Pold2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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319 records found for search term Pold2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156418213	CV1914574	single nucleotide variant	NM_006230.4(POLD2):c.-6G>A	not provided [RCV002611392]	uncertain significance	7	44122059	44122059	Human		name
597958355	CV3814810	single nucleotide variant	NM_006230.4(POLD2):c.-7T>C	not provided [RCV005162935]	likely benign	7	44122060	44122060	Human		name
156130695	CV2022725	single nucleotide variant	NM_006230.4(POLD2):c.-91C>T	not provided [RCV002740553]	benign	7	44123545	44123545	Human		name
156078171	CV2025801	single nucleotide variant	NM_006230.4(POLD2):c.-76G>C	not provided [RCV002760537]	benign	7	44123530	44123530	Human		name
156288566	CV2047095	single nucleotide variant	NM_006230.4(POLD2):c.-43C>T	not provided [RCV002770669]	likely benign	7	44122096	44122096	Human		name
155941929	CV2076037	single nucleotide variant	NM_006230.4(POLD2):c.-67C>A	not provided [RCV002861837]	likely benign	7	44123521	44123521	Human		name
156232489	CV2093883	single nucleotide variant	NM_006230.4(POLD2):c.-86G>A	not provided [RCV002894607]	uncertain significance	7	44123540	44123540	Human		name
155933163	CV2142327	single nucleotide variant	NM_006230.4(POLD2):c.-51C>T	not provided [RCV002993531]	uncertain significance	7	44122104	44122104	Human		name
156019545	CV2174050	single nucleotide variant	NM_006230.4(POLD2):c.-36G>A	not provided [RCV003035658]	uncertain significance	7	44122089	44122089	Human		name
405179506	CV3027688	single nucleotide variant	NM_006230.4(POLD2):c.-88G>A	not provided [RCV003705395]	likely benign	7	44123542	44123542	Human		name
405067503	CV3030909	single nucleotide variant	NM_006230.4(POLD2):c.-64G>C	not provided [RCV003698119]	likely benign	7	44123518	44123518	Human		name
405071000	CV3034382	single nucleotide variant	NM_006230.4(POLD2):c.-77C>A	not provided [RCV003698320]	uncertain significance	7	44123531	44123531	Human		name
405071790	CV3034439	single nucleotide variant	NM_006230.4(POLD2):c.-18C>A	not provided [RCV003698365]	uncertain significance	7	44122071	44122071	Human		name
405222261	CV3038734	single nucleotide variant	NM_006230.4(POLD2):c.-80T>C	not provided [RCV003710150]	uncertain significance	7	44123534	44123534	Human		name
405206526	CV3039998	single nucleotide variant	NM_006230.4(POLD2):c.-65C>T	not provided [RCV003708076]	uncertain significance	7	44123519	44123519	Human		name
402481185	CV3041557	single nucleotide variant	NM_006230.4(POLD2):c.-62C>T	not provided [RCV003712856]	uncertain significance	7	44123516	44123516	Human		name
597894199	CV3773269	single nucleotide variant	NM_006230.4(POLD2):c.-67C>T	not provided [RCV005111176]	likely benign	7	44123521	44123521	Human		name
597938428	CV3788270	single nucleotide variant	NM_006230.4(POLD2):c.-80T>G	not provided [RCV005132945]	uncertain significance	7	44123534	44123534	Human		name
597942507	CV3815612	single nucleotide variant	NM_006230.4(POLD2):c.-77C>T	not provided [RCV005159301]	uncertain significance	7	44123531	44123531	Human		name
597913167	CV3833762	deletion	NM_006230.4(POLD2):c.-51del	not provided [RCV005183121]	uncertain significance	7	44122104	44122104	Human		name
155959065	CV1900103	single nucleotide variant	NM_006230.4(POLD2):c.343-8C>T	not provided [RCV003095747]	likely benign	7	44117750	44117750	Human		name
156259335	CV2026068	single nucleotide variant	NM_006230.4(POLD2):c.861+7G>A	not provided [RCV002746253]	likely benign	7	44116423	44116423	Human		name
156037744	CV2030100	single nucleotide variant	NM_006230.4(POLD2):c.467-5C>T	not provided [RCV002736064]	likely benign	7	44117252	44117252	Human		name
156217197	CV2087245	single nucleotide variant	NM_006230.4(POLD2):c.220+4A>C	not provided [RCV002875723]	uncertain significance	7	44121830	44121830	Human		name
156200732	CV2092481	single nucleotide variant	NM_006230.4(POLD2):c.862-4C>G	not provided [RCV002917778]	benign	7	44116276	44116276	Human		name
156330269	CV2094744	single nucleotide variant	NM_006230.4(POLD2):c.467-6C>T	not provided [RCV002899880]	benign	7	44117253	44117253	Human		name
155931571	CV2096096	single nucleotide variant	NM_006230.4(POLD2):c.221-4C>T	not provided [RCV002903857]	benign	7	44118068	44118068	Human		name
155938043	CV2135151	deletion	NM_006230.4(POLD2):c.467-9del	not provided [RCV002993868]	likely benign	7	44117256	44117256	Human		name
156085392	CV2184440	single nucleotide variant	NM_006230.4(POLD2):c.582-5C>T	not provided [RCV003054170]	likely benign	7	44117020	44117020	Human		name
402474745	CV2858067	single nucleotide variant	NM_006230.4(POLD2):c.221-9G>C	not provided [RCV003543088]	likely benign	7	44118073	44118073	Human		name
405100417	CV2938224	single nucleotide variant	NM_006230.4(POLD2):c.781-4C>T	not provided [RCV003665863]	likely benign	7	44116514	44116514	Human		name
405127701	CV2939602	single nucleotide variant	NM_006230.4(POLD2):c.862-3C>T	not provided [RCV003672050]	uncertain significance	7	44116275	44116275	Human		name
405089454	CV2939664	single nucleotide variant	NM_006230.4(POLD2):c.582-4G>A	not provided [RCV003665184]	likely benign	7	44117019	44117019	Human		name
405117996	CV2955778	single nucleotide variant	NM_006230.4(POLD2):c.-56-5C>T	not provided [RCV003671159]	likely benign	7	44122114	44122114	Human		name
405118615	CV3030511	single nucleotide variant	NM_006230.4(POLD2):c.-57+8G>T	not provided [RCV003700510]	likely benign	7	44123503	44123503	Human		name
402522411	CV3126998	single nucleotide variant	NM_006230.4(POLD2):c.466+7A>C	not provided [RCV003824916]	likely benign	7	44117612	44117612	Human		name
597832024	CV3830889	single nucleotide variant	NM_006230.4(POLD2):c.-57+9G>A	not provided [RCV005170287]	likely benign	7	44123502	44123502	Human		name
597932948	CV3844577	single nucleotide variant	NM_006230.4(POLD2):c.-56-4G>C	not provided [RCV005186084]	uncertain significance	7	44122113	44122113	Human		name
156154100	CV2023216	single nucleotide variant	NM_006230.4(POLD2):c.-57+20A>G	not provided [RCV002741317]	likely benign	7	44123491	44123491	Human		name
156255079	CV2025904	single nucleotide variant	NM_006230.4(POLD2):c.581+16C>T	not provided [RCV002746120]	likely benign	7	44117117	44117117	Human		name
156256589	CV2025962	single nucleotide variant	NM_006230.4(POLD2):c.781-14G>C	not provided [RCV002746167]	benign	7	44116524	44116524	Human		name
156172334	CV2026299	single nucleotide variant	NM_006230.4(POLD2):c.780+11C>T	not provided [RCV002765356]	likely benign	7	44116806	44116806	Human		name
155990979	CV2026967	single nucleotide variant	NM_006230.4(POLD2):c.220+11G>A	not provided [RCV002755748]	likely benign	7	44121823	44121823	Human		name
155910681	CV2032956	single nucleotide variant	NM_006230.4(POLD2):c.582-13C>T	not provided [RCV002750112]	likely benign	7	44117028	44117028	Human		name
155910998	CV2033042	single nucleotide variant	NM_006230.4(POLD2):c.-57+10G>A	not provided [RCV002750135]	likely benign	7	44123501	44123501	Human		name
156223226	CV2064134	single nucleotide variant	NM_006230.4(POLD2):c.221-12C>A	not provided [RCV002829768]	likely benign	7	44118076	44118076	Human		name
156090358	CV2080241	single nucleotide variant	NM_006230.4(POLD2):c.1019+9C>T	not provided [RCV002847692]	uncertain significance	7	44116106	44116106	Human		name
155961027	CV2080449	single nucleotide variant	NM_006230.4(POLD2):c.1020-9G>C	not provided [RCV002862859]	likely benign	7	44115902	44115902	Human		name
156110933	CV2082173	single nucleotide variant	NM_006230.4(POLD2):c.1249+1G>C	not provided [RCV002848450]	uncertain significance	7	44115294	44115294	Human		name
156102354	CV2149177	single nucleotide variant	NM_006230.4(POLD2):c.581+16C>A	not provided [RCV003021094]	likely benign	7	44117117	44117117	Human		name
155947868	CV2151003	single nucleotide variant	NM_006230.4(POLD2):c.466+10C>T	not provided [RCV003014678]	likely benign	7	44117609	44117609	Human		name
155986761	CV2159766	single nucleotide variant	NM_006230.4(POLD2):c.861+14G>C	not provided [RCV003034134]	uncertain significance	7	44116416	44116416	Human		name
156315783	CV2161353	single nucleotide variant	NM_006230.4(POLD2):c.581+14C>A	not provided [RCV003046294]	likely benign	7	44117119	44117119	Human		name
156323163	CV2162964	single nucleotide variant	NM_006230.4(POLD2):c.467-10T>C	not provided [RCV003029311]	likely benign	7	44117257	44117257	Human		name
155954514	CV2166350	single nucleotide variant	NM_006230.4(POLD2):c.343-18C>T	not provided [RCV003015027]	likely benign	7	44117760	44117760	Human		name
402479025	CV2853853	single nucleotide variant	NM_006230.4(POLD2):c.343-12T>C	not provided [RCV003543814]	uncertain significance	7	44117754	44117754	Human		name
405213670	CV2924972	single nucleotide variant	NM_006230.4(POLD2):c.221-10C>T	not provided [RCV003567509]	likely benign	7	44118074	44118074	Human		name
402517451	CV2936521	single nucleotide variant	NM_006230.4(POLD2):c.862-20C>T	not provided [RCV003663060]	likely benign	7	44116292	44116292	Human		name
405114742	CV2953026	single nucleotide variant	NM_006230.4(POLD2):c.343-13C>T	not provided [RCV003666783]	likely benign	7	44117755	44117755	Human		name
405162381	CV2960401	single nucleotide variant	NM_006230.4(POLD2):c.780+17G>A	not provided [RCV003674777]	likely benign	7	44116800	44116800	Human		name
405056594	CV3023380	single nucleotide variant	NM_006230.4(POLD2):c.466+13A>G	not provided [RCV003697382]	likely benign	7	44117606	44117606	Human		name
405120900	CV3024524	single nucleotide variant	NM_006230.4(POLD2):c.466+14T>C	not provided [RCV003700748]	uncertain significance	7	44117605	44117605	Human		name
405150732	CV3031261	single nucleotide variant	NM_006230.4(POLD2):c.-57+14A>G	not provided [RCV003703230]	likely benign	7	44123497	44123497	Human		name
405183791	CV3040134	single nucleotide variant	NM_006230.4(POLD2):c.221-12C>T	not provided [RCV003705809]	likely benign	7	44118076	44118076	Human		name
597861949	CV3766422	single nucleotide variant	NM_006230.4(POLD2):c.-56-16C>G	not provided [RCV005106147]	likely benign	7	44122125	44122125	Human		name
597965731	CV3793830	deletion	NM_006230.4(POLD2):c.-57+11del	not provided [RCV005140212]	likely benign	7	44123500	44123500	Human		name
597897199	CV3806782	single nucleotide variant	NM_006230.4(POLD2):c.862-14C>T	not provided [RCV005152169]	likely benign	7	44116286	44116286	Human		name
597954825	CV3809342	single nucleotide variant	NM_006230.4(POLD2):c.467-14C>T	not provided [RCV005162066]	likely benign	7	44117261	44117261	Human		name
597892311	CV3809773	single nucleotide variant	NM_006230.4(POLD2):c.862-11G>A	not provided [RCV005151494]	likely benign	7	44116283	44116283	Human		name
597863974	CV3814112	single nucleotide variant	NM_006230.4(POLD2):c.-57+11T>A	not provided [RCV005147181]	likely benign	7	44123500	44123500	Human		name
597976434	CV3829595	single nucleotide variant	NM_006230.4(POLD2):c.-57+17G>A	not provided [RCV005169862]	likely benign	7	44123494	44123494	Human		name
597883436	CV3834773	deletion	NM_006230.4(POLD2):c.1249+9del	not provided [RCV005178496]	benign	7	44115286	44115286	Human		name
156028371	CV2022516	single nucleotide variant	NM_006230.4(POLD2):c.1148-11T>C	not provided [RCV002735697]	benign	7	44115407	44115407	Human		name
156157548	CV2096711	single nucleotide variant	NM_006230.4(POLD2):c.1249+20G>A	not provided [RCV002872536]	likely benign	7	44115275	44115275	Human		name
156167903	CV2102361	single nucleotide variant	NM_006230.4(POLD2):c.1249+12C>T	not provided [RCV002891233]	likely benign	7	44115283	44115283	Human		name
156047729	CV2154125	single nucleotide variant	NM_006230.4(POLD2):c.1147+15C>T	not provided [RCV003019290]	likely benign	7	44115751	44115751	Human		name
405208518	CV2874172	single nucleotide variant	NM_006230.4(POLD2):c.1020-16G>C	not provided [RCV003552127]	likely benign	7	44115909	44115909	Human		name
405118479	CV2955851	single nucleotide variant	NM_006230.4(POLD2):c.1148-12C>T	not provided [RCV003671208]	likely benign	7	44115408	44115408	Human		name
405026449	CV2999963	single nucleotide variant	NM_006230.4(POLD2):c.1147+11C>T	not provided [RCV003695248]	likely benign	7	44115755	44115755	Human		name
405151653	CV3031440	single nucleotide variant	NM_006230.4(POLD2):c.1249+17G>C	not provided [RCV003703337]	likely benign	7	44115278	44115278	Human		name
402502881	CV3032539	single nucleotide variant	NM_006230.4(POLD2):c.1148-15C>T	not provided [RCV003714924]	likely benign	7	44115411	44115411	Human		name
597923531	CV3808526	single nucleotide variant	NM_006230.4(POLD2):c.1250-17A>G	not provided [RCV005156040]	likely benign	7	44114962	44114962	Human		name
8590830	CV125539	single nucleotide variant	NM_001127218.2(POLD2):c.220+481T>C	Lung cancer [RCV000106058]	uncertain significance	7	44121353	44121353	Human		name
156336183	CV1906050	microsatellite	NM_006230.4(POLD2):c.343-11_343-10del	not provided [RCV003090080]	benign	7	44117752	44117753	Human		name
156097607	CV2183671	single nucleotide variant	NM_006230.4(POLD2):c.78G>A (p.Arg26=)	not provided [RCV003054601]	likely benign	7	44121976	44121976	Human		name
404993593	CV2995936	single nucleotide variant	NM_006230.4(POLD2):c.39A>G (p.Leu13=)	not provided [RCV003692524]	likely benign	7	44122015	44122015	Human		name
597933359	CV3810700	single nucleotide variant	NM_006230.4(POLD2):c.51A>G (p.Pro17=)	not provided [RCV005157409]	likely benign	7	44122003	44122003	Human		name
156174845	CV2051914	single nucleotide variant	NM_006230.4(POLD2):c.171C>T (p.Arg57=)	not provided [RCV002828108]	likely benign	7	44121883	44121883	Human		name
405146050	CV2885251	single nucleotide variant	NM_006230.4(POLD2):c.144G>T (p.Arg48=)	not provided [RCV003561346]	likely benign	7	44121910	44121910	Human		name
405059731	CV2928935	single nucleotide variant	NM_006230.4(POLD2):c.135C>T (p.Ser45=)	not provided [RCV003580290]	likely benign	7	44121919	44121919	Human		name
402485547	CV2944921	single nucleotide variant	NM_006230.4(POLD2):c.20C>T (p.Ala7Val)	not provided [RCV003659965]	uncertain significance	7	44122034	44122034	Human		name
405120979	CV2952407	single nucleotide variant	NM_006230.4(POLD2):c.171C>G (p.Arg57=)	not provided [RCV003671470]	likely benign	7	44121883	44121883	Human		name
405221771	CV3158172	single nucleotide variant	NM_006230.4(POLD2):c.15G>C (p.Gln5His)	not provided [RCV003863667]\|not specified [RCV004369544]	uncertain significance	7	44122039	44122039	Human		name
597968306	CV3820894	single nucleotide variant	NM_006230.4(POLD2):c.147G>A (p.Gln49=)	not provided [RCV005165735]	likely benign	7	44121907	44121907	Human		name
156223497	CV1879454	single nucleotide variant	NM_006230.4(POLD2):c.684C>T (p.Asp228=)	not provided [RCV003059036]	likely benign	7	44116913	44116913	Human		name
156313160	CV1896547	single nucleotide variant	NM_006230.4(POLD2):c.558C>T (p.Pro186=)	not provided [RCV003088568]	likely benign	7	44117156	44117156	Human		name
156359513	CV1904244	single nucleotide variant	NM_006230.4(POLD2):c.861C>T (p.Ser287=)	not provided [RCV002581630]	uncertain significance	7	44116430	44116430	Human		name
156412460	CV1904448	single nucleotide variant	NM_006230.4(POLD2):c.915G>A (p.Thr305=)	not provided [RCV002587829]	likely benign	7	44116219	44116219	Human		name
156378140	CV1906824	single nucleotide variant	NM_006230.4(POLD2):c.618C>T (p.Gly206=)	not provided [RCV003093045]	likely benign	7	44116979	44116979	Human		name
156103559	CV1907283	single nucleotide variant	NM_006230.4(POLD2):c.600C>T (p.Ser200=)	not provided [RCV003080696]	likely benign	7	44116997	44116997	Human		name
156272723	CV1915436	single nucleotide variant	NM_006230.4(POLD2):c.465G>A (p.Thr155=)	not provided [RCV002628157]	uncertain significance	7	44117620	44117620	Human		name
156356502	CV1917623	single nucleotide variant	NM_006230.4(POLD2):c.891C>T (p.Gly297=)	not provided [RCV002632374]	likely benign	7	44116243	44116243	Human		name
156406972	CV1917940	single nucleotide variant	NM_006230.4(POLD2):c.372T>C (p.Ser124=)	not provided [RCV002606759]	likely benign	7	44117713	44117713	Human		name
156397224	CV1934296	single nucleotide variant	NM_006230.4(POLD2):c.876G>T (p.Val292=)	not provided [RCV002655049]	likely benign	7	44116258	44116258	Human		name
156436896	CV1936714	single nucleotide variant	NM_006230.4(POLD2):c.597G>A (p.Val199=)	not provided [RCV003106420]	likely benign	7	44117000	44117000	Human		name
156442410	CV1938690	single nucleotide variant	NM_006230.4(POLD2):c.711C>T (p.His237=)	not provided [RCV003112751]	likely benign	7	44116886	44116886	Human		name
156440452	CV1943503	single nucleotide variant	NM_006230.4(POLD2):c.705C>T (p.Ala235=)	not provided [RCV003110487]	likely benign	7	44116892	44116892	Human		name
156264629	CV2030350	single nucleotide variant	NM_006230.4(POLD2):c.306G>A (p.Pro102=)	not provided [RCV002746427]	likely benign	7	44117979	44117979	Human		name
156169681	CV2041486	single nucleotide variant	NM_006230.4(POLD2):c.315C>T (p.Pro105=)	not provided [RCV002741821]	likely benign	7	44117970	44117970	Human		name
155938899	CV2041525	single nucleotide variant	NM_006230.4(POLD2):c.816C>T (p.Ser272=)	not provided [RCV002775061]	likely benign	7	44116475	44116475	Human		name
156321544	CV2067605	single nucleotide variant	NM_006230.4(POLD2):c.942C>T (p.Cys314=)	not provided [RCV002834731]	likely benign	7	44116192	44116192	Human		name
156078675	CV2083588	single nucleotide variant	NM_006230.4(POLD2):c.345C>T (p.His115=)	not provided [RCV002847313]	likely benign	7	44117740	44117740	Human		name
156117573	CV2086596	single nucleotide variant	NM_006230.4(POLD2):c.936C>T (p.His312=)	not provided [RCV002871136]	likely benign	7	44116198	44116198	Human		name
155960192	CV2088945	single nucleotide variant	NM_006230.4(POLD2):c.321C>T (p.Ile107=)	not provided [RCV002880979]	likely benign	7	44117964	44117964	Human		name
155993082	CV2095587	single nucleotide variant	NM_006230.4(POLD2):c.492C>T (p.Ser164=)	not provided [RCV002908255]	benign	7	44117222	44117222	Human		name
155995855	CV2095751	single nucleotide variant	NM_006230.4(POLD2):c.462T>G (p.Val154=)	not provided [RCV002908380]	likely benign	7	44117623	44117623	Human		name
156081272	CV2098682	single nucleotide variant	NM_006230.4(POLD2):c.336C>T (p.Ser112=)	not provided [RCV002912712]	benign	7	44117949	44117949	Human		name
155921765	CV2102442	single nucleotide variant	NM_006230.4(POLD2):c.354C>T (p.Leu118=)	not provided [RCV002903387]	likely benign	7	44117731	44117731	Human		name
156100577	CV2107343	single nucleotide variant	NM_006230.4(POLD2):c.537T>C (p.Ala179=)	not provided [RCV002927036]	likely benign	7	44117177	44117177	Human		name
156128500	CV2112459	single nucleotide variant	NM_006230.4(POLD2):c.393C>T (p.Asp131=)	not provided [RCV002928102]	benign	7	44117692	44117692	Human		name
156295061	CV2119187	single nucleotide variant	NM_006230.4(POLD2):c.850C>T (p.Leu284=)	not provided [RCV002961885]	benign	7	44116441	44116441	Human		name
156313576	CV2120179	single nucleotide variant	NM_006230.4(POLD2):c.450G>T (p.Val150=)	not provided [RCV002962760]	benign	7	44117635	44117635	Human		name
156097255	CV2135865	single nucleotide variant	NM_006230.4(POLD2):c.804C>G (p.Thr268=)	not provided [RCV002979841]	likely benign	7	44116487	44116487	Human		name
156316895	CV2140365	single nucleotide variant	NM_006230.4(POLD2):c.879C>T (p.Asp293=)	not provided [RCV003011442]	likely benign	7	44116255	44116255	Human		name
156023878	CV2145491	single nucleotide variant	NM_006230.4(POLD2):c.636G>T (p.Leu212=)	not provided [RCV003018360]	likely benign	7	44116961	44116961	Human		name
155993615	CV2147770	single nucleotide variant	NM_006230.4(POLD2):c.741C>T (p.Leu247=)	not provided [RCV003016947]	likely benign	7	44116856	44116856	Human		name
155919823	CV2152261	single nucleotide variant	NM_006230.4(POLD2):c.669G>A (p.Thr223=)	not provided [RCV003013124]	likely benign	7	44116928	44116928	Human		name
155967309	CV2156143	single nucleotide variant	NM_006230.4(POLD2):c.918C>A (p.Leu306=)	not provided [RCV003015766]	likely benign	7	44116216	44116216	Human		name
156366571	CV2177088	single nucleotide variant	NM_006230.4(POLD2):c.74C>T (p.Ala25Val)	not provided [RCV003049387]	uncertain significance	7	44121980	44121980	Human		name
156101570	CV2180098	single nucleotide variant	NM_006230.4(POLD2):c.732T>A (p.Ala244=)	not provided [RCV003054746]	likely benign	7	44116865	44116865	Human		name
401908735	CV2828422	single nucleotide variant	NM_006230.4(POLD2):c.636G>A (p.Leu212=)	not provided [RCV003423558]	likely benign	7	44116961	44116961	Human		name
402489333	CV2866522	single nucleotide variant	NM_006230.4(POLD2):c.627C>T (p.Gly209=)	not provided [RCV003572854]	likely benign	7	44116970	44116970	Human		name
405190093	CV2871226	single nucleotide variant	NM_006230.4(POLD2):c.975C>G (p.Leu325=)	not provided [RCV003550323]	likely benign	7	44116159	44116159	Human		name
405134549	CV2955629	single nucleotide variant	NM_006230.4(POLD2):c.459G>A (p.Leu153=)	not provided [RCV003668675]	likely benign	7	44117626	44117626	Human		name
405206273	CV2994186	single nucleotide variant	NM_006230.4(POLD2):c.966C>T (p.Tyr322=)	not provided [RCV003678777]	likely benign	7	44116168	44116168	Human		name
402499207	CV3038327	single nucleotide variant	NM_006230.4(POLD2):c.457C>T (p.Leu153=)	not provided [RCV003714564]	uncertain significance	7	44117628	44117628	Human		name
405243879	CV3072178	single nucleotide variant	NM_006230.4(POLD2):c.951G>A (p.Pro317=)	not provided [RCV003737897]	likely benign	7	44116183	44116183	Human		name
405156873	CV3163429	single nucleotide variant	NM_006230.4(POLD2):c.729C>T (p.Leu243=)	not provided [RCV003856675]	likely benign	7	44116868	44116868	Human		name
402467955	CV3174218	single nucleotide variant	NM_006230.4(POLD2):c.501C>T (p.Asp167=)	not provided [RCV003873501]	likely benign	7	44117213	44117213	Human		name
597852428	CV3758572	single nucleotide variant	NM_006230.4(POLD2):c.891C>G (p.Gly297=)	not provided [RCV005088131]	likely benign	7	44116243	44116243	Human		name
597877619	CV3766811	single nucleotide variant	NM_006230.4(POLD2):c.531C>T (p.Cys177=)	not provided [RCV005108751]	likely benign	7	44117183	44117183	Human		name
597909599	CV3806327	single nucleotide variant	NM_006230.4(POLD2):c.726C>T (p.Ile242=)	not provided [RCV005153894]	likely benign	7	44116871	44116871	Human		name
597963309	CV3819585	single nucleotide variant	NM_006230.4(POLD2):c.504C>T (p.Asp168=)	not provided [RCV005164301]	likely benign	7	44117210	44117210	Human		name
597859223	CV3822458	single nucleotide variant	NM_006230.4(POLD2):c.702C>T (p.Ser234=)	not provided [RCV005174756]	likely benign	7	44116895	44116895	Human		name
597957355	CV3838465	single nucleotide variant	NM_006230.4(POLD2):c.765G>A (p.Arg255=)	not provided [RCV005191840]	likely benign	7	44116832	44116832	Human		name
597885969	CV3842257	single nucleotide variant	NM_006230.4(POLD2):c.972G>A (p.Thr324=)	not provided [RCV005178892]	likely benign	7	44116162	44116162	Human		name
597958050	CV3849051	single nucleotide variant	NM_006230.4(POLD2):c.651G>A (p.Leu217=)	not provided [RCV005192052]	likely benign	7	44116946	44116946	Human		name
156383639	CV1870586	single nucleotide variant	NM_006230.4(POLD2):c.1365C>T (p.Phe455=)	not provided [RCV003067380]	likely benign	7	44114830	44114830	Human		name
156320327	CV1897783	single nucleotide variant	NM_006230.4(POLD2):c.131G>A (p.Arg44His)	not provided [RCV002579198]\|not specified [RCV004073435]	uncertain significance	7	44121923	44121923	Human		name
156368960	CV1905005	single nucleotide variant	NM_006230.4(POLD2):c.1119C>T (p.His373=)	not provided [RCV002582279]	likely benign	7	44115794	44115794	Human		name
156375521	CV1917534	single nucleotide variant	NM_006230.4(POLD2):c.1176G>A (p.Pro392=)	not provided [RCV002603544]	likely benign	7	44115368	44115368	Human		name
156356333	CV1917575	single nucleotide variant	NM_006230.4(POLD2):c.142C>T (p.Arg48Trp)	not provided [RCV002632362]\|not specified [RCV004069046]	uncertain significance	7	44121912	44121912	Human		name
156418798	CV1918780	single nucleotide variant	NM_006230.4(POLD2):c.203G>A (p.Arg68Gln)	not provided [RCV002612007]\|not specified [RCV004070533]	uncertain significance	7	44121851	44121851	Human		name
156059307	CV2034435	single nucleotide variant	NM_006230.4(POLD2):c.192C>A (p.Phe64Leu)	not provided [RCV002736780]	uncertain significance	7	44121862	44121862	Human		name
156165001	CV2045107	single nucleotide variant	NM_006230.4(POLD2):c.130C>T (p.Arg44Cys)	not provided [RCV002741682]	uncertain significance	7	44121924	44121924	Human		name
156002350	CV2057519	single nucleotide variant	NM_006230.4(POLD2):c.1194C>T (p.Cys398=)	not provided [RCV002819715]	likely benign	7	44115350	44115350	Human		name
156268783	CV2059733	single nucleotide variant	NM_006230.4(POLD2):c.142C>G (p.Arg48Gly)	not provided [RCV002806586]	uncertain significance	7	44121912	44121912	Human		name
156018377	CV2061775	single nucleotide variant	NM_006230.4(POLD2):c.202C>G (p.Arg68Gly)	not provided [RCV002820492]	uncertain significance	7	44121852	44121852	Human		name
156113653	CV2093069	single nucleotide variant	NM_006230.4(POLD2):c.1341C>T (p.Cys447=)	not provided [RCV002913882]	benign\|likely benign	7	44114854	44114854	Human		name
156330596	CV2094769	single nucleotide variant	NM_006230.4(POLD2):c.1302G>A (p.Thr434=)	not provided [RCV002899901]	benign	7	44114893	44114893	Human		name
156318942	CV2111850	single nucleotide variant	NM_006230.4(POLD2):c.1044C>T (p.Asn348=)	not provided [RCV002937623]	likely benign	7	44115869	44115869	Human		name
155942021	CV2114968	single nucleotide variant	NM_006230.4(POLD2):c.1197G>A (p.Pro399=)	not provided [RCV002904535]	benign	7	44115347	44115347	Human		name
156102052	CV2117246	single nucleotide variant	NM_006230.4(POLD2):c.1005C>T (p.Thr335=)	not provided [RCV002952775]	benign	7	44116129	44116129	Human		name
156151788	CV2131805	single nucleotide variant	NM_006230.4(POLD2):c.241A>C (p.Lys81Gln)	not provided [RCV002982679]	uncertain significance	7	44118044	44118044	Human		name
155977378	CV2146650	single nucleotide variant	NM_006230.4(POLD2):c.117C>G (p.Phe39Leu)	not provided [RCV003016215]	uncertain significance	7	44121937	44121937	Human		name
155974385	CV2148937	single nucleotide variant	NM_006230.4(POLD2):c.170G>A (p.Arg57His)	not provided [RCV003016086]	uncertain significance	7	44121884	44121884	Human		name
155979807	CV2157201	single nucleotide variant	NM_006230.4(POLD2):c.1398G>T (p.Gly466=)	not provided [RCV003016322]	likely benign	7	44114797	44114797	Human		name
156073243	CV2163770	single nucleotide variant	NM_006230.4(POLD2):c.124G>A (p.Gly42Arg)	not provided [RCV003020103]	uncertain significance	7	44121930	44121930	Human		name
156402950	CV2189652	single nucleotide variant	NM_006230.4(POLD2):c.1374G>A (p.Glu458=)	not provided [RCV003052499]	likely benign	7	44114821	44114821	Human		name
156251881	CV2311328	single nucleotide variant	NM_006230.4(POLD2):c.271T>C (p.Cys91Arg)	not specified [RCV004166398]	uncertain significance	7	44118014	44118014	Human		name
405225952	CV2882229	single nucleotide variant	NM_006230.4(POLD2):c.112C>T (p.Pro38Ser)	not provided [RCV003554636]	uncertain significance	7	44121942	44121942	Human		name
405226588	CV2882246	single nucleotide variant	NM_006230.4(POLD2):c.1270C>T (p.Leu424=)	not provided [RCV003554641]	likely benign	7	44114925	44114925	Human		name
405139363	CV2903641	single nucleotide variant	NM_006230.4(POLD2):c.1095G>A (p.Leu365=)	not provided [RCV003560719]	likely benign	7	44115818	44115818	Human		name
402524155	CV2940285	single nucleotide variant	NM_006230.4(POLD2):c.227G>C (p.Gly76Ala)	not provided [RCV003663424]	uncertain significance	7	44118058	44118058	Human		name
405118770	CV2955900	single nucleotide variant	NM_006230.4(POLD2):c.220G>A (p.Gly74Ser)	not provided [RCV003671236]	uncertain significance	7	44121834	44121834	Human		name
405155931	CV2960805	single nucleotide variant	NM_006230.4(POLD2):c.1122C>T (p.Ile374=)	not provided [RCV003670375]	uncertain significance	7	44115791	44115791	Human		name
405226733	CV2967199	single nucleotide variant	NM_006230.4(POLD2):c.1242C>T (p.Ile414=)	not provided [RCV003681551]	likely benign	7	44115302	44115302	Human		name
405243914	CV2971798	deletion	NM_006230.4(POLD2):c.922del (p.Gln308fs)	not provided [RCV003684709]	uncertain significance	7	44116212	44116212	Human		name
405065033	CV3020809	single nucleotide variant	NM_006230.4(POLD2):c.1308C>T (p.Thr436=)	not provided [RCV003697964]	likely benign	7	44114887	44114887	Human		name
405119150	CV3030624	single nucleotide variant	NM_006230.4(POLD2):c.1281T>C (p.Thr427=)	not provided [RCV003700567]	likely benign	7	44114914	44114914	Human		name
402487754	CV3034126	single nucleotide variant	NM_006230.4(POLD2):c.198G>C (p.Glu66Asp)	not provided [RCV003713448]	uncertain significance	7	44121856	44121856	Human		name
405222511	CV3038776	single nucleotide variant	NM_006230.4(POLD2):c.202C>T (p.Arg68Trp)	not provided [RCV003710182]	uncertain significance	7	44121852	44121852	Human		name
402505992	CV3039080	single nucleotide variant	NM_006230.4(POLD2):c.118C>T (p.Arg40Trp)	not provided [RCV003715204]	uncertain significance	7	44121936	44121936	Human		name
405199408	CV3056624	single nucleotide variant	NM_006230.4(POLD2):c.1359G>A (p.Ser453=)	not provided [RCV003730602]	likely benign	7	44114836	44114836	Human		name
405230601	CV3073307	single nucleotide variant	NM_006230.4(POLD2):c.1215C>G (p.Gly405=)	not provided [RCV003734829]	likely benign	7	44115329	44115329	Human		name
405238145	CV3077882	single nucleotide variant	NM_006230.4(POLD2):c.1104C>T (p.Thr368=)	not provided [RCV003736300]	likely benign	7	44115809	44115809	Human		name
405184075	CV3124134	single nucleotide variant	NM_006230.4(POLD2):c.104C>T (p.Ser35Phe)	not provided [RCV003820332]	uncertain significance	7	44121950	44121950	Human		name
407480705	CV3463994	single nucleotide variant	NM_006230.4(POLD2):c.250G>C (p.Glu84Gln)	not specified [RCV004664450]	uncertain significance	7	44118035	44118035	Human		name
597897182	CV3806780	single nucleotide variant	NM_006230.4(POLD2):c.1377C>T (p.Asp459=)	not provided [RCV005152167]	likely benign	7	44114818	44114818	Human		name
597960492	CV3811904	single nucleotide variant	NM_006230.4(POLD2):c.1017C>T (p.Val339=)	not provided [RCV005163557]	uncertain significance	7	44116117	44116117	Human		name
598243878	CV3907325	single nucleotide variant	NM_006230.4(POLD2):c.295A>G (p.Lys99Glu)	not specified [RCV005258131]	uncertain significance	7	44117990	44117990	Human		name
126732956	CV1000594	single nucleotide variant	NM_006230.4(POLD2):c.905C>A (p.Thr302Asn)	not provided [RCV001310965]	uncertain significance	7	44116229	44116229	Human		name
127284549	CV1108693	single nucleotide variant	NM_006230.4(POLD2):c.877G>A (p.Asp293Asn)	not provided [RCV001449568]	uncertain significance	7	44116257	44116257	Human		name
156397217	CV1871035	single nucleotide variant	NM_006230.4(POLD2):c.758A>G (p.Gln253Arg)	not provided [RCV003068758]	uncertain significance	7	44116839	44116839	Human		name
156405575	CV1884482	single nucleotide variant	NM_006230.4(POLD2):c.641G>A (p.Gly214Asp)	not provided [RCV003070066]	uncertain significance	7	44116956	44116956	Human		name
156123091	CV1892693	single nucleotide variant	NM_006230.4(POLD2):c.502G>C (p.Asp168His)	not provided [RCV003081524]\|not specified [RCV004071761]	uncertain significance	7	44117212	44117212	Human		name
156362769	CV1899171	single nucleotide variant	NM_006230.4(POLD2):c.493G>T (p.Val165Leu)	not provided [RCV003091824]\|not specified [RCV004073167]	uncertain significance	7	44117221	44117221	Human		name
155952199	CV1900017	single nucleotide variant	NM_006230.4(POLD2):c.712G>A (p.Val238Ile)	not provided [RCV003088492]\|not specified [RCV004073260]	uncertain significance	7	44116885	44116885	Human		name
156372371	CV1901553	single nucleotide variant	NM_006230.4(POLD2):c.305C>G (p.Pro102Arg)	not provided [RCV002582527]	uncertain significance	7	44117980	44117980	Human		name
156368916	CV1905002	single nucleotide variant	NM_006230.4(POLD2):c.880G>A (p.Val294Met)	not provided [RCV002582275]\|not specified [RCV004068765]	uncertain significance	7	44116254	44116254	Human		name
156362497	CV1905129	single nucleotide variant	NM_006230.4(POLD2):c.950C>T (p.Pro317Leu)	not provided [RCV002602599]	uncertain significance	7	44116184	44116184	Human		name
156315568	CV1907349	single nucleotide variant	NM_006230.4(POLD2):c.703G>A (p.Ala235Thr)	not provided [RCV003088700]	uncertain significance	7	44116894	44116894	Human		name
156207945	CV1913318	single nucleotide variant	NM_006230.4(POLD2):c.464C>T (p.Thr155Met)	not provided [RCV002595956]	uncertain significance	7	44117621	44117621	Human		name
156446529	CV1947876	single nucleotide variant	NM_006230.4(POLD2):c.527A>G (p.Tyr176Cys)	not provided [RCV003118038]	uncertain significance	7	44117187	44117187	Human		name
156032697	CV2029849	single nucleotide variant	NM_006230.4(POLD2):c.908A>G (p.Asn303Ser)	not provided [RCV002735871]	uncertain significance	7	44116226	44116226	Human		name
156191322	CV2037965	single nucleotide variant	NM_006230.4(POLD2):c.575C>G (p.Thr192Arg)	not provided [RCV002765920]	uncertain significance	7	44117139	44117139	Human		name
155945849	CV2039631	single nucleotide variant	NM_006230.4(POLD2):c.566C>A (p.Pro189Gln)	not provided [RCV002775474]	uncertain significance	7	44117148	44117148	Human		name
155938133	CV2045225	single nucleotide variant	NM_006230.4(POLD2):c.719G>A (p.Arg240Gln)	not provided [RCV002775016]	uncertain significance	7	44116878	44116878	Human		name
156203663	CV2092617	single nucleotide variant	NM_006230.4(POLD2):c.368G>A (p.Arg123Gln)	not provided [RCV002917881]	uncertain significance	7	44117717	44117717	Human		name
156324351	CV2101306	single nucleotide variant	NM_006230.4(POLD2):c.305C>A (p.Pro102Gln)	not provided [RCV002899521]	uncertain significance	7	44117980	44117980	Human		name
156285715	CV2114852	single nucleotide variant	NM_006230.4(POLD2):c.326G>A (p.Arg109Gln)	not provided [RCV002921943]	uncertain significance	7	44117959	44117959	Human		name
155901756	CV2126982	single nucleotide variant	NM_006230.4(POLD2):c.601G>A (p.Gly201Ser)	not provided [RCV002967465]	uncertain significance	7	44116996	44116996	Human		name
155931778	CV2129195	single nucleotide variant	NM_006230.4(POLD2):c.565C>G (p.Pro189Ala)	not provided [RCV002970669]	uncertain significance	7	44117149	44117149	Human		name
155933408	CV2138509	single nucleotide variant	NM_006230.4(POLD2):c.362C>T (p.Pro121Leu)	not provided [RCV002993545]	benign\|conflicting interpretations of pathogenicity	7	44117723	44117723	Human		name
156028864	CV2139343	single nucleotide variant	NM_006230.4(POLD2):c.493G>A (p.Val165Met)	not provided [RCV002999050]	uncertain significance	7	44117221	44117221	Human		name
155983120	CV2140638	single nucleotide variant	NM_006230.4(POLD2):c.619G>A (p.Gly207Ser)	not provided [RCV002996201]\|not specified [RCV004847938]	uncertain significance	7	44116978	44116978	Human		name
155964015	CV2140968	single nucleotide variant	NM_006230.4(POLD2):c.367C>T (p.Arg123Trp)	not provided [RCV003015608]	uncertain significance	7	44117718	44117718	Human		name
156360633	CV2158761	single nucleotide variant	NM_006230.4(POLD2):c.740T>A (p.Leu247His)	not provided [RCV003031540]	uncertain significance	7	44116857	44116857	Human		name
156395607	CV2178061	single nucleotide variant	NM_006230.4(POLD2):c.374A>G (p.Lys125Arg)	not provided [RCV003051818]	uncertain significance	7	44117711	44117711	Human		name
156282540	CV2186934	single nucleotide variant	NM_006230.4(POLD2):c.347A>G (p.Asn116Ser)	not provided [RCV003044827]	uncertain significance	7	44117738	44117738	Human		name
155935489	CV2225612	single nucleotide variant	NM_006230.4(POLD2):c.730G>A (p.Ala244Thr)	not provided [RCV005099602]\|not specified [RCV004100984]	uncertain significance	7	44116867	44116867	Human		name
156279052	CV2227726	single nucleotide variant	NM_006230.4(POLD2):c.718C>T (p.Arg240Trp)	not specified [RCV004094112]	uncertain significance	7	44116879	44116879	Human		name
155920661	CV2240396	single nucleotide variant	NM_006230.4(POLD2):c.556C>A (p.Pro186Thr)	not specified [RCV004117294]	uncertain significance	7	44117158	44117158	Human		name
156048535	CV2241678	single nucleotide variant	NM_006230.4(POLD2):c.557C>T (p.Pro186Leu)	not specified [RCV004106625]	uncertain significance	7	44117157	44117157	Human		name
156242966	CV2283231	single nucleotide variant	NM_006230.4(POLD2):c.999G>C (p.Gln333His)	not specified [RCV004145903]	uncertain significance	7	44116135	44116135	Human		name
402525103	CV2868476	single nucleotide variant	NM_006230.4(POLD2):c.920C>T (p.Pro307Leu)	not provided [RCV003548050]	uncertain significance	7	44116214	44116214	Human		name
405026466	CV2889892	single nucleotide variant	NM_006230.4(POLD2):c.724A>C (p.Ile242Leu)	not provided [RCV003578018]	uncertain significance	7	44116873	44116873	Human		name
405113937	CV2896606	single nucleotide variant	NM_006230.4(POLD2):c.971C>T (p.Thr324Met)	not provided [RCV003558266]	uncertain significance	7	44116163	44116163	Human		name
402474122	CV2919644	single nucleotide variant	NM_006230.4(POLD2):c.632G>C (p.Ser211Thr)	not provided [RCV003571131]	uncertain significance	7	44116965	44116965	Human		name
405184299	CV2920422	single nucleotide variant	NM_006230.4(POLD2):c.831G>T (p.Lys277Asn)	not provided [RCV003564305]	uncertain significance	7	44116460	44116460	Human		name
405193371	CV2928379	single nucleotide variant	NM_006230.4(POLD2):c.559G>A (p.Ala187Thr)	not provided [RCV003565040]	uncertain significance	7	44117155	44117155	Human		name
402524201	CV2940319	single nucleotide variant	NM_006230.4(POLD2):c.797A>G (p.Lys266Arg)	not provided [RCV003663449]	uncertain significance	7	44116494	44116494	Human		name
405078574	CV2945404	single nucleotide variant	NM_006230.4(POLD2):c.721G>A (p.Val241Ile)	not provided [RCV003664434]	uncertain significance	7	44116876	44116876	Human		name
402490597	CV2949017	single nucleotide variant	NM_006230.4(POLD2):c.545C>T (p.Ala182Val)	not provided [RCV003660508]	uncertain significance	7	44117169	44117169	Human		name
405118496	CV2949792	single nucleotide variant	NM_006230.4(POLD2):c.560C>T (p.Ala187Val)	not provided [RCV003667183]	uncertain significance	7	44117154	44117154	Human		name
405135850	CV2958110	single nucleotide variant	NM_006230.4(POLD2):c.701G>A (p.Ser234Asn)	not provided [RCV003672810]	uncertain significance	7	44116896	44116896	Human		name
402494599	CV2978492	duplication	NM_006230.4(POLD2):c.1393dup (p.Leu465fs)	not provided [RCV003714119]	uncertain significance	7	44114801	44114802	Human		name
405248018	CV2983898	single nucleotide variant	NM_006230.4(POLD2):c.682G>A (p.Asp228Asn)	not provided [RCV003685862]	uncertain significance	7	44116915	44116915	Human		name
402482164	CV3001246	single nucleotide variant	NM_006230.4(POLD2):c.992C>T (p.Pro331Leu)	not provided [RCV003686698]	uncertain significance	7	44116142	44116142	Human		name
405182435	CV3024475	single nucleotide variant	NM_006230.4(POLD2):c.731C>A (p.Ala244Asp)	not provided [RCV003705671]	uncertain significance	7	44116866	44116866	Human		name
402502229	CV3035600	single nucleotide variant	NM_006230.4(POLD2):c.534T>G (p.Phe178Leu)	not provided [RCV003714863]	uncertain significance	7	44117180	44117180	Human		name
405222330	CV3038746	single nucleotide variant	NM_006230.4(POLD2):c.394G>A (p.Glu132Lys)	not provided [RCV003710159]	uncertain significance	7	44117691	44117691	Human		name
405246181	CV3047980	single nucleotide variant	NM_006230.4(POLD2):c.874G>A (p.Val292Met)	not provided [RCV003720484]	uncertain significance	7	44116260	44116260	Human		name
405036847	CV3057574	single nucleotide variant	NM_006230.4(POLD2):c.541C>A (p.Leu181Ile)	not provided [RCV003739596]	uncertain significance	7	44117173	44117173	Human		name
405211276	CV3059168	single nucleotide variant	NM_006230.4(POLD2):c.776A>G (p.Asn259Ser)	not provided [RCV003732046]	uncertain significance	7	44116821	44116821	Human		name
405191957	CV3070037	single nucleotide variant	NM_006230.4(POLD2):c.337G>A (p.Glu113Lys)	not provided [RCV003729806]	uncertain significance	7	44117948	44117948	Human		name
405197090	CV3168223	single nucleotide variant	NM_006230.4(POLD2):c.325C>T (p.Arg109Trp)	not provided [RCV003860355]\|not specified [RCV004848000]	uncertain significance	7	44117960	44117960	Human		name
405212594	CV3169781	single nucleotide variant	NM_006230.4(POLD2):c.562C>A (p.Pro188Thr)	not provided [RCV003862380]	uncertain significance	7	44117152	44117152	Human		name
402482356	CV3170785	single nucleotide variant	NM_006230.4(POLD2):c.892G>A (p.Glu298Lys)	not provided [RCV003875987]	uncertain significance	7	44116242	44116242	Human		name
402474410	CV3182747	single nucleotide variant	NM_006230.4(POLD2):c.421C>T (p.Arg141Cys)	not provided [RCV003874990]	uncertain significance	7	44117664	44117664	Human		name
405658811	CV3373333	single nucleotide variant	NM_006230.4(POLD2):c.607G>A (p.Gly203Ser)	not specified [RCV004512194]	uncertain significance	7	44116990	44116990	Human		name
405658814	CV3373334	single nucleotide variant	NM_006230.4(POLD2):c.685G>A (p.Glu229Lys)	not specified [RCV004512195]	uncertain significance	7	44116912	44116912	Human		name
407480714	CV3463996	single nucleotide variant	NM_006230.4(POLD2):c.395A>G (p.Glu132Gly)	not provided [RCV005102382]\|not specified [RCV004664452]	uncertain significance	7	44117690	44117690	Human		name
597900734	CV3741112	single nucleotide variant	NM_006230.4(POLD2):c.502G>A (p.Asp168Asn)	not provided [RCV005072275]	uncertain significance	7	44117212	44117212	Human		name
597929972	CV3745790	single nucleotide variant	NM_006230.4(POLD2):c.566C>T (p.Pro189Leu)	not provided [RCV005075775]	uncertain significance	7	44117148	44117148	Human		name
597943694	CV3765872	single nucleotide variant	NM_006230.4(POLD2):c.559G>C (p.Ala187Pro)	not provided [RCV005119250]	uncertain significance	7	44117155	44117155	Human		name
597874940	CV3766242	single nucleotide variant	NM_006230.4(POLD2):c.914C>T (p.Thr305Met)	not provided [RCV005108374]	uncertain significance	7	44116220	44116220	Human		name
597878176	CV3776252	single nucleotide variant	NM_006230.4(POLD2):c.668C>T (p.Thr223Met)	not provided [RCV005123780]	uncertain significance	7	44116929	44116929	Human		name
597935107	CV3777164	single nucleotide variant	NM_006230.4(POLD2):c.611T>G (p.Leu204Arg)	not provided [RCV005117323]	uncertain significance	7	44116986	44116986	Human		name
597931680	CV3789281	single nucleotide variant	NM_006230.4(POLD2):c.785A>G (p.Lys262Arg)	not provided [RCV005131562]	uncertain significance	7	44116506	44116506	Human		name
597962917	CV3795864	single nucleotide variant	NM_006230.4(POLD2):c.422G>A (p.Arg141His)	not provided [RCV005139354]	uncertain significance	7	44117663	44117663	Human		name
597915934	CV3814654	single nucleotide variant	NM_006230.4(POLD2):c.335G>T (p.Ser112Ile)	not provided [RCV005154969]	uncertain significance	7	44117950	44117950	Human		name
597958550	CV3814840	single nucleotide variant	NM_006230.4(POLD2):c.497G>A (p.Arg166Lys)	not provided [RCV005162965]	uncertain significance	7	44117217	44117217	Human		name
597929544	CV3816269	single nucleotide variant	NM_006230.4(POLD2):c.757C>T (p.Gln253Ter)	not provided [RCV005156850]	uncertain significance	7	44116840	44116840	Human		name
597857389	CV3816739	single nucleotide variant	NM_006230.4(POLD2):c.737A>G (p.Asn246Ser)	not provided [RCV005146312]	uncertain significance	7	44116860	44116860	Human		name
597957018	CV3818118	single nucleotide variant	NM_006230.4(POLD2):c.553A>C (p.Lys185Gln)	not provided [RCV005162569]	uncertain significance	7	44117161	44117161	Human		name
597878982	CV3826186	single nucleotide variant	NM_006230.4(POLD2):c.632G>A (p.Ser211Asn)	not provided [RCV005177882]	uncertain significance	7	44116965	44116965	Human		name
597898405	CV3826626	single nucleotide variant	NM_006230.4(POLD2):c.322C>G (p.Leu108Val)	not provided [RCV005180759]	uncertain significance	7	44117963	44117963	Human		name
597909748	CV3830092	single nucleotide variant	NM_006230.4(POLD2):c.896T>C (p.Phe299Ser)	not provided [RCV005182662]	uncertain significance	7	44116238	44116238	Human		name
597971368	CV3833003	single nucleotide variant	NM_006230.4(POLD2):c.308T>C (p.Leu103Pro)	not provided [RCV005166900]	uncertain significance	7	44117977	44117977	Human		name
597912093	CV3850623	single nucleotide variant	NM_006230.4(POLD2):c.671G>A (p.Gly224Glu)	not provided [RCV005203771]	uncertain significance	7	44116926	44116926	Human		name
597916691	CV3851637	single nucleotide variant	NM_006230.4(POLD2):c.635T>A (p.Leu212Gln)	not provided [RCV005204398]	uncertain significance	7	44116962	44116962	Human		name
597934190	CV3858734	deletion	NM_006230.4(POLD2):c.1158del (p.Phe387fs)	not provided [RCV005207204]	uncertain significance	7	44115386	44115386	Human		name
598243887	CV3907326	single nucleotide variant	NM_006230.4(POLD2):c.738C>A (p.Asn246Lys)	not specified [RCV005258132]	uncertain significance	7	44116859	44116859	Human		name
598243896	CV3907327	single nucleotide variant	NM_006230.4(POLD2):c.623G>A (p.Gly208Glu)	not specified [RCV005258133]	uncertain significance	7	44116974	44116974	Human		name
156372924	CV1921006	single nucleotide variant	NM_006230.4(POLD2):c.1309G>A (p.Ala437Thr)	not provided [RCV002603331]\|not specified [RCV004661577]	uncertain significance	7	44114886	44114886	Human		name
156446559	CV1947904	single nucleotide variant	NM_006230.4(POLD2):c.1327C>T (p.Arg443Cys)	not provided [RCV003118068]	uncertain significance	7	44114868	44114868	Human		name
156352715	CV2015474	single nucleotide variant	NM_006230.4(POLD2):c.1397G>A (p.Gly466Glu)	not provided [RCV002720303]	uncertain significance	7	44114798	44114798	Human		name
155934426	CV2035287	single nucleotide variant	NM_006230.4(POLD2):c.1328G>A (p.Arg443His)	not provided [RCV002751347]	uncertain significance	7	44114867	44114867	Human		name
156196143	CV2038261	single nucleotide variant	NM_006230.4(POLD2):c.1374G>C (p.Glu458Asp)	not provided [RCV002766073]	uncertain significance	7	44114821	44114821	Human		name
156174501	CV2051878	single nucleotide variant	NM_006230.4(POLD2):c.1142C>T (p.Thr381Ile)	not provided [RCV002828097]	uncertain significance	7	44115771	44115771	Human		name
156130235	CV2084847	single nucleotide variant	NM_006230.4(POLD2):c.1378G>C (p.Asp460His)	not provided [RCV002871607]	uncertain significance	7	44114817	44114817	Human		name
156109348	CV2085766	single nucleotide variant	NM_006230.4(POLD2):c.1097A>G (p.Glu366Gly)	not provided [RCV002848387]	uncertain significance	7	44115816	44115816	Human		name
156090732	CV2092993	single nucleotide variant	NM_006230.4(POLD2):c.1358C>T (p.Ser453Leu)	not provided [RCV002926670]	uncertain significance	7	44114837	44114837	Human		name
156142175	CV2113071	single nucleotide variant	NM_006230.4(POLD2):c.1061G>A (p.Arg354Gln)	not provided [RCV002914949]	uncertain significance	7	44115852	44115852	Human		name
156194850	CV2113597	single nucleotide variant	NM_006230.4(POLD2):c.1145T>A (p.Leu382Gln)	not provided [RCV002957174]	uncertain significance	7	44115768	44115768	Human		name
156309835	CV2119915	single nucleotide variant	NM_006230.4(POLD2):c.1300A>G (p.Thr434Ala)	not provided [RCV002962555]	uncertain significance	7	44114895	44114895	Human		name
155987466	CV2137044	single nucleotide variant	NM_006230.4(POLD2):c.1301C>G (p.Thr434Arg)	not provided [RCV002996400]	uncertain significance	7	44114894	44114894	Human		name
156197642	CV2159126	single nucleotide variant	NM_006230.4(POLD2):c.1307C>T (p.Thr436Ile)	not provided [RCV003041860]	uncertain significance	7	44114888	44114888	Human		name
156075984	CV2173492	single nucleotide variant	NM_006230.4(POLD2):c.1402G>A (p.Gly468Ser)	not provided [RCV003053866]	uncertain significance	7	44114793	44114793	Human		name
156175100	CV2181403	single nucleotide variant	NM_006230.4(POLD2):c.1366G>A (p.Gly456Arg)	not provided [RCV003057344]	uncertain significance	7	44114829	44114829	Human		name
156038801	CV2260087	single nucleotide variant	NM_006230.4(POLD2):c.1049G>C (p.Ser350Thr)	not specified [RCV004119091]	uncertain significance	7	44115864	44115864	Human		name
401717956	CV2704100	single nucleotide variant	NM_006230.4(POLD2):c.1114C>T (p.Arg372Cys)	not provided [RCV003549045]\|not specified [RCV004308968]	uncertain significance	7	44115799	44115799	Human		name
401899751	CV2762140	single nucleotide variant	NM_006230.4(POLD2):c.1369G>A (p.Ala457Thr)	not provided [RCV005104073]\|not specified [RCV004341954]	uncertain significance	7	44114826	44114826	Human		name
405067551	CV2936775	single nucleotide variant	NM_006230.4(POLD2):c.1060C>T (p.Arg354Ter)	not provided [RCV003659219]	uncertain significance	7	44115853	44115853	Human		name
405112768	CV2939041	single nucleotide variant	NM_006230.4(POLD2):c.1196C>T (p.Pro399Leu)	not provided [RCV003666527]	uncertain significance	7	44115348	44115348	Human		name
405127341	CV2939574	single nucleotide variant	NM_006230.4(POLD2):c.1205A>G (p.Tyr402Cys)	not provided [RCV003672030]	uncertain significance	7	44115339	44115339	Human		name
405246125	CV2965705	single nucleotide variant	NM_006230.4(POLD2):c.1045G>A (p.Val349Met)	not provided [RCV003685348]	uncertain significance	7	44115868	44115868	Human		name
405193689	CV2975122	single nucleotide variant	NM_006230.4(POLD2):c.1072A>G (p.Met358Val)	not provided [RCV003677441]	uncertain significance	7	44115841	44115841	Human		name
405216466	CV2978065	single nucleotide variant	NM_006230.4(POLD2):c.1397G>C (p.Gly466Ala)	not provided [RCV003709385]	uncertain significance	7	44114798	44114798	Human		name
405178755	CV3027606	single nucleotide variant	NM_006230.4(POLD2):c.1060C>G (p.Arg354Gly)	not provided [RCV003705332]	uncertain significance	7	44115853	44115853	Human		name
405169441	CV3029252	single nucleotide variant	NM_006230.4(POLD2):c.1235C>T (p.Ser412Phe)	not provided [RCV003704565]	uncertain significance	7	44115309	44115309	Human		name
405205099	CV3033640	single nucleotide variant	NM_006230.4(POLD2):c.1220C>T (p.Thr407Ile)	not provided [RCV003707901]	uncertain significance	7	44115324	44115324	Human		name
402486076	CV3033916	single nucleotide variant	NM_006230.4(POLD2):c.1383C>G (p.Asp461Glu)	not provided [RCV003713308]	uncertain significance	7	44114812	44114812	Human		name
405085728	CV3047731	single nucleotide variant	NM_006230.4(POLD2):c.1247G>A (p.Arg416Gln)	not provided [RCV003717456]	uncertain significance	7	44115297	44115297	Human		name
405133821	CV3051825	single nucleotide variant	NM_006230.4(POLD2):c.1108C>T (p.Arg370Trp)	not provided [RCV003725064]	uncertain significance	7	44115805	44115805	Human		name
405244947	CV3054832	single nucleotide variant	NM_006230.4(POLD2):c.1378G>A (p.Asp460Asn)	not provided [RCV003720141]\|not specified [RCV004374035]	uncertain significance	7	44114817	44114817	Human		name
405206013	CV3068299	single nucleotide variant	NM_006230.4(POLD2):c.1220C>A (p.Thr407Asn)	not provided [RCV003731318]\|not specified [RCV004847987]	uncertain significance	7	44115324	44115324	Human		name
405658805	CV3373331	single nucleotide variant	NM_006230.4(POLD2):c.1318G>A (p.Val440Met)	not specified [RCV004512192]	uncertain significance	7	44114877	44114877	Human		name
597745116	CV3591010	single nucleotide variant	NM_006230.4(POLD2):c.1240A>G (p.Ile414Val)	not provided [RCV005107720]\|not specified [RCV004845285]	likely benign\|uncertain significance	7	44115304	44115304	Human		name
597859951	CV3770022	single nucleotide variant	NM_006230.4(POLD2):c.1199A>G (p.His400Arg)	not provided [RCV005105874]	uncertain significance	7	44115345	44115345	Human		name
597858440	CV3816710	single nucleotide variant	NM_006230.4(POLD2):c.1253C>G (p.Pro418Arg)	not provided [RCV005146283]	uncertain significance	7	44114942	44114942	Human		name
597876878	CV3825698	single nucleotide variant	NM_006230.4(POLD2):c.1247G>C (p.Arg416Pro)	not provided [RCV005177572]	uncertain significance	7	44115297	44115297	Human		name
597910298	CV3830172	single nucleotide variant	NM_006230.4(POLD2):c.1109G>A (p.Arg370Gln)	not provided [RCV005182742]	uncertain significance	7	44115804	44115804	Human		name
597971673	CV3833141	single nucleotide variant	NM_006230.4(POLD2):c.1079A>G (p.Asp360Gly)	not provided [RCV005167038]	uncertain significance	7	44115834	44115834	Human		name
405204038	CV3033405	deletion	NM_006230.4(POLD2):c.133_135del (p.Ser45del)	not provided [RCV003707769]	uncertain significance	7	44121919	44121921	Human		name
156245165	CV2029353	duplication	NM_006230.4(POLD2):c.1400dup (p.Ter470LeuextTer?)	not provided [RCV002745802]	uncertain significance	7	44114794	44114795	Human		name
156377155	CV2189117	deletion	NM_006230.4(POLD2):c.100_105del (p.Asn34_Ser35del)	not provided [RCV003050199]	uncertain significance	7	44121949	44121954	Human		name
156108577	CV2058117	duplication	NM_006230.4(POLD2):c.1378_1381dup (p.Asp461delinsGlyTer)	not provided [RCV002824831]	uncertain significance	7	44114813	44114814	Human		name

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