Tinag Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

101 records found for search term Tinag

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15156257	CV722074	single nucleotide variant	NM_014464.4(TINAG):c.33T>G (p.Ser11=)	not provided [RCV000880590]	benign	6	54308583	54308583	Human		name
8632118	CV87324	single nucleotide variant	NM_014464.3(TINAG):c.58G>A (p.Glu20Lys)	Malignant melanoma [RCV000067415]	not provided	6	54308608	54308608	Human		name
156185255	CV2239388	single nucleotide variant	NM_014464.4(TINAG):c.148G>C (p.Ala50Pro)	not specified [RCV004114122]	uncertain significance	6	54308698	54308698	Human		name
156273794	CV2320211	single nucleotide variant	NM_014464.4(TINAG):c.283T>C (p.Cys95Arg)	not specified [RCV004169831]	uncertain significance	6	54308833	54308833	Human		name
405768741	CV3345950	single nucleotide variant	NM_014464.4(TINAG):c.137G>C (p.Arg46Pro)	not specified [RCV004469912]	uncertain significance	6	54308687	54308687	Human		name
407458447	CV3475714	single nucleotide variant	NM_014464.4(TINAG):c.296A>G (p.Lys99Arg)	not specified [RCV004686823]	uncertain significance	6	54308846	54308846	Human		name
598176677	CV3924273	single nucleotide variant	NM_014464.4(TINAG):c.209G>A (p.Cys70Tyr)	not specified [RCV005285680]	uncertain significance	6	54308759	54308759	Human		name
598176685	CV3924274	single nucleotide variant	NM_014464.4(TINAG):c.191A>G (p.Glu64Gly)	not specified [RCV005285681]	uncertain significance	6	54308741	54308741	Human		name
155922399	CV2207481	single nucleotide variant	NM_014464.4(TINAG):c.871A>G (p.Arg291Gly)	not specified [RCV004089959]	uncertain significance	6	54347489	54347489	Human		name
155920597	CV2210844	single nucleotide variant	NM_014464.4(TINAG):c.975G>T (p.Arg325Ser)	not specified [RCV004085931]	uncertain significance	6	54349791	54349791	Human		name
156383521	CV2220084	single nucleotide variant	NM_014464.4(TINAG):c.481A>G (p.Ile161Val)	not specified [RCV004093957]	uncertain significance	6	54321358	54321358	Human		name
155916013	CV2239631	single nucleotide variant	NM_014464.4(TINAG):c.326C>T (p.Pro109Leu)	not specified [RCV004108186]	uncertain significance	6	54308876	54308876	Human		name
155992826	CV2252027	single nucleotide variant	NM_014464.4(TINAG):c.625G>A (p.Ala209Thr)	not specified [RCV004122064]	uncertain significance	6	54343226	54343226	Human		name
156013882	CV2359180	single nucleotide variant	NM_014464.4(TINAG):c.664G>A (p.Val222Ile)	not specified [RCV004214534]	likely benign	6	54343265	54343265	Human		name
155930123	CV2361055	single nucleotide variant	NM_014464.4(TINAG):c.499G>A (p.Gly167Arg)	not specified [RCV004216251]	uncertain significance	6	54321376	54321376	Human		name
329373269	CV2434166	single nucleotide variant	NM_014464.4(TINAG):c.913G>A (p.Ala305Thr)	not specified [RCV004250061]	uncertain significance	6	54349729	54349729	Human		name
329399415	CV2446984	single nucleotide variant	NM_014464.4(TINAG):c.427T>A (p.Ser143Thr)	not specified [RCV004257823]	uncertain significance	6	54321304	54321304	Human		name
329361386	CV2459392	single nucleotide variant	NM_014464.4(TINAG):c.953A>G (p.Asn318Ser)	not specified [RCV004275088]	likely benign	6	54349769	54349769	Human		name
329376454	CV2472034	single nucleotide variant	NM_014464.4(TINAG):c.868G>A (p.Asp290Asn)	not specified [RCV004283180]	uncertain significance	6	54347486	54347486	Human		name
401865260	CV2768734	single nucleotide variant	NM_014464.4(TINAG):c.712A>G (p.Lys238Glu)	not specified [RCV004346574]	uncertain significance	6	54343313	54343313	Human		name
405768752	CV3345952	single nucleotide variant	NM_014464.4(TINAG):c.325C>G (p.Pro109Ala)	not specified [RCV004469914]	uncertain significance	6	54308875	54308875	Human		name
405768755	CV3345953	single nucleotide variant	NM_014464.4(TINAG):c.622A>T (p.Thr208Ser)	not specified [RCV004469915]	uncertain significance	6	54326914	54326914	Human		name
405768760	CV3345954	single nucleotide variant	NM_014464.4(TINAG):c.682C>T (p.Pro228Ser)	not specified [RCV004469916]	uncertain significance	6	54343283	54343283	Human		name
405768767	CV3345955	single nucleotide variant	NM_014464.4(TINAG):c.715A>C (p.Asn239His)	not specified [RCV004469917]	uncertain significance	6	54343316	54343316	Human		name
405768771	CV3345956	single nucleotide variant	NM_014464.4(TINAG):c.718T>C (p.Cys240Arg)	not specified [RCV004469918]	uncertain significance	6	54343319	54343319	Human		name
405768774	CV3345957	single nucleotide variant	NM_014464.4(TINAG):c.965T>C (p.Met322Thr)	not specified [RCV004469919]	uncertain significance	6	54349781	54349781	Human		name
405768780	CV3345958	single nucleotide variant	NM_014464.4(TINAG):c.988G>A (p.Gly330Arg)	not specified [RCV004469920]	uncertain significance	6	54349804	54349804	Human		name
597774217	CV3610068	single nucleotide variant	NM_014464.4(TINAG):c.719G>T (p.Cys240Phe)	not specified [RCV004872240]	uncertain significance	6	54343320	54343320	Human		name
597774221	CV3610069	single nucleotide variant	NM_014464.4(TINAG):c.850T>C (p.Cys284Arg)	not specified [RCV004872241]	uncertain significance	6	54347468	54347468	Human		name
597774228	CV3610071	single nucleotide variant	NM_014464.4(TINAG):c.304T>C (p.Cys102Arg)	not specified [RCV004872243]	uncertain significance	6	54308854	54308854	Human		name
597774236	CV3610074	single nucleotide variant	NM_014464.4(TINAG):c.387G>C (p.Glu129Asp)	not specified [RCV004872245]	uncertain significance	6	54320610	54320610	Human		name
597774244	CV3610076	single nucleotide variant	NM_014464.4(TINAG):c.601C>T (p.Leu201Phe)	not specified [RCV004872247]	uncertain significance	6	54326893	54326893	Human		name
597774248	CV3610077	single nucleotide variant	NM_014464.4(TINAG):c.926T>C (p.Leu309Pro)	not specified [RCV004872248]	uncertain significance	6	54349742	54349742	Human		name
598176692	CV3924275	single nucleotide variant	NM_014464.4(TINAG):c.727T>A (p.Ser243Thr)	not specified [RCV005285682]	uncertain significance	6	54343328	54343328	Human		name
598197884	CV3924276	single nucleotide variant	NM_014464.4(TINAG):c.610A>G (p.Met204Val)	not specified [RCV005289637]	uncertain significance	6	54326902	54326902	Human		name
8632119	CV87325	single nucleotide variant	NM_014464.3(TINAG):c.698G>A (p.Gly233Asp)	Malignant melanoma [RCV000067416]	not provided	6	54343299	54343299	Human		name
156229626	CV2267707	single nucleotide variant	NM_014464.4(TINAG):c.1372G>A (p.Asp458Asn)	not specified [RCV004134244]	uncertain significance	6	54389866	54389866	Human		name
155921194	CV2276262	single nucleotide variant	NM_014464.4(TINAG):c.1082A>T (p.Glu361Val)	not specified [RCV004144021]	uncertain significance	6	54351353	54351353	Human		name
156079366	CV2351180	single nucleotide variant	NM_014464.4(TINAG):c.1012T>C (p.Cys338Arg)	not specified [RCV004214031]	uncertain significance	6	54349828	54349828	Human		name
155982587	CV2351678	single nucleotide variant	NM_014464.4(TINAG):c.1024G>A (p.Val342Ile)	not specified [RCV004195387]	likely benign	6	54349840	54349840	Human		name
156200483	CV2362954	single nucleotide variant	NM_014464.4(TINAG):c.1294T>G (p.Trp432Gly)	not specified [RCV004209054]	uncertain significance	6	54380569	54380569	Human		name
155931514	CV2370939	single nucleotide variant	NM_014464.4(TINAG):c.1222C>T (p.Leu408Phe)	not specified [RCV004218666]	uncertain significance	6	54354608	54354608	Human		name
156061487	CV2380241	single nucleotide variant	NM_014464.4(TINAG):c.1360G>A (p.Val454Ile)	not specified [RCV004224599]	uncertain significance	6	54389854	54389854	Human		name
329364708	CV2443777	single nucleotide variant	NM_014464.4(TINAG):c.1226A>G (p.Gln409Arg)	not specified [RCV004256073]	likely benign	6	54354612	54354612	Human		name
329381821	CV2467373	single nucleotide variant	NM_014464.4(TINAG):c.1145A>G (p.Glu382Gly)	not specified [RCV004285161]	uncertain significance	6	54354531	54354531	Human		name
404994852	CV2851270	single nucleotide variant	NM_014464.4(TINAG):c.1354C>T (p.Arg452Ter)	not provided [RCV003491671]	uncertain significance	6	54389848	54389848	Human		name
405768712	CV3345945	single nucleotide variant	NM_014464.4(TINAG):c.1063T>C (p.Tyr355His)	not specified [RCV004469907]	uncertain significance	6	54349879	54349879	Human		name
405768717	CV3345946	single nucleotide variant	NM_014464.4(TINAG):c.1117C>T (p.Pro373Ser)	not specified [RCV004469908]	uncertain significance	6	54351388	54351388	Human		name
405768729	CV3345948	single nucleotide variant	NM_014464.4(TINAG):c.1165A>T (p.Thr389Ser)	not specified [RCV004469910]	uncertain significance	6	54354551	54354551	Human		name
405768735	CV3345949	single nucleotide variant	NM_014464.4(TINAG):c.1355G>A (p.Arg452Gln)	not specified [RCV004469911]	uncertain significance	6	54389849	54389849	Human		name
405768746	CV3345951	single nucleotide variant	NM_014464.4(TINAG):c.1412C>T (p.Thr471Met)	not specified [RCV004469913]	uncertain significance	6	54389906	54389906	Human		name
407520507	CV3475715	single nucleotide variant	NM_014464.4(TINAG):c.1028A>G (p.Glu343Gly)	not specified [RCV004676982]	uncertain significance	6	54349844	54349844	Human		name
597774224	CV3610070	single nucleotide variant	NM_014464.4(TINAG):c.1103T>C (p.Ile368Thr)	not specified [RCV004872242]	uncertain significance	6	54351374	54351374	Human		name
597774232	CV3610073	single nucleotide variant	NM_014464.4(TINAG):c.1246A>T (p.Thr416Ser)	not specified [RCV004872244]	uncertain significance	6	54354632	54354632	Human		name
597774240	CV3610075	single nucleotide variant	NM_014464.4(TINAG):c.1279C>G (p.Gln427Glu)	not specified [RCV004872246]	uncertain significance	6	54380554	54380554	Human		name
597774251	CV3610078	single nucleotide variant	NM_014464.4(TINAG):c.1020C>A (p.Asn340Lys)	not specified [RCV004872249]	uncertain significance	6	54349836	54349836	Human		name
597774259	CV3610081	single nucleotide variant	NM_022164.3(TINAGL1):c.8G>A (p.Arg3Gln)	not specified [RCV004872251]	uncertain significance	1	31577156	31577156	Human		name
15163766	CV746424	single nucleotide variant	NM_022164.3(TINAGL1):c.84C>T (p.Arg28=)	not provided [RCV000926211]	likely benign	1	31577232	31577232	Human		name
156062223	CV2392095	single nucleotide variant	NM_022164.3(TINAGL1):c.56C>T (p.Ala19Val)	not specified [RCV004237990]	uncertain significance	1	31577204	31577204	Human		name
401729270	CV2690122	single nucleotide variant	NM_022164.3(TINAGL1):c.83G>A (p.Arg28His)	not specified [RCV004300352]	uncertain significance	1	31577231	31577231	Human		name
401927390	CV2812587	single nucleotide variant	NM_022164.3(TINAGL1):c.717C>T (p.Ser239=)	not provided [RCV003406279]	likely benign	1	31584896	31584896	Human		name
405768817	CV3345964	single nucleotide variant	NM_022164.3(TINAGL1):c.67C>G (p.Gln23Glu)	not specified [RCV004469926]	uncertain significance	1	31577215	31577215	Human		name
598197891	CV3924277	single nucleotide variant	NM_022164.3(TINAGL1):c.38C>T (p.Pro13Leu)	not specified [RCV005289638]	likely benign	1	31577186	31577186	Human		name
156400125	CV2198984	single nucleotide variant	NM_022164.3(TINAGL1):c.191T>G (p.Leu64Arg)	not specified [RCV004080394]	uncertain significance	1	31577339	31577339	Human		name
156028268	CV2238211	single nucleotide variant	NM_022164.3(TINAGL1):c.133G>A (p.Gly45Ser)	not specified [RCV004113303]	uncertain significance	1	31577281	31577281	Human		name
156183182	CV2243241	single nucleotide variant	NM_022164.3(TINAGL1):c.181G>T (p.Asp61Tyr)	not specified [RCV004110129]	uncertain significance	1	31577329	31577329	Human		name
156274542	CV2334115	single nucleotide variant	NM_022164.3(TINAGL1):c.289C>T (p.Pro97Ser)	not specified [RCV004183630]	uncertain significance	1	31577437	31577437	Human		name
156137867	CV2354486	single nucleotide variant	NM_022164.3(TINAGL1):c.122G>A (p.Arg41Gln)	not specified [RCV004202473]	uncertain significance	1	31577270	31577270	Human		name
156057788	CV2383260	single nucleotide variant	NM_022164.3(TINAGL1):c.128C>T (p.Ala43Val)	not specified [RCV004222313]	uncertain significance	1	31577276	31577276	Human		name
401770942	CV2700773	single nucleotide variant	NM_022164.3(TINAGL1):c.136C>T (p.Arg46Trp)	not specified [RCV004307058]	uncertain significance	1	31577284	31577284	Human		name
405768788	CV3345959	single nucleotide variant	NM_022164.3(TINAGL1):c.137G>A (p.Arg46Gln)	not specified [RCV004469921]	uncertain significance	1	31577285	31577285	Human		name
597774255	CV3610079	single nucleotide variant	NM_022164.3(TINAGL1):c.178G>A (p.Asp60Asn)	not specified [RCV004872250]	uncertain significance	1	31577326	31577326	Human		name
598197899	CV3924278	single nucleotide variant	NM_022164.3(TINAGL1):c.164G>A (p.Cys55Tyr)	not specified [RCV005289639]	uncertain significance	1	31577312	31577312	Human		name
156355771	CV2324545	single nucleotide variant	NM_022164.3(TINAGL1):c.986A>G (p.Asn329Ser)	not specified [RCV004179018]	uncertain significance	1	31585279	31585279	Human		name
156066210	CV2348997	single nucleotide variant	NM_022164.3(TINAGL1):c.904G>A (p.Glu302Lys)	not specified [RCV004203424]	likely benign	1	31585197	31585197	Human		name
155937255	CV2373505	single nucleotide variant	NM_022164.3(TINAGL1):c.335A>C (p.Tyr112Ser)	not specified [RCV004222620]	uncertain significance	1	31579228	31579228	Human		name
156042571	CV2387851	single nucleotide variant	NM_022164.3(TINAGL1):c.847C>T (p.Arg283Cys)	not specified [RCV004236408]	uncertain significance	1	31585026	31585026	Human		name
155999028	CV2393494	single nucleotide variant	NM_022164.3(TINAGL1):c.593A>G (p.Asn198Ser)	not specified [RCV004228983]	uncertain significance	1	31584688	31584688	Human		name
329385107	CV2435261	single nucleotide variant	NM_022164.3(TINAGL1):c.887C>T (p.Ser296Leu)	not specified [RCV004252894]	uncertain significance	1	31585180	31585180	Human		name
329375723	CV2441090	single nucleotide variant	NM_022164.3(TINAGL1):c.388A>G (p.Asn130Asp)	not specified [RCV004263497]	uncertain significance	1	31583162	31583162	Human		name
401758318	CV2678600	single nucleotide variant	NM_022164.3(TINAGL1):c.941G>A (p.Arg314Gln)	not specified [RCV004292605]	uncertain significance	1	31585234	31585234	Human		name
401742755	CV2715310	single nucleotide variant	NM_022164.3(TINAGL1):c.943G>A (p.Ala315Thr)	not specified [RCV004324646]	uncertain significance	1	31585236	31585236	Human		name
401782354	CV2719301	single nucleotide variant	NM_022164.3(TINAGL1):c.949G>T (p.Gly317Cys)	not specified [RCV004324939]	uncertain significance	1	31585242	31585242	Human		name
405768799	CV3345961	single nucleotide variant	NM_022164.3(TINAGL1):c.329G>A (p.Arg110His)	not specified [RCV004469923]	uncertain significance	1	31579222	31579222	Human		name
405768804	CV3345962	single nucleotide variant	NM_022164.3(TINAGL1):c.454C>G (p.Gln152Glu)	not specified [RCV004469924]	uncertain significance	1	31583228	31583228	Human		name
407520509	CV3475716	single nucleotide variant	NM_022164.3(TINAGL1):c.587T>C (p.Val196Ala)	not specified [RCV004676983]	uncertain significance	1	31584682	31584682	Human		name
407520512	CV3475717	single nucleotide variant	NM_022164.3(TINAGL1):c.335A>T (p.Tyr112Phe)	not specified [RCV004676984]	uncertain significance	1	31579228	31579228	Human		name
407520516	CV3475718	single nucleotide variant	NM_022164.3(TINAGL1):c.500G>T (p.Gly167Val)	not specified [RCV004676985]	uncertain significance	1	31583493	31583493	Human		name
407520522	CV3475720	single nucleotide variant	NM_022164.3(TINAGL1):c.356G>T (p.Trp119Leu)	not specified [RCV004676987]	uncertain significance	1	31579249	31579249	Human		name
598176698	CV3924279	single nucleotide variant	NM_022164.3(TINAGL1):c.821G>A (p.Arg274His)	not specified [RCV005285683]	likely benign	1	31585000	31585000	Human		name
598197913	CV3924281	single nucleotide variant	NM_022164.3(TINAGL1):c.893G>A (p.Arg298His)	not specified [RCV005289641]	likely benign	1	31585186	31585186	Human		name
598197919	CV3924282	single nucleotide variant	NM_022164.3(TINAGL1):c.718G>A (p.Asp240Asn)	not specified [RCV005289642]	uncertain significance	1	31584897	31584897	Human		name
598197927	CV3924284	single nucleotide variant	NM_022164.3(TINAGL1):c.584C>A (p.Thr195Lys)	not specified [RCV005289643]	uncertain significance	1	31584679	31584679	Human		name
156031890	CV2239259	single nucleotide variant	NM_022164.3(TINAGL1):c.1331A>G (p.Asn444Ser)	not specified [RCV004112227]	uncertain significance	1	31586906	31586906	Human		name
156270319	CV2398666	single nucleotide variant	NM_022164.3(TINAGL1):c.1235T>C (p.Leu412Pro)	not specified [RCV004240014]	uncertain significance	1	31586727	31586727	Human		name
329354261	CV2437732	single nucleotide variant	NM_022164.3(TINAGL1):c.1392G>C (p.Met464Ile)	not specified [RCV004261041]	uncertain significance	1	31586967	31586967	Human		name
401732975	CV2702315	single nucleotide variant	NM_022164.3(TINAGL1):c.1328T>C (p.Val443Ala)	not specified [RCV004314641]	likely benign	1	31586903	31586903	Human		name
405768793	CV3345960	single nucleotide variant	NM_022164.3(TINAGL1):c.1390A>G (p.Met464Val)	not specified [RCV004469922]	uncertain significance	1	31586965	31586965	Human		name
407520519	CV3475719	single nucleotide variant	NM_022164.3(TINAGL1):c.1333G>A (p.Glu445Lys)	not specified [RCV004676986]	uncertain significance	1	31586908	31586908	Human		name
597774263	CV3610082	single nucleotide variant	NM_022164.3(TINAGL1):c.1324G>A (p.Gly442Ser)	not specified [RCV004872252]	uncertain significance	1	31586899	31586899	Human		name
598176702	CV3924283	single nucleotide variant	NM_022164.3(TINAGL1):c.1321C>T (p.Arg441Cys)	not specified [RCV005285684]	uncertain significance	1	31586896	31586896	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message