Spats2 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

100 records found for search term Spats2

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8654034	CV130609	single nucleotide variant	NM_023071.3(SPATS2):c.-243-33163A>T	Lung cancer [RCV000111096]	uncertain significance	12	49427607	49427607	Human		name
329354736	CV2448946	single nucleotide variant	NM_023071.4(SPATS2):c.61A>G (p.Thr21Ala)	not specified [RCV004264031]	uncertain significance	12	49484625	49484625	Human		name
329363253	CV2464994	single nucleotide variant	NM_023071.4(SPATS2):c.43T>G (p.Phe15Val)	not specified [RCV004284906]	uncertain significance	12	49484607	49484607	Human		name
401752251	CV2710670	single nucleotide variant	NM_023071.4(SPATS2):c.74A>G (p.Gln25Arg)	not specified [RCV004319574]	uncertain significance	12	49484638	49484638	Human		name
15158964	CV713556	single nucleotide variant	NM_023071.4(SPATS2):c.64G>A (p.Val22Ile)	not provided [RCV000969622]	benign	12	49484628	49484628	Human		name
156203771	CV2234652	single nucleotide variant	NM_023071.4(SPATS2):c.287C>T (p.Pro96Leu)	not specified [RCV004102611]	uncertain significance	12	49494763	49494763	Human		name
155901269	CV2294399	single nucleotide variant	NM_023071.4(SPATS2):c.115G>A (p.Val39Ile)	not specified [RCV004159909]	uncertain significance	12	49489474	49489474	Human		name
401752815	CV2682946	single nucleotide variant	NM_023071.4(SPATS2):c.113C>T (p.Ala38Val)	not specified [RCV004283737]	uncertain significance	12	49489472	49489472	Human		name
407511130	CV3481606	single nucleotide variant	NM_023071.4(SPATS2):c.140G>A (p.Ser47Asn)	not specified [RCV004672922]	uncertain significance	12	49489499	49489499	Human		name
155920362	CV2210788	single nucleotide variant	NM_023071.4(SPATS2):c.540G>C (p.Gln180His)	not specified [RCV004085881]	uncertain significance	12	49496846	49496846	Human		name
156238403	CV2221171	single nucleotide variant	NM_023071.4(SPATS2):c.910C>T (p.Leu304Phe)	not specified [RCV004094618]	uncertain significance	12	49519084	49519084	Human		name
156234731	CV2245368	single nucleotide variant	NM_023071.4(SPATS2):c.674A>C (p.Asp225Ala)	not specified [RCV004109163]	uncertain significance	12	49496980	49496980	Human		name
156103205	CV2352352	single nucleotide variant	NM_023071.4(SPATS2):c.860C>T (p.Ala287Val)	not specified [RCV004200822]	uncertain significance	12	49514575	49514575	Human		name
401724309	CV2681377	single nucleotide variant	NM_023071.4(SPATS2):c.416A>G (p.Asn139Ser)	not specified [RCV004291924]	uncertain significance	12	49494892	49494892	Human		name
401731949	CV2684634	single nucleotide variant	NM_023071.4(SPATS2):c.788T>C (p.Met263Thr)	not specified [RCV004293733]	uncertain significance	12	49500154	49500154	Human		name
401858238	CV2766423	single nucleotide variant	NM_023071.4(SPATS2):c.787A>G (p.Met263Val)	not specified [RCV004345266]	uncertain significance	12	49500153	49500153	Human		name
401890947	CV2778529	single nucleotide variant	NM_023071.4(SPATS2):c.452T>G (p.Leu151Trp)	not specified [RCV004344187]	uncertain significance	12	49494928	49494928	Human		name
405716471	CV3326623	single nucleotide variant	NM_023071.4(SPATS2):c.605C>G (p.Pro202Arg)	not specified [RCV004462574]	uncertain significance	12	49496911	49496911	Human		name
405716484	CV3326625	single nucleotide variant	NM_023071.4(SPATS2):c.721T>C (p.Ser241Pro)	not specified [RCV004462576]	uncertain significance	12	49500087	49500087	Human		name
405716491	CV3326626	single nucleotide variant	NM_023071.4(SPATS2):c.757G>A (p.Ala253Thr)	not specified [RCV004462577]	uncertain significance	12	49500123	49500123	Human		name
407525563	CV3481603	single nucleotide variant	NM_023071.4(SPATS2):c.298G>A (p.Ala100Thr)	not specified [RCV004679317]	uncertain significance	12	49494774	49494774	Human		name
407525565	CV3481605	single nucleotide variant	NM_023071.4(SPATS2):c.512C>T (p.Thr171Met)	not specified [RCV004679318]	likely benign	12	49494988	49494988	Human		name
597767853	CV3608085	single nucleotide variant	NM_023071.4(SPATS2):c.944A>G (p.Lys315Arg)	not specified [RCV004870915]	uncertain significance	12	49519118	49519118	Human		name
597767860	CV3608086	single nucleotide variant	NM_023071.4(SPATS2):c.314G>A (p.Gly105Asp)	not specified [RCV004870916]	uncertain significance	12	49494790	49494790	Human		name
597767868	CV3608088	single nucleotide variant	NM_023071.4(SPATS2):c.415A>G (p.Asn139Asp)	not specified [RCV004870918]	uncertain significance	12	49494891	49494891	Human		name
597767873	CV3608089	single nucleotide variant	NM_023071.4(SPATS2):c.974A>C (p.Glu325Ala)	not specified [RCV004870919]	uncertain significance	12	49519148	49519148	Human		name
597767876	CV3608090	single nucleotide variant	NM_023071.4(SPATS2):c.781G>C (p.Glu261Gln)	not specified [RCV004870920]	uncertain significance	12	49500147	49500147	Human		name
597767881	CV3608091	single nucleotide variant	NM_023071.4(SPATS2):c.772G>T (p.Val258Leu)	not specified [RCV004870921]	uncertain significance	12	49500138	49500138	Human		name
597742620	CV3608094	single nucleotide variant	NM_023071.4(SPATS2):c.767G>A (p.Arg256Gln)	not specified [RCV004865118]	uncertain significance	12	49500133	49500133	Human		name
156077822	CV2198257	single nucleotide variant	NM_023071.4(SPATS2):c.1423C>T (p.Arg475Cys)	not specified [RCV004079835]	uncertain significance	12	49526040	49526040	Human		name
156065474	CV2287369	single nucleotide variant	NM_023071.4(SPATS2):c.1211C>A (p.Ser404Tyr)	not specified [RCV004146982]	uncertain significance	12	49524781	49524781	Human		name
155918702	CV2362686	single nucleotide variant	NM_023071.4(SPATS2):c.1248C>A (p.Asn416Lys)	not specified [RCV004215331]	uncertain significance	12	49524818	49524818	Human		name
156051301	CV2386306	single nucleotide variant	NM_023071.4(SPATS2):c.1445A>G (p.Tyr482Cys)	not specified [RCV004228649]	uncertain significance	12	49526062	49526062	Human		name
329357366	CV2427687	single nucleotide variant	NM_023071.4(SPATS2):c.1100C>T (p.Ser367Leu)	not specified [RCV004252475]	uncertain significance	12	49522842	49522842	Human		name
401751844	CV2672596	single nucleotide variant	NM_023071.4(SPATS2):c.1405C>T (p.Arg469Trp)	not specified [RCV004287627]	uncertain significance	12	49526022	49526022	Human		name
401756497	CV2687179	single nucleotide variant	NM_023071.4(SPATS2):c.1500T>G (p.Ile500Met)	not specified [RCV004298128]	uncertain significance	12	49526117	49526117	Human		name
405716458	CV3326621	single nucleotide variant	NM_023071.4(SPATS2):c.1079C>A (p.Thr360Asn)	not specified [RCV004462572]	uncertain significance	12	49522821	49522821	Human		name
407525561	CV3481601	single nucleotide variant	NM_023071.4(SPATS2):c.1385A>G (p.Asn462Ser)	not specified [RCV004679316]	likely benign	12	49526002	49526002	Human		name
407511136	CV3481602	single nucleotide variant	NM_023071.4(SPATS2):c.1528A>G (p.Thr510Ala)	not specified [RCV004672920]	uncertain significance	12	49526145	49526145	Human		name
407511133	CV3481604	single nucleotide variant	NM_023071.4(SPATS2):c.1181G>C (p.Ser394Thr)	not specified [RCV004672921]	uncertain significance	12	49524751	49524751	Human		name
597742607	CV3608084	single nucleotide variant	NM_023071.4(SPATS2):c.1453G>C (p.Gly485Arg)	not specified [RCV004865116]	uncertain significance	12	49526070	49526070	Human		name
597767863	CV3608087	single nucleotide variant	NM_023071.4(SPATS2):c.1348G>A (p.Gly450Arg)	not specified [RCV004870917]	uncertain significance	12	49525965	49525965	Human		name
597767886	CV3608092	single nucleotide variant	NM_023071.4(SPATS2):c.1429A>G (p.Arg477Gly)	not specified [RCV004870922]	uncertain significance	12	49526046	49526046	Human		name
597742614	CV3608093	single nucleotide variant	NM_023071.4(SPATS2):c.1385A>T (p.Asn462Ile)	not specified [RCV004865117]	uncertain significance	12	49526002	49526002	Human		name
598262501	CV3919031	single nucleotide variant	NM_023071.4(SPATS2):c.1474C>G (p.Pro492Ala)	not specified [RCV005280201]	uncertain significance	12	49526091	49526091	Human		name
598262505	CV3919032	single nucleotide variant	NM_023071.4(SPATS2):c.1346G>A (p.Arg449Gln)	not specified [RCV005280202]	uncertain significance	12	49525963	49525963	Human		name
8576928	CV111297	single nucleotide variant	NM_001100422.1(SPATS2L):c.788+8644C>T	Lung cancer [RCV000091820]	uncertain significance	2	200449428	200449428	Human		name
156180016	CV2258390	single nucleotide variant	NM_001100423.2(SPATS2L):c.10C>G (p.Leu4Val)	not specified [RCV004115597]	uncertain significance	2	200389254	200389254	Human		name
597767894	CV3608096	single nucleotide variant	NM_001100423.2(SPATS2L):c.69C>A (p.Asn23Lys)	not specified [RCV004870924]	uncertain significance	2	200412340	200412340	Human		name
598262520	CV3919036	single nucleotide variant	NM_001100423.2(SPATS2L):c.67A>T (p.Asn23Tyr)	not specified [RCV005280206]	uncertain significance	2	200412338	200412338	Human		name
329359910	CV2462370	single nucleotide variant	NM_001100423.2(SPATS2L):c.262G>T (p.Val88Leu)	not specified [RCV004268135]	uncertain significance	2	200419313	200419313	Human		name
401746883	CV2698724	single nucleotide variant	NM_001100423.2(SPATS2L):c.272C>G (p.Pro91Arg)	not specified [RCV004301180]	uncertain significance	2	200419323	200419323	Human		name
405716567	CV3326634	single nucleotide variant	NM_001100423.2(SPATS2L):c.269G>T (p.Arg90Met)	not specified [RCV004462585]	uncertain significance	2	200419320	200419320	Human		name
405716574	CV3326635	single nucleotide variant	NM_001100423.2(SPATS2L):c.293C>T (p.Pro98Leu)	not specified [RCV004462586]	uncertain significance	2	200419344	200419344	Human		name
407511127	CV3481607	single nucleotide variant	NM_001100423.2(SPATS2L):c.202A>G (p.Asn68Asp)	not specified [RCV004672923]	uncertain significance	2	200419253	200419253	Human		name
597767904	CV3608099	single nucleotide variant	NM_001100423.2(SPATS2L):c.175T>C (p.Trp59Arg)	not specified [RCV004870926]	uncertain significance	2	200416405	200416405	Human		name
156202488	CV2234499	single nucleotide variant	NM_001100423.2(SPATS2L):c.748G>A (p.Val250Met)	not specified [RCV004100697]	uncertain significance	2	200440744	200440744	Human		name
156079612	CV2259216	single nucleotide variant	NM_001100423.2(SPATS2L):c.336G>C (p.Glu112Asp)	not specified [RCV004122242]	uncertain significance	2	200419387	200419387	Human		name
156193276	CV2325810	single nucleotide variant	NM_001100423.2(SPATS2L):c.809C>T (p.Ser270Leu)	not specified [RCV004173693]	uncertain significance	2	200459789	200459789	Human		name
401731441	CV2674374	single nucleotide variant	NM_001100423.2(SPATS2L):c.418C>T (p.Pro140Ser)	not specified [RCV004289244]	uncertain significance	2	200419469	200419469	Human		name
401744174	CV2680907	single nucleotide variant	NM_001100423.2(SPATS2L):c.925A>T (p.Met309Leu)	not specified [RCV004295982]	uncertain significance	2	200467367	200467367	Human		name
401739594	CV2704584	single nucleotide variant	NM_001100423.2(SPATS2L):c.518G>C (p.Arg173Thr)	not specified [RCV004313626]	uncertain significance	2	200439194	200439194	Human		name
401899989	CV2780152	single nucleotide variant	NM_001100423.2(SPATS2L):c.439G>A (p.Val147Ile)	not specified [RCV004355808]	uncertain significance	2	200419490	200419490	Human		name
405716590	CV3326637	single nucleotide variant	NM_001100423.2(SPATS2L):c.718G>A (p.Val240Ile)	not specified [RCV004462588]	uncertain significance	2	200440714	200440714	Human		name
405716597	CV3326638	single nucleotide variant	NM_001100423.2(SPATS2L):c.865C>T (p.Arg289Cys)	not specified [RCV004462589]	uncertain significance	2	200467307	200467307	Human		name
407511120	CV3481609	single nucleotide variant	NM_001100423.2(SPATS2L):c.979T>C (p.Tyr327His)	not specified [RCV004672925]	uncertain significance	2	200469935	200469935	Human		name
597742626	CV3608098	single nucleotide variant	NM_001100423.2(SPATS2L):c.532C>A (p.Gln178Lys)	not specified [RCV004865119]	uncertain significance	2	200439208	200439208	Human		name
597767913	CV3608101	single nucleotide variant	NM_001100423.2(SPATS2L):c.560C>T (p.Pro187Leu)	not specified [RCV004870928]	uncertain significance	2	200439236	200439236	Human		name
597767919	CV3608102	single nucleotide variant	NM_001100423.2(SPATS2L):c.386C>T (p.Pro129Leu)	not specified [RCV004870929]	uncertain significance	2	200419437	200419437	Human		name
598262508	CV3919033	single nucleotide variant	NM_001100423.2(SPATS2L):c.410T>C (p.Leu137Pro)	not specified [RCV005280203]	likely benign	2	200419461	200419461	Human		name
598262512	CV3919034	single nucleotide variant	NM_001100423.2(SPATS2L):c.388C>T (p.Arg130Cys)	not specified [RCV005280204]	uncertain significance	2	200419439	200419439	Human		name
598262516	CV3919035	single nucleotide variant	NM_001100423.2(SPATS2L):c.599A>G (p.Asn200Ser)	not specified [RCV005280205]	uncertain significance	2	200439275	200439275	Human		name
598262527	CV3919038	single nucleotide variant	NM_001100423.2(SPATS2L):c.937G>A (p.Glu313Lys)	not specified [RCV005280208]	uncertain significance	2	200467379	200467379	Human		name
598262531	CV3919039	single nucleotide variant	NM_001100423.2(SPATS2L):c.748G>T (p.Val250Leu)	not specified [RCV005280209]	uncertain significance	2	200440744	200440744	Human		name
598262535	CV3919040	single nucleotide variant	NM_001100423.2(SPATS2L):c.607G>A (p.Ala203Thr)	not specified [RCV005280210]	uncertain significance	2	200439283	200439283	Human		name
15202013	CV719514	single nucleotide variant	NM_001100423.2(SPATS2L):c.449G>A (p.Gly150Asp)	not provided [RCV000891358]	likely benign	2	200439125	200439125	Human		name
156238229	CV2207092	single nucleotide variant	NM_001100423.2(SPATS2L):c.1553C>T (p.Ser518Leu)	not specified [RCV004085694]	uncertain significance	2	200477907	200477907	Human		name
156114789	CV2273210	single nucleotide variant	NM_001100423.2(SPATS2L):c.1426C>T (p.His476Tyr)	not specified [RCV004138142]	uncertain significance	2	200477780	200477780	Human		name
156271487	CV2312416	single nucleotide variant	NM_001100423.2(SPATS2L):c.1424C>T (p.Pro475Leu)	not specified [RCV004167104]	uncertain significance	2	200477778	200477778	Human		name
156297766	CV2329006	single nucleotide variant	NM_001100423.2(SPATS2L):c.1423C>T (p.Pro475Ser)	not specified [RCV004180295]	uncertain significance	2	200477777	200477777	Human		name
155918823	CV2333075	single nucleotide variant	NM_001100423.2(SPATS2L):c.1284T>G (p.Asn428Lys)	not specified [RCV004194370]	uncertain significance	2	200477638	200477638	Human		name
155965980	CV2396018	single nucleotide variant	NM_001100423.2(SPATS2L):c.1000G>A (p.Ala334Thr)	not specified [RCV004237563]	uncertain significance	2	200469956	200469956	Human		name
329373816	CV2452682	single nucleotide variant	NM_001100423.2(SPATS2L):c.1303C>T (p.Arg435Trp)	not specified [RCV004275242]	uncertain significance	2	200477657	200477657	Human		name
401888463	CV2761442	single nucleotide variant	NM_001100423.2(SPATS2L):c.1405C>A (p.His469Asn)	not specified [RCV004334619]	uncertain significance	2	200477759	200477759	Human		name
401867153	CV2780401	single nucleotide variant	NM_001100423.2(SPATS2L):c.1432G>A (p.Gly478Ser)	not specified [RCV004357796]	uncertain significance	2	200477786	200477786	Human		name
401896401	CV2781260	single nucleotide variant	NM_001100423.2(SPATS2L):c.1033A>G (p.Lys345Glu)	not specified [RCV004352293]	uncertain significance	2	200469989	200469989	Human		name
401878002	CV2786931	single nucleotide variant	NM_001100423.2(SPATS2L):c.1145G>A (p.Gly382Glu)	not specified [RCV004366069]	uncertain significance	2	200472916	200472916	Human		name
405716498	CV3326627	single nucleotide variant	NM_001100423.2(SPATS2L):c.1004C>T (p.Ala335Val)	not specified [RCV004462578]	uncertain significance	2	200469960	200469960	Human		name
405716519	CV3326629	single nucleotide variant	NM_001100423.2(SPATS2L):c.1214C>G (p.Pro405Arg)	not specified [RCV004462580]	uncertain significance	2	200472985	200472985	Human		name
405716527	CV3326630	single nucleotide variant	NM_001100423.2(SPATS2L):c.1286G>C (p.Gly429Ala)	not specified [RCV004462581]	uncertain significance	2	200477640	200477640	Human		name
405716539	CV3326631	single nucleotide variant	NM_001100423.2(SPATS2L):c.1408G>A (p.Glu470Lys)	not specified [RCV004462582]	uncertain significance	2	200477762	200477762	Human		name
405716549	CV3326632	single nucleotide variant	NM_001100423.2(SPATS2L):c.1570C>G (p.Arg524Gly)	not specified [RCV004462583]	uncertain significance	2	200477924	200477924	Human		name
405716558	CV3326633	single nucleotide variant	NM_001100423.2(SPATS2L):c.1583G>A (p.Gly528Asp)	not specified [RCV004462584]	uncertain significance	2	200477937	200477937	Human		name
407511124	CV3481608	single nucleotide variant	NM_001100423.2(SPATS2L):c.1274A>G (p.Asn425Ser)	not specified [RCV004672924]	uncertain significance	2	200473045	200473045	Human		name
407511117	CV3481610	single nucleotide variant	NM_001100423.2(SPATS2L):c.1243G>T (p.Ala415Ser)	not specified [RCV004672926]	uncertain significance	2	200473014	200473014	Human		name
597767890	CV3608095	single nucleotide variant	NM_001100423.2(SPATS2L):c.1529G>A (p.Arg510Gln)	not specified [RCV004870923]	uncertain significance	2	200477883	200477883	Human		name
597767899	CV3608097	single nucleotide variant	NM_001100423.2(SPATS2L):c.1250C>T (p.Pro417Leu)	not specified [RCV004870925]	uncertain significance	2	200473021	200473021	Human		name
597767909	CV3608100	single nucleotide variant	NM_001100423.2(SPATS2L):c.1402C>T (p.Arg468Cys)	not specified [RCV004870927]	uncertain significance	2	200477756	200477756	Human		name
597742632	CV3608103	single nucleotide variant	NM_001100423.2(SPATS2L):c.1253C>G (p.Ser418Cys)	not specified [RCV004865120]	uncertain significance	2	200473024	200473024	Human		name
598262523	CV3919037	single nucleotide variant	NM_001100423.2(SPATS2L):c.1304G>A (p.Arg435Gln)	not specified [RCV005280207]	uncertain significance	2	200477658	200477658	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