ClinVar Miner

List of variants in gene POLD1 reported as likely benign by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_002691.4(POLD1):c.1419G>A (p.Thr473=) rs763643495
NM_002691.4(POLD1):c.1596C>T (p.Ala532=) rs550441767
NM_002691.4(POLD1):c.1626C>T (p.Pro542=) rs201208120
NM_002691.4(POLD1):c.1665C>T (p.Val555=) rs150238541
NM_002691.4(POLD1):c.2103C>T (p.Tyr701=) rs201483538
NM_002691.4(POLD1):c.2251-8G>A rs56051075
NM_002691.4(POLD1):c.2598C>T (p.Asp866=) rs773567499
NM_002691.4(POLD1):c.2967G>A (p.Thr989=) rs3218752
NM_002691.4(POLD1):c.3054G>A (p.Val1018=) rs369613619
NM_002691.4(POLD1):c.3249G>A (p.Lys1083=) rs760214407
NM_002691.4(POLD1):c.378C>T (p.Arg126=) rs145324823
NM_002691.4(POLD1):c.639C>T (p.Thr213=) rs139949679
NM_002691.4(POLD1):c.714G>A (p.Thr238=) rs149096523
NM_002691.4(POLD1):c.80A>T (p.Asp27Val) rs150066950
NM_002691.4(POLD1):c.885G>C (p.Val295=) rs201946114
NM_002691.4(POLD1):c.894C>T (p.His298=) rs1442547881

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