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
Download table as spreadsheet
HGVS dbSNP
NM_001256849.1(POLD1):c.1017G>A (p.Ser339=) rs373404887
NM_001256849.1(POLD1):c.1065C>A (p.Leu355=) rs1555790429
NM_001256849.1(POLD1):c.1137+10G>A rs367666867
NM_001256849.1(POLD1):c.1138-8A>G rs41544624
NM_001256849.1(POLD1):c.1275C>T (p.Ala425=) rs3219392
NM_001256849.1(POLD1):c.1383+8C>T rs374719944
NM_001256849.1(POLD1):c.1383+9G>C rs767098823
NM_001256849.1(POLD1):c.1461G>A (p.Glu487=) rs149728120
NM_001256849.1(POLD1):c.1494+5C>T rs565428379
NM_001256849.1(POLD1):c.1626C>T (p.Pro542=) rs201208120
NM_001256849.1(POLD1):c.1665C>T (p.Val555=) rs150238541
NM_001256849.1(POLD1):c.1719G>C (p.Val573=) rs1555791509
NM_001256849.1(POLD1):c.1785C>T (p.Asp595=) rs769563176
NM_001256849.1(POLD1):c.1824G>A (p.Pro608=) rs372002045
NM_001256849.1(POLD1):c.1932C>G (p.Asp644Glu) rs80214209
NM_001256849.1(POLD1):c.2007-4G>A rs202035484
NM_001256849.1(POLD1):c.2016C>T (p.Ala672=) rs761142119
NM_001256849.1(POLD1):c.208G>A (p.Val70Ile) rs147911699
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.2155-8C>T rs759802920
NM_001256849.1(POLD1):c.2163G>A (p.Thr721=) rs763876339
NM_001256849.1(POLD1):c.2169C>T (p.Phe723=) rs753797045
NM_001256849.1(POLD1):c.2275G>A (p.Val759Ile) rs145473716
NM_001256849.1(POLD1):c.2389-9C>G rs552399406
NM_001256849.1(POLD1):c.2700C>T (p.His900=) rs769965495
NM_001256849.1(POLD1):c.2727G>A (p.Lys909=) rs753176146
NM_001256849.1(POLD1):c.2910C>T (p.Phe970=) rs757740787
NM_001256849.1(POLD1):c.2958G>C (p.Gly986=) rs878854547
NM_001256849.1(POLD1):c.3054G>A (p.Val1018=) rs369613619
NM_001256849.1(POLD1):c.3218+5G>A rs569395274
NM_001256849.1(POLD1):c.324G>T (p.Ala108=) rs20582
NM_001256849.1(POLD1):c.357C>T (p.Arg119=) rs561258266
NM_001256849.1(POLD1):c.371T>C (p.Val124Ala) rs199993010
NM_001256849.1(POLD1):c.432C>T (p.Phe144=) rs550836711
NM_001256849.1(POLD1):c.433G>A (p.Ala145Thr) rs137953986
NM_001256849.1(POLD1):c.581C>G (p.Ser194Cys) rs144656348
NM_001256849.1(POLD1):c.657C>T (p.Leu219=) rs777751728
NM_001256849.1(POLD1):c.714G>A (p.Thr238=) rs149096523
NM_001256849.1(POLD1):c.758+8C>G rs377133822
NM_001256849.1(POLD1):c.773C>T (p.Thr258Met) rs76131127
NM_001256849.1(POLD1):c.778A>G (p.Ile260Val) rs8105725
NM_001256849.1(POLD1):c.783C>T (p.Val261=) rs34269084
NM_001256849.1(POLD1):c.841-10A>G rs140160345
NM_001256849.1(POLD1):c.864G>A (p.Ala288=) rs781735549
NM_001256849.1(POLD1):c.885G>C (p.Val295=) rs201946114
NM_001256849.1(POLD1):c.933C>T (p.Arg311=) rs749278926
NM_001256849.1(POLD1):c.971-4G>A rs200144991

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.