ClinVar Miner

List of variants in gene POLD1 reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP
NM_001256849.1(POLD1):c.1157G>A (p.Arg386His) rs764023083
NM_001256849.1(POLD1):c.1240A>G (p.Lys414Glu) rs1555790592
NM_001256849.1(POLD1):c.1517G>A (p.Arg506His) rs140379348
NM_001256849.1(POLD1):c.1552C>A (p.Leu518Met) rs149043082
NM_001256849.1(POLD1):c.1573C>T (p.Arg525Trp) rs201804732
NM_001256849.1(POLD1):c.1696G>A (p.Glu566Lys) rs372429157
NM_001256849.1(POLD1):c.1735G>A (p.Glu579Lys) rs1354117345
NM_001256849.1(POLD1):c.1955G>A (p.Arg652Gln) rs778037523
NM_001256849.1(POLD1):c.203G>A (p.Gly68Glu) rs144707871
NM_001256849.1(POLD1):c.2052G>C (p.Gln684His) rs144143245
NM_001256849.1(POLD1):c.2154+2T>C rs1555792026
NM_001256849.1(POLD1):c.2275G>A (p.Val759Ile) rs145473716
NM_001256849.1(POLD1):c.2326C>T (p.Arg776Trp) rs780138978
NM_001256849.1(POLD1):c.2797G>T (p.Val933Leu) rs764785216
NM_001256849.1(POLD1):c.2824C>G (p.Pro942Ala) rs1203736050
NM_001256849.1(POLD1):c.2953+12C>T rs3218776
NM_001256849.1(POLD1):c.2954G>C (p.Arg985Pro) rs749159160
NM_001256849.1(POLD1):c.3023G>A (p.Arg1008His) rs763747258
NM_001256849.1(POLD1):c.487G>T (p.Asp163Tyr) rs753299061
NM_001256849.1(POLD1):c.632G>A (p.Arg211His) rs373192520
NM_001256849.1(POLD1):c.758+5G>A rs760003191
NM_001256849.1(POLD1):c.868G>A (p.Val290Met) rs748657880

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.