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90 records found for search term Stk31
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401925630CV2828349single nucleotide variantNM_031414.5(STK31):c.9C>A (p.Val3=)not provided [RCV003436683]likely benign72371029423710294Humanname
156027357CV2242448single nucleotide variantNM_031414.5(STK31):c.23C>T (p.Ser8Phe)not specified [RCV004111444]uncertain significance72371030823710308Humanname
329377639CV2462724single nucleotide variantNM_031414.5(STK31):c.26G>A (p.Arg9Lys)not specified [RCV004278654]uncertain significance72371031123710311Humanname
407496347CV3485513single nucleotide variantNM_031414.5(STK31):c.23C>A (p.Ser8Tyr)not specified [RCV004668115]uncertain significance72371030823710308Humanname
597747711CV3614864single nucleotide variantNM_031414.5(STK31):c.14G>T (p.Gly5Val)not specified [RCV004866122]uncertain significance72371029923710299Humanname
329387595CV2470857single nucleotide variantNM_031414.5(STK31):c.38C>T (p.Thr13Met)not specified [RCV004276063]uncertain significance72371032323710323Humanname
597747690CV3614858single nucleotide variantNM_031414.5(STK31):c.62T>C (p.Ile21Thr)not specified [RCV004866117]uncertain significance72371211023712110Humanname
401864707CV2761015single nucleotide variantNM_031414.5(STK31):c.158A>G (p.Asn53Ser)not provided [RCV004707825]|not specified [RCV004338685]likely benign72371748823717488Humanname
407496350CV3485514single nucleotide variantNM_031414.5(STK31):c.223G>A (p.Val75Ile)not specified [RCV004668116]uncertain significance72371755323717553Humanname
8632528CV87736single nucleotide variantNM_031414.4(STK31):c.169G>A (p.Asp57Asn)Malignant melanoma [RCV000067828]not provided72371749923717499Humanname
8632530CV87738single nucleotide variantNM_031414.4(STK31):c.2502C>T (p.Val834=)Malignant melanoma [RCV000067830]not provided72378799423787994Humanname
156387585CV2221551single nucleotide variantNM_031414.5(STK31):c.848G>C (p.Ser283Thr)not specified [RCV004096815]uncertain significance72373690923736909Humanname
156273377CV2323627single nucleotide variantNM_031414.5(STK31):c.652A>G (p.Thr218Ala)not specified [RCV004165815]uncertain significance72373570623735706Humanname
156183697CV2327983single nucleotide variantNM_031414.5(STK31):c.946G>C (p.Glu316Gln)not specified [RCV004179296]uncertain significance72373700723737007Humanname
329387334CV2436394single nucleotide variantNM_031414.5(STK31):c.314G>A (p.Ser105Asn)not specified [RCV004251786]uncertain significance72372730523727305Humanname
401752204CV2710538single nucleotide variantNM_031414.5(STK31):c.738A>T (p.Arg246Ser)not specified [RCV004319463]uncertain significance72373579223735792Humanname
401767850CV2727299single nucleotide variantNM_031414.5(STK31):c.751A>G (p.Thr251Ala)not specified [RCV004327412]likely benign72373580523735805Humanname
405741180CV3334525single nucleotide variantNM_031414.5(STK31):c.874G>C (p.Gly292Arg)not specified [RCV004465738]uncertain significance72373693523736935Humanname
407496338CV3485511single nucleotide variantNM_031414.5(STK31):c.985T>A (p.Leu329Met)not specified [RCV004668113]uncertain significance72373704623737046Humanname
407496343CV3485512single nucleotide variantNM_031414.5(STK31):c.414T>G (p.Ser138Arg)not specified [RCV004668114]uncertain significance72372918023729180Humanname
597747680CV3614856single nucleotide variantNM_031414.5(STK31):c.413G>A (p.Ser138Asn)not specified [RCV004866115]uncertain significance72372917923729179Humanname
597747700CV3614860single nucleotide variantNM_031414.5(STK31):c.671A>G (p.Lys224Arg)not specified [RCV004866119]uncertain significance72373572523735725Humanname
597747727CV3614867single nucleotide variantNM_031414.5(STK31):c.484G>A (p.Gly162Ser)not specified [RCV004866125]uncertain significance72373553823735538Humanname
8632529CV87737single nucleotide variantNM_031414.4(STK31):c.478G>A (p.Asp160Asn)Malignant melanoma [RCV000067829]not provided72372924423729244Humanname
156249157CV2199426single nucleotide variantNM_031414.5(STK31):c.2383T>A (p.Phe795Ile)not specified [RCV004070989]uncertain significance72378661623786616Humanname
156228741CV2199427single nucleotide variantNM_031414.5(STK31):c.2384T>A (p.Phe795Tyr)not specified [RCV004070990]uncertain significance72378661723786617Humanname
156332603CV2214465single nucleotide variantNM_031414.5(STK31):c.2788A>G (p.Ile930Val)not specified [RCV004088522]uncertain significance72381517123815171Humanname
156114935CV2225222single nucleotide variantNM_031414.5(STK31):c.1864A>G (p.Lys622Glu)not specified [RCV004095017]uncertain significance72377217723772177Humanname
156065896CV2240330single nucleotide variantNM_031414.5(STK31):c.2722G>C (p.Gly908Arg)not specified [RCV004112884]uncertain significance72379090823790908Humanname
156140665CV2280844single nucleotide variantNM_031414.5(STK31):c.1019A>C (p.Gln340Pro)not specified [RCV004145100]uncertain significance72375271823752718Humanname
156273897CV2293711single nucleotide variantNM_031414.5(STK31):c.1976C>A (p.Pro659His)not specified [RCV004154999]likely benign72378142923781429Humanname
156152294CV2307620single nucleotide variantNM_031414.5(STK31):c.2279A>C (p.Tyr760Ser)not specified [RCV004168041]uncertain significance72378651223786512Humanname
156194646CV2322164single nucleotide variantNM_031414.5(STK31):c.2520G>C (p.Gln840His)not specified [RCV004175946]uncertain significance72378801223788012Humanname
156282794CV2348886single nucleotide variantNM_031414.5(STK31):c.1552G>A (p.Ala518Thr)not specified [RCV004203322]uncertain significance72376913023769130Humanname
155920867CV2350577single nucleotide variantNM_031414.5(STK31):c.1240A>T (p.Ile414Leu)not specified [RCV004204928]uncertain significance72375442123754421Humanname
156140280CV2351281single nucleotide variantNM_031414.5(STK31):c.1399C>T (p.Arg467Cys)not specified [RCV004214127]uncertain significance72376290623762906Humanname
156198317CV2357843single nucleotide variantNM_031414.5(STK31):c.1639G>A (p.Ala547Thr)not specified [RCV004205127]likely benign72376968223769682Humanname
156091787CV2389501single nucleotide variantNM_031414.5(STK31):c.1829T>C (p.Ile610Thr)not specified [RCV004243580]uncertain significance72377112023771120Humanname
329388763CV2469557single nucleotide variantNM_031414.5(STK31):c.2456C>G (p.Ala819Gly)not specified [RCV004282995]uncertain significance72378689323786893Humanname
401720592CV2673390single nucleotide variantNM_031414.5(STK31):c.2843A>G (p.Lys948Arg)not specified [RCV004288368]uncertain significance72383214923832149Humanname
401779831CV2676699single nucleotide variantNM_031414.5(STK31):c.2038C>G (p.Gln680Glu)not specified [RCV004290876]uncertain significance72378149123781491Humanname
401766229CV2679615single nucleotide variantNM_031414.5(STK31):c.2668G>C (p.Gly890Arg)not specified [RCV004282094]uncertain significance72379085423790854Humanname
401733018CV2691178single nucleotide variantNM_031414.5(STK31):c.2659A>G (p.Met887Val)not specified [RCV004302955]uncertain significance72379084523790845Humanname
401746251CV2695532single nucleotide variantNM_031414.5(STK31):c.2206A>T (p.Met736Leu)not specified [RCV004305711]uncertain significance72378553523785535Humanname
401737132CV2699737single nucleotide variantNM_031414.5(STK31):c.1448G>A (p.Gly483Glu)not specified [RCV004308398]uncertain significance72376902623769026Humanname
401741451CV2713510single nucleotide variantNM_031414.5(STK31):c.2663T>C (p.Met888Thr)not specified [RCV004319111]uncertain significance72379084923790849Humanname
401780895CV2716952single nucleotide variantNM_031414.5(STK31):c.2592C>A (p.Asn864Lys)not specified [RCV004330037]uncertain significance72378808423788084Humanname
401876881CV2754536single nucleotide variantNM_031414.5(STK31):c.1521G>T (p.Glu507Asp)not specified [RCV004336740]uncertain significance72376909923769099Humanname
401861528CV2756330single nucleotide variantNM_031414.5(STK31):c.1621T>C (p.Ser541Pro)not specified [RCV004342876]likely benign72376966423769664Humanname
401925631CV2828350single nucleotide variantNM_031414.5(STK31):c.1153C>T (p.Arg385Cys)not provided [RCV003436684]likely benign72375433423754334Humanname
405741056CV3334506single nucleotide variantNM_031414.5(STK31):c.1052A>G (p.His351Arg)not specified [RCV004465719]uncertain significance72375275123752751Humanname
405741070CV3334508single nucleotide variantNM_031414.5(STK31):c.1064C>T (p.Thr355Ile)not specified [RCV004465721]uncertain significance72375276323752763Humanname
405741076CV3334509single nucleotide variantNM_031414.5(STK31):c.1085C>A (p.Thr362Asn)not specified [RCV004465722]uncertain significance72375278423752784Humanname
405741086CV3334510single nucleotide variantNM_031414.5(STK31):c.1141G>A (p.Asp381Asn)not specified [RCV004465723]likely benign72375432223754322Humanname
405741091CV3334511single nucleotide variantNM_031414.5(STK31):c.1454C>A (p.Ala485Asp)not specified [RCV004465724]uncertain significance72376903223769032Humanname
405741103CV3334513single nucleotide variantNM_031414.5(STK31):c.1757G>T (p.Ser586Ile)not specified [RCV004465726]uncertain significance72377104823771048Humanname
405741109CV3334514single nucleotide variantNM_031414.5(STK31):c.1870C>T (p.Pro624Ser)not specified [RCV004465727]uncertain significance72377218323772183Humanname
405741115CV3334515single nucleotide variantNM_031414.5(STK31):c.1903A>T (p.Thr635Ser)not specified [RCV004465728]uncertain significance72377221623772216Humanname
405741122CV3334516single nucleotide variantNM_031414.5(STK31):c.2073G>A (p.Met691Ile)not specified [RCV004465729]uncertain significance72378358823783588Humanname
405741134CV3334518single nucleotide variantNM_031414.5(STK31):c.2570A>G (p.Gln857Arg)not specified [RCV004465731]uncertain significance72378806223788062Humanname
405741148CV3334520single nucleotide variantNM_031414.5(STK31):c.2810A>G (p.Lys937Arg)not specified [RCV004465733]uncertain significance72381519323815193Humanname
407496334CV3485508single nucleotide variantNM_031414.5(STK31):c.1649A>G (p.Asn550Ser)not specified [RCV004668112]uncertain significance72376969223769692Humanname
407530128CV3485509single nucleotide variantNM_031414.5(STK31):c.2015C>T (p.Thr672Ile)not specified [RCV004681670]uncertain significance72378146823781468Humanname
407530129CV3485510single nucleotide variantNM_031414.5(STK31):c.2896G>C (p.Val966Leu)not specified [RCV004681671]uncertain significance72383220223832202Humanname
596947063CV3547127single nucleotide variantNM_031414.5(STK31):c.2936C>G (p.Ser979Ter)not provided [RCV004810935]likely benign72383224223832242Humanname
597794473CV3614852single nucleotide variantNM_031414.5(STK31):c.2651C>T (p.Ser884Leu)not specified [RCV004877864]uncertain significance72379083723790837Humanname
597747673CV3614854single nucleotide variantNM_031414.5(STK31):c.1089A>C (p.Arg363Ser)not specified [RCV004866113]uncertain significance72375278823752788Humanname
597747677CV3614855single nucleotide variantNM_031414.5(STK31):c.1273A>G (p.Ile425Val)not specified [RCV004866114]uncertain significance72375445423754454Humanname
597747685CV3614857single nucleotide variantNM_031414.5(STK31):c.2131G>A (p.Gly711Arg)not specified [RCV004866116]uncertain significance72378364623783646Humanname
597747695CV3614859single nucleotide variantNM_031414.5(STK31):c.1663C>G (p.Leu555Val)not specified [RCV004866118]uncertain significance72376970623769706Humanname
597747707CV3614862single nucleotide variantNM_031414.5(STK31):c.1408A>C (p.Thr470Pro)not specified [RCV004866121]uncertain significance72376291523762915Humanname
597747716CV3614865single nucleotide variantNM_031414.5(STK31):c.1644G>A (p.Met548Ile)not specified [RCV004866123]likely benign72376968723769687Humanname
597747722CV3614866single nucleotide variantNM_031414.5(STK31):c.1870C>A (p.Pro624Thr)not specified [RCV004866124]uncertain significance72377218323772183Humanname
598207566CV3919696single nucleotide variantNM_031414.5(STK31):c.2500G>A (p.Val834Ile)not specified [RCV005291304]uncertain significance72378799223787992Humanname
598251509CV3919697single nucleotide variantNM_031414.5(STK31):c.2552T>C (p.Ile851Thr)not specified [RCV005277902]uncertain significance72378804423788044Humanname
598207572CV3919698single nucleotide variantNM_031414.5(STK31):c.2071A>G (p.Met691Val)not specified [RCV005291305]uncertain significance72378358623783586Humanname
598251514CV3919699single nucleotide variantNM_031414.5(STK31):c.1436A>G (p.Glu479Gly)not specified [RCV005277903]uncertain significance72376901423769014Humanname
598251519CV3919700single nucleotide variantNM_031414.5(STK31):c.1885T>G (p.Leu629Val)not specified [RCV005277904]uncertain significance72377219823772198Humanname
598251523CV3919701single nucleotide variantNM_031414.5(STK31):c.1400G>A (p.Arg467His)not specified [RCV005277905]uncertain significance72376290723762907Humanname
598207578CV3919702single nucleotide variantNM_031414.5(STK31):c.2863A>T (p.Ile955Leu)not specified [RCV005291306]uncertain significance72383216923832169Humanname
598251528CV3919703single nucleotide variantNM_031414.5(STK31):c.1642A>G (p.Met548Val)not specified [RCV005277906]likely benign72376968523769685Humanname
598207585CV3919704single nucleotide variantNM_031414.5(STK31):c.1048A>T (p.Asn350Tyr)not specified [RCV005291307]uncertain significance72375274723752747Humanname
8626392CV81536single nucleotide variantNM_031414.4(STK31):c.2248G>A (p.Val750Ile)Malignant melanoma [RCV000061614]not provided72378557723785577Humanname
8626393CV81537single nucleotide variantNM_031414.4(STK31):c.2308G>A (p.Val770Met)Malignant melanoma [RCV000061615]not provided72378654123786541Humanname
8626394CV81538single nucleotide variantNM_031414.4(STK31):c.2647G>A (p.Ala883Thr)Malignant melanoma [RCV000061616]not provided72379083323790833Humanname
8632531CV87739single nucleotide variantNM_031414.4(STK31):c.2989G>A (p.Glu997Lys)Malignant melanoma [RCV000067831]not provided72383229523832295Humanname
405741155CV3334521single nucleotide variantNM_031414.5(STK31):c.3003G>C (p.Glu1001Asp)not specified [RCV004465734]uncertain significance72383230923832309Humanname
405741162CV3334522single nucleotide variantNM_031414.5(STK31):c.3011A>G (p.Asp1004Gly)not specified [RCV004465735]uncertain significance72383231723832317Humanname
405741169CV3334523single nucleotide variantNM_031414.5(STK31):c.3017G>A (p.Cys1006Tyr)not specified [RCV004465736]likely benign72383232323832323Humanname
597747702CV3614861single nucleotide variantNM_031414.5(STK31):c.3020T>C (p.Met1007Thr)not specified [RCV004866120]uncertain significance72383232623832326Humanname