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57 records found for search term Lrrc49
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156133704CV2216876single nucleotide variantNM_017691.5(LRRC49):c.35G>A (p.Arg12Gln)not specified [RCV004083294]uncertain significance157089292970892929Humanname
597633212CV3693481single nucleotide variantNM_017691.5(LRRC49):c.61C>T (p.Leu21Phe)not specified [RCV004940122]uncertain significance157089359670893596Humanname
156226559CV2203144single nucleotide variantNM_017691.5(LRRC49):c.200A>G (p.His67Arg)not specified [RCV004070846]uncertain significance157090092870900928Humanname
156044182CV2305895single nucleotide variantNM_017691.5(LRRC49):c.166C>G (p.Leu56Val)not specified [RCV004167684]uncertain significance157089590970895909Humanname
156233759CV2346229single nucleotide variantNM_017691.5(LRRC49):c.283T>A (p.Leu95Met)not specified [RCV004203725]uncertain significance157090101170901011Humanname
407501046CV3456546single nucleotide variantNM_017691.5(LRRC49):c.248G>A (p.Arg83His)not specified [RCV004644772]uncertain significance157090097670900976Humanname
407468184CV3456547single nucleotide variantNM_017691.5(LRRC49):c.158A>G (p.Gln53Arg)not specified [RCV004636183]uncertain significance157089590170895901Humanname
156297664CV2240878single nucleotide variantNM_017691.5(LRRC49):c.404A>C (p.Lys135Thr)not specified [RCV004102166]uncertain significance157090465970904659Humanname
156000587CV2287402single nucleotide variantNM_017691.5(LRRC49):c.976C>T (p.Arg326Trp)not specified [RCV004147009]uncertain significance157098015570980155Humanname
155924861CV2348227single nucleotide variantNM_017691.5(LRRC49):c.509A>C (p.Lys170Thr)not specified [RCV004191270]uncertain significance157091154070911540Humanname
156143764CV2358602single nucleotide variantNM_017691.5(LRRC49):c.920C>T (p.Thr307Met)not specified [RCV004207479]uncertain significance157096393170963931Humanname
155968234CV2391434single nucleotide variantNM_017691.5(LRRC49):c.831T>A (p.Asp277Glu)not specified [RCV004239829]uncertain significance157096384270963842Humanname
329373958CV2452736single nucleotide variantNM_017691.5(LRRC49):c.886A>G (p.Met296Val)not specified [RCV004275283]uncertain significance157096389770963897Humanname
401760017CV2698709single nucleotide variantNM_017691.5(LRRC49):c.896G>A (p.Arg299His)not specified [RCV004301168]uncertain significance157096390770963907Humanname
401750271CV2715571single nucleotide variantNM_017691.5(LRRC49):c.934C>T (p.Arg312Cys)not specified [RCV004326964]uncertain significance157098011370980113Humanname
405656000CV3287864single nucleotide variantNM_017691.5(LRRC49):c.347T>C (p.Leu116Ser)not specified [RCV004415652]uncertain significance157090460270904602Humanname
405656001CV3287865single nucleotide variantNM_017691.5(LRRC49):c.377G>A (p.Arg126Gln)not specified [RCV004415653]uncertain significance157090463270904632Humanname
405656004CV3287866single nucleotide variantNM_017691.5(LRRC49):c.683A>C (p.Asn228Thr)not specified [RCV004415654]uncertain significance157091916570919165Humanname
405656006CV3287867single nucleotide variantNM_017691.5(LRRC49):c.940G>A (p.Ala314Thr)not specified [RCV004415655]uncertain significance157098011970980119Humanname
407501037CV3456544single nucleotide variantNM_017691.5(LRRC49):c.469T>C (p.Cys157Arg)not specified [RCV004644770]uncertain significance157090472470904724Humanname
407501060CV3456551single nucleotide variantNM_017691.5(LRRC49):c.376C>T (p.Arg126Trp)not specified [RCV004644776]uncertain significance157090463170904631Humanname
597633223CV3693479single nucleotide variantNM_017691.5(LRRC49):c.367T>G (p.Phe123Val)not specified [RCV004940120]uncertain significance157090462270904622Humanname
597633198CV3693484single nucleotide variantNM_017691.5(LRRC49):c.497A>C (p.Asn166Thr)not specified [RCV004940125]uncertain significance157090475270904752Humanname
156270567CV2195172single nucleotide variantNM_017691.5(LRRC49):c.1924A>G (p.Ile642Val)not specified [RCV004080120]uncertain significance157104947571049475Humanname
156177281CV2220386single nucleotide variantNM_017691.5(LRRC49):c.1460T>C (p.Leu487Pro)not specified [RCV004095796]uncertain significance157100985971009859Humanname
156076861CV2230245single nucleotide variantNM_017691.5(LRRC49):c.1841A>G (p.Tyr614Cys)not specified [RCV004099865]uncertain significance157103731671037316Humanname
156206358CV2249949single nucleotide variantNM_017691.5(LRRC49):c.1764A>C (p.Glu588Asp)not specified [RCV004122921]uncertain significance157103723971037239Humanname
156098037CV2306427single nucleotide variantNM_017691.5(LRRC49):c.1610T>C (p.Met537Thr)not specified [RCV004157054]uncertain significance157101282071012820Humanname
329396414CV2462651single nucleotide variantNM_017691.5(LRRC49):c.1190A>G (p.Asn397Ser)not specified [RCV004278589]uncertain significance157100839971008399Humanname
401730221CV2680050single nucleotide variantNM_017691.5(LRRC49):c.1363G>A (p.Val455Ile)not specified [RCV004286546]uncertain significance157100857271008572Humanname
401745198CV2693204single nucleotide variantNM_017691.5(LRRC49):c.1588A>C (p.Thr530Pro)not specified [RCV004293132]uncertain significance157100998771009987Humanname
401761826CV2726922single nucleotide variantNM_017691.5(LRRC49):c.1713A>T (p.Gln571His)not specified [RCV004323206]uncertain significance157103718871037188Humanname
401898889CV2792089single nucleotide variantNM_017691.5(LRRC49):c.1175T>C (p.Leu392Pro)not specified [RCV004361318]uncertain significance157100838471008384Humanname
405655982CV3287857single nucleotide variantNM_017691.5(LRRC49):c.1103C>T (p.Ser368Phe)not specified [RCV004415645]uncertain significance157098419170984191Humanname
405655984CV3287858single nucleotide variantNM_017691.5(LRRC49):c.1128G>T (p.Gln376His)not specified [RCV004415646]uncertain significance157098421670984216Humanname
405655990CV3287860single nucleotide variantNM_017691.5(LRRC49):c.1316G>A (p.Gly439Glu)not specified [RCV004415648]uncertain significance157100852571008525Humanname
405655992CV3287861single nucleotide variantNM_017691.5(LRRC49):c.1471C>T (p.Arg491Cys)not specified [RCV004415649]uncertain significance157100987071009870Humanname
405655994CV3287862single nucleotide variantNM_017691.5(LRRC49):c.1498C>G (p.Pro500Ala)not specified [RCV004415650]uncertain significance157100989771009897Humanname
405655997CV3287863single nucleotide variantNM_017691.5(LRRC49):c.1678C>G (p.Leu560Val)not specified [RCV004415651]uncertain significance157101288871012888Humanname
407501032CV3456543single nucleotide variantNM_017691.5(LRRC49):c.1370T>G (p.Val457Gly)not specified [RCV004644769]uncertain significance157100857971008579Humanname
407501041CV3456545single nucleotide variantNM_017691.5(LRRC49):c.1438A>T (p.Met480Leu)not specified [RCV004644771]uncertain significance157100983771009837Humanname
407501051CV3456549single nucleotide variantNM_017691.5(LRRC49):c.1120C>T (p.Pro374Ser)not specified [RCV004644774]uncertain significance157098420870984208Humanname
407501056CV3456550single nucleotide variantNM_017691.5(LRRC49):c.1052T>G (p.Leu351Trp)not specified [RCV004644775]uncertain significance157098414070984140Humanname
407501064CV3456552single nucleotide variantNM_017691.5(LRRC49):c.1495G>T (p.Asp499Tyr)not specified [RCV004644777]uncertain significance157100989471009894Humanname
597633238CV3693476single nucleotide variantNM_017691.5(LRRC49):c.2021A>G (p.Tyr674Cys)not specified [RCV004940117]uncertain significance157104957271049572Humanname
597633233CV3693477single nucleotide variantNM_017691.5(LRRC49):c.1626G>T (p.Arg542Ser)not specified [RCV004940118]uncertain significance157101283671012836Humanname
597633227CV3693478single nucleotide variantNM_017691.5(LRRC49):c.1101T>A (p.Asp367Glu)not specified [RCV004940119]uncertain significance157098418970984189Humanname
597633217CV3693480single nucleotide variantNM_017691.5(LRRC49):c.1057C>G (p.Gln353Glu)not specified [RCV004940121]uncertain significance157098414570984145Humanname
597633209CV3693482single nucleotide variantNM_017691.5(LRRC49):c.1619C>G (p.Ala540Gly)not specified [RCV004940123]uncertain significance157101282971012829Humanname
597633204CV3693483single nucleotide variantNM_017691.5(LRRC49):c.1181C>T (p.Ser394Leu)not specified [RCV004940124]uncertain significance157100839071008390Humanname
597633192CV3693486single nucleotide variantNM_017691.5(LRRC49):c.1350A>T (p.Glu450Asp)not specified [RCV004940126]uncertain significance157100855971008559Humanname
598251140CV3984743single nucleotide variantNM_017691.5(LRRC49):c.1763A>G (p.Glu588Gly)not specified [RCV005366629]uncertain significance157103723871037238Humanname
598222544CV3984744single nucleotide variantNM_017691.5(LRRC49):c.1588A>G (p.Thr530Ala)not specified [RCV005379906]uncertain significance157100998771009987Humanname
598251145CV3984745single nucleotide variantNM_017691.5(LRRC49):c.1475G>A (p.Arg492His)not specified [RCV005366630]uncertain significance157100987471009874Humanname
598251150CV3984746single nucleotide variantNM_017691.5(LRRC49):c.1675C>T (p.Arg559Cys)not specified [RCV005366631]uncertain significance157101288571012885Humanname
8635554CV90776single nucleotide variantNM_001199017.2(LRRC49):c.1377C>T (p.Ile459=)Malignant melanoma [RCV000070874]not provided157100857171008571Humanname
8635555CV90777single nucleotide variantNM_001199017.2(LRRC49):c.1947G>A (p.Met649Ile)Malignant melanoma [RCV000070875]not provided157104948371049483Humanname