Pdzrn3 Variant Search Result - Rat Genome Database

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132 records found for search term Pdzrn3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15198507	CV777280	duplication	NM_015009.3(PDZRN3):c.1417-2dup	not provided [RCV000956776]	benign	3	73388070	73388071	Human		name
14350115	CV590847	single nucleotide variant	NM_015009.3(PDZRN3):c.1417-10T>C	Short stature [RCV000736216]	likely pathogenic	3	73388079	73388079	Human	2	name
15187195	CV777399	single nucleotide variant	NM_015009.3(PDZRN3):c.1636-10G>C	not provided [RCV000953515]	benign	3	73384940	73384940	Human		name
8578773	CV113161	single nucleotide variant	NM_015009.2(PDZRN3):c.919-3667T>C	Lung cancer [RCV000093684]	uncertain significance	3	73408062	73408062	Human		name
8578774	CV113162	single nucleotide variant	NM_015009.2(PDZRN3):c.919-87739G>T	Lung cancer [RCV000093685]	uncertain significance	3	73492134	73492134	Human		name
405789880	CV3372197	single nucleotide variant	NM_015009.3(PDZRN3):c.7T>G (p.Phe3Val)	not specified [RCV004505616]	uncertain significance	3	73624819	73624819	Human		name
405789839	CV3372187	single nucleotide variant	NM_015009.3(PDZRN3):c.25G>A (p.Asp9Asn)	not specified [RCV004505606]	uncertain significance	3	73624801	73624801	Human		name
156077202	CV2281643	single nucleotide variant	NM_015009.3(PDZRN3):c.31G>T (p.Asp11Tyr)	not specified [RCV004153935]	uncertain significance	3	73624795	73624795	Human		name
401922305	CV2827560	single nucleotide variant	NM_015009.3(PDZRN3):c.786T>C (p.Asn262=)	not provided [RCV003433669]	likely benign	3	73608622	73608622	Human		name
405789867	CV3372194	single nucleotide variant	NM_015009.3(PDZRN3):c.65A>G (p.His22Arg)	not specified [RCV004505613]	uncertain significance	3	73624761	73624761	Human		name
15186165	CV698287	single nucleotide variant	NM_015009.3(PDZRN3):c.924C>T (p.Asn308=)	not provided [RCV000953201]	benign	3	73404390	73404390	Human		name
155947338	CV2234802	single nucleotide variant	NM_015009.3(PDZRN3):c.182C>T (p.Ser61Leu)	not specified [RCV004111238]	uncertain significance	3	73624644	73624644	Human		name
401922304	CV2827559	single nucleotide variant	NM_015009.3(PDZRN3):c.2445C>T (p.Pro815=)	not provided [RCV003433668]	likely benign	3	73384121	73384121	Human		name
407463808	CV3470539	single nucleotide variant	NM_015009.3(PDZRN3):c.286C>G (p.Gln96Glu)	not specified [RCV004659786]	uncertain significance	3	73624540	73624540	Human		name
597721579	CV3579343	single nucleotide variant	NM_015009.3(PDZRN3):c.209C>T (p.Pro70Leu)	not specified [RCV004841959]	uncertain significance	3	73624617	73624617	Human		name
15186160	CV698286	single nucleotide variant	NM_015009.3(PDZRN3):c.1452T>C (p.Ala484=)	not provided [RCV000953200]	benign	3	73388034	73388034	Human		name
15153998	CV734291	single nucleotide variant	NM_015009.3(PDZRN3):c.1002G>A (p.Gln334=)	not provided [RCV000901869]	likely benign	3	73404312	73404312	Human		name
10448552	CV204614	single nucleotide variant	NM_015009.3(PDZRN3):c.820G>A (p.Asp274Asn)	Childhood-onset schizophrenia [RCV000202335]	likely pathogenic	3	73602452	73602452	Human	1	name
155962632	CV2285678	single nucleotide variant	NM_015009.3(PDZRN3):c.727G>A (p.Glu243Lys)	not specified [RCV004141530]	uncertain significance	3	73608681	73608681	Human		name
156095805	CV2297399	single nucleotide variant	NM_015009.3(PDZRN3):c.398C>T (p.Ala133Val)	not specified [RCV004153342]	uncertain significance	3	73624428	73624428	Human		name
156363772	CV2330042	single nucleotide variant	NM_015009.3(PDZRN3):c.433G>A (p.Gly145Ser)	not specified [RCV004185534]	uncertain significance	3	73624393	73624393	Human		name
329368707	CV2428112	single nucleotide variant	NM_015009.3(PDZRN3):c.803C>T (p.Pro268Leu)	not specified [RCV004254484]	uncertain significance	3	73608605	73608605	Human		name
329354759	CV2448974	single nucleotide variant	NM_015009.3(PDZRN3):c.686C>G (p.Ser229Trp)	not specified [RCV004264058]	uncertain significance	3	73624140	73624140	Human		name
329368681	CV2453247	single nucleotide variant	NM_015009.3(PDZRN3):c.407C>G (p.Ala136Gly)	not specified [RCV004266890]	uncertain significance	3	73624419	73624419	Human		name
329399328	CV2470045	single nucleotide variant	NM_015009.3(PDZRN3):c.928A>G (p.Arg310Gly)	not specified [RCV004287316]	uncertain significance	3	73404386	73404386	Human		name
401889759	CV2763373	single nucleotide variant	NM_015009.3(PDZRN3):c.446C>T (p.Pro149Leu)	not specified [RCV004349264]	uncertain significance	3	73624380	73624380	Human		name
401898239	CV2790986	single nucleotide variant	NM_015009.3(PDZRN3):c.911T>G (p.Ile304Ser)	not specified [RCV004354608]	uncertain significance	3	73602361	73602361	Human		name
405789856	CV3372191	single nucleotide variant	NM_015009.3(PDZRN3):c.392G>A (p.Arg131His)	not specified [RCV004505610]	uncertain significance	3	73624434	73624434	Human		name
405789860	CV3372192	single nucleotide variant	NM_015009.3(PDZRN3):c.544A>G (p.Lys182Glu)	not specified [RCV004505611]	uncertain significance	3	73624282	73624282	Human		name
405789864	CV3372193	single nucleotide variant	NM_015009.3(PDZRN3):c.618G>C (p.Gln206His)	not specified [RCV004505612]	uncertain significance	3	73624208	73624208	Human		name
405789871	CV3372195	single nucleotide variant	NM_015009.3(PDZRN3):c.700G>C (p.Val234Leu)	not specified [RCV004505614]	uncertain significance	3	73624126	73624126	Human		name
405789875	CV3372196	single nucleotide variant	NM_015009.3(PDZRN3):c.713C>G (p.Pro238Arg)	not specified [RCV004505615]	uncertain significance	3	73624113	73624113	Human		name
407463804	CV3470538	single nucleotide variant	NM_015009.3(PDZRN3):c.352G>T (p.Gly118Cys)	not specified [RCV004659785]	uncertain significance	3	73624474	73624474	Human		name
407528694	CV3470545	single nucleotide variant	NM_015009.3(PDZRN3):c.343G>A (p.Ala115Thr)	not specified [RCV004655651]	uncertain significance	3	73624483	73624483	Human		name
407463829	CV3470546	single nucleotide variant	NM_015009.3(PDZRN3):c.377T>G (p.Val126Gly)	not specified [RCV004659791]	uncertain significance	3	73624449	73624449	Human		name
597721360	CV3579325	single nucleotide variant	NM_015009.3(PDZRN3):c.800G>A (p.Arg267Gln)	not specified [RCV004841942]	uncertain significance	3	73608608	73608608	Human		name
597721371	CV3579326	single nucleotide variant	NM_015009.3(PDZRN3):c.760C>T (p.Arg254Trp)	not specified [RCV004841943]	uncertain significance	3	73608648	73608648	Human		name
597721382	CV3579327	single nucleotide variant	NM_015009.3(PDZRN3):c.662C>T (p.Thr221Ile)	not specified [RCV004841944]	uncertain significance	3	73624164	73624164	Human		name
597721422	CV3579330	single nucleotide variant	NM_015009.3(PDZRN3):c.991A>C (p.Ile331Leu)	not specified [RCV004841947]	uncertain significance	3	73404323	73404323	Human		name
597721542	CV3579340	single nucleotide variant	NM_015009.3(PDZRN3):c.769G>A (p.Gly257Ser)	not specified [RCV004841956]	uncertain significance	3	73608639	73608639	Human		name
597721566	CV3579342	single nucleotide variant	NM_015009.3(PDZRN3):c.868G>A (p.Gly290Arg)	not specified [RCV004841958]	uncertain significance	3	73602404	73602404	Human		name
597721603	CV3579345	single nucleotide variant	NM_015009.3(PDZRN3):c.819C>A (p.His273Gln)	not specified [RCV004841961]	likely benign	3	73602453	73602453	Human		name
598261072	CV4002749	single nucleotide variant	NM_015009.3(PDZRN3):c.547G>T (p.Ala183Ser)	not specified [RCV005386822]	uncertain significance	3	73624279	73624279	Human		name
598261087	CV4002753	single nucleotide variant	NM_015009.3(PDZRN3):c.652A>G (p.Lys218Glu)	not specified [RCV005386825]	uncertain significance	3	73624174	73624174	Human		name
598261094	CV4002754	single nucleotide variant	NM_015009.3(PDZRN3):c.508A>G (p.Asn170Asp)	not specified [RCV005386826]	uncertain significance	3	73624318	73624318	Human		name
156253904	CV2193161	single nucleotide variant	NM_015009.3(PDZRN3):c.2005G>A (p.Gly669Ser)	not specified [RCV004071159]	likely benign	3	73384561	73384561	Human		name
156323222	CV2201563	single nucleotide variant	NM_015009.3(PDZRN3):c.1939C>T (p.Arg647Cys)	not specified [RCV004080053]	uncertain significance	3	73384627	73384627	Human		name
156377309	CV2207034	single nucleotide variant	NM_015009.3(PDZRN3):c.2543G>T (p.Ser848Ile)	not specified [RCV004085647]	uncertain significance	3	73384023	73384023	Human		name
156380288	CV2208088	single nucleotide variant	NM_015009.3(PDZRN3):c.2659A>G (p.Ile887Val)	not specified [RCV004086775]	uncertain significance	3	73383907	73383907	Human		name
156381081	CV2219126	single nucleotide variant	NM_015009.3(PDZRN3):c.2393C>T (p.Thr798Met)	not specified [RCV004087283]	uncertain significance	3	73384173	73384173	Human		name
156338027	CV2224886	single nucleotide variant	NM_015009.3(PDZRN3):c.2512A>G (p.Lys838Glu)	not specified [RCV004092971]	uncertain significance	3	73384054	73384054	Human		name
156225146	CV2226107	single nucleotide variant	NM_015009.3(PDZRN3):c.1138G>A (p.Val380Met)	not specified [RCV004105523]	uncertain significance	3	73404176	73404176	Human		name
155988711	CV2234244	single nucleotide variant	NM_015009.3(PDZRN3):c.2329A>G (p.Asn777Asp)	not specified [RCV004106320]	uncertain significance	3	73384237	73384237	Human		name
155988722	CV2234245	single nucleotide variant	NM_015009.3(PDZRN3):c.2332T>A (p.Ser778Thr)	not specified [RCV004106321]	uncertain significance	3	73384234	73384234	Human		name
155988735	CV2234246	single nucleotide variant	NM_015009.3(PDZRN3):c.2333C>A (p.Ser778Tyr)	not specified [RCV004106322]	uncertain significance	3	73384233	73384233	Human		name
155916501	CV2239755	single nucleotide variant	NM_015009.3(PDZRN3):c.1127C>G (p.Pro376Arg)	not specified [RCV004108288]	uncertain significance	3	73404187	73404187	Human		name
156073167	CV2263726	single nucleotide variant	NM_015009.3(PDZRN3):c.2559G>C (p.Gln853His)	not specified [RCV004136017]	uncertain significance	3	73384007	73384007	Human		name
156154655	CV2266093	single nucleotide variant	NM_015009.3(PDZRN3):c.2161C>G (p.Leu721Val)	not specified [RCV004128692]	uncertain significance	3	73384405	73384405	Human		name
156049301	CV2271788	single nucleotide variant	NM_015009.3(PDZRN3):c.2538C>G (p.Ser846Arg)	not specified [RCV004130626]	uncertain significance	3	73384028	73384028	Human		name
156273096	CV2283777	single nucleotide variant	NM_015009.3(PDZRN3):c.1820C>A (p.Thr607Asn)	not specified [RCV004142297]	uncertain significance	3	73384746	73384746	Human		name
156011986	CV2291206	single nucleotide variant	NM_015009.3(PDZRN3):c.2165A>C (p.His722Pro)	not specified [RCV004153502]	uncertain significance	3	73384401	73384401	Human		name
156088321	CV2295501	single nucleotide variant	NM_015009.3(PDZRN3):c.1037C>T (p.Thr346Met)	not specified [RCV004160608]	uncertain significance	3	73404277	73404277	Human		name
156094247	CV2309997	single nucleotide variant	NM_015009.3(PDZRN3):c.2571C>A (p.Ser857Arg)	not specified [RCV004163138]	uncertain significance	3	73383995	73383995	Human		name
156052580	CV2312355	single nucleotide variant	NM_015009.3(PDZRN3):c.1556T>C (p.Phe519Ser)	not specified [RCV004167056]	uncertain significance	3	73385748	73385748	Human		name
156168175	CV2315367	single nucleotide variant	NM_015009.3(PDZRN3):c.1639A>C (p.Lys547Gln)	not specified [RCV004167339]	uncertain significance	3	73384927	73384927	Human		name
156052009	CV2336703	single nucleotide variant	NM_015009.3(PDZRN3):c.2539C>T (p.Arg847Trp)	not specified [RCV004196943]	uncertain significance	3	73384027	73384027	Human		name
155984269	CV2344739	single nucleotide variant	NM_015009.3(PDZRN3):c.1321G>A (p.Asp441Asn)	not specified [RCV004190895]	uncertain significance	3	73391050	73391050	Human		name
155990806	CV2372100	single nucleotide variant	NM_015009.3(PDZRN3):c.1708G>A (p.Gly570Ser)	not specified [RCV004221760]	uncertain significance	3	73384858	73384858	Human		name
156162155	CV2398323	single nucleotide variant	NM_015009.3(PDZRN3):c.1181A>G (p.His394Arg)	not specified [RCV004235225]	uncertain significance	3	73400995	73400995	Human		name
329367985	CV2442604	single nucleotide variant	NM_015009.3(PDZRN3):c.2735C>T (p.Pro912Leu)	not specified [RCV004264963]	uncertain significance	3	73383831	73383831	Human		name
329388805	CV2447885	single nucleotide variant	NM_015009.3(PDZRN3):c.1219C>A (p.His407Asn)	not specified [RCV004260699]	uncertain significance	3	73400957	73400957	Human		name
329395767	CV2454541	single nucleotide variant	NM_015009.3(PDZRN3):c.1316C>G (p.Thr439Arg)	not specified [RCV004268028]	uncertain significance	3	73391055	73391055	Human		name
401720660	CV2673420	single nucleotide variant	NM_015009.3(PDZRN3):c.1442G>A (p.Arg481His)	not specified [RCV004288395]	uncertain significance	3	73388044	73388044	Human		name
401747368	CV2679082	single nucleotide variant	NM_015009.3(PDZRN3):c.2549C>A (p.Thr850Lys)	not specified [RCV004295077]	uncertain significance	3	73384017	73384017	Human		name
401749498	CV2712377	single nucleotide variant	NM_015009.3(PDZRN3):c.2618T>C (p.Ile873Thr)	not specified [RCV004313858]	uncertain significance	3	73383948	73383948	Human		name
401768282	CV2720025	single nucleotide variant	NM_015009.3(PDZRN3):c.1841G>A (p.Gly614Asp)	not specified [RCV004323603]	uncertain significance	3	73384725	73384725	Human		name
401753532	CV2722502	single nucleotide variant	NM_015009.3(PDZRN3):c.1831G>A (p.Asp611Asn)	not specified [RCV004322889]	uncertain significance	3	73384735	73384735	Human		name
401729409	CV2733028	single nucleotide variant	NM_015009.3(PDZRN3):c.1878T>G (p.Ile626Met)	not specified [RCV004331199]	uncertain significance	3	73384688	73384688	Human		name
401874790	CV2781245	single nucleotide variant	NM_015009.3(PDZRN3):c.2189A>C (p.Asn730Thr)	not specified [RCV004352279]	uncertain significance	3	73384377	73384377	Human		name
401866901	CV2792556	single nucleotide variant	NM_015009.3(PDZRN3):c.2850C>G (p.Ile950Met)	not specified [RCV004363591]	uncertain significance	3	73383716	73383716	Human		name
405789793	CV3372176	single nucleotide variant	NM_015009.3(PDZRN3):c.1002G>T (p.Gln334His)	not specified [RCV004505595]	uncertain significance	3	73404312	73404312	Human		name
405789797	CV3372177	single nucleotide variant	NM_015009.3(PDZRN3):c.1081G>A (p.Asp361Asn)	not specified [RCV004505596]	uncertain significance	3	73404233	73404233	Human		name
405789801	CV3372178	single nucleotide variant	NM_015009.3(PDZRN3):c.1534A>C (p.Met512Leu)	not specified [RCV004505597]	uncertain significance	3	73385770	73385770	Human		name
405789805	CV3372179	single nucleotide variant	NM_015009.3(PDZRN3):c.1766A>G (p.Asn589Ser)	not specified [RCV004505598]	uncertain significance	3	73384800	73384800	Human		name
405789808	CV3372180	single nucleotide variant	NM_015009.3(PDZRN3):c.1787C>T (p.Ser596Phe)	not specified [RCV004505599]	uncertain significance	3	73384779	73384779	Human		name
405789814	CV3372181	single nucleotide variant	NM_015009.3(PDZRN3):c.1922A>C (p.Asp641Ala)	not specified [RCV004505600]	uncertain significance	3	73384644	73384644	Human		name
405789819	CV3372182	single nucleotide variant	NM_015009.3(PDZRN3):c.1934G>A (p.Arg645His)	not specified [RCV004505601]	uncertain significance	3	73384632	73384632	Human		name
405790057	CV3372183	single nucleotide variant	NM_015009.3(PDZRN3):c.2078G>A (p.Arg693His)	not specified [RCV004505602]	uncertain significance	3	73384488	73384488	Human		name
405789827	CV3372184	single nucleotide variant	NM_015009.3(PDZRN3):c.2286G>C (p.Glu762Asp)	not specified [RCV004505603]	uncertain significance	3	73384280	73384280	Human		name
405789831	CV3372185	single nucleotide variant	NM_015009.3(PDZRN3):c.2519G>T (p.Arg840Leu)	not specified [RCV004505604]	uncertain significance	3	73384047	73384047	Human		name
405789842	CV3372188	single nucleotide variant	NM_015009.3(PDZRN3):c.2633A>G (p.Gln878Arg)	not specified [RCV004505607]	uncertain significance	3	73383933	73383933	Human		name
405789846	CV3372189	single nucleotide variant	NM_015009.3(PDZRN3):c.2735C>A (p.Pro912His)	not specified [RCV004505608]	uncertain significance	3	73383831	73383831	Human		name
405789852	CV3372190	single nucleotide variant	NM_015009.3(PDZRN3):c.2848A>G (p.Ile950Val)	not specified [RCV004505609]	uncertain significance	3	73383718	73383718	Human		name
407463795	CV3470536	single nucleotide variant	NM_015009.3(PDZRN3):c.1875C>A (p.Phe625Leu)	not specified [RCV004659783]	uncertain significance	3	73384691	73384691	Human		name
407463799	CV3470537	single nucleotide variant	NM_015009.3(PDZRN3):c.2528G>A (p.Ser843Asn)	not specified [RCV004659784]	uncertain significance	3	73384038	73384038	Human		name
407528689	CV3470540	single nucleotide variant	NM_015009.3(PDZRN3):c.1608G>T (p.Met536Ile)	not specified [RCV004655649]	uncertain significance	3	73385696	73385696	Human		name
407463813	CV3470541	single nucleotide variant	NM_015009.3(PDZRN3):c.2570G>A (p.Ser857Asn)	not specified [RCV004659787]	uncertain significance	3	73383996	73383996	Human		name
407528692	CV3470542	single nucleotide variant	NM_015009.3(PDZRN3):c.2785G>A (p.Gly929Arg)	not specified [RCV004655650]	uncertain significance	3	73383781	73383781	Human		name
407463817	CV3470543	single nucleotide variant	NM_015009.3(PDZRN3):c.1441C>T (p.Arg481Cys)	not specified [RCV004659788]	uncertain significance	3	73388045	73388045	Human		name
407463821	CV3470544	single nucleotide variant	NM_015009.3(PDZRN3):c.2755A>G (p.Met919Val)	not specified [RCV004659789]	uncertain significance	3	73383811	73383811	Human		name
597721397	CV3579328	single nucleotide variant	NM_015009.3(PDZRN3):c.2533G>A (p.Gly845Arg)	not specified [RCV004841945]	uncertain significance	3	73384033	73384033	Human		name
597721408	CV3579329	single nucleotide variant	NM_015009.3(PDZRN3):c.1536G>A (p.Met512Ile)	not specified [RCV004841946]	uncertain significance	3	73385768	73385768	Human		name
597721435	CV3579331	single nucleotide variant	NM_015009.3(PDZRN3):c.2697G>C (p.Gln899His)	not specified [RCV004841948]	uncertain significance	3	73383869	73383869	Human		name
597721448	CV3579332	single nucleotide variant	NM_015009.3(PDZRN3):c.2165A>T (p.His722Leu)	not specified [RCV004841949]	uncertain significance	3	73384401	73384401	Human		name
597721462	CV3579333	single nucleotide variant	NM_015009.3(PDZRN3):c.2096G>C (p.Cys699Ser)	not specified [RCV004841950]	uncertain significance	3	73384470	73384470	Human		name
597721475	CV3579334	single nucleotide variant	NM_015009.3(PDZRN3):c.2650A>T (p.Met884Leu)	not specified [RCV004841951]	uncertain significance	3	73383916	73383916	Human		name
597721487	CV3579335	single nucleotide variant	NM_015009.3(PDZRN3):c.1201G>T (p.Asp401Tyr)	not specified [RCV004841952]	uncertain significance	3	73400975	73400975	Human		name
597721501	CV3579336	single nucleotide variant	NM_015009.3(PDZRN3):c.2993G>A (p.Ser998Asn)	not specified [RCV004841953]	uncertain significance	3	73383573	73383573	Human		name
597721514	CV3579337	single nucleotide variant	NM_015009.3(PDZRN3):c.1588G>A (p.Glu530Lys)	not specified [RCV004841954]	uncertain significance	3	73385716	73385716	Human		name
597721527	CV3579338	single nucleotide variant	NM_015009.3(PDZRN3):c.1027A>G (p.Lys343Glu)	not specified [RCV004841955]	uncertain significance	3	73404287	73404287	Human		name
597721555	CV3579341	single nucleotide variant	NM_015009.3(PDZRN3):c.2099T>A (p.Leu700Gln)	not specified [RCV004841957]	uncertain significance	3	73384467	73384467	Human		name
597721592	CV3579344	single nucleotide variant	NM_015009.3(PDZRN3):c.1475A>G (p.Glu492Gly)	not specified [RCV004841960]	uncertain significance	3	73388011	73388011	Human		name
597721616	CV3579346	single nucleotide variant	NM_015009.3(PDZRN3):c.2131C>G (p.Leu711Val)	not specified [RCV004841962]	uncertain significance	3	73384435	73384435	Human		name
598196531	CV4002739	single nucleotide variant	NM_015009.3(PDZRN3):c.2605A>G (p.Lys869Glu)	not specified [RCV005397729]	uncertain significance	3	73383961	73383961	Human		name
598261027	CV4002740	single nucleotide variant	NM_015009.3(PDZRN3):c.1856C>T (p.Pro619Leu)	not specified [RCV005386813]	uncertain significance	3	73384710	73384710	Human		name
598261032	CV4002741	single nucleotide variant	NM_015009.3(PDZRN3):c.2342G>A (p.Arg781Lys)	not specified [RCV005386814]	uncertain significance	3	73384224	73384224	Human		name
598261037	CV4002742	single nucleotide variant	NM_015009.3(PDZRN3):c.1151A>G (p.Tyr384Cys)	not specified [RCV005386815]	uncertain significance	3	73404163	73404163	Human		name
598261042	CV4002743	single nucleotide variant	NM_015009.3(PDZRN3):c.1820C>T (p.Thr607Ile)	not specified [RCV005386816]	uncertain significance	3	73384746	73384746	Human		name
598261047	CV4002744	single nucleotide variant	NM_015009.3(PDZRN3):c.2554A>G (p.Ser852Gly)	not specified [RCV005386817]	uncertain significance	3	73384012	73384012	Human		name
598261057	CV4002746	single nucleotide variant	NM_015009.3(PDZRN3):c.2988G>A (p.Met996Ile)	not specified [RCV005386819]	uncertain significance	3	73383578	73383578	Human		name
598261062	CV4002747	single nucleotide variant	NM_015009.3(PDZRN3):c.2686G>A (p.Ala896Thr)	not specified [RCV005386820]	uncertain significance	3	73383880	73383880	Human		name
598261067	CV4002748	single nucleotide variant	NM_015009.3(PDZRN3):c.1133C>T (p.Pro378Leu)	not specified [RCV005386821]	uncertain significance	3	73404181	73404181	Human		name
598261078	CV4002750	single nucleotide variant	NM_015009.3(PDZRN3):c.1595A>C (p.His532Pro)	not specified [RCV005386823]	uncertain significance	3	73385709	73385709	Human		name
598261082	CV4002751	single nucleotide variant	NM_015009.3(PDZRN3):c.2377G>C (p.Gly793Arg)	not specified [RCV005386824]	uncertain significance	3	73384189	73384189	Human		name
598196537	CV4002752	single nucleotide variant	NM_015009.3(PDZRN3):c.1565A>T (p.Asp522Val)	not specified [RCV005397730]	uncertain significance	3	73385739	73385739	Human		name
14350194	CV590846	single nucleotide variant	NM_015009.3(PDZRN3):c.2101A>C (p.Ser701Arg)	Short stature [RCV000736215]	likely pathogenic	3	73384465	73384465	Human	2	name
15106126	CV709036	single nucleotide variant	NM_015009.3(PDZRN3):c.1987G>A (p.Gly663Ser)	not provided [RCV000960015]	benign	3	73384579	73384579	Human		name
8625662	CV80786	single nucleotide variant	NM_015009.2(PDZRN3):c.1479T>A (p.Asn493Lys)	Malignant melanoma [RCV000060863]	not provided	3	73388007	73388007	Human		name
8630944	CV86100	single nucleotide variant	NM_015009.2(PDZRN3):c.2740C>T (p.Pro914Ser)	Malignant melanoma [RCV000066184]	not provided	3	73383826	73383826	Human		name
8630945	CV86101	single nucleotide variant	NM_015009.3(PDZRN3):c.2443C>T (p.Pro815Ser)	not specified [RCV004659790]	uncertain significance\|not provided	3	73384123	73384123	Human		name
407528695	CV3470547	single nucleotide variant	NM_015009.3(PDZRN3):c.3025G>A (p.Ala1009Thr)	not specified [RCV004655652]	uncertain significance	3	73383541	73383541	Human		name
8625661	CV80785	single nucleotide variant	NM_015009.2(PDZRN3):c.3148T>C (p.Ser1050Pro)	Malignant melanoma [RCV000060862]	not provided	3	73383418	73383418	Human		name

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