Fpr2 Variant Search Result - Rat Genome Database

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34 records found for search term Fpr2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
243053606	CV2404685	single nucleotide variant	NM_001005738.2(FPR2):c.-15+1402C>T	Lung adenocarcinoma [RCV003129712]	uncertain significance	19	51762632	51762632	Human	2	name
401740533	CV2702345	single nucleotide variant	NM_001005738.2(FPR2):c.77G>A (p.Arg26Gln)	not specified [RCV004316874]	likely benign	19	51768735	51768735	Human		name
597727678	CV3669881	single nucleotide variant	NM_001005738.2(FPR2):c.79A>C (p.Ile27Leu)	not specified [RCV004919480]	uncertain significance	19	51768737	51768737	Human		name
597727702	CV3669884	single nucleotide variant	NM_001005738.2(FPR2):c.95T>C (p.Val32Ala)	not specified [RCV004919483]	uncertain significance	19	51768753	51768753	Human		name
155963139	CV2197766	single nucleotide variant	NM_001005738.2(FPR2):c.254T>C (p.Met85Thr)	not specified [RCV004074964]	uncertain significance	19	51768912	51768912	Human		name
156235749	CV2268026	single nucleotide variant	NM_001005738.2(FPR2):c.283T>C (p.Trp95Arg)	not specified [RCV004136581]	uncertain significance	19	51768941	51768941	Human		name
156201028	CV2313117	single nucleotide variant	NM_001005738.2(FPR2):c.118G>A (p.Gly40Arg)	not specified [RCV004161385]	uncertain significance	19	51768776	51768776	Human		name
405762572	CV3250805	single nucleotide variant	NM_001005738.2(FPR2):c.169C>T (p.Arg57Cys)	not specified [RCV004394511]	uncertain significance	19	51768827	51768827	Human		name
405762577	CV3250806	single nucleotide variant	NM_001005738.2(FPR2):c.175G>A (p.Val59Ile)	not specified [RCV004394512]	uncertain significance	19	51768833	51768833	Human		name
405762582	CV3250807	single nucleotide variant	NM_001005738.2(FPR2):c.224C>T (p.Thr75Met)	not specified [RCV004394513]	uncertain significance	19	51768882	51768882	Human		name
407494494	CV3442845	single nucleotide variant	NM_001005738.2(FPR2):c.100G>A (p.Gly34Arg)	not specified [RCV004621337]	uncertain significance	19	51768758	51768758	Human		name
15122158	CV716657	single nucleotide variant	NM_001005738.2(FPR2):c.220T>C (p.Phe74Leu)	not provided [RCV000963025]	benign\|likely benign	19	51768878	51768878	Human		name
8636976	CV92201	single nucleotide variant	NM_001005738.1(FPR2):c.160C>T (p.Arg54Trp)	Malignant melanoma [RCV000072299]	not provided	19	51768818	51768818	Human		name
156027627	CV2242475	single nucleotide variant	NM_001005738.2(FPR2):c.442G>A (p.Gly148Arg)	not specified [RCV004111466]	uncertain significance	19	51769100	51769100	Human		name
156073651	CV2299242	single nucleotide variant	NM_001005738.2(FPR2):c.734C>T (p.Ala245Val)	not specified [RCV004152573]	uncertain significance	19	51769392	51769392	Human		name
156040824	CV2310836	single nucleotide variant	NM_001005738.2(FPR2):c.736G>A (p.Val246Met)	not specified [RCV004163883]	uncertain significance	19	51769394	51769394	Human		name
155975033	CV2341498	single nucleotide variant	NM_001005738.2(FPR2):c.753C>G (p.Phe251Leu)	not specified [RCV004188891]	uncertain significance	19	51769411	51769411	Human		name
155923987	CV2347603	single nucleotide variant	NM_001005738.2(FPR2):c.888C>G (p.Cys296Trp)	not specified [RCV004200541]	uncertain significance	19	51769546	51769546	Human		name
156174996	CV2377210	single nucleotide variant	NM_001005738.2(FPR2):c.933G>C (p.Glu311Asp)	not specified [RCV004231880]	uncertain significance	19	51769591	51769591	Human		name
329353091	CV2471462	single nucleotide variant	NM_001005738.2(FPR2):c.638C>T (p.Pro213Leu)	not specified [RCV004280460]	uncertain significance	19	51769296	51769296	Human		name
401780974	CV2681844	single nucleotide variant	NM_001005738.2(FPR2):c.816G>C (p.Leu272Phe)	not specified [RCV004296839]	uncertain significance	19	51769474	51769474	Human		name
401764863	CV2701469	single nucleotide variant	NM_001005738.2(FPR2):c.383T>G (p.Leu128Arg)	not specified [RCV004312138]	uncertain significance	19	51769041	51769041	Human		name
401783615	CV2723768	single nucleotide variant	NM_001005738.2(FPR2):c.907G>C (p.Val303Leu)	not specified [RCV004325927]	uncertain significance	19	51769565	51769565	Human		name
405762589	CV3250808	single nucleotide variant	NM_001005738.2(FPR2):c.523T>C (p.Tyr175His)	not specified [RCV004394514]	uncertain significance	19	51769181	51769181	Human		name
405762597	CV3250809	single nucleotide variant	NM_001005738.2(FPR2):c.796G>A (p.Val266Ile)	not specified [RCV004394515]	uncertain significance	19	51769454	51769454	Human		name
405762603	CV3250810	single nucleotide variant	NM_001005738.2(FPR2):c.859A>G (p.Thr287Ala)	not specified [RCV004394516]	uncertain significance	19	51769517	51769517	Human		name
405762609	CV3250811	single nucleotide variant	NM_001005738.2(FPR2):c.904T>C (p.Tyr302His)	not specified [RCV004394517]	uncertain significance	19	51769562	51769562	Human		name
407494490	CV3442844	single nucleotide variant	NM_001005738.2(FPR2):c.346A>G (p.Ile116Val)	not specified [RCV004621336]	uncertain significance	19	51769004	51769004	Human		name
597727669	CV3669880	single nucleotide variant	NM_001005738.2(FPR2):c.742G>T (p.Ala248Ser)	not specified [RCV004919479]	uncertain significance	19	51769400	51769400	Human		name
597727687	CV3669882	single nucleotide variant	NM_001005738.2(FPR2):c.406C>T (p.His136Tyr)	not specified [RCV004919481]	uncertain significance	19	51769064	51769064	Human		name
597727695	CV3669883	single nucleotide variant	NM_001005738.2(FPR2):c.896C>G (p.Pro299Arg)	not specified [RCV004919482]	uncertain significance	19	51769554	51769554	Human		name
598229981	CV3970074	single nucleotide variant	NM_001005738.2(FPR2):c.409C>T (p.Arg137Cys)	not specified [RCV005342165]	uncertain significance	19	51769067	51769067	Human		name
598229988	CV3970075	single nucleotide variant	NM_001005738.2(FPR2):c.589A>G (p.Met197Val)	not specified [RCV005342166]	uncertain significance	19	51769247	51769247	Human		name
598229995	CV3970076	single nucleotide variant	NM_001005738.2(FPR2):c.591G>A (p.Met197Ile)	not specified [RCV005342167]	uncertain significance	19	51769249	51769249	Human		name

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