ClinVar Miner

List of variants in gene POLE reported as benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP
NM_006231.3(POLE):c.1020+124A>G
NM_006231.3(POLE):c.1226+45C>T
NM_006231.3(POLE):c.1227-149T>C
NM_006231.3(POLE):c.1323G>A (p.Pro441=) rs116573514
NM_006231.3(POLE):c.2027-61T>C
NM_006231.3(POLE):c.2083T>A (p.Phe695Ile) rs5744799
NM_006231.3(POLE):c.2089C>T (p.Pro697Ser) rs5744800
NM_006231.3(POLE):c.2174-8G>A rs117409343
NM_006231.3(POLE):c.2320-13A>G rs75329753
NM_006231.3(POLE):c.2340G>A (p.Ser780=) rs5744822
NM_006231.3(POLE):c.2469-15G>A rs5744833
NM_006231.3(POLE):c.2469-227C>T
NM_006231.3(POLE):c.2550C>T (p.Ile850=) rs5744834
NM_006231.3(POLE):c.2562-48T>C
NM_006231.3(POLE):c.286-96G>A
NM_006231.3(POLE):c.2928C>T (p.Arg976=) rs5744845
NM_006231.3(POLE):c.3060+189C>T
NM_006231.3(POLE):c.3126G>A (p.Lys1042=) rs5744856
NM_006231.3(POLE):c.3156G>A (p.Thr1052=) rs5744857
NM_006231.3(POLE):c.3265_3275+15dup rs1555225627
NM_006231.3(POLE):c.3275+92T>C
NM_006231.3(POLE):c.3276-186_3276-185insACAC
NM_006231.3(POLE):c.3379-5T>C rs5744886
NM_006231.3(POLE):c.3582+17A>G rs5744889
NM_006231.3(POLE):c.3583-164T>C
NM_006231.3(POLE):c.3796-58A>G
NM_006231.3(POLE):c.4149+152C>T
NM_006231.3(POLE):c.4150-107C>T
NM_006231.3(POLE):c.4150-90dup
NM_006231.3(POLE):c.4187A>G (p.Asn1396Ser) rs5744934
NM_006231.3(POLE):c.4259C>T (p.Ala1420Val) rs41561818
NM_006231.3(POLE):c.4290+102A>T
NM_006231.3(POLE):c.4290+5C>T rs5744936
NM_006231.3(POLE):c.4444+4T>A rs5744941
NM_006231.3(POLE):c.4445-33C>T
NM_006231.3(POLE):c.4530A>G (p.Ala1510=) rs5744944
NM_006231.3(POLE):c.4552-10G>T rs5744946
NM_006231.3(POLE):c.4952+17_4952+19dupCGT rs571641918
NM_006231.3(POLE):c.5334C>T (p.Ala1778=) rs11146986
NM_006231.3(POLE):c.5553-43T>C
NM_006231.3(POLE):c.5583A>C (p.Ser1861=) rs5744972
NM_006231.3(POLE):c.5678+4C>T rs5744973
NM_006231.3(POLE):c.5678+78C>G
NM_006231.3(POLE):c.5679-127G>A
NM_006231.3(POLE):c.5679-82A>G
NM_006231.3(POLE):c.5707C>T (p.Leu1903=) rs5744990
NM_006231.3(POLE):c.5804G>A (p.Cys1935Tyr) rs5744991
NM_006231.3(POLE):c.5812-123G>A
NM_006231.3(POLE):c.5812-21G>A
NM_006231.3(POLE):c.6005-212A>G
NM_006231.3(POLE):c.62+15C>T rs2075784
NM_006231.3(POLE):c.62+97T>G
NM_006231.3(POLE):c.6252A>G (p.Ser2084=) rs5745022
NM_006231.3(POLE):c.63-139_63-135del
NM_006231.3(POLE):c.63-223G>A
NM_006231.3(POLE):c.6330+15G>A rs5745023
NM_006231.3(POLE):c.6330+18C>T rs5745024
NM_006231.3(POLE):c.6330+19G>A rs5745025
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.6657+16C>T rs5745075
NM_006231.3(POLE):c.6658-200C>T
NM_006231.3(POLE):c.6763A>T (p.Ile2255Phe) rs73155056
NM_006231.3(POLE):c.721-54A>G
NM_006231.3(POLE):c.755C>T (p.Ala252Val) rs5744751
NM_006231.3(POLE):c.801+78A>G
NM_006231.3(POLE):c.802-71T>C
NM_006231.3(POLE):c.910-157A>G
NM_006231.3(POLE):c.910-6G>C rs4077170
NM_006231.3(POLE):c.91G>T (p.Ala31Ser) rs34047482

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