Farp1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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112 records found for search term Farp1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8583425	CV117987	single nucleotide variant	NM_001001715.3(FARP1):c.-23-4256A>T	Lung cancer [RCV000098507]	uncertain significance	13	98208964	98208964	Human		name
8583424	CV117986	single nucleotide variant	NM_001001715.3(FARP1):c.-24+30007G>T	Lung cancer [RCV000098506]	uncertain significance	13	98173499	98173499	Human		name
8583426	CV117988	single nucleotide variant	NM_001286839.1(FARP1):c.171+56617G>C	Lung cancer [RCV000098508]	uncertain significance	13	98270030	98270030	Human		name
329372555	CV2451542	single nucleotide variant	NM_005766.4(FARP1):c.19A>G (p.Arg7Gly)	not specified [RCV004274484]	uncertain significance	13	98213261	98213261	Human		name
329358991	CV2425325	single nucleotide variant	NM_005766.4(FARP1):c.62G>A (p.Gly21Glu)	not specified [RCV004250990]	uncertain significance	13	98213304	98213304	Human		name
401934108	CV2813970	single nucleotide variant	NM_005766.4(FARP1):c.450G>A (p.Thr150=)	not provided [RCV003410991]	likely benign	13	98377872	98377872	Human		name
597695038	CV3672094	single nucleotide variant	NM_005766.4(FARP1):c.80G>C (p.Arg27Pro)	not specified [RCV004915729]	uncertain significance	13	98213322	98213322	Human		name
156280132	CV2325418	single nucleotide variant	NM_005766.4(FARP1):c.275C>T (p.Thr92Met)	not specified [RCV004177779]	uncertain significance	13	98343865	98343865	Human		name
401910118	CV2813971	single nucleotide variant	NM_005766.4(FARP1):c.2163G>T (p.Thr721=)	not provided [RCV003398352]	likely benign	13	98435595	98435595	Human		name
405867589	CV2842318	single nucleotide variant	NM_005766.4(FARP1):c.1461G>A (p.Ser487=)	EBV-positive nodal T- and NK-cell lymphoma [RCV004560267]	likely benign	13	98409384	98409384	Human		name
407492548	CV3432117	single nucleotide variant	NM_005766.4(FARP1):c.122C>G (p.Ser41Cys)	not specified [RCV004620815]	uncertain significance	13	98213364	98213364	Human		name
407492552	CV3432118	single nucleotide variant	NM_005766.4(FARP1):c.257C>G (p.Pro86Arg)	not specified [RCV004620816]	uncertain significance	13	98343847	98343847	Human		name
15185475	CV702749	single nucleotide variant	NM_005766.4(FARP1):c.2424T>C (p.Tyr808=)	not provided [RCV000952995]	benign	13	98439187	98439187	Human		name
15199920	CV702750	single nucleotide variant	NM_005766.4(FARP1):c.2583C>T (p.Ser861=)	not provided [RCV000957181]	benign	13	98440189	98440189	Human		name
8635097	CV90319	single nucleotide variant	NM_005766.3(FARP1):c.1266G>A (p.Pro422=)	Malignant melanoma [RCV000070417]	not provided	13	98395328	98395328	Human		name
156063586	CV2272367	single nucleotide variant	NM_005766.4(FARP1):c.449C>T (p.Thr150Met)	not specified [RCV004133293]	uncertain significance	13	98377871	98377871	Human		name
156284067	CV2334734	single nucleotide variant	NM_005766.4(FARP1):c.610A>G (p.Ile204Val)	not specified [RCV004188713]	uncertain significance	13	98384843	98384843	Human		name
156343945	CV2364198	single nucleotide variant	NM_005766.4(FARP1):c.364C>T (p.Pro122Ser)	not specified [RCV004223437]	uncertain significance	13	98368161	98368161	Human		name
401746838	CV2691995	single nucleotide variant	NM_005766.4(FARP1):c.595T>A (p.Phe199Ile)	not specified [RCV004301722]	uncertain significance	13	98384828	98384828	Human		name
401741713	CV2710075	single nucleotide variant	NM_005766.4(FARP1):c.672G>A (p.Met224Ile)	not specified [RCV004315135]	uncertain significance	13	98385727	98385727	Human		name
401721829	CV2710183	single nucleotide variant	NM_005766.4(FARP1):c.662G>A (p.Arg221Gln)	not specified [RCV004315225]	uncertain significance	13	98385717	98385717	Human		name
405762945	CV3253078	single nucleotide variant	NM_005766.4(FARP1):c.304G>A (p.Val102Met)	not specified [RCV004383794]	uncertain significance	13	98365422	98365422	Human		name
407492531	CV3432112	single nucleotide variant	NM_005766.4(FARP1):c.841C>T (p.Arg281Trp)	not specified [RCV004620810]	uncertain significance	13	98388464	98388464	Human		name
407492543	CV3432116	single nucleotide variant	NM_005766.4(FARP1):c.800G>A (p.Arg267Gln)	not specified [RCV004620814]	uncertain significance	13	98388423	98388423	Human		name
407492567	CV3432122	single nucleotide variant	NM_005766.4(FARP1):c.521C>A (p.Ala174Asp)	not specified [RCV004620820]	uncertain significance	13	98384754	98384754	Human		name
407492575	CV3432124	single nucleotide variant	NM_005766.4(FARP1):c.335T>G (p.Val112Gly)	not specified [RCV004620822]	uncertain significance	13	98368132	98368132	Human		name
597695094	CV3672100	single nucleotide variant	NM_005766.4(FARP1):c.842G>A (p.Arg281Gln)	not specified [RCV004915734]	uncertain significance	13	98388465	98388465	Human		name
598213027	CV3966095	single nucleotide variant	NM_005766.4(FARP1):c.589G>A (p.Val197Met)	not specified [RCV005339186]	uncertain significance	13	98384822	98384822	Human		name
598213042	CV3966097	single nucleotide variant	NM_005766.4(FARP1):c.890C>T (p.Ala297Val)	not specified [RCV005339188]	uncertain significance	13	98389991	98389991	Human		name
156400660	CV2199330	single nucleotide variant	NM_005766.4(FARP1):c.1484A>G (p.Asn495Ser)	not specified [RCV004082676]	uncertain significance	13	98409407	98409407	Human		name
156141689	CV2199959	single nucleotide variant	NM_005766.4(FARP1):c.1976G>A (p.Arg659Gln)	not specified [RCV004074130]	uncertain significance	13	98431113	98431113	Human		name
156333532	CV2220847	single nucleotide variant	NM_005766.4(FARP1):c.1264C>G (p.Pro422Ala)	not specified [RCV004092278]	uncertain significance	13	98395326	98395326	Human		name
156293123	CV2233514	single nucleotide variant	NM_005766.4(FARP1):c.2122G>A (p.Ala708Thr)	not specified [RCV004099997]	uncertain significance	13	98431259	98431259	Human		name
156028239	CV2238209	single nucleotide variant	NM_005766.4(FARP1):c.2522G>C (p.Arg841Pro)	not specified [RCV004113301]	uncertain significance	13	98440128	98440128	Human		name
155976856	CV2246097	single nucleotide variant	NM_005766.4(FARP1):c.2870C>G (p.Thr957Arg)	not specified [RCV004114002]	uncertain significance	13	98446171	98446171	Human		name
156208235	CV2250103	single nucleotide variant	NM_005766.4(FARP1):c.1289C>G (p.Pro430Arg)	not specified [RCV004116923]	uncertain significance	13	98395351	98395351	Human		name
155969030	CV2262068	single nucleotide variant	NM_005766.4(FARP1):c.1197A>T (p.Glu399Asp)	not specified [RCV004126542]	uncertain significance	13	98395259	98395259	Human		name
156255579	CV2264739	single nucleotide variant	NM_005766.4(FARP1):c.2837G>A (p.Ser946Asn)	not specified [RCV004132723]	uncertain significance	13	98446138	98446138	Human		name
156367900	CV2266895	single nucleotide variant	NM_005766.4(FARP1):c.1154T>C (p.Val385Ala)	not specified [RCV004131559]	uncertain significance	13	98393708	98393708	Human		name
155973595	CV2269855	single nucleotide variant	NM_005766.4(FARP1):c.2945C>T (p.Ser982Leu)	not specified [RCV004127085]	uncertain significance	13	98446706	98446706	Human		name
156265040	CV2275367	single nucleotide variant	NM_005766.4(FARP1):c.2152G>C (p.Ala718Pro)	not specified [RCV004135252]	uncertain significance	13	98435584	98435584	Human		name
156118166	CV2278982	single nucleotide variant	NM_005766.4(FARP1):c.1685T>C (p.Ile562Thr)	not specified [RCV004145671]	uncertain significance	13	98410816	98410816	Human		name
156004536	CV2290186	single nucleotide variant	NM_005766.4(FARP1):c.1568C>G (p.Pro523Arg)	not specified [RCV004152845]	uncertain significance	13	98409491	98409491	Human		name
156363451	CV2329890	single nucleotide variant	NM_005766.4(FARP1):c.1465G>T (p.Gly489Trp)	not specified [RCV004183348]	uncertain significance	13	98409388	98409388	Human		name
155912582	CV2332385	single nucleotide variant	NM_005766.4(FARP1):c.1831G>A (p.Gly611Ser)	not specified [RCV004182542]	uncertain significance	13	98424576	98424576	Human		name
156071098	CV2337734	single nucleotide variant	NM_005766.4(FARP1):c.2483G>A (p.Arg828Gln)	not specified [RCV004183755]	uncertain significance	13	98440010	98440010	Human		name
156342917	CV2368646	single nucleotide variant	NM_005766.4(FARP1):c.2633C>A (p.Ser878Tyr)	not specified [RCV004221420]	uncertain significance	13	98440673	98440673	Human		name
156346112	CV2373025	single nucleotide variant	NM_005766.4(FARP1):c.2381C>T (p.Thr794Met)	not specified [RCV004224052]	uncertain significance	13	98439144	98439144	Human		name
156211331	CV2378274	single nucleotide variant	NM_005766.4(FARP1):c.1816C>G (p.Leu606Val)	not specified [RCV004226309]	uncertain significance	13	98412024	98412024	Human		name
156134117	CV2383096	single nucleotide variant	NM_005766.4(FARP1):c.1046A>C (p.Asp349Ala)	not specified [RCV004217668]	uncertain significance	13	98390838	98390838	Human		name
155968844	CV2391505	single nucleotide variant	NM_005766.4(FARP1):c.2284C>T (p.Arg762Cys)	not specified [RCV004239891]	uncertain significance	13	98438813	98438813	Human		name
329385135	CV2435269	single nucleotide variant	NM_005766.4(FARP1):c.1469G>T (p.Gly490Val)	not specified [RCV004252902]	uncertain significance	13	98409392	98409392	Human		name
329389255	CV2448834	single nucleotide variant	NM_005766.4(FARP1):c.1574C>T (p.Thr525Met)	not specified [RCV004261520]	uncertain significance	13	98409497	98409497	Human		name
329359646	CV2462154	single nucleotide variant	NM_005766.4(FARP1):c.1741A>G (p.Lys581Glu)	not specified [RCV004266175]	uncertain significance	13	98411949	98411949	Human		name
401719587	CV2675626	single nucleotide variant	NM_005766.4(FARP1):c.2557A>G (p.Met853Val)	not specified [RCV004287882]	uncertain significance	13	98440163	98440163	Human		name
401719837	CV2675697	single nucleotide variant	NM_005766.4(FARP1):c.1595G>A (p.Arg532Gln)	not specified [RCV004287948]	uncertain significance	13	98409518	98409518	Human		name
401761342	CV2689114	single nucleotide variant	NM_005766.4(FARP1):c.1091A>G (p.Lys364Arg)	not specified [RCV004305877]	uncertain significance	13	98393645	98393645	Human		name
401733299	CV2691261	single nucleotide variant	NM_005766.4(FARP1):c.2897C>T (p.Ser966Leu)	not specified [RCV004303025]	uncertain significance	13	98446198	98446198	Human		name
401749082	CV2694563	single nucleotide variant	NM_005766.4(FARP1):c.2764G>A (p.Val922Ile)	not specified [RCV004298688]	uncertain significance	13	98440804	98440804	Human		name
401861902	CV2766488	single nucleotide variant	NM_005766.4(FARP1):c.2719C>T (p.Arg907Cys)	not specified [RCV004347111]	uncertain significance	13	98440759	98440759	Human		name
401897966	CV2769868	single nucleotide variant	NM_005766.4(FARP1):c.1255G>A (p.Ala419Thr)	not specified [RCV004353719]	uncertain significance	13	98395317	98395317	Human		name
401867419	CV2773562	single nucleotide variant	NM_005766.4(FARP1):c.2402T>G (p.Val801Gly)	not specified [RCV004355970]	uncertain significance	13	98439165	98439165	Human		name
401895592	CV2778219	single nucleotide variant	NM_005766.4(FARP1):c.2285G>A (p.Arg762His)	not specified [RCV004349939]	uncertain significance	13	98438814	98438814	Human		name
405762725	CV3253066	single nucleotide variant	NM_005766.4(FARP1):c.1105C>G (p.His369Asp)	not specified [RCV004383782]	uncertain significance	13	98393659	98393659	Human		name
405762878	CV3253067	single nucleotide variant	NM_005766.4(FARP1):c.1460C>T (p.Ser487Leu)	not specified [RCV004383783]	uncertain significance	13	98409383	98409383	Human		name
405762884	CV3253068	single nucleotide variant	NM_005766.4(FARP1):c.1466G>C (p.Gly489Ala)	not specified [RCV004383784]	uncertain significance	13	98409389	98409389	Human		name
405762890	CV3253069	single nucleotide variant	NM_005766.4(FARP1):c.2060A>C (p.His687Pro)	not specified [RCV004383785]	uncertain significance	13	98431197	98431197	Human		name
405762897	CV3253070	single nucleotide variant	NM_005766.4(FARP1):c.2093G>C (p.Arg698Pro)	not specified [RCV004383786]	uncertain significance	13	98431230	98431230	Human		name
405762903	CV3253071	single nucleotide variant	NM_005766.4(FARP1):c.2244T>G (p.Ile748Met)	not specified [RCV004383787]	uncertain significance	13	98435676	98435676	Human		name
405762908	CV3253072	single nucleotide variant	NM_005766.4(FARP1):c.2372G>C (p.Arg791Pro)	not specified [RCV004383788]	uncertain significance	13	98439135	98439135	Human		name
405762920	CV3253074	single nucleotide variant	NM_005766.4(FARP1):c.2648C>G (p.Thr883Ser)	not specified [RCV004383790]	uncertain significance	13	98440688	98440688	Human		name
405762923	CV3253075	single nucleotide variant	NM_005766.4(FARP1):c.2733G>T (p.Met911Ile)	not specified [RCV004383791]	uncertain significance	13	98440773	98440773	Human		name
405762932	CV3253076	single nucleotide variant	NM_005766.4(FARP1):c.2739C>A (p.His913Gln)	not specified [RCV004383792]	uncertain significance	13	98440779	98440779	Human		name
405762939	CV3253077	single nucleotide variant	NM_005766.4(FARP1):c.2890T>C (p.Tyr964His)	not specified [RCV004383793]	uncertain significance	13	98446191	98446191	Human		name
407492534	CV3432113	single nucleotide variant	NM_005766.4(FARP1):c.2417C>T (p.Pro806Leu)	not specified [RCV004620811]	uncertain significance	13	98439180	98439180	Human		name
407492537	CV3432114	single nucleotide variant	NM_005766.4(FARP1):c.1330G>C (p.Ala444Pro)	not specified [RCV004620812]	uncertain significance	13	98395392	98395392	Human		name
407492540	CV3432115	single nucleotide variant	NM_005766.4(FARP1):c.1486G>A (p.Val496Met)	not specified [RCV004620813]	uncertain significance	13	98409409	98409409	Human		name
407492556	CV3432119	single nucleotide variant	NM_005766.4(FARP1):c.1186A>G (p.Thr396Ala)	not specified [RCV004620817]	uncertain significance	13	98395248	98395248	Human		name
407492560	CV3432120	single nucleotide variant	NM_005766.4(FARP1):c.1337C>T (p.Ala446Val)	not specified [RCV004620818]	likely benign	13	98395399	98395399	Human		name
407492571	CV3432123	single nucleotide variant	NM_005766.4(FARP1):c.2083G>C (p.Val695Leu)	not specified [RCV004620821]	uncertain significance	13	98431220	98431220	Human		name
407492579	CV3432125	single nucleotide variant	NM_005766.4(FARP1):c.2788G>A (p.Ala930Thr)	not specified [RCV004620823]	uncertain significance	13	98440828	98440828	Human		name
407492583	CV3432126	single nucleotide variant	NM_005766.4(FARP1):c.1933A>G (p.Ser645Gly)	not specified [RCV004620824]	uncertain significance	13	98431070	98431070	Human		name
597694955	CV3672086	single nucleotide variant	NM_005766.4(FARP1):c.1463A>G (p.Gln488Arg)	not specified [RCV004915721]	uncertain significance	13	98409386	98409386	Human		name
597694965	CV3672087	single nucleotide variant	NM_005766.4(FARP1):c.2114C>T (p.Pro705Leu)	not specified [RCV004915722]	uncertain significance	13	98431251	98431251	Human		name
597694974	CV3672088	single nucleotide variant	NM_005766.4(FARP1):c.2371C>T (p.Arg791Trp)	not specified [RCV004915723]	uncertain significance	13	98439134	98439134	Human		name
597694996	CV3672090	single nucleotide variant	NM_005766.4(FARP1):c.2593G>A (p.Ala865Thr)	not specified [RCV004915725]	likely benign	13	98440199	98440199	Human		name
597695008	CV3672091	single nucleotide variant	NM_005766.4(FARP1):c.2258T>C (p.Leu753Pro)	not specified [RCV004915726]	uncertain significance	13	98435690	98435690	Human		name
597695019	CV3672092	single nucleotide variant	NM_005766.4(FARP1):c.2189C>T (p.Thr730Met)	not specified [RCV004915727]	uncertain significance	13	98435621	98435621	Human		name
597695028	CV3672093	single nucleotide variant	NM_005766.4(FARP1):c.2353G>A (p.Val785Ile)	not specified [RCV004915728]	uncertain significance	13	98439116	98439116	Human		name
597695049	CV3672095	single nucleotide variant	NM_005766.4(FARP1):c.1871G>A (p.Gly624Asp)	not specified [RCV004915730]	uncertain significance	13	98424616	98424616	Human		name
597695059	CV3672097	single nucleotide variant	NM_005766.4(FARP1):c.1784A>T (p.His595Leu)	not specified [RCV004915731]	uncertain significance	13	98411992	98411992	Human		name
597695070	CV3672098	single nucleotide variant	NM_005766.4(FARP1):c.2330G>A (p.Arg777His)	not specified [RCV004915732]	uncertain significance	13	98438859	98438859	Human		name
597695081	CV3672099	single nucleotide variant	NM_005766.4(FARP1):c.1049A>G (p.Tyr350Cys)	not specified [RCV004915733]	uncertain significance	13	98390841	98390841	Human		name
597695103	CV3672101	single nucleotide variant	NM_005766.4(FARP1):c.1706C>G (p.Thr569Arg)	not specified [RCV004915735]	uncertain significance	13	98411914	98411914	Human		name
597695115	CV3672102	single nucleotide variant	NM_005766.4(FARP1):c.1922T>C (p.Leu641Pro)	not specified [RCV004915736]	uncertain significance	13	98431059	98431059	Human		name
597695125	CV3672103	single nucleotide variant	NM_005766.4(FARP1):c.2246G>A (p.Gly749Asp)	not specified [RCV004915737]	uncertain significance	13	98435678	98435678	Human		name
598213009	CV3966092	single nucleotide variant	NM_005766.4(FARP1):c.2843G>T (p.Gly948Val)	not specified [RCV005339183]	uncertain significance	13	98446144	98446144	Human		name
598213015	CV3966093	single nucleotide variant	NM_005766.4(FARP1):c.1529C>T (p.Ser510Phe)	not specified [RCV005339184]	uncertain significance	13	98409452	98409452	Human		name
598213022	CV3966094	single nucleotide variant	NM_005766.4(FARP1):c.1400C>T (p.Pro467Leu)	not specified [RCV005339185]	uncertain significance	13	98395462	98395462	Human		name
598213035	CV3966096	single nucleotide variant	NM_005766.4(FARP1):c.1100A>G (p.Lys367Arg)	not specified [RCV005339187]	uncertain significance	13	98393654	98393654	Human		name
598213050	CV3966098	single nucleotide variant	NM_005766.4(FARP1):c.1216G>C (p.Gly406Arg)	not specified [RCV005339189]	uncertain significance	13	98395278	98395278	Human		name
598213056	CV3966099	single nucleotide variant	NM_005766.4(FARP1):c.1366A>G (p.Lys456Glu)	not specified [RCV005339190]	uncertain significance	13	98395428	98395428	Human		name
598213062	CV3966100	single nucleotide variant	NM_005766.4(FARP1):c.1703G>C (p.Ser568Thr)	not specified [RCV005339191]	uncertain significance	13	98411911	98411911	Human		name
598213069	CV3966101	single nucleotide variant	NM_005766.4(FARP1):c.1196A>G (p.Glu399Gly)	not specified [RCV005339192]	uncertain significance	13	98395258	98395258	Human		name
598213074	CV3966102	single nucleotide variant	NM_005766.4(FARP1):c.1013G>A (p.Arg338Gln)	not specified [RCV005339193]	uncertain significance	13	98390114	98390114	Human		name
598213079	CV3966103	single nucleotide variant	NM_005766.4(FARP1):c.1493T>G (p.Leu498Trp)	not specified [RCV005339194]	uncertain significance	13	98409416	98409416	Human		name
598213084	CV3966104	single nucleotide variant	NM_005766.4(FARP1):c.2243T>C (p.Ile748Thr)	not specified [RCV005339195]	uncertain significance	13	98435675	98435675	Human		name
598213090	CV3966105	single nucleotide variant	NM_005766.4(FARP1):c.2500A>G (p.Ile834Val)	not specified [RCV005339196]	uncertain significance	13	98440027	98440027	Human		name
598213095	CV3966106	single nucleotide variant	NM_005766.4(FARP1):c.2205G>T (p.Glu735Asp)	not specified [RCV005339197]	uncertain significance	13	98435637	98435637	Human		name
329397680	CV2456482	single nucleotide variant	NM_005766.4(FARP1):c.3089C>T (p.Ser1030Phe)	not specified [RCV004275629]	uncertain significance	13	98448268	98448268	Human		name
405762950	CV3253079	single nucleotide variant	NM_005766.4(FARP1):c.3111G>C (p.Leu1037Phe)	not specified [RCV004383795]	uncertain significance	13	98448290	98448290	Human		name
597694985	CV3672089	single nucleotide variant	NM_005766.4(FARP1):c.3098G>A (p.Arg1033Gln)	not specified [RCV004915724]	uncertain significance	13	98448277	98448277	Human		name

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