ClinVar Miner

List of variants in gene POLG reported as uncertain significance for not specified

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Total variants: 43
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HGVS dbSNP
NM_002693.2(POLG):c.-170T>A rs796052915
NM_002693.2(POLG):c.101A>T (p.Asp34Val) rs779409525
NM_002693.2(POLG):c.1174C>G (p.Leu392Val) rs145289229
NM_002693.2(POLG):c.131A>G (p.Gln44Arg) rs757120802
NM_002693.2(POLG):c.1328G>A (p.Arg443His) rs796052903
NM_002693.2(POLG):c.1381_1382delinsTC (p.Lys461Ser) rs796052920
NM_002693.2(POLG):c.1402A>G (p.Asn468Asp) rs145843073
NM_002693.2(POLG):c.1493A>C (p.Lys498Thr) rs769637557
NM_002693.2(POLG):c.1509_1510delinsTG (p.Lys504Glu) rs796052909
NM_002693.2(POLG):c.1550G>T (p.Gly517Val) rs61752783
NM_002693.2(POLG):c.158_159delinsCT (p.Gln53Pro) rs1064795981
NM_002693.2(POLG):c.1612_1613delinsTT (p.Glu538Leu) rs796052921
NM_002693.2(POLG):c.1760C>T (p.Pro587Leu) rs113994096
NM_002693.2(POLG):c.1761G>A (p.Pro587=) rs374805003
NM_002693.2(POLG):c.176C>T (p.Pro59Leu) rs1057518590
NM_002693.2(POLG):c.1837C>T (p.His613Tyr) rs147407423
NM_002693.2(POLG):c.1850G>A (p.Arg617His) rs779961986
NM_002693.2(POLG):c.2177A>G (p.Lys726Arg) rs774599342
NM_002693.2(POLG):c.2207A>G (p.Asn736Ser) rs138457939
NM_002693.2(POLG):c.2372_2373delinsTC (p.Ala791Val) rs1555452985
NM_002693.2(POLG):c.2468G>A (p.Arg823His) rs751172552
NM_002693.2(POLG):c.2509T>C (p.Tyr837His) rs544828395
NM_002693.2(POLG):c.2510A>G (p.Tyr837Cys) rs778190998
NM_002693.2(POLG):c.2597G>A (p.Arg866Gln) rs779723962
NM_002693.2(POLG):c.2606G>A (p.Arg869Gln) rs1356604153
NM_002693.2(POLG):c.2620T>A (p.Leu874Met) rs758402960
NM_002693.2(POLG):c.2724C>T (p.Ala908=) rs377390914
NM_002693.2(POLG):c.2986C>T (p.Arg996Trp) rs202229893
NM_002693.2(POLG):c.3098C>T (p.Ala1033Val) rs551708243
NM_002693.2(POLG):c.3176A>G (p.Asn1059Ser) rs201192905
NM_002693.2(POLG):c.32G>A rs765472726
NM_002693.2(POLG):c.3323A>G (p.Tyr1108Cys) rs765949668
NM_002693.2(POLG):c.3498C>T (p.Tyr1166=) rs1427798436
NM_002693.2(POLG):c.3519G>A (p.Leu1173=) rs953889846
NM_002693.2(POLG):c.3559C>T (p.Arg1187Trp) rs369544574
NM_002693.2(POLG):c.3564C>T (p.Cys1188=) rs146584956
NM_002693.2(POLG):c.3582C>T (p.Thr1194=) rs1555452247
NM_002693.2(POLG):c.391T>C (p.Tyr131His) rs562847013
NM_002693.2(POLG):c.559G>C (p.Val187Leu) rs1555454261
NM_002693.2(POLG):c.752C>T (p.Thr251Ile) rs113994094
NM_002693.2(POLG):c.803G>C (p.Gly268Ala) rs61752784
NM_002693.2(POLG):c.826G>A (p.Ala276Thr) rs778531134
NM_002693.2(POLG):c.970C>A (p.Pro324Thr) rs2307437

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