Synj2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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179 records found for search term Synj2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401921029	CV2828075	single nucleotide variant	NM_003898.4(SYNJ2):c.1717+3G>A	not provided [RCV003432143]	likely benign	6	158066638	158066638	Human		name
15100853	CV777559	single nucleotide variant	NM_003898.4(SYNJ2):c.1127+10G>A	not provided [RCV000958977]	benign	6	158062174	158062174	Human		name
156235651	CV2268007	single nucleotide variant	NM_003898.4(SYNJ2):c.10A>G (p.Ser4Gly)	not specified [RCV004136564]	uncertain significance	6	157981971	157981971	Human		name
597779898	CV3618812	single nucleotide variant	NM_003898.4(SYNJ2):c.76C>G (p.Arg26Gly)	not specified [RCV004873691]	uncertain significance	6	157982037	157982037	Human		name
598180495	CV3923340	single nucleotide variant	NM_003898.4(SYNJ2):c.29T>G (p.Leu10Arg)	not specified [RCV005286562]	uncertain significance	6	157981990	157981990	Human		name
156331079	CV2220477	single nucleotide variant	NM_003898.4(SYNJ2):c.268A>G (p.Arg90Gly)	not specified [RCV004097707]	uncertain significance	6	158028809	158028809	Human		name
156264014	CV2289769	single nucleotide variant	NM_003898.4(SYNJ2):c.181T>A (p.Tyr61Asn)	not specified [RCV004150454]	uncertain significance	6	158017257	158017257	Human		name
156360938	CV2329714	single nucleotide variant	NM_003898.4(SYNJ2):c.122C>T (p.Thr41Met)	not specified [RCV004180818]	uncertain significance	6	157982083	157982083	Human		name
401921100	CV2828074	single nucleotide variant	NM_003898.4(SYNJ2):c.1680C>T (p.Leu560=)	not provided [RCV003432142]	likely benign	6	158066598	158066598	Human		name
401916218	CV2828076	single nucleotide variant	NM_003898.4(SYNJ2):c.2544G>A (p.Ala848=)	not provided [RCV003429016]	likely benign	6	158078258	158078258	Human		name
401921031	CV2828077	single nucleotide variant	NM_003898.4(SYNJ2):c.2745C>T (p.Leu915=)	not provided [RCV003432144]	likely benign	6	158081286	158081286	Human		name
405725605	CV3334684	single nucleotide variant	NM_003898.4(SYNJ2):c.187T>A (p.Cys63Ser)	not specified [RCV004463724]	uncertain significance	6	158017263	158017263	Human		name
405869658	CV3397887	single nucleotide variant	NM_003898.4(SYNJ2):c.179C>T (p.Ala60Val)	Meniere disease [RCV004573530]	uncertain significance	6	158017255	158017255	Human	1	name
597779906	CV3618814	single nucleotide variant	NM_003898.4(SYNJ2):c.231C>G (p.Ser77Arg)	not specified [RCV004873693]	uncertain significance	6	158028772	158028772	Human		name
597780172	CV3618816	single nucleotide variant	NM_003898.4(SYNJ2):c.125T>C (p.Leu42Pro)	not specified [RCV004873695]	uncertain significance	6	157982086	157982086	Human		name
597779928	CV3618821	single nucleotide variant	NM_003898.4(SYNJ2):c.278A>G (p.Asp93Gly)	not specified [RCV004873699]	uncertain significance	6	158028819	158028819	Human		name
15144536	CV735500	single nucleotide variant	NM_003898.4(SYNJ2):c.1920A>G (p.Pro640=)	not provided [RCV000900018]	likely benign	6	158069653	158069653	Human		name
156335673	CV2228425	single nucleotide variant	NM_003898.4(SYNJ2):c.883T>C (p.Tyr295His)	not specified [RCV004098400]	uncertain significance	6	158059282	158059282	Human		name
155990327	CV2256333	single nucleotide variant	NM_003898.4(SYNJ2):c.895G>A (p.Val299Met)	not specified [RCV004116792]	uncertain significance	6	158059294	158059294	Human		name
155929448	CV2278126	single nucleotide variant	NM_003898.4(SYNJ2):c.530G>C (p.Cys177Ser)	not specified [RCV004141336]	uncertain significance	6	158033499	158033499	Human		name
155962524	CV2388250	single nucleotide variant	NM_003898.4(SYNJ2):c.763G>A (p.Val255Ile)	not specified [RCV004234708]	uncertain significance	6	158043367	158043367	Human		name
329386691	CV2455979	single nucleotide variant	NM_003898.4(SYNJ2):c.905A>G (p.Asn302Ser)	not specified [RCV004279236]	uncertain significance	6	158059304	158059304	Human		name
329363233	CV2464979	single nucleotide variant	NM_003898.4(SYNJ2):c.891G>T (p.Gln297His)	not specified [RCV004284894]	uncertain significance	6	158059290	158059290	Human		name
329382915	CV2465473	single nucleotide variant	NM_003898.4(SYNJ2):c.532T>C (p.Cys178Arg)	not specified [RCV004281238]	uncertain significance	6	158033501	158033501	Human		name
329393087	CV2469295	single nucleotide variant	NM_003898.4(SYNJ2):c.925G>A (p.Gly309Arg)	not specified [RCV004280631]	uncertain significance	6	158059324	158059324	Human		name
401733785	CV2713216	single nucleotide variant	NM_003898.4(SYNJ2):c.949T>G (p.Phe317Val)	not specified [RCV004316750]	uncertain significance	6	158059348	158059348	Human		name
401762385	CV2714121	single nucleotide variant	NM_003898.4(SYNJ2):c.535G>A (p.Asp179Asn)	not specified [RCV004317376]	uncertain significance	6	158033504	158033504	Human		name
401873452	CV2761470	single nucleotide variant	NM_003898.4(SYNJ2):c.638G>A (p.Arg213His)	not specified [RCV004334644]	uncertain significance	6	158033607	158033607	Human		name
401921032	CV2828078	single nucleotide variant	NM_003898.4(SYNJ2):c.3306T>A (p.Pro1102=)	not provided [RCV003432145]	likely benign	6	158086952	158086952	Human		name
401916221	CV2828079	single nucleotide variant	NM_003898.4(SYNJ2):c.4002G>A (p.Pro1334=)	not provided [RCV003429017]	likely benign	6	158095875	158095875	Human		name
405725815	CV3334709	single nucleotide variant	NM_003898.4(SYNJ2):c.434G>A (p.Arg145His)	not specified [RCV004463749]	uncertain significance	6	158028975	158028975	Human		name
405725833	CV3334711	single nucleotide variant	NM_003898.4(SYNJ2):c.502G>T (p.Val168Leu)	not specified [RCV004463751]	uncertain significance	6	158033471	158033471	Human		name
405725849	CV3334713	single nucleotide variant	NM_003898.4(SYNJ2):c.623G>A (p.Arg208His)	not specified [RCV004463753]	uncertain significance	6	158033592	158033592	Human		name
405725857	CV3334714	single nucleotide variant	NM_003898.4(SYNJ2):c.979G>A (p.Ala327Thr)	not specified [RCV004463754]	uncertain significance	6	158062016	158062016	Human		name
405725867	CV3334715	single nucleotide variant	NM_003898.4(SYNJ2):c.994A>G (p.Met332Val)	not specified [RCV004463755]	uncertain significance	6	158062031	158062031	Human		name
405869659	CV3397888	single nucleotide variant	NM_003898.4(SYNJ2):c.559G>A (p.Gly187Arg)	Meniere disease [RCV004573531]	uncertain significance	6	158033528	158033528	Human	1	name
405869660	CV3397889	single nucleotide variant	NM_003898.4(SYNJ2):c.901G>A (p.Val301Met)	Meniere disease [RCV004573532]	uncertain significance	6	158059300	158059300	Human	1	name
407505658	CV3478283	single nucleotide variant	NM_003898.4(SYNJ2):c.650G>A (p.Arg217His)	not specified [RCV004670897]	uncertain significance	6	158033619	158033619	Human		name
407505665	CV3478285	single nucleotide variant	NM_003898.4(SYNJ2):c.809A>C (p.His270Pro)	not specified [RCV004670899]	uncertain significance	6	158054980	158054980	Human		name
407505672	CV3478291	single nucleotide variant	NM_003898.4(SYNJ2):c.845C>T (p.Pro282Leu)	not specified [RCV004670901]	uncertain significance	6	158055016	158055016	Human		name
597779894	CV3618811	single nucleotide variant	NM_003898.4(SYNJ2):c.853G>A (p.Asp285Asn)	not specified [RCV004873690]	uncertain significance	6	158055024	158055024	Human		name
598180482	CV3923338	single nucleotide variant	NM_003898.4(SYNJ2):c.662G>A (p.Arg221His)	not specified [RCV005286560]	uncertain significance	6	158033631	158033631	Human		name
598180509	CV3923343	single nucleotide variant	NM_003898.4(SYNJ2):c.842C>T (p.Ala281Val)	not specified [RCV005286564]	uncertain significance	6	158055013	158055013	Human		name
598180554	CV3923350	single nucleotide variant	NM_003898.4(SYNJ2):c.625G>A (p.Val209Ile)	not specified [RCV005286570]	likely benign	6	158033594	158033594	Human		name
598180560	CV3923351	single nucleotide variant	NM_003898.4(SYNJ2):c.319C>T (p.Leu107Phe)	not specified [RCV005286571]	uncertain significance	6	158028860	158028860	Human		name
598180567	CV3923352	single nucleotide variant	NM_003898.4(SYNJ2):c.721A>G (p.Met241Val)	not specified [RCV005286572]	uncertain significance	6	158043325	158043325	Human		name
598180588	CV3923355	single nucleotide variant	NM_003898.4(SYNJ2):c.332C>A (p.Ala111Asp)	not specified [RCV005286575]	uncertain significance	6	158028873	158028873	Human		name
598180601	CV3923358	single nucleotide variant	NM_003898.4(SYNJ2):c.876G>T (p.Lys292Asn)	not specified [RCV005286577]	uncertain significance	6	158059275	158059275	Human		name
155925685	CV2230485	single nucleotide variant	NM_003898.4(SYNJ2):c.1849C>T (p.Arg617Cys)	not specified [RCV004097461]	uncertain significance	6	158069582	158069582	Human		name
11051302	CV225809	single nucleotide variant	NM_003898.4(SYNJ2):c.2557T>C (p.Ser853Pro)	not specified [RCV000209855]	uncertain significance	6	158078271	158078271	Human		name
156257074	CV2264848	single nucleotide variant	NM_003898.4(SYNJ2):c.2386C>T (p.Arg796Cys)	not specified [RCV004134606]	uncertain significance	6	158076719	158076719	Human		name
156208412	CV2298122	single nucleotide variant	NM_003898.4(SYNJ2):c.2353G>A (p.Gly785Ser)	not specified [RCV004159788]	uncertain significance	6	158076686	158076686	Human		name
156197965	CV2334439	single nucleotide variant	NM_003898.4(SYNJ2):c.2851G>A (p.Val951Met)	not specified [RCV004188413]	uncertain significance	6	158081496	158081496	Human		name
156337210	CV2343023	single nucleotide variant	NM_003898.4(SYNJ2):c.1108G>T (p.Gly370Trp)	not specified [RCV004192625]	uncertain significance	6	158062145	158062145	Human		name
156014565	CV2360143	single nucleotide variant	NM_003898.4(SYNJ2):c.2938C>T (p.Arg980Trp)	not specified [RCV004215415]	uncertain significance	6	158083501	158083501	Human		name
156386477	CV2364755	single nucleotide variant	NM_003898.4(SYNJ2):c.1631A>C (p.Gln544Pro)	not specified [RCV004219629]	uncertain significance	6	158066549	158066549	Human		name
156256318	CV2368689	single nucleotide variant	NM_003898.4(SYNJ2):c.1517C>T (p.Ala506Val)	not specified [RCV004214582]	uncertain significance	6	158064983	158064983	Human		name
156168744	CV2373821	single nucleotide variant	NM_003898.4(SYNJ2):c.1397G>A (p.Arg466Gln)	not specified [RCV004224757]	uncertain significance	6	158064863	158064863	Human		name
156035740	CV2373930	single nucleotide variant	NM_003898.4(SYNJ2):c.2065G>A (p.Gly689Arg)	not specified [RCV004227067]	uncertain significance	6	158071726	158071726	Human		name
156039200	CV2390292	single nucleotide variant	NM_003898.4(SYNJ2):c.1708G>A (p.Asp570Asn)	not specified [RCV004240658]	uncertain significance	6	158066626	158066626	Human		name
156187330	CV2397867	single nucleotide variant	NM_003898.4(SYNJ2):c.1637G>A (p.Arg546Gln)	Meniere disease [RCV004572839]\|not specified [RCV004239336]	uncertain significance	6	158066555	158066555	Human	1	name
156102619	CV2400144	single nucleotide variant	NM_003898.4(SYNJ2):c.2539C>T (p.Arg847Cys)	not specified [RCV004242946]	uncertain significance	6	158078253	158078253	Human		name
156104944	CV2400330	single nucleotide variant	NM_003898.4(SYNJ2):c.1148G>A (p.Arg383Gln)	not specified [RCV004244389]	uncertain significance	6	158063811	158063811	Human		name
329357849	CV2427858	single nucleotide variant	NM_003898.4(SYNJ2):c.1469A>G (p.Tyr490Cys)	not specified [RCV004252631]	uncertain significance	6	158064935	158064935	Human		name
329370546	CV2435639	single nucleotide variant	NM_003898.4(SYNJ2):c.2447C>T (p.Thr816Ile)	not specified [RCV004254883]	uncertain significance	6	158076780	158076780	Human		name
329362481	CV2444787	single nucleotide variant	NM_003898.4(SYNJ2):c.2525T>C (p.Leu842Pro)	not specified [RCV004259031]	uncertain significance	6	158078239	158078239	Human		name
329376864	CV2455243	single nucleotide variant	NM_003898.4(SYNJ2):c.1259T>C (p.Val420Ala)	not provided [RCV003456576]\|not specified [RCV004274462]	likely benign	6	158064650	158064650	Human		name
329390473	CV2459276	single nucleotide variant	NM_003898.4(SYNJ2):c.1513A>G (p.Thr505Ala)	not specified [RCV004274707]	uncertain significance	6	158064979	158064979	Human		name
329392220	CV2470483	single nucleotide variant	NM_003898.4(SYNJ2):c.1384C>T (p.Arg462Trp)	not specified [RCV004273503]	uncertain significance	6	158064850	158064850	Human		name
329352803	CV2470549	single nucleotide variant	NM_003898.4(SYNJ2):c.1975G>A (p.Gly659Arg)	not specified [RCV004273554]	uncertain significance	6	158071636	158071636	Human		name
401739854	CV2683187	single nucleotide variant	NM_003898.4(SYNJ2):c.1385G>C (p.Arg462Pro)	not specified [RCV004286183]	uncertain significance	6	158064851	158064851	Human		name
401749261	CV2694601	single nucleotide variant	NM_003898.4(SYNJ2):c.1592G>A (p.Arg531Gln)	not specified [RCV004298719]	uncertain significance	6	158066510	158066510	Human		name
401743727	CV2696854	single nucleotide variant	NM_003898.4(SYNJ2):c.1126C>T (p.Arg376Cys)	not specified [RCV004290819]	uncertain significance	6	158062163	158062163	Human		name
401770289	CV2711054	single nucleotide variant	NM_003898.4(SYNJ2):c.1957A>T (p.Thr653Ser)	not specified [RCV004310747]	uncertain significance	6	158071618	158071618	Human		name
401777773	CV2718331	single nucleotide variant	NM_003898.4(SYNJ2):c.2947G>T (p.Asp983Tyr)	not specified [RCV004318168]	uncertain significance	6	158083510	158083510	Human		name
401772441	CV2719643	single nucleotide variant	NM_003898.4(SYNJ2):c.2087G>C (p.Arg696Pro)	not specified [RCV004327306]	uncertain significance	6	158071748	158071748	Human		name
401754741	CV2719963	single nucleotide variant	NM_003898.4(SYNJ2):c.2641G>C (p.Val881Leu)	not specified [RCV004329349]	uncertain significance	6	158081182	158081182	Human		name
401746578	CV2731868	single nucleotide variant	NM_003898.4(SYNJ2):c.2924G>A (p.Arg975Gln)	not specified [RCV004333116]	likely benign	6	158083487	158083487	Human		name
401872336	CV2754343	single nucleotide variant	NM_003898.4(SYNJ2):c.2641G>T (p.Val881Leu)	not specified [RCV004334519]	uncertain significance	6	158081182	158081182	Human		name
401890019	CV2763593	single nucleotide variant	NM_003898.4(SYNJ2):c.2057T>G (p.Leu686Arg)	not specified [RCV004343103]	uncertain significance	6	158071718	158071718	Human		name
405725785	CV3334681	single nucleotide variant	NM_003898.4(SYNJ2):c.1090T>G (p.Phe364Val)	not specified [RCV004463721]	uncertain significance	6	158062127	158062127	Human		name
405725589	CV3334682	single nucleotide variant	NM_003898.4(SYNJ2):c.1361T>C (p.Val454Ala)	not specified [RCV004463722]	uncertain significance	6	158064827	158064827	Human		name
405725596	CV3334683	single nucleotide variant	NM_003898.4(SYNJ2):c.1600A>T (p.Met534Leu)	not specified [RCV004463723]	uncertain significance	6	158066518	158066518	Human		name
405725616	CV3334685	single nucleotide variant	NM_003898.4(SYNJ2):c.2110A>G (p.Thr704Ala)	not specified [RCV004463725]	uncertain significance	6	158071771	158071771	Human		name
405725624	CV3334686	single nucleotide variant	NM_003898.4(SYNJ2):c.2116A>C (p.Lys706Gln)	not specified [RCV004463726]	uncertain significance	6	158071777	158071777	Human		name
405725634	CV3334687	single nucleotide variant	NM_003898.4(SYNJ2):c.2119C>T (p.Leu707Phe)	not specified [RCV004463727]	uncertain significance	6	158071780	158071780	Human		name
405725642	CV3334688	single nucleotide variant	NM_003898.4(SYNJ2):c.2153A>G (p.His718Arg)	not specified [RCV004463728]	uncertain significance	6	158074599	158074599	Human		name
405725648	CV3334689	single nucleotide variant	NM_003898.4(SYNJ2):c.2176G>A (p.Asp726Asn)	not specified [RCV004463729]	uncertain significance	6	158074622	158074622	Human		name
405725656	CV3334690	single nucleotide variant	NM_003898.4(SYNJ2):c.2395G>A (p.Ala799Thr)	not specified [RCV004463730]	uncertain significance	6	158076728	158076728	Human		name
405725665	CV3334691	single nucleotide variant	NM_003898.4(SYNJ2):c.2593G>A (p.Glu865Lys)	not specified [RCV004463731]	uncertain significance	6	158081134	158081134	Human		name
405725672	CV3334692	single nucleotide variant	NM_003898.4(SYNJ2):c.2621G>A (p.Arg874Gln)	not specified [RCV004463732]	uncertain significance	6	158081162	158081162	Human		name
405725689	CV3334694	single nucleotide variant	NM_003898.4(SYNJ2):c.2750A>G (p.Gln917Arg)	not specified [RCV004463734]	uncertain significance	6	158081291	158081291	Human		name
405725698	CV3334695	single nucleotide variant	NM_003898.4(SYNJ2):c.2813C>T (p.Thr938Ile)	not specified [RCV004463735]	uncertain significance	6	158081458	158081458	Human		name
405725707	CV3334696	single nucleotide variant	NM_003898.4(SYNJ2):c.2957C>A (p.Ala986Asp)	not specified [RCV004463736]	uncertain significance	6	158083520	158083520	Human		name
405725715	CV3334697	single nucleotide variant	NM_003898.4(SYNJ2):c.2962G>C (p.Val988Leu)	not specified [RCV004463737]	uncertain significance	6	158083525	158083525	Human		name
405871540	CV3397890	single nucleotide variant	NM_003898.4(SYNJ2):c.1850G>A (p.Arg617His)	Meniere disease [RCV004574889]	uncertain significance	6	158069583	158069583	Human	1	name
407505662	CV3478284	single nucleotide variant	NM_003898.4(SYNJ2):c.2230C>T (p.Arg744Cys)	not specified [RCV004670898]	uncertain significance	6	158074676	158074676	Human		name
407530302	CV3478286	single nucleotide variant	NM_003898.4(SYNJ2):c.1777G>T (p.Ala593Ser)	not specified [RCV004681841]	uncertain significance	6	158068706	158068706	Human		name
407505669	CV3478287	single nucleotide variant	NM_003898.4(SYNJ2):c.2462A>G (p.Asn821Ser)	not specified [RCV004670900]	uncertain significance	6	158078176	158078176	Human		name
407530304	CV3478288	single nucleotide variant	NM_003898.4(SYNJ2):c.1937T>C (p.Ile646Thr)	not specified [RCV004681842]	uncertain significance	6	158069670	158069670	Human		name
407530306	CV3478289	single nucleotide variant	NM_003898.4(SYNJ2):c.1939A>G (p.Arg647Gly)	not specified [RCV004681843]	uncertain significance	6	158069672	158069672	Human		name
407530308	CV3478290	single nucleotide variant	NM_003898.4(SYNJ2):c.1974G>C (p.Met658Ile)	not specified [RCV004681844]	uncertain significance	6	158071635	158071635	Human		name
597771698	CV3618800	single nucleotide variant	NM_003898.4(SYNJ2):c.1202C>T (p.Ala401Val)	not specified [RCV004871696]	uncertain significance	6	158063865	158063865	Human		name
597771703	CV3618801	single nucleotide variant	NM_003898.4(SYNJ2):c.2312A>G (p.Glu771Gly)	not specified [RCV004871697]	uncertain significance	6	158076645	158076645	Human		name
597771708	CV3618802	single nucleotide variant	NM_003898.4(SYNJ2):c.2497G>A (p.Val833Ile)	not specified [RCV004871698]	uncertain significance	6	158078211	158078211	Human		name
597771716	CV3618804	single nucleotide variant	NM_003898.4(SYNJ2):c.1697C>T (p.Ser566Leu)	not specified [RCV004871700]	uncertain significance	6	158066615	158066615	Human		name
597771726	CV3618806	single nucleotide variant	NM_003898.4(SYNJ2):c.1683C>G (p.Asp561Glu)	not specified [RCV004871702]	uncertain significance	6	158066601	158066601	Human		name
597771730	CV3618808	single nucleotide variant	NM_003898.4(SYNJ2):c.1265G>A (p.Arg422His)	not specified [RCV004871703]	uncertain significance	6	158064656	158064656	Human		name
597771735	CV3618809	single nucleotide variant	NM_003898.4(SYNJ2):c.2945G>A (p.Arg982Gln)	not specified [RCV004871704]	uncertain significance	6	158083508	158083508	Human		name
597779902	CV3618813	single nucleotide variant	NM_003898.4(SYNJ2):c.2939G>A (p.Arg980Gln)	not specified [RCV004873692]	uncertain significance	6	158083502	158083502	Human		name
597779910	CV3618815	single nucleotide variant	NM_003898.4(SYNJ2):c.2453G>A (p.Gly818Glu)	not specified [RCV004873694]	uncertain significance	6	158078167	158078167	Human		name
597779920	CV3618818	single nucleotide variant	NM_003898.4(SYNJ2):c.2056C>G (p.Leu686Val)	not specified [RCV004873697]	uncertain significance	6	158071717	158071717	Human		name
597794665	CV3618823	single nucleotide variant	NM_003898.4(SYNJ2):c.1368G>T (p.Lys456Asn)	not specified [RCV004877931]	uncertain significance	6	158064834	158064834	Human		name
598180488	CV3923339	single nucleotide variant	NM_003898.4(SYNJ2):c.1855C>T (p.His619Tyr)	not specified [RCV005286561]	uncertain significance	6	158069588	158069588	Human		name
598180503	CV3923341	single nucleotide variant	NM_003898.4(SYNJ2):c.2002G>A (p.Val668Ile)	not specified [RCV005286563]	uncertain significance	6	158071663	158071663	Human		name
598264006	CV3923342	single nucleotide variant	NM_003898.4(SYNJ2):c.1954G>A (p.Asp652Asn)	not specified [RCV005280678]	uncertain significance	6	158071615	158071615	Human		name
598180524	CV3923346	single nucleotide variant	NM_003898.4(SYNJ2):c.2621G>C (p.Arg874Pro)	not specified [RCV005286566]	uncertain significance	6	158081162	158081162	Human		name
598180539	CV3923348	single nucleotide variant	NM_003898.4(SYNJ2):c.1531C>T (p.Pro511Ser)	not specified [RCV005286568]	uncertain significance	6	158066449	158066449	Human		name
598180580	CV3923354	single nucleotide variant	NM_003898.4(SYNJ2):c.2978A>T (p.Asn993Ile)	not specified [RCV005286574]	uncertain significance	6	158083541	158083541	Human		name
598264012	CV3923357	single nucleotide variant	NM_003898.4(SYNJ2):c.2045T>C (p.Ile682Thr)	not specified [RCV005280680]	uncertain significance	6	158071706	158071706	Human		name
598264019	CV3923359	single nucleotide variant	NM_003898.4(SYNJ2):c.1858A>G (p.Arg620Gly)	not specified [RCV005280681]	uncertain significance	6	158069591	158069591	Human		name
598264025	CV3923360	single nucleotide variant	NM_003898.4(SYNJ2):c.2123G>A (p.Cys708Tyr)	not specified [RCV005280682]	uncertain significance	6	158071784	158071784	Human		name
598180609	CV3923361	single nucleotide variant	NM_003898.4(SYNJ2):c.2410G>T (p.Val804Leu)	not specified [RCV005286578]	uncertain significance	6	158076743	158076743	Human		name
156269999	CV2195127	single nucleotide variant	NM_003898.4(SYNJ2):c.4366G>A (p.Ala1456Thr)	not specified [RCV004078033]	uncertain significance	6	158096239	158096239	Human		name
156399931	CV2202311	single nucleotide variant	NM_003898.4(SYNJ2):c.3988C>G (p.Pro1330Ala)	not specified [RCV004078241]	uncertain significance	6	158095861	158095861	Human		name
156399215	CV2204985	single nucleotide variant	NM_003898.4(SYNJ2):c.3542G>A (p.Arg1181Gln)	not specified [RCV004077605]	uncertain significance	6	158089924	158089924	Human		name
156190050	CV2206006	single nucleotide variant	NM_003898.4(SYNJ2):c.3686G>A (p.Arg1229His)	not specified [RCV004078423]	uncertain significance	6	158093046	158093046	Human		name
156116444	CV2209085	single nucleotide variant	NM_003898.4(SYNJ2):c.3502A>G (p.Ile1168Val)	not specified [RCV004093317]	uncertain significance	6	158089884	158089884	Human		name
156253126	CV2212513	single nucleotide variant	NM_003898.4(SYNJ2):c.3337C>G (p.Pro1113Ala)	not specified [RCV004091397]	uncertain significance	6	158086983	158086983	Human		name
156375102	CV2213494	single nucleotide variant	NM_003898.4(SYNJ2):c.3556G>A (p.Ala1186Thr)	not specified [RCV004087461]	uncertain significance	6	158089938	158089938	Human		name
156069674	CV2232257	single nucleotide variant	NM_003898.4(SYNJ2):c.3214G>A (p.Ala1072Thr)	not specified [RCV004105040]	uncertain significance	6	158086860	158086860	Human		name
156269819	CV2240220	single nucleotide variant	NM_003898.4(SYNJ2):c.3070G>A (p.Asp1024Asn)	not specified [RCV004112794]	uncertain significance	6	158084036	158084036	Human		name
156302426	CV2241766	single nucleotide variant	NM_003898.4(SYNJ2):c.3008T>G (p.Phe1003Cys)	not specified [RCV004106702]	uncertain significance	6	158083571	158083571	Human		name
156036643	CV2243599	single nucleotide variant	NM_003898.4(SYNJ2):c.4120G>A (p.Ala1374Thr)	not specified [RCV004114328]	likely benign	6	158095993	158095993	Human		name
155999588	CV2257655	single nucleotide variant	NM_003898.4(SYNJ2):c.3085C>T (p.Pro1029Ser)	not specified [RCV004127751]	uncertain significance	6	158084051	158084051	Human		name
155999601	CV2257656	single nucleotide variant	NM_003898.4(SYNJ2):c.3143C>A (p.Thr1048Lys)	not specified [RCV004127752]	uncertain significance	6	158084109	158084109	Human		name
156395863	CV2325969	single nucleotide variant	NM_003898.4(SYNJ2):c.3322C>T (p.Pro1108Ser)	not specified [RCV004176182]	uncertain significance	6	158086968	158086968	Human		name
155901646	CV2345846	single nucleotide variant	NM_003898.4(SYNJ2):c.3229C>T (p.Leu1077Phe)	not specified [RCV004198890]	uncertain significance	6	158086875	158086875	Human		name
155925231	CV2348327	single nucleotide variant	NM_003898.4(SYNJ2):c.3777G>C (p.Gln1259His)	not specified [RCV004193525]	uncertain significance	6	158095650	158095650	Human		name
155932760	CV2364463	single nucleotide variant	NM_003898.4(SYNJ2):c.3337C>A (p.Pro1113Thr)	not specified [RCV004216941]	uncertain significance	6	158086983	158086983	Human		name
156266213	CV2372444	single nucleotide variant	NM_003898.4(SYNJ2):c.3832G>A (p.Val1278Met)	not specified [RCV004219248]	uncertain significance	6	158095705	158095705	Human		name
156185059	CV2377799	single nucleotide variant	NM_003898.4(SYNJ2):c.3796G>A (p.Gly1266Arg)	not specified [RCV004230379]	uncertain significance	6	158095669	158095669	Human		name
156052589	CV2386659	single nucleotide variant	NM_003898.4(SYNJ2):c.3638C>T (p.Pro1213Leu)	not specified [RCV004230999]	uncertain significance	6	158092998	158092998	Human		name
329355713	CV2445589	single nucleotide variant	NM_003898.4(SYNJ2):c.4000C>G (p.Pro1334Ala)	not specified [RCV004259676]	uncertain significance	6	158095873	158095873	Human		name
401742821	CV2677688	single nucleotide variant	NM_003898.4(SYNJ2):c.3334C>G (p.Pro1112Ala)	not specified [RCV004291773]	uncertain significance	6	158086980	158086980	Human		name
401747081	CV2679002	single nucleotide variant	NM_003898.4(SYNJ2):c.3950C>G (p.Ala1317Gly)	not specified [RCV004295013]	uncertain significance	6	158095823	158095823	Human		name
401758314	CV2704420	single nucleotide variant	NM_003898.4(SYNJ2):c.3355G>A (p.Val1119Met)	not specified [RCV004311383]	uncertain significance	6	158088671	158088671	Human		name
401899877	CV2755795	single nucleotide variant	NM_003898.4(SYNJ2):c.3812G>A (p.Ser1271Asn)	not specified [RCV004342168]	uncertain significance	6	158095685	158095685	Human		name
401890366	CV2755834	single nucleotide variant	NM_003898.4(SYNJ2):c.3213C>G (p.Asp1071Glu)	not specified [RCV004342204]	uncertain significance	6	158086859	158086859	Human		name
401889455	CV2756592	single nucleotide variant	NM_003898.4(SYNJ2):c.3821C>G (p.Ala1274Gly)	not specified [RCV004345115]	uncertain significance	6	158095694	158095694	Human		name
405725724	CV3334698	single nucleotide variant	NM_003898.4(SYNJ2):c.3080A>G (p.Asn1027Ser)	not specified [RCV004463738]	likely benign	6	158084046	158084046	Human		name
405725737	CV3334700	single nucleotide variant	NM_003898.4(SYNJ2):c.3344C>T (p.Thr1115Ile)	not specified [RCV004463740]	uncertain significance	6	158088660	158088660	Human		name
405725745	CV3334701	single nucleotide variant	NM_003898.4(SYNJ2):c.3670C>T (p.Pro1224Ser)	not specified [RCV004463741]	uncertain significance	6	158093030	158093030	Human		name
405725760	CV3334703	single nucleotide variant	NM_003898.4(SYNJ2):c.3839C>T (p.Ala1280Val)	not specified [RCV004463743]	likely benign	6	158095712	158095712	Human		name
405725767	CV3334704	single nucleotide variant	NM_003898.4(SYNJ2):c.3845G>A (p.Arg1282Gln)	not specified [RCV004463744]	likely benign	6	158095718	158095718	Human		name
405725777	CV3334705	single nucleotide variant	NM_003898.4(SYNJ2):c.3892G>T (p.Ala1298Ser)	not specified [RCV004463745]	uncertain significance	6	158095765	158095765	Human		name
405726920	CV3334706	single nucleotide variant	NM_003898.4(SYNJ2):c.4066C>T (p.Leu1356Phe)	not specified [RCV004463746]	uncertain significance	6	158095939	158095939	Human		name
405725792	CV3334707	single nucleotide variant	NM_003898.4(SYNJ2):c.4090A>G (p.Ser1364Gly)	not specified [RCV004463747]	uncertain significance	6	158095963	158095963	Human		name
405725801	CV3334708	single nucleotide variant	NM_003898.4(SYNJ2):c.4321A>G (p.Thr1441Ala)	not specified [RCV004463748]	uncertain significance	6	158096194	158096194	Human		name
405725827	CV3334710	single nucleotide variant	NM_003898.4(SYNJ2):c.4412C>G (p.Thr1471Ser)	not specified [RCV004463750]	uncertain significance	6	158096285	158096285	Human		name
407530300	CV3478281	single nucleotide variant	NM_003898.4(SYNJ2):c.3346G>A (p.Gly1116Ser)	not specified [RCV004681840]	uncertain significance	6	158088662	158088662	Human		name
407505654	CV3478282	single nucleotide variant	NM_003898.4(SYNJ2):c.3457C>T (p.Pro1153Ser)	not specified [RCV004670896]	uncertain significance	6	158089839	158089839	Human		name
597771711	CV3618803	single nucleotide variant	NM_003898.4(SYNJ2):c.4334A>G (p.Lys1445Arg)	not specified [RCV004871699]	uncertain significance	6	158096207	158096207	Human		name
597771721	CV3618805	single nucleotide variant	NM_003898.4(SYNJ2):c.3118G>A (p.Asp1040Asn)	not specified [RCV004871701]	uncertain significance	6	158084084	158084084	Human		name
597771740	CV3618810	single nucleotide variant	NM_003898.4(SYNJ2):c.3335C>A (p.Pro1112His)	not specified [RCV004871705]	uncertain significance	6	158086981	158086981	Human		name
597780179	CV3618817	single nucleotide variant	NM_003898.4(SYNJ2):c.3878A>G (p.Gln1293Arg)	not specified [RCV004873696]	uncertain significance	6	158095751	158095751	Human		name
597794660	CV3618819	single nucleotide variant	NM_003898.4(SYNJ2):c.3797G>A (p.Gly1266Glu)	not specified [RCV004877930]	uncertain significance	6	158095670	158095670	Human		name
597779924	CV3618820	single nucleotide variant	NM_003898.4(SYNJ2):c.4034A>C (p.His1345Pro)	not specified [RCV004873698]	uncertain significance	6	158095907	158095907	Human		name
597779932	CV3618822	single nucleotide variant	NM_003898.4(SYNJ2):c.3746C>T (p.Pro1249Leu)	not specified [RCV004873700]	uncertain significance	6	158095619	158095619	Human		name
598180476	CV3923337	single nucleotide variant	NM_003898.4(SYNJ2):c.3391G>A (p.Gly1131Ser)	not specified [RCV005286559]	uncertain significance	6	158088707	158088707	Human		name
598180517	CV3923345	single nucleotide variant	NM_003898.4(SYNJ2):c.3689G>A (p.Arg1230Gln)	not specified [RCV005286565]	uncertain significance	6	158093049	158093049	Human		name
598180532	CV3923347	single nucleotide variant	NM_003898.4(SYNJ2):c.3851C>G (p.Pro1284Arg)	not specified [RCV005286567]	uncertain significance	6	158095724	158095724	Human		name
598180546	CV3923349	single nucleotide variant	NM_003898.4(SYNJ2):c.3307C>T (p.Arg1103Trp)	not specified [RCV005286569]	uncertain significance	6	158086953	158086953	Human		name
598180595	CV3923356	single nucleotide variant	NM_003898.4(SYNJ2):c.3524A>G (p.Glu1175Gly)	not specified [RCV005286576]	uncertain significance	6	158089906	158089906	Human		name
15164691	CV710284	single nucleotide variant	NM_003898.4(SYNJ2):c.4129G>A (p.Val1377Ile)	not provided [RCV000970782]	benign	6	158096002	158096002	Human		name
8631898	CV87104	single nucleotide variant	NM_003898.3(SYNJ2):c.3574G>A (p.Glu1192Lys)	Malignant melanoma [RCV000067195]	not provided	6	158092934	158092934	Human		name
156282472	CV2363128	single nucleotide variant	NM_018373.3(SYNJ2BP):c.424C>T (p.Arg142Trp)	not specified [RCV004211251]	uncertain significance	14	70373005	70373005	Human		name
401889446	CV2758117	single nucleotide variant	NM_018373.3(SYNJ2BP):c.398T>C (p.Val133Ala)	not specified [RCV004341497]	uncertain significance	14	70373031	70373031	Human		name
156348113	CV2383043	single nucleotide variant	NM_001202547.2(SYNJ2BP-COX16):c.256C>T (p.Arg86Cys)	not specified [RCV004217624]	uncertain significance	14	70375717	70375717	Human		name

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