Scly Variant Search Result - Rat Genome Database

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76 records found for search term Scly

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156205928	CV2297920	single nucleotide variant	NM_016510.7(SCLY):c.-6G>T	not specified [RCV004157849]	uncertain significance	2	238061049	238061049	Human		name
15144493	CV778860	single nucleotide variant	NM_016510.7(SCLY):c.612+7C>T	not provided [RCV000966842]	benign	2	238081843	238081843	Human		name
156167816	CV2373731	single nucleotide variant	NM_016510.7(SCLY):c.32C>T (p.Ala11Val)	not specified [RCV004222805]	uncertain significance	2	238061086	238061086	Human		name
405744190	CV3317329	single nucleotide variant	NM_016510.7(SCLY):c.34C>G (p.Pro12Ala)	not specified [RCV004452850]	uncertain significance	2	238061088	238061088	Human		name
598196959	CV3910355	single nucleotide variant	NM_016510.7(SCLY):c.47C>G (p.Ala16Gly)	not specified [RCV005268034]	uncertain significance	2	238061101	238061101	Human		name
598196965	CV3910356	single nucleotide variant	NM_016510.7(SCLY):c.35C>G (p.Pro12Arg)	not specified [RCV005268035]	likely benign	2	238061089	238061089	Human		name
156141011	CV2199901	single nucleotide variant	NM_016510.7(SCLY):c.206G>T (p.Arg69Ile)	not specified [RCV004074085]	uncertain significance	2	238068068	238068068	Human		name
156196461	CV2297350	single nucleotide variant	NM_016510.7(SCLY):c.211G>A (p.Ala71Thr)	not specified [RCV004153005]	uncertain significance	2	238068073	238068073	Human		name
401760641	CV2718906	single nucleotide variant	NM_016510.7(SCLY):c.260G>T (p.Gly87Val)	not specified [RCV004322508]	uncertain significance	2	238068122	238068122	Human		name
401877091	CV2793344	single nucleotide variant	NM_016510.7(SCLY):c.235C>T (p.Arg79Trp)	not specified [RCV004362155]	uncertain significance	2	238068097	238068097	Human		name
405744155	CV3317323	single nucleotide variant	NM_016510.7(SCLY):c.150G>T (p.Met50Ile)	not specified [RCV004452844]	uncertain significance	2	238064417	238064417	Human		name
405744160	CV3317324	single nucleotide variant	NM_016510.7(SCLY):c.191C>T (p.Pro64Leu)	not specified [RCV004452845]	likely benign	2	238064458	238064458	Human		name
405744166	CV3317325	single nucleotide variant	NM_016510.7(SCLY):c.218A>G (p.Asp73Gly)	not specified [RCV004452846]	uncertain significance	2	238068080	238068080	Human		name
405744171	CV3317326	single nucleotide variant	NM_016510.7(SCLY):c.292G>A (p.Gly98Arg)	not specified [RCV004452847]	uncertain significance	2	238068154	238068154	Human		name
597691610	CV3597963	single nucleotide variant	NM_016510.7(SCLY):c.290C>T (p.Ser97Phe)	not specified [RCV004858932]	uncertain significance	2	238068152	238068152	Human		name
598196980	CV3910358	single nucleotide variant	NM_016510.7(SCLY):c.115A>G (p.Thr39Ala)	not specified [RCV005268037]	uncertain significance	2	238064382	238064382	Human		name
598196987	CV3910359	single nucleotide variant	NM_016510.7(SCLY):c.267A>T (p.Lys89Asn)	not specified [RCV005268038]	uncertain significance	2	238068129	238068129	Human		name
15128923	CV717978	single nucleotide variant	NM_016510.7(SCLY):c.1233G>A (p.Arg411=)	not provided [RCV000964169]	benign	2	238098250	238098250	Human		name
15165292	CV717979	single nucleotide variant	NM_016510.7(SCLY):c.1275C>T (p.Ala425=)	not provided [RCV000970918]	benign	2	238098292	238098292	Human		name
15144484	CV717980	single nucleotide variant	NM_016510.7(SCLY):c.258A>G (p.Ile86Met)	not provided [RCV000966841]	benign	2	238068120	238068120	Human		name
15195596	CV729834	single nucleotide variant	NM_016510.7(SCLY):c.1161G>C (p.Ala387=)	not provided [RCV000889545]	likely benign	2	238096853	238096853	Human		name
156082733	CV2205462	single nucleotide variant	NM_016510.7(SCLY):c.868C>T (p.Arg290Trp)	not specified [RCV004082404]	uncertain significance	2	238083338	238083338	Human		name
156114307	CV2268547	single nucleotide variant	NM_016510.7(SCLY):c.724C>A (p.Arg242Ser)	not specified [RCV004123968]	uncertain significance	2	238082156	238082156	Human		name
156250582	CV2273305	single nucleotide variant	NM_016510.7(SCLY):c.661G>A (p.Val221Met)	not specified [RCV004132097]	uncertain significance	2	238082093	238082093	Human		name
156061969	CV2351373	single nucleotide variant	NM_016510.7(SCLY):c.583C>G (p.Leu195Val)	not specified [RCV004193071]	uncertain significance	2	238081807	238081807	Human		name
155908144	CV2354574	single nucleotide variant	NM_016510.7(SCLY):c.430G>C (p.Glu144Gln)	not specified [RCV004202549]	uncertain significance	2	238069423	238069423	Human		name
156213022	CV2385822	single nucleotide variant	NM_016510.7(SCLY):c.727G>A (p.Val243Met)	not specified [RCV004226873]	uncertain significance	2	238082159	238082159	Human		name
329375310	CV2431453	single nucleotide variant	NM_016510.7(SCLY):c.535G>A (p.Asp179Asn)	not specified [RCV004254617]	uncertain significance	2	238081759	238081759	Human		name
329371590	CV2432022	single nucleotide variant	NM_016510.7(SCLY):c.500C>T (p.Pro167Leu)	not specified [RCV004249174]	uncertain significance	2	238081724	238081724	Human		name
329374141	CV2443732	single nucleotide variant	NM_016510.7(SCLY):c.925G>A (p.Ala309Thr)	not specified [RCV004256031]	uncertain significance	2	238093864	238093864	Human		name
401741144	CV2680339	single nucleotide variant	NM_016510.7(SCLY):c.688G>A (p.Val230Met)	not specified [RCV004288591]	likely benign	2	238082120	238082120	Human		name
401774488	CV2713499	single nucleotide variant	NM_016510.7(SCLY):c.635G>C (p.Arg212Pro)	not specified [RCV004319102]	uncertain significance	2	238082067	238082067	Human		name
401783232	CV2716191	single nucleotide variant	NM_016510.7(SCLY):c.926C>G (p.Ala309Gly)	not specified [RCV004323422]	uncertain significance	2	238093865	238093865	Human		name
401768090	CV2727378	single nucleotide variant	NM_016510.7(SCLY):c.628A>C (p.Ser210Arg)	not specified [RCV004327477]	uncertain significance	2	238082060	238082060	Human		name
401877257	CV2764559	single nucleotide variant	NM_016510.7(SCLY):c.901A>G (p.Met301Val)	not specified [RCV004339114]	uncertain significance	2	238091234	238091234	Human		name
401895922	CV2779641	single nucleotide variant	NM_016510.7(SCLY):c.499C>G (p.Pro167Ala)	not specified [RCV004351344]	uncertain significance	2	238081723	238081723	Human		name
405744132	CV3317320	single nucleotide variant	NM_016510.7(SCLY):c.979C>T (p.Arg327Cys)	not specified [RCV004452841]	uncertain significance	2	238093918	238093918	Human		name
405744180	CV3317327	single nucleotide variant	NM_016510.7(SCLY):c.299C>G (p.Thr100Ser)	not specified [RCV004452848]	uncertain significance	2	238068161	238068161	Human		name
405744196	CV3317330	single nucleotide variant	NM_016510.7(SCLY):c.899C>T (p.Pro300Leu)	not specified [RCV004452851]	uncertain significance	2	238091232	238091232	Human		name
405744208	CV3317331	single nucleotide variant	NM_016510.7(SCLY):c.946T>C (p.Cys316Arg)	not specified [RCV004452852]	uncertain significance	2	238093885	238093885	Human		name
407461436	CV3480017	single nucleotide variant	NM_016510.7(SCLY):c.553C>T (p.Arg185Cys)	not specified [RCV004658712]	uncertain significance	2	238081777	238081777	Human		name
597691461	CV3597948	single nucleotide variant	NM_016510.7(SCLY):c.733G>A (p.Val245Met)	not specified [RCV004858917]	uncertain significance	2	238082165	238082165	Human		name
597691482	CV3597950	single nucleotide variant	NM_016510.7(SCLY):c.869G>A (p.Arg290Gln)	not specified [RCV004858919]	uncertain significance	2	238083339	238083339	Human		name
597691493	CV3597951	single nucleotide variant	NM_016510.7(SCLY):c.977T>C (p.Val326Ala)	not specified [RCV004858920]	uncertain significance	2	238093916	238093916	Human		name
597691525	CV3597954	single nucleotide variant	NM_016510.7(SCLY):c.980G>A (p.Arg327His)	not specified [RCV004858923]	uncertain significance	2	238093919	238093919	Human		name
597691535	CV3597955	single nucleotide variant	NM_016510.7(SCLY):c.695C>T (p.Thr232Met)	not specified [RCV004858924]	uncertain significance	2	238082127	238082127	Human		name
597691554	CV3597957	single nucleotide variant	NM_016510.7(SCLY):c.554G>A (p.Arg185His)	not specified [RCV004858926]	uncertain significance	2	238081778	238081778	Human		name
597691563	CV3597958	single nucleotide variant	NM_016510.7(SCLY):c.299C>T (p.Thr100Ile)	not specified [RCV004858927]	uncertain significance	2	238068161	238068161	Human		name
597691584	CV3597960	single nucleotide variant	NM_016510.7(SCLY):c.967A>G (p.Met323Val)	not specified [RCV004858929]	uncertain significance	2	238093906	238093906	Human		name
597691593	CV3597961	single nucleotide variant	NM_016510.7(SCLY):c.748G>A (p.Val250Met)	not specified [RCV004858930]	uncertain significance	2	238082180	238082180	Human		name
597691601	CV3597962	single nucleotide variant	NM_016510.7(SCLY):c.949G>A (p.Glu317Lys)	not specified [RCV004858931]	uncertain significance	2	238093888	238093888	Human		name
598196928	CV3910350	single nucleotide variant	NM_016510.7(SCLY):c.566G>A (p.Arg189His)	not specified [RCV005268029]	uncertain significance	2	238081790	238081790	Human		name
598196936	CV3910351	single nucleotide variant	NM_016510.7(SCLY):c.446G>A (p.Arg149Gln)	not specified [RCV005268030]	uncertain significance	2	238069439	238069439	Human		name
598196947	CV3910353	single nucleotide variant	NM_016510.7(SCLY):c.605T>C (p.Ile202Thr)	not specified [RCV005268032]	uncertain significance	2	238081829	238081829	Human		name
15195938	CV706441	single nucleotide variant	NM_016510.7(SCLY):c.827T>C (p.Phe276Ser)	not provided [RCV000956060]	benign	2	238083297	238083297	Human		name
15144499	CV717977	single nucleotide variant	NM_016510.7(SCLY):c.976G>A (p.Val326Ile)	not provided [RCV000966843]	benign	2	238093915	238093915	Human		name
156185425	CV2195561	single nucleotide variant	NM_016510.7(SCLY):c.1229C>A (p.Ala410Asp)	not specified [RCV004082776]	uncertain significance	2	238098246	238098246	Human		name
155919539	CV2202655	single nucleotide variant	NM_016510.7(SCLY):c.1156G>T (p.Ala386Ser)	not specified [RCV004082907]	uncertain significance	2	238096848	238096848	Human		name
156247167	CV2215308	single nucleotide variant	NM_016510.7(SCLY):c.1208A>G (p.Tyr403Cys)	not specified [RCV004087339]	likely benign	2	238098225	238098225	Human		name
156334085	CV2333337	single nucleotide variant	NM_016510.7(SCLY):c.1316C>T (p.Ala439Val)	not specified [RCV004190051]	uncertain significance	2	238098333	238098333	Human		name
156228647	CV2397563	single nucleotide variant	NM_016510.7(SCLY):c.1187C>T (p.Pro396Leu)	not specified [RCV004237025]	uncertain significance	2	238098204	238098204	Human		name
155931142	CV2399790	single nucleotide variant	NM_016510.7(SCLY):c.1090C>T (p.Arg364Trp)	not specified [RCV004245600]	uncertain significance	2	238094504	238094504	Human		name
329398248	CV2464942	single nucleotide variant	NM_016510.7(SCLY):c.1055C>G (p.Thr352Ser)	not specified [RCV004284866]	uncertain significance	2	238094469	238094469	Human		name
401762556	CV2719973	single nucleotide variant	NM_016510.7(SCLY):c.1078A>C (p.Asn360His)	not specified [RCV004323558]	uncertain significance	2	238094492	238094492	Human		name
401896613	CV2791760	single nucleotide variant	NM_016510.7(SCLY):c.1276G>A (p.Glu426Lys)	not specified [RCV004353080]	uncertain significance	2	238098293	238098293	Human		name
405744140	CV3317321	single nucleotide variant	NM_016510.7(SCLY):c.1169C>T (p.Ser390Leu)	not specified [RCV004452842]	uncertain significance	2	238096861	238096861	Human		name
405744148	CV3317322	single nucleotide variant	NM_016510.7(SCLY):c.1285C>T (p.Leu429Phe)	not specified [RCV004452843]	uncertain significance	2	238098302	238098302	Human		name
407461440	CV3480018	single nucleotide variant	NM_016510.7(SCLY):c.1177G>A (p.Gly393Arg)	not specified [RCV004658713]	uncertain significance	2	238096869	238096869	Human		name
597691472	CV3597949	single nucleotide variant	NM_016510.7(SCLY):c.1133G>A (p.Arg378Gln)	not specified [RCV004858918]	uncertain significance	2	238096825	238096825	Human		name
597691503	CV3597952	single nucleotide variant	NM_016510.7(SCLY):c.1312G>A (p.Val438Met)	not specified [RCV004858921]	uncertain significance	2	238098329	238098329	Human		name
597691513	CV3597953	single nucleotide variant	NM_016510.7(SCLY):c.1228G>A (p.Ala410Thr)	not specified [RCV004858922]	uncertain significance	2	238098245	238098245	Human		name
597691545	CV3597956	single nucleotide variant	NM_016510.7(SCLY):c.1237G>A (p.Ala413Thr)	not specified [RCV004858925]	uncertain significance	2	238098254	238098254	Human		name
597691573	CV3597959	single nucleotide variant	NM_016510.7(SCLY):c.1186C>G (p.Pro396Ala)	not specified [RCV004858928]	uncertain significance	2	238098203	238098203	Human		name
597691620	CV3597964	single nucleotide variant	NM_016510.7(SCLY):c.1100G>A (p.Arg367Gln)	not specified [RCV004858933]	likely benign	2	238094514	238094514	Human		name
598196942	CV3910352	single nucleotide variant	NM_016510.7(SCLY):c.1097C>G (p.Pro366Arg)	not specified [RCV005268031]	uncertain significance	2	238094511	238094511	Human		name
598196973	CV3910357	single nucleotide variant	NM_016510.7(SCLY):c.1278G>T (p.Glu426Asp)	not specified [RCV005268036]	uncertain significance	2	238098295	238098295	Human		name

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