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Variants search result for Homo sapiens
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57 records found for search term Ifi44l
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401927873CV2808974single nucleotide variantNM_006820.4(IFI44L):c.1325-2A>Gnot provided [RCV003406572]uncertain significance17864177378641773Humanname
15153258CV758929single nucleotide variantNM_006820.4(IFI44L):c.528-10A>Gnot provided [RCV000924027]likely benign17862971078629710Humanname
401927871CV2808973single nucleotide variantNM_006820.4(IFI44L):c.99T>C (p.His33=)not provided [RCV003406571]likely benign17862801478628014Humanname
155985939CV2282464single nucleotide variantNM_006820.4(IFI44L):c.14C>T (p.Thr5Ile)not specified [RCV004133267]uncertain significance17862792978627929Humanname
155927843CV2218484single nucleotide variantNM_006820.4(IFI44L):c.61A>T (p.Asn21Tyr)not specified [RCV004090764]uncertain significance17862797678627976Humanname
156306245CV2359887single nucleotide variantNM_006820.4(IFI44L):c.98A>C (p.His33Pro)not specified [RCV004212738]uncertain significance17862801378628013Humanname
401781502CV2682019single nucleotide variantNM_006820.4(IFI44L):c.56T>A (p.Leu19His)not specified [RCV004290086]uncertain significance17862797178627971Humanname
156166602CV2283971single nucleotide variantNM_006820.4(IFI44L):c.173A>G (p.Tyr58Cys)not specified [RCV004144280]uncertain significance17862808878628088Humanname
155980739CV2336956single nucleotide variantNM_006820.4(IFI44L):c.107G>A (p.Ser36Asn)not specified [RCV004192730]uncertain significance17862802278628022Humanname
329395882CV2454674single nucleotide variantNM_006820.4(IFI44L):c.122T>C (p.Val41Ala)not specified [RCV004268126]uncertain significance17862803778628037Humanname
405792009CV3267415single nucleotide variantNM_006820.4(IFI44L):c.137G>A (p.Arg46His)not specified [RCV004400051]likely benign17862805278628052Humanname
597763160CV3683212single nucleotide variantNM_006820.4(IFI44L):c.211A>G (p.Asn71Asp)not specified [RCV004926270]uncertain significance17862812678628126Humanname
598267882CV3979161single nucleotide variantNM_006820.4(IFI44L):c.278C>G (p.Thr93Ser)not specified [RCV005349593]uncertain significance17862819378628193Humanname
15176120CV707527single nucleotide variantNM_006820.4(IFI44L):c.176A>G (p.Asn59Ser)not provided [RCV000973112]likely benign17862809178628091Humanname
15112114CV719094single nucleotide variantNM_006820.4(IFI44L):c.1317G>A (p.Glu439=)not provided [RCV000894403]benign17864160278641602Humanname
150534799CV1311624single nucleotide variantNM_006820.4(IFI44L):c.873T>A (p.Tyr291Ter)Multisystem inflammatory syndrome in children [RCV001779434]risk factor17863548678635486Human1name
156248237CV2203070single nucleotide variantNM_006820.4(IFI44L):c.958G>A (p.Ala320Thr)not specified [RCV004069318]uncertain significance17863711378637113Humanname
156186756CV2232695single nucleotide variantNM_006820.4(IFI44L):c.502A>G (p.Ile168Val)not specified [RCV004101355]uncertain significance17862897478628974Humanname
156185176CV2239370single nucleotide variantNM_006820.4(IFI44L):c.932C>G (p.Ser311Cys)not specified [RCV004114105]uncertain significance17863708778637087Humanname
156297622CV2240874single nucleotide variantNM_006820.4(IFI44L):c.443G>A (p.Arg148His)not specified [RCV004102163]uncertain significance17862835878628358Humanname
155915763CV2339202single nucleotide variantNM_006820.4(IFI44L):c.475G>C (p.Glu159Gln)not specified [RCV004191446]uncertain significance17862839078628390Humanname
329385555CV2462035single nucleotide variantNM_006820.4(IFI44L):c.953G>C (p.Cys318Ser)not specified [RCV004272213]uncertain significance17863710878637108Humanname
401731253CV2674312single nucleotide variantNM_006820.4(IFI44L):c.818G>T (p.Gly273Val)not specified [RCV004289190]uncertain significance17863543178635431Humanname
401749200CV2692996single nucleotide variantNM_006820.4(IFI44L):c.550G>C (p.Asp184His)not specified [RCV004306505]uncertain significance17862974278629742Humanname
401778503CV2732571single nucleotide variantNM_006820.4(IFI44L):c.817G>A (p.Gly273Arg)not specified [RCV004332581]uncertain significance17863543078635430Humanname
405792012CV3267416single nucleotide variantNM_006820.4(IFI44L):c.317A>G (p.Lys106Arg)not specified [RCV004400052]uncertain significance17862823278628232Humanname
405792015CV3267417single nucleotide variantNM_006820.4(IFI44L):c.779T>G (p.Leu260Trp)not specified [RCV004400053]uncertain significance17863539278635392Humanname
407466149CV3440546single nucleotide variantNM_006820.4(IFI44L):c.530A>G (p.His177Arg)not specified [RCV004635557]uncertain significance17862972278629722Humanname
597763126CV3683204single nucleotide variantNM_006820.4(IFI44L):c.443G>T (p.Arg148Leu)not specified [RCV004926263]likely benign17862835878628358Humanname
597763131CV3683205single nucleotide variantNM_006820.4(IFI44L):c.718G>A (p.Glu240Lys)not specified [RCV004926264]uncertain significance17862991078629910Humanname
597763140CV3683208single nucleotide variantNM_006820.4(IFI44L):c.470G>A (p.Arg157Gln)not specified [RCV004926266]uncertain significance17862838578628385Humanname
597763144CV3683209single nucleotide variantNM_006820.4(IFI44L):c.646T>C (p.Ser216Pro)not specified [RCV004926267]uncertain significance17862983878629838Humanname
597763150CV3683210single nucleotide variantNM_006820.4(IFI44L):c.886C>A (p.Arg296Ser)not specified [RCV004926268]uncertain significance17863704178637041Humanname
597763155CV3683211single nucleotide variantNM_006820.4(IFI44L):c.305A>G (p.Asn102Ser)not specified [RCV004926269]uncertain significance17862822078628220Humanname
597763164CV3683213single nucleotide variantNM_006820.4(IFI44L):c.991C>A (p.Leu331Ile)not specified [RCV004926271]uncertain significance17863714678637146Humanname
598267862CV3979158single nucleotide variantNM_006820.4(IFI44L):c.811G>A (p.Gly271Arg)not specified [RCV005349590]uncertain significance17863542478635424Humanname
598267887CV3979162single nucleotide variantNM_006820.4(IFI44L):c.356C>A (p.Thr119Lys)not specified [RCV005349594]uncertain significance17862827178628271Humanname
15153323CV707528single nucleotide variantNM_006820.4(IFI44L):c.442C>T (p.Arg148Cys)not provided [RCV000968523]benign17862835778628357Humanname
15112108CV719093single nucleotide variantNM_006820.4(IFI44L):c.887G>A (p.Arg296His)not provided [RCV000894402]benign17863704278637042Humanname
156028310CV2238216single nucleotide variantNM_006820.4(IFI44L):c.1301A>G (p.Glu434Gly)not specified [RCV004113308]uncertain significance17864158678641586Humanname
156166437CV2270416single nucleotide variantNM_006820.4(IFI44L):c.1280G>A (p.Arg427Gln)not specified [RCV004137393]uncertain significance17864156578641565Humanname
155992420CV2281205single nucleotide variantNM_006820.4(IFI44L):c.1091G>A (p.Ser364Asn)not specified [RCV004147455]uncertain significance17864106378641063Humanname
156326956CV2332031single nucleotide variantNM_006820.4(IFI44L):c.1340C>T (p.Ala447Val)not specified [RCV004189085]likely benign17864179078641790Humanname
156008797CV2361914single nucleotide variantNM_006820.4(IFI44L):c.1081G>A (p.Asp361Asn)not specified [RCV004207687]likely benign17864105378641053Humanname
329362234CV2448450single nucleotide variantNM_006820.4(IFI44L):c.1198A>T (p.Met400Leu)not specified [RCV004256729]uncertain significance17864148378641483Humanname
329374217CV2463441single nucleotide variantNM_006820.4(IFI44L):c.1282G>T (p.Ala428Ser)not specified [RCV004277273]uncertain significance17864156778641567Humanname
401732198CV2708714single nucleotide variantNM_006820.4(IFI44L):c.1005G>A (p.Met335Ile)not specified [RCV004307686]uncertain significance17863716078637160Humanname
401730448CV2711312single nucleotide variantNM_006820.4(IFI44L):c.1183A>G (p.Ile395Val)not specified [RCV004313086]uncertain significance17864146878641468Humanname
401880134CV2769936single nucleotide variantNM_006820.4(IFI44L):c.1184T>C (p.Ile395Thr)not specified [RCV004353774]uncertain significance17864146978641469Humanname
405792000CV3267412single nucleotide variantNM_006820.4(IFI44L):c.1088G>A (p.Cys363Tyr)not specified [RCV004400048]uncertain significance17864106078641060Humanname
405792003CV3267413single nucleotide variantNM_006820.4(IFI44L):c.1147C>T (p.Arg383Trp)not specified [RCV004400049]uncertain significance17864111978641119Humanname
405792006CV3267414single nucleotide variantNM_006820.4(IFI44L):c.1163A>G (p.His388Arg)not specified [RCV004400050]uncertain significance17864144878641448Humanname
407466153CV3440547single nucleotide variantNM_006820.4(IFI44L):c.1118A>G (p.Asn373Ser)not specified [RCV004635558]uncertain significance17864109078641090Humanname
598267870CV3979159single nucleotide variantNM_006820.4(IFI44L):c.1279C>T (p.Arg427Trp)not specified [RCV005349591]uncertain significance17864156478641564Humanname
598267876CV3979160single nucleotide variantNM_006820.4(IFI44L):c.1181C>T (p.Pro394Leu)not specified [RCV005349592]uncertain significance17864146678641466Humanname
598267894CV3979163single nucleotide variantNM_006820.4(IFI44L):c.1319A>G (p.Glu440Gly)not specified [RCV005349595]uncertain significance17864160478641604Humanname
598206487CV3979164single nucleotide variantNM_006820.4(IFI44L):c.1154T>C (p.Met385Thr)not specified [RCV005337792]uncertain significance17864143978641439Humanname