ClinVar Miner

List of variants in gene POLG reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 95
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HGVS dbSNP
NM_002693.2(POLG):c.1023+13T>G rs201874835
NM_002693.2(POLG):c.1066C>T (p.Leu356=) rs371431444
NM_002693.2(POLG):c.1126C>T (p.Leu376=) rs116165908
NM_002693.2(POLG):c.1250+188A>G
NM_002693.2(POLG):c.1251-43C>T rs2307444
NM_002693.2(POLG):c.1251-88dup
NM_002693.2(POLG):c.126_128GCA[10] (p.Gln55del) rs41550117
NM_002693.2(POLG):c.126_128GCA[12] (p.Gln55dup) rs41550117
NM_002693.2(POLG):c.126_128GCA[13] (p.Gln54_Gln55dup) rs41550117
NM_002693.2(POLG):c.126_128GCA[14] (p.Gln53_Gln55dup) rs41550117
NM_002693.2(POLG):c.126_128GCA[6] (p.Gln51_Gln55del) rs41550117
NM_002693.2(POLG):c.126_128GCA[7] (p.Gln52_Gln55del) rs41550117
NM_002693.2(POLG):c.126_128GCA[8] (p.Gln53_Gln55del) rs41550117
NM_002693.2(POLG):c.1275C>T (p.Ala425=) rs147404477
NM_002693.2(POLG):c.128A>G (p.Gln43Arg) rs28567406
NM_002693.2(POLG):c.1311C>T (p.Val437=) rs62640035
NM_002693.2(POLG):c.1386G>A (p.Ser462=) rs62640034
NM_002693.2(POLG):c.1515G>A (p.Lys505=) rs796052880
NM_002693.2(POLG):c.1550G>T (p.Gly517Val) rs61752783
NM_002693.2(POLG):c.156G>A (p.Gln52=) rs587781117
NM_002693.2(POLG):c.1585+11T>C rs201566815
NM_002693.2(POLG):c.159A>G (p.Gln53=) rs587781118
NM_002693.2(POLG):c.162G>A (p.Gln54=) rs796052878
NM_002693.2(POLG):c.1636C>T (p.Arg546Cys) rs2307447
NM_002693.2(POLG):c.1674C>G (p.Leu558=) rs552085869
NM_002693.2(POLG):c.1712+10G>A rs55962804
NM_002693.2(POLG):c.1712+110T>C
NM_002693.2(POLG):c.1712+177C>T
NM_002693.2(POLG):c.1712+238C>T
NM_002693.2(POLG):c.1713-5C>T rs148494026
NM_002693.2(POLG):c.1743C>T (p.Asp581=) rs140743000
NM_002693.2(POLG):c.1890C>T (p.Asn630=) rs148658588
NM_002693.2(POLG):c.1949+20G>C rs371964664
NM_002693.2(POLG):c.1950-9T>C rs780378329
NM_002693.2(POLG):c.1984G>A (p.Glu662Lys) rs2307450
NM_002693.2(POLG):c.2028G>A (p.Ala676=) rs373550219
NM_002693.2(POLG):c.2071-14T>G rs150088708
NM_002693.2(POLG):c.2109C>A (p.Ala703=) rs2307429
NM_002693.2(POLG):c.2109C>T (p.Ala703=) rs2307429
NM_002693.2(POLG):c.2157+11C>T rs56411159
NM_002693.2(POLG):c.2157+15G>A rs766521182
NM_002693.2(POLG):c.2220C>T (p.Asn740=) rs141538857
NM_002693.2(POLG):c.2254C>T (p.Leu752=) rs41564016
NM_002693.2(POLG):c.2265+236G>A
NM_002693.2(POLG):c.2266-153C>T
NM_002693.2(POLG):c.2266-19C>T rs780096431
NM_002693.2(POLG):c.2266-227A>G
NM_002693.2(POLG):c.2426+281A>G
NM_002693.2(POLG):c.2427-12C>G rs199815957
NM_002693.2(POLG):c.2427-240C>T
NM_002693.2(POLG):c.2480+17G>A rs762669285
NM_002693.2(POLG):c.2481-6C>T rs752226219
NM_002693.2(POLG):c.2481-7C>T rs2307448
NM_002693.2(POLG):c.2487C>T (p.Pro829=) rs147563527
NM_002693.2(POLG):c.2492A>G (p.Tyr831Cys) rs41549716
NM_002693.2(POLG):c.2541C>T (p.Ala847=) rs143810171
NM_002693.2(POLG):c.2599-14C>T rs587781115
NM_002693.2(POLG):c.2601T>C (p.Pro867=) rs201749977
NM_002693.2(POLG):c.264C>T (p.Phe88=) rs144439703
NM_002693.2(POLG):c.2724C>T (p.Ala908=) rs377390914
NM_002693.2(POLG):c.2735-15C>T rs41544115
NM_002693.2(POLG):c.2735-7C>G rs200372494
NM_002693.2(POLG):c.2853C>T (p.Tyr951=) rs41546712
NM_002693.2(POLG):c.2981+206C>A
NM_002693.2(POLG):c.2981+283A>C
NM_002693.2(POLG):c.2982-331G>T
NM_002693.2(POLG):c.2982-332T>G
NM_002693.2(POLG):c.3104+8C>A rs754615624
NM_002693.2(POLG):c.3105-16_3105-15delGT rs146915033
NM_002693.2(POLG):c.3198G>A (p.Thr1066=) rs61752780
NM_002693.2(POLG):c.3216C>G (p.Thr1072=) rs146936870
NM_002693.2(POLG):c.3274-19G>A rs116925016
NM_002693.2(POLG):c.3294T>C (p.Asn1098=) rs374224714
NM_002693.2(POLG):c.3450C>T (p.Ala1150=) rs774880085
NM_002693.2(POLG):c.3451C>T (p.Leu1151=) rs769193603
NM_002693.2(POLG):c.3482+6C>T rs55779802
NM_002693.2(POLG):c.3482+7G>A rs200309191
NM_002693.2(POLG):c.3483-14T>C rs587781119
NM_002693.2(POLG):c.3483-164A>C
NM_002693.2(POLG):c.3483-19T>G rs2307438
NM_002693.2(POLG):c.3561G>C (p.Arg1187=) rs62640037
NM_002693.2(POLG):c.3564C>T (p.Cys1188=) rs146584956
NM_002693.2(POLG):c.3597C>A (p.Thr1199=) rs2307443
NM_002693.2(POLG):c.659+11G>T rs3087379
NM_002693.2(POLG):c.659+284G>C
NM_002693.2(POLG):c.660-11A>G rs369731644
NM_002693.2(POLG):c.660-290T>C
NM_002693.2(POLG):c.798G>T (p.Val266=) rs143631183
NM_002693.2(POLG):c.852C>T (p.Ile284=) rs41540414
NM_002693.2(POLG):c.856-11C>T rs375058609
NM_002693.2(POLG):c.856-5_856-3del rs200056162
NM_002693.2(POLG):c.87C>T (p.Ser29=) rs587781116
NM_002693.2(POLG):c.948G>A (p.Lys316=) rs61756401
NM_002693.2(POLG):c.970C>T (p.Pro324Ser) rs2307437
NM_002693.2(POLG):c.975C>A (p.Pro325=) rs551973680

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