_721-8delGT rs752682384
NM_006231.3(POLE):c.776G>A (p.Arg259His) rs61732929
NM_006231.3(POLE):c.909+20G>A rs750593090

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