Ifit1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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89 records found for search term Ifit1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405792078	CV3267437	single nucleotide variant	NM_001548.5(IFIT1):c.7A>C (p.Thr3Pro)	not specified [RCV004400073]	uncertain significance	10	89402282	89402282	Human		name
401889639	CV2766778	single nucleotide variant	NM_001548.5(IFIT1):c.17A>T (p.Asp6Val)	not specified [RCV004349167]	uncertain significance	10	89402292	89402292	Human		name
15156540	CV724111	single nucleotide variant	NM_001548.5(IFIT1):c.141C>T (p.Asp47=)	not provided [RCV000880650]	benign	10	89402416	89402416	Human		name
401855857	CV2757557	single nucleotide variant	NM_001548.5(IFIT1):c.43G>C (p.Glu15Gln)	not specified [RCV004340931]	uncertain significance	10	89402318	89402318	Human		name
405792059	CV3267431	single nucleotide variant	NM_001548.5(IFIT1):c.31A>G (p.Lys11Glu)	not specified [RCV004400067]	uncertain significance	10	89402306	89402306	Human		name
156239111	CV2217178	single nucleotide variant	NM_001548.5(IFIT1):c.290C>T (p.Thr97Ile)	not specified [RCV004087635]	uncertain significance	10	89402565	89402565	Human		name
329353536	CV2466852	single nucleotide variant	NM_001548.5(IFIT1):c.149A>G (p.Tyr50Cys)	not specified [RCV004282627]	uncertain significance	10	89402424	89402424	Human		name
401756344	CV2687101	single nucleotide variant	NM_001548.5(IFIT1):c.163C>T (p.His55Tyr)	not specified [RCV004304413]	uncertain significance	10	89402438	89402438	Human		name
598206497	CV3979170	single nucleotide variant	NM_001548.5(IFIT1):c.128T>C (p.Ile43Thr)	not specified [RCV005337794]	uncertain significance	10	89402403	89402403	Human		name
156246241	CV2196173	single nucleotide variant	NM_001548.5(IFIT1):c.779T>A (p.Phe260Tyr)	not specified [RCV004073531]	uncertain significance	10	89403054	89403054	Human		name
156149320	CV2200910	single nucleotide variant	NM_001548.5(IFIT1):c.933A>T (p.Arg311Ser)	not specified [RCV004081526]	uncertain significance	10	89403208	89403208	Human		name
156248473	CV2222001	single nucleotide variant	NM_001548.5(IFIT1):c.398G>A (p.Arg133His)	not specified [RCV004599462]	uncertain significance	10	89402673	89402673	Human		name
155941574	CV2229197	single nucleotide variant	NM_001548.5(IFIT1):c.808G>A (p.Ala270Thr)	not specified [RCV004101016]	uncertain significance	10	89403083	89403083	Human		name
155968945	CV2312902	single nucleotide variant	NM_001548.5(IFIT1):c.832T>G (p.Leu278Val)	not specified [RCV004171388]	uncertain significance	10	89403107	89403107	Human		name
155986060	CV2345457	single nucleotide variant	NM_001548.5(IFIT1):c.341C>T (p.Ala114Val)	not specified [RCV004198229]	uncertain significance	10	89402616	89402616	Human		name
156216613	CV2386081	single nucleotide variant	NM_001548.5(IFIT1):c.365A>G (p.Glu122Gly)	not specified [RCV004229138]	uncertain significance	10	89402640	89402640	Human		name
329372751	CV2428635	single nucleotide variant	NM_001548.5(IFIT1):c.730C>G (p.Leu244Val)	not specified [RCV004255436]	uncertain significance	10	89403005	89403005	Human		name
401781794	CV2678287	single nucleotide variant	NM_001548.5(IFIT1):c.427T>C (p.Cys143Arg)	not specified [RCV004290282]	uncertain significance	10	89402702	89402702	Human		name
401753974	CV2685121	single nucleotide variant	NM_001548.5(IFIT1):c.545C>T (p.Ala182Val)	not specified [RCV004289689]	uncertain significance	10	89402820	89402820	Human		name
401745423	CV2728995	single nucleotide variant	NM_001548.5(IFIT1):c.785G>A (p.Arg262Gln)	not specified [RCV004331694]	uncertain significance	10	89403060	89403060	Human		name
405792062	CV3267432	single nucleotide variant	NM_001548.5(IFIT1):c.476G>A (p.Arg159Gln)	not specified [RCV004400068]	uncertain significance	10	89402751	89402751	Human		name
405792065	CV3267433	single nucleotide variant	NM_001548.5(IFIT1):c.613C>T (p.Pro205Ser)	not specified [RCV004400069]	uncertain significance	10	89402888	89402888	Human		name
405792068	CV3267434	single nucleotide variant	NM_001548.5(IFIT1):c.665T>G (p.Leu222Arg)	not specified [RCV004400070]	uncertain significance	10	89402940	89402940	Human		name
405792072	CV3267435	single nucleotide variant	NM_001548.5(IFIT1):c.748C>G (p.Gln250Glu)	not specified [RCV004400071]	uncertain significance	10	89403023	89403023	Human		name
405792075	CV3267436	single nucleotide variant	NM_001548.5(IFIT1):c.770C>T (p.Ala257Val)	not specified [RCV004400072]	uncertain significance	10	89403045	89403045	Human		name
407466167	CV3440550	single nucleotide variant	NM_001548.5(IFIT1):c.508G>A (p.Val170Met)	not specified [RCV004635561]	uncertain significance	10	89402783	89402783	Human		name
597763181	CV3683225	single nucleotide variant	NM_001548.5(IFIT1):c.661G>T (p.Val221Phe)	not specified [RCV004926275]	uncertain significance	10	89402936	89402936	Human		name
597763191	CV3683227	single nucleotide variant	NM_001548.5(IFIT1):c.364G>A (p.Glu122Lys)	not specified [RCV004926277]	uncertain significance	10	89402639	89402639	Human		name
597763196	CV3683228	single nucleotide variant	NM_001548.5(IFIT1):c.892C>G (p.Gln298Glu)	not specified [RCV004926278]	uncertain significance	10	89403167	89403167	Human		name
597763199	CV3683229	single nucleotide variant	NM_001548.5(IFIT1):c.343C>G (p.Gln115Glu)	not specified [RCV004926279]	uncertain significance	10	89402618	89402618	Human		name
597763208	CV3683231	single nucleotide variant	NM_001548.5(IFIT1):c.655A>G (p.Ile219Val)	not specified [RCV004926281]	uncertain significance	10	89402930	89402930	Human		name
598267924	CV3979172	single nucleotide variant	NM_001548.5(IFIT1):c.981T>G (p.Phe327Leu)	not specified [RCV005349601]	uncertain significance	10	89403256	89403256	Human		name
405792047	CV3267427	single nucleotide variant	NM_001548.5(IFIT1):c.1039G>A (p.Ala347Thr)	not specified [RCV004400063]	uncertain significance	10	89403314	89403314	Human		name
405792050	CV3267428	single nucleotide variant	NM_001548.5(IFIT1):c.1042A>G (p.Arg348Gly)	not specified [RCV004400064]	uncertain significance	10	89403317	89403317	Human		name
405792053	CV3267429	single nucleotide variant	NM_001548.5(IFIT1):c.1049A>G (p.Tyr350Cys)	not specified [RCV004400065]	uncertain significance	10	89403324	89403324	Human		name
405792056	CV3267430	single nucleotide variant	NM_001548.5(IFIT1):c.1181C>A (p.Ser394Tyr)	not specified [RCV004400066]	uncertain significance	10	89403456	89403456	Human		name
407466171	CV3440551	single nucleotide variant	NM_001548.5(IFIT1):c.1167A>C (p.Glu389Asp)	not specified [RCV004635562]	uncertain significance	10	89403442	89403442	Human		name
597763186	CV3683226	single nucleotide variant	NM_001548.5(IFIT1):c.1196T>G (p.Ile399Ser)	not specified [RCV004926276]	uncertain significance	10	89403471	89403471	Human		name
597763204	CV3683230	single nucleotide variant	NM_001548.5(IFIT1):c.1192G>A (p.Ala398Thr)	not specified [RCV004926280]	uncertain significance	10	89403467	89403467	Human		name
597763213	CV3683232	single nucleotide variant	NM_001548.5(IFIT1):c.1190A>G (p.Asn397Ser)	not specified [RCV004926282]	uncertain significance	10	89403465	89403465	Human		name
598267930	CV3979173	single nucleotide variant	NM_001548.5(IFIT1):c.1381G>A (p.Glu461Lys)	not specified [RCV005349602]	uncertain significance	10	89403656	89403656	Human		name
407466183	CV3440554	single nucleotide variant	NM_001010987.2(IFIT1B):c.24G>C (p.Lys8Asn)	not specified [RCV004635565]	likely benign	10	89383337	89383337	Human		name
156247279	CV2396885	single nucleotide variant	NM_001010987.2(IFIT1B):c.149A>G (p.Tyr50Cys)	not specified [RCV004234009]	uncertain significance	10	89383462	89383462	Human		name
405792098	CV3267444	single nucleotide variant	NM_001010987.2(IFIT1B):c.181G>T (p.Val61Leu)	not specified [RCV004400080]	uncertain significance	10	89383494	89383494	Human		name
597763231	CV3683237	single nucleotide variant	NM_001010987.2(IFIT1B):c.235G>A (p.Glu79Lys)	not specified [RCV004926286]	uncertain significance	10	89383548	89383548	Human		name
597763243	CV3683240	single nucleotide variant	NM_001010987.2(IFIT1B):c.278G>A (p.Arg93Lys)	not specified [RCV004926289]	uncertain significance	10	89383591	89383591	Human		name
598267958	CV3979180	single nucleotide variant	NM_001010987.2(IFIT1B):c.260C>A (p.Ala87Asp)	not specified [RCV005349607]	uncertain significance	10	89383573	89383573	Human		name
156136521	CV2284822	single nucleotide variant	NM_001010987.2(IFIT1B):c.625G>T (p.Ala209Ser)	not specified [RCV004142997]	uncertain significance	10	89383938	89383938	Human		name
156174832	CV2345971	single nucleotide variant	NM_001010987.2(IFIT1B):c.871A>G (p.Met291Val)	not specified [RCV004199005]	uncertain significance	10	89384184	89384184	Human		name
155905804	CV2357187	single nucleotide variant	NM_001010987.2(IFIT1B):c.559C>T (p.Arg187Cys)	not specified [RCV004206973]	uncertain significance	10	89383872	89383872	Human		name
156255586	CV2359422	single nucleotide variant	NM_001010987.2(IFIT1B):c.578C>T (p.Thr193Ile)	not specified [RCV004214744]	likely benign	10	89383891	89383891	Human		name
329398953	CV2471812	single nucleotide variant	NM_001010987.2(IFIT1B):c.921C>G (p.Asn307Lys)	not specified [RCV004280849]	uncertain significance	10	89384234	89384234	Human		name
401727488	CV2681056	single nucleotide variant	NM_001010987.2(IFIT1B):c.407T>C (p.Met136Thr)	not specified [RCV004296117]	uncertain significance	10	89383720	89383720	Human		name
401733010	CV2685399	single nucleotide variant	NM_001010987.2(IFIT1B):c.899T>C (p.Ile300Thr)	not specified [RCV004294434]	uncertain significance	10	89384212	89384212	Human		name
401740255	CV2705938	single nucleotide variant	NM_001010987.2(IFIT1B):c.436G>C (p.Gly146Arg)	not specified [RCV004320863]	uncertain significance	10	89383749	89383749	Human		name
401874469	CV2773983	single nucleotide variant	NM_001010987.2(IFIT1B):c.934G>A (p.Gly312Arg)	not specified [RCV004358395]	uncertain significance	10	89384247	89384247	Human		name
401884851	CV2786597	single nucleotide variant	NM_001010987.2(IFIT1B):c.781T>C (p.Tyr261His)	not specified [RCV004363737]	uncertain significance	10	89384094	89384094	Human		name
405792101	CV3267445	single nucleotide variant	NM_001010987.2(IFIT1B):c.334G>A (p.Ala112Thr)	not specified [RCV004400081]	uncertain significance	10	89383647	89383647	Human		name
405792103	CV3267446	single nucleotide variant	NM_001010987.2(IFIT1B):c.411G>C (p.Glu137Asp)	not specified [RCV004400082]	uncertain significance	10	89383724	89383724	Human		name
405792107	CV3267447	single nucleotide variant	NM_001010987.2(IFIT1B):c.492T>G (p.Phe164Leu)	not specified [RCV004400083]	uncertain significance	10	89383805	89383805	Human		name
405792110	CV3267448	single nucleotide variant	NM_001010987.2(IFIT1B):c.545C>T (p.Ala182Val)	not specified [RCV004400084]	uncertain significance	10	89383858	89383858	Human		name
405792116	CV3267450	single nucleotide variant	NM_001010987.2(IFIT1B):c.832T>G (p.Leu278Val)	not specified [RCV004400086]	uncertain significance	10	89384145	89384145	Human		name
407466175	CV3440552	single nucleotide variant	NM_001010987.2(IFIT1B):c.634C>A (p.Leu212Ile)	not specified [RCV004635563]	uncertain significance	10	89383947	89383947	Human		name
597763221	CV3683234	single nucleotide variant	NM_001010987.2(IFIT1B):c.338A>C (p.Glu113Ala)	not specified [RCV004926284]	uncertain significance	10	89383651	89383651	Human		name
597763226	CV3683236	single nucleotide variant	NM_001010987.2(IFIT1B):c.571T>C (p.Phe191Leu)	not specified [RCV004926285]	uncertain significance	10	89383884	89383884	Human		name
597763236	CV3683238	single nucleotide variant	NM_001010987.2(IFIT1B):c.653A>G (p.Tyr218Cys)	not specified [RCV004926287]	uncertain significance	10	89383966	89383966	Human		name
597763239	CV3683239	single nucleotide variant	NM_001010987.2(IFIT1B):c.793G>C (p.Gly265Arg)	not specified [RCV004926288]	uncertain significance	10	89384106	89384106	Human		name
597763248	CV3683241	single nucleotide variant	NM_001010987.2(IFIT1B):c.906C>G (p.Ile302Met)	not specified [RCV004926290]	uncertain significance	10	89384219	89384219	Human		name
598267935	CV3979174	single nucleotide variant	NM_001010987.2(IFIT1B):c.788G>C (p.Arg263Thr)	not specified [RCV005349603]	uncertain significance	10	89384101	89384101	Human		name
598267940	CV3979175	single nucleotide variant	NM_001010987.2(IFIT1B):c.890C>T (p.Ala297Val)	not specified [RCV005349604]	uncertain significance	10	89384203	89384203	Human		name
598267951	CV3979177	single nucleotide variant	NM_001010987.2(IFIT1B):c.437G>A (p.Gly146Glu)	not specified [RCV005349606]	uncertain significance	10	89383750	89383750	Human		name
598206507	CV3979179	single nucleotide variant	NM_001010987.2(IFIT1B):c.347C>A (p.Thr116Asn)	not specified [RCV005337796]	uncertain significance	10	89383660	89383660	Human		name
15106264	CV724110	single nucleotide variant	NM_001010987.2(IFIT1B):c.563T>C (p.Leu188Pro)	not provided [RCV000893246]	benign	10	89383876	89383876	Human		name
155969300	CV2213311	single nucleotide variant	NM_001010987.2(IFIT1B):c.1223T>G (p.Ile408Arg)	not specified [RCV004085522]	uncertain significance	10	89384536	89384536	Human		name
155974921	CV2235792	single nucleotide variant	NM_001010987.2(IFIT1B):c.1138A>T (p.Ile380Phe)	not specified [RCV004111916]	uncertain significance	10	89384451	89384451	Human		name
156329677	CV2342439	single nucleotide variant	NM_001010987.2(IFIT1B):c.1381G>A (p.Glu461Lys)	not specified [RCV004194044]	uncertain significance	10	89384694	89384694	Human		name
401778518	CV2709209	single nucleotide variant	NM_001010987.2(IFIT1B):c.1157G>A (p.Arg386His)	not specified [RCV004316381]	uncertain significance	10	89384470	89384470	Human		name
401884848	CV2786596	single nucleotide variant	NM_001010987.2(IFIT1B):c.1177A>C (p.Lys393Gln)	not specified [RCV004363736]	uncertain significance	10	89384490	89384490	Human		name
405792081	CV3267438	single nucleotide variant	NM_001010987.2(IFIT1B):c.1003T>A (p.Leu335Ile)	not specified [RCV004400074]	uncertain significance	10	89384316	89384316	Human		name
405792083	CV3267439	single nucleotide variant	NM_001010987.2(IFIT1B):c.1166A>C (p.Glu389Ala)	not specified [RCV004400075]	uncertain significance	10	89384479	89384479	Human		name
405792086	CV3267440	single nucleotide variant	NM_001010987.2(IFIT1B):c.1283G>T (p.Arg428Ile)	not specified [RCV004400076]	uncertain significance	10	89384596	89384596	Human		name
405792089	CV3267441	single nucleotide variant	NM_001010987.2(IFIT1B):c.1309G>A (p.Val437Met)	not specified [RCV004400077]	uncertain significance	10	89384622	89384622	Human		name
405792092	CV3267442	single nucleotide variant	NM_001010987.2(IFIT1B):c.1333C>T (p.Leu445Phe)	not specified [RCV004400078]	likely benign	10	89384646	89384646	Human		name
405792095	CV3267443	single nucleotide variant	NM_001010987.2(IFIT1B):c.1352G>A (p.Gly451Glu)	not specified [RCV004400079]	uncertain significance	10	89384665	89384665	Human		name
407475602	CV3494739	single nucleotide variant	NM_001010987.2(IFIT1B):c.1102C>T (p.Arg368Cys)	not specified [RCV004690638]	likely benign	10	89384415	89384415	Human		name
597763218	CV3683233	single nucleotide variant	NM_001010987.2(IFIT1B):c.1046C>T (p.Thr349Met)	not specified [RCV004926283]	likely benign	10	89384359	89384359	Human		name
598267946	CV3979176	single nucleotide variant	NM_001010987.2(IFIT1B):c.1417A>G (p.Ile473Val)	not specified [RCV005349605]	uncertain significance	10	89384730	89384730	Human		name
598206502	CV3979178	single nucleotide variant	NM_001010987.2(IFIT1B):c.1354G>C (p.Glu452Gln)	not specified [RCV005337795]	uncertain significance	10	89384667	89384667	Human		name
14696135	CV612403	single nucleotide variant	NM_001010987.2(IFIT1B):c.1153G>A (p.Gly385Ser)	High myopia [RCV000785681]	uncertain significance	10	89384466	89384466	Human	2	name

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