Bfar Variant Search Result - Rat Genome Database

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41 records found for search term Bfar

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407472645	CV3427540	single nucleotide variant	NM_016561.3(BFAR):c.26T>C (p.Val9Ala)	not specified [RCV004600191]	uncertain significance	16	14644372	14644372	Human		name
8635674	CV90896	single nucleotide variant	NM_016561.2(BFAR):c.120C>T (p.Ile40=)	Malignant melanoma [RCV000070994]	not provided	16	14644466	14644466	Human		name
401855956	CV2754155	single nucleotide variant	NM_016561.3(BFAR):c.70G>A (p.Gly24Ser)	not specified [RCV004334348]	likely benign	16	14644416	14644416	Human		name
598161165	CV3949374	single nucleotide variant	NM_016561.3(BFAR):c.34A>G (p.Met12Val)	not specified [RCV005306954]	uncertain significance	16	14644380	14644380	Human		name
156276699	CV2230577	single nucleotide variant	NM_016561.3(BFAR):c.164G>A (p.Arg55His)	not specified [RCV004097542]	uncertain significance	16	14644510	14644510	Human		name
156218737	CV2253978	single nucleotide variant	NM_016561.3(BFAR):c.194C>T (p.Ser65Leu)	not specified [RCV004127647]	uncertain significance	16	14644540	14644540	Human		name
156134612	CV2260178	single nucleotide variant	NM_016561.3(BFAR):c.134C>T (p.Thr45Ile)	not specified [RCV004120955]	uncertain significance	16	14644480	14644480	Human		name
405728612	CV3298233	single nucleotide variant	NM_016561.3(BFAR):c.101G>A (p.Cys34Tyr)	not specified [RCV004429054]	uncertain significance	16	14644447	14644447	Human		name
405728626	CV3298235	single nucleotide variant	NM_016561.3(BFAR):c.295A>G (p.Ile99Val)	not specified [RCV004429056]	uncertain significance	16	14648419	14648419	Human		name
405728635	CV3298236	single nucleotide variant	NM_016561.3(BFAR):c.297T>G (p.Ile99Met)	not specified [RCV004429057]	uncertain significance	16	14648421	14648421	Human		name
597737963	CV3636545	single nucleotide variant	NM_016561.3(BFAR):c.269C>T (p.Ala90Val)	not specified [RCV004890038]	uncertain significance	16	14648393	14648393	Human		name
598276732	CV3949376	single nucleotide variant	NM_016561.3(BFAR):c.285T>G (p.Phe95Leu)	not specified [RCV005305866]	uncertain significance	16	14648409	14648409	Human		name
156133535	CV2195960	single nucleotide variant	NM_016561.3(BFAR):c.870C>G (p.Asp290Glu)	not specified [RCV004072214]	uncertain significance	16	14661978	14661978	Human		name
156305593	CV2252633	single nucleotide variant	NM_016561.3(BFAR):c.733C>T (p.Arg245Cys)	not specified [RCV004118505]	uncertain significance	16	14655160	14655160	Human		name
156036139	CV2253292	single nucleotide variant	NM_016561.3(BFAR):c.628G>C (p.Val210Leu)	not specified [RCV004122825]	uncertain significance	16	14649963	14649963	Human		name
155955567	CV2303922	single nucleotide variant	NM_016561.3(BFAR):c.815T>C (p.Leu272Pro)	not specified [RCV004168200]	uncertain significance	16	14661923	14661923	Human		name
156210376	CV2309696	single nucleotide variant	NM_016561.3(BFAR):c.382C>T (p.Pro128Ser)	not specified [RCV004160830]	uncertain significance	16	14648506	14648506	Human		name
156078401	CV2318725	single nucleotide variant	NM_016561.3(BFAR):c.985T>C (p.Trp329Arg)	not specified [RCV004175659]	uncertain significance	16	14664896	14664896	Human		name
156274156	CV2319957	single nucleotide variant	NM_016561.3(BFAR):c.373G>C (p.Asp125His)	not specified [RCV004167832]	uncertain significance	16	14648497	14648497	Human		name
329381132	CV2464524	single nucleotide variant	NM_016561.3(BFAR):c.758C>A (p.Pro253His)	not specified [RCV004276436]	uncertain significance	16	14655185	14655185	Human		name
401730406	CV2711275	single nucleotide variant	NM_016561.3(BFAR):c.391C>G (p.Pro131Ala)	not specified [RCV004313058]	uncertain significance	16	14648515	14648515	Human		name
401857265	CV2762536	single nucleotide variant	NM_016561.3(BFAR):c.776A>G (p.Glu259Gly)	not specified [RCV004338070]	uncertain significance	16	14655203	14655203	Human		name
401858019	CV2774147	single nucleotide variant	NM_016561.3(BFAR):c.736G>A (p.Val246Ile)	not specified [RCV004345737]	uncertain significance	16	14655163	14655163	Human		name
405728648	CV3298237	single nucleotide variant	NM_016561.3(BFAR):c.514G>C (p.Asp172His)	not specified [RCV004429058]	uncertain significance	16	14649849	14649849	Human		name
405728657	CV3298238	single nucleotide variant	NM_016561.3(BFAR):c.758C>G (p.Pro253Arg)	not specified [RCV004429059]	uncertain significance	16	14655185	14655185	Human		name
405728666	CV3298239	single nucleotide variant	NM_016561.3(BFAR):c.974C>T (p.Thr325Met)	not specified [RCV004429060]	uncertain significance	16	14664885	14664885	Human		name
407472636	CV3427538	single nucleotide variant	NM_016561.3(BFAR):c.410A>G (p.Asn137Ser)	not specified [RCV004600189]	uncertain significance	16	14648534	14648534	Human		name
407472640	CV3427539	single nucleotide variant	NM_016561.3(BFAR):c.713C>T (p.Ala238Val)	not specified [RCV004600190]	uncertain significance	16	14655140	14655140	Human		name
597737968	CV3636546	single nucleotide variant	NM_016561.3(BFAR):c.347T>C (p.Leu116Pro)	not specified [RCV004890039]	uncertain significance	16	14648471	14648471	Human		name
598161170	CV3949375	single nucleotide variant	NM_016561.3(BFAR):c.511C>T (p.His171Tyr)	not specified [RCV005306955]	uncertain significance	16	14649846	14649846	Human		name
598276734	CV3949379	single nucleotide variant	NM_016561.3(BFAR):c.911C>T (p.Pro304Leu)	not specified [RCV005305868]	uncertain significance	16	14662019	14662019	Human		name
15200592	CV703494	single nucleotide variant	NM_016561.3(BFAR):c.734G>A (p.Arg245His)	not provided [RCV000957375]	benign	16	14655161	14655161	Human		name
8635675	CV90897	single nucleotide variant	NM_016561.2(BFAR):c.793C>T (p.Pro265Ser)	Malignant melanoma [RCV000070995]	not provided	16	14661901	14661901	Human		name
155917975	CV2275143	single nucleotide variant	NM_016561.3(BFAR):c.1143G>T (p.Trp381Cys)	not specified [RCV004136942]	uncertain significance	16	14665054	14665054	Human		name
155990969	CV2384095	single nucleotide variant	NM_016561.3(BFAR):c.1010C>G (p.Ser337Cys)	not specified [RCV004227501]	uncertain significance	16	14664921	14664921	Human		name
401870096	CV2772617	single nucleotide variant	NM_016561.3(BFAR):c.1145C>T (p.Ser382Leu)	not specified [RCV004355368]	uncertain significance	16	14665056	14665056	Human		name
405728619	CV3298234	single nucleotide variant	NM_016561.3(BFAR):c.1327C>T (p.Arg443Trp)	not specified [RCV004429055]	uncertain significance	16	14667801	14667801	Human		name
407472648	CV3427541	single nucleotide variant	NM_016561.3(BFAR):c.1218T>A (p.Phe406Leu)	not specified [RCV004600192]	uncertain significance	16	14667692	14667692	Human		name
598161160	CV3949373	single nucleotide variant	NM_016561.3(BFAR):c.1004A>C (p.Lys335Thr)	not specified [RCV005306953]	uncertain significance	16	14664915	14664915	Human		name
598161175	CV3949378	single nucleotide variant	NM_016561.3(BFAR):c.1051T>C (p.Trp351Arg)	not specified [RCV005306956]	uncertain significance	16	14664962	14664962	Human		name
598161180	CV3949380	single nucleotide variant	NM_016561.3(BFAR):c.1298T>C (p.Ile433Thr)	not specified [RCV005306957]	uncertain significance	16	14667772	14667772	Human		name

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