ClinVar Miner

List of variants in gene POLG reported as uncertain significance for Seizures

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Total variants: 24
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HGVS dbSNP
NM_002693.2(POLG):c.1402A>G (p.Asn468Asp) rs145843073
NM_002693.2(POLG):c.1736G>A (p.Arg579Gln)
NM_002693.2(POLG):c.1837C>T (p.His613Tyr) rs147407423
NM_002693.2(POLG):c.1991G>A (p.Gly664Glu) rs773073959
NM_002693.2(POLG):c.2021G>A (p.Gly674Asp) rs200257554
NM_002693.2(POLG):c.2069C>T (p.Thr690Met)
NM_002693.2(POLG):c.2197C>T (p.His733Tyr)
NM_002693.2(POLG):c.2207A>G (p.Asn736Ser) rs138457939
NM_002693.2(POLG):c.2218A>G (p.Asn740Asp) rs78347903
NM_002693.2(POLG):c.2369G>A (p.Arg790His) rs191490663
NM_002693.2(POLG):c.260T>C (p.Ile87Thr)
NM_002693.2(POLG):c.3095C>G (p.Thr1032Ser)
NM_002693.2(POLG):c.3131T>C (p.Val1044Ala) rs150233690
NM_002693.2(POLG):c.3139C>T (p.Arg1047Trp) rs181860632
NM_002693.2(POLG):c.3204C>G (p.Asp1068Glu) rs1057523186
NM_002693.2(POLG):c.3274-4C>T rs760343963
NM_002693.2(POLG):c.328C>T (p.His110Tyr) rs139599587
NM_002693.2(POLG):c.337T>G (p.Trp113Gly)
NM_002693.2(POLG):c.377G>A (p.Arg126His)
NM_002693.2(POLG):c.431A>G (p.Gln144Arg)
NM_002693.2(POLG):c.460G>A (p.Ala154Thr) rs753858440
NM_002693.2(POLG):c.551C>T (p.Ala184Val)
NM_002693.2(POLG):c.578G>A (p.Arg193Gln) rs3176162
NM_002693.2(POLG):c.803G>C (p.Gly268Ala) rs61752784

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