ClinVar Miner

List of variants in gene POLD1 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP
NM_001256849.1(POLD1):c.2007-4G>A rs202035484
NM_001256849.1(POLD1):c.3218+10A>G rs2463239
NM_001256849.1(POLD1):c.463+8G>T rs1726802
NM_001256849.1(POLD1):c.56G>A (p.Arg19His) rs3218773
NM_001308632.1(POLD1):c.1539_1548delGAAGGATGCCinsAAAGGATGCT (p.Leu513_Ala516=) rs1555791361
NM_001308632.1(POLD1):c.3297-25_3297-20dup
NM_002691.3(POLD1):c.1148C>T (p.Thr383Ile) rs201654210
NM_002691.3(POLD1):c.1173C>T (p.Asp391=) rs2230244
NM_002691.3(POLD1):c.1275C>T (p.Ala425=) rs3219392
NM_002691.3(POLD1):c.1485C>T (p.Thr495=) rs2230245
NM_002691.3(POLD1):c.1539G>A (p.Leu513=) rs2230246
NM_002691.3(POLD1):c.1548C>T (p.Ala516=) rs2230247
NM_002691.3(POLD1):c.1620C>T (p.Gly540=) rs140216790
NM_002691.3(POLD1):c.1665C>T (p.Val555=) rs150238541
NM_002691.3(POLD1):c.1713C>T (p.Pro571=) rs2230248
NM_002691.3(POLD1):c.1761C>T (p.Ile587=) rs3218755
NM_002691.3(POLD1):c.1860G>A (p.Thr620=) rs1726790
NM_002691.3(POLD1):c.1977C>T (p.Ile659=) rs45605236
NM_002691.3(POLD1):c.2103C>T (p.Tyr701=) rs201483538
NM_002691.3(POLD1):c.2154+13_2154+14insA rs3218767
NM_002691.3(POLD1):c.2244T>C (p.Ser748=) rs1274607
NM_002691.3(POLD1):c.2337G>A (p.Ala779=) rs147108748
NM_002691.3(POLD1):c.234C>G (p.Arg78=) rs2228665
NM_002691.3(POLD1):c.2546G>A (p.Arg849His) rs3218775
NM_002691.3(POLD1):c.2628C>T (p.Ile876=) rs75874199
NM_002691.3(POLD1):c.2700C>T (p.His900=) rs769965495
NM_002691.3(POLD1):c.2718-12A>G rs3219433
NM_002691.3(POLD1):c.2862G>C (p.Thr954=) rs3219440
NM_002691.3(POLD1):c.2953+12C>T rs3218776
NM_002691.3(POLD1):c.2967G>A (p.Thr989=) rs3218752
NM_002691.3(POLD1):c.3121-19C>T rs3212330
NM_002691.3(POLD1):c.3218+9C>T rs3219448
NM_002691.3(POLD1):c.3218+9_3218+10invCA
NM_002691.3(POLD1):c.3219-15_3219-10dup
NM_002691.3(POLD1):c.3219-21_3219-10dupTGCCCCTGCCCC rs3219456
NM_002691.3(POLD1):c.324G>A (p.Ala108=) rs20582
NM_002691.3(POLD1):c.324G>T (p.Ala108=) rs20582
NM_002691.3(POLD1):c.33C>T (p.Pro11=) rs3218768
NM_002691.3(POLD1):c.356G>A (p.Arg119His) rs1726801
NM_002691.3(POLD1):c.378C>T (p.Arg126=) rs145324823
NM_002691.3(POLD1):c.463+9C>T rs1673046
NM_002691.3(POLD1):c.518G>A (p.Ser173Asn) rs1726803
NM_002691.3(POLD1):c.624G>A (p.Pro208=) rs78996304
NM_002691.3(POLD1):c.783C>T (p.Val261=) rs34269084
NM_002691.3(POLD1):c.810T>C (p.Ala270=) rs1143666
NM_002691.3(POLD1):c.841-10A>G rs140160345
NM_002691.3(POLD1):c.849G>T (p.Gln283His) rs113282414
NM_002691.3(POLD1):c.88C>T (p.Arg30Trp) rs3218772
NM_002691.3(POLD1):c.945C>T (p.Phe315=) rs150116169
NM_002691.3(POLD1):c.971-12C>T rs1673044
NM_002691.3(POLD1):c.971-4G>A rs200144991

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