ClinVar Miner

List of variants in gene POLD1 reported as uncertain significance by PreventionGenetics

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Total variants: 27
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HGVS dbSNP
NM_001256849.1(POLD1):c.208G>T (p.Val70Phe) rs147911699
NM_002691.3(POLD1):c.1054C>T (p.Arg352Cys) rs762330164
NM_002691.3(POLD1):c.1055G>A (p.Arg352His) rs556862476
NM_002691.3(POLD1):c.1234A>G (p.Thr412Ala) rs1038164521
NM_002691.3(POLD1):c.1495-15_1495-14delCGinsGA rs1064794332
NM_002691.3(POLD1):c.1681C>T (p.Arg561Trp) rs368738479
NM_002691.3(POLD1):c.1795G>A (p.Ala599Thr) rs149569984
NM_002691.3(POLD1):c.2017G>A (p.Glu673Lys) rs61751955
NM_002691.3(POLD1):c.2052G>C (p.Gln684His) rs144143245
NM_002691.3(POLD1):c.208G>A (p.Val70Ile) rs147911699
NM_002691.3(POLD1):c.2290G>A (p.Gly764Ser) rs148838746
NM_002691.3(POLD1):c.241C>T (p.Arg81Trp)
NM_002691.3(POLD1):c.245C>T (p.Pro82Leu) rs201006221
NM_002691.3(POLD1):c.2560G>T (p.Asp854Tyr) rs373650022
NM_002691.3(POLD1):c.2599G>A (p.Val867Ile) rs367680864
NM_002691.3(POLD1):c.2758G>A (p.Asp920Asn) rs1060501811
NM_002691.3(POLD1):c.3016G>A (p.Ala1006Thr) rs376197467
NM_002691.3(POLD1):c.3136G>T (p.Ala1046Ser) rs751088347
NM_002691.3(POLD1):c.455C>T (p.Ala152Val) rs41563714
NM_002691.3(POLD1):c.49C>T (p.Arg17Trp) rs570461545
NM_002691.3(POLD1):c.521G>A (p.Arg174Gln) rs141976385
NM_002691.3(POLD1):c.530G>A (p.Arg177His) rs3218750
NM_002691.3(POLD1):c.584G>A (p.Arg195Gln) rs1555789938
NM_002691.3(POLD1):c.758+5G>A rs760003191
NM_002691.3(POLD1):c.835_837delGAG (p.Glu279del) rs746341854
NM_002691.3(POLD1):c.866A>G (p.Asp289Gly) rs878854558
NM_002691.3(POLD1):c.883G>A (p.Val295Met) rs199545019

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