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Variants search result for Homo sapiens
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63 records found for search term Trim46
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598274199CV3935492single nucleotide variantNM_025058.5(TRIM46):c.24G>C (p.Gln8His)not specified [RCV005303805]uncertain significance1155173990155173990Humanname
329395248CV2458238single nucleotide variantNM_025058.5(TRIM46):c.78C>A (p.Asn26Lys)not specified [RCV004265897]uncertain significance1155175400155175400Humanname
401889725CV2763346single nucleotide variantNM_025058.5(TRIM46):c.32C>A (p.Thr11Asn)not specified [RCV004349242]uncertain significance1155173998155173998Humanname
598202835CV3935497single nucleotide variantNM_025058.5(TRIM46):c.28T>C (p.Phe10Leu)not specified [RCV005290440]uncertain significance1155173994155173994Humanname
329357251CV2453501single nucleotide variantNM_025058.5(TRIM46):c.202G>C (p.Gly68Arg)not specified [RCV004269191]uncertain significance1155175524155175524Humanname
401863639CV2770770single nucleotide variantNM_025058.5(TRIM46):c.260G>A (p.Arg87His)not specified [RCV004349809]uncertain significance1155175582155175582Humanname
405796528CV3337029single nucleotide variantNM_025058.5(TRIM46):c.254C>T (p.Ser85Phe)not specified [RCV004475890]uncertain significance1155175576155175576Humanname
407453905CV3490553single nucleotide variantNM_025058.5(TRIM46):c.268C>A (p.Arg90Ser)not specified [RCV004684707]uncertain significance1155175590155175590Humanname
407461463CV3490555single nucleotide variantNM_025058.5(TRIM46):c.1944G>A (p.Ser648=)not specified [RCV004687659]likely benign1155183854155183854Humanname
597801911CV3617809single nucleotide variantNM_025058.5(TRIM46):c.236C>G (p.Ser79Cys)not specified [RCV004880966]uncertain significance1155175558155175558Humanname
15186921CV696138single nucleotide variantNM_025058.5(TRIM46):c.1383C>T (p.His461=)not provided [RCV000953429]benign1155179729155179729Humanname
155973771CV2334474single nucleotide variantNM_025058.5(TRIM46):c.424C>T (p.Arg142Trp)not specified [RCV004188443]uncertain significance1155175986155175986Humanname
156062239CV2392096single nucleotide variantNM_025058.5(TRIM46):c.860C>T (p.Thr287Met)not specified [RCV004237991]uncertain significance1155177241155177241Humanname
329372692CV2451609single nucleotide variantNM_025058.5(TRIM46):c.923A>C (p.Gln308Pro)not specified [RCV004274536]uncertain significance1155178015155178015Humanname
329396839CV2459064single nucleotide variantNM_025058.5(TRIM46):c.341C>T (p.Pro114Leu)not specified [RCV004272532]uncertain significance1155175903155175903Humanname
405796531CV3337030single nucleotide variantNM_025058.5(TRIM46):c.300C>A (p.Asp100Glu)not specified [RCV004475891]uncertain significance1155175622155175622Humanname
405796534CV3337031single nucleotide variantNM_025058.5(TRIM46):c.464G>A (p.Arg155His)not specified [RCV004475892]uncertain significance1155176026155176026Humanname
405796540CV3337033single nucleotide variantNM_025058.5(TRIM46):c.860C>A (p.Thr287Lys)not specified [RCV004475894]uncertain significance1155177241155177241Humanname
407453903CV3490551single nucleotide variantNM_025058.5(TRIM46):c.953G>A (p.Arg318Gln)not specified [RCV004684706]uncertain significance1155178045155178045Humanname
407461459CV3490552single nucleotide variantNM_025058.5(TRIM46):c.368C>T (p.Pro123Leu)not specified [RCV004687658]uncertain significance1155175930155175930Humanname
597801899CV3617803single nucleotide variantNM_025058.5(TRIM46):c.895G>A (p.Val299Met)not specified [RCV004880960]uncertain significance1155177276155177276Humanname
597801901CV3617804single nucleotide variantNM_025058.5(TRIM46):c.425G>A (p.Arg142Gln)not specified [RCV004880961]uncertain significance1155175987155175987Humanname
597801903CV3617805single nucleotide variantNM_025058.5(TRIM46):c.781A>G (p.Thr261Ala)not specified [RCV004880962]uncertain significance1155177043155177043Humanname
597801907CV3617807single nucleotide variantNM_025058.5(TRIM46):c.395C>G (p.Ala132Gly)not specified [RCV004880964]uncertain significance1155175957155175957Humanname
597801913CV3617810single nucleotide variantNM_025058.5(TRIM46):c.794G>A (p.Ser265Asn)not specified [RCV004880967]uncertain significance1155177056155177056Humanname
598202787CV3935486single nucleotide variantNM_025058.5(TRIM46):c.955G>A (p.Gly319Arg)not specified [RCV005290432]uncertain significance1155178047155178047Humanname
598202794CV3935487single nucleotide variantNM_025058.5(TRIM46):c.905C>T (p.Thr302Ile)not specified [RCV005290433]uncertain significance1155177286155177286Humanname
598202817CV3935493single nucleotide variantNM_025058.5(TRIM46):c.476G>A (p.Arg159Gln)not specified [RCV005290437]uncertain significance1155176038155176038Humanname
598274201CV3935496single nucleotide variantNM_025058.5(TRIM46):c.494G>A (p.Ser165Asn)not specified [RCV005303806]uncertain significance1155176056155176056Humanname
598202840CV3935498single nucleotide variantNM_025058.5(TRIM46):c.765C>G (p.His255Gln)not specified [RCV005290441]uncertain significance1155177027155177027Humanname
8624717CV79831single nucleotide variantNM_025058.4(TRIM46):c.385C>T (p.Pro129Ser)Malignant melanoma [RCV000059907]not provided1155175947155175947Humanname
8628966CV84109single nucleotide variantNM_025058.4(TRIM46):c.307G>A (p.Asp103Asn)Malignant melanoma [RCV000064190]not provided1155175629155175629Humanname
156128798CV2238483single nucleotide variantNM_025058.5(TRIM46):c.2141T>G (p.Leu714Trp)not specified [RCV004113535]uncertain significance1155184051155184051Humanname
156167920CV2320052single nucleotide variantNM_025058.5(TRIM46):c.2011G>A (p.Ala671Thr)not specified [RCV004167910]uncertain significance1155183921155183921Humanname
155998749CV2393462single nucleotide variantNM_025058.5(TRIM46):c.1172G>A (p.Arg391Gln)not specified [RCV004228954]uncertain significance1155178500155178500Humanname
329376569CV2428465single nucleotide variantNM_025058.5(TRIM46):c.1033C>T (p.Arg345Cys)not specified [RCV004253257]uncertain significance1155178125155178125Humanname
329359898CV2446465single nucleotide variantNM_025058.5(TRIM46):c.1445G>A (p.Arg482Gln)not specified [RCV004249580]uncertain significance1155179791155179791Humanname
329393717CV2472037single nucleotide variantNM_025058.5(TRIM46):c.1613G>A (p.Arg538His)not specified [RCV004283183]uncertain significance1155181876155181876Humanname
401729535CV2690315single nucleotide variantNM_025058.5(TRIM46):c.2243G>T (p.Arg748Met)not specified [RCV004302310]uncertain significance1155184153155184153Humanname
401731499CV2693835single nucleotide variantNM_025058.5(TRIM46):c.1417G>A (p.Ala473Thr)not specified [RCV004300143]uncertain significance1155179763155179763Humanname
401743763CV2696861single nucleotide variantNM_025058.5(TRIM46):c.1042G>A (p.Ala348Thr)not specified [RCV004290826]uncertain significance1155178134155178134Humanname
401752001CV2703173single nucleotide variantNM_025058.5(TRIM46):c.1183G>A (p.Ala395Thr)not specified [RCV004315241]uncertain significance1155178511155178511Humanname
401879309CV2791383single nucleotide variantNM_025058.5(TRIM46):c.1363C>G (p.His455Asp)not specified [RCV004358785]uncertain significance1155179709155179709Humanname
405796500CV3337021single nucleotide variantNM_025058.5(TRIM46):c.1198C>T (p.Arg400Trp)not specified [RCV004475882]uncertain significance1155178526155178526Humanname
405796508CV3337023single nucleotide variantNM_025058.5(TRIM46):c.1592T>G (p.Leu531Arg)not specified [RCV004475884]uncertain significance1155181855155181855Humanname
405796511CV3337024single nucleotide variantNM_025058.5(TRIM46):c.1606G>A (p.Asp536Asn)not specified [RCV004475885]uncertain significance1155181869155181869Humanname
405796514CV3337025single nucleotide variantNM_025058.5(TRIM46):c.1621G>A (p.Ala541Thr)not specified [RCV004475886]likely benign1155181884155181884Humanname
405796517CV3337026single nucleotide variantNM_025058.5(TRIM46):c.1628G>A (p.Arg543Gln)not specified [RCV004475887]uncertain significance1155181891155181891Humanname
405796520CV3337027single nucleotide variantNM_025058.5(TRIM46):c.2102G>T (p.Arg701Leu)not specified [RCV004475888]uncertain significance1155184012155184012Humanname
405796525CV3337028single nucleotide variantNM_025058.5(TRIM46):c.2191A>G (p.Ile731Val)not specified [RCV004475889]uncertain significance1155184101155184101Humanname
407453892CV3490547single nucleotide variantNM_025058.5(TRIM46):c.1403G>A (p.Arg468His)not specified [RCV004684702]uncertain significance1155179749155179749Humanname
407453895CV3490548single nucleotide variantNM_025058.5(TRIM46):c.1171C>G (p.Arg391Gly)not specified [RCV004684703]uncertain significance1155178499155178499Humanname
407453897CV3490549single nucleotide variantNM_025058.5(TRIM46):c.2044G>A (p.Gly682Ser)not specified [RCV004684704]likely benign1155183954155183954Humanname
407453900CV3490550single nucleotide variantNM_025058.5(TRIM46):c.1789G>A (p.Ala597Thr)not specified [RCV004684705]uncertain significance1155182052155182052Humanname
407453908CV3490554single nucleotide variantNM_025058.5(TRIM46):c.1705C>T (p.Arg569Trp)not specified [RCV004684708]uncertain significance1155181968155181968Humanname
597801905CV3617806single nucleotide variantNM_025058.5(TRIM46):c.1202C>T (p.Pro401Leu)not specified [RCV004880963]uncertain significance1155178530155178530Humanname
597801909CV3617808single nucleotide variantNM_025058.5(TRIM46):c.1234C>T (p.Leu412Phe)not specified [RCV004880965]uncertain significance1155178562155178562Humanname
598274196CV3935488single nucleotide variantNM_025058.5(TRIM46):c.2255T>C (p.Ile752Thr)not specified [RCV005303804]uncertain significance1155184165155184165Humanname
598202799CV3935489single nucleotide variantNM_025058.5(TRIM46):c.1609A>G (p.Ser537Gly)not specified [RCV005290434]likely benign1155181872155181872Humanname
598202805CV3935490single nucleotide variantNM_025058.5(TRIM46):c.1999G>T (p.Ala667Ser)not specified [RCV005290435]uncertain significance1155183909155183909Humanname
598202823CV3935494single nucleotide variantNM_025058.5(TRIM46):c.1966A>G (p.Ile656Val)not specified [RCV005290438]uncertain significance1155183876155183876Humanname
598202829CV3935495single nucleotide variantNM_025058.5(TRIM46):c.1406C>T (p.Thr469Met)not specified [RCV005290439]uncertain significance1155179752155179752Humanname
8574916CV109255single nucleotide variantNM_001256599.1(TRIM46):c.1999C>T (p.Arg667Cys)Lung cancer [RCV000089780]uncertain significance1155183978155183978Humanname