ClinVar Miner

List of variants in gene POLD1 reported as uncertain significance by Counsyl

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Total variants: 34
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HGVS dbSNP
NM_001256849.1(POLD1):c.-3A>C rs1254845405
NM_001256849.1(POLD1):c.1171dup (p.Asp391fs) rs1555790567
NM_001256849.1(POLD1):c.1225C>T (p.Arg409Trp) rs778135510
NM_001256849.1(POLD1):c.125_136del (p.Glu42_Glu45del) rs1300269779
NM_001256849.1(POLD1):c.1371G>T (p.Met457Ile) rs1457008478
NM_001256849.1(POLD1):c.1514G>A (p.Arg505His) rs1043752384
NM_001256849.1(POLD1):c.151_156CAGGAG[1] (p.51_52QE[1]) rs760207160
NM_001256849.1(POLD1):c.1773dup (p.Gly592fs) rs1555791532
NM_001256849.1(POLD1):c.1786G>A (p.Val596Ile) rs773180520
NM_001256849.1(POLD1):c.17G>A (p.Arg6Gln) rs778275831
NM_001256849.1(POLD1):c.2052G>C (p.Gln684His) rs144143245
NM_001256849.1(POLD1):c.208G>T (p.Val70Phe) rs147911699
NM_001256849.1(POLD1):c.2154+4G>A rs373416476
NM_001256849.1(POLD1):c.2275G>A (p.Val759Ile) rs145473716
NM_001256849.1(POLD1):c.2429C>T (p.Ala810Val) rs765981178
NM_001256849.1(POLD1):c.2443_2445TCC[1] (p.Ser816del) rs763850764
NM_001256849.1(POLD1):c.245C>T (p.Pro82Leu) rs201006221
NM_001256849.1(POLD1):c.269A>G (p.Gln90Arg) rs778838312
NM_001256849.1(POLD1):c.2803G>A (p.Ala935Thr) rs555452657
NM_001256849.1(POLD1):c.2T>A (p.Met1Lys) rs1057517594
NM_001256849.1(POLD1):c.3068-2A>G rs1555793565
NM_001256849.1(POLD1):c.3074_3076dup (p.Cys1026_Glu1027insLeu) rs1555793570
NM_001256849.1(POLD1):c.317-2A>G rs761230747
NM_001256849.1(POLD1):c.3305del (p.Pro1102fs) rs761614971
NM_001256849.1(POLD1):c.358G>C (p.Gly120Arg) rs746234949
NM_001256849.1(POLD1):c.469G>A (p.Gly157Arg) rs774568050
NM_001256849.1(POLD1):c.55C>T (p.Arg19Cys) rs368033860
NM_001256849.1(POLD1):c.583C>T (p.Arg195Ter) rs377690809
NM_001256849.1(POLD1):c.590-2A>G rs758877520
NM_001256849.1(POLD1):c.758G>A (p.Arg253Gln) rs1366413924
NM_001256849.1(POLD1):c.835_837del (p.Glu279del) rs746341854
NM_001256849.1(POLD1):c.961G>A (p.Gly321Ser) rs41554817
NM_001256849.1(POLD1):c.980C>T (p.Pro327Leu) rs397514633
NM_001256849.1:c.2887_2888ins7

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