ClinVar Miner

List of variants in gene POLD1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002691.4(POLD1):c.961G>A (p.Gly321Ser) rs41554817 0.00029
NM_002691.4(POLD1):c.2861C>G (p.Thr954Arg) rs374016016 0.00026
NM_002691.4(POLD1):c.353C>T (p.Ser118Phe) rs780604625 0.00016
NM_002691.4(POLD1):c.1574G>A (p.Arg525Gln) rs372190244 0.00008
NM_002691.4(POLD1):c.713C>T (p.Thr238Met) rs553342844 0.00007
NM_002691.4(POLD1):c.245C>T (p.Pro82Leu) rs201006221 0.00006
NM_002691.4(POLD1):c.2467C>T (p.Arg823Cys) rs376946722 0.00006
NM_002691.4(POLD1):c.301A>T (p.Ile101Phe) rs140858857 0.00006
NM_002691.4(POLD1):c.3038T>C (p.Ile1013Thr) rs368439344 0.00006
NM_002691.4(POLD1):c.34G>A (p.Gly12Arg) rs772197667 0.00006
NM_002691.4(POLD1):c.496C>T (p.Arg166Trp) rs376236497 0.00006
NM_002691.4(POLD1):c.1322C>T (p.Thr441Met) rs376711125 0.00005
NM_002691.4(POLD1):c.1363G>A (p.Val455Met) rs762670703 0.00004
NM_002691.4(POLD1):c.1930G>A (p.Asp644Asn) rs763465385 0.00004
NM_002691.4(POLD1):c.2290G>A (p.Gly764Ser) rs148838746 0.00004
NM_002691.4(POLD1):c.1157G>A (p.Arg386His) rs764023083 0.00003
NM_002691.4(POLD1):c.1918A>G (p.Thr640Ala) rs201212113 0.00002
NM_002691.4(POLD1):c.2197C>G (p.Gln733Glu) rs1471359934 0.00002
NM_002691.4(POLD1):c.2563C>T (p.Arg855Ter) rs768048535 0.00002
NM_002691.4(POLD1):c.3167C>T (p.Thr1056Met) rs772397517 0.00002
NM_002691.4(POLD1):c.376C>T (p.Arg126Cys) rs864622753 0.00002
NM_002691.4(POLD1):c.1291A>G (p.Ile431Val) rs752444746 0.00001
NM_002691.4(POLD1):c.1516C>T (p.Arg506Cys) rs528292347 0.00001
NM_002691.4(POLD1):c.1717G>T (p.Val573Leu) rs760616076 0.00001
NM_002691.4(POLD1):c.1811C>A (p.Ser604Tyr) rs1060501807 0.00001
NM_002691.4(POLD1):c.1867C>T (p.Arg623Trp) rs768773535 0.00001
NM_002691.4(POLD1):c.203G>A (p.Gly68Glu) rs144707871 0.00001
NM_002691.4(POLD1):c.2142G>A (p.Leu714=) rs1060501816 0.00001
NM_002691.4(POLD1):c.2760C>G (p.Asp920Glu) rs1057521209 0.00001
NM_002691.4(POLD1):c.2953C>T (p.Arg985Trp) rs780926432 0.00001
NM_002691.4(POLD1):c.590-2A>G rs758877520 0.00001
NM_002691.4(POLD1):c.820G>A (p.Ala274Thr) rs878854557 0.00001
NM_002691.4(POLD1):c.866A>G (p.Asp289Gly) rs878854558 0.00001
NM_002691.4(POLD1):c.965G>A (p.Arg322His) rs980303681 0.00001
NM_002691.4(POLD1):c.1294C>G (p.Arg432Gly) rs774130423
NM_002691.4(POLD1):c.1366C>G (p.Gln456Glu) rs878854520
NM_002691.4(POLD1):c.208G>T (p.Val70Phe) rs147911699
NM_002691.4(POLD1):c.223A>G (p.Ile75Val) rs940296193
NM_002691.4(POLD1):c.2959dup rs756872503
NM_002691.4(POLD1):c.3298G>A (p.Gly1100Arg) rs1060501837
NM_002691.4(POLD1):c.343C>T (p.Pro115Ser) rs754917939
NM_002691.4(POLD1):c.364G>A (p.Val122Met) rs141579552
NM_002691.4(POLD1):c.652C>T (p.Arg218Cys) rs1295943468

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.