Spred3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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47 records found for search term Spred3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15194467	CV756958	single nucleotide variant	NM_001394336.1(SPRED3):c.153C>T (p.His51=)	not provided [RCV000911134]	benign	19	38390455	38390455	Human		name
598272482	CV3915601	single nucleotide variant	NM_001394336.1(SPRED3):c.92T>A (p.Val31Glu)	not specified [RCV005282637]	uncertain significance	19	38390394	38390394	Human		name
598239267	CV3915603	single nucleotide variant	NM_001394336.1(SPRED3):c.74G>T (p.Gly25Val)	not specified [RCV005275980]	uncertain significance	19	38390376	38390376	Human		name
401742749	CV2715309	single nucleotide variant	NM_001394336.1(SPRED3):c.106G>A (p.Gly36Arg)	not specified [RCV004324645]	uncertain significance	19	38390408	38390408	Human		name
407525732	CV3478007	single nucleotide variant	NM_001394336.1(SPRED3):c.131G>C (p.Arg44Pro)	not specified [RCV004679403]	uncertain significance	19	38390433	38390433	Human		name
407525734	CV3478009	single nucleotide variant	NM_001394336.1(SPRED3):c.124G>T (p.Gly42Trp)	not specified [RCV004679404]	uncertain significance	19	38390426	38390426	Human		name
407516040	CV3478010	single nucleotide variant	NM_001394336.1(SPRED3):c.125G>T (p.Gly42Val)	not specified [RCV004675156]	uncertain significance	19	38390427	38390427	Human		name
597769173	CV3607838	single nucleotide variant	NM_001394336.1(SPRED3):c.122G>T (p.Gly41Val)	not specified [RCV004871190]	uncertain significance	19	38390424	38390424	Human		name
597679585	CV3607840	single nucleotide variant	NM_001394336.1(SPRED3):c.176A>G (p.Lys59Arg)	not specified [RCV004857296]	uncertain significance	19	38390478	38390478	Human		name
597769183	CV3607841	single nucleotide variant	NM_001394336.1(SPRED3):c.131G>A (p.Arg44His)	not specified [RCV004871192]	uncertain significance	19	38390433	38390433	Human		name
597769187	CV3607844	single nucleotide variant	NM_001394336.1(SPRED3):c.125G>A (p.Gly42Glu)	not specified [RCV004871193]	uncertain significance	19	38390427	38390427	Human		name
156242726	CV2210753	single nucleotide variant	NM_001394336.1(SPRED3):c.656G>A (p.Gly219Asp)	not specified [RCV004085849]	uncertain significance	19	38395568	38395568	Human		name
155993294	CV2252225	single nucleotide variant	NM_001394336.1(SPRED3):c.593C>T (p.Thr198Met)	not specified [RCV004116098]	uncertain significance	19	38395505	38395505	Human		name
156213057	CV2257342	single nucleotide variant	NM_001394336.1(SPRED3):c.951G>C (p.Glu317Asp)	not specified [RCV004125437]	uncertain significance	19	38395863	38395863	Human		name
156256615	CV2277594	single nucleotide variant	NM_001394336.1(SPRED3):c.841T>A (p.Ser281Thr)	not specified [RCV004147063]	uncertain significance	19	38395753	38395753	Human		name
155905435	CV2303108	single nucleotide variant	NM_001394336.1(SPRED3):c.812C>T (p.Pro271Leu)	not specified [RCV004156886]	uncertain significance	19	38395724	38395724	Human		name
155954125	CV2303257	single nucleotide variant	NM_001394336.1(SPRED3):c.680G>C (p.Gly227Ala)	not specified [RCV004159009]	uncertain significance	19	38395592	38395592	Human		name
156262235	CV2314833	single nucleotide variant	NM_001394336.1(SPRED3):c.700C>G (p.Leu234Val)	not specified [RCV004170952]	uncertain significance	19	38395612	38395612	Human		name
155901084	CV2345735	single nucleotide variant	NM_001394336.1(SPRED3):c.865C>A (p.Pro289Thr)	not specified [RCV004205671]	uncertain significance	19	38395777	38395777	Human		name
155968421	CV2391456	single nucleotide variant	NM_001394336.1(SPRED3):c.562G>A (p.Ala188Thr)	not specified [RCV004239849]	uncertain significance	19	38394781	38394781	Human		name
329355839	CV2430507	single nucleotide variant	NM_001394336.1(SPRED3):c.553C>T (p.Arg185Cys)	not specified [RCV004252093]	uncertain significance	19	38394772	38394772	Human		name
401766555	CV2676208	single nucleotide variant	NM_001394336.1(SPRED3):c.830G>C (p.Gly277Ala)	not specified [RCV004286255]	uncertain significance	19	38395742	38395742	Human		name
401735192	CV2699194	single nucleotide variant	NM_001394336.1(SPRED3):c.548G>T (p.Arg183Leu)	not specified [RCV004303689]	uncertain significance	19	38394767	38394767	Human		name
401776753	CV2711333	single nucleotide variant	NM_001394336.1(SPRED3):c.887G>T (p.Arg296Leu)	not specified [RCV004313103]	uncertain significance	19	38395799	38395799	Human		name
405738064	CV3333855	single nucleotide variant	NM_001394336.1(SPRED3):c.440A>G (p.Asp147Gly)	not specified [RCV004465255]	uncertain significance	19	38394659	38394659	Human		name
405738070	CV3333856	single nucleotide variant	NM_001394336.1(SPRED3):c.442T>G (p.Ser148Ala)	not specified [RCV004465256]	uncertain significance	19	38394661	38394661	Human		name
405738077	CV3333857	single nucleotide variant	NM_001394336.1(SPRED3):c.443C>A (p.Ser148Tyr)	not specified [RCV004465257]	uncertain significance	19	38394662	38394662	Human		name
405738084	CV3333858	single nucleotide variant	NM_001394336.1(SPRED3):c.724G>T (p.Ala242Ser)	not specified [RCV004465258]	uncertain significance	19	38395636	38395636	Human		name
405738090	CV3333859	single nucleotide variant	NM_001394336.1(SPRED3):c.779C>T (p.Ala260Val)	not specified [RCV004465259]	uncertain significance	19	38395691	38395691	Human		name
407516032	CV3478005	single nucleotide variant	NM_001394336.1(SPRED3):c.655G>A (p.Gly219Ser)	not specified [RCV004675153]	uncertain significance	19	38395567	38395567	Human		name
407516034	CV3478006	single nucleotide variant	NM_001394336.1(SPRED3):c.542C>A (p.Pro181His)	not specified [RCV004675154]	uncertain significance	19	38394761	38394761	Human		name
407516037	CV3478008	single nucleotide variant	NM_001394336.1(SPRED3):c.634G>A (p.Gly212Ser)	not specified [RCV004675155]	uncertain significance	19	38395546	38395546	Human		name
407525737	CV3478011	single nucleotide variant	NM_001394336.1(SPRED3):c.525C>A (p.Phe175Leu)	not specified [RCV004679405]	uncertain significance	19	38394744	38394744	Human		name
597769169	CV3607837	single nucleotide variant	NM_001394336.1(SPRED3):c.877G>A (p.Glu293Lys)	not specified [RCV004871189]	uncertain significance	19	38395789	38395789	Human		name
597769177	CV3607839	single nucleotide variant	NM_001394336.1(SPRED3):c.326C>T (p.Ala109Val)	not specified [RCV004871191]	uncertain significance	19	38392094	38392094	Human		name
597679602	CV3607843	single nucleotide variant	NM_001394336.1(SPRED3):c.790G>A (p.Glu264Lys)	not specified [RCV004857298]	uncertain significance	19	38395702	38395702	Human		name
598272477	CV3915598	single nucleotide variant	NM_001394336.1(SPRED3):c.557C>T (p.Ser186Phe)	not specified [RCV005282636]	uncertain significance	19	38394776	38394776	Human		name
598239254	CV3915599	single nucleotide variant	NM_001394336.1(SPRED3):c.758G>A (p.Gly253Asp)	not specified [RCV005275978]	uncertain significance	19	38395670	38395670	Human		name
598239260	CV3915600	single nucleotide variant	NM_001394336.1(SPRED3):c.545A>G (p.Gln182Arg)	not specified [RCV005275979]	uncertain significance	19	38394764	38394764	Human		name
598272486	CV3915602	single nucleotide variant	NM_001394336.1(SPRED3):c.692C>T (p.Pro231Leu)	not specified [RCV005282638]	uncertain significance	19	38395604	38395604	Human		name
156374425	CV2198444	single nucleotide variant	NM_001394336.1(SPRED3):c.1090G>A (p.Ala364Thr)	not specified [RCV004081973]	uncertain significance	19	38396002	38396002	Human		name
156332729	CV2220730	single nucleotide variant	NM_001394336.1(SPRED3):c.1121C>T (p.Ser374Phe)	not specified [RCV004097898]	uncertain significance	19	38396033	38396033	Human		name
156017534	CV2222904	single nucleotide variant	NM_001394336.1(SPRED3):c.1003G>T (p.Ala335Ser)	not specified [RCV004101720]	uncertain significance	19	38395915	38395915	Human		name
329371247	CV2431932	single nucleotide variant	NM_001394336.1(SPRED3):c.1171T>C (p.Trp391Arg)	not specified [RCV004249091]	uncertain significance	19	38396083	38396083	Human		name
405738047	CV3333853	single nucleotide variant	NM_001394336.1(SPRED3):c.1082C>G (p.Pro361Arg)	not specified [RCV004465253]	uncertain significance	19	38395994	38395994	Human		name
405738055	CV3333854	single nucleotide variant	NM_001394336.1(SPRED3):c.1184G>T (p.Arg395Leu)	not specified [RCV004465254]	uncertain significance	19	38396096	38396096	Human		name
597679595	CV3607842	single nucleotide variant	NM_001394336.1(SPRED3):c.1153C>T (p.Pro385Ser)	not specified [RCV004857297]	uncertain significance	19	38396065	38396065	Human		name

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