ClinVar Miner

List of variants in gene POLD1 reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP
NM_002691.4(POLD1):c.1017G>A (p.Ser339=) rs373404887
NM_002691.4(POLD1):c.1065C>A (p.Leu355=) rs1555790429
NM_002691.4(POLD1):c.1137+10G>A rs367666867
NM_002691.4(POLD1):c.1138-8A>G rs41544624
NM_002691.4(POLD1):c.1275C>T (p.Ala425=) rs3219392
NM_002691.4(POLD1):c.1383+9G>C rs767098823
NM_002691.4(POLD1):c.1461G>A (p.Glu487=) rs149728120
NM_002691.4(POLD1):c.1719G>C (p.Val573=) rs1555791509
NM_002691.4(POLD1):c.1794C>T (p.Ile598=) rs369152704
NM_002691.4(POLD1):c.1824G>A (p.Pro608=) rs372002045
NM_002691.4(POLD1):c.1932C>G (p.Asp644Glu) rs80214209
NM_002691.4(POLD1):c.2007-4G>A rs202035484
NM_002691.4(POLD1):c.2016C>T (p.Ala672=) rs761142119
NM_002691.4(POLD1):c.2052G>C (p.Gln684His) rs144143245
NM_002691.4(POLD1):c.208G>A (p.Val70Ile) rs147911699
NM_002691.4(POLD1):c.2136G>A (p.Pro712=) rs765207547
NM_002691.4(POLD1):c.2155-8C>T rs759802920
NM_002691.4(POLD1):c.2169C>T (p.Phe723=) rs753797045
NM_002691.4(POLD1):c.2275G>A (p.Val759Ile) rs145473716
NM_002691.4(POLD1):c.2346G>A (p.Val782=) rs1406011948
NM_002691.4(POLD1):c.2389-9C>G rs552399406
NM_002691.4(POLD1):c.2598C>T (p.Asp866=) rs773567499
NM_002691.4(POLD1):c.2700C>T (p.His900=) rs769965495
NM_002691.4(POLD1):c.2727G>A (p.Lys909=) rs753176146
NM_002691.4(POLD1):c.2910C>T (p.Phe970=) rs757740787
NM_002691.4(POLD1):c.2958G>C (p.Gly986=) rs878854547
NM_002691.4(POLD1):c.3054G>A (p.Val1018=) rs369613619
NM_002691.4(POLD1):c.3231C>T (p.Pro1077=) rs770660636
NM_002691.4(POLD1):c.324G>T (p.Ala108=) rs20582
NM_002691.4(POLD1):c.3291G>A (p.Arg1097=) rs753235009
NM_002691.4(POLD1):c.357C>T (p.Arg119=) rs561258266
NM_002691.4(POLD1):c.432C>T (p.Phe144=) rs550836711
NM_002691.4(POLD1):c.433G>A (p.Ala145Thr) rs137953986
NM_002691.4(POLD1):c.447C>T (p.Tyr149=) rs527915939
NM_002691.4(POLD1):c.455C>T (p.Ala152Val) rs41563714
NM_002691.4(POLD1):c.581C>G (p.Ser194Cys) rs144656348
NM_002691.4(POLD1):c.657C>T (p.Leu219=) rs777751728
NM_002691.4(POLD1):c.714G>A (p.Thr238=) rs149096523
NM_002691.4(POLD1):c.732C>T (p.Tyr244=) rs778836055
NM_002691.4(POLD1):c.758+8C>G rs377133822
NM_002691.4(POLD1):c.773C>T (p.Thr258Met) rs76131127
NM_002691.4(POLD1):c.778A>G (p.Ile260Val) rs8105725
NM_002691.4(POLD1):c.783C>T (p.Val261=) rs34269084
NM_002691.4(POLD1):c.841-10A>G rs140160345
NM_002691.4(POLD1):c.864G>A (p.Ala288=) rs781735549
NM_002691.4(POLD1):c.885G>C (p.Val295=) rs201946114
NM_002691.4(POLD1):c.933C>T (p.Arg311=) rs749278926
NM_002691.4(POLD1):c.971-4G>A rs200144991

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