ClinVar Miner

List of variants in gene POLE reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP
NM_006231.3(POLE):c.*18G>T rs573406234
NM_006231.3(POLE):c.-15G>A rs554140626
NM_006231.3(POLE):c.1106+9G>A
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.1308C>T (p.Pro436=) rs755627156
NM_006231.3(POLE):c.1347G>A (p.Thr449=) rs142373951
NM_006231.3(POLE):c.1360-6C>T rs139836643
NM_006231.3(POLE):c.1405C>T (p.Leu469=) rs368303888
NM_006231.3(POLE):c.1419C>T (p.Tyr473=) rs369961557
NM_006231.3(POLE):c.1467C>T (p.Pro489=) rs995585765
NM_006231.3(POLE):c.1560A>G (p.Gln520=) rs201841065
NM_006231.3(POLE):c.1590C>T (p.Asp530=) rs1040269464
NM_006231.3(POLE):c.1695C>T (p.Ala565=) rs139748472
NM_006231.3(POLE):c.16G>C (p.Gly6Arg) rs202220778
NM_006231.3(POLE):c.1707C>T (p.Phe569=) rs147438050
NM_006231.3(POLE):c.1795-13G>A rs749522265
NM_006231.3(POLE):c.1863C>G (p.Leu621=) rs767326433
NM_006231.3(POLE):c.1866C>T (p.Ile622=) rs1060504068
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.2090C>G (p.Pro697Arg) rs36120395
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.2442C>T (p.Ser814=) rs377036799
NM_006231.3(POLE):c.2468+10C>T rs5744823
NM_006231.3(POLE):c.2864+8T>C rs878854856
NM_006231.3(POLE):c.2865-4dup rs369732588
NM_006231.3(POLE):c.3015T>C (p.Ser1005=) rs376781169
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.3379-12C>T rs187618435
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+6G>A rs113307290
NM_006231.3(POLE):c.3582+7G>A rs558837073
NM_006231.3(POLE):c.3645C>T (p.Phe1215=) rs758716323
NM_006231.3(POLE):c.369G>A (p.Lys123=) rs1328407908
NM_006231.3(POLE):c.4047G>A (p.Ala1349=) rs201746181
NM_006231.3(POLE):c.4150-17C>T rs758539843
NM_006231.3(POLE):c.4150-6C>T rs756837862
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.4291-12C>T rs564807391
NM_006231.3(POLE):c.4353G>A (p.Leu1451=) rs769149466
NM_006231.3(POLE):c.4494G>A (p.Ala1498=) rs777611171
NM_006231.3(POLE):c.4534G>A (p.Val1512Ile) rs147354120
NM_006231.3(POLE):c.48T>C (p.Asp16=) rs1057523833
NM_006231.3(POLE):c.4941C>T (p.Phe1647=) rs145639967
NM_006231.3(POLE):c.5007C>T (p.Ser1669=) rs146761597
NM_006231.3(POLE):c.5135C>T (p.Ala1712Val) rs5744950
NM_006231.3(POLE):c.5173+10C>T rs371098994
NM_006231.3(POLE):c.5173+17A>G rs368209692
NM_006231.3(POLE):c.5173+18C>T rs201587262
NM_006231.3(POLE):c.519C>T (p.Ala173=) rs187690610
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.5379-19C>T rs376722984
NM_006231.3(POLE):c.5478G>T (p.Arg1826=) rs537648186
NM_006231.3(POLE):c.5570A>G (p.Lys1857Arg) rs5744971
NM_006231.3(POLE):c.561C>T (p.Tyr187=) rs143938822
NM_006231.3(POLE):c.6004+11A>G rs201591857
NM_006231.3(POLE):c.6018C>T (p.Ala2006=) rs111709550
NM_006231.3(POLE):c.6039C>T (p.Asp2013=) rs371563366
NM_006231.3(POLE):c.6177C>T (p.Leu2059=)
NM_006231.3(POLE):c.6271C>T (p.Pro2091Ser) rs572252265
NM_006231.3(POLE):c.6417C>T (p.Ser2139=) rs766935890
NM_006231.3(POLE):c.6453C>T (p.Tyr2151=) rs116076060
NM_006231.3(POLE):c.6495C>T (p.Arg2165=) rs114778730
NM_006231.3(POLE):c.6531+18C>T
NM_006231.3(POLE):c.6532-14C>G
NM_006231.3(POLE):c.6658-19C>G rs5745081
NM_006231.3(POLE):c.6658-7C>A rs531482240
NM_006231.3(POLE):c.6675C>T (p.Arg2225=) rs149973644
NM_006231.3(POLE):c.6678G>A (p.Gly2226=) rs1162754521
NM_006231.3(POLE):c.776G>A (p.Arg259His) rs61732929

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