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57 records found for search term Icam5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407465814CV3444361single nucleotide variantNM_003259.4(ICAM5):c.38T>G (p.Leu13Arg)not specified [RCV004635450]uncertain significance191029008110290081Humanname
8636591CV91816single nucleotide variantNM_003259.3(ICAM5):c.417C>T (p.Thr139=)Malignant melanoma [RCV000071914]not provided191029155310291553Humanname
598257301CV3978969single nucleotide variantNM_003259.4(ICAM5):c.265G>A (p.Asp89Asn)not specified [RCV005346972]uncertain significance191029125410291254Humanname
598257338CV3978977single nucleotide variantNM_003259.4(ICAM5):c.274G>A (p.Glu92Lys)not specified [RCV005346979]uncertain significance191029126310291263Humanname
156075004CV2248214single nucleotide variantNM_003259.4(ICAM5):c.881A>T (p.Gln294Leu)not specified [RCV004117604]uncertain significance191029224210292242Humanname
156160865CV2272545single nucleotide variantNM_003259.4(ICAM5):c.574C>T (p.His192Tyr)not specified [RCV004133442]uncertain significance191029171010291710Humanname
156053575CV2308587single nucleotide variantNM_003259.4(ICAM5):c.880C>G (p.Gln294Glu)not specified [RCV004167150]uncertain significance191029224110292241Humanname
155901425CV2345804single nucleotide variantNM_003259.4(ICAM5):c.448C>A (p.Arg150Ser)not specified [RCV004205728]uncertain significance191029158410291584Humanname
401748822CV2694511single nucleotide variantNM_003259.4(ICAM5):c.740T>C (p.Val247Ala)not specified [RCV004298645]uncertain significance191029210110292101Humanname
401754266CV2717320single nucleotide variantNM_003259.4(ICAM5):c.770C>T (p.Ala257Val)not specified [RCV004330204]uncertain significance191029213110292131Humanname
401781960CV2722358single nucleotide variantNM_003259.4(ICAM5):c.977T>G (p.Leu326Arg)not specified [RCV004322768]uncertain significance191029262710292627Humanname
405781738CV3267192single nucleotide variantNM_003259.4(ICAM5):c.364C>T (p.Arg122Cys)not specified [RCV004397758]uncertain significance191029150010291500Humanname
405781744CV3267193single nucleotide variantNM_003259.4(ICAM5):c.449G>A (p.Arg150His)not specified [RCV004397759]uncertain significance191029158510291585Humanname
405781751CV3267194single nucleotide variantNM_003259.4(ICAM5):c.701C>T (p.Ala234Val)not specified [RCV004397760]uncertain significance191029206210292062Humanname
405781757CV3267195single nucleotide variantNM_003259.4(ICAM5):c.722T>C (p.Val241Ala)not specified [RCV004397761]uncertain significance191029208310292083Humanname
407510974CV3444362single nucleotide variantNM_003259.4(ICAM5):c.478G>C (p.Gly160Arg)not specified [RCV004626311]uncertain significance191029161410291614Humanname
407465827CV3444366single nucleotide variantNM_003259.4(ICAM5):c.398C>A (p.Pro133Gln)not specified [RCV004635453]uncertain significance191029153410291534Humanname
597783991CV3682946single nucleotide variantNM_003259.4(ICAM5):c.524G>A (p.Arg175Gln)not specified [RCV004931560]uncertain significance191029166010291660Humanname
597784003CV3682949single nucleotide variantNM_003259.4(ICAM5):c.431T>C (p.Val144Ala)not specified [RCV004931563]uncertain significance191029156710291567Humanname
597784014CV3682953single nucleotide variantNM_003259.4(ICAM5):c.982A>G (p.Thr328Ala)not specified [RCV004931566]uncertain significance191029263210292632Humanname
598257308CV3978970single nucleotide variantNM_003259.4(ICAM5):c.337C>T (p.Leu113Phe)not specified [RCV005346973]uncertain significance191029132610291326Humanname
598206235CV3978976single nucleotide variantNM_003259.4(ICAM5):c.628G>A (p.Gly210Arg)not specified [RCV005337744]uncertain significance191029176410291764Humanname
598257343CV3978978single nucleotide variantNM_003259.4(ICAM5):c.403G>A (p.Gly135Ser)not specified [RCV005346980]uncertain significance191029153910291539Humanname
156057251CV2239062single nucleotide variantNM_003259.4(ICAM5):c.1369C>G (p.Leu457Val)not specified [RCV004112068]uncertain significance191029315010293150Humanname
156035630CV2282994single nucleotide variantNM_003259.4(ICAM5):c.2752G>T (p.Ala918Ser)not specified [RCV004143623]uncertain significance191029659310296593Humanname
156279030CV2285021single nucleotide variantNM_003259.4(ICAM5):c.1765G>A (p.Gly589Arg)not specified [RCV004143447]uncertain significance191029409310294093Humanname
156098934CV2306501single nucleotide variantNM_003259.4(ICAM5):c.1355T>C (p.Leu452Pro)not specified [RCV004157117]uncertain significance191029313610293136Humanname
156089806CV2344536single nucleotide variantNM_003259.4(ICAM5):c.1895C>T (p.Pro632Leu)not specified [RCV004195270]uncertain significance191029422310294223Humanname
156244247CV2347135single nucleotide variantNM_003259.4(ICAM5):c.2717G>A (p.Gly906Asp)not specified [RCV004204613]uncertain significance191029655810296558Humanname
156224810CV2352611single nucleotide variantNM_003259.4(ICAM5):c.1120G>A (p.Glu374Lys)not specified [RCV004198644]uncertain significance191029277010292770Humanname
156143398CV2383851single nucleotide variantNM_003259.4(ICAM5):c.1841C>A (p.Ala614Asp)not specified [RCV004231714]uncertain significance191029416910294169Humanname
156056723CV2396274single nucleotide variantNM_003259.4(ICAM5):c.1728G>T (p.Glu576Asp)not specified [RCV004240223]uncertain significance191029405610294056Humanname
329378155CV2460871single nucleotide variantNM_003259.4(ICAM5):c.1870C>T (p.Pro624Ser)not specified [RCV004271176]likely benign191029419810294198Humanname
401759692CV2698593single nucleotide variantNM_003259.4(ICAM5):c.2674G>C (p.Gly892Arg)not specified [RCV004299076]uncertain significance191029651510296515Humanname
401770915CV2726300single nucleotide variantNM_003259.4(ICAM5):c.1982G>A (p.Ser661Asn)not specified [RCV004326742]uncertain significance191029431010294310Humanname
401770928CV2726304single nucleotide variantNM_003259.4(ICAM5):c.1983C>A (p.Ser661Arg)not specified [RCV004326746]uncertain significance191029431110294311Humanname
401885335CV2768097single nucleotide variantNM_003259.4(ICAM5):c.2713G>A (p.Gly905Arg)not specified [RCV004348327]uncertain significance191029655410296554Humanname
401886260CV2771706single nucleotide variantNM_003259.4(ICAM5):c.2078G>A (p.Arg693Gln)not specified [RCV004350496]uncertain significance191029448810294488Humanname
405781709CV3267187single nucleotide variantNM_003259.4(ICAM5):c.1622G>C (p.Arg541Pro)not specified [RCV004397753]uncertain significance191029385410293854Humanname
405781713CV3267188single nucleotide variantNM_003259.4(ICAM5):c.1873C>T (p.Pro625Ser)not specified [RCV004397754]uncertain significance191029420110294201Humanname
405781720CV3267189single nucleotide variantNM_003259.4(ICAM5):c.2128C>T (p.Pro710Ser)not specified [RCV004397755]uncertain significance191029453810294538Humanname
405781725CV3267190single nucleotide variantNM_003259.4(ICAM5):c.2248G>A (p.Glu750Lys)not specified [RCV004397756]uncertain significance191029536310295363Humanname
405781732CV3267191single nucleotide variantNM_003259.4(ICAM5):c.2489G>A (p.Arg830His)not specified [RCV004397757]uncertain significance191029560410295604Humanname
407465819CV3444363single nucleotide variantNM_003259.4(ICAM5):c.2717G>T (p.Gly906Val)not specified [RCV004635451]uncertain significance191029655810296558Humanname
407510977CV3444364single nucleotide variantNM_003259.4(ICAM5):c.1387G>A (p.Ala463Thr)not specified [RCV004626312]uncertain significance191029316810293168Humanname
407465823CV3444365single nucleotide variantNM_003259.4(ICAM5):c.1069G>A (p.Val357Ile)not specified [RCV004635452]likely benign191029271910292719Humanname
597783987CV3682945single nucleotide variantNM_003259.4(ICAM5):c.1331C>T (p.Ala444Val)not specified [RCV004931559]uncertain significance191029311210293112Humanname
597783995CV3682947single nucleotide variantNM_003259.4(ICAM5):c.2258C>T (p.Ala753Val)not specified [RCV004931561]uncertain significance191029537310295373Humanname
597783999CV3682948single nucleotide variantNM_003259.4(ICAM5):c.1544T>A (p.Val515Glu)not specified [RCV004931562]uncertain significance191029377610293776Humanname
597784008CV3682951single nucleotide variantNM_003259.4(ICAM5):c.1233C>A (p.Asp411Glu)not specified [RCV004931564]uncertain significance191029301410293014Humanname
597784010CV3682952single nucleotide variantNM_003259.4(ICAM5):c.2656G>C (p.Gly886Arg)not specified [RCV004931565]uncertain significance191029649710296497Humanname
598257297CV3978968single nucleotide variantNM_003259.4(ICAM5):c.1906A>G (p.Arg636Gly)not specified [RCV005346971]uncertain significance191029423410294234Humanname
598257315CV3978972single nucleotide variantNM_003259.4(ICAM5):c.2357G>C (p.Gly786Ala)not specified [RCV005346975]uncertain significance191029547210295472Humanname
598257320CV3978973single nucleotide variantNM_003259.4(ICAM5):c.2746G>C (p.Val916Leu)not specified [RCV005346976]uncertain significance191029658710296587Humanname
598257326CV3978974single nucleotide variantNM_003259.4(ICAM5):c.2072C>T (p.Ala691Val)not specified [RCV005346977]uncertain significance191029448210294482Humanname
598257332CV3978975single nucleotide variantNM_003259.4(ICAM5):c.2132A>G (p.Glu711Gly)not specified [RCV005346978]uncertain significance191029454210294542Humanname
41405789CV982143single nucleotide variantNM_003259.4(ICAM5):c.2198C>T (p.Thr733Met)not provided [RCV001810567]uncertain significance191029460810294608Humanname