Vsig4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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60 records found for search term Vsig4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405269017	CV3199178	single nucleotide variant	NM_007268.3(VSIG4):c.*127C>T	VSIG4-related disorder [RCV003912279]	likely benign	X	66022136	66022136	Human		name , trait , alternate_id
405260450	CV3204111	single nucleotide variant	NM_007268.3(VSIG4):c.56-4T>C	VSIG4-related disorder [RCV003943981]	likely benign	X	66033834	66033834	Human		name , trait , alternate_id
401927206	CV2829156	single nucleotide variant	NM_007268.3(VSIG4):c.758-7T>C	not provided [RCV003438436]	likely benign	X	66027533	66027533	Human		name
405268770	CV3199079	single nucleotide variant	NM_007268.3(VSIG4):c.56-10G>A	VSIG4-related disorder [RCV003912184]	likely benign	X	66033840	66033840	Human		name , trait , alternate_id
405266300	CV3213113	single nucleotide variant	NM_007268.3(VSIG4):c.757+8T>C	VSIG4-related disorder [RCV003969270]	likely benign	X	66028042	66028042	Human		name , trait , alternate_id
15153755	CV760890	single nucleotide variant	NM_007268.3(VSIG4):c.694+7G>A	not provided [RCV000924119]	likely benign	X	66032461	66032461	Human		name
15120454	CV745191	single nucleotide variant	NM_007268.3(VSIG4):c.413-10T>G	not provided [RCV000895897]	benign	X	66032759	66032759	Human		name
597687538	CV3626775	single nucleotide variant	NM_007268.3(VSIG4):c.7A>C (p.Ile3Leu)	not specified [RCV004884268]	likely benign	X	66039992	66039992	Human		name
150412368	CV1196396	single nucleotide variant	NM_007268.3(VSIG4):c.94C>T (p.Pro32Ser)	not provided [RCV001574056]	likely benign	X	66033792	66033792	Human		name
156247568	CV2215348	single nucleotide variant	NM_007268.3(VSIG4):c.58C>T (p.Arg20Cys)	VSIG4-related disorder [RCV003963729]\|not provided [RCV003435897]\|not specified [RCV004089161]	likely benign\|uncertain significance	X	66033828	66033828	Human		name , trait , alternate_id
156387178	CV2221430	single nucleotide variant	NM_007268.3(VSIG4):c.43G>T (p.Val15Leu)	not specified [RCV004096721]	uncertain significance	X	66039956	66039956	Human		name
405284841	CV3190894	single nucleotide variant	NM_007268.3(VSIG4):c.408G>A (p.Gln136=)	VSIG4-related disorder [RCV003909458]	likely benign	X	66033478	66033478	Human		name , trait , alternate_id
405294769	CV3212050	single nucleotide variant	NM_007268.3(VSIG4):c.31G>A (p.Gly11Arg)	VSIG4-related disorder [RCV003934720]	benign	X	66039968	66039968	Human		name , trait , alternate_id
405265966	CV3215823	single nucleotide variant	NM_007268.3(VSIG4):c.669C>T (p.Ser223=)	VSIG4-related disorder [RCV003946970]	likely benign	X	66032493	66032493	Human		name , trait , alternate_id
405278180	CV3216432	single nucleotide variant	NM_007268.3(VSIG4):c.603G>A (p.Ala201=)	VSIG4-related disorder [RCV003954372]	likely benign	X	66032559	66032559	Human		name , trait , alternate_id
405663527	CV3342315	single nucleotide variant	NM_007268.3(VSIG4):c.91G>A (p.Gly31Arg)	not specified [RCV004485011]	uncertain significance	X	66033795	66033795	Human		name
598217939	CV3926147	single nucleotide variant	NM_007268.3(VSIG4):c.34C>A (p.His12Asn)	not specified [RCV005293108]	uncertain significance	X	66039965	66039965	Human		name
156170432	CV2317140	single nucleotide variant	NM_007268.3(VSIG4):c.114T>A (p.Asn38Lys)	not specified [RCV004174610]	uncertain significance	X	66033772	66033772	Human		name
405663513	CV3342312	single nucleotide variant	NM_007268.3(VSIG4):c.290C>T (p.Ser97Phe)	not specified [RCV004485008]	uncertain significance	X	66033596	66033596	Human		name
597687520	CV3626772	single nucleotide variant	NM_007268.3(VSIG4):c.151C>G (p.Gln51Glu)	not specified [RCV004884266]	uncertain significance	X	66033735	66033735	Human		name
598255966	CV3926145	single nucleotide variant	NM_007268.3(VSIG4):c.200T>C (p.Ile67Thr)	not specified [RCV005299529]	uncertain significance	X	66033686	66033686	Human		name
598217957	CV3926149	single nucleotide variant	NM_007268.3(VSIG4):c.140A>T (p.Gln47Leu)	not specified [RCV005293110]	uncertain significance	X	66033746	66033746	Human		name
598255977	CV3926152	single nucleotide variant	NM_007268.3(VSIG4):c.179G>A (p.Arg60His)	not specified [RCV005299531]	uncertain significance	X	66033707	66033707	Human		name
15107618	CV717844	single nucleotide variant	NM_007268.3(VSIG4):c.274G>T (p.Val92Phe)	not provided [RCV000960327]	benign	X	66033612	66033612	Human		name
150411275	CV1196395	single nucleotide variant	NM_007268.3(VSIG4):c.644G>A (p.Gly215Asp)	not provided [RCV001573592]	uncertain significance	X	66032518	66032518	Human		name
156350682	CV2316251	single nucleotide variant	NM_007268.3(VSIG4):c.730C>G (p.Pro244Ala)	not specified [RCV004174283]	uncertain significance	X	66028077	66028077	Human		name
155984802	CV2344903	single nucleotide variant	NM_007268.3(VSIG4):c.480G>T (p.Arg160Ser)	not specified [RCV004191038]	uncertain significance	X	66032682	66032682	Human		name
156067806	CV2345837	single nucleotide variant	NM_007268.3(VSIG4):c.669C>A (p.Ser223Arg)	not specified [RCV004198882]	uncertain significance	X	66032493	66032493	Human		name
156346853	CV2353767	single nucleotide variant	NM_007268.3(VSIG4):c.793A>T (p.Thr265Ser)	not specified [RCV004201775]	uncertain significance	X	66027491	66027491	Human		name
156070486	CV2356009	single nucleotide variant	NM_007268.3(VSIG4):c.736A>T (p.Thr246Ser)	not specified [RCV004201384]	uncertain significance	X	66028071	66028071	Human		name
156206962	CV2360370	single nucleotide variant	NM_007268.3(VSIG4):c.613G>A (p.Asp205Asn)	not specified [RCV004208701]	uncertain significance	X	66032549	66032549	Human		name
156266393	CV2372462	single nucleotide variant	NM_007268.3(VSIG4):c.722C>T (p.Thr241Ile)	not specified [RCV004219262]	uncertain significance	X	66028085	66028085	Human		name
156074250	CV2376958	single nucleotide variant	NM_007268.3(VSIG4):c.364G>C (p.Gly122Arg)	not specified [RCV004229646]	uncertain significance	X	66033522	66033522	Human		name
401765908	CV2683466	single nucleotide variant	NM_007268.3(VSIG4):c.794C>T (p.Thr265Ile)	not specified [RCV004288224]	uncertain significance	X	66027490	66027490	Human		name
401879971	CV2783051	single nucleotide variant	NM_007268.3(VSIG4):c.302G>A (p.Ser101Asn)	not specified [RCV004363421]	likely benign	X	66033584	66033584	Human		name
405258513	CV3203882	single nucleotide variant	NM_007268.3(VSIG4):c.322C>T (p.Arg108Trp)	VSIG4-related disorder [RCV003942044]	benign	X	66033564	66033564	Human		name , trait , alternate_id
405271547	CV3209433	single nucleotide variant	NM_007268.3(VSIG4):c.590T>A (p.Leu197His)	VSIG4-related disorder [RCV003949756]	likely benign	X	66032572	66032572	Human		name , trait , alternate_id
405663518	CV3342313	single nucleotide variant	NM_007268.3(VSIG4):c.698C>T (p.Ser233Phe)	not specified [RCV004485009]	uncertain significance	X	66028109	66028109	Human		name
405663934	CV3342314	single nucleotide variant	NM_007268.3(VSIG4):c.764C>G (p.Ser255Cys)	not specified [RCV004485010]	uncertain significance	X	66027520	66027520	Human		name
405663532	CV3342316	single nucleotide variant	NM_007268.3(VSIG4):c.947T>C (p.Val316Ala)	not specified [RCV004485012]	uncertain significance	X	66022856	66022856	Human		name
407450493	CV3491509	single nucleotide variant	NM_007268.3(VSIG4):c.584C>A (p.Thr195Asn)	not specified [RCV004683319]	uncertain significance	X	66032578	66032578	Human		name
407450496	CV3491510	single nucleotide variant	NM_007268.3(VSIG4):c.883T>C (p.Cys295Arg)	not specified [RCV004683320]	uncertain significance	X	66025082	66025082	Human		name
407450498	CV3491511	single nucleotide variant	NM_007268.3(VSIG4):c.343G>A (p.Val115Ile)	not specified [RCV004683321]	uncertain significance	X	66033543	66033543	Human		name
408384428	CV3505320	single nucleotide variant	NM_007268.3(VSIG4):c.472G>C (p.Gly158Arg)	VSIG4-related disorder [RCV004731802]	uncertain significance	X	66032690	66032690	Human		name , trait , alternate_id
597687488	CV3626768	single nucleotide variant	NM_007268.3(VSIG4):c.400C>T (p.Arg134Cys)	not specified [RCV004884263]	uncertain significance	X	66033486	66033486	Human		name
597699718	CV3626769	single nucleotide variant	NM_007268.3(VSIG4):c.581G>A (p.Ser194Asn)	not specified [RCV004885526]	uncertain significance	X	66032581	66032581	Human		name
597687497	CV3626770	single nucleotide variant	NM_007268.3(VSIG4):c.842G>A (p.Ser281Asn)	not specified [RCV004884264]	uncertain significance	X	66025123	66025123	Human		name
597699726	CV3626773	single nucleotide variant	NM_007268.3(VSIG4):c.724G>A (p.Glu242Lys)	not specified [RCV004885527]	uncertain significance	X	66028083	66028083	Human		name
597687529	CV3626774	single nucleotide variant	NM_007268.3(VSIG4):c.637G>A (p.Ala213Thr)	not specified [RCV004884267]	uncertain significance	X	66032525	66032525	Human		name
598255972	CV3926146	single nucleotide variant	NM_007268.3(VSIG4):c.401G>A (p.Arg134His)	not specified [RCV005299530]	uncertain significance	X	66033485	66033485	Human		name
598217946	CV3926148	single nucleotide variant	NM_007268.3(VSIG4):c.922C>T (p.Arg308Trp)	not specified [RCV005293109]	uncertain significance	X	66025043	66025043	Human		name
598217972	CV3926151	single nucleotide variant	NM_007268.3(VSIG4):c.742A>T (p.Thr248Ser)	not specified [RCV005293112]	uncertain significance	X	66028065	66028065	Human		name
155930025	CV2366483	single nucleotide variant	NM_007268.3(VSIG4):c.1135C>T (p.Arg379Cys)	not specified [RCV004208460]	uncertain significance	X	66022328	66022328	Human		name
156052227	CV2388449	single nucleotide variant	NM_007268.3(VSIG4):c.1132G>A (p.Ala378Thr)	not specified [RCV004237309]	uncertain significance	X	66022331	66022331	Human		name
329354423	CV2448149	single nucleotide variant	NM_007268.3(VSIG4):c.1175C>A (p.Ala392Asp)	not specified [RCV004263366]	uncertain significance	X	66022288	66022288	Human		name
407450491	CV3491508	single nucleotide variant	NM_007268.3(VSIG4):c.1030T>C (p.Ser344Pro)	not specified [RCV004683318]	likely benign	X	66022433	66022433	Human		name
408384014	CV3506168	single nucleotide variant	NM_007268.3(VSIG4):c.1186A>C (p.Lys396Gln)	VSIG4-related disorder [RCV004731430]	uncertain significance	X	66022277	66022277	Human		name , trait , alternate_id
597687506	CV3626771	single nucleotide variant	NM_007268.3(VSIG4):c.1116G>C (p.Gln372His)	not specified [RCV004884265]	uncertain significance	X	66022347	66022347	Human		name
598217964	CV3926150	single nucleotide variant	NM_007268.3(VSIG4):c.1175C>T (p.Ala392Val)	not specified [RCV005293111]	uncertain significance	X	66022288	66022288	Human		name
15107613	CV717843	single nucleotide variant	NM_007268.3(VSIG4):c.1148C>T (p.Thr383Ile)	not provided [RCV000960326]	benign	X	66022315	66022315	Human		name

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