ClinVar Miner

List of variants in gene POLE reported as benign by Integrated Genetics/Laboratory Corporation of America

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP
NM_006231.3(POLE):c.1007A>G (p.Asn336Ser) rs5744760
NM_006231.3(POLE):c.1323G>A (p.Pro441=) rs116573514
NM_006231.3(POLE):c.1359+9G>A rs75135381
NM_006231.3(POLE):c.2083T>A (p.Phe695Ile) rs5744799
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.2468+10C>T rs5744823
NM_006231.3(POLE):c.2469-15G>A rs5744833
NM_006231.3(POLE):c.2550C>T (p.Ile850=) rs5744834
NM_006231.3(POLE):c.2561+6T>C rs116231808
NM_006231.3(POLE):c.2928C>T (p.Arg976=) rs5744845
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.3379-5T>C rs5744886
NM_006231.3(POLE):c.3582+17A>G rs5744889
NM_006231.3(POLE):c.4184A>G (p.Tyr1395Cys) rs5744933
NM_006231.3(POLE):c.4187A>G (p.Asn1396Ser) rs5744934
NM_006231.3(POLE):c.4290+5C>T rs5744936
NM_006231.3(POLE):c.4444+4T>A rs5744941
NM_006231.3(POLE):c.4523G>A (p.Arg1508His) rs142508245
NM_006231.3(POLE):c.4530A>G (p.Ala1510=) rs5744944
NM_006231.3(POLE):c.4552-10G>T rs5744946
NM_006231.3(POLE):c.5135C>T (p.Ala1712Val) rs5744950
NM_006231.3(POLE):c.5334C>T (p.Ala1778=) rs11146986
NM_006231.3(POLE):c.5570A>G (p.Lys1857Arg) rs5744971
NM_006231.3(POLE):c.5583A>C (p.Ser1861=) rs5744972
NM_006231.3(POLE):c.5678+4C>T rs5744973
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.62+15C>T rs2075784
NM_006231.3(POLE):c.6252A>G (p.Ser2084=) rs5745022
NM_006231.3(POLE):c.6330+15G>A rs5745023
NM_006231.3(POLE):c.6418G>A (p.Glu2140Lys) rs5745066
NM_006231.3(POLE):c.6453C>T (p.Tyr2151=) rs116076060
NM_006231.3(POLE):c.6494G>A (p.Arg2165His) rs5745068
NM_006231.3(POLE):c.6539C>T (p.Ala2180Val) rs552452448
NM_006231.3(POLE):c.6657+16C>T rs5745075
NM_006231.3(POLE):c.6817A>T (p.Thr2273Ser) rs73481453
NM_006231.3(POLE):c.755C>T (p.Ala252Val) rs5744751
NM_006231.3(POLE):c.846C>T (p.Pro282=) rs5744758
NM_006231.3(POLE):c.861T>A (p.Asp287Glu) rs139075637
NM_006231.3(POLE):c.910-6G>C rs4077170
NM_006231.3(POLE):c.91G>T (p.Ala31Ser) rs34047482

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.