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Variants search result for Homo sapiens
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59 records found for search term Trim25
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8585457CV120044single nucleotide variantNM_005082.4(TRIM25):c.598-466C>GLung cancer [RCV000100564]uncertain significance175690902956909029Humanname
597801654CV3617647single nucleotide variantNM_005082.5(TRIM25):c.13T>C (p.Cys5Arg)not specified [RCV004880830]uncertain significance175691397656913976Humanname
597801648CV3617644single nucleotide variantNM_005082.5(TRIM25):c.71T>C (p.Val24Ala)not specified [RCV004880827]uncertain significance175691391856913918Humanname
597801650CV3617645single nucleotide variantNM_005082.5(TRIM25):c.70G>A (p.Val24Ile)not specified [RCV004880828]uncertain significance175691391956913919Humanname
597801657CV3617649single nucleotide variantNM_005082.5(TRIM25):c.41C>T (p.Ser14Phe)not specified [RCV004880832]uncertain significance175691394856913948Humanname
15136084CV715579single nucleotide variantNM_005082.5(TRIM25):c.648G>A (p.Ala216=)not provided [RCV000965393]benign175690851356908513Humanname
156367760CV2203578single nucleotide variantNM_005082.5(TRIM25):c.287C>A (p.Ala96Asp)not specified [RCV004072774]uncertain significance175691370256913702Humanname
405789954CV3336841single nucleotide variantNM_005082.5(TRIM25):c.142T>A (p.Tyr48Asn)not specified [RCV004473720]uncertain significance175691384756913847Humanname
405789961CV3336843single nucleotide variantNM_005082.5(TRIM25):c.247C>T (p.Arg83Trp)not specified [RCV004473722]uncertain significance175691374256913742Humanname
405789968CV3336845single nucleotide variantNM_005082.5(TRIM25):c.280G>A (p.Ala94Thr)not specified [RCV004473724]uncertain significance175691370956913709Humanname
598274068CV3935388single nucleotide variantNM_005082.5(TRIM25):c.190C>T (p.His64Tyr)not specified [RCV005303744]uncertain significance175691379956913799Humanname
598274070CV3935389single nucleotide variantNM_005082.5(TRIM25):c.193A>C (p.Lys65Gln)not specified [RCV005303745]uncertain significance175691379656913796Humanname
15169144CV704241single nucleotide variantNM_005082.5(TRIM25):c.1725G>A (p.Thr575=)not provided [RCV000949401]benign175689186856891868Humanname
15191282CV740897single nucleotide variantNM_005082.5(TRIM25):c.1650C>T (p.Cys550=)not provided [RCV000910200]likely benign175689194356891943Humanname
155962994CV2197710single nucleotide variantNM_005082.5(TRIM25):c.440C>T (p.Pro147Leu)not specified [RCV004074915]uncertain significance175691354956913549Humanname
156244006CV2207186single nucleotide variantNM_005082.5(TRIM25):c.562C>T (p.Pro188Ser)not specified [RCV004087920]uncertain significance175691342756913427Humanname
156141880CV2208466single nucleotide variantNM_005082.5(TRIM25):c.566C>T (p.Ala189Val)not specified [RCV004091003]likely benign175691342356913423Humanname
156298866CV2248562single nucleotide variantNM_005082.5(TRIM25):c.451G>C (p.Asp151His)not specified [RCV004121758]uncertain significance175691353856913538Humanname
401724549CV2677915single nucleotide variantNM_005082.5(TRIM25):c.688G>A (p.Val230Met)not specified [RCV004294402]uncertain significance175690847356908473Humanname
401773773CV2702429single nucleotide variantNM_005082.5(TRIM25):c.893G>A (p.Ser298Asn)not specified [RCV004316942]uncertain significance175690428956904289Humanname
405789972CV3336846single nucleotide variantNM_005082.5(TRIM25):c.529C>G (p.His177Asp)not specified [RCV004473725]uncertain significance175691346056913460Humanname
405789976CV3336847single nucleotide variantNM_005082.5(TRIM25):c.626T>A (p.Met209Lys)not specified [RCV004473726]uncertain significance175690853556908535Humanname
405789980CV3336848single nucleotide variantNM_005082.5(TRIM25):c.673A>G (p.Asn225Asp)not specified [RCV004473727]uncertain significance175690848856908488Humanname
405789985CV3336849single nucleotide variantNM_005082.5(TRIM25):c.691C>T (p.Arg231Trp)not specified [RCV004473728]uncertain significance175690847056908470Humanname
405789989CV3336850single nucleotide variantNM_005082.5(TRIM25):c.712G>A (p.Val238Met)not specified [RCV004473729]likely benign175690447056904470Humanname
405789992CV3336851single nucleotide variantNM_005082.5(TRIM25):c.760G>A (p.Ala254Thr)not specified [RCV004473730]uncertain significance175690442256904422Humanname
405789995CV3336852single nucleotide variantNM_005082.5(TRIM25):c.995A>G (p.Lys332Arg)not specified [RCV004473731]uncertain significance175690151156901511Humanname
407461424CV3492759single nucleotide variantNM_005082.5(TRIM25):c.631A>G (p.Ser211Gly)not specified [RCV004687649]likely benign175690853056908530Humanname
597801640CV3617640single nucleotide variantNM_005082.5(TRIM25):c.808G>T (p.Val270Phe)not specified [RCV004880823]uncertain significance175690437456904374Humanname
597801642CV3617641single nucleotide variantNM_005082.5(TRIM25):c.620C>G (p.Thr207Ser)not specified [RCV004880824]uncertain significance175690854156908541Humanname
597801646CV3617643single nucleotide variantNM_005082.5(TRIM25):c.371C>T (p.Ala124Val)not specified [RCV004880826]uncertain significance175691361856913618Humanname
597801652CV3617646single nucleotide variantNM_005082.5(TRIM25):c.431C>G (p.Pro144Arg)not specified [RCV004880829]uncertain significance175691355856913558Humanname
597801656CV3617648single nucleotide variantNM_005082.5(TRIM25):c.869C>A (p.Thr290Asn)not specified [RCV004880831]uncertain significance175690431356904313Humanname
598202527CV3935387single nucleotide variantNM_005082.5(TRIM25):c.695T>G (p.Met232Arg)not specified [RCV005290392]uncertain significance175690448756904487Humanname
598202552CV3935393single nucleotide variantNM_005082.5(TRIM25):c.302C>G (p.Pro101Arg)not specified [RCV005290395]uncertain significance175691368756913687Humanname
15201491CV704242single nucleotide variantNM_005082.5(TRIM25):c.553A>G (p.Thr185Ala)not provided [RCV000957637]benign175691343656913436Humanname
156088787CV2202012single nucleotide variantNM_005082.5(TRIM25):c.1634A>G (p.Asn545Ser)not specified [RCV004075934]uncertain significance175689195956891959Humanname
156280625CV2206418single nucleotide variantNM_005082.5(TRIM25):c.1591G>A (p.Gly531Arg)not specified [RCV004078740]uncertain significance175689200256892002Humanname
156063173CV2277371single nucleotide variantNM_005082.5(TRIM25):c.1480A>G (p.Arg494Gly)not specified [RCV004144791]uncertain significance175689211356892113Humanname
156396200CV2326149single nucleotide variantNM_005082.5(TRIM25):c.1781C>T (p.Ala594Val)not specified [RCV004180421]uncertain significance175689181256891812Humanname
156334658CV2333416single nucleotide variantNM_005082.5(TRIM25):c.1127C>T (p.Ser376Phe)not specified [RCV004190122]uncertain significance175689914156899141Humanname
155986605CV2345537single nucleotide variantNM_005082.5(TRIM25):c.1369A>G (p.Ile457Val)not specified [RCV004198298]likely benign175689222456892224Humanname
155925903CV2365663single nucleotide variantNM_005082.5(TRIM25):c.1745A>G (p.Asn582Ser)not specified [RCV004214218]uncertain significance175689184856891848Humanname
155954209CV2379163single nucleotide variantNM_005082.5(TRIM25):c.1117A>G (p.Thr373Ala)not specified [RCV004235953]uncertain significance175689915156899151Humanname
329367333CV2427361single nucleotide variantNM_005082.5(TRIM25):c.1284C>A (p.Ser428Arg)not specified [RCV004248217]uncertain significance175689542256895422Humanname
329360252CV2458650single nucleotide variantNM_005082.5(TRIM25):c.1408G>A (p.Val470Met)not specified [RCV004268320]uncertain significance175689218556892185Humanname
401772521CV2712773single nucleotide variantNM_005082.5(TRIM25):c.1461C>A (p.Asn487Lys)not specified [RCV004310114]uncertain significance175689213256892132Humanname
405789951CV3336840single nucleotide variantNM_005082.5(TRIM25):c.1270G>T (p.Ala424Ser)not specified [RCV004473719]uncertain significance175689543656895436Humanname
405789957CV3336842single nucleotide variantNM_005082.5(TRIM25):c.1667C>G (p.Thr556Ser)not specified [RCV004473721]uncertain significance175689192656891926Humanname
407453640CV3492755single nucleotide variantNM_005082.5(TRIM25):c.1211C>T (p.Pro404Leu)not specified [RCV004684617]uncertain significance175689557456895574Humanname
407453642CV3492756single nucleotide variantNM_005082.5(TRIM25):c.1256G>C (p.Gly419Ala)not specified [RCV004684618]uncertain significance175689552956895529Humanname
407453645CV3492758single nucleotide variantNM_005082.5(TRIM25):c.1114T>C (p.Ser372Pro)not specified [RCV004684619]uncertain significance175689915456899154Humanname
407453648CV3492760single nucleotide variantNM_005082.5(TRIM25):c.1795C>A (p.Leu599Met)not specified [RCV004684620]uncertain significance175689179856891798Humanname
597801638CV3617639single nucleotide variantNM_005082.5(TRIM25):c.1249C>A (p.Gln417Lys)not specified [RCV004880822]uncertain significance175689553656895536Humanname
597801644CV3617642single nucleotide variantNM_005082.5(TRIM25):c.1012C>T (p.His338Tyr)not specified [RCV004880825]likely benign175690149456901494Humanname
598202536CV3935390single nucleotide variantNM_005082.5(TRIM25):c.1804A>G (p.Lys602Glu)not specified [RCV005290393]uncertain significance175689178956891789Humanname
598274072CV3935391single nucleotide variantNM_005082.5(TRIM25):c.1108C>A (p.Pro370Thr)not specified [RCV005303746]uncertain significance175689916056899160Humanname
598202546CV3935392single nucleotide variantNM_005082.5(TRIM25):c.1596C>A (p.Ser532Arg)not specified [RCV005290394]uncertain significance175689199756891997Humanname
598274074CV3935394single nucleotide variantNM_005082.5(TRIM25):c.1756G>C (p.Gly586Arg)not specified [RCV005303747]uncertain significance175689183756891837Humanname