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44 records found for search term Usp39
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405800709CV3338214single nucleotide variantNM_006590.4(USP39):c.7G>A (p.Gly3Ser)not specified [RCV004477413]likely benign28561620285616202Humanname
405800695CV3338207single nucleotide variantNM_006590.4(USP39):c.23A>G (p.Glu8Gly)not specified [RCV004477406]uncertain significance28561621885616218Humanname
156081945CV2301126single nucleotide variantNM_006590.4(USP39):c.74C>T (p.Ser25Phe)not specified [RCV004160042]uncertain significance28561626985616269Humanname
401912186CV2812061single nucleotide variantNM_006590.4(USP39):c.300G>C (p.Arg100=)not provided [RCV003427087]likely benign28561925185619251Humanname
405800701CV3338210single nucleotide variantNM_006590.4(USP39):c.31G>A (p.Gly11Ser)not specified [RCV004477409]uncertain significance28561622685616226Humanname
405800703CV3338211single nucleotide variantNM_006590.4(USP39):c.40C>T (p.Arg14Cys)not specified [RCV004477410]uncertain significance28561623585616235Humanname
598125280CV3881527single nucleotide variantNM_006590.4(USP39):c.570G>A (p.Thr190=)not specified [RCV005232433]uncertain significance28562378285623782Humanname
598275306CV3932843single nucleotide variantNM_006590.4(USP39):c.64C>G (p.Arg22Gly)not specified [RCV005304440]uncertain significance28561625985616259Humanname
156231688CV2199681single nucleotide variantNM_006590.4(USP39):c.226C>T (p.Arg76Cys)not specified [RCV004072417]uncertain significance28561642185616421Humanname
156136668CV2239703single nucleotide variantNM_006590.4(USP39):c.134G>A (p.Gly45Asp)not specified [RCV004108247]uncertain significance28561632985616329Humanname
155925850CV2258635single nucleotide variantNM_006590.4(USP39):c.119C>T (p.Ala40Val)not specified [RCV004117892]uncertain significance28561631485616314Humanname
156175064CV2326991single nucleotide variantNM_006590.4(USP39):c.173G>T (p.Ser58Ile)not specified [RCV004178586]uncertain significance28561636885616368Humanname
156076413CV2375036single nucleotide variantNM_006590.4(USP39):c.232G>A (p.Val78Ile)not specified [RCV004230087]uncertain significance28561642785616427Humanname
401772143CV2687427single nucleotide variantNM_006590.4(USP39):c.157G>C (p.Glu53Gln)not specified [RCV004300672]uncertain significance28561635285616352Humanname
405800686CV3338202single nucleotide variantNM_006590.4(USP39):c.124A>C (p.Ser42Arg)not specified [RCV004477401]uncertain significance28561631985616319Humanname
407528823CV3487616single nucleotide variantNM_006590.4(USP39):c.149T>C (p.Val50Ala)not specified [RCV004680586]uncertain significance28561634485616344Humanname
407528825CV3487617single nucleotide variantNM_006590.4(USP39):c.145C>T (p.Arg49Cys)not specified [RCV004680587]uncertain significance28561634085616340Humanname
597798908CV3623040single nucleotide variantNM_006590.4(USP39):c.110A>T (p.Glu37Val)not specified [RCV004879416]uncertain significance28561630585616305Humanname
597798912CV3623043single nucleotide variantNM_006590.4(USP39):c.137G>C (p.Ser46Thr)not specified [RCV004879418]uncertain significance28561633285616332Humanname
597798916CV3623045single nucleotide variantNM_006590.4(USP39):c.205T>G (p.Phe69Val)not specified [RCV004879420]uncertain significance28561640085616400Humanname
156355675CV2324527single nucleotide variantNM_006590.4(USP39):c.993C>G (p.His331Gln)not specified [RCV004179004]uncertain significance28563609685636096Humanname
156081441CV2333772single nucleotide variantNM_006590.4(USP39):c.944A>G (p.Lys315Arg)not specified [RCV004181279]uncertain significance28563094185630941Humanname
405800697CV3338208single nucleotide variantNM_006590.4(USP39):c.307C>T (p.Arg103Cys)not specified [RCV004477407]uncertain significance28561925885619258Humanname
405800705CV3338212single nucleotide variantNM_006590.4(USP39):c.432A>T (p.Gln144His)not specified [RCV004477411]uncertain significance28562157885621578Humanname
405800707CV3338213single nucleotide variantNM_006590.4(USP39):c.788A>G (p.Lys263Arg)not specified [RCV004477412]uncertain significance28563078585630785Humanname
407528827CV3487618single nucleotide variantNM_006590.4(USP39):c.958G>T (p.Val320Phe)not specified [RCV004680588]uncertain significance28563606185636061Humanname
597798910CV3623041single nucleotide variantNM_006590.4(USP39):c.566T>C (p.Ile189Thr)not specified [RCV004879417]uncertain significance28562377885623778Humanname
597798914CV3623044single nucleotide variantNM_006590.4(USP39):c.784A>G (p.Ile262Val)not specified [RCV004879419]uncertain significance28563078185630781Humanname
597724024CV3623047single nucleotide variantNM_006590.4(USP39):c.755A>G (p.Tyr252Cys)not specified [RCV004888133]uncertain significance28563075285630752Humanname
156275676CV2202781single nucleotide variantNM_006590.4(USP39):c.1681A>G (p.Asn561Asp)not specified [RCV004083019]uncertain significance28564879185648791Humanname
156035779CV2208247single nucleotide variantNM_006590.4(USP39):c.1326G>C (p.Gln442His)not specified [RCV004088698]uncertain significance28564101785641017Humanname
155973814CV2239037single nucleotide variantNM_006590.4(USP39):c.1670A>G (p.Asn557Ser)not specified [RCV004109915]uncertain significance28564878085648780Humanname
156094560CV2300308single nucleotide variantNM_006590.4(USP39):c.1013A>G (p.Lys338Arg)not specified [RCV004153259]uncertain significance28563611685636116Humanname
156056486CV2320620single nucleotide variantNM_006590.4(USP39):c.1603A>G (p.Thr535Ala)not specified [RCV004172235]uncertain significance28564796985647969Humanname
156129867CV2364766single nucleotide variantNM_006590.4(USP39):c.1531G>C (p.Glu511Gln)not specified [RCV004219639]uncertain significance28564505185645051Humanname
156000175CV2383179single nucleotide variantNM_006590.4(USP39):c.1690G>C (p.Gly564Arg)not specified [RCV004220192]uncertain significance28564880085648800Humanname
401739814CV2684181single nucleotide variantNM_006590.4(USP39):c.1531G>A (p.Glu511Lys)not specified [RCV004288852]uncertain significance28564505185645051Humanname
405800684CV3338201single nucleotide variantNM_006590.4(USP39):c.1028C>G (p.Thr343Ser)not specified [RCV004477400]uncertain significance28563736985637369Humanname
405800688CV3338203single nucleotide variantNM_006590.4(USP39):c.1381A>T (p.Asn461Tyr)not specified [RCV004477402]uncertain significance28564107285641072Humanname
405800690CV3338204single nucleotide variantNM_006590.4(USP39):c.1432G>A (p.Val478Met)not specified [RCV004477403]uncertain significance28564495285644952Humanname
405800691CV3338205single nucleotide variantNM_006590.4(USP39):c.1490A>G (p.Tyr497Cys)not specified [RCV004477404]uncertain significance28564501085645010Humanname
597724004CV3623042single nucleotide variantNM_006590.4(USP39):c.1390G>A (p.Val464Ile)not specified [RCV004888131]uncertain significance28564108185641081Humanname
597724014CV3623046single nucleotide variantNM_006590.4(USP39):c.1604C>T (p.Thr535Ile)not specified [RCV004888132]uncertain significance28564797085647970Humanname
598204262CV3932841single nucleotide variantNM_006590.4(USP39):c.1167G>T (p.Met389Ile)not specified [RCV005290663]uncertain significance28563927485639274Humanname