Slc2a3 Variant Search Result - Rat Genome Database

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48 records found for search term Slc2a3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15171980	CV730889	single nucleotide variant	NM_006931.3(SLC2A3):c.511-8G>A	not provided [RCV000883753]	likely benign	12	7930650	7930650	Human		name
15202876	CV760264	single nucleotide variant	NM_006931.3(SLC2A3):c.1272+9A>T	not provided [RCV000913591]	likely benign	12	7922812	7922812	Human		name
15176219	CV778058	single nucleotide variant	NM_006931.3(SLC2A3):c.1068+4G>A	not provided [RCV000950775]	benign	12	7924406	7924406	Human		name
597764888	CV3602887	single nucleotide variant	NM_006931.3(SLC2A3):c.33A>C (p.Ile11=)	not specified [RCV004870229]	likely benign	12	7933885	7933885	Human		name
15107003	CV725284	single nucleotide variant	NM_006931.3(SLC2A3):c.486C>A (p.Ile162=)	not provided [RCV000893391]	likely benign	12	7931269	7931269	Human		name
156252099	CV2232372	single nucleotide variant	NM_006931.3(SLC2A3):c.131A>C (p.Lys44Thr)	not specified [RCV004099004]	uncertain significance	12	7933125	7933125	Human		name
156254387	CV2358781	single nucleotide variant	NM_006931.3(SLC2A3):c.149G>C (p.Gly50Ala)	not specified [RCV004212135]	likely benign	12	7933107	7933107	Human		name
329377637	CV2449883	single nucleotide variant	NM_006931.3(SLC2A3):c.229G>C (p.Gly77Arg)	not specified [RCV004268968]	uncertain significance	12	7933027	7933027	Human		name
405783227	CV3332508	single nucleotide variant	NM_006931.3(SLC2A3):c.155C>T (p.Ala52Val)	not specified [RCV004459026]	uncertain significance	12	7933101	7933101	Human		name
405783233	CV3332509	single nucleotide variant	NM_006931.3(SLC2A3):c.280A>G (p.Met94Val)	not specified [RCV004459027]	uncertain significance	12	7931475	7931475	Human		name
407451446	CV3474228	single nucleotide variant	NM_006931.3(SLC2A3):c.179C>T (p.Thr60Met)	not specified [RCV004683669]	uncertain significance	12	7933077	7933077	Human		name
596947878	CV3547465	single nucleotide variant	NM_006931.3(SLC2A3):c.1464T>C (p.Pro488=)	not provided [RCV004811769]	likely benign	12	7921440	7921440	Human		name
598169951	CV3914630	single nucleotide variant	NM_006931.3(SLC2A3):c.260G>A (p.Arg87His)	not specified [RCV005284427]	uncertain significance	12	7932996	7932996	Human		name
15163480	CV738872	single nucleotide variant	NM_006931.3(SLC2A3):c.160C>T (p.Pro54Ser)	not provided [RCV000903782]	likely benign	12	7933096	7933096	Human		name
15106911	CV769313	single nucleotide variant	NM_006931.3(SLC2A3):c.1266C>T (p.Ser422=)	not provided [RCV000937869]	benign	12	7922827	7922827	Human		name
156311672	CV2260211	single nucleotide variant	NM_006931.3(SLC2A3):c.466A>T (p.Thr156Ser)	not specified [RCV004120985]	uncertain significance	12	7931289	7931289	Human		name
156282048	CV2295166	single nucleotide variant	NM_006931.3(SLC2A3):c.811A>G (p.Ile271Val)	not specified [RCV004158263]	uncertain significance	12	7929734	7929734	Human		name
156205587	CV2311422	single nucleotide variant	NM_006931.3(SLC2A3):c.843G>T (p.Gln281His)	not specified [RCV004168269]	uncertain significance	12	7929702	7929702	Human		name
156304355	CV2341513	single nucleotide variant	NM_006931.3(SLC2A3):c.490G>A (p.Val164Ile)	not specified [RCV004188905]	likely benign	12	7931265	7931265	Human		name
156248246	CV2357121	single nucleotide variant	NM_006931.3(SLC2A3):c.745A>G (p.Met249Val)	not specified [RCV004206916]	uncertain significance	12	7929800	7929800	Human		name
329362440	CV2444710	single nucleotide variant	NM_006931.3(SLC2A3):c.554C>T (p.Pro185Leu)	not specified [RCV004258964]	uncertain significance	12	7930599	7930599	Human		name
329371081	CV2461942	single nucleotide variant	NM_006931.3(SLC2A3):c.826C>T (p.Leu276Phe)	not specified [RCV004271844]	uncertain significance	12	7929719	7929719	Human		name
401740630	CV2679769	single nucleotide variant	NM_006931.3(SLC2A3):c.319T>C (p.Phe107Leu)	not specified [RCV004282233]	likely benign	12	7931436	7931436	Human		name
401753803	CV2685064	single nucleotide variant	NM_006931.3(SLC2A3):c.445G>C (p.Ala149Pro)	not specified [RCV004289643]	uncertain significance	12	7931310	7931310	Human		name
401760423	CV2718835	single nucleotide variant	NM_006931.3(SLC2A3):c.812T>C (p.Ile271Thr)	not specified [RCV004328579]	uncertain significance	12	7929733	7929733	Human		name
405783242	CV3332510	single nucleotide variant	NM_006931.3(SLC2A3):c.641T>C (p.Ile214Thr)	not specified [RCV004459028]	uncertain significance	12	7930512	7930512	Human		name
405783254	CV3332512	single nucleotide variant	NM_006931.3(SLC2A3):c.998C>T (p.Thr333Ile)	not specified [RCV004459030]	uncertain significance	12	7924480	7924480	Human		name
407451449	CV3474229	single nucleotide variant	NM_006931.3(SLC2A3):c.557T>A (p.Leu186Gln)	not specified [RCV004683670]	uncertain significance	12	7930596	7930596	Human		name
597764890	CV3602888	single nucleotide variant	NM_006931.3(SLC2A3):c.642T>G (p.Ile214Met)	not specified [RCV004870230]	uncertain significance	12	7930511	7930511	Human		name
597701615	CV3602890	single nucleotide variant	NM_006931.3(SLC2A3):c.439C>T (p.Pro147Ser)	not specified [RCV004860005]	uncertain significance	12	7931316	7931316	Human		name
598169954	CV3914631	single nucleotide variant	NM_006931.3(SLC2A3):c.411T>G (p.Phe137Leu)	not specified [RCV005284428]	uncertain significance	12	7931344	7931344	Human		name
598169960	CV3914634	single nucleotide variant	NM_006931.3(SLC2A3):c.958G>A (p.Val320Ile)	not specified [RCV005284430]	uncertain significance	12	7925852	7925852	Human		name
155925621	CV2230475	single nucleotide variant	NM_006931.3(SLC2A3):c.1204A>G (p.Met402Val)	not specified [RCV004097451]	uncertain significance	12	7922889	7922889	Human		name
156169624	CV2247330	single nucleotide variant	NM_006931.3(SLC2A3):c.1109T>C (p.Ile370Thr)	not specified [RCV004108676]	uncertain significance	12	7922984	7922984	Human		name
156265584	CV2389076	single nucleotide variant	NM_006931.3(SLC2A3):c.1127T>G (p.Phe376Cys)	not specified [RCV004235414]	uncertain significance	12	7922966	7922966	Human		name
401735101	CV2690777	single nucleotide variant	NM_006931.3(SLC2A3):c.1286C>G (p.Ala429Gly)	not specified [RCV004298495]	uncertain significance	12	7921618	7921618	Human		name
401736941	CV2717853	single nucleotide variant	NM_006931.3(SLC2A3):c.1226A>G (p.Asn409Ser)	not specified [RCV004321827]	uncertain significance	12	7922867	7922867	Human		name
405783216	CV3332506	single nucleotide variant	NM_006931.3(SLC2A3):c.1361G>A (p.Arg454His)	not specified [RCV004459024]	uncertain significance	12	7921543	7921543	Human		name
405783222	CV3332507	single nucleotide variant	NM_006931.3(SLC2A3):c.1459G>A (p.Glu487Lys)	not specified [RCV004459025]	uncertain significance	12	7921445	7921445	Human		name
407509809	CV3474230	single nucleotide variant	NM_006931.3(SLC2A3):c.1449G>T (p.Met483Ile)	not specified [RCV004672496]	uncertain significance	12	7921455	7921455	Human		name
597701574	CV3602883	single nucleotide variant	NM_006931.3(SLC2A3):c.1324T>G (p.Phe442Val)	not specified [RCV004860000]	uncertain significance	12	7921580	7921580	Human		name
597701582	CV3602884	single nucleotide variant	NM_006931.3(SLC2A3):c.1387C>T (p.Arg463Trp)	not specified [RCV004860001]	uncertain significance	12	7921517	7921517	Human		name
597701589	CV3602885	single nucleotide variant	NM_006931.3(SLC2A3):c.1267G>A (p.Ala423Thr)	not specified [RCV004860002]	uncertain significance	12	7922826	7922826	Human		name
597701598	CV3602886	single nucleotide variant	NM_006931.3(SLC2A3):c.1435G>A (p.Gly479Ser)	not specified [RCV004860003]	uncertain significance	12	7921469	7921469	Human		name
597701606	CV3602889	single nucleotide variant	NM_006931.3(SLC2A3):c.1288T>C (p.Tyr430His)	not specified [RCV004860004]	uncertain significance	12	7921616	7921616	Human		name
597764894	CV3602891	single nucleotide variant	NM_006931.3(SLC2A3):c.1202C>G (p.Ala401Gly)	not specified [RCV004870231]	uncertain significance	12	7922891	7922891	Human		name
598169957	CV3914632	single nucleotide variant	NM_006931.3(SLC2A3):c.1388G>A (p.Arg463Gln)	not specified [RCV005284429]	uncertain significance	12	7921516	7921516	Human		name
598237041	CV3914633	single nucleotide variant	NM_006931.3(SLC2A3):c.1192C>T (p.Arg398Cys)	not specified [RCV005275575]	uncertain significance	12	7922901	7922901	Human		name

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