Sorcs3 Variant Search Result - Rat Genome Database

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140 records found for search term Sorcs3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15159473	CV777846	single nucleotide variant	NM_014978.3(SORCS3):c.696-10T>G	not provided [RCV000947283]	benign	10	104915823	104915823	Human		name
8651480	CV128055	single nucleotide variant	NM_014978.2(SORCS3):c.954+2668G>C	Lung cancer [RCV000108542]	uncertain significance	10	104980161	104980161	Human		name
8651478	CV128053	single nucleotide variant	NM_014978.2(SORCS3):c.795+11861G>T	Lung cancer [RCV000108540]	uncertain significance	10	104927793	104927793	Human		name
8651479	CV128054	single nucleotide variant	NM_014978.2(SORCS3):c.795+14424A>T	Lung cancer [RCV000108541]	uncertain significance	10	104930356	104930356	Human		name
8651481	CV128056	single nucleotide variant	NM_014978.2(SORCS3):c.954+22901T>A	Lung cancer [RCV000108543]	uncertain significance	10	105000394	105000394	Human		name
8651482	CV128057	single nucleotide variant	NM_014978.2(SORCS3):c.1029-4261C>A	Lung cancer [RCV000108544]	uncertain significance	10	105085514	105085514	Human		name
8651483	CV128058	single nucleotide variant	NM_014978.2(SORCS3):c.2869-4030C>A	Lung cancer [RCV000108545]	uncertain significance	10	105241512	105241512	Human		name
405289001	CV3204914	single nucleotide variant	NM_014978.3(SORCS3):c.250C>A (p.Arg84=)	SORCS3-related disorder [RCV003961559]	likely benign	10	104641577	104641577	Human		name , trait , alternate_id
405773697	CV3333361	single nucleotide variant	NM_014978.3(SORCS3):c.59C>G (p.Thr20Arg)	not specified [RCV004457430]	uncertain significance	10	104641386	104641386	Human		name
15154048	CV712144	single nucleotide variant	NM_014978.3(SORCS3):c.94G>A (p.Gly32Ser)	not provided [RCV000968663]	benign	10	104641421	104641421	Human		name
15112912	CV723755	single nucleotide variant	NM_014978.3(SORCS3):c.35G>A (p.Arg12Lys)	not provided [RCV000894559]	benign	10	104641362	104641362	Human		name
8633481	CV88696	single nucleotide variant	NM_014978.2(SORCS3):c.639C>T (p.Ile213=)	Malignant melanoma [RCV000068791]	not provided	10	104842803	104842803	Human		name
8633482	CV88697	single nucleotide variant	NM_014978.2(SORCS3):c.792G>A (p.Arg264=)	Malignant melanoma [RCV000068792]	not provided	10	104915929	104915929	Human		name
156242065	CV2261990	single nucleotide variant	NM_014978.3(SORCS3):c.137C>T (p.Pro46Leu)	not specified [RCV004126479]	uncertain significance	10	104641464	104641464	Human		name
155923767	CV2280376	single nucleotide variant	NM_014978.3(SORCS3):c.115G>A (p.Ala39Thr)	not specified [RCV004140562]	uncertain significance	10	104641442	104641442	Human		name
156154196	CV2328619	single nucleotide variant	NM_014978.3(SORCS3):c.152C>T (p.Ser51Leu)	not specified [RCV004177871]	uncertain significance	10	104641479	104641479	Human		name
156154215	CV2328620	single nucleotide variant	NM_014978.3(SORCS3):c.264G>T (p.Glu88Asp)	not specified [RCV004177872]	uncertain significance	10	104641591	104641591	Human		name
156056857	CV2343499	single nucleotide variant	NM_014978.3(SORCS3):c.134G>A (p.Arg45His)	not specified [RCV004197567]	uncertain significance	10	104641461	104641461	Human		name
155938520	CV2380790	single nucleotide variant	NM_014978.3(SORCS3):c.238G>C (p.Val80Leu)	not specified [RCV004218352]	uncertain significance	10	104641565	104641565	Human		name
401907768	CV2809604	single nucleotide variant	NM_014978.3(SORCS3):c.1980G>A (p.Val660=)	not provided [RCV003422865]	likely benign	10	105178144	105178144	Human		name
401907770	CV2809605	single nucleotide variant	NM_014978.3(SORCS3):c.2080C>A (p.Arg694=)	not provided [RCV003422866]	likely benign	10	105200069	105200069	Human		name
401907771	CV2809606	single nucleotide variant	NM_014978.3(SORCS3):c.2691C>T (p.Asn897=)	not provided [RCV003422867]	likely benign	10	105217079	105217079	Human		name
597756187	CV3603682	single nucleotide variant	NM_014978.3(SORCS3):c.248G>C (p.Arg83Pro)	not specified [RCV004868337]	uncertain significance	10	104641575	104641575	Human		name
597756191	CV3603683	single nucleotide variant	NM_014978.3(SORCS3):c.198C>G (p.Ser66Arg)	not specified [RCV004868338]	uncertain significance	10	104641525	104641525	Human		name
15171063	CV701161	single nucleotide variant	NM_014978.3(SORCS3):c.1056G>A (p.Ala352=)	not provided [RCV000949765]	benign	10	105089802	105089802	Human		name
15138574	CV712145	single nucleotide variant	NM_014978.3(SORCS3):c.1131C>T (p.Ala377=)	not provided [RCV000965815]	benign	10	105105434	105105434	Human		name
8626768	CV81912	single nucleotide variant	NM_014978.2(SORCS3):c.1791G>A (p.Gly597=)	Malignant melanoma [RCV000061991]	not provided	10	105164361	105164361	Human		name
8633485	CV88700	single nucleotide variant	NM_014978.2(SORCS3):c.2154G>A (p.Arg718=)	Malignant melanoma [RCV000068795]	not provided	10	105201146	105201146	Human		name
155976700	CV2218609	single nucleotide variant	NM_014978.3(SORCS3):c.320G>T (p.Gly107Val)	not specified [RCV004090869]	uncertain significance	10	104641647	104641647	Human		name
155976710	CV2218610	single nucleotide variant	NM_014978.3(SORCS3):c.322A>T (p.Thr108Ser)	not specified [RCV004090870]	uncertain significance	10	104641649	104641649	Human		name
156338531	CV2224952	single nucleotide variant	NM_014978.3(SORCS3):c.877C>T (p.Leu293Phe)	not specified [RCV004094802]	uncertain significance	10	104977416	104977416	Human		name
156157301	CV2262388	single nucleotide variant	NM_014978.3(SORCS3):c.306G>C (p.Gln102His)	not specified [RCV004128836]	uncertain significance	10	104641633	104641633	Human		name
156071315	CV2289736	single nucleotide variant	NM_014978.3(SORCS3):c.595G>T (p.Ala199Ser)	not specified [RCV004150429]	uncertain significance	10	104641922	104641922	Human		name
156057684	CV2305172	single nucleotide variant	NM_014978.3(SORCS3):c.523G>A (p.Gly175Arg)	not specified [RCV004171111]	uncertain significance	10	104641850	104641850	Human		name
329365719	CV2441072	single nucleotide variant	NM_014978.3(SORCS3):c.874C>T (p.Arg292Trp)	not specified [RCV004261437]	uncertain significance	10	104977413	104977413	Human		name
329378176	CV2459062	single nucleotide variant	NM_014978.3(SORCS3):c.555C>A (p.Ser185Arg)	not specified [RCV004272531]	uncertain significance	10	104641882	104641882	Human		name
401747853	CV2696808	single nucleotide variant	NM_014978.3(SORCS3):c.739G>A (p.Val247Met)	not specified [RCV004290778]	uncertain significance	10	104915876	104915876	Human		name
401762352	CV2723409	single nucleotide variant	NM_014978.3(SORCS3):c.581C>T (p.Ser194Leu)	not specified [RCV004329614]	uncertain significance	10	104641908	104641908	Human		name
401860030	CV2765442	single nucleotide variant	NM_014978.3(SORCS3):c.945G>C (p.Leu315Phe)	not specified [RCV004341760]	uncertain significance	10	104977484	104977484	Human		name
405292658	CV3192565	single nucleotide variant	NM_014978.3(SORCS3):c.967A>G (p.Met323Val)	SORCS3-related disorder [RCV003929816]	likely benign	10	105043067	105043067	Human		name , trait , alternate_id
405773685	CV3333359	single nucleotide variant	NM_014978.3(SORCS3):c.505A>C (p.Lys169Gln)	not specified [RCV004457428]	uncertain significance	10	104641832	104641832	Human		name
405773690	CV3333360	single nucleotide variant	NM_014978.3(SORCS3):c.589A>T (p.Asn197Tyr)	not specified [RCV004457429]	uncertain significance	10	104641916	104641916	Human		name
405773703	CV3333362	single nucleotide variant	NM_014978.3(SORCS3):c.808A>T (p.Ser270Cys)	not specified [RCV004457431]	uncertain significance	10	104977347	104977347	Human		name
407504494	CV3485012	single nucleotide variant	NM_014978.3(SORCS3):c.390G>T (p.Arg130Ser)	not specified [RCV004670537]	uncertain significance	10	104641717	104641717	Human		name
407504498	CV3485013	single nucleotide variant	NM_014978.3(SORCS3):c.391A>C (p.Ser131Arg)	not specified [RCV004670538]	uncertain significance	10	104641718	104641718	Human		name
407504504	CV3485016	single nucleotide variant	NM_014978.3(SORCS3):c.608G>T (p.Trp203Leu)	not specified [RCV004670540]	uncertain significance	10	104641935	104641935	Human		name
407525372	CV3485018	single nucleotide variant	NM_014978.3(SORCS3):c.481G>A (p.Ala161Thr)	not specified [RCV004679195]	uncertain significance	10	104641808	104641808	Human		name
407504511	CV3485019	single nucleotide variant	NM_014978.3(SORCS3):c.368C>T (p.Ala123Val)	not specified [RCV004670542]	uncertain significance	10	104641695	104641695	Human		name
407504519	CV3485022	single nucleotide variant	NM_014978.3(SORCS3):c.605A>G (p.His202Arg)	not specified [RCV004670545]	uncertain significance	10	104641932	104641932	Human		name
407504527	CV3485024	single nucleotide variant	NM_014978.3(SORCS3):c.428G>C (p.Gly143Ala)	not specified [RCV004670547]	uncertain significance	10	104641755	104641755	Human		name
407504539	CV3485028	single nucleotide variant	NM_014978.3(SORCS3):c.508G>A (p.Ala170Thr)	not specified [RCV004670551]	uncertain significance	10	104641835	104641835	Human		name
597741492	CV3603675	single nucleotide variant	NM_014978.3(SORCS3):c.875G>A (p.Arg292Gln)	not specified [RCV004864877]	uncertain significance	10	104977414	104977414	Human		name
597756195	CV3603684	single nucleotide variant	NM_014978.3(SORCS3):c.307G>A (p.Val103Met)	not specified [RCV004868339]	uncertain significance	10	104641634	104641634	Human		name
597756199	CV3603686	single nucleotide variant	NM_014978.3(SORCS3):c.644C>T (p.Thr215Met)	not specified [RCV004868340]	uncertain significance	10	104842808	104842808	Human		name
597756202	CV3603687	single nucleotide variant	NM_014978.3(SORCS3):c.922G>A (p.Asp308Asn)	not specified [RCV004868341]	uncertain significance	10	104977461	104977461	Human		name
597756217	CV3603691	single nucleotide variant	NM_014978.3(SORCS3):c.982C>T (p.Arg328Trp)	not specified [RCV004868345]	uncertain significance	10	105043082	105043082	Human		name
597741502	CV3603692	single nucleotide variant	NM_014978.3(SORCS3):c.643A>G (p.Thr215Ala)	not specified [RCV004864879]	uncertain significance	10	104842807	104842807	Human		name
597756220	CV3603693	single nucleotide variant	NM_014978.3(SORCS3):c.436T>A (p.Trp146Arg)	not specified [RCV004868346]	likely benign	10	104641763	104641763	Human		name
597756225	CV3603696	single nucleotide variant	NM_014978.3(SORCS3):c.565G>T (p.Ala189Ser)	not specified [RCV004868347]	uncertain significance	10	104641892	104641892	Human		name
598246688	CV3911929	single nucleotide variant	NM_014978.3(SORCS3):c.781A>G (p.Thr261Ala)	not specified [RCV005277166]	uncertain significance	10	104915918	104915918	Human		name
598246719	CV3911933	single nucleotide variant	NM_014978.3(SORCS3):c.781A>T (p.Thr261Ser)	not specified [RCV005277170]	uncertain significance	10	104915918	104915918	Human		name
15202990	CV701162	single nucleotide variant	NM_014978.3(SORCS3):c.3297G>A (p.Pro1099=)	not provided [RCV000958155]	benign	10	105255761	105255761	Human		name
15146550	CV712146	single nucleotide variant	NM_014978.3(SORCS3):c.3558G>A (p.Thr1186=)	not provided [RCV000967181]	benign	10	105262445	105262445	Human		name
156173907	CV2194382	single nucleotide variant	NM_014978.3(SORCS3):c.1831G>A (p.Val611Ile)	not specified [RCV004079486]	uncertain significance	10	105167279	105167279	Human		name
156097562	CV2206847	single nucleotide variant	NM_014978.3(SORCS3):c.2923G>A (p.Asp975Asn)	not specified [RCV004083520]	likely benign	10	105245596	105245596	Human		name
156111138	CV2207845	single nucleotide variant	NM_014978.3(SORCS3):c.2695C>G (p.Leu899Val)	not specified [RCV004084277]	uncertain significance	10	105217083	105217083	Human		name
155920566	CV2210837	single nucleotide variant	NM_014978.3(SORCS3):c.2033G>C (p.Arg678Pro)	not specified [RCV004085926]	uncertain significance	10	105200022	105200022	Human		name
156069688	CV2232262	single nucleotide variant	NM_014978.3(SORCS3):c.2431G>A (p.Ala811Thr)	not specified [RCV004105045]	uncertain significance	10	105214497	105214497	Human		name
156020325	CV2270260	single nucleotide variant	NM_014978.3(SORCS3):c.2464C>T (p.Arg822Trp)	not specified [RCV004135479]	uncertain significance	10	105214530	105214530	Human		name
155909925	CV2303487	single nucleotide variant	NM_014978.3(SORCS3):c.1057G>A (p.Asp353Asn)	not specified [RCV004161593]	uncertain significance	10	105089803	105089803	Human		name
155962861	CV2308203	single nucleotide variant	NM_014978.3(SORCS3):c.1196A>C (p.Glu399Ala)	not specified [RCV004164705]	uncertain significance	10	105105499	105105499	Human		name
155962871	CV2308204	single nucleotide variant	NM_014978.3(SORCS3):c.1589C>T (p.Pro530Leu)	not specified [RCV004164706]	uncertain significance	10	105157244	105157244	Human		name
156303122	CV2331744	single nucleotide variant	NM_014978.3(SORCS3):c.1935G>C (p.Lys645Asn)	not specified [RCV004184369]	uncertain significance	10	105178099	105178099	Human		name
156043567	CV2342322	single nucleotide variant	NM_014978.3(SORCS3):c.1327G>A (p.Glu443Lys)	not specified [RCV004191889]	uncertain significance	10	105147641	105147641	Human		name
156071476	CV2353165	single nucleotide variant	NM_014978.3(SORCS3):c.2119C>T (p.Leu707Phe)	not specified [RCV004203638]	uncertain significance	10	105200108	105200108	Human		name
156073971	CV2376940	single nucleotide variant	NM_014978.3(SORCS3):c.1861G>A (p.Val621Met)	not specified [RCV004229628]	uncertain significance	10	105167309	105167309	Human		name
155954353	CV2379193	single nucleotide variant	NM_014978.3(SORCS3):c.2002A>C (p.Ile668Leu)	not specified [RCV004235981]	uncertain significance	10	105178166	105178166	Human		name
156187734	CV2395293	single nucleotide variant	NM_014978.3(SORCS3):c.2465G>A (p.Arg822Gln)	not specified [RCV004239390]	uncertain significance	10	105214531	105214531	Human		name
401747325	CV2698841	single nucleotide variant	NM_014978.3(SORCS3):c.1999C>T (p.His667Tyr)	not specified [RCV004301278]	uncertain significance	10	105178163	105178163	Human		name
401735963	CV2703003	single nucleotide variant	NM_014978.3(SORCS3):c.2780G>T (p.Arg927Ile)	not specified [RCV004321314]	uncertain significance	10	105223161	105223161	Human		name
401750968	CV2715826	single nucleotide variant	NM_014978.3(SORCS3):c.2785A>G (p.Lys929Glu)	not specified [RCV004328948]	uncertain significance	10	105223166	105223166	Human		name
401766086	CV2718001	single nucleotide variant	NM_014978.3(SORCS3):c.2633G>T (p.Gly878Val)	not specified [RCV004321944]	uncertain significance	10	105217021	105217021	Human		name
401893333	CV2765231	single nucleotide variant	NM_014978.3(SORCS3):c.2134C>G (p.Pro712Ala)	not specified [RCV004339758]	uncertain significance	10	105201126	105201126	Human		name
401877311	CV2769410	single nucleotide variant	NM_014978.3(SORCS3):c.2063A>G (p.Tyr688Cys)	not specified [RCV004357397]	uncertain significance	10	105200052	105200052	Human		name
401898715	CV2782621	single nucleotide variant	NM_014978.3(SORCS3):c.1628T>A (p.Leu543Gln)	not specified [RCV004359645]	uncertain significance	10	105157283	105157283	Human		name
401920520	CV2796525	single nucleotide variant	NM_014978.3(SORCS3):c.2545G>A (p.Glu849Lys)	SORCS3-related disorder [RCV003402561]	uncertain significance	10	105214611	105214611	Human		name , trait , alternate_id
405282994	CV3216882	single nucleotide variant	NM_014978.3(SORCS3):c.2400C>A (p.Asn800Lys)	SORCS3-related disorder [RCV003979050]	likely benign	10	105214466	105214466	Human		name , trait , alternate_id
405773607	CV3333345	single nucleotide variant	NM_014978.3(SORCS3):c.1055C>T (p.Ala352Val)	not specified [RCV004457414]	uncertain significance	10	105089801	105089801	Human		name
405773612	CV3333346	single nucleotide variant	NM_014978.3(SORCS3):c.1476G>T (p.Leu492Phe)	not specified [RCV004457415]	uncertain significance	10	105147790	105147790	Human		name
405773625	CV3333348	single nucleotide variant	NM_014978.3(SORCS3):c.1790G>C (p.Gly597Ala)	not specified [RCV004457417]	uncertain significance	10	105164360	105164360	Human		name
405773631	CV3333349	single nucleotide variant	NM_014978.3(SORCS3):c.2533A>G (p.Ile845Val)	not specified [RCV004457418]	uncertain significance	10	105214599	105214599	Human		name
405773637	CV3333350	single nucleotide variant	NM_014978.3(SORCS3):c.2776A>G (p.Ile926Val)	not specified [RCV004457419]	uncertain significance	10	105223157	105223157	Human		name
405773647	CV3333352	single nucleotide variant	NM_014978.3(SORCS3):c.2912C>A (p.Ala971Glu)	not specified [RCV004457421]	uncertain significance	10	105245585	105245585	Human		name
405773650	CV3333353	single nucleotide variant	NM_014978.3(SORCS3):c.2912C>G (p.Ala971Gly)	not specified [RCV004457422]	uncertain significance	10	105245585	105245585	Human		name
407504501	CV3485014	single nucleotide variant	NM_014978.3(SORCS3):c.2797A>G (p.Ile933Val)	not specified [RCV004670539]	uncertain significance	10	105223178	105223178	Human		name
407504508	CV3485017	single nucleotide variant	NM_014978.3(SORCS3):c.1078C>T (p.Arg360Trp)	not specified [RCV004670541]	uncertain significance	10	105089824	105089824	Human		name
407504513	CV3485020	single nucleotide variant	NM_014978.3(SORCS3):c.1262C>T (p.Ala421Val)	not specified [RCV004670543]	uncertain significance	10	105139446	105139446	Human		name
407504517	CV3485021	single nucleotide variant	NM_014978.3(SORCS3):c.2686G>A (p.Glu896Lys)	not specified [RCV004670544]	uncertain significance	10	105217074	105217074	Human		name
407504530	CV3485025	single nucleotide variant	NM_014978.3(SORCS3):c.1192G>A (p.Asp398Asn)	not specified [RCV004670548]	uncertain significance	10	105105495	105105495	Human		name
597756165	CV3603676	single nucleotide variant	NM_014978.3(SORCS3):c.1397C>T (p.Thr466Met)	not specified [RCV004868331]	uncertain significance	10	105147711	105147711	Human		name
597756169	CV3603677	single nucleotide variant	NM_014978.3(SORCS3):c.1219A>G (p.Thr407Ala)	not specified [RCV004868332]	uncertain significance	10	105139403	105139403	Human		name
597756173	CV3603678	single nucleotide variant	NM_014978.3(SORCS3):c.1468A>G (p.Ile490Val)	not specified [RCV004868333]	uncertain significance	10	105147782	105147782	Human		name
597756177	CV3603679	single nucleotide variant	NM_014978.3(SORCS3):c.2692A>G (p.Asn898Asp)	not specified [RCV004868334]	uncertain significance	10	105217080	105217080	Human		name
597741497	CV3603685	single nucleotide variant	NM_014978.3(SORCS3):c.1063G>C (p.Val355Leu)	not specified [RCV004864878]	uncertain significance	10	105089809	105089809	Human		name
597756205	CV3603688	single nucleotide variant	NM_014978.3(SORCS3):c.2246A>G (p.Asn749Ser)	not specified [RCV004868342]	uncertain significance	10	105201238	105201238	Human		name
597756213	CV3603690	single nucleotide variant	NM_014978.3(SORCS3):c.2957C>T (p.Ala986Val)	not specified [RCV004868344]	uncertain significance	10	105245630	105245630	Human		name
597741507	CV3603694	single nucleotide variant	NM_014978.3(SORCS3):c.2833C>G (p.Leu945Val)	not specified [RCV004864880]	uncertain significance	10	105223214	105223214	Human		name
597741512	CV3603695	single nucleotide variant	NM_014978.3(SORCS3):c.1595T>G (p.Val532Gly)	not specified [RCV004864881]	uncertain significance	10	105157250	105157250	Human		name
597756228	CV3603697	single nucleotide variant	NM_014978.3(SORCS3):c.1081A>T (p.Thr361Ser)	not specified [RCV004868348]	uncertain significance	10	105089827	105089827	Human		name
597756231	CV3603698	single nucleotide variant	NM_014978.3(SORCS3):c.2858A>G (p.Asn953Ser)	not specified [RCV004868349]	uncertain significance	10	105223239	105223239	Human		name
597756235	CV3603699	single nucleotide variant	NM_014978.3(SORCS3):c.1592A>T (p.Asp531Val)	not specified [RCV004868350]	uncertain significance	10	105157247	105157247	Human		name
598246694	CV3911930	single nucleotide variant	NM_014978.3(SORCS3):c.1252C>G (p.Arg418Gly)	not specified [RCV005277167]	uncertain significance	10	105139436	105139436	Human		name
598246701	CV3911931	single nucleotide variant	NM_014978.3(SORCS3):c.1387A>G (p.Ile463Val)	not specified [RCV005277168]	uncertain significance	10	105147701	105147701	Human		name
598246710	CV3911932	single nucleotide variant	NM_014978.3(SORCS3):c.1400G>A (p.Arg467His)	not specified [RCV005277169]	uncertain significance	10	105147714	105147714	Human		name
598246726	CV3911934	single nucleotide variant	NM_014978.3(SORCS3):c.1616T>C (p.Val539Ala)	not specified [RCV005277171]	uncertain significance	10	105157271	105157271	Human		name
15160957	CV723756	single nucleotide variant	NM_014978.3(SORCS3):c.1528G>A (p.Asp510Asn)	not provided [RCV000881482]	benign	10	105157183	105157183	Human		name
8626767	CV81911	single nucleotide variant	NM_014978.2(SORCS3):c.1151C>T (p.Pro384Leu)	Malignant melanoma [RCV000061990]	not provided	10	105105454	105105454	Human		name
8633483	CV88698	single nucleotide variant	NM_014978.3(SORCS3):c.1031C>T (p.Ser344Leu)	not specified [RCV004336088]	uncertain significance\|not provided	10	105089777	105089777	Human		name
8633484	CV88699	single nucleotide variant	NM_014978.2(SORCS3):c.1693T>C (p.Ser565Pro)	Malignant melanoma [RCV000068794]	not provided	10	105158955	105158955	Human		name
156398406	CV2200756	single nucleotide variant	NM_014978.3(SORCS3):c.3593C>T (p.Thr1198Met)	not specified [RCV004081402]	uncertain significance	10	105262480	105262480	Human		name
155993775	CV2286337	single nucleotide variant	NM_014978.3(SORCS3):c.3602T>G (p.Ile1201Arg)	not specified [RCV004146284]	uncertain significance	10	105262489	105262489	Human		name
156170477	CV2312509	single nucleotide variant	NM_014978.3(SORCS3):c.3064A>G (p.Arg1022Gly)	not specified [RCV004167468]	uncertain significance	10	105247290	105247290	Human		name
401721978	CV2680767	single nucleotide variant	NM_014978.3(SORCS3):c.3596G>A (p.Arg1199Gln)	not specified [RCV004293418]	uncertain significance	10	105262483	105262483	Human		name
401722366	CV2706487	single nucleotide variant	NM_014978.3(SORCS3):c.3094G>A (p.Ala1032Thr)	not specified [RCV004317302]	uncertain significance	10	105247320	105247320	Human		name
405773656	CV3333354	single nucleotide variant	NM_014978.3(SORCS3):c.3193A>G (p.Asn1065Asp)	not specified [RCV004457423]	uncertain significance	10	105252862	105252862	Human		name
405773669	CV3333356	single nucleotide variant	NM_014978.3(SORCS3):c.3532C>T (p.Pro1178Ser)	not specified [RCV004457425]	uncertain significance	10	105262419	105262419	Human		name
405773673	CV3333357	single nucleotide variant	NM_014978.3(SORCS3):c.3632A>G (p.Glu1211Gly)	not specified [RCV004457426]	uncertain significance	10	105263337	105263337	Human		name
405773679	CV3333358	single nucleotide variant	NM_014978.3(SORCS3):c.3633A>C (p.Glu1211Asp)	not specified [RCV004457427]	uncertain significance	10	105263338	105263338	Human		name
407504524	CV3485023	single nucleotide variant	NM_014978.3(SORCS3):c.3472C>G (p.Gln1158Glu)	not specified [RCV004670546]	uncertain significance	10	105262359	105262359	Human		name
407504536	CV3485027	single nucleotide variant	NM_014978.3(SORCS3):c.3409G>T (p.Gly1137Cys)	not specified [RCV004670550]	uncertain significance	10	105256890	105256890	Human		name
597756180	CV3603680	single nucleotide variant	NM_014978.3(SORCS3):c.3155T>C (p.Leu1052Pro)	not specified [RCV004868335]	uncertain significance	10	105252824	105252824	Human		name
597756183	CV3603681	single nucleotide variant	NM_014978.3(SORCS3):c.3160A>C (p.Thr1054Pro)	not specified [RCV004868336]	uncertain significance	10	105252829	105252829	Human		name
597756209	CV3603689	single nucleotide variant	NM_014978.3(SORCS3):c.3085A>G (p.Ile1029Val)	not specified [RCV004868343]	uncertain significance	10	105247311	105247311	Human		name
597756239	CV3603700	single nucleotide variant	NM_014978.3(SORCS3):c.3601A>T (p.Ile1201Leu)	not specified [RCV004868351]	uncertain significance	10	105262488	105262488	Human		name
597741517	CV3603701	single nucleotide variant	NM_014978.3(SORCS3):c.3137T>C (p.Ile1046Thr)	not specified [RCV004864882]	uncertain significance	10	105252806	105252806	Human		name
598246732	CV3911935	single nucleotide variant	NM_014978.3(SORCS3):c.3257A>C (p.Asn1086Thr)	not specified [RCV005277172]	uncertain significance	10	105255721	105255721	Human		name
15189304	CV701163	single nucleotide variant	NM_014978.3(SORCS3):c.3515G>A (p.Ser1172Asn)	not provided [RCV000954135]	benign	10	105262402	105262402	Human		name
21070570	CV792533	single nucleotide variant	NM_014978.3(SORCS3):c.3110C>G (p.Thr1037Ser)	not provided [RCV000991040]	uncertain significance	10	105252779	105252779	Human		name
8626769	CV81913	single nucleotide variant	NM_014978.2(SORCS3):c.3298G>A (p.Gly1100Arg)	Malignant melanoma [RCV000061992]	not provided	10	105255762	105255762	Human		name
8633486	CV88701	single nucleotide variant	NM_014978.2(SORCS3):c.3501G>A (p.Met1167Ile)	Malignant melanoma [RCV000068796]	not provided	10	105262388	105262388	Human		name

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