Oas2 Variant Search Result - Rat Genome Database

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66 records found for search term Oas2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405731582	CV3362921	single nucleotide variant	NM_002535.3(OAS2):c.*1174T>C	not specified [RCV004496459]	uncertain significance	12	113010429	113010429	Human		name
597666456	CV3566944	single nucleotide variant	NM_002535.3(OAS2):c.*1161A>C	not specified [RCV004835727]	uncertain significance	12	113010416	113010416	Human		name
598194379	CV4001158	single nucleotide variant	NM_002535.3(OAS2):c.17C>T (p.Ser6Phe)	not specified [RCV005374708]	uncertain significance	12	112978625	112978625	Human		name
15121895	CV738454	single nucleotide variant	NM_002535.3(OAS2):c.150G>A (p.Gln50=)	not provided [RCV000896146]	benign	12	112978758	112978758	Human		name
155981153	CV2343749	single nucleotide variant	NM_002535.3(OAS2):c.37G>A (p.Ala13Thr)	not specified [RCV004190771]	uncertain significance	12	112978645	112978645	Human		name
15195275	CV753106	single nucleotide variant	NM_002535.3(OAS2):c.429G>A (p.Leu143=)	not provided [RCV000911369]	likely benign	12	112987289	112987289	Human		name
156073636	CV2229999	single nucleotide variant	NM_002535.3(OAS2):c.167G>A (p.Gly56Glu)	not specified [RCV004105804]	uncertain significance	12	112978775	112978775	Human		name
156091224	CV2256568	single nucleotide variant	NM_002535.3(OAS2):c.112G>A (p.Val38Met)	not specified [RCV004118763]	uncertain significance	12	112978720	112978720	Human		name
156364062	CV2341794	single nucleotide variant	NM_002535.3(OAS2):c.187T>G (p.Tyr63Asp)	not specified [RCV004184751]	uncertain significance	12	112987047	112987047	Human		name
401874495	CV2774002	single nucleotide variant	NM_002535.3(OAS2):c.142C>T (p.Pro48Ser)	not specified [RCV004358410]	uncertain significance	12	112978750	112978750	Human		name
401877767	CV2786778	single nucleotide variant	NM_002535.3(OAS2):c.268C>G (p.Gln90Glu)	not specified [RCV004365949]	uncertain significance	12	112987128	112987128	Human		name
401877769	CV2786779	single nucleotide variant	NM_002535.3(OAS2):c.291C>G (p.Ile97Met)	not specified [RCV004365950]	uncertain significance	12	112987151	112987151	Human		name
407522530	CV3459208	single nucleotide variant	NM_002535.3(OAS2):c.194G>A (p.Arg65Gln)	not specified [RCV004652876]	uncertain significance	12	112987054	112987054	Human		name
598159497	CV4001160	single nucleotide variant	NM_002535.3(OAS2):c.274A>G (p.Arg92Gly)	not specified [RCV005390177]	uncertain significance	12	112987134	112987134	Human		name
15171278	CV713344	single nucleotide variant	NM_002535.3(OAS2):c.1857C>T (p.Thr619=)	not provided [RCV000972166]	benign	12	113007905	113007905	Human		name
15135221	CV713345	single nucleotide variant	NM_002535.3(OAS2):c.2016G>T (p.Gly672=)	not provided [RCV000965252]	benign	12	113009207	113009207	Human		name
156033898	CV2256561	single nucleotide variant	NM_002535.3(OAS2):c.463C>A (p.Pro155Thr)	not specified [RCV004118757]	uncertain significance	12	112995310	112995310	Human		name
156184172	CV2292212	single nucleotide variant	NM_002535.3(OAS2):c.770G>T (p.Cys257Phe)	not specified [RCV004148256]	uncertain significance	12	112997662	112997662	Human		name
156282746	CV2334614	single nucleotide variant	NM_002535.3(OAS2):c.665C>T (p.Pro222Leu)	not specified [RCV004188601]	uncertain significance	12	112997557	112997557	Human		name
156144203	CV2393661	single nucleotide variant	NM_002535.3(OAS2):c.472T>C (p.Trp158Arg)	not specified [RCV004231469]	uncertain significance	12	112995319	112995319	Human		name
329400486	CV2438387	single nucleotide variant	NM_002535.3(OAS2):c.467G>T (p.Ser156Ile)	not specified [RCV004259545]	uncertain significance	12	112995314	112995314	Human		name
329402404	CV2454248	single nucleotide variant	NM_002535.3(OAS2):c.809A>T (p.Asn270Ile)	not specified [RCV004265723]	uncertain significance	12	112997701	112997701	Human		name
401745503	CV2693269	single nucleotide variant	NM_002535.3(OAS2):c.751G>A (p.Val251Ile)	not specified [RCV004295238]	likely benign	12	112997643	112997643	Human		name
401781338	CV2726497	single nucleotide variant	NM_002535.3(OAS2):c.354C>G (p.Phe118Leu)	not specified [RCV004328683]	uncertain significance	12	112987214	112987214	Human		name
405731588	CV3362922	single nucleotide variant	NM_002535.3(OAS2):c.349A>G (p.Asn117Asp)	not specified [RCV004496460]	uncertain significance	12	112987209	112987209	Human		name
407522527	CV3459207	single nucleotide variant	NM_002535.3(OAS2):c.797T>C (p.Met266Thr)	not specified [RCV004652875]	likely benign	12	112997689	112997689	Human		name
407478446	CV3459209	single nucleotide variant	NM_002535.3(OAS2):c.742G>A (p.Val248Ile)	not specified [RCV004639001]	likely benign	12	112997634	112997634	Human		name
407522534	CV3459210	single nucleotide variant	NM_002535.3(OAS2):c.893C>T (p.Thr298Ile)	not specified [RCV004652877]	uncertain significance	12	112998295	112998295	Human		name
407522537	CV3459212	single nucleotide variant	NM_002535.3(OAS2):c.710G>A (p.Cys237Tyr)	not specified [RCV004652878]	uncertain significance	12	112997602	112997602	Human		name
597666449	CV3566943	single nucleotide variant	NM_002535.3(OAS2):c.688G>A (p.Val230Met)	not specified [RCV004835726]	uncertain significance	12	112997580	112997580	Human		name
597666471	CV3566946	single nucleotide variant	NM_002535.3(OAS2):c.670G>A (p.Ala224Thr)	not specified [RCV004835729]	uncertain significance	12	112997562	112997562	Human		name
598194364	CV4001156	single nucleotide variant	NM_002535.3(OAS2):c.332C>T (p.Thr111Met)	not specified [RCV005374706]	uncertain significance	12	112987192	112987192	Human		name
598194402	CV4001162	single nucleotide variant	NM_002535.3(OAS2):c.608T>C (p.Ile203Thr)	not specified [RCV005374711]	uncertain significance	12	112995455	112995455	Human		name
156397435	CV2200492	single nucleotide variant	NM_002535.3(OAS2):c.1603C>T (p.Arg535Trp)	not specified [RCV004078848]	uncertain significance	12	113006547	113006547	Human		name
155960440	CV2204216	single nucleotide variant	NM_002535.3(OAS2):c.1234G>A (p.Val412Ile)	not specified [RCV004077012]	uncertain significance	12	113004988	113004988	Human		name
156254972	CV2209690	single nucleotide variant	NM_002535.3(OAS2):c.1597C>T (p.Arg533Cys)	not specified [RCV004093730]	uncertain significance	12	113006541	113006541	Human		name
156018414	CV2233128	single nucleotide variant	NM_002535.3(OAS2):c.1345G>A (p.Glu449Lys)	not specified [RCV004103743]	uncertain significance	12	113005099	113005099	Human		name
155961096	CV2249589	single nucleotide variant	NM_002535.3(OAS2):c.1801C>G (p.Gln601Glu)	not specified [RCV004120606]	uncertain significance	12	113007849	113007849	Human		name
156135577	CV2256918	single nucleotide variant	NM_002535.3(OAS2):c.1827G>C (p.Trp609Cys)	not specified [RCV004121118]	uncertain significance	12	113007875	113007875	Human		name
156014596	CV2272173	single nucleotide variant	NM_002535.3(OAS2):c.1538C>T (p.Ser513Leu)	not specified [RCV004124943]	uncertain significance	12	113006482	113006482	Human		name
156274180	CV2279698	single nucleotide variant	NM_002535.3(OAS2):c.1294G>A (p.Val432Ile)	not specified [RCV004144318]	likely benign	12	113005048	113005048	Human		name
156092424	CV2300137	single nucleotide variant	NM_002535.3(OAS2):c.1246A>C (p.Asn416His)	not specified [RCV004151327]	uncertain significance	12	113005000	113005000	Human		name
156036229	CV2303664	single nucleotide variant	NM_002535.3(OAS2):c.1712T>C (p.Leu571Pro)	not specified [RCV004161738]	uncertain significance	12	113007760	113007760	Human		name
156328805	CV2332314	single nucleotide variant	NM_002535.3(OAS2):c.1244A>G (p.His415Arg)	not specified [RCV004182484]	uncertain significance	12	113004998	113004998	Human		name
156115126	CV2349265	single nucleotide variant	NM_002535.3(OAS2):c.1237G>T (p.Val413Leu)	not specified [RCV004199212]	uncertain significance	12	113004991	113004991	Human		name
156247907	CV2357094	single nucleotide variant	NM_002535.3(OAS2):c.1948C>T (p.Arg650Cys)	not specified [RCV004206894]	uncertain significance	12	113009139	113009139	Human		name
156392101	CV2378279	single nucleotide variant	NM_002535.3(OAS2):c.1025C>T (p.Thr342Met)	not specified [RCV004226314]	uncertain significance	12	113002948	113002948	Human		name
329377176	CV2435835	single nucleotide variant	NM_002535.3(OAS2):c.1727C>T (p.Ala576Val)	not specified [RCV004255075]	uncertain significance	12	113007775	113007775	Human		name
329388959	CV2448538	single nucleotide variant	NM_002535.3(OAS2):c.1043T>C (p.Leu348Pro)	not specified [RCV004259220]	uncertain significance	12	113002966	113002966	Human		name
401741852	CV2677451	single nucleotide variant	NM_002535.3(OAS2):c.1282C>T (p.Arg428Trp)	not specified [RCV004289520]	uncertain significance	12	113005036	113005036	Human		name
401731579	CV2701436	single nucleotide variant	NM_002535.3(OAS2):c.1543C>T (p.Leu515Phe)	not specified [RCV004311792]	likely benign	12	113006487	113006487	Human		name
401735442	CV2702776	single nucleotide variant	NM_002535.3(OAS2):c.1192G>A (p.Ala398Thr)	not specified [RCV004319343]	uncertain significance	12	113004946	113004946	Human		name
401779873	CV2725749	single nucleotide variant	NM_002535.3(OAS2):c.1225G>A (p.Ala409Thr)	not specified [RCV004322438]	uncertain significance	12	113004979	113004979	Human		name
401869160	CV2766916	single nucleotide variant	NM_002535.3(OAS2):c.1148G>T (p.Arg383Leu)	not specified [RCV004343307]	uncertain significance	12	113003071	113003071	Human		name
401895334	CV2786375	single nucleotide variant	NM_002535.3(OAS2):c.1279G>A (p.Glu427Lys)	not specified [RCV004361970]	uncertain significance	12	113005033	113005033	Human		name
405731540	CV3362915	single nucleotide variant	NM_002535.3(OAS2):c.1322C>T (p.Ala441Val)	not specified [RCV004496453]	uncertain significance	12	113005076	113005076	Human		name
405731547	CV3362916	single nucleotide variant	NM_002535.3(OAS2):c.1501G>A (p.Glu501Lys)	not specified [RCV004496454]	likely benign	12	113006445	113006445	Human		name
405731558	CV3362918	single nucleotide variant	NM_002535.3(OAS2):c.1547C>T (p.Pro516Leu)	not specified [RCV004496456]	likely benign	12	113006491	113006491	Human		name
405731563	CV3362919	single nucleotide variant	NM_002535.3(OAS2):c.1696A>G (p.Lys566Glu)	not specified [RCV004496457]	uncertain significance	12	113007744	113007744	Human		name
405731573	CV3362920	single nucleotide variant	NM_002535.3(OAS2):c.1858G>A (p.Val620Met)	not specified [RCV004496458]	uncertain significance	12	113007906	113007906	Human		name
407478450	CV3459211	single nucleotide variant	NM_002535.3(OAS2):c.2032C>A (p.Pro678Thr)	not specified [RCV004639002]	uncertain significance	12	113009223	113009223	Human		name
597666440	CV3566942	single nucleotide variant	NM_002535.3(OAS2):c.1918G>A (p.Glu640Lys)	not specified [RCV004835725]	uncertain significance	12	113009109	113009109	Human		name
597666464	CV3566945	single nucleotide variant	NM_002535.3(OAS2):c.1720A>G (p.Ile574Val)	not specified [RCV004835728]	likely benign	12	113007768	113007768	Human		name
598194357	CV4001155	single nucleotide variant	NM_002535.3(OAS2):c.1097T>C (p.Ile366Thr)	not specified [RCV005374705]	uncertain significance	12	113003020	113003020	Human		name
598194385	CV4001159	single nucleotide variant	NM_002535.3(OAS2):c.2048C>T (p.Pro683Leu)	not specified [RCV005374709]	uncertain significance	12	113009239	113009239	Human		name
598194393	CV4001161	single nucleotide variant	NM_002535.3(OAS2):c.1334A>C (p.Glu445Ala)	not specified [RCV005374710]	uncertain significance	12	113005088	113005088	Human		name

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