ClinVar Miner

List of variants in gene POLE reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP
NM_006231.3(POLE):c.-6G>A rs534524789
NM_006231.3(POLE):c.1188G>A (p.Glu396=) rs371717068
NM_006231.3(POLE):c.1227-8C>T rs537816213
NM_006231.3(POLE):c.123G>A (p.Thr41=) rs5744734
NM_006231.3(POLE):c.1288G>A (p.Ala430Thr) rs140566004
NM_006231.3(POLE):c.1308C>T (p.Pro436=) rs755627156
NM_006231.3(POLE):c.1347G>A (p.Thr449=) rs142373951
NM_006231.3(POLE):c.1359+9G>A rs75135381
NM_006231.3(POLE):c.1360-6C>T rs139836643
NM_006231.3(POLE):c.1419C>T (p.Tyr473=) rs369961557
NM_006231.3(POLE):c.1470C>T (p.Asp490=) rs5744777
NM_006231.3(POLE):c.155G>A (p.Arg52Gln) rs372459649
NM_006231.3(POLE):c.1590C>T (p.Asp530=) rs1040269464
NM_006231.3(POLE):c.16G>C (p.Gly6Arg) rs202220778
NM_006231.3(POLE):c.1740C>T (p.His580=) rs114972594
NM_006231.3(POLE):c.1836C>T (p.Asp612=) rs116456858
NM_006231.3(POLE):c.1863C>G (p.Leu621=) rs767326433
NM_006231.3(POLE):c.1905C>T (p.Ile635=) rs145203544
NM_006231.3(POLE):c.1924-6del rs758112633
NM_006231.3(POLE):c.1926C>T (p.Pro642=) rs779747873
NM_006231.3(POLE):c.2026+9C>T rs373790607
NM_006231.3(POLE):c.207C>G (p.Thr69=) rs146986360
NM_006231.3(POLE):c.2089C>T (p.Pro697Ser) rs5744800
NM_006231.3(POLE):c.2106G>T (p.Gly702=) rs5744801
NM_006231.3(POLE):c.2172G>A (p.Ala724=) rs372240734
NM_006231.3(POLE):c.2340G>C (p.Ser780=) rs5744822
NM_006231.3(POLE):c.2561+6T>C rs116231808
NM_006231.3(POLE):c.2602C>T (p.Leu868=) rs115830215
NM_006231.3(POLE):c.2865-17dup rs369732588
NM_006231.3(POLE):c.2886C>T (p.Asp962=) rs757682919
NM_006231.3(POLE):c.3049C>T (p.Leu1017=) rs371831931
NM_006231.3(POLE):c.3054C>T (p.Tyr1018=) rs201249963
NM_006231.3(POLE):c.3135T>C (p.Asp1045=) rs748871390
NM_006231.3(POLE):c.318T>C (p.Ile106=) rs770759936
NM_006231.3(POLE):c.3411G>A (p.Leu1137=) rs368920055
NM_006231.3(POLE):c.3489C>T (p.His1163=) rs5744888
NM_006231.3(POLE):c.351A>G (p.Ser117=) rs199773841
NM_006231.3(POLE):c.3582+7G>A rs558837073
NM_006231.3(POLE):c.363C>T (p.Ser121=) rs1555230177
NM_006231.3(POLE):c.3645C>T (p.Phe1215=) rs758716323
NM_006231.3(POLE):c.3738G>A (p.Thr1246=) rs545161424
NM_006231.3(POLE):c.3747G>A (p.Val1249=) rs80290414
NM_006231.3(POLE):c.3851G>A (p.Arg1284Gln) rs149462407
NM_006231.3(POLE):c.4057A>G (p.Ser1353Gly) rs141619382
NM_006231.3(POLE):c.4101C>T (p.Tyr1367=) rs780694561
NM_006231.3(POLE):c.4206G>A (p.Val1402=) rs773786700
NM_006231.3(POLE):c.4245C>T (p.Asn1415=) rs778896278
NM_006231.3(POLE):c.4259C>T (p.Ala1420Val) rs41561818
NM_006231.3(POLE):c.4269C>T (p.Ile1423=) rs761413102
NM_006231.3(POLE):c.4602C>T (p.His1534=) rs749126952
NM_006231.3(POLE):c.4645C>G (p.Pro1549Ala) rs147500308
NM_006231.3(POLE):c.4827G>A (p.Val1609=) rs770382974
NM_006231.3(POLE):c.5007C>T (p.Ser1669=) rs146761597
NM_006231.3(POLE):c.5124C>T (p.Phe1708=) rs114891564
NM_006231.3(POLE):c.5173+10C>T rs371098994
NM_006231.3(POLE):c.519C>T (p.Ala173=) rs187690610
NM_006231.3(POLE):c.51C>G (p.Gly17=) rs780436496
NM_006231.3(POLE):c.5313G>T (p.Thr1771=) rs201803493
NM_006231.3(POLE):c.5346C>T (p.Tyr1782=) rs761902063
NM_006231.3(POLE):c.5478G>T (p.Arg1826=) rs537648186
NM_006231.3(POLE):c.5496T>C (p.Leu1832=) rs147543146
NM_006231.3(POLE):c.561C>T (p.Tyr187=) rs143938822
NM_006231.3(POLE):c.600C>T (p.Val200=) rs878854888
NM_006231.3(POLE):c.6018C>T (p.Ala2006=) rs111709550
NM_006231.3(POLE):c.6271C>T (p.Pro2091Ser) rs572252265
NM_006231.3(POLE):c.6331-8C>T rs769766403
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.6658-7C>A rs531482240
NM_006231.3(POLE):c.6678G>A (p.Gly2226=) rs1162754521
NM_006231.3(POLE):c.6763A>T (p.Ile2255Phe) rs73155056
NM_006231.3(POLE):c.6766G>A (p.Gly2256Arg) rs116323660
NM_006231.3(POLE):c.6804G>A (p.Ser2268=) rs544223319
NM_006231.3(POLE):c.6820C>G (p.Leu2274Val) rs148788180
NM_006231.3(POLE):c.747A>G (p.Arg249=) rs1002061657
NM_006231.3(POLE):c.776G>A (p.Arg259His) rs61732929
NM_006231.3(POLE):c.779G>A (p.Arg260Gln) rs5744752
NM_006231.3(POLE):c.846C>T (p.Pro282=) rs5744758

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