Bub3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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441 records found for search term Bub3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405277224	CV3217708	single nucleotide variant	NM_004725.4(BUB3):c.266-7T>C	BUB3-related disorder [RCV003974773]	benign	10	123157722	123157722	Human		name , trait , alternate_id
15187407	CV744553	single nucleotide variant	NM_004725.4(BUB3):c.972-7C>T	not provided [RCV000909081]	benign	10	123163813	123163813	Human		name
155708036	CV1822410	single nucleotide variant	NM_004725.4(BUB3):c.6C>T (p.Thr2=)	not specified [RCV004055125]	likely benign	10	123154923	123154923	Human		name
401868213	CV2787351	single nucleotide variant	NM_004725.4(BUB3):c.6C>G (p.Thr2=)	not specified [RCV004366253]	likely benign	10	123154923	123154923	Human		name
155719438	CV1837368	single nucleotide variant	NM_004725.4(BUB3):c.15C>T (p.Asn5=)	not specified [RCV004057414]	likely benign	10	123154932	123154932	Human		name
155692721	CV1845772	single nucleotide variant	NM_004725.4(BUB3):c.25C>T (p.Leu9=)	not specified [RCV004062888]	likely benign	10	123154942	123154942	Human		name
155716090	CV1785090	single nucleotide variant	NM_004725.4(BUB3):c.30C>T (p.Asn10=)	not specified [RCV004048332]	likely benign	10	123154947	123154947	Human		name
155664429	CV1786014	single nucleotide variant	NM_004725.4(BUB3):c.33G>A (p.Gln11=)	not specified [RCV004047927]	likely benign	10	123154950	123154950	Human		name
155664231	CV1786475	single nucleotide variant	NM_004725.4(BUB3):c.36A>G (p.Pro12=)	not specified [RCV004049699]	likely benign	10	123154953	123154953	Human		name
155696897	CV1793902	single nucleotide variant	NM_004725.4(BUB3):c.39C>T (p.Pro13=)	not specified [RCV004050575]	likely benign	10	123154956	123154956	Human		name
155674365	CV1810131	single nucleotide variant	NM_004725.4(BUB3):c.54C>T (p.Ser18=)	not specified [RCV004053157]	likely benign	10	123154971	123154971	Human		name
155704270	CV1810658	single nucleotide variant	NM_004725.4(BUB3):c.57C>G (p.Ser19=)	not specified [RCV004054109]	likely benign	10	123154974	123154974	Human		name
155665771	CV1813903	single nucleotide variant	NM_004725.4(BUB3):c.7G>A (p.Gly3Ser)	not specified [RCV004055371]	uncertain significance	10	123154924	123154924	Human		name
155697939	CV1816809	single nucleotide variant	NM_004725.4(BUB3):c.81C>G (p.Ser27=)	not specified [RCV004055539]	likely benign	10	123154998	123154998	Human		name
155710817	CV1817762	single nucleotide variant	NM_004725.4(BUB3):c.90G>T (p.Leu30=)	not specified [RCV004055001]	likely benign	10	123155007	123155007	Human		name
155728919	CV1822699	single nucleotide variant	NM_004725.4(BUB3):c.72C>G (p.Pro24=)	not specified [RCV004055865]	likely benign	10	123154989	123154989	Human		name
155713057	CV1824366	single nucleotide variant	NM_004725.4(BUB3):c.84G>A (p.Gln28=)	not specified [RCV004056197]	likely benign	10	123155001	123155001	Human		name
155690995	CV1825092	single nucleotide variant	NM_004725.4(BUB3):c.93T>A (p.Leu31=)	not specified [RCV004056775]	likely benign	10	123155010	123155010	Human		name
155702229	CV1825307	single nucleotide variant	NM_004725.4(BUB3):c.96C>A (p.Val32=)	not specified [RCV004057536]	likely benign	10	123155013	123155013	Human		name
155702273	CV1825313	single nucleotide variant	NM_004725.4(BUB3):c.96C>T (p.Val32=)	not specified [RCV004057537]	likely benign	10	123155013	123155013	Human		name
155731056	CV1825883	single nucleotide variant	NM_004725.4(BUB3):c.99C>T (p.Ser33=)	not specified [RCV004057757]	likely benign	10	123155016	123155016	Human		name
329363352	CV2429075	single nucleotide variant	NM_004725.4(BUB3):c.39C>G (p.Pro13=)	not specified [RCV004247522]	likely benign	10	123154956	123154956	Human		name
329363361	CV2429078	single nucleotide variant	NM_004725.4(BUB3):c.75C>T (p.Asn25=)	not specified [RCV004247525]	likely benign	10	123154992	123154992	Human		name
329389732	CV2467995	single nucleotide variant	NM_004725.4(BUB3):c.78C>T (p.Thr26=)	not specified [RCV004281422]	likely benign	10	123154995	123154995	Human		name
329389751	CV2468005	single nucleotide variant	NM_004725.4(BUB3):c.36A>C (p.Pro12=)	not specified [RCV004281428]	likely benign	10	123154953	123154953	Human		name
329389755	CV2468008	single nucleotide variant	NM_004725.4(BUB3):c.88C>T (p.Leu30=)	not specified [RCV004281429]	likely benign	10	123155005	123155005	Human		name
401775014	CV2723948	single nucleotide variant	NM_004725.4(BUB3):c.93T>G (p.Leu31=)	not specified [RCV004326117]	likely benign	10	123155010	123155010	Human		name
401868197	CV2787345	single nucleotide variant	NM_004725.4(BUB3):c.72C>A (p.Pro24=)	not specified [RCV004366248]	likely benign	10	123154989	123154989	Human		name
405690720	CV3386887	single nucleotide variant	NM_004725.4(BUB3):c.87C>T (p.Phe29=)	not specified [RCV004519248]	likely benign	10	123155004	123155004	Human		name
407490147	CV3418014	single nucleotide variant	NM_004725.4(BUB3):c.42G>A (p.Glu14=)	not specified [RCV004604326]	likely benign	10	123154959	123154959	Human		name
155666401	CV1793112	single nucleotide variant	NM_004725.4(BUB3):c.114C>G (p.Ser38=)	not specified [RCV004049297]	likely benign	10	123155031	123155031	Human		name
155666646	CV1793180	single nucleotide variant	NM_004725.4(BUB3):c.114C>T (p.Ser38=)	not specified [RCV004049308]	likely benign	10	123155031	123155031	Human		name
155739037	CV1801542	single nucleotide variant	NM_004725.4(BUB3):c.117G>T (p.Val39=)	not specified [RCV004051512]	likely benign	10	123155034	123155034	Human		name
155745354	CV1802784	single nucleotide variant	NM_004725.4(BUB3):c.11C>G (p.Ser4Cys)	not specified [RCV004052448]	uncertain significance	10	123154928	123154928	Human		name
155679809	CV1807058	single nucleotide variant	NM_004725.4(BUB3):c.120T>C (p.Arg40=)	not specified [RCV004054192]	likely benign	10	123155037	123155037	Human		name
155698883	CV1824484	single nucleotide variant	NM_004725.4(BUB3):c.126C>T (p.Tyr42=)	not specified [RCV004054839]	likely benign	10	123155043	123155043	Human		name
155732100	CV1826367	single nucleotide variant	NM_004725.4(BUB3):c.102C>T (p.Ser34=)	not specified [RCV004058806]	likely benign	10	123155019	123155019	Human		name
155689030	CV1826630	single nucleotide variant	NM_004725.4(BUB3):c.141C>T (p.Asn47=)	not specified [RCV004057229]	likely benign	10	123155058	123155058	Human		name
155691349	CV1827273	single nucleotide variant	NM_004725.4(BUB3):c.150G>A (p.Arg50=)	not specified [RCV004058587]	likely benign	10	123155067	123155067	Human		name
155691422	CV1827285	single nucleotide variant	NM_004725.4(BUB3):c.150G>T (p.Arg50=)	not specified [RCV004058589]	likely benign	10	123155067	123155067	Human		name
155701127	CV1828575	single nucleotide variant	NM_004725.4(BUB3):c.174C>T (p.Ala58=)	not specified [RCV004061278]	likely benign	10	123155091	123155091	Human		name
155720084	CV1830678	single nucleotide variant	NM_004725.4(BUB3):c.156G>A (p.Lys52=)	not specified [RCV004059189]	likely benign	10	123155073	123155073	Human		name
155738006	CV1831850	single nucleotide variant	NM_004725.4(BUB3):c.180G>A (p.Leu60=)	not specified [RCV004059315]	likely benign	10	123155097	123155097	Human		name
155738016	CV1831858	single nucleotide variant	NM_004725.4(BUB3):c.180G>C (p.Leu60=)	not specified [RCV004059320]	likely benign	10	123155097	123155097	Human		name
155709629	CV1832692	single nucleotide variant	NM_004725.4(BUB3):c.138C>G (p.Ala46=)	not specified [RCV004057074]	likely benign	10	123155055	123155055	Human		name
155707218	CV1833380	single nucleotide variant	NM_004725.4(BUB3):c.153C>G (p.Leu51=)	not specified [RCV004059006]	likely benign	10	123155070	123155070	Human		name
155707244	CV1833384	single nucleotide variant	NM_004725.4(BUB3):c.153C>T (p.Leu51=)	not specified [RCV004059008]	likely benign	10	123155070	123155070	Human		name
155700373	CV1836729	single nucleotide variant	NM_004725.4(BUB3):c.144C>G (p.Ser48=)	not specified [RCV004057897]	likely benign	10	123155061	123155061	Human		name
155745146	CV1838029	single nucleotide variant	NM_004725.4(BUB3):c.168C>A (p.Thr56=)	not specified [RCV004059925]	likely benign	10	123155085	123155085	Human		name
155724292	CV1838034	single nucleotide variant	NM_004725.4(BUB3):c.168C>T (p.Thr56=)	not specified [RCV004059927]	likely benign	10	123155085	123155085	Human		name
155731267	CV1838590	single nucleotide variant	NM_004725.4(BUB3):c.177C>G (p.Val59=)	not specified [RCV004061434]	likely benign	10	123155094	123155094	Human		name
155733436	CV1842617	single nucleotide variant	NM_004725.4(BUB3):c.189C>G (p.Ala63=)	not specified [RCV004060749]	likely benign	10	123155106	123155106	Human		name
155676566	CV1843687	single nucleotide variant	NM_004725.4(BUB3):c.204G>C (p.Thr68=)	not specified [RCV004059638]	likely benign	10	123155666	123155666	Human		name
155695439	CV1844626	single nucleotide variant	NM_004725.4(BUB3):c.225A>C (p.Leu75=)	not specified [RCV004061940]	likely benign	10	123155687	123155687	Human		name
155717259	CV1844892	single nucleotide variant	NM_004725.4(BUB3):c.235T>C (p.Leu79=)	not specified [RCV004063292]	likely benign	10	123155697	123155697	Human		name
155692696	CV1845765	single nucleotide variant	NM_004725.4(BUB3):c.25C>A (p.Leu9Met)	not specified [RCV004062884]	uncertain significance	10	123154942	123154942	Human		name
155684070	CV1849512	single nucleotide variant	NM_004725.4(BUB3):c.198T>C (p.Asp66=)	not specified [RCV004061676]	likely benign	10	123155660	123155660	Human		name
155685753	CV1850303	single nucleotide variant	NM_004725.4(BUB3):c.210C>A (p.Ala70=)	not specified [RCV004060359]	likely benign	10	123155672	123155672	Human		name
155684833	CV1850758	single nucleotide variant	NM_004725.4(BUB3):c.228T>C (p.Asp76=)	not specified [RCV004062569]	likely benign	10	123155690	123155690	Human		name
155678926	CV1854087	single nucleotide variant	NM_004725.4(BUB3):c.273T>C (p.Leu91=)	not specified [RCV004064074]	likely benign	10	123157736	123157736	Human		name
155664117	CV1855124	single nucleotide variant	NM_004725.4(BUB3):c.282C>A (p.Thr94=)	not specified [RCV004062355]	likely benign	10	123157745	123157745	Human		name
155689683	CV1856515	single nucleotide variant	NM_004725.4(BUB3):c.297C>T (p.Ile99=)	not specified [RCV004065416]	likely benign	10	123157760	123157760	Human		name
329363981	CV2429081	single nucleotide variant	NM_004725.4(BUB3):c.102C>G (p.Ser34=)	not specified [RCV004247528]	likely benign	10	123155019	123155019	Human		name
329363995	CV2429085	single nucleotide variant	NM_004725.4(BUB3):c.153C>A (p.Leu51=)	not specified [RCV004247532]	likely benign	10	123155070	123155070	Human		name
329389786	CV2465557	single nucleotide variant	NM_004725.4(BUB3):c.111G>A (p.Thr37=)	not specified [RCV004281439]	likely benign	10	123155028	123155028	Human		name
329389759	CV2468010	single nucleotide variant	NM_004725.4(BUB3):c.171C>T (p.Gly57=)	not specified [RCV004281430]	likely benign	10	123155088	123155088	Human		name
329389782	CV2468022	single nucleotide variant	NM_004725.4(BUB3):c.258T>C (p.Thr86=)	not specified [RCV004281437]	likely benign	10	123155720	123155720	Human		name
401899086	CV2786041	single nucleotide variant	NM_004725.4(BUB3):c.148C>A (p.Arg50=)	not specified [RCV004359865]	likely benign	10	123155065	123155065	Human		name
405690372	CV3386851	single nucleotide variant	NM_004725.4(BUB3):c.129T>C (p.Asp43=)	not specified [RCV004519214]	likely benign	10	123155046	123155046	Human		name
405690380	CV3386852	single nucleotide variant	NM_004725.4(BUB3):c.135G>A (p.Pro45=)	not specified [RCV004519215]	likely benign	10	123155052	123155052	Human		name
405690385	CV3386853	single nucleotide variant	NM_004725.4(BUB3):c.144C>T (p.Ser48=)	not specified [RCV004519216]	likely benign	10	123155061	123155061	Human		name
405690421	CV3386859	single nucleotide variant	NM_004725.4(BUB3):c.255C>T (p.Asn85=)	not specified [RCV004519222]	likely benign	10	123155717	123155717	Human		name
407490115	CV3418005	single nucleotide variant	NM_004725.4(BUB3):c.246T>C (p.His82=)	not specified [RCV004604318]	likely benign	10	123155708	123155708	Human		name
407490127	CV3418008	single nucleotide variant	NM_004725.4(BUB3):c.186C>T (p.Cys62=)	not specified [RCV004604321]	likely benign	10	123155103	123155103	Human		name
407490144	CV3418013	single nucleotide variant	NM_004725.4(BUB3):c.291C>T (p.Ala97=)	not specified [RCV004604325]	likely benign	10	123157754	123157754	Human		name
597792909	CV3643665	single nucleotide variant	NM_004725.4(BUB3):c.111G>T (p.Thr37=)	not specified [RCV004902801]	likely benign	10	123155028	123155028	Human		name
597750036	CV3643669	single nucleotide variant	NM_004725.4(BUB3):c.250T>C (p.Leu84=)	not specified [RCV004892479]	likely benign	10	123155712	123155712	Human		name
597792918	CV3643670	single nucleotide variant	NM_004725.4(BUB3):c.183C>T (p.Asp61=)	not specified [RCV004902804]	likely benign	10	123155100	123155100	Human		name
597792935	CV3643683	single nucleotide variant	NM_004725.4(BUB3):c.264A>G (p.Gln88=)	not specified [RCV004902810]	likely benign	10	123155726	123155726	Human		name
597792938	CV3643684	single nucleotide variant	NM_004725.4(BUB3):c.177C>T (p.Val59=)	not specified [RCV004902811]	likely benign	10	123155094	123155094	Human		name
597750077	CV3643692	single nucleotide variant	NM_004725.4(BUB3):c.114C>A (p.Ser38=)	not specified [RCV004892487]	likely benign	10	123155031	123155031	Human		name
155664333	CV1785987	single nucleotide variant	NM_004725.4(BUB3):c.339T>C (p.Thr113=)	not specified [RCV004047921]	likely benign	10	123157802	123157802	Human		name
155686726	CV1787271	single nucleotide variant	NM_004725.4(BUB3):c.390T>C (p.Asn130=)	not specified [RCV004050381]	likely benign	10	123157853	123157853	Human		name
155704987	CV1787700	single nucleotide variant	NM_004725.4(BUB3):c.40G>A (p.Glu14Lys)	not specified [RCV004051330]	uncertain significance	10	123154957	123154957	Human		name
155701211	CV1788254	single nucleotide variant	NM_004725.4(BUB3):c.318A>G (p.Pro106=)	not specified [RCV004048877]	likely benign	10	123157781	123157781	Human		name
155722502	CV1790010	single nucleotide variant	NM_004725.4(BUB3):c.384T>C (p.Pro128=)	not specified [RCV004048213]	likely benign	10	123157847	123157847	Human		name
155726268	CV1791044	single nucleotide variant	NM_004725.4(BUB3):c.420A>G (p.Val140=)	not specified [RCV004051892]	likely benign	10	123160409	123160409	Human		name
155742126	CV1791255	single nucleotide variant	NM_004725.4(BUB3):c.438T>C (p.Ser146=)	not specified [RCV004050615]	likely benign	10	123160427	123160427	Human		name
155717439	CV1792271	single nucleotide variant	NM_004725.4(BUB3):c.330G>A (p.Val110=)	not specified [RCV004049519]	likely benign	10	123157793	123157793	Human		name
155677208	CV1792843	single nucleotide variant	NM_004725.4(BUB3):c.360T>C (p.Val120=)	not specified [RCV004049242]	likely benign	10	123157823	123157823	Human		name
155744525	CV1793090	single nucleotide variant	NM_004725.4(BUB3):c.363A>G (p.Lys121=)	not specified [RCV004049293]	likely benign	10	123157826	123157826	Human		name
155721125	CV1793376	single nucleotide variant	NM_004725.4(BUB3):c.37C>A (p.Pro13Thr)	not specified [RCV004048111]	uncertain significance	10	123154954	123154954	Human		name
155676441	CV1796140	single nucleotide variant	NM_004725.4(BUB3):c.35C>A (p.Pro12Gln)	not specified [RCV004049209]	uncertain significance	10	123154952	123154952	Human		name
155736372	CV1798742	single nucleotide variant	NM_004725.4(BUB3):c.46G>A (p.Gly16Ser)	not specified [RCV004052002]	uncertain significance	10	123154963	123154963	Human		name
155739711	CV1799149	single nucleotide variant	NM_004725.4(BUB3):c.493C>A (p.Arg165=)	not specified [RCV004050260]	likely benign	10	123160482	123160482	Human		name
155724113	CV1799388	single nucleotide variant	NM_004725.4(BUB3):c.516G>A (p.Gln172=)	not specified [RCV004051633]	likely benign	10	123160505	123160505	Human		name
155697419	CV1800952	single nucleotide variant	NM_004725.4(BUB3):c.603C>T (p.Gly201=)	not specified [RCV004052616]	likely benign	10	123162262	123162262	Human		name
155697629	CV1800991	single nucleotide variant	NM_004725.4(BUB3):c.604C>A (p.Arg202=)	not specified [RCV004052629]	likely benign	10	123162263	123162263	Human		name
155735413	CV1801642	single nucleotide variant	NM_004725.4(BUB3):c.462A>G (p.Thr154=)	not specified [RCV004051533]	likely benign	10	123160451	123160451	Human		name
155734261	CV1802244	single nucleotide variant	NM_004725.4(BUB3):c.489C>T (p.Asp163=)	not specified [RCV004050175]	likely benign	10	123160478	123160478	Human		name
155713413	CV1802447	single nucleotide variant	NM_004725.4(BUB3):c.510G>A (p.Val170=)	not specified [RCV004051027]	likely benign	10	123160499	123160499	Human		name
155666322	CV1804286	single nucleotide variant	NM_004725.4(BUB3):c.624G>A (p.Leu208=)	not specified [RCV004053444]	likely benign	10	123162283	123162283	Human		name
155724541	CV1804701	single nucleotide variant	NM_004725.4(BUB3):c.654G>A (p.Lys218=)	not specified [RCV004054390]	likely benign	10	123162313	123162313	Human		name
155738066	CV1804995	single nucleotide variant	NM_004725.4(BUB3):c.456G>A (p.Val152=)	not specified [RCV004051442]	likely benign	10	123160445	123160445	Human		name
155710884	CV1805874	single nucleotide variant	NM_004725.4(BUB3):c.504T>C (p.Gly168=)	not specified [RCV004050946]	likely benign	10	123160493	123160493	Human		name
155712016	CV1806044	single nucleotide variant	NM_004725.4(BUB3):c.507C>T (p.Tyr169=)	not specified [RCV004050983]	likely benign	10	123160496	123160496	Human		name
155745001	CV1806413	single nucleotide variant	NM_004725.4(BUB3):c.532C>T (p.Leu178=)	not specified [RCV004052405]	likely benign	10	123160521	123160521	Human		name
155743284	CV1806712	single nucleotide variant	NM_004725.4(BUB3):c.558A>G (p.Arg186=)	not specified [RCV004053566]	likely benign	10	123160547	123160547	Human		name
155705943	CV1807438	single nucleotide variant	NM_004725.4(BUB3):c.612A>C (p.Ala204=)	not specified [RCV004053288]	likely benign	10	123162271	123162271	Human		name
155711328	CV1807847	single nucleotide variant	NM_004725.4(BUB3):c.642A>G (p.Val214=)	not specified [RCV004053974]	likely benign	10	123162301	123162301	Human		name
155711344	CV1807850	single nucleotide variant	NM_004725.4(BUB3):c.642A>T (p.Val214=)	not specified [RCV004053975]	likely benign	10	123162301	123162301	Human		name
155730684	CV1808479	single nucleotide variant	NM_004725.4(BUB3):c.450G>A (p.Leu150=)	not specified [RCV004050826]	likely benign	10	123160439	123160439	Human		name
155709453	CV1808898	single nucleotide variant	NM_004725.4(BUB3):c.474A>G (p.Arg158=)	not specified [RCV004052065]	likely benign	10	123160463	123160463	Human		name
155740356	CV1809349	single nucleotide variant	NM_004725.4(BUB3):c.498C>T (p.Asn166=)	not specified [RCV004050330]	likely benign	10	123160487	123160487	Human		name
155742268	CV1809703	single nucleotide variant	NM_004725.4(BUB3):c.522G>A (p.Arg174=)	not specified [RCV004052240]	likely benign	10	123160511	123160511	Human		name
155735526	CV1809908	single nucleotide variant	NM_004725.4(BUB3):c.525G>A (p.Glu175=)	not specified [RCV004052295]	likely benign	10	123160514	123160514	Human		name
155679440	CV1810884	single nucleotide variant	NM_004725.4(BUB3):c.582T>C (p.Tyr194=)	not specified [RCV004054158]	likely benign	10	123162241	123162241	Human		name
155726248	CV1811910	single nucleotide variant	NM_004725.4(BUB3):c.660C>T (p.Ala220=)	not specified [RCV004054456]	likely benign	10	123162319	123162319	Human		name
155715960	CV1812433	single nucleotide variant	NM_004725.4(BUB3):c.693T>C (p.Ile231=)	not specified [RCV004052982]	likely benign	10	123162352	123162352	Human		name
155742413	CV1813701	single nucleotide variant	NM_004725.4(BUB3):c.795C>T (p.Asn265=)	not specified [RCV004054810]	likely benign	10	123162652	123162652	Human		name
155708948	CV1814009	single nucleotide variant	NM_004725.4(BUB3):c.831G>A (p.Thr277=)	not specified [RCV004056042]	likely benign	10	123162688	123162688	Human		name
155730912	CV1814236	single nucleotide variant	NM_004725.4(BUB3):c.837C>T (p.Ile279=)	not specified [RCV004056091]	likely benign	10	123162694	123162694	Human		name
155690133	CV1814621	single nucleotide variant	NM_004725.4(BUB3):c.882G>A (p.Ala294=)	not specified [RCV004056745]	likely benign	10	123162739	123162739	Human		name
155690167	CV1814628	single nucleotide variant	NM_004725.4(BUB3):c.882G>C (p.Ala294=)	not specified [RCV004056747]	likely benign	10	123162739	123162739	Human		name
155677524	CV1815095	single nucleotide variant	NM_004725.4(BUB3):c.681A>G (p.Lys227=)	not specified [RCV004052833]	likely benign	10	123162340	123162340	Human		name
155714340	CV1815260	single nucleotide variant	NM_004725.4(BUB3):c.684A>G (p.Glu228=)	not specified [RCV004052872]	likely benign	10	123162343	123162343	Human		name
155679999	CV1815844	single nucleotide variant	NM_004725.4(BUB3):c.71C>G (p.Pro24Arg)	not specified [RCV004055747]	uncertain significance	10	123154988	123154988	Human		name
155688040	CV1817528	single nucleotide variant	NM_004725.4(BUB3):c.870G>A (p.Thr290=)	not specified [RCV004056656]	likely benign	10	123162727	123162727	Human		name
155711453	CV1817844	single nucleotide variant	NM_004725.4(BUB3):c.912A>C (p.Thr304=)	not specified [RCV004055017]	likely benign	10	123162769	123162769	Human		name
155712204	CV1817935	single nucleotide variant	NM_004725.4(BUB3):c.915A>G (p.Glu305=)	not specified [RCV004055040]	likely benign	10	123162772	123162772	Human		name
155668030	CV1818080	single nucleotide variant	NM_004725.4(BUB3):c.957A>G (p.Ala319=)	not specified [RCV004056926]	likely benign	10	123162814	123162814	Human		name
155701404	CV1818367	single nucleotide variant	NM_004725.4(BUB3):c.966A>G (p.Lys322=)	not specified [RCV004056991]	likely benign	10	123162823	123162823	Human		name
155701987	CV1818485	single nucleotide variant	NM_004725.4(BUB3):c.969C>G (p.Pro323=)	not specified [RCV004057018]	likely benign	10	123162826	123162826	Human		name
155727796	CV1818929	single nucleotide variant	NM_004725.4(BUB3):c.705C>T (p.Tyr235=)	not specified [RCV004055199]	likely benign	10	123162364	123162364	Human		name
155708536	CV1819262	single nucleotide variant	NM_004725.4(BUB3):c.711C>T (p.Val237=)	not specified [RCV004055274]	likely benign	10	123162370	123162370	Human		name
155673571	CV1820281	single nucleotide variant	NM_004725.4(BUB3):c.813A>G (p.Gln271=)	not specified [RCV004055487]	likely benign	10	123162670	123162670	Human		name
155674404	CV1820398	single nucleotide variant	NM_004725.4(BUB3):c.816C>T (p.Phe272=)	BUB3-related disorder [RCV004758230]\|not specified [RCV004055512]	likely benign	10	123162673	123162673	Human		name , trait , alternate_id
155714533	CV1820818	single nucleotide variant	NM_004725.4(BUB3):c.858T>C (p.Asn286=)	not specified [RCV004056534]	likely benign	10	123162715	123162715	Human		name
155700511	CV1821089	single nucleotide variant	NM_004725.4(BUB3):c.900A>G (p.Glu300=)	not specified [RCV004054922]	likely benign	10	123162757	123162757	Human		name
155710156	CV1821309	single nucleotide variant	NM_004725.4(BUB3):c.906T>C (p.Asp302=)	not specified [RCV004054966]	likely benign	10	123162763	123162763	Human		name
155691465	CV1821350	single nucleotide variant	NM_004725.4(BUB3):c.945A>G (p.Gln315=)	not specified [RCV004056820]	likely benign	10	123162802	123162802	Human		name
155691725	CV1821459	single nucleotide variant	NM_004725.4(BUB3):c.948G>A (p.Val316=)	not specified [RCV004056848]	likely benign	10	123162805	123162805	Human		name
155692354	CV1821579	single nucleotide variant	NM_004725.4(BUB3):c.951A>G (p.Thr317=)	not specified [RCV004056875]	likely benign	10	123162808	123162808	Human		name
155707711	CV1823133	single nucleotide variant	NM_004725.4(BUB3):c.762T>C (p.Ser254=)	not specified [RCV004056479]	likely benign	10	123162619	123162619	Human		name
155728969	CV1823429	single nucleotide variant	NM_004725.4(BUB3):c.76A>G (p.Thr26Ala)	not specified [RCV004054595]	uncertain significance	10	123154993	123154993	Human		name
155729001	CV1823435	single nucleotide variant	NM_004725.4(BUB3):c.76A>T (p.Thr26Ser)	not specified [RCV004054598]	uncertain significance	10	123154993	123154993	Human		name
155667339	CV1823843	single nucleotide variant	NM_004725.4(BUB3):c.807G>A (p.Leu269=)	not specified [RCV004055427]	likely benign	10	123162664	123162664	Human		name
155667349	CV1823845	single nucleotide variant	NM_004725.4(BUB3):c.807G>C (p.Leu269=)	not specified [RCV004055428]	likely benign	10	123162664	123162664	Human		name
155742916	CV1823994	single nucleotide variant	NM_004725.4(BUB3):c.840A>G (p.Ala280=)	not specified [RCV004056120]	likely benign	10	123162697	123162697	Human		name
155713091	CV1824371	single nucleotide variant	NM_004725.4(BUB3):c.84G>C (p.Gln28His)	not specified [RCV004056201]	uncertain significance	10	123155001	123155001	Human		name
155690595	CV1824390	single nucleotide variant	NM_004725.4(BUB3):c.885A>C (p.Ser295=)	not specified [RCV004056763]	likely benign	10	123162742	123162742	Human		name
155723118	CV1824392	single nucleotide variant	NM_004725.4(BUB3):c.885A>G (p.Ser295=)	not specified [RCV004056764]	likely benign	10	123162742	123162742	Human		name
155698820	CV1824468	single nucleotide variant	NM_004725.4(BUB3):c.888A>C (p.Ser296=)	not specified [RCV004054835]	likely benign	10	123162745	123162745	Human		name
155723328	CV1824471	single nucleotide variant	NM_004725.4(BUB3):c.888A>T (p.Ser296=)	not specified [RCV004054837]	likely benign	10	123162745	123162745	Human		name
155684062	CV1825271	single nucleotide variant	NM_004725.4(BUB3):c.930T>G (p.Gly310=)	not specified [RCV004055674]	likely benign	10	123162787	123162787	Human		name
329363355	CV2429076	single nucleotide variant	NM_004725.4(BUB3):c.933C>T (p.Ile311=)	not specified [RCV004247523]	likely benign	10	123162790	123162790	Human		name
329389670	CV2467985	single nucleotide variant	NM_004725.4(BUB3):c.519C>T (p.Arg173=)	not specified [RCV004281418]	likely benign	10	123160508	123160508	Human		name
329389730	CV2467994	single nucleotide variant	NM_004725.4(BUB3):c.408G>A (p.Gln136=)	not specified [RCV004281421]	likely benign	10	123157871	123157871	Human		name
329389737	CV2467998	single nucleotide variant	NM_004725.4(BUB3):c.561G>A (p.Ala187=)	not specified [RCV004281424]	likely benign	10	123160550	123160550	Human		name
329389762	CV2468012	single nucleotide variant	NM_004725.4(BUB3):c.537A>G (p.Lys179=)	not specified [RCV004281431]	likely benign	10	123160526	123160526	Human		name
329389766	CV2468014	single nucleotide variant	NM_004725.4(BUB3):c.37C>T (p.Pro13Ser)	not specified [RCV004281432]	uncertain significance	10	123154954	123154954	Human		name
329389773	CV2468018	single nucleotide variant	NM_004725.4(BUB3):c.94G>A (p.Val32Ile)	not specified [RCV004281433]	uncertain significance	10	123155011	123155011	Human		name
329389779	CV2468021	single nucleotide variant	NM_004725.4(BUB3):c.963A>G (p.Thr321=)	not specified [RCV004281436]	likely benign	10	123162820	123162820	Human		name
401719687	CV2701237	single nucleotide variant	NM_004725.4(BUB3):c.74A>G (p.Asn25Ser)	not specified [RCV004309810]	uncertain significance	10	123154991	123154991	Human		name
401753017	CV2720599	single nucleotide variant	NM_004725.4(BUB3):c.552C>T (p.Cys184=)	not specified [RCV004327974]	likely benign	10	123160541	123160541	Human		name
401765239	CV2733577	single nucleotide variant	NM_004725.4(BUB3):c.38C>A (p.Pro13His)	not specified [RCV004330425]	uncertain significance	10	123154955	123154955	Human		name
401765241	CV2733578	single nucleotide variant	NM_004725.4(BUB3):c.366G>A (p.Leu122=)	not specified [RCV004330426]	likely benign	10	123157829	123157829	Human		name
401765243	CV2733579	single nucleotide variant	NM_004725.4(BUB3):c.66C>A (p.Phe22Leu)	not specified [RCV004330427]	uncertain significance	10	123154983	123154983	Human		name
401765247	CV2733581	single nucleotide variant	NM_004725.4(BUB3):c.87C>G (p.Phe29Leu)	not specified [RCV004330429]	uncertain significance	10	123155004	123155004	Human		name
401765250	CV2733583	single nucleotide variant	NM_004725.4(BUB3):c.426C>G (p.Thr142=)	not specified [RCV004330430]	likely benign	10	123160415	123160415	Human		name
401868202	CV2787347	single nucleotide variant	NM_004725.4(BUB3):c.98C>G (p.Ser33Cys)	not specified [RCV004366250]	uncertain significance	10	123155015	123155015	Human		name
401868211	CV2787350	single nucleotide variant	NM_004725.4(BUB3):c.47G>T (p.Gly16Val)	not specified [RCV004366252]	uncertain significance	10	123154964	123154964	Human		name
401868220	CV2787353	single nucleotide variant	NM_004725.4(BUB3):c.768C>A (p.Gly256=)	not specified [RCV004366255]	likely benign	10	123162625	123162625	Human		name
401881141	CV2789531	single nucleotide variant	NM_004725.4(BUB3):c.930T>C (p.Gly310=)	BUB3-related disorder [RCV003906710]\|not specified [RCV004360141]	likely benign	10	123162787	123162787	Human		name , trait , alternate_id
401881323	CV2789572	single nucleotide variant	NM_004725.4(BUB3):c.66C>G (p.Phe22Leu)	not specified [RCV004360177]	uncertain significance	10	123154983	123154983	Human		name
405690441	CV3386863	single nucleotide variant	NM_004725.4(BUB3):c.41A>G (p.Glu14Gly)	not specified [RCV004519226]	uncertain significance	10	123154958	123154958	Human		name
405690454	CV3386865	single nucleotide variant	NM_004725.4(BUB3):c.435G>C (p.Val145=)	not specified [RCV004519228]	likely benign	10	123160424	123160424	Human		name
405690459	CV3386866	single nucleotide variant	NM_004725.4(BUB3):c.477G>A (p.Val159=)	not specified [RCV004519229]	likely benign	10	123160466	123160466	Human		name
405690464	CV3386867	single nucleotide variant	NM_004725.4(BUB3):c.483G>A (p.Val161=)	not specified [RCV004519230]	likely benign	10	123160472	123160472	Human		name
405690470	CV3386868	single nucleotide variant	NM_004725.4(BUB3):c.540C>T (p.Tyr180=)	not specified [RCV004519231]	likely benign	10	123160529	123160529	Human		name
405690657	CV3386875	single nucleotide variant	NM_004725.4(BUB3):c.579T>G (p.Gly193=)	not specified [RCV004519237]	likely benign	10	123162238	123162238	Human		name
405690661	CV3386877	single nucleotide variant	NM_004725.4(BUB3):c.627C>T (p.Asp209=)	not specified [RCV004519238]	likely benign	10	123162286	123162286	Human		name
405690667	CV3386878	single nucleotide variant	NM_004725.4(BUB3):c.633C>T (p.Ser211=)	not specified [RCV004519239]	likely benign	10	123162292	123162292	Human		name
405690673	CV3386879	single nucleotide variant	NM_004725.4(BUB3):c.657T>C (p.Tyr219=)	not specified [RCV004519240]	likely benign	10	123162316	123162316	Human		name
405690678	CV3386880	single nucleotide variant	NM_004725.4(BUB3):c.676C>T (p.Leu226=)	not specified [RCV004519241]	likely benign	10	123162335	123162335	Human		name
405690689	CV3386882	single nucleotide variant	NM_004725.4(BUB3):c.738C>T (p.His246=)	not specified [RCV004519243]	likely benign	10	123162397	123162397	Human		name
405690707	CV3386885	single nucleotide variant	NM_004725.4(BUB3):c.83A>T (p.Gln28Leu)	not specified [RCV004519246]	uncertain significance	10	123155000	123155000	Human		name
405690735	CV3386891	single nucleotide variant	NM_004725.4(BUB3):c.912A>T (p.Thr304=)	not specified [RCV004519251]	likely benign	10	123162769	123162769	Human		name
405690753	CV3386894	single nucleotide variant	NM_004725.4(BUB3):c.936C>T (p.Phe312=)	not specified [RCV004519254]	likely benign	10	123162793	123162793	Human		name
407490131	CV3418010	single nucleotide variant	NM_004725.4(BUB3):c.393T>C (p.Ala131=)	not specified [RCV004604322]	likely benign	10	123157856	123157856	Human		name
407490155	CV3418016	single nucleotide variant	NM_004725.4(BUB3):c.930T>A (p.Gly310=)	not specified [RCV004604328]	likely benign	10	123162787	123162787	Human		name
407490203	CV3418031	single nucleotide variant	NM_004725.4(BUB3):c.342A>C (p.Gly114=)	not specified [RCV004604340]	likely benign	10	123157805	123157805	Human		name
407490225	CV3418038	single nucleotide variant	NM_004725.4(BUB3):c.34C>T (p.Pro12Ser)	not specified [RCV004604347]	uncertain significance	10	123154951	123154951	Human		name
407490228	CV3418039	single nucleotide variant	NM_004725.4(BUB3):c.38C>T (p.Pro13Leu)	not specified [RCV004604348]	uncertain significance	10	123154955	123154955	Human		name
597792900	CV3643660	single nucleotide variant	NM_004725.4(BUB3):c.62A>G (p.Lys21Arg)	not specified [RCV004902798]	uncertain significance	10	123154979	123154979	Human		name
597792912	CV3643666	single nucleotide variant	NM_004725.4(BUB3):c.29A>G (p.Asn10Ser)	not specified [RCV004902802]	uncertain significance	10	123154946	123154946	Human		name
597750041	CV3643672	single nucleotide variant	NM_004725.4(BUB3):c.34C>A (p.Pro12Thr)	not specified [RCV004892480]	uncertain significance	10	123154951	123154951	Human		name
597792923	CV3643674	single nucleotide variant	NM_004725.4(BUB3):c.612A>G (p.Ala204=)	not specified [RCV004902806]	likely benign	10	123162271	123162271	Human		name
597750060	CV3643678	single nucleotide variant	NM_004725.4(BUB3):c.570C>T (p.Asn190=)	not specified [RCV004892484]	likely benign	10	123160559	123160559	Human		name
597750065	CV3643680	single nucleotide variant	NM_004725.4(BUB3):c.777T>C (p.Asn259=)	not specified [RCV004892485]	likely benign	10	123162634	123162634	Human		name
597792941	CV3643685	single nucleotide variant	NM_004725.4(BUB3):c.975A>G (p.Ser325=)	not specified [RCV004902812]	likely benign	10	123163823	123163823	Human		name
597792949	CV3643688	single nucleotide variant	NM_004725.4(BUB3):c.612A>T (p.Ala204=)	not specified [RCV004902815]	likely benign	10	123162271	123162271	Human		name
597792955	CV3643690	single nucleotide variant	NM_004725.4(BUB3):c.834C>T (p.Ser278=)	not specified [RCV004902817]	likely benign	10	123162691	123162691	Human		name
15197247	CV723826	single nucleotide variant	NM_004725.4(BUB3):c.591C>T (p.Ser197=)	not provided [RCV000890004]\|not specified [RCV004028392]	likely benign	10	123162250	123162250	Human		name
15098005	CV752014	single nucleotide variant	NM_004725.4(BUB3):c.942C>T (p.Arg314=)	not provided [RCV000914145]\|not specified [RCV004029372]	likely benign	10	123162799	123162799	Human		name
15177599	CV767657	single nucleotide variant	NM_004725.4(BUB3):c.805C>T (p.Leu269=)	not provided [RCV000929197]\|not specified [RCV004029544]	likely benign	10	123162662	123162662	Human		name
15112487	CV783554	single nucleotide variant	NM_004725.4(BUB3):c.594T>C (p.Ser198=)	not provided [RCV000977828]\|not specified [RCV004030003]	likely benign	10	123162253	123162253	Human		name
155663728	CV1785776	single nucleotide variant	NM_004725.4(BUB3):c.113C>T (p.Ser38Phe)	not specified [RCV004047863]	uncertain significance	10	123155030	123155030	Human		name
155687216	CV1796867	single nucleotide variant	NM_004725.4(BUB3):c.115G>A (p.Val39Met)	not specified [RCV004050437]	uncertain significance	10	123155032	123155032	Human		name
155687435	CV1796939	single nucleotide variant	NM_004725.4(BUB3):c.115G>C (p.Val39Leu)	not specified [RCV004050455]	uncertain significance	10	123155032	123155032	Human		name
155672579	CV1801077	single nucleotide variant	NM_004725.4(BUB3):c.121C>G (p.Leu41Val)	not specified [RCV004053495]	uncertain significance	10	123155038	123155038	Human		name
155745037	CV1806431	single nucleotide variant	NM_004725.4(BUB3):c.119G>A (p.Arg40His)	not specified [RCV004052410]	uncertain significance	10	123155036	123155036	Human		name
155740199	CV1809266	single nucleotide variant	NM_004725.4(BUB3):c.118C>G (p.Arg40Gly)	not specified [RCV004050314]	uncertain significance	10	123155035	123155035	Human		name
155698104	CV1811887	single nucleotide variant	NM_004725.4(BUB3):c.101C>A (p.Ser34Tyr)	not specified [RCV004054451]	uncertain significance	10	123155018	123155018	Human		name
155667397	CV1812124	single nucleotide variant	NM_004725.4(BUB3):c.101C>G (p.Ser34Cys)	not specified [RCV004054506]	uncertain significance	10	123155018	123155018	Human		name
155737461	CV1819902	single nucleotide variant	NM_004725.4(BUB3):c.124T>C (p.Tyr42His)	not specified [RCV004054647]	uncertain significance	10	123155041	123155041	Human		name
155669611	CV1822113	single nucleotide variant	NM_004725.4(BUB3):c.101C>T (p.Ser34Phe)	not specified [RCV004052738]	uncertain significance	10	123155018	123155018	Human		name
155677948	CV1826264	single nucleotide variant	NM_004725.4(BUB3):c.134C>A (p.Pro45Gln)	not specified [RCV004058778]	uncertain significance	10	123155051	123155051	Human		name
155677950	CV1826265	single nucleotide variant	NM_004725.4(BUB3):c.134C>G (p.Pro45Arg)	not specified [RCV004058779]	uncertain significance	10	123155051	123155051	Human		name
155677960	CV1826268	single nucleotide variant	NM_004725.4(BUB3):c.134C>T (p.Pro45Leu)	not specified [RCV004058780]	uncertain significance	10	123155051	123155051	Human		name
155717997	CV1827668	single nucleotide variant	NM_004725.4(BUB3):c.158A>G (p.Tyr53Cys)	not specified [RCV004057345]	uncertain significance	10	123155075	123155075	Human		name
155730089	CV1828379	single nucleotide variant	NM_004725.4(BUB3):c.173C>T (p.Ala58Val)	not specified [RCV004061217]	uncertain significance	10	123155090	123155090	Human		name
155709827	CV1830897	single nucleotide variant	NM_004725.4(BUB3):c.163C>T (p.His55Tyr)	not specified [RCV004058130]	uncertain significance	10	123155080	123155080	Human		name
155680563	CV1832907	single nucleotide variant	NM_004725.4(BUB3):c.139A>G (p.Asn47Asp)	not specified [RCV004057122]	uncertain significance	10	123155056	123155056	Human		name
155701894	CV1833007	single nucleotide variant	NM_004725.4(BUB3):c.145A>C (p.Met49Leu)	not specified [RCV004057947]	uncertain significance	10	123155062	123155062	Human		name
155701924	CV1833011	single nucleotide variant	NM_004725.4(BUB3):c.145A>T (p.Met49Leu)	not specified [RCV004057948]	uncertain significance	10	123155062	123155062	Human		name
155732688	CV1834076	single nucleotide variant	NM_004725.4(BUB3):c.162G>C (p.Gln54His)	not specified [RCV004058071]	uncertain significance	10	123155079	123155079	Human		name
155720884	CV1834502	single nucleotide variant	NM_004725.4(BUB3):c.170G>A (p.Gly57Asp)	not specified [RCV004060565]	uncertain significance	10	123155087	123155087	Human		name
155714859	CV1834866	single nucleotide variant	NM_004725.4(BUB3):c.178C>G (p.Leu60Val)	not specified [RCV004059218]	uncertain significance	10	123155095	123155095	Human		name
155746678	CV1835259	single nucleotide variant	NM_004725.4(BUB3):c.187G>A (p.Ala63Thr)	not specified [RCV004060154]	uncertain significance	10	123155104	123155104	Human		name
155732699	CV1835429	single nucleotide variant	NM_004725.4(BUB3):c.188C>A (p.Ala63Asp)	not specified [RCV004060199]	uncertain significance	10	123155105	123155105	Human		name
155744960	CV1837799	single nucleotide variant	NM_004725.4(BUB3):c.167C>G (p.Thr56Ser)	not specified [RCV004059870]	uncertain significance	10	123155084	123155084	Human		name
155730832	CV1838213	single nucleotide variant	NM_004725.4(BUB3):c.175G>C (p.Val59Leu)	not specified [RCV004061333]	uncertain significance	10	123155092	123155092	Human		name
155677360	CV1839988	single nucleotide variant	NM_004725.4(BUB3):c.205C>T (p.His69Tyr)	not specified [RCV004059674]	uncertain significance	10	123155667	123155667	Human		name
155722184	CV1840769	single nucleotide variant	NM_004725.4(BUB3):c.217G>C (p.Gly73Arg)	not specified [RCV004061141]	uncertain significance	10	123155679	123155679	Human		name
155696293	CV1840983	single nucleotide variant	NM_004725.4(BUB3):c.226G>T (p.Asp76Tyr)	not specified [RCV004062503]	uncertain significance	10	123155688	123155688	Human		name
155739021	CV1842873	single nucleotide variant	NM_004725.4(BUB3):c.190T>C (p.Phe64Leu)	not specified [RCV004060816]	uncertain significance	10	123155107	123155107	Human		name
155744230	CV1843013	single nucleotide variant	NM_004725.4(BUB3):c.106G>C (p.Asp36His)	not specified [RCV004060960]	uncertain significance	10	123155023	123155023	Human		name
155674529	CV1843123	single nucleotide variant	NM_004725.4(BUB3):c.194A>C (p.Tyr65Ser)	not specified [RCV004060989]	uncertain significance	10	123155111	123155111	Human		name
155674545	CV1843125	single nucleotide variant	NM_004725.4(BUB3):c.194A>G (p.Tyr65Cys)	not specified [RCV004060990]	uncertain significance	10	123155111	123155111	Human		name
155670427	CV1843514	single nucleotide variant	NM_004725.4(BUB3):c.203C>T (p.Thr68Met)	not specified [RCV004059594]	uncertain significance	10	123155665	123155665	Human		name
155671369	CV1847354	single nucleotide variant	NM_004725.4(BUB3):c.221G>C (p.Gly74Ala)	not specified [RCV004061797]	uncertain significance	10	123155683	123155683	Human		name
155694571	CV1848125	single nucleotide variant	NM_004725.4(BUB3):c.243G>A (p.Met81Ile)	not specified [RCV004063818]	uncertain significance	10	123155705	123155705	Human		name
155677573	CV1848275	single nucleotide variant	NM_004725.4(BUB3):c.244C>A (p.His82Asn)	not specified [RCV004063857]	uncertain significance	10	123155706	123155706	Human		name
155710921	CV1848277	single nucleotide variant	NM_004725.4(BUB3):c.244C>T (p.His82Tyr)	not specified [RCV004063859]	uncertain significance	10	123155706	123155706	Human		name
155677782	CV1848416	single nucleotide variant	NM_004725.4(BUB3):c.245A>G (p.His82Arg)	not specified [RCV004063893]	uncertain significance	10	123155707	123155707	Human		name
155691356	CV1848720	single nucleotide variant	NM_004725.4(BUB3):c.256A>G (p.Thr86Ala)	not specified [RCV004062773]	uncertain significance	10	123155718	123155718	Human		name
155715198	CV1849366	single nucleotide variant	NM_004725.4(BUB3):c.271C>A (p.Leu91Ile)	not specified [RCV004064004]	uncertain significance	10	123157734	123157734	Human		name
155684873	CV1849970	single nucleotide variant	NM_004725.4(BUB3):c.208G>A (p.Ala70Thr)	not specified [RCV004060295]	uncertain significance	10	123155670	123155670	Human		name
155688484	CV1850381	single nucleotide variant	NM_004725.4(BUB3):c.218G>A (p.Gly73Glu)	not specified [RCV004061175]	uncertain significance	10	123155680	123155680	Human		name
155680608	CV1853270	single nucleotide variant	NM_004725.4(BUB3):c.277G>T (p.Gly93Trp)	not specified [RCV004064201]	uncertain significance	10	123157740	123157740	Human		name
155688022	CV1853760	single nucleotide variant	NM_004725.4(BUB3):c.295A>G (p.Ile99Val)	not specified [RCV004065355]	uncertain significance	10	123157758	123157758	Human		name
155664811	CV1855271	single nucleotide variant	NM_004725.4(BUB3):c.283C>T (p.His95Tyr)	not specified [RCV004062381]	uncertain significance	10	123157746	123157746	Human		name
155674099	CV1855723	single nucleotide variant	NM_004725.4(BUB3):c.287A>T (p.Asp96Val)	not specified [RCV004063022]	uncertain significance	10	123157750	123157750	Human		name
156152795	CV2394895	single nucleotide variant	NM_004725.4(BUB3):c.185G>T (p.Cys62Phe)	not specified [RCV004234551]	uncertain significance	10	123155102	123155102	Human		name
329363984	CV2429082	single nucleotide variant	NM_004725.4(BUB3):c.266A>G (p.Glu89Gly)	not specified [RCV004247529]	uncertain significance	10	123157729	123157729	Human		name
329363989	CV2429083	single nucleotide variant	NM_004725.4(BUB3):c.129T>A (p.Asp43Glu)	not specified [RCV004247530]	uncertain significance	10	123155046	123155046	Human		name
329389794	CV2465561	single nucleotide variant	NM_004725.4(BUB3):c.110C>T (p.Thr37Met)	not specified [RCV004281443]	uncertain significance	10	123155027	123155027	Human		name
329389632	CV2467966	single nucleotide variant	NM_004725.4(BUB3):c.137C>T (p.Ala46Val)	not specified [RCV004281413]	uncertain significance	10	123155054	123155054	Human		name
329389636	CV2467968	single nucleotide variant	NM_004725.4(BUB3):c.275T>C (p.Val92Ala)	not specified [RCV004281415]	uncertain significance	10	123157738	123157738	Human		name
329389721	CV2467990	single nucleotide variant	NM_004725.4(BUB3):c.136G>C (p.Ala46Pro)	not specified [RCV004281419]	uncertain significance	10	123155053	123155053	Human		name
329389777	CV2468020	single nucleotide variant	NM_004725.4(BUB3):c.140A>G (p.Asn47Ser)	not specified [RCV004281435]	uncertain significance	10	123155057	123155057	Human		name
401753014	CV2720598	single nucleotide variant	NM_004725.4(BUB3):c.128A>G (p.Asp43Gly)	not specified [RCV004327973]	uncertain significance	10	123155045	123155045	Human		name
401775011	CV2723947	single nucleotide variant	NM_004725.4(BUB3):c.220G>A (p.Gly74Arg)	not specified [RCV004326116]	uncertain significance	10	123155682	123155682	Human		name
401881168	CV2789542	single nucleotide variant	NM_004725.4(BUB3):c.151C>T (p.Leu51Phe)	not specified [RCV004360149]	uncertain significance	10	123155068	123155068	Human		name
405731472	CV3294854	single nucleotide variant	NM_004725.4(BUB3):c.264A>C (p.Gln88His)	not specified [RCV004429399]	uncertain significance	10	123155726	123155726	Human		name
405690390	CV3386854	single nucleotide variant	NM_004725.4(BUB3):c.157T>A (p.Tyr53Asn)	not specified [RCV004519217]	uncertain significance	10	123155074	123155074	Human		name
405690398	CV3386855	single nucleotide variant	NM_004725.4(BUB3):c.179T>C (p.Leu60Pro)	not specified [RCV004519218]	uncertain significance	10	123155096	123155096	Human		name
405690403	CV3386856	single nucleotide variant	NM_004725.4(BUB3):c.181G>C (p.Asp61His)	not specified [RCV004519219]	uncertain significance	10	123155098	123155098	Human		name
405690408	CV3386857	single nucleotide variant	NM_004725.4(BUB3):c.230A>G (p.His77Arg)	not specified [RCV004519220]	uncertain significance	10	123155692	123155692	Human		name
405690416	CV3386858	single nucleotide variant	NM_004725.4(BUB3):c.240A>T (p.Lys80Asn)	not specified [RCV004519221]	uncertain significance	10	123155702	123155702	Human		name
405690425	CV3386860	single nucleotide variant	NM_004725.4(BUB3):c.264A>T (p.Gln88His)	not specified [RCV004519223]	uncertain significance	10	123155726	123155726	Human		name
407490124	CV3418007	single nucleotide variant	NM_004725.4(BUB3):c.243G>T (p.Met81Ile)	not specified [RCV004604320]	uncertain significance	10	123155705	123155705	Human		name
407500761	CV3418009	single nucleotide variant	NM_004725.4(BUB3):c.169G>C (p.Gly57Arg)	not specified [RCV004607211]	uncertain significance	10	123155086	123155086	Human		name
407490165	CV3418018	single nucleotide variant	NM_004725.4(BUB3):c.271C>T (p.Leu91Phe)	not specified [RCV004604330]	uncertain significance	10	123157734	123157734	Human		name
407490179	CV3418022	single nucleotide variant	NM_004725.4(BUB3):c.146T>C (p.Met49Thr)	not specified [RCV004604333]	uncertain significance	10	123155063	123155063	Human		name
407490188	CV3418024	single nucleotide variant	NM_004725.4(BUB3):c.165C>G (p.His55Gln)	not specified [RCV004604335]	uncertain significance	10	123155082	123155082	Human		name
407490194	CV3418026	single nucleotide variant	NM_004725.4(BUB3):c.161A>G (p.Gln54Arg)	not specified [RCV004604337]	uncertain significance	10	123155078	123155078	Human		name
407490222	CV3418037	single nucleotide variant	NM_004725.4(BUB3):c.206A>G (p.His69Arg)	not specified [RCV004604346]	uncertain significance	10	123155668	123155668	Human		name
597750031	CV3643664	single nucleotide variant	NM_004725.4(BUB3):c.118C>T (p.Arg40Cys)	not specified [RCV004892478]	uncertain significance	10	123155035	123155035	Human		name
597750051	CV3643676	single nucleotide variant	NM_004725.4(BUB3):c.200C>T (p.Pro67Leu)	not specified [RCV004892482]	uncertain significance	10	123155662	123155662	Human		name
597750070	CV3643681	single nucleotide variant	NM_004725.4(BUB3):c.136G>A (p.Ala46Thr)	not specified [RCV004892486]	uncertain significance	10	123155053	123155053	Human		name
597792952	CV3643689	single nucleotide variant	NM_004725.4(BUB3):c.266A>C (p.Glu89Ala)	not specified [RCV004902816]	uncertain significance	10	123157729	123157729	Human		name
597792964	CV3643694	single nucleotide variant	NM_004725.4(BUB3):c.260A>G (p.Asp87Gly)	not specified [RCV004902820]	uncertain significance	10	123155722	123155722	Human		name
597792967	CV3643695	single nucleotide variant	NM_004725.4(BUB3):c.233A>G (p.Gln78Arg)	not specified [RCV004902821]	uncertain significance	10	123155695	123155695	Human		name
597792969	CV3643696	single nucleotide variant	NM_004725.4(BUB3):c.106G>A (p.Asp36Asn)	not specified [RCV004902822]	uncertain significance	10	123155023	123155023	Human		name
597792978	CV3643699	single nucleotide variant	NM_004725.4(BUB3):c.209C>G (p.Ala70Gly)	not specified [RCV004902825]	uncertain significance	10	123155671	123155671	Human		name
155709952	CV1785579	single nucleotide variant	NM_004725.4(BUB3):c.323T>G (p.Val108Gly)	not specified [RCV004049321]	uncertain significance	10	123157786	123157786	Human		name
155704413	CV1787591	single nucleotide variant	NM_004725.4(BUB3):c.408G>T (p.Gln136His)	not specified [RCV004599295]	uncertain significance	10	123157871	123157871	Human		name
155741279	CV1790725	single nucleotide variant	NM_004725.4(BUB3):c.416A>C (p.Lys139Thr)	not specified [RCV004051819]	uncertain significance	10	123157879	123157879	Human		name
155741574	CV1791117	single nucleotide variant	NM_004725.4(BUB3):c.436T>C (p.Ser146Pro)	not specified [RCV004050074]	uncertain significance	10	123160425	123160425	Human		name
155699927	CV1791809	single nucleotide variant	NM_004725.4(BUB3):c.316C>A (p.Pro106Thr)	not specified [RCV004048823]	uncertain significance	10	123157779	123157779	Human		name
155704810	CV1792038	single nucleotide variant	NM_004725.4(BUB3):c.328G>A (p.Val110Met)	not specified [RCV004049467]	uncertain significance	10	123157791	123157791	Human		name
155717110	CV1792145	single nucleotide variant	NM_004725.4(BUB3):c.329T>C (p.Val110Ala)	not specified [RCV004049492]	uncertain significance	10	123157792	123157792	Human		name
155683475	CV1792455	single nucleotide variant	NM_004725.4(BUB3):c.344G>T (p.Ser115Ile)	not specified [RCV004048556]	uncertain significance	10	123157807	123157807	Human		name
155696658	CV1793799	single nucleotide variant	NM_004725.4(BUB3):c.398C>T (p.Thr133Ile)	not specified [RCV004050544]	uncertain significance	10	123157861	123157861	Human		name
155686979	CV1796786	single nucleotide variant	NM_004725.4(BUB3):c.392C>T (p.Ala131Val)	not specified [RCV004050420]	uncertain significance	10	123157855	123157855	Human		name
155728138	CV1798259	single nucleotide variant	NM_004725.4(BUB3):c.445C>T (p.Arg149Trp)	not specified [RCV004050739]	uncertain significance	10	123160434	123160434	Human		name
155724496	CV1799438	single nucleotide variant	NM_004725.4(BUB3):c.517C>G (p.Arg173Gly)	not specified [RCV004051643]	uncertain significance	10	123160506	123160506	Human		name
155746574	CV1800232	single nucleotide variant	NM_004725.4(BUB3):c.570C>G (p.Asn190Lys)	not specified [RCV004053735]	uncertain significance	10	123160559	123160559	Human		name
155682639	CV1801010	single nucleotide variant	NM_004725.4(BUB3):c.627C>A (p.Asp209Glu)	not specified [RCV004053474]	uncertain significance	10	123162286	123162286	Human		name
155682754	CV1801079	single nucleotide variant	NM_004725.4(BUB3):c.628C>G (p.Pro210Ala)	not specified [RCV004053496]	uncertain significance	10	123162287	123162287	Human		name
155683365	CV1801330	single nucleotide variant	NM_004725.4(BUB3):c.632G>T (p.Ser211Ile)	not specified [RCV004053846]	uncertain significance	10	123162291	123162291	Human		name
155738911	CV1801507	single nucleotide variant	NM_004725.4(BUB3):c.460A>G (p.Thr154Ala)	not specified [RCV004051506]	uncertain significance	10	123160449	123160449	Human		name
155735777	CV1801811	single nucleotide variant	NM_004725.4(BUB3):c.464C>T (p.Ala155Val)	not specified [RCV004051574]	uncertain significance	10	123160453	123160453	Human		name
155733133	CV1801977	single nucleotide variant	NM_004725.4(BUB3):c.485G>T (p.Trp162Leu)	not specified [RCV004050115]	uncertain significance	10	123160474	123160474	Human		name
155738434	CV1805150	single nucleotide variant	NM_004725.4(BUB3):c.458G>T (p.Gly153Val)	not specified [RCV004051472]	uncertain significance	10	123160447	123160447	Human		name
155721055	CV1805494	single nucleotide variant	NM_004725.4(BUB3):c.481G>C (p.Val161Leu)	not specified [RCV004052184]	uncertain significance	10	123160470	123160470	Human		name
155743175	CV1806660	single nucleotide variant	NM_004725.4(BUB3):c.557G>A (p.Arg186Gln)	not specified [RCV004053549]	uncertain significance	10	123160546	123160546	Human		name
155680247	CV1807167	single nucleotide variant	NM_004725.4(BUB3):c.586T>A (p.Leu196Ile)	not specified [RCV004054209]	uncertain significance	10	123162245	123162245	Human		name
155729122	CV1808324	single nucleotide variant	NM_004725.4(BUB3):c.448C>G (p.Leu150Val)	not specified [RCV004050785]	uncertain significance	10	123160437	123160437	Human		name
155672928	CV1809595	single nucleotide variant	NM_004725.4(BUB3):c.501G>A (p.Met167Ile)	not specified [RCV004050901]	uncertain significance	10	123160490	123160490	Human		name
155669822	CV1810034	single nucleotide variant	NM_004725.4(BUB3):c.548G>C (p.Arg183Pro)	not specified [RCV004053136]	uncertain significance	10	123160537	123160537	Human		name
155669826	CV1810035	single nucleotide variant	NM_004725.4(BUB3):c.548G>T (p.Arg183Leu)	not specified [RCV004053137]	uncertain significance	10	123160537	123160537	Human		name
155676417	CV1810459	single nucleotide variant	NM_004725.4(BUB3):c.555A>G (p.Ile185Met)	not specified [RCV004053230]	uncertain significance	10	123160544	123160544	Human		name
155697913	CV1810942	single nucleotide variant	NM_004725.4(BUB3):c.605G>A (p.Arg202Gln)	not specified [RCV004052645]	uncertain significance	10	123162264	123162264	Human		name
155715357	CV1812199	single nucleotide variant	NM_004725.4(BUB3):c.689A>G (p.Asn230Ser)	not specified [RCV004052931]	uncertain significance	10	123162348	123162348	Human		name
155680625	CV1812682	single nucleotide variant	NM_004725.4(BUB3):c.722C>G (p.Ser241Cys)	not specified [RCV004055787]	uncertain significance	10	123162381	123162381	Human		name
155728707	CV1813021	single nucleotide variant	NM_004725.4(BUB3):c.729C>A (p.His243Gln)	not specified [RCV004055852]	uncertain significance	10	123162388	123162388	Human		name
155747473	CV1813696	single nucleotide variant	NM_004725.4(BUB3):c.795C>A (p.Asn265Lys)	not specified [RCV004054808]	uncertain significance	10	123162652	123162652	Human		name
155730150	CV1814118	single nucleotide variant	NM_004725.4(BUB3):c.834C>G (p.Ser278Arg)	not specified [RCV004056062]	uncertain significance	10	123162691	123162691	Human		name
155730339	CV1814158	single nucleotide variant	NM_004725.4(BUB3):c.835A>G (p.Ile279Val)	not specified [RCV004056072]	uncertain significance	10	123162692	123162692	Human		name
155730711	CV1814207	single nucleotide variant	NM_004725.4(BUB3):c.836T>G (p.Ile279Ser)	not specified [RCV004056085]	uncertain significance	10	123162693	123162693	Human		name
155688895	CV1814385	single nucleotide variant	NM_004725.4(BUB3):c.875C>T (p.Ala292Val)	not specified [RCV004056687]	uncertain significance	10	123162732	123162732	Human		name
155722514	CV1814451	single nucleotide variant	NM_004725.4(BUB3):c.877A>T (p.Ile293Leu)	not specified [RCV004056705]	uncertain significance	10	123162734	123162734	Human		name
155683427	CV1815017	single nucleotide variant	NM_004725.4(BUB3):c.928G>A (p.Gly310Ser)	not specified [RCV004055655]	uncertain significance	10	123162785	123162785	Human		name
155683534	CV1815037	single nucleotide variant	NM_004725.4(BUB3):c.929G>A (p.Gly310Asp)	not specified [RCV004055661]	uncertain significance	10	123162786	123162786	Human		name
155670914	CV1815535	single nucleotide variant	NM_004725.4(BUB3):c.713A>G (p.Asn238Ser)	not specified [RCV004055290]	uncertain significance	10	123162372	123162372	Human		name
155679921	CV1815827	single nucleotide variant	NM_004725.4(BUB3):c.719T>C (p.Ile240Thr)	not specified [RCV004055743]	uncertain significance	10	123162378	123162378	Human		name
155697005	CV1816221	single nucleotide variant	NM_004725.4(BUB3):c.751A>G (p.Thr251Ala)	not specified [RCV004056357]	uncertain significance	10	123162410	123162410	Human		name
155742242	CV1816604	single nucleotide variant	NM_004725.4(BUB3):c.787C>G (p.Pro263Ala)	not specified [RCV004054742]	uncertain significance	10	123162644	123162644	Human		name
155747118	CV1816648	single nucleotide variant	NM_004725.4(BUB3):c.788C>A (p.Pro263Gln)	not specified [RCV004054753]	uncertain significance	10	123162645	123162645	Human		name
155698386	CV1816908	single nucleotide variant	NM_004725.4(BUB3):c.821G>A (p.Arg274Gln)	not specified [RCV004055555]	uncertain significance	10	123162678	123162678	Human		name
155707199	CV1817013	single nucleotide variant	NM_004725.4(BUB3):c.824A>G (p.Tyr275Cys)	not specified [RCV004055568]	uncertain significance	10	123162681	123162681	Human		name
155707593	CV1817087	single nucleotide variant	NM_004725.4(BUB3):c.826C>A (p.Pro276Thr)	not specified [RCV004055585]	uncertain significance	10	123162683	123162683	Human		name
155708067	CV1817183	single nucleotide variant	NM_004725.4(BUB3):c.829A>G (p.Thr277Ala)	not specified [RCV004056011]	uncertain significance	10	123162686	123162686	Human		name
155721470	CV1817260	single nucleotide variant	NM_004725.4(BUB3):c.863G>C (p.Gly288Ala)	not specified [RCV004056577]	uncertain significance	10	123162720	123162720	Human		name
155687701	CV1817428	single nucleotide variant	NM_004725.4(BUB3):c.868A>G (p.Thr290Ala)	not specified [RCV004056628]	uncertain significance	10	123162725	123162725	Human		name
155711836	CV1817891	single nucleotide variant	NM_004725.4(BUB3):c.913G>C (p.Glu305Gln)	not specified [RCV004055030]	uncertain significance	10	123162770	123162770	Human		name
155672607	CV1818413	single nucleotide variant	NM_004725.4(BUB3):c.967C>G (p.Pro323Ala)	not specified [RCV004057002]	uncertain significance	10	123162824	123162824	Human		name
155701600	CV1818416	single nucleotide variant	NM_004725.4(BUB3):c.967C>T (p.Pro323Ser)	not specified [RCV004057003]	uncertain significance	10	123162824	123162824	Human		name
155670291	CV1819144	single nucleotide variant	NM_004725.4(BUB3):c.709G>A (p.Val237Ile)	not specified [RCV004055251]	uncertain significance	10	123162368	123162368	Human		name
155666629	CV1819557	single nucleotide variant	NM_004725.4(BUB3):c.741T>A (p.Asn247Lys)	not specified [RCV004056265]	uncertain significance	10	123162400	123162400	Human		name
155729946	CV1819784	single nucleotide variant	NM_004725.4(BUB3):c.772G>T (p.Val258Leu)	not specified [RCV004054622]	uncertain significance	10	123162629	123162629	Human		name
155737466	CV1819907	single nucleotide variant	NM_004725.4(BUB3):c.775A>G (p.Asn259Asp)	not specified [RCV004054649]	uncertain significance	10	123162632	123162632	Human		name
155737651	CV1820057	single nucleotide variant	NM_004725.4(BUB3):c.778A>T (p.Ile260Phe)	not specified [RCV004054682]	uncertain significance	10	123162635	123162635	Human		name
155713682	CV1820604	single nucleotide variant	NM_004725.4(BUB3):c.852C>G (p.Phe284Leu)	not specified [RCV004056225]	uncertain significance	10	123162709	123162709	Human		name
155714331	CV1820768	single nucleotide variant	NM_004725.4(BUB3):c.857A>G (p.Asn286Ser)	not specified [RCV004056520]	uncertain significance	10	123162714	123162714	Human		name
155727378	CV1822532	single nucleotide variant	NM_004725.4(BUB3):c.701T>C (p.Ile234Thr)	not specified [RCV004055148]	uncertain significance	10	123162360	123162360	Human		name
155717240	CV1822914	single nucleotide variant	NM_004725.4(BUB3):c.733A>C (p.Ile245Leu)	not specified [RCV004055914]	uncertain significance	10	123162392	123162392	Human		name
155717930	CV1823068	single nucleotide variant	NM_004725.4(BUB3):c.736C>T (p.His246Tyr)	not specified [RCV004055949]	uncertain significance	10	123162395	123162395	Human		name
155708119	CV1823204	single nucleotide variant	NM_004725.4(BUB3):c.764A>T (p.Asp255Val)	not specified [RCV004056490]	uncertain significance	10	123162621	123162621	Human		name
155667210	CV1823816	single nucleotide variant	NM_004725.4(BUB3):c.806T>C (p.Leu269Pro)	not specified [RCV004055419]	uncertain significance	10	123162663	123162663	Human		name
155711738	CV1824184	single nucleotide variant	NM_004725.4(BUB3):c.845T>A (p.Leu282His)	not specified [RCV004056160]	uncertain significance	10	123162702	123162702	Human		name
155699030	CV1824520	single nucleotide variant	NM_004725.4(BUB3):c.889T>C (p.Tyr297His)	not specified [RCV004054845]	uncertain significance	10	123162746	123162746	Human		name
155684515	CV1824904	single nucleotide variant	NM_004725.4(BUB3):c.934T>A (p.Phe312Ile)	not specified [RCV004055704]	uncertain significance	10	123162791	123162791	Human		name
155690818	CV1825048	single nucleotide variant	NM_004725.4(BUB3):c.939T>G (p.Ile313Met)	not specified [RCV004055731]	uncertain significance	10	123162796	123162796	Human		name
155691130	CV1825119	single nucleotide variant	NM_004725.4(BUB3):c.940C>T (p.Arg314Cys)	not specified [RCV004056784]	uncertain significance	10	123162797	123162797	Human		name
155691216	CV1825142	single nucleotide variant	NM_004725.4(BUB3):c.941G>A (p.Arg314His)	not specified [RCV004056791]	uncertain significance	10	123162798	123162798	Human		name
155684114	CV1825287	single nucleotide variant	NM_004725.4(BUB3):c.931A>G (p.Ile311Val)	not specified [RCV004055681]	uncertain significance	10	123162788	123162788	Human		name
155703155	CV1825504	single nucleotide variant	NM_004725.4(BUB3):c.974C>T (p.Ser325Leu)	not specified [RCV004057573]	uncertain significance	10	123163822	123163822	Human		name
155673497	CV1825563	single nucleotide variant	NM_004725.4(BUB3):c.976C>A (p.Pro326Thr)	not specified [RCV004057586]	uncertain significance	10	123163824	123163824	Human		name
155673515	CV1825566	single nucleotide variant	NM_004725.4(BUB3):c.976C>T (p.Pro326Ser)	not specified [RCV004057587]	uncertain significance	10	123163824	123163824	Human		name
155697969	CV1854971	single nucleotide variant	NM_004725.4(BUB3):c.305T>G (p.Val102Gly)	not specified [RCV004066410]	uncertain significance	10	123157768	123157768	Human		name
329363358	CV2429077	single nucleotide variant	NM_004725.4(BUB3):c.632G>A (p.Ser211Asn)	not specified [RCV004247524]	uncertain significance	10	123162291	123162291	Human		name
329363975	CV2429079	single nucleotide variant	NM_004725.4(BUB3):c.979T>C (p.Cys327Arg)	not specified [RCV004247526]	uncertain significance	10	123163827	123163827	Human		name
329363978	CV2429080	single nucleotide variant	NM_004725.4(BUB3):c.716C>G (p.Ala239Gly)	not specified [RCV004247527]	uncertain significance	10	123162375	123162375	Human		name
329363992	CV2429084	single nucleotide variant	NM_004725.4(BUB3):c.493C>T (p.Arg165Trp)	not specified [RCV004247531]	uncertain significance	10	123160482	123160482	Human		name
329364192	CV2429086	single nucleotide variant	NM_004725.4(BUB3):c.740A>G (p.Asn247Ser)	not specified [RCV004247533]	uncertain significance	10	123162399	123162399	Human		name
329363363	CV2429087	single nucleotide variant	NM_004725.4(BUB3):c.539A>G (p.Tyr180Cys)	not specified [RCV004247534]	uncertain significance	10	123160528	123160528	Human		name
329364001	CV2429088	single nucleotide variant	NM_004725.4(BUB3):c.322G>C (p.Val108Leu)	not specified [RCV004247535]	uncertain significance	10	123157785	123157785	Human		name
329363366	CV2429089	single nucleotide variant	NM_004725.4(BUB3):c.398C>A (p.Thr133Asn)	not specified [RCV004247536]	uncertain significance	10	123157861	123157861	Human		name
329389784	CV2465556	single nucleotide variant	NM_004725.4(BUB3):c.354G>C (p.Gln118His)	not specified [RCV004281438]	uncertain significance	10	123157817	123157817	Human		name
329389787	CV2465558	single nucleotide variant	NM_004725.4(BUB3):c.890A>G (p.Tyr297Cys)	not specified [RCV004281440]	uncertain significance	10	123162747	123162747	Human		name
329389789	CV2465559	single nucleotide variant	NM_004725.4(BUB3):c.493C>G (p.Arg165Gly)	not specified [RCV004281441]	uncertain significance	10	123160482	123160482	Human		name
329389791	CV2465560	single nucleotide variant	NM_004725.4(BUB3):c.788C>T (p.Pro263Leu)	not specified [RCV004281442]	uncertain significance	10	123162645	123162645	Human		name
329389629	CV2467964	single nucleotide variant	NM_004725.4(BUB3):c.911C>G (p.Thr304Arg)	not specified [RCV004281412]	uncertain significance	10	123162768	123162768	Human		name
329389634	CV2467967	single nucleotide variant	NM_004725.4(BUB3):c.901A>G (p.Met301Val)	not specified [RCV004281414]	uncertain significance	10	123162758	123162758	Human		name
329389647	CV2467974	single nucleotide variant	NM_004725.4(BUB3):c.319G>A (p.Glu107Lys)	not specified [RCV004281416]	uncertain significance	10	123157782	123157782	Human		name
329389655	CV2467978	single nucleotide variant	NM_004725.4(BUB3):c.742A>G (p.Thr248Ala)	not specified [RCV004281417]	uncertain significance	10	123162401	123162401	Human		name
329389743	CV2468001	single nucleotide variant	NM_004725.4(BUB3):c.820C>T (p.Arg274Trp)	not specified [RCV004281427]	uncertain significance	10	123162677	123162677	Human		name
329389775	CV2468019	single nucleotide variant	NM_004725.4(BUB3):c.865A>G (p.Thr289Ala)	not specified [RCV004281434]	uncertain significance	10	123162722	123162722	Human		name
401765245	CV2733580	single nucleotide variant	NM_004725.4(BUB3):c.553A>C (p.Ile185Leu)	not specified [RCV004330428]	uncertain significance	10	123160542	123160542	Human		name
401765252	CV2733584	single nucleotide variant	NM_004725.4(BUB3):c.871C>T (p.Leu291Phe)	not specified [RCV004330431]	uncertain significance	10	123162728	123162728	Human		name
401866742	CV2782929	single nucleotide variant	NM_004725.4(BUB3):c.698A>G (p.Gln233Arg)	not specified [RCV004361727]	uncertain significance	10	123162357	123162357	Human		name
401880204	CV2783130	single nucleotide variant	NM_004725.4(BUB3):c.676C>G (p.Leu226Val)	not specified [RCV004363483]	uncertain significance	10	123162335	123162335	Human		name
401868194	CV2787344	single nucleotide variant	NM_004725.4(BUB3):c.920C>T (p.Pro307Leu)	not specified [RCV004366247]	uncertain significance	10	123162777	123162777	Human		name
401868199	CV2787346	single nucleotide variant	NM_004725.4(BUB3):c.735C>G (p.Ile245Met)	not specified [RCV004366249]	uncertain significance	10	123162394	123162394	Human		name
401868205	CV2787348	single nucleotide variant	NM_004725.4(BUB3):c.430T>G (p.Ser144Ala)	not specified [RCV004366251]	uncertain significance	10	123160419	123160419	Human		name
401868216	CV2787352	single nucleotide variant	NM_004725.4(BUB3):c.335T>C (p.Val112Ala)	not specified [RCV004366254]	uncertain significance	10	123157798	123157798	Human		name
401868224	CV2787354	single nucleotide variant	NM_004725.4(BUB3):c.592T>G (p.Ser198Ala)	not specified [RCV004366256]	uncertain significance	10	123162251	123162251	Human		name
401868228	CV2787355	single nucleotide variant	NM_004725.4(BUB3):c.508G>A (p.Val170Met)	not specified [RCV004366257]	uncertain significance	10	123160497	123160497	Human		name
401881267	CV2789552	single nucleotide variant	NM_004725.4(BUB3):c.929G>C (p.Gly310Ala)	not specified [RCV004360158]	uncertain significance	10	123162786	123162786	Human		name
401881294	CV2789562	single nucleotide variant	NM_004725.4(BUB3):c.343A>G (p.Ser115Gly)	not specified [RCV004360167]	uncertain significance	10	123157806	123157806	Human		name
405731484	CV3294855	single nucleotide variant	NM_004725.4(BUB3):c.778A>G (p.Ile260Val)	not specified [RCV004429400]	uncertain significance	10	123162635	123162635	Human		name
405690432	CV3386861	single nucleotide variant	NM_004725.4(BUB3):c.320A>C (p.Glu107Ala)	not specified [RCV004519224]	uncertain significance	10	123157783	123157783	Human		name
405690437	CV3386862	single nucleotide variant	NM_004725.4(BUB3):c.404C>G (p.Ser135Cys)	not specified [RCV004519225]	uncertain significance	10	123157867	123157867	Human		name
405690448	CV3386864	single nucleotide variant	NM_004725.4(BUB3):c.427C>G (p.Leu143Val)	not specified [RCV004519227]	uncertain significance	10	123160416	123160416	Human		name
405690475	CV3386869	single nucleotide variant	NM_004725.4(BUB3):c.543G>C (p.Gln181His)	not specified [RCV004519232]	uncertain significance	10	123160532	123160532	Human		name
405690481	CV3386870	single nucleotide variant	NM_004725.4(BUB3):c.547C>A (p.Arg183Ser)	not specified [RCV004519233]	uncertain significance	10	123160536	123160536	Human		name
405690487	CV3386871	single nucleotide variant	NM_004725.4(BUB3):c.553A>T (p.Ile185Leu)	not specified [RCV004519234]	uncertain significance	10	123160542	123160542	Human		name
405690642	CV3386872	single nucleotide variant	NM_004725.4(BUB3):c.554T>C (p.Ile185Thr)	not specified [RCV004519235]	uncertain significance	10	123160543	123160543	Human		name
405690650	CV3386873	single nucleotide variant	NM_004725.4(BUB3):c.564T>G (p.Phe188Leu)	not specified [RCV004519236]	uncertain significance	10	123160553	123160553	Human		name
405690684	CV3386881	single nucleotide variant	NM_004725.4(BUB3):c.686A>G (p.Asn229Ser)	not specified [RCV004519242]	uncertain significance	10	123162345	123162345	Human		name
405690702	CV3386884	single nucleotide variant	NM_004725.4(BUB3):c.817C>T (p.His273Tyr)	not specified [RCV004519245]	uncertain significance	10	123162674	123162674	Human		name
405690716	CV3386886	single nucleotide variant	NM_004725.4(BUB3):c.854G>A (p.Ser285Asn)	not specified [RCV004519247]	uncertain significance	10	123162711	123162711	Human		name
405690726	CV3386888	single nucleotide variant	NM_004725.4(BUB3):c.881C>A (p.Ala294Glu)	not specified [RCV004519249]	uncertain significance	10	123162738	123162738	Human		name
405690729	CV3386889	single nucleotide variant	NM_004725.4(BUB3):c.892A>G (p.Met298Val)	not specified [RCV004519250]	uncertain significance	10	123162749	123162749	Human		name
405690740	CV3386892	single nucleotide variant	NM_004725.4(BUB3):c.923A>C (p.Glu308Ala)	not specified [RCV004519252]	uncertain significance	10	123162780	123162780	Human		name
405690746	CV3386893	single nucleotide variant	NM_004725.4(BUB3):c.934T>G (p.Phe312Val)	not specified [RCV004519253]	uncertain significance	10	123162791	123162791	Human		name
407490136	CV3418011	single nucleotide variant	NM_004725.4(BUB3):c.307G>A (p.Glu103Lys)	not specified [RCV004604323]	uncertain significance	10	123157770	123157770	Human		name
407490140	CV3418012	single nucleotide variant	NM_004725.4(BUB3):c.425C>T (p.Thr142Ile)	not specified [RCV004604324]	uncertain significance	10	123160414	123160414	Human		name
407490160	CV3418017	single nucleotide variant	NM_004725.4(BUB3):c.422A>G (p.Tyr141Cys)	not specified [RCV004604329]	uncertain significance	10	123160411	123160411	Human		name
407500765	CV3418019	single nucleotide variant	NM_004725.4(BUB3):c.439G>A (p.Gly147Arg)	not specified [RCV004607212]	uncertain significance	10	123160428	123160428	Human		name
407490169	CV3418020	single nucleotide variant	NM_004725.4(BUB3):c.634C>T (p.Pro212Ser)	not specified [RCV004604331]	uncertain significance	10	123162293	123162293	Human		name
407490174	CV3418021	single nucleotide variant	NM_004725.4(BUB3):c.548G>A (p.Arg183His)	not specified [RCV004604332]	uncertain significance	10	123160537	123160537	Human		name
407490191	CV3418025	single nucleotide variant	NM_004725.4(BUB3):c.772G>A (p.Val258Ile)	not specified [RCV004604336]	uncertain significance	10	123162629	123162629	Human		name
407500771	CV3418027	single nucleotide variant	NM_004725.4(BUB3):c.916C>T (p.His306Tyr)	not specified [RCV004607213]	uncertain significance	10	123162773	123162773	Human		name
407500775	CV3418028	single nucleotide variant	NM_004725.4(BUB3):c.653A>T (p.Lys218Met)	not specified [RCV004607214]	uncertain significance	10	123162312	123162312	Human		name
407490197	CV3418029	single nucleotide variant	NM_004725.4(BUB3):c.538T>C (p.Tyr180His)	not specified [RCV004604338]	uncertain significance	10	123160527	123160527	Human		name
407490200	CV3418030	single nucleotide variant	NM_004725.4(BUB3):c.527C>A (p.Ser176Tyr)	not specified [RCV004604339]	uncertain significance	10	123160516	123160516	Human		name
407490206	CV3418032	single nucleotide variant	NM_004725.4(BUB3):c.382C>G (p.Pro128Ala)	not specified [RCV004604341]	uncertain significance	10	123157845	123157845	Human		name
407490209	CV3418033	single nucleotide variant	NM_004725.4(BUB3):c.475G>C (p.Val159Leu)	not specified [RCV004604342]	uncertain significance	10	123160464	123160464	Human		name
407490215	CV3418035	single nucleotide variant	NM_004725.4(BUB3):c.905A>G (p.Asp302Gly)	not specified [RCV004604344]	uncertain significance	10	123162762	123162762	Human		name
407490219	CV3418036	single nucleotide variant	NM_004725.4(BUB3):c.433G>A (p.Val145Met)	not specified [RCV004604345]	uncertain significance	10	123160422	123160422	Human		name
407490232	CV3418040	single nucleotide variant	NM_004725.4(BUB3):c.553A>G (p.Ile185Val)	not specified [RCV004604349]	uncertain significance	10	123160542	123160542	Human		name
407490235	CV3418041	single nucleotide variant	NM_004725.4(BUB3):c.685A>T (p.Asn229Tyr)	not specified [RCV004604350]	uncertain significance	10	123162344	123162344	Human		name
597792903	CV3643661	single nucleotide variant	NM_004725.4(BUB3):c.547C>T (p.Arg183Cys)	not specified [RCV004902799]	uncertain significance	10	123160536	123160536	Human		name
597792906	CV3643663	single nucleotide variant	NM_004725.4(BUB3):c.389A>G (p.Asn130Ser)	not specified [RCV004902800]	uncertain significance	10	123157852	123157852	Human		name
597792915	CV3643667	single nucleotide variant	NM_004725.4(BUB3):c.362A>G (p.Lys121Arg)	not specified [RCV004902803]	uncertain significance	10	123157825	123157825	Human		name
597792921	CV3643671	single nucleotide variant	NM_004725.4(BUB3):c.575A>G (p.Gln192Arg)	not specified [RCV004902805]	uncertain significance	10	123160564	123160564	Human		name
597750046	CV3643673	single nucleotide variant	NM_004725.4(BUB3):c.525G>T (p.Glu175Asp)	not specified [RCV004892481]	uncertain significance	10	123160514	123160514	Human		name
597792926	CV3643675	single nucleotide variant	NM_004725.4(BUB3):c.560C>G (p.Ala187Gly)	not specified [RCV004902807]	uncertain significance	10	123160549	123160549	Human		name
597750055	CV3643677	single nucleotide variant	NM_004725.4(BUB3):c.629C>G (p.Pro210Arg)	not specified [RCV004892483]	uncertain significance	10	123162288	123162288	Human		name
597792929	CV3643679	single nucleotide variant	NM_004725.4(BUB3):c.780T>G (p.Ile260Met)	not specified [RCV004902808]	uncertain significance	10	123162637	123162637	Human		name
597792932	CV3643682	single nucleotide variant	NM_004725.4(BUB3):c.317C>T (p.Pro106Leu)	not specified [RCV004902809]	uncertain significance	10	123157780	123157780	Human		name
597792943	CV3643686	single nucleotide variant	NM_004725.4(BUB3):c.496A>G (p.Asn166Asp)	not specified [RCV004902813]	uncertain significance	10	123160485	123160485	Human		name
597792958	CV3643691	single nucleotide variant	NM_004725.4(BUB3):c.794A>G (p.Asn265Ser)	not specified [RCV004902818]	uncertain significance	10	123162651	123162651	Human		name
597792961	CV3643693	single nucleotide variant	NM_004725.4(BUB3):c.733A>G (p.Ile245Val)	not specified [RCV004902819]	uncertain significance	10	123162392	123162392	Human		name
597792972	CV3643697	single nucleotide variant	NM_004725.4(BUB3):c.862G>A (p.Gly288Arg)	not specified [RCV004902823]	uncertain significance	10	123162719	123162719	Human		name
597792975	CV3643698	single nucleotide variant	NM_004725.4(BUB3):c.298A>G (p.Arg100Gly)	not specified [RCV004902824]	uncertain significance	10	123157761	123157761	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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