ClinVar Miner

List of variants in gene POLG reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 20
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HGVS dbSNP
NM_002693.2(POLG):c.1174C>G (p.Leu392Val) rs145289229
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.126_128GCA[9] (p.Gln54_Gln55del) rs41550117
NM_002693.2(POLG):c.134A>G (p.Gln45Arg) rs201016638
NM_002693.2(POLG):c.1389G>A (p.Leu463=) rs150828914
NM_002693.2(POLG):c.1550G>T (p.Gly517Val) rs61752783
NM_002693.2(POLG):c.1743C>T (p.Asp581=) rs140743000
NM_002693.2(POLG):c.2051A>G (p.Asn684Ser) rs202244328
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.2541C>T (p.Ala847=) rs143810171
NM_002693.2(POLG):c.264C>T (p.Phe88=) rs144439703
NM_002693.2(POLG):c.2853C>T (p.Tyr951=) rs41546712
NM_002693.2(POLG):c.3198G>A (p.Thr1066=) rs61752780
NM_002693.2(POLG):c.3450C>T (p.Ala1150=) rs774880085
NM_002693.2(POLG):c.472T>C (p.Leu158=) rs1567194008
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.975C>A (p.Pro325=) rs551973680

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