Pdyn Variant Search Result - Rat Genome Database

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200 records found for search term Pdyn

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
11652414	CV334875	single nucleotide variant	NM_024411.5(PDYN):c.-42A>T	Spinocerebellar ataxia type 23 [RCV000304722]	uncertain significance	20	1992606	1992606	Human	1	name
28890820	CV885856	single nucleotide variant	NM_024411.5(PDYN):c.*78A>G	Spinocerebellar ataxia type 23 [RCV001139161]	benign	20	1980245	1980245	Human	1	name
28890823	CV885857	single nucleotide variant	NM_024411.5(PDYN):c.*65C>G	Spinocerebellar ataxia type 23 [RCV001139162]	uncertain significance	20	1980258	1980258	Human	1	name
28890826	CV885858	single nucleotide variant	NM_024411.5(PDYN):c.*33A>C	Spinocerebellar ataxia type 23 [RCV001139163]	likely benign	20	1980290	1980290	Human	1	name
28883786	CV885867	single nucleotide variant	NM_024411.5(PDYN):c.-43G>A	Spinocerebellar ataxia type 23 [RCV001137021]	uncertain significance	20	1992607	1992607	Human	1	name
11612909	CV334850	single nucleotide variant	NM_024411.5(PDYN):c.*743T>C	Spinocerebellar ataxia type 23 [RCV000263533]\|not provided [RCV004717352]	benign	20	1979580	1979580	Human	1	name
11661741	CV334857	single nucleotide variant	NM_024411.5(PDYN):c.*522C>T	Spinocerebellar ataxia type 23 [RCV000379350]	uncertain significance	20	1979801	1979801	Human	1	name
11616007	CV334867	single nucleotide variant	NM_024411.5(PDYN):c.*346G>A	Spinocerebellar ataxia type 23 [RCV000290894]\|not provided [RCV004694595]	uncertain significance	20	1979977	1979977	Human	1	name
11620134	CV334880	single nucleotide variant	NM_024411.4(PDYN):c.-382C>T	Autosomal dominant cerebellar ataxia [RCV000333444]	likely benign	20	1994213	1994213	Human	1	name
11632213	CV344728	single nucleotide variant	NM_024411.5(PDYN):c.*836C>G	Spinocerebellar ataxia type 23 [RCV000400841]	benign\|likely benign	20	1979487	1979487	Human	1	name
11630606	CV344729	single nucleotide variant	NM_024411.5(PDYN):c.*771T>C	Spinocerebellar ataxia type 23 [RCV000353637]\|not provided [RCV004717351]	benign	20	1979552	1979552	Human	1	name
11630785	CV344733	single nucleotide variant	NM_024411.5(PDYN):c.*656T>C	Spinocerebellar ataxia type 23 [RCV000359519]\|not provided [RCV004717353]	benign\|likely benign	20	1979667	1979667	Human	1	name
11645296	CV344736	single nucleotide variant	NM_024411.5(PDYN):c.*561C>T	Spinocerebellar ataxia type 23 [RCV000264902]	uncertain significance	20	1979762	1979762	Human	1	name
11631625	CV344742	single nucleotide variant	NM_024411.5(PDYN):c.*356T>C	Spinocerebellar ataxia type 23 [RCV000384132]\|not provided [RCV004717354]	benign\|likely benign	20	1979967	1979967	Human	1	name
11656315	CV344744	single nucleotide variant	NM_024411.5(PDYN):c.*261C>T	Spinocerebellar ataxia type 23 [RCV000331910]	uncertain significance	20	1980062	1980062	Human	1	name
11631085	CV344752	single nucleotide variant	NM_024411.4(PDYN):c.-358G>A	Autosomal dominant cerebellar ataxia [RCV000368252]	uncertain significance	20	1994189	1994189	Human	1	name
11631790	CV344754	single nucleotide variant	NM_024411.4(PDYN):c.-402C>G	Autosomal dominant cerebellar ataxia [RCV000388020]	uncertain significance	20	1994233	1994233	Human	1	name
11631705	CV349710	single nucleotide variant	NM_024411.5(PDYN):c.*231C>G	Spinocerebellar ataxia type 23 [RCV000386330]\|not provided [RCV002263613]	benign\|uncertain significance	20	1980092	1980092	Human	1	name
11660081	CV349714	single nucleotide variant	NM_024411.5(PDYN):c.-162A>G	Spinocerebellar ataxia type 23 [RCV000364098]	uncertain significance	20	1993993	1993993	Human	1	name
11626746	CV349717	single nucleotide variant	NM_024411.4(PDYN):c.-241G>C	Autosomal dominant cerebellar ataxia [RCV000269505]	uncertain significance	20	1994072	1994072	Human	1	name
11655910	CV349719	single nucleotide variant	NM_024411.4(PDYN):c.-286G>C	Autosomal dominant cerebellar ataxia [RCV000329214]	uncertain significance	20	1994117	1994117	Human	1	name
11630583	CV350697	single nucleotide variant	NM_024411.5(PDYN):c.*847T>C	Spinocerebellar ataxia type 23 [RCV000352319]	uncertain significance	20	1979476	1979476	Human	1	name
11651441	CV350698	single nucleotide variant	NM_024411.5(PDYN):c.*827A>G	Spinocerebellar ataxia type 23 [RCV000298858]	uncertain significance	20	1979496	1979496	Human	1	name
11629494	CV350702	single nucleotide variant	NM_024411.5(PDYN):c.*556C>T	Spinocerebellar ataxia type 23 [RCV000324808]	benign\|likely benign	20	1979767	1979767	Human	1	name
11629499	CV350705	single nucleotide variant	NM_024411.5(PDYN):c.*369A>G	Spinocerebellar ataxia type 23 [RCV000324951]	benign\|likely benign	20	1979954	1979954	Human	1	name
11628207	CV350706	single nucleotide variant	NM_024411.5(PDYN):c.*138A>G	Spinocerebellar ataxia type 23 [RCV000296775]\|not provided [RCV001709608]	benign\|likely benign	20	1980185	1980185	Human	1	name
11630522	CV350709	single nucleotide variant	NM_024411.5(PDYN):c.*103C>T	Spinocerebellar ataxia type 23 [RCV000351495]\|not provided [RCV004694596]	uncertain significance	20	1980220	1980220	Human	1	name
11627013	CV350714	single nucleotide variant	NM_024411.4(PDYN):c.-381A>G	Autosomal dominant cerebellar ataxia [RCV000273681]	benign	20	1994212	1994212	Human	1	name
28897664	CV885847	single nucleotide variant	NM_024411.5(PDYN):c.*872C>A	Spinocerebellar ataxia type 23 [RCV001141669]	uncertain significance	20	1979451	1979451	Human	1	name
28897669	CV885848	single nucleotide variant	NM_024411.5(PDYN):c.*760G>C	Spinocerebellar ataxia type 23 [RCV001141670]\|not provided [RCV003438674]	benign\|uncertain significance	20	1979563	1979563	Human	1	name
28902221	CV885849	single nucleotide variant	NM_024411.5(PDYN):c.*671T>C	Spinocerebellar ataxia type 23 [RCV001143492]	uncertain significance	20	1979652	1979652	Human	1	name
28902224	CV885850	single nucleotide variant	NM_024411.5(PDYN):c.*670A>T	Spinocerebellar ataxia type 23 [RCV001143493]	uncertain significance	20	1979653	1979653	Human	1	name
28902228	CV885851	single nucleotide variant	NM_024411.5(PDYN):c.*636G>C	Spinocerebellar ataxia type 23 [RCV001143494]	uncertain significance	20	1979687	1979687	Human	1	name
28883422	CV885852	single nucleotide variant	NM_024411.5(PDYN):c.*556C>A	Spinocerebellar ataxia type 23 [RCV001136917]	uncertain significance	20	1979767	1979767	Human	1	name
28883425	CV885853	single nucleotide variant	NM_024411.5(PDYN):c.*389A>T	Spinocerebellar ataxia type 23 [RCV001136918]	uncertain significance	20	1979934	1979934	Human	1	name
28883429	CV885854	single nucleotide variant	NM_024411.5(PDYN):c.*320C>T	Spinocerebellar ataxia type 23 [RCV001136919]	uncertain significance	20	1980003	1980003	Human	1	name
28890816	CV885855	single nucleotide variant	NM_024411.5(PDYN):c.*225T>C	Spinocerebellar ataxia type 23 [RCV001139160]	benign	20	1980098	1980098	Human	1	name
155268219	CV1705301	single nucleotide variant	NM_024411.5(PDYN):c.129+1G>A	not provided [RCV002285906]	uncertain significance	20	1982955	1982955	Human		name
156225438	CV2080783	single nucleotide variant	NM_024411.5(PDYN):c.129+3A>G	not provided [RCV002876033]	uncertain significance	20	1982953	1982953	Human		name
401919661	CV2827037	single nucleotide variant	NM_024411.5(PDYN):c.-19-9C>T	not provided [RCV003431226]	uncertain significance	20	1983112	1983112	Human		name
11644921	CV334842	single nucleotide variant	NM_024411.5(PDYN):c.*1532C>T	Spinocerebellar ataxia type 23 [RCV000262123]	uncertain significance	20	1978791	1978791	Human	1	name
11621300	CV334848	single nucleotide variant	NM_024411.5(PDYN):c.*1071G>A	Spinocerebellar ataxia type 23 [RCV000346631]\|not provided [RCV003437076]	benign\|uncertain significance	20	1979252	1979252	Human	1	name
11629394	CV344718	single nucleotide variant	NM_024411.5(PDYN):c.*1443G>A	Spinocerebellar ataxia type 23 [RCV000321841]\|not provided [RCV004717349]	benign\|likely benign	20	1978880	1978880	Human	1	name
11632233	CV344725	single nucleotide variant	NM_024411.5(PDYN):c.*1030C>T	Spinocerebellar ataxia type 23 [RCV000401555]\|not provided [RCV004717350]	benign	20	1979293	1979293	Human	1	name
11631388	CV349705	single nucleotide variant	NM_024411.5(PDYN):c.*1396C>T	Spinocerebellar ataxia type 23 [RCV000376552]	benign\|likely benign	20	1978927	1978927	Human	1	name
11657498	CV349706	single nucleotide variant	NM_024411.5(PDYN):c.*1274T>G	Spinocerebellar ataxia type 23 [RCV000341566]	uncertain significance	20	1979049	1979049	Human	1	name
11631619	CV349709	single nucleotide variant	NM_024411.5(PDYN):c.*1238A>T	Autosomal dominant cerebellar ataxia [RCV000382262]	likely benign	20	1979085	1979085	Human	1	name
11627642	CV350693	single nucleotide variant	NM_024411.5(PDYN):c.*1394C>A	Spinocerebellar ataxia type 23 [RCV000286614]	benign\|likely benign	20	1978929	1978929	Human	1	name
11627752	CV350695	single nucleotide variant	NM_024411.5(PDYN):c.*1157T>G	Spinocerebellar ataxia type 23 [RCV000287865]	uncertain significance	20	1979166	1979166	Human	1	name
11628898	CV350696	single nucleotide variant	NM_024411.5(PDYN):c.*1029A>G	Spinocerebellar ataxia type 23 [RCV000311521]	benign\|likely benign	20	1979294	1979294	Human	1	name
14693671	CV620917	single nucleotide variant	NM_024411.5(PDYN):c.-19-1G>C	not specified [RCV003323721]	uncertain significance	20	1983104	1983104	Human		name
15177320	CV776925	single nucleotide variant	NM_024411.5(PDYN):c.129+8T>C	not provided [RCV000929127]	likely benign	20	1982948	1982948	Human		name
28883067	CV885843	single nucleotide variant	NM_024411.5(PDYN):c.*1457C>G	Spinocerebellar ataxia type 23 [RCV001136814]	benign	20	1978866	1978866	Human	1	name
28883070	CV885844	single nucleotide variant	NM_024411.5(PDYN):c.*1394C>T	Spinocerebellar ataxia type 23 [RCV001136815]	uncertain significance	20	1978929	1978929	Human	1	name
28890496	CV885845	single nucleotide variant	NM_024411.5(PDYN):c.*1336G>C	Spinocerebellar ataxia type 23 [RCV001139057]	uncertain significance	20	1978987	1978987	Human	1	name
28890498	CV885846	single nucleotide variant	NM_024411.5(PDYN):c.*1065C>T	Spinocerebellar ataxia type 23 [RCV001139058]	uncertain significance	20	1979258	1979258	Human	1	name
126913450	CV1038755	single nucleotide variant	NM_024411.5(PDYN):c.-80+226T>C	not provided [RCV001357385]	uncertain significance	20	1993685	1993685	Human		name
150501710	CV1224261	single nucleotide variant	NM_024411.5(PDYN):c.130-171G>A	not provided [RCV001620902]	benign	20	1981129	1981129	Human		name
150462400	CV1253368	single nucleotide variant	NM_024411.5(PDYN):c.129+189C>T	not provided [RCV001669697]	benign	20	1982767	1982767	Human		name
150515545	CV1285577	single nucleotide variant	NM_024411.5(PDYN):c.-19-246T>C	not provided [RCV001723030]	benign	20	1983349	1983349	Human		name
11628369	CV350701	deletion	NM_024411.5(PDYN):c.700_703del	Autosomal dominant cerebellar ataxia [RCV000300116]	uncertain significance	20	1979620	1979623	Human	1	name
156367269	CV2190330	single nucleotide variant	NM_024411.5(PDYN):c.2T>C (p.Met1Thr)	not provided [RCV003066034]	uncertain significance	20	1983083	1983083	Human		name
21067100	CV793819	single nucleotide variant	NM_024411.5(PDYN):c.72G>A (p.Ser24=)	not provided [RCV000992515]	benign	20	1983013	1983013	Human		name
41406936	CV983198	single nucleotide variant	NM_024411.5(PDYN):c.67C>T (p.Leu23=)	PDYN-related disorder [RCV003928823]\|not provided [RCV002070093]\|not specified [RCV001289122]	benign\|likely benign	20	1983018	1983018	Human	1	name , trait , alternate_id
152166025	CV1618228	single nucleotide variant	NM_024411.5(PDYN):c.192C>T (p.Ser64=)	not provided [RCV002204362]	likely benign	20	1980896	1980896	Human		name
152124889	CV1640489	single nucleotide variant	NM_024411.5(PDYN):c.162G>T (p.Leu54=)	not provided [RCV002176054]	likely benign	20	1980926	1980926	Human		name
152162908	CV1648074	single nucleotide variant	NM_024411.5(PDYN):c.162G>A (p.Leu54=)	not provided [RCV002123522]	likely benign	20	1980926	1980926	Human		name
156033486	CV1932527	single nucleotide variant	NM_024411.5(PDYN):c.120C>T (p.Ile40=)	not provided [RCV002637268]	likely benign	20	1982965	1982965	Human		name
402473325	CV3172157	single nucleotide variant	NM_024411.5(PDYN):c.294C>A (p.Leu98=)	not provided [RCV003874760]	likely benign	20	1980794	1980794	Human		name
597857682	CV3793470	single nucleotide variant	NM_024411.5(PDYN):c.17T>C (p.Leu6Pro)	not provided [RCV005132126]	uncertain significance	20	1983068	1983068	Human		name
13216853	CV430285	deletion	NM_024411.5(PDYN):c.34del (p.Leu12fs)	not provided [RCV003766842]\|not specified [RCV000504081]	uncertain significance	20	1983051	1983051	Human		name
15189004	CV742279	single nucleotide variant	NM_024411.5(PDYN):c.138C>T (p.Ser46=)	not provided [RCV000909527]	likely benign	20	1980950	1980950	Human		name
15193066	CV773013	single nucleotide variant	NM_024411.5(PDYN):c.198G>A (p.Leu66=)	not provided [RCV000933262]	likely benign	20	1980890	1980890	Human		name
28902490	CV885865	single nucleotide variant	NM_024411.5(PDYN):c.244T>C (p.Leu82=)	Spinocerebellar ataxia type 23 [RCV001143593]	uncertain significance	20	1980844	1980844	Human	1	name
150432296	CV1246244	single nucleotide variant	NM_024411.5(PDYN):c.459T>C (p.Asp153=)	not specified [RCV001663657]	likely benign	20	1980629	1980629	Human		name
150432299	CV1246245	single nucleotide variant	NM_024411.5(PDYN):c.732G>A (p.Pro244=)	not specified [RCV001663658]	benign	20	1980356	1980356	Human		name
150438611	CV1274807	single nucleotide variant	NM_024411.5(PDYN):c.74G>A (p.Arg25Gln)	not provided [RCV001703080]	likely benign\|uncertain significance	20	1983011	1983011	Human		name
151350619	CV1325733	single nucleotide variant	NM_024411.5(PDYN):c.80C>G (p.Ser27Cys)	not specified [RCV001815078]	uncertain significance	20	1983005	1983005	Human		name
151878587	CV1376046	single nucleotide variant	NM_024411.5(PDYN):c.71C>T (p.Ser24Leu)	not provided [RCV002019852]	uncertain significance	20	1983014	1983014	Human		name
153303357	CV1686195	single nucleotide variant	NM_024411.5(PDYN):c.80C>T (p.Ser27Phe)	not provided [RCV002261628]	uncertain significance	20	1983005	1983005	Human		name
155801806	CV1864117	single nucleotide variant	NM_024411.5(PDYN):c.68T>G (p.Leu23Arg)	not provided [RCV002475069]	uncertain significance	20	1983017	1983017	Human		name
156347460	CV1868475	single nucleotide variant	NM_024411.5(PDYN):c.65G>A (p.Cys22Tyr)	not provided [RCV003064594]	uncertain significance	20	1983020	1983020	Human		name
155952088	CV1922022	single nucleotide variant	NM_024411.5(PDYN):c.59C>T (p.Ala20Val)	Inborn genetic diseases [RCV004961118]\|not provided [RCV002616279]	uncertain significance	20	1983026	1983026	Human	1	name
156449655	CV1941987	single nucleotide variant	NM_024411.5(PDYN):c.73C>T (p.Arg25Trp)	Inborn genetic diseases [RCV005382602]\|not provided [RCV003121781]	conflicting interpretations of pathogenicity\|uncertain significance	20	1983012	1983012	Human	1	name
156213209	CV1963096	single nucleotide variant	NM_024411.5(PDYN):c.489C>T (p.Leu163=)	not provided [RCV002575231]	likely benign	20	1980599	1980599	Human		name
156294336	CV2111572	single nucleotide variant	NM_024411.5(PDYN):c.88G>A (p.Ala30Thr)	not provided [RCV002922283]	uncertain significance	20	1982997	1982997	Human		name
156351349	CV2157539	single nucleotide variant	NM_024411.5(PDYN):c.41T>A (p.Met14Lys)	not provided [RCV003030897]	uncertain significance	20	1983044	1983044	Human		name
156274037	CV2164270	single nucleotide variant	NM_024411.5(PDYN):c.618C>G (p.Arg206=)	not provided [RCV003027090]	likely benign	20	1980470	1980470	Human		name
401919572	CV2827036	single nucleotide variant	NM_024411.5(PDYN):c.393G>A (p.Arg131=)	not provided [RCV003431225]	likely benign	20	1980695	1980695	Human		name
402489532	CV2861911	single nucleotide variant	NM_024411.5(PDYN):c.528G>A (p.Gly176=)	not provided [RCV003544712]	likely benign	20	1980560	1980560	Human		name
405033479	CV2922767	single nucleotide variant	NM_024411.5(PDYN):c.708G>A (p.Val236=)	not provided [RCV003578535]	likely benign	20	1980380	1980380	Human		name
405078598	CV2945409	single nucleotide variant	NM_024411.5(PDYN):c.378G>A (p.Leu126=)	not provided [RCV003664436]	likely benign	20	1980710	1980710	Human		name
405252541	CV3047351	single nucleotide variant	NM_024411.5(PDYN):c.729T>C (p.Asp243=)	not provided [RCV003722259]	likely benign	20	1980359	1980359	Human		name
11646299	CV334858	indel	NM_024411.5(PDYN):c.449_459delinsTAA	Autosomal dominant cerebellar ataxia [RCV000269910]	uncertain significance	20	1979864	1979874	Human		name
11625360	CV334872	single nucleotide variant	NM_024411.5(PDYN):c.600T>C (p.His200=)	Spinocerebellar ataxia type 23 [RCV000606402]\|not provided [RCV001523416]\|not specified [RCV001289121]	benign	20	1980488	1980488	Human	1	name
11628521	CV344746	single nucleotide variant	NM_024411.5(PDYN):c.483C>G (p.Leu161=)	Spinocerebellar ataxia type 23 [RCV000303380]\|not provided [RCV003105874]	likely benign\|uncertain significance	20	1980605	1980605	Human	1	name
11631940	CV344751	single nucleotide variant	NM_024411.5(PDYN):c.405C>T (p.Asp135=)	Spinocerebellar ataxia type 23 [RCV000392614]\|not provided [RCV002057727]	likely benign\|uncertain significance	20	1980683	1980683	Human	1	name
407463725	CV3470487	single nucleotide variant	NM_024411.5(PDYN):c.67C>G (p.Leu23Val)	Inborn genetic diseases [RCV004659765]	uncertain significance	20	1983018	1983018	Human	1	name
11662896	CV349713	single nucleotide variant	NM_024411.5(PDYN):c.501C>T (p.Asp167=)	Spinocerebellar ataxia type 23 [RCV000390192]	uncertain significance	20	1980587	1980587	Human	1	name
597911187	CV3844814	single nucleotide variant	NM_024411.5(PDYN):c.612C>T (p.Tyr204=)	not provided [RCV005186320]	likely benign	20	1980476	1980476	Human		name
598260694	CV4002655	single nucleotide variant	NM_024411.5(PDYN):c.98C>T (p.Thr33Ile)	Inborn genetic diseases [RCV005386744]	uncertain significance	20	1982987	1982987	Human	1	name
13531501	CV512442	single nucleotide variant	NM_024411.5(PDYN):c.53C>T (p.Thr18Ile)	Inborn genetic diseases [RCV000623384]	uncertain significance	20	1983032	1983032	Human	1	name
13810645	CV577833	single nucleotide variant	NM_024411.5(PDYN):c.691C>A (p.Arg231=)	Spinocerebellar ataxia type 23 [RCV001141783]\|not provided [RCV000712516]\|not specified [RCV004997236]	likely benign\|uncertain significance	20	1980397	1980397	Human	1	name
15169524	CV716867	single nucleotide variant	NM_024411.5(PDYN):c.607C>T (p.Leu203=)	not provided [RCV000971829]	likely benign	20	1980481	1980481	Human		name
15157432	CV742277	single nucleotide variant	NM_024411.5(PDYN):c.582C>T (p.Asp194=)	Spinocerebellar ataxia type 23 [RCV001141785]\|not provided [RCV000902527]\|not specified [RCV001289119]	benign\|likely benign\|uncertain significance	20	1980506	1980506	Human	1	name
15155778	CV742278	single nucleotide variant	NM_024411.5(PDYN):c.300G>T (p.Gly100=)	not provided [RCV000902204]	likely benign	20	1980788	1980788	Human		name
15149384	CV757391	single nucleotide variant	NM_024411.5(PDYN):c.561A>C (p.Ser187=)	not provided [RCV000923276]	likely benign	20	1980527	1980527	Human		name
15106190	CV757392	single nucleotide variant	NM_024411.5(PDYN):c.444T>C (p.Asp148=)	not provided [RCV000915698]	likely benign	20	1980644	1980644	Human		name
21068111	CV797955	single nucleotide variant	NM_024411.5(PDYN):c.41T>C (p.Met14Thr)	not provided [RCV000997731]	uncertain significance	20	1983044	1983044	Human		name
28902485	CV885863	single nucleotide variant	NM_024411.5(PDYN):c.456C>T (p.Asn152=)	Spinocerebellar ataxia type 23 [RCV001143591]\|not provided [RCV001473757]	likely benign	20	1980632	1980632	Human	1	name
28883780	CV885866	single nucleotide variant	NM_024411.5(PDYN):c.86G>T (p.Cys29Phe)	Spinocerebellar ataxia type 23 [RCV001137020]	uncertain significance	20	1982999	1982999	Human	1	name
41406934	CV983199	single nucleotide variant	NM_024411.5(PDYN):c.40A>G (p.Met14Val)	not provided [RCV002070092]\|not specified [RCV001289116]	benign	20	1983045	1983045	Human		name
150543933	CV1309884	single nucleotide variant	NM_024411.5(PDYN):c.146G>A (p.Cys49Tyr)	not provided [RCV003237626]	uncertain significance	20	1980942	1980942	Human		name
151748480	CV1478851	single nucleotide variant	NM_024411.5(PDYN):c.209C>T (p.Thr70Ile)	not provided [RCV002023114]	uncertain significance	20	1980879	1980879	Human		name
153304994	CV1687441	single nucleotide variant	NM_024411.5(PDYN):c.135C>G (p.Cys45Trp)	not provided [RCV002263261]	uncertain significance	20	1980953	1980953	Human		name
10044801	CV188054	single nucleotide variant	NM_024411.5(PDYN):c.217A>G (p.Thr73Ala)	Spinocerebellar ataxia type 23 [RCV000170442]	likely pathogenic\|uncertain significance	20	1980871	1980871	Human	1	name
156446317	CV1951354	single nucleotide variant	NM_024411.5(PDYN):c.271C>T (p.Pro91Ser)	Inborn genetic diseases [RCV004245961]\|not provided [RCV003117289]	likely benign\|uncertain significance	20	1980817	1980817	Human	1	name
156115599	CV2035501	single nucleotide variant	NM_024411.5(PDYN):c.154G>A (p.Ala52Thr)	not provided [RCV002785578]	uncertain significance	20	1980934	1980934	Human		name
155996125	CV2056435	single nucleotide variant	NM_024411.5(PDYN):c.104A>G (p.Asp35Gly)	not provided [RCV002819430]	uncertain significance	20	1982981	1982981	Human		name
156028421	CV2109083	single nucleotide variant	NM_024411.5(PDYN):c.137C>T (p.Ser46Phe)	not provided [RCV002909951]	uncertain significance	20	1980951	1980951	Human		name
401894286	CV2780594	single nucleotide variant	NM_024411.5(PDYN):c.293T>C (p.Leu98Pro)	Inborn genetic diseases [RCV003371339]	uncertain significance	20	1980795	1980795	Human	1	name
401962701	CV2845323	single nucleotide variant	NM_024411.5(PDYN):c.149A>G (p.Gln50Arg)	not provided [RCV003482784]	uncertain significance	20	1980939	1980939	Human		name
401962702	CV2845324	single nucleotide variant	NM_024411.5(PDYN):c.275A>G (p.Tyr92Cys)	not provided [RCV003482785]	uncertain significance	20	1980813	1980813	Human		name
596926380	CV3539817	deletion	NM_024411.5(PDYN):c.751del (p.Leu251fs)	not provided [RCV004790808]	uncertain significance	20	1980337	1980337	Human		name
597713425	CV3579230	single nucleotide variant	NM_024411.5(PDYN):c.250A>G (p.Ser84Gly)	Inborn genetic diseases [RCV004959439]	uncertain significance	20	1980838	1980838	Human	1	name
597865938	CV3794337	single nucleotide variant	NM_024411.5(PDYN):c.220C>G (p.Leu74Val)	not provided [RCV005140513]	uncertain significance	20	1980868	1980868	Human		name
597925410	CV3859448	single nucleotide variant	NM_024411.5(PDYN):c.209C>A (p.Thr70Asn)	not provided [RCV005200104]	uncertain significance	20	1980879	1980879	Human		name
13479203	CV442266	single nucleotide variant	NM_024411.5(PDYN):c.268G>A (p.Gly90Arg)	Inborn genetic diseases [RCV002527505]\|not provided [RCV000516917]	benign\|likely benign\|uncertain significance	20	1980820	1980820	Human	1	name
13485762	CV442267	single nucleotide variant	NM_024411.5(PDYN):c.121A>G (p.Asn41Asp)	PDYN-related disorder [RCV003905304]\|not provided [RCV000904758]\|not specified [RCV000518822]	benign\|likely benign	20	1982964	1982964	Human	1	name , trait , alternate_id
13482040	CV442268	single nucleotide variant	NM_024411.5(PDYN):c.106G>T (p.Gly36Cys)	Spinocerebellar ataxia type 23 [RCV002490885]\|not provided [RCV000900279]\|not specified [RCV000517756]	benign\|likely benign	20	1982979	1982979	Human	1	name
14693670	CV620654	deletion	NM_024411.5(PDYN):c.496del (p.Glu166fs)	Spinocerebellar ataxia type 23 [RCV000779343]	uncertain significance	20	1980592	1980592	Human		name
28902487	CV885864	single nucleotide variant	NM_024411.5(PDYN):c.257C>T (p.Ser86Leu)	Spinocerebellar ataxia type 23 [RCV001143592]\|not provided [RCV002559386]	uncertain significance	20	1980831	1980831	Human	1	name
150432293	CV1246243	single nucleotide variant	NM_024411.5(PDYN):c.321G>T (p.Glu107Asp)	not provided [RCV001663656]	uncertain significance	20	1980767	1980767	Human		name
151757693	CV1288085	single nucleotide variant	NM_024411.5(PDYN):c.635G>A (p.Arg212Gln)	Spinocerebellar ataxia type 23 [RCV001849208]\|not provided [RCV002261376]\|not specified [RCV004998957]	likely benign\|uncertain significance	20	1980453	1980453	Human	1	name
151350700	CV1325752	single nucleotide variant	NM_024411.5(PDYN):c.394G>T (p.Gly132Cys)	not specified [RCV001815097]	uncertain significance	20	1980694	1980694	Human		name
151353336	CV1326427	single nucleotide variant	NM_024411.5(PDYN):c.437T>A (p.Met146Lys)	not provided [RCV001816301]	uncertain significance	20	1980651	1980651	Human		name
151883717	CV1338120	single nucleotide variant	NM_024411.5(PDYN):c.731C>T (p.Pro244Leu)	not provided [RCV001962189]	uncertain significance	20	1980357	1980357	Human		name
151830802	CV1343501	single nucleotide variant	NM_024411.5(PDYN):c.347C>G (p.Ser116Ter)	not provided [RCV001920470]	uncertain significance	20	1980741	1980741	Human		name
151724547	CV1357030	single nucleotide variant	NM_024411.5(PDYN):c.695G>A (p.Arg232His)	not provided [RCV001966418]	uncertain significance	20	1980393	1980393	Human		name
151855467	CV1372878	single nucleotide variant	NM_024411.5(PDYN):c.584G>A (p.Gly195Glu)	not provided [RCV001996483]	uncertain significance	20	1980504	1980504	Human		name
151738328	CV1379158	single nucleotide variant	NM_024411.5(PDYN):c.530G>A (p.Gly177Asp)	not provided [RCV001911675]	uncertain significance	20	1980558	1980558	Human		name
151755619	CV1387873	single nucleotide variant	NM_024411.5(PDYN):c.746G>A (p.Gly249Glu)	not provided [RCV001969637]	uncertain significance	20	1980342	1980342	Human		name
151753680	CV1471178	single nucleotide variant	NM_024411.5(PDYN):c.727G>A (p.Asp243Asn)	not provided [RCV001948404]	uncertain significance	20	1980361	1980361	Human		name
151765697	CV1495926	single nucleotide variant	NM_024411.5(PDYN):c.568G>T (p.Ala190Ser)	Inborn genetic diseases [RCV004656681]\|not provided [RCV001873951]	uncertain significance	20	1980520	1980520	Human	1	name
155748869	CV1772480	single nucleotide variant	NM_024411.5(PDYN):c.623G>A (p.Gly208Glu)	not provided [RCV002304004]	uncertain significance	20	1980465	1980465	Human		name
155707684	CV1778442	single nucleotide variant	NM_024411.5(PDYN):c.385A>C (p.Lys129Gln)	not provided [RCV002296045]	uncertain significance	20	1980703	1980703	Human		name
155797067	CV1863162	single nucleotide variant	NM_024411.5(PDYN):c.630C>G (p.Phe210Leu)	Spinocerebellar ataxia type 23 [RCV002470436]	uncertain significance	20	1980458	1980458	Human	1	name
156211268	CV1909767	single nucleotide variant	NM_024411.5(PDYN):c.539G>A (p.Arg180His)	not provided [RCV002596072]	uncertain significance	20	1980549	1980549	Human		name
155948559	CV1921780	single nucleotide variant	NM_024411.5(PDYN):c.490G>A (p.Ala164Thr)	Inborn genetic diseases [RCV002616089]\|not provided [RCV002616088]	likely benign\|uncertain significance	20	1980598	1980598	Human	1	name
156437645	CV1947655	single nucleotide variant	NM_024411.5(PDYN):c.365T>C (p.Leu122Pro)	not provided [RCV003107185]	uncertain significance	20	1980723	1980723	Human		name
156221277	CV1981305	single nucleotide variant	NM_024411.5(PDYN):c.457G>A (p.Asp153Asn)	not provided [RCV002626455]	uncertain significance	20	1980631	1980631	Human		name
10403742	CV208643	single nucleotide variant	NM_024411.5(PDYN):c.583G>A (p.Gly195Arg)	not specified [RCV000193293]	uncertain significance	20	1980505	1980505	Human		name
156107834	CV2096527	single nucleotide variant	NM_024411.5(PDYN):c.422C>T (p.Ala141Val)	not provided [RCV002913655]	uncertain significance	20	1980666	1980666	Human		name
156258368	CV2098797	single nucleotide variant	NM_024411.5(PDYN):c.637C>T (p.Arg213Cys)	not provided [RCV002895491]	uncertain significance	20	1980451	1980451	Human		name
155912992	CV2148619	single nucleotide variant	NM_024411.5(PDYN):c.338C>G (p.Pro113Arg)	not provided [RCV002991456]	uncertain significance	20	1980750	1980750	Human		name
156307942	CV2249451	single nucleotide variant	NM_024411.5(PDYN):c.509A>T (p.Glu170Val)	Inborn genetic diseases [RCV002808705]	uncertain significance	20	1980579	1980579	Human	1	name
156292191	CV2296770	single nucleotide variant	NM_024411.5(PDYN):c.723G>C (p.Gln241His)	Inborn genetic diseases [RCV002878965]	uncertain significance	20	1980365	1980365	Human	1	name
243059316	CV2405956	single nucleotide variant	NM_024411.5(PDYN):c.718T>A (p.Ser240Thr)	Spinocerebellar ataxia type 23 [RCV003134789]	uncertain significance	20	1980370	1980370	Human	1	name
401798891	CV2742660	single nucleotide variant	NM_024411.5(PDYN):c.430G>C (p.Glu144Gln)	not provided [RCV003325105]	uncertain significance	20	1980658	1980658	Human		name
401919569	CV2827034	single nucleotide variant	NM_024411.5(PDYN):c.644G>A (p.Arg215His)	not provided [RCV003431224]	uncertain significance	20	1980444	1980444	Human		name
401961169	CV2844550	single nucleotide variant	NM_024411.5(PDYN):c.653T>C (p.Leu218Pro)	not provided [RCV003480346]	uncertain significance	20	1980435	1980435	Human		name
401962703	CV2845325	single nucleotide variant	NM_024411.5(PDYN):c.565G>A (p.Val189Met)	not provided [RCV003482786]	uncertain significance	20	1980523	1980523	Human		name
405123595	CV2885154	single nucleotide variant	NM_024411.5(PDYN):c.476G>A (p.Gly159Asp)	not provided [RCV003559317]	uncertain significance	20	1980612	1980612	Human		name
405085250	CV2943101	single nucleotide variant	NM_024411.5(PDYN):c.538C>A (p.Arg180Ser)	not provided [RCV003664905]	uncertain significance	20	1980550	1980550	Human		name
405016436	CV2991606	single nucleotide variant	NM_024411.5(PDYN):c.660G>A (p.Trp220Ter)	not provided [RCV003694443]	uncertain significance	20	1980428	1980428	Human		name
405205980	CV2997664	single nucleotide variant	NM_024411.5(PDYN):c.650A>G (p.Lys217Arg)	not provided [RCV003678652]	uncertain significance	20	1980438	1980438	Human		name
405077681	CV3136965	single nucleotide variant	NM_024411.5(PDYN):c.596G>C (p.Gly199Ala)	Inborn genetic diseases [RCV005387274]\|not provided [RCV003833863]	uncertain significance	20	1980492	1980492	Human	1	name
405061395	CV3148345	single nucleotide variant	NM_024411.5(PDYN):c.566T>G (p.Val189Gly)	not provided [RCV003850301]	uncertain significance	20	1980522	1980522	Human		name
405127446	CV3167074	single nucleotide variant	NM_024411.5(PDYN):c.547C>A (p.Pro183Thr)	not provided [RCV003854329]	uncertain significance	20	1980541	1980541	Human		name
11622262	CV334873	single nucleotide variant	NM_024411.5(PDYN):c.436A>C (p.Met146Leu)	Spinocerebellar ataxia type 23 [RCV000624990]\|not provided [RCV000891825]\|not specified [RCV001289117]	benign\|likely benign	20	1980652	1980652	Human	1	name
8565718	CV33497	single nucleotide variant	NM_024411.5(PDYN):c.414G>T (p.Arg138Ser)	Spinocerebellar ataxia type 23 [RCV000018094]\|not provided [RCV001268483]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity	20	1980674	1980674	Human	1	name
8565719	CV33498	single nucleotide variant	NM_024411.5(PDYN):c.643C>T (p.Arg215Cys)	Spinocerebellar ataxia type 23 [RCV000018095]	pathogenic	20	1980445	1980445	Human	1	name
8565720	CV33499	single nucleotide variant	NM_024411.5(PDYN):c.632T>C (p.Leu211Ser)	Spinocerebellar ataxia type 23 [RCV000018096]\|not provided [RCV000992514]	pathogenic\|uncertain significance	20	1980456	1980456	Human	1	name
8565721	CV33500	single nucleotide variant	NM_024411.5(PDYN):c.634C>T (p.Arg212Trp)	Spinocerebellar ataxia type 23 [RCV000018097]	pathogenic\|likely pathogenic	20	1980454	1980454	Human	1	name
405789494	CV3372083	single nucleotide variant	NM_024411.5(PDYN):c.503C>A (p.Pro168His)	Inborn genetic diseases [RCV004505502]	uncertain significance	20	1980585	1980585	Human	1	name
407528625	CV3470486	single nucleotide variant	NM_024411.5(PDYN):c.692G>A (p.Arg231Gln)	Inborn genetic diseases [RCV004655617]	uncertain significance	20	1980396	1980396	Human	1	name
407528626	CV3470488	single nucleotide variant	NM_024411.5(PDYN):c.557G>C (p.Ser186Thr)	Inborn genetic diseases [RCV004655618]	uncertain significance	20	1980531	1980531	Human	1	name
11627285	CV350710	single nucleotide variant	NM_024411.5(PDYN):c.575A>T (p.Glu192Val)	Spinocerebellar ataxia type 23 [RCV000279003]\|not provided [RCV000421771]\|not specified [RCV001289118]	benign\|likely benign	20	1980513	1980513	Human	1	name
11630027	CV350712	single nucleotide variant	NM_024411.5(PDYN):c.520C>T (p.Arg174Cys)	Spinocerebellar ataxia type 23 [RCV000338758]\|not provided [RCV001865228]\|not specified [RCV000518013]	likely benign\|uncertain significance	20	1980568	1980568	Human	1	name
596921207	CV3534768	single nucleotide variant	NM_024411.5(PDYN):c.380A>G (p.Glu127Gly)	not provided [RCV004784325]	uncertain significance	20	1980708	1980708	Human		name
597648918	CV3579226	single nucleotide variant	NM_024411.5(PDYN):c.566T>C (p.Val189Ala)	Inborn genetic diseases [RCV004959436]\|not provided [RCV005000593]	uncertain significance	20	1980522	1980522	Human	1	name
597713416	CV3579227	single nucleotide variant	NM_024411.5(PDYN):c.728A>T (p.Asp243Val)	Inborn genetic diseases [RCV004959437]	uncertain significance	20	1980360	1980360	Human	1	name
597713420	CV3579228	single nucleotide variant	NM_024411.5(PDYN):c.352A>C (p.Lys118Gln)	Inborn genetic diseases [RCV004959438]	uncertain significance	20	1980736	1980736	Human	1	name
597713433	CV3579231	single nucleotide variant	NM_024411.5(PDYN):c.529G>A (p.Gly177Ser)	Inborn genetic diseases [RCV004959440]	uncertain significance	20	1980559	1980559	Human	1	name
597713439	CV3579232	single nucleotide variant	NM_024411.5(PDYN):c.580G>T (p.Asp194Tyr)	Inborn genetic diseases [RCV004959441]	uncertain significance	20	1980508	1980508	Human	1	name
597650191	CV3730474	single nucleotide variant	NM_024411.5(PDYN):c.626G>A (p.Gly209Asp)	not provided [RCV005000763]	uncertain significance	20	1980462	1980462	Human		name
598260690	CV4002654	single nucleotide variant	NM_024411.5(PDYN):c.578G>C (p.Gly193Ala)	Inborn genetic diseases [RCV005386743]	uncertain significance	20	1980510	1980510	Human	1	name
13211371	CV426328	single nucleotide variant	NM_024411.5(PDYN):c.674G>A (p.Arg225His)	not provided [RCV000497351]	uncertain significance	20	1980414	1980414	Human		name
13477121	CV442263	single nucleotide variant	NM_024411.5(PDYN):c.716G>A (p.Arg239Gln)	Spinocerebellar ataxia type 23 [RCV005398737]\|not provided [RCV000905914]\|not specified [RCV000516280]	benign\|likely benign	20	1980372	1980372	Human	1	name
13482465	CV442264	single nucleotide variant	NM_024411.5(PDYN):c.712A>G (p.Thr238Ala)	not provided [RCV000884160]\|not specified [RCV000517871]	benign	20	1980376	1980376	Human		name
13477376	CV442265	single nucleotide variant	NM_024411.5(PDYN):c.527G>A (p.Gly176Glu)	not provided [RCV000516350]	uncertain significance	20	1980561	1980561	Human		name
13810642	CV577834	single nucleotide variant	NM_024411.5(PDYN):c.405C>A (p.Asp135Glu)	not provided [RCV000712514]	uncertain significance	20	1980683	1980683	Human		name
28880065	CV860632	single nucleotide variant	NM_024411.5(PDYN):c.616C>T (p.Arg206Cys)	Spinocerebellar ataxia type 23 [RCV001141784]\|not provided [RCV001091282]	uncertain significance	20	1980472	1980472	Human	1	name
28890829	CV885859	single nucleotide variant	NM_024411.5(PDYN):c.724G>A (p.Glu242Lys)	Inborn genetic diseases [RCV003163305]\|Spinocerebellar ataxia type 23 [RCV001139164]\|not provided [RCV005093619]	uncertain significance	20	1980364	1980364	Human	2	name
28897968	CV885860	single nucleotide variant	NM_024411.5(PDYN):c.691C>T (p.Arg231Trp)	Inborn genetic diseases [RCV005394762]\|Spinocerebellar ataxia type 23 [RCV001141782]	uncertain significance	20	1980397	1980397	Human	2	name
28897975	CV885861	single nucleotide variant	NM_024411.5(PDYN):c.571G>T (p.Gly191Trp)	Inborn genetic diseases [RCV002557013]\|Spinocerebellar ataxia type 23 [RCV001141786]\|not provided [RCV002473206]	uncertain significance	20	1980517	1980517	Human	2	name
28897979	CV885862	single nucleotide variant	NM_024411.5(PDYN):c.538C>T (p.Arg180Cys)	Spinocerebellar ataxia type 23 [RCV001141787]\|not provided [RCV004694877]	uncertain significance	20	1980550	1980550	Human	1	name
41406935	CV983197	single nucleotide variant	NM_024411.5(PDYN):c.592A>T (p.Met198Leu)	not provided [RCV001289120]	uncertain significance	20	1980496	1980496	Human		name
10406876	CV208642	deletion	NM_024411.5(PDYN):c.658_659del (p.Trp220fs)	Spinocerebellar ataxia type 23 [RCV000991062]\|not provided [RCV000712515]\|not specified [RCV000194525]	conflicting interpretations of pathogenicity\|uncertain significance	20	1980429	1980430	Human	1	name
401930361	CV2827035	duplication	NM_024411.5(PDYN):c.519_527dup (p.Gly176_Gly177insArgTyrGly)	not provided [RCV003440313]	uncertain significance	20	1980560	1980561	Human		name

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