S1pr4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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65 records found for search term S1pr4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401908216	CV2815150	single nucleotide variant	NM_003775.4(S1PR4):c.12G>A (p.Thr4=)	not provided [RCV003423188]	likely benign	19	3178804	3178804	Human		name
401908218	CV2815151	single nucleotide variant	NM_003775.4(S1PR4):c.261C>T (p.Asn87=)	not provided [RCV003423189]	likely benign	19	3179053	3179053	Human		name
401906827	CV2815152	single nucleotide variant	NM_003775.4(S1PR4):c.291G>A (p.Ala97=)	not provided [RCV003421729]	likely benign	19	3179083	3179083	Human		name
15176493	CV704901	single nucleotide variant	NM_003775.4(S1PR4):c.285G>A (p.Thr95=)	not provided [RCV000950837]	benign\|likely benign	19	3179077	3179077	Human		name
156345868	CV2356405	single nucleotide variant	NM_003775.4(S1PR4):c.50C>T (p.Ala17Val)	not specified [RCV004206206]	uncertain significance	19	3178842	3178842	Human		name
329379319	CV2443365	single nucleotide variant	NM_003775.4(S1PR4):c.68G>A (p.Arg23Gln)	not specified [RCV004260164]	uncertain significance	19	3178860	3178860	Human		name
401783326	CV2716286	single nucleotide variant	NM_003775.4(S1PR4):c.86A>G (p.Tyr29Cys)	not specified [RCV004325288]	uncertain significance	19	3178878	3178878	Human		name
401861583	CV2756359	single nucleotide variant	NM_003775.4(S1PR4):c.55G>A (p.Gly19Ser)	not specified [RCV004342904]	likely benign	19	3178847	3178847	Human		name
401908219	CV2815153	single nucleotide variant	NM_003775.4(S1PR4):c.345C>T (p.Pro115=)	not provided [RCV003423190]	likely benign	19	3179137	3179137	Human		name
597734869	CV3597928	single nucleotide variant	NM_003775.4(S1PR4):c.35C>T (p.Ser12Phe)	not specified [RCV004863561]	uncertain significance	19	3178827	3178827	Human		name
155958693	CV2313827	single nucleotide variant	NM_003775.4(S1PR4):c.215C>A (p.Thr72Asn)	not specified [RCV004164152]	uncertain significance	19	3179007	3179007	Human		name
156386017	CV2364632	single nucleotide variant	NM_003775.4(S1PR4):c.109G>A (p.Gly37Arg)	not specified [RCV004219524]	uncertain significance	19	3178901	3178901	Human		name
155930511	CV2366792	single nucleotide variant	NM_003775.4(S1PR4):c.149G>A (p.Arg50Gln)	not specified [RCV004210782]	uncertain significance	19	3178941	3178941	Human		name
401729839	CV2731776	single nucleotide variant	NM_003775.4(S1PR4):c.233G>A (p.Arg78Gln)	not specified [RCV004333032]	uncertain significance	19	3179025	3179025	Human		name
405702449	CV3310194	single nucleotide variant	NM_003775.4(S1PR4):c.158C>T (p.Ser53Leu)	not specified [RCV004447272]	uncertain significance	19	3178950	3178950	Human		name
597734815	CV3597917	single nucleotide variant	NM_003775.4(S1PR4):c.148C>T (p.Arg50Trp)	not specified [RCV004863551]	uncertain significance	19	3178940	3178940	Human		name
597734820	CV3597918	single nucleotide variant	NM_003775.4(S1PR4):c.236G>A (p.Arg79His)	not specified [RCV004863552]	uncertain significance	19	3179028	3179028	Human		name
597734831	CV3597920	single nucleotide variant	NM_003775.4(S1PR4):c.166G>A (p.Ala56Thr)	not specified [RCV004863554]	uncertain significance	19	3178958	3178958	Human		name
597734841	CV3597922	single nucleotide variant	NM_003775.4(S1PR4):c.261C>G (p.Asn87Lys)	not specified [RCV004863556]	uncertain significance	19	3179053	3179053	Human		name
597734852	CV3597924	single nucleotide variant	NM_003775.4(S1PR4):c.112C>T (p.Arg38Cys)	not specified [RCV004863558]	uncertain significance	19	3178904	3178904	Human		name
598207747	CV3910257	single nucleotide variant	NM_003775.4(S1PR4):c.289G>A (p.Ala97Thr)	not specified [RCV005270092]	uncertain significance	19	3179081	3179081	Human		name
15136261	CV741764	single nucleotide variant	NM_003775.4(S1PR4):c.1116G>A (p.Arg372=)	not provided [RCV000898599]	benign	19	3179908	3179908	Human		name
156082481	CV2205442	single nucleotide variant	NM_003775.4(S1PR4):c.722C>T (p.Ala241Val)	not specified [RCV004082386]	uncertain significance	19	3179514	3179514	Human		name
155934452	CV2225300	single nucleotide variant	NM_003775.4(S1PR4):c.301G>A (p.Ala101Thr)	not specified [RCV004098943]	uncertain significance	19	3179093	3179093	Human		name
156075564	CV2248255	single nucleotide variant	NM_003775.4(S1PR4):c.314T>C (p.Leu105Pro)	not specified [RCV004119425]	uncertain significance	19	3179106	3179106	Human		name
156257987	CV2277701	single nucleotide variant	NM_003775.4(S1PR4):c.335G>A (p.Arg112His)	not specified [RCV004147147]	uncertain significance	19	3179127	3179127	Human		name
155945324	CV2292047	single nucleotide variant	NM_003775.4(S1PR4):c.607C>T (p.Arg203Cys)	not specified [RCV004160324]	uncertain significance	19	3179399	3179399	Human		name
156090868	CV2300005	single nucleotide variant	NM_003775.4(S1PR4):c.529G>A (p.Gly177Arg)	not specified [RCV004151218]	uncertain significance	19	3179321	3179321	Human		name
156270828	CV2333798	single nucleotide variant	NM_003775.4(S1PR4):c.716G>A (p.Arg239His)	not specified [RCV004181300]	uncertain significance	19	3179508	3179508	Human		name
156165982	CV2348646	single nucleotide variant	NM_003775.4(S1PR4):c.608G>A (p.Arg203His)	not specified [RCV004195868]	uncertain significance	19	3179400	3179400	Human		name
156144791	CV2358686	single nucleotide variant	NM_003775.4(S1PR4):c.743G>A (p.Arg248His)	not specified [RCV004209604]	uncertain significance	19	3179535	3179535	Human		name
156104595	CV2400303	single nucleotide variant	NM_003775.4(S1PR4):c.391G>A (p.Ala131Thr)	not specified [RCV004244363]	uncertain significance	19	3179183	3179183	Human		name
329364605	CV2443733	single nucleotide variant	NM_003775.4(S1PR4):c.346G>A (p.Ala116Thr)	not specified [RCV004256032]	uncertain significance	19	3179138	3179138	Human		name
401740563	CV2679753	single nucleotide variant	NM_003775.4(S1PR4):c.640G>A (p.Gly214Ser)	not specified [RCV004282218]	likely benign	19	3179432	3179432	Human		name
401883398	CV2761084	single nucleotide variant	NM_003775.4(S1PR4):c.484G>A (p.Val162Ile)	not specified [RCV004338743]	uncertain significance	19	3179276	3179276	Human		name
401875031	CV2791026	single nucleotide variant	NM_003775.4(S1PR4):c.970T>C (p.Cys324Arg)	not specified [RCV004354637]	uncertain significance	19	3179762	3179762	Human		name
405702211	CV3310195	single nucleotide variant	NM_003775.4(S1PR4):c.422G>A (p.Gly141Glu)	not specified [RCV004447273]	uncertain significance	19	3179214	3179214	Human		name
405702153	CV3310196	single nucleotide variant	NM_003775.4(S1PR4):c.463G>A (p.Gly155Arg)	not specified [RCV004447274]	uncertain significance	19	3179255	3179255	Human		name
405702160	CV3310197	single nucleotide variant	NM_003775.4(S1PR4):c.464G>C (p.Gly155Ala)	not specified [RCV004447275]	uncertain significance	19	3179256	3179256	Human		name
405702172	CV3310198	single nucleotide variant	NM_003775.4(S1PR4):c.692A>C (p.Gln231Pro)	not specified [RCV004447277]	uncertain significance	19	3179484	3179484	Human		name
405702179	CV3310199	single nucleotide variant	NM_003775.4(S1PR4):c.823G>T (p.Val275Phe)	not specified [RCV004447278]	uncertain significance	19	3179615	3179615	Human		name
405702191	CV3310200	single nucleotide variant	NM_003775.4(S1PR4):c.998G>T (p.Gly333Val)	not specified [RCV004447279]	uncertain significance	19	3179790	3179790	Human		name
407514154	CV3473365	single nucleotide variant	NM_003775.4(S1PR4):c.683G>A (p.Arg228His)	not specified [RCV004674424]	uncertain significance	19	3179475	3179475	Human		name
407468966	CV3473368	single nucleotide variant	NM_003775.4(S1PR4):c.463G>C (p.Gly155Arg)	not specified [RCV004661313]	uncertain significance	19	3179255	3179255	Human		name
407514158	CV3473369	single nucleotide variant	NM_003775.4(S1PR4):c.754A>G (p.Thr252Ala)	not specified [RCV004674426]	uncertain significance	19	3179546	3179546	Human		name
597734826	CV3597919	single nucleotide variant	NM_003775.4(S1PR4):c.446G>A (p.Arg149Gln)	not specified [RCV004863553]	uncertain significance	19	3179238	3179238	Human		name
597734836	CV3597921	single nucleotide variant	NM_003775.4(S1PR4):c.562T>A (p.Cys188Ser)	not specified [RCV004863555]	uncertain significance	19	3179354	3179354	Human		name
597734847	CV3597923	single nucleotide variant	NM_003775.4(S1PR4):c.388G>A (p.Ala130Thr)	not specified [RCV004863557]	uncertain significance	19	3179180	3179180	Human		name
597734859	CV3597926	single nucleotide variant	NM_003775.4(S1PR4):c.497T>C (p.Ile166Thr)	not specified [RCV004863559]	uncertain significance	19	3179289	3179289	Human		name
597734864	CV3597927	single nucleotide variant	NM_003775.4(S1PR4):c.699C>G (p.Ser233Arg)	not specified [RCV004863560]	uncertain significance	19	3179491	3179491	Human		name
597734874	CV3597929	single nucleotide variant	NM_003775.4(S1PR4):c.524T>C (p.Leu175Pro)	not specified [RCV004863562]	uncertain significance	19	3179316	3179316	Human		name
598207754	CV3910258	single nucleotide variant	NM_003775.4(S1PR4):c.833C>T (p.Ser278Phe)	not specified [RCV005270093]	uncertain significance	19	3179625	3179625	Human		name
598207768	CV3910260	single nucleotide variant	NM_003775.4(S1PR4):c.913A>G (p.Ile305Val)	not specified [RCV005270095]	uncertain significance	19	3179705	3179705	Human		name
8628266	CV83410	single nucleotide variant	NM_003775.4(S1PR4):c.643G>A (p.Val215Ile)	not specified [RCV004447276]	likely benign\|not provided	19	3179435	3179435	Human		name
156029992	CV2206183	single nucleotide variant	NM_003775.4(S1PR4):c.1109G>A (p.Arg370Gln)	not specified [RCV004080622]	uncertain significance	19	3179901	3179901	Human		name
156344544	CV2346110	single nucleotide variant	NM_003775.4(S1PR4):c.1113G>C (p.Met371Ile)	not specified [RCV004201573]	uncertain significance	19	3179905	3179905	Human		name
329360132	CV2446605	single nucleotide variant	NM_003775.4(S1PR4):c.1054G>A (p.Asp352Asn)	not specified [RCV004251496]	uncertain significance	19	3179846	3179846	Human		name
405702460	CV3310192	single nucleotide variant	NM_003775.4(S1PR4):c.1018C>T (p.Arg340Trp)	not specified [RCV004447270]	uncertain significance	19	3179810	3179810	Human		name
405702454	CV3310193	single nucleotide variant	NM_003775.4(S1PR4):c.1115G>A (p.Arg372Gln)	not specified [RCV004447271]	uncertain significance	19	3179907	3179907	Human		name
407468960	CV3473364	single nucleotide variant	NM_003775.4(S1PR4):c.1003G>A (p.Gly335Arg)	not specified [RCV004661311]	uncertain significance	19	3179795	3179795	Human		name
407468963	CV3473366	single nucleotide variant	NM_003775.4(S1PR4):c.1112T>A (p.Met371Lys)	not specified [RCV004661312]	uncertain significance	19	3179904	3179904	Human		name
407514156	CV3473367	single nucleotide variant	NM_003775.4(S1PR4):c.1114C>T (p.Arg372Trp)	not specified [RCV004674425]	uncertain significance	19	3179906	3179906	Human		name
597734808	CV3597916	single nucleotide variant	NM_003775.4(S1PR4):c.1145G>A (p.Arg382Gln)	not specified [RCV004863550]	uncertain significance	19	3179937	3179937	Human		name
598207741	CV3910256	single nucleotide variant	NM_003775.4(S1PR4):c.1027G>A (p.Glu343Lys)	not specified [RCV005270091]	uncertain significance	19	3179819	3179819	Human		name
598207760	CV3910259	single nucleotide variant	NM_003775.4(S1PR4):c.1087G>A (p.Gly363Ser)	not specified [RCV005270094]	uncertain significance	19	3179879	3179879	Human		name

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