Fscb Variant Search Result - Rat Genome Database

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101 records found for search term Fscb

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15184501	CV702874	single nucleotide variant	NM_032135.4(FSCB):c.273C>T (p.Thr91=)	not provided [RCV000952723]	benign	14	44506715	44506715	Human		name
155916094	CV2197220	single nucleotide variant	NM_032135.4(FSCB):c.74C>G (p.Pro25Arg)	not specified [RCV004079005]	uncertain significance	14	44506914	44506914	Human		name
156230821	CV2264234	single nucleotide variant	NM_032135.4(FSCB):c.95G>T (p.Gly32Val)	not specified [RCV004138163]	uncertain significance	14	44506893	44506893	Human		name
401735531	CV2672676	single nucleotide variant	NM_032135.4(FSCB):c.91A>G (p.Ile31Val)	not specified [RCV004287691]	uncertain significance	14	44506897	44506897	Human		name
597769195	CV3677370	single nucleotide variant	NM_032135.4(FSCB):c.32T>C (p.Ile11Thr)	not specified [RCV004928042]	likely benign	14	44506956	44506956	Human		name
598231858	CV3966494	single nucleotide variant	NM_032135.4(FSCB):c.59C>A (p.Pro20Gln)	not specified [RCV005342486]	uncertain significance	14	44506929	44506929	Human		name
8635219	CV90441	single nucleotide variant	NM_032135.3(FSCB):c.94G>A (p.Gly32Ser)	Malignant melanoma [RCV000070539]	not provided	14	44506894	44506894	Human		name
401774048	CV2691498	single nucleotide variant	NM_032135.4(FSCB):c.293C>T (p.Ser98Leu)	not specified [RCV004305341]	uncertain significance	14	44506695	44506695	Human		name
401901984	CV2810380	single nucleotide variant	NM_032135.4(FSCB):c.1905G>A (p.Gln635=)	not provided [RCV003393400]	likely benign	14	44505083	44505083	Human		name
405782163	CV3261214	single nucleotide variant	NM_032135.4(FSCB):c.214T>C (p.Ser72Pro)	not specified [RCV004386963]	uncertain significance	14	44506774	44506774	Human		name
598231830	CV3966489	single nucleotide variant	NM_032135.4(FSCB):c.116G>A (p.Gly39Asp)	not specified [RCV005342481]	uncertain significance	14	44506872	44506872	Human		name
598231846	CV3966492	single nucleotide variant	NM_032135.4(FSCB):c.274G>A (p.Val92Met)	not specified [RCV005342484]	uncertain significance	14	44506714	44506714	Human		name
15190696	CV725666	single nucleotide variant	NM_032135.4(FSCB):c.1533A>G (p.Pro511=)	not provided [RCV000888171]	likely benign	14	44505455	44505455	Human		name
156150463	CV2197717	single nucleotide variant	NM_032135.4(FSCB):c.526A>G (p.Lys176Glu)	not specified [RCV004074922]	uncertain significance	14	44506462	44506462	Human		name
156117992	CV2209211	single nucleotide variant	NM_032135.4(FSCB):c.524C>T (p.Thr175Ile)	not specified [RCV004093406]	uncertain significance	14	44506464	44506464	Human		name
156019424	CV2301847	single nucleotide variant	NM_032135.4(FSCB):c.407G>A (p.Arg136His)	not specified [RCV004156641]	uncertain significance	14	44506581	44506581	Human		name
156197940	CV2400802	single nucleotide variant	NM_032135.4(FSCB):c.857C>T (p.Ala286Val)	not specified [RCV004242461]	uncertain significance	14	44506131	44506131	Human		name
329379592	CV2443475	single nucleotide variant	NM_032135.4(FSCB):c.751A>G (p.Lys251Glu)	not specified [RCV004262310]	uncertain significance	14	44506237	44506237	Human		name
401879069	CV2754765	single nucleotide variant	NM_032135.4(FSCB):c.917C>T (p.Ala306Val)	not specified [RCV004341249]	uncertain significance	14	44506071	44506071	Human		name
401860266	CV2765507	single nucleotide variant	NM_032135.4(FSCB):c.505A>G (p.Arg169Gly)	not specified [RCV004341817]	uncertain significance	14	44506483	44506483	Human		name
401865170	CV2768692	single nucleotide variant	NM_032135.4(FSCB):c.383T>A (p.Met128Lys)	not specified [RCV004344538]	uncertain significance	14	44506605	44506605	Human		name
401894682	CV2785175	single nucleotide variant	NM_032135.4(FSCB):c.325C>T (p.Pro109Ser)	not specified [RCV004355169]	uncertain significance	14	44506663	44506663	Human		name
405782169	CV3261215	single nucleotide variant	NM_032135.4(FSCB):c.674G>A (p.Gly225Asp)	not specified [RCV004386964]	likely benign	14	44506314	44506314	Human		name
405782175	CV3261216	single nucleotide variant	NM_032135.4(FSCB):c.737G>T (p.Gly246Val)	not specified [RCV004386965]	uncertain significance	14	44506251	44506251	Human		name
407495523	CV3443124	single nucleotide variant	NM_032135.4(FSCB):c.545T>G (p.Leu182Arg)	not specified [RCV004621616]	likely benign	14	44506443	44506443	Human		name
407495527	CV3443125	single nucleotide variant	NM_032135.4(FSCB):c.370G>A (p.Val124Ile)	not specified [RCV004621617]	uncertain significance	14	44506618	44506618	Human		name
407495549	CV3443130	single nucleotide variant	NM_032135.4(FSCB):c.385G>T (p.Asp129Tyr)	not specified [RCV004621622]	uncertain significance	14	44506603	44506603	Human		name
597741801	CV3677360	single nucleotide variant	NM_032135.4(FSCB):c.399G>C (p.Gln133His)	not specified [RCV004921749]	uncertain significance	14	44506589	44506589	Human		name
597769178	CV3677361	single nucleotide variant	NM_032135.4(FSCB):c.406C>T (p.Arg136Cys)	not specified [RCV004928038]	likely benign	14	44506582	44506582	Human		name
597741837	CV3677376	single nucleotide variant	NM_032135.4(FSCB):c.788A>G (p.Glu263Gly)	not specified [RCV004921757]	uncertain significance	14	44506200	44506200	Human		name
598231825	CV3966488	single nucleotide variant	NM_032135.4(FSCB):c.560C>T (p.Ser187Leu)	not specified [RCV005342480]	uncertain significance	14	44506428	44506428	Human		name
598231877	CV3966497	single nucleotide variant	NM_032135.4(FSCB):c.667A>G (p.Lys223Glu)	not specified [RCV005342489]	uncertain significance	14	44506321	44506321	Human		name
15118136	CV714128	single nucleotide variant	NM_032135.4(FSCB):c.420G>A (p.Trp140Ter)	not provided [RCV000962322]	likely benign	14	44506568	44506568	Human		name
15160662	CV725667	single nucleotide variant	NM_032135.4(FSCB):c.355C>T (p.Pro119Ser)	not provided [RCV000881427]	likely benign	14	44506633	44506633	Human		name
156378725	CV2207787	single nucleotide variant	NM_032135.4(FSCB):c.2014C>G (p.Pro672Ala)	not specified [RCV004084223]	uncertain significance	14	44504974	44504974	Human		name
156152000	CV2209324	single nucleotide variant	NM_032135.4(FSCB):c.1810G>A (p.Glu604Lys)	not specified [RCV004093504]	uncertain significance	14	44505178	44505178	Human		name
156330961	CV2210734	single nucleotide variant	NM_032135.4(FSCB):c.1996G>A (p.Ala666Thr)	not specified [RCV004085832]	uncertain significance	14	44504992	44504992	Human		name
156334912	CV2214836	single nucleotide variant	NM_032135.4(FSCB):c.1858G>A (p.Ala620Thr)	not specified [RCV004090629]	uncertain significance	14	44505130	44505130	Human		name
156295357	CV2239657	single nucleotide variant	NM_032135.4(FSCB):c.2444A>G (p.His815Arg)	not specified [RCV004108207]	uncertain significance	14	44504544	44504544	Human		name
156154718	CV2242349	single nucleotide variant	NM_032135.4(FSCB):c.1492G>A (p.Glu498Lys)	not specified [RCV004111356]	uncertain significance	14	44505496	44505496	Human		name
156273547	CV2247680	single nucleotide variant	NM_032135.4(FSCB):c.1042G>C (p.Ala348Pro)	not specified [RCV004115093]	uncertain significance	14	44505946	44505946	Human		name
156040885	CV2261336	single nucleotide variant	NM_032135.4(FSCB):c.1261C>G (p.Leu421Val)	not specified [RCV004129984]	uncertain significance	14	44505727	44505727	Human		name
156162411	CV2272682	single nucleotide variant	NM_032135.4(FSCB):c.1846G>A (p.Glu616Lys)	not specified [RCV004135344]	uncertain significance	14	44505142	44505142	Human		name
156076587	CV2291533	single nucleotide variant	NM_032135.4(FSCB):c.2064G>T (p.Glu688Asp)	not specified [RCV004155839]	uncertain significance	14	44504924	44504924	Human		name
155940194	CV2294040	single nucleotide variant	NM_032135.4(FSCB):c.1294G>T (p.Ala432Ser)	not specified [RCV004149427]	uncertain significance	14	44505694	44505694	Human		name
155978443	CV2321487	single nucleotide variant	NM_032135.4(FSCB):c.1081G>A (p.Glu361Lys)	not specified [RCV004177458]	uncertain significance	14	44505907	44505907	Human		name
156169198	CV2337349	single nucleotide variant	NM_032135.4(FSCB):c.2032G>T (p.Ala678Ser)	not specified [RCV004187796]	uncertain significance	14	44504956	44504956	Human		name
156067310	CV2356654	single nucleotide variant	NM_032135.4(FSCB):c.1154G>A (p.Arg385Gln)	not provided [RCV004703306]\|not specified [RCV004202016]	likely benign	14	44505834	44505834	Human		name
155931154	CV2361364	single nucleotide variant	NM_032135.4(FSCB):c.2032G>A (p.Ala678Thr)	not specified [RCV004218566]	uncertain significance	14	44504956	44504956	Human		name
156010183	CV2362090	single nucleotide variant	NM_032135.4(FSCB):c.1409C>T (p.Ala470Val)	not provided [RCV004695695]\|not specified [RCV004209897]	uncertain significance	14	44505579	44505579	Human		name
156086919	CV2366337	single nucleotide variant	NM_032135.4(FSCB):c.1153C>T (p.Arg385Trp)	not specified [RCV004212393]	uncertain significance	14	44505835	44505835	Human		name
329361067	CV2436639	single nucleotide variant	NM_032135.4(FSCB):c.1069G>C (p.Glu357Gln)	not specified [RCV004258015]	uncertain significance	14	44505919	44505919	Human		name
329361070	CV2436640	single nucleotide variant	NM_032135.4(FSCB):c.1441G>A (p.Glu481Lys)	not specified [RCV004258016]	uncertain significance	14	44505547	44505547	Human		name
401758394	CV2694081	single nucleotide variant	NM_032135.4(FSCB):c.1163C>T (p.Ser388Leu)	not specified [RCV004302515]	uncertain significance	14	44505825	44505825	Human		name
401719838	CV2705537	single nucleotide variant	NM_032135.4(FSCB):c.1138C>T (p.Leu380Phe)	not specified [RCV004318406]	uncertain significance	14	44505850	44505850	Human		name
401768751	CV2716718	single nucleotide variant	NM_032135.4(FSCB):c.1738T>C (p.Ser580Pro)	not specified [RCV004327766]	likely benign	14	44505250	44505250	Human		name
401737018	CV2717898	single nucleotide variant	NM_032135.4(FSCB):c.1883A>C (p.Glu628Ala)	not specified [RCV004321864]	uncertain significance	14	44505105	44505105	Human		name
401869386	CV2772383	single nucleotide variant	NM_032135.4(FSCB):c.1165G>A (p.Ala389Thr)	not specified [RCV004355180]	uncertain significance	14	44505823	44505823	Human		name
401877323	CV2790129	single nucleotide variant	NM_032135.4(FSCB):c.1028C>T (p.Ser343Phe)	not specified [RCV004364067]	uncertain significance	14	44505960	44505960	Human		name
405782106	CV3261205	single nucleotide variant	NM_032135.4(FSCB):c.1076C>T (p.Pro359Leu)	not specified [RCV004386954]	uncertain significance	14	44505912	44505912	Human		name
405782116	CV3261207	single nucleotide variant	NM_032135.4(FSCB):c.1210G>A (p.Ala404Thr)	not specified [RCV004386956]	uncertain significance	14	44505778	44505778	Human		name
405782123	CV3261208	single nucleotide variant	NM_032135.4(FSCB):c.1243C>T (p.Pro415Ser)	not specified [RCV004386957]	uncertain significance	14	44505745	44505745	Human		name
405782129	CV3261209	single nucleotide variant	NM_032135.4(FSCB):c.2007A>T (p.Glu669Asp)	not specified [RCV004386958]	uncertain significance	14	44504981	44504981	Human		name
405782136	CV3261210	single nucleotide variant	NM_032135.4(FSCB):c.2014C>T (p.Pro672Ser)	not specified [RCV004386959]	likely benign	14	44504974	44504974	Human		name
405782142	CV3261211	single nucleotide variant	NM_032135.4(FSCB):c.2021C>T (p.Pro674Leu)	not specified [RCV004386960]	uncertain significance	14	44504967	44504967	Human		name
405782151	CV3261212	single nucleotide variant	NM_032135.4(FSCB):c.2068A>G (p.Thr690Ala)	not specified [RCV004386961]	likely benign	14	44504920	44504920	Human		name
405782157	CV3261213	single nucleotide variant	NM_032135.4(FSCB):c.2072C>T (p.Pro691Leu)	not specified [RCV004386962]	uncertain significance	14	44504916	44504916	Human		name
407495503	CV3443120	single nucleotide variant	NM_032135.4(FSCB):c.2012A>G (p.Gln671Arg)	not specified [RCV004621612]	uncertain significance	14	44504976	44504976	Human		name
407495508	CV3443121	single nucleotide variant	NM_032135.4(FSCB):c.1964C>T (p.Pro655Leu)	not specified [RCV004621613]	uncertain significance	14	44505024	44505024	Human		name
407495513	CV3443122	single nucleotide variant	NM_032135.4(FSCB):c.2006A>G (p.Glu669Gly)	not specified [RCV004621614]	uncertain significance	14	44504982	44504982	Human		name
407495531	CV3443126	single nucleotide variant	NM_032135.4(FSCB):c.1891C>T (p.Pro631Ser)	not specified [RCV004621618]	uncertain significance	14	44505097	44505097	Human		name
407495536	CV3443127	single nucleotide variant	NM_032135.4(FSCB):c.1782G>C (p.Gln594His)	not specified [RCV004621619]	uncertain significance	14	44505206	44505206	Human		name
407495540	CV3443128	single nucleotide variant	NM_032135.4(FSCB):c.1174G>T (p.Ala392Ser)	not specified [RCV004621620]	uncertain significance	14	44505814	44505814	Human		name
407495544	CV3443129	single nucleotide variant	NM_032135.4(FSCB):c.1517C>A (p.Ala506Asp)	not specified [RCV004621621]	uncertain significance	14	44505471	44505471	Human		name
407495553	CV3443131	single nucleotide variant	NM_032135.4(FSCB):c.1837C>A (p.Pro613Thr)	not specified [RCV004621623]	uncertain significance	14	44505151	44505151	Human		name
407495933	CV3443132	single nucleotide variant	NM_032135.4(FSCB):c.1562C>T (p.Ala521Val)	not specified [RCV004621624]	uncertain significance	14	44505426	44505426	Human		name
407495563	CV3443133	single nucleotide variant	NM_032135.4(FSCB):c.1898A>G (p.Glu633Gly)	not specified [RCV004621625]	uncertain significance	14	44505090	44505090	Human		name
597769172	CV3677357	single nucleotide variant	NM_032135.4(FSCB):c.1384C>T (p.Pro462Ser)	not specified [RCV004928037]	uncertain significance	14	44505604	44505604	Human		name
597741792	CV3677358	single nucleotide variant	NM_032135.4(FSCB):c.2014C>A (p.Pro672Thr)	not specified [RCV004921747]	uncertain significance	14	44504974	44504974	Human		name
597741796	CV3677359	single nucleotide variant	NM_032135.4(FSCB):c.2033C>A (p.Ala678Asp)	not specified [RCV004921748]	uncertain significance	14	44504955	44504955	Human		name
597741805	CV3677362	single nucleotide variant	NM_032135.4(FSCB):c.2009T>C (p.Val670Ala)	not specified [RCV004921750]	uncertain significance	14	44504979	44504979	Human		name
597741810	CV3677363	single nucleotide variant	NM_032135.4(FSCB):c.1175C>T (p.Ala392Val)	not specified [RCV004921751]	uncertain significance	14	44505813	44505813	Human		name
597741815	CV3677364	single nucleotide variant	NM_032135.4(FSCB):c.1343C>T (p.Thr448Ile)	not specified [RCV004921752]	uncertain significance	14	44505645	44505645	Human		name
597741819	CV3677365	single nucleotide variant	NM_032135.4(FSCB):c.1297C>T (p.Pro433Ser)	not specified [RCV004921753]	uncertain significance	14	44505691	44505691	Human		name
597769182	CV3677366	single nucleotide variant	NM_032135.4(FSCB):c.2017C>A (p.Pro673Thr)	not specified [RCV004928039]	uncertain significance	14	44504971	44504971	Human		name
597741823	CV3677367	single nucleotide variant	NM_032135.4(FSCB):c.1489G>A (p.Glu497Lys)	not specified [RCV004921754]	uncertain significance	14	44505499	44505499	Human		name
597769186	CV3677368	single nucleotide variant	NM_032135.4(FSCB):c.1597G>T (p.Ala533Ser)	not specified [RCV004928040]	uncertain significance	14	44505391	44505391	Human		name
597769190	CV3677369	single nucleotide variant	NM_032135.4(FSCB):c.2059G>A (p.Ala687Thr)	not specified [RCV004928041]	uncertain significance	14	44504929	44504929	Human		name
597741828	CV3677371	single nucleotide variant	NM_032135.4(FSCB):c.2062G>A (p.Glu688Lys)	not specified [RCV004921755]	uncertain significance	14	44504926	44504926	Human		name
597741833	CV3677372	single nucleotide variant	NM_032135.4(FSCB):c.1439C>T (p.Thr480Met)	not specified [RCV004921756]	uncertain significance	14	44505549	44505549	Human		name
597769200	CV3677373	single nucleotide variant	NM_032135.4(FSCB):c.1030G>T (p.Val344Leu)	not specified [RCV004928043]	uncertain significance	14	44505958	44505958	Human		name
597769209	CV3677377	single nucleotide variant	NM_032135.4(FSCB):c.1345C>G (p.Pro449Ala)	not specified [RCV004928045]	uncertain significance	14	44505643	44505643	Human		name
597741842	CV3677378	single nucleotide variant	NM_032135.4(FSCB):c.2056C>T (p.Pro686Ser)	not specified [RCV004921758]	uncertain significance	14	44504932	44504932	Human		name
598231836	CV3966490	single nucleotide variant	NM_032135.4(FSCB):c.1071G>T (p.Glu357Asp)	not specified [RCV005342482]	uncertain significance	14	44505917	44505917	Human		name
598231841	CV3966491	single nucleotide variant	NM_032135.4(FSCB):c.2043A>T (p.Glu681Asp)	not specified [RCV005342483]	uncertain significance	14	44504945	44504945	Human		name
598231853	CV3966493	single nucleotide variant	NM_032135.4(FSCB):c.2275G>C (p.Glu759Gln)	not specified [RCV005342485]	uncertain significance	14	44504713	44504713	Human		name
598231865	CV3966495	single nucleotide variant	NM_032135.4(FSCB):c.2150A>T (p.His717Leu)	not specified [RCV005342487]	uncertain significance	14	44504838	44504838	Human		name
598231870	CV3966496	single nucleotide variant	NM_032135.4(FSCB):c.1306G>C (p.Glu436Gln)	not specified [RCV005342488]	uncertain significance	14	44505682	44505682	Human		name
598231884	CV3966498	single nucleotide variant	NM_032135.4(FSCB):c.1249G>A (p.Val417Ile)	not specified [RCV005342490]	uncertain significance	14	44505739	44505739	Human		name
15200023	CV702872	deletion	NM_032135.4(FSCB):c.2032_2067del (p.Ala678_Glu689del)	not provided [RCV000957210]	likely benign	14	44504921	44504956	Human		name
15160840	CV702873	microsatellite	NM_032135.4(FSCB):c.2036_2037insCTCTGAAGTTCAGCCTCCACCAGCTGAGGAGGCCCC (p.Pro679_Ala680insSerGluValGlnProProProAlaGluGluAlaPro)	not provided [RCV000947564]	benign	14	44504951	44504952	Human		name

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