Fgr Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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36 records found for search term Fgr

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15165213	CV777097	single nucleotide variant	NM_005248.3(FGR):c.533-8C>G	not provided [RCV000948535]	benign	1	27617014	27617014	Human		name
150463913	CV1237701	single nucleotide variant	NM_005248.3(FGR):c.762C>T (p.Asp254=)	not provided [RCV001649707]	benign	1	27615765	27615765	Human		name
155930240	CV2224691	single nucleotide variant	NM_005248.3(FGR):c.88G>A (p.Ala30Thr)	not specified [RCV004092527]	uncertain significance	1	27623829	27623829	Human		name
405760698	CV3250313	single nucleotide variant	NM_005248.3(FGR):c.56C>T (p.Ala19Val)	not specified [RCV004394205]	likely benign	1	27623861	27623861	Human		name
15174526	CV696673	single nucleotide variant	NM_005248.3(FGR):c.366C>T (p.Ser122=)	not provided [RCV000950364]	benign	1	27621621	27621621	Human		name
156075250	CV2273278	single nucleotide variant	NM_005248.3(FGR):c.155A>G (p.Asn52Ser)	not specified [RCV004132070]	uncertain significance	1	27623762	27623762	Human		name
401874019	CV2773632	single nucleotide variant	NM_005248.3(FGR):c.235G>T (p.Val79Leu)	not specified [RCV004356324]	uncertain significance	1	27623136	27623136	Human		name
401891707	CV2780683	single nucleotide variant	NM_005248.3(FGR):c.212T>G (p.Ile71Ser)	not specified [RCV004352026]	uncertain significance	1	27623705	27623705	Human		name
405760662	CV3250307	single nucleotide variant	NM_005248.3(FGR):c.125G>A (p.Arg42Gln)	not specified [RCV004394199]	likely benign	1	27623792	27623792	Human		name
405760687	CV3250311	single nucleotide variant	NM_005248.3(FGR):c.179C>T (p.Ala60Val)	not specified [RCV004394203]	uncertain significance	1	27623738	27623738	Human		name
598242052	CV3955615	single nucleotide variant	NM_005248.3(FGR):c.178G>A (p.Ala60Thr)	not specified [RCV005344455]	uncertain significance	1	27623739	27623739	Human		name
598242057	CV3955616	single nucleotide variant	NM_005248.3(FGR):c.103G>T (p.Gly35Trp)	not specified [RCV005344456]	uncertain significance	1	27623814	27623814	Human		name
156173501	CV2284098	single nucleotide variant	NM_005248.3(FGR):c.928A>T (p.Met310Leu)	not specified [RCV004144696]	uncertain significance	1	27615524	27615524	Human		name
156086442	CV2295335	single nucleotide variant	NM_005248.3(FGR):c.675C>G (p.His225Gln)	not specified [RCV004158696]	uncertain significance	1	27616864	27616864	Human		name
155963134	CV2388351	single nucleotide variant	NM_005248.3(FGR):c.980A>C (p.Glu327Ala)	not specified [RCV004234802]	uncertain significance	1	27615472	27615472	Human		name
401737488	CV2695815	single nucleotide variant	NM_005248.3(FGR):c.482C>T (p.Pro161Leu)	not specified [RCV004308099]	uncertain significance	1	27617243	27617243	Human		name
401724767	CV2714964	single nucleotide variant	NM_005248.3(FGR):c.302G>A (p.Gly101Asp)	not specified [RCV004322286]	uncertain significance	1	27623069	27623069	Human		name
401737749	CV2718202	single nucleotide variant	NM_005248.3(FGR):c.650A>G (p.Asn217Ser)	not specified [RCV004315897]	likely benign	1	27616889	27616889	Human		name
401878931	CV2754887	single nucleotide variant	NM_005248.3(FGR):c.860A>C (p.Lys287Thr)	not specified [RCV004341361]	uncertain significance	1	27615592	27615592	Human		name
405760692	CV3250312	single nucleotide variant	NM_005248.3(FGR):c.471G>C (p.Gln157His)	not specified [RCV004394204]	uncertain significance	1	27617254	27617254	Human		name
407501824	CV3439199	single nucleotide variant	NM_005248.3(FGR):c.774C>G (p.Ile258Met)	not specified [RCV004623341]	uncertain significance	1	27615753	27615753	Human		name
407501828	CV3439200	single nucleotide variant	NM_005248.3(FGR):c.856A>G (p.Thr286Ala)	not specified [RCV004623342]	uncertain significance	1	27615596	27615596	Human		name
597752265	CV3672796	single nucleotide variant	NM_005248.3(FGR):c.446T>C (p.Ile149Thr)	not specified [RCV004923883]	uncertain significance	1	27617279	27617279	Human		name
40888542	CV971611	single nucleotide variant	NM_005248.3(FGR):c.352C>T (p.Arg118Trp)	not provided [RCV001263546]	uncertain significance	1	27621635	27621635	Human		name
156252315	CV2268385	single nucleotide variant	NM_005248.3(FGR):c.1393C>T (p.Arg465Trp)	not specified [RCV004132525]	uncertain significance	1	27613111	27613111	Human		name
156268333	CV2275614	single nucleotide variant	NM_005248.3(FGR):c.1351C>T (p.Leu451Phe)	not specified [RCV004137244]	uncertain significance	1	27613249	27613249	Human		name
156140888	CV2280866	single nucleotide variant	NM_005248.3(FGR):c.1327T>C (p.Ser443Pro)	not specified [RCV004145119]	uncertain significance	1	27613273	27613273	Human		name
401727340	CV2684588	single nucleotide variant	NM_005248.3(FGR):c.1322T>G (p.Val441Gly)	not specified [RCV004293696]	uncertain significance	1	27613278	27613278	Human		name
401774759	CV2688277	single nucleotide variant	NM_005248.3(FGR):c.1183G>A (p.Ala395Thr)	not specified [RCV004299287]	uncertain significance	1	27614496	27614496	Human		name
401748668	CV2704369	single nucleotide variant	NM_005248.3(FGR):c.1489C>G (p.Leu497Val)	not specified [RCV004311340]	uncertain significance	1	27613015	27613015	Human		name
405760667	CV3250308	single nucleotide variant	NM_005248.3(FGR):c.1379C>T (p.Pro460Leu)	not specified [RCV004394200]	uncertain significance	1	27613221	27613221	Human		name
405760681	CV3250310	single nucleotide variant	NM_005248.3(FGR):c.1562C>T (p.Pro521Leu)	not specified [RCV004394202]	uncertain significance	1	27612942	27612942	Human		name
407501817	CV3439198	single nucleotide variant	NM_005248.3(FGR):c.1184C>T (p.Ala395Val)	not specified [RCV004623340]	likely benign	1	27614495	27614495	Human		name
597752260	CV3672795	single nucleotide variant	NM_005248.3(FGR):c.1486C>T (p.Arg496Cys)	not specified [RCV004923882]	uncertain significance	1	27613018	27613018	Human		name
8624973	CV80092	single nucleotide variant	NM_001042729.1(FGR):c.891C>T (p.Thr297=)	Malignant melanoma [RCV000060168]	not provided	1	27615561	27615561	Human		name
40888543	CV971612	single nucleotide variant	NM_005248.3(FGR):c.1573C>T (p.Pro525Ser)	not provided [RCV001263547]	uncertain significance	1	27612931	27612931	Human		name

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