ClinVar Miner

List of variants in gene POLD1 reported as likely benign by PreventionGenetics

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Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP
NM_001256849.1(POLD1):c.1137+9C>T rs373860178
NM_001256849.1(POLD1):c.1138-8A>G rs41544624
NM_001256849.1(POLD1):c.1182C>T (p.Thr394=) rs377462923
NM_001256849.1(POLD1):c.1243-15G>T rs3218763
NM_001256849.1(POLD1):c.1560G>A (p.Leu520=) rs200345841
NM_001256849.1(POLD1):c.156G>A (p.Glu52=) rs370359745
NM_001256849.1(POLD1):c.1626C>T (p.Pro542=) rs201208120
NM_001256849.1(POLD1):c.1746G>A (p.Thr582=) rs749873325
NM_001256849.1(POLD1):c.1775+12G>C
NM_001256849.1(POLD1):c.1794C>T (p.Ile598=) rs369152704
NM_001256849.1(POLD1):c.1869G>T (p.Arg623=) rs748380365
NM_001256849.1(POLD1):c.2007-4G>A rs202035484
NM_001256849.1(POLD1):c.2007-5C>T rs199506387
NM_001256849.1(POLD1):c.2100A>G (p.Val700=) rs772468675
NM_001256849.1(POLD1):c.2103C>T (p.Tyr701=) rs201483538
NM_001256849.1(POLD1):c.2136G>A (p.Pro712=) rs765207547
NM_001256849.1(POLD1):c.2163G>A (p.Thr721=) rs763876339
NM_001256849.1(POLD1):c.2275G>A (p.Val759Ile) rs145473716
NM_001256849.1(POLD1):c.2334C>T (p.Ala778=) rs1472994995
NM_001256849.1(POLD1):c.2457C>T (p.Asp819=) rs777433056
NM_001256849.1(POLD1):c.2565-17G>A rs200576676
NM_001256849.1(POLD1):c.2717+11G>A rs753506843
NM_001256849.1(POLD1):c.2718-4G>A rs755348897
NM_001256849.1(POLD1):c.2727G>A (p.Lys909=) rs753176146
NM_001256849.1(POLD1):c.2787C>T (p.Ala929=) rs1057522848
NM_001256849.1(POLD1):c.2802C>T (p.Ala934=) rs762628311
NM_001256849.1(POLD1):c.2955G>T (p.Arg985=) rs770495723
NM_001256849.1(POLD1):c.3054G>A (p.Val1018=) rs369613619
NM_001256849.1(POLD1):c.3068-14C>T rs3218758
NM_001256849.1(POLD1):c.3121-14G>A rs367766963
NM_001256849.1(POLD1):c.317-10dup rs1568618625
NM_001256849.1(POLD1):c.3192C>T (p.Ser1064=) rs773088677
NM_001256849.1(POLD1):c.3204C>T (p.Asp1068=) rs759019419
NM_001256849.1(POLD1):c.3219-19C>A rs374168125
NM_001256849.1(POLD1):c.3249G>A (p.Lys1083=) rs760214407
NM_001256849.1(POLD1):c.3291G>A (p.Arg1097=) rs753235009
NM_001256849.1(POLD1):c.433G>A (p.Ala145Thr) rs137953986
NM_001256849.1(POLD1):c.438C>G (p.Pro146=) rs374926513
NM_001256849.1(POLD1):c.55C>T (p.Arg19Cys) rs368033860
NM_001256849.1(POLD1):c.581C>G (p.Ser194Cys) rs144656348
NM_001256849.1(POLD1):c.590-10C>G rs762015952
NM_001256849.1(POLD1):c.773C>T (p.Thr258Met) rs76131127
NM_001256849.1(POLD1):c.780C>T (p.Ile260=) rs762155346
NM_001256849.1(POLD1):c.80A>T (p.Asp27Val) rs150066950
NM_001256849.1(POLD1):c.846G>A (p.Thr282=) rs780498642
NM_001256849.1(POLD1):c.84A>G (p.Ala28=) rs1568614799
NM_001256849.1(POLD1):c.864G>A (p.Ala288=) rs781735549
NM_001256849.1(POLD1):c.900G>C (p.Pro300=) rs142407935
NM_001256849.1(POLD1):c.945C>T (p.Phe315=) rs150116169
NM_001256849.1(POLD1):c.971-19G>A rs56022846
NM_002691.3(POLD1):c.2154+20delG rs1568631645

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