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Variants search result for Homo sapiens
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57 records found for search term Chrna9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401923386CV2822499single nucleotide variantNM_017581.4(CHRNA9):c.234T>C (p.Thr78=)not provided [RCV003435007]likely benign44033723340337233Humanname
405672142CV3297318single nucleotide variantNM_017581.4(CHRNA9):c.23T>C (p.Ile8Thr)not specified [RCV004441499]uncertain significance44033549040335490Humanname
407455882CV3422871single nucleotide variantNM_017581.4(CHRNA9):c.22A>T (p.Ile8Phe)not specified [RCV004610500]uncertain significance44033548940335489Humanname
401923284CV2822500single nucleotide variantNM_017581.4(CHRNA9):c.675G>A (p.Pro225=)not provided [RCV003435008]likely benign44034919140349191Humanname
405672168CV3297323single nucleotide variantNM_017581.4(CHRNA9):c.56G>C (p.Arg19Thr)not specified [RCV004441504]uncertain significance44033552340335523Humanname
15119791CV734638single nucleotide variantNM_017581.4(CHRNA9):c.99G>C (p.Lys33Asn)not provided [RCV000895786]likely benign44033586140335861Humanname
8625788CV80912single nucleotide variantNM_017581.3(CHRNA9):c.83G>A (p.Gly28Glu)Malignant melanoma [RCV000060989]not provided44033584540335845Humanname
8625789CV80913single nucleotide variantNM_017581.3(CHRNA9):c.312C>T (p.Ser104=)Malignant melanoma [RCV000060990]not provided44033731140337311Humanname
8631173CV86329single nucleotide variantNM_017581.3(CHRNA9):c.549G>A (p.Val183=)Malignant melanoma [RCV000066420]not provided44034906540349065Humanname
155984445CV2344787single nucleotide variantNM_017581.4(CHRNA9):c.188C>T (p.Thr63Met)not specified [RCV004190935]uncertain significance44033595040335950Humanname
155931140CV2362473single nucleotide variantNM_017581.4(CHRNA9):c.167T>C (p.Leu56Pro)not specified [RCV004213093]uncertain significance44033592940335929Humanname
407455877CV3422869single nucleotide variantNM_017581.4(CHRNA9):c.194C>T (p.Ser65Phe)not specified [RCV004610498]uncertain significance44033595640335956Humanname
156079751CV2198410single nucleotide variantNM_017581.4(CHRNA9):c.543T>G (p.Asn181Lys)not specified [RCV004081944]uncertain significance44034905940349059Humanname
156334662CV2214798single nucleotide variantNM_017581.4(CHRNA9):c.505T>C (p.Cys169Arg)not specified [RCV004090600]uncertain significance44034902140349021Humanname
155924072CV2217800single nucleotide variantNM_017581.4(CHRNA9):c.937T>C (p.Ser313Pro)not specified [RCV004083975]uncertain significance44035401740354017Humanname
156118504CV2279056single nucleotide variantNM_017581.4(CHRNA9):c.320T>A (p.Ile107Asn)not specified [RCV004145736]uncertain significance44033731940337319Humanname
156073005CV2331551single nucleotide variantNM_017581.4(CHRNA9):c.956T>C (p.Met319Thr)not specified [RCV004182152]uncertain significance44035403640354036Humanname
156386642CV2364807single nucleotide variantNM_017581.4(CHRNA9):c.574G>A (p.Gly192Arg)not specified [RCV004219673]uncertain significance44034909040349090Humanname
155931423CV2370917single nucleotide variantNM_017581.4(CHRNA9):c.913G>A (p.Ala305Thr)not specified [RCV004218647]uncertain significance44035399340353993Humanname
156263121CV2377122single nucleotide variantNM_017581.4(CHRNA9):c.374A>T (p.Asp125Val)not specified [RCV004229792]uncertain significance44034889040348890Humanname
156214342CV2385912single nucleotide variantNM_017581.4(CHRNA9):c.412C>T (p.Arg138Trp)not specified [RCV004226950]uncertain significance44034892840348928Humanname
329397007CV2459817single nucleotide variantNM_017581.4(CHRNA9):c.466G>T (p.Val156Leu)not specified [RCV004279322]uncertain significance44034898240348982Humanname
401742528CV2673806single nucleotide variantNM_017581.4(CHRNA9):c.326G>C (p.Ser109Thr)not specified [RCV004293190]uncertain significance44033732540337325Humanname
401757877CV2731514single nucleotide variantNM_017581.4(CHRNA9):c.985G>A (p.Glu329Lys)not specified [RCV004330864]uncertain significance44035406540354065Humanname
405672148CV3297319single nucleotide variantNM_017581.4(CHRNA9):c.298G>C (p.Asp100His)not specified [RCV004441500]uncertain significance44033729740337297Humanname
405672154CV3297320single nucleotide variantNM_017581.4(CHRNA9):c.301G>A (p.Gly101Ser)not specified [RCV004441501]uncertain significance44033730040337300Humanname
405672159CV3297321single nucleotide variantNM_017581.4(CHRNA9):c.334G>T (p.Val112Leu)not specified [RCV004441502]uncertain significance44033733340337333Humanname
405672163CV3297322single nucleotide variantNM_017581.4(CHRNA9):c.422G>A (p.Gly141Glu)not specified [RCV004441503]uncertain significance44034893840348938Humanname
405672172CV3297324single nucleotide variantNM_017581.4(CHRNA9):c.728A>T (p.Asn243Ile)not specified [RCV004441505]uncertain significance44034924440349244Humanname
597770601CV3653377single nucleotide variantNM_017581.4(CHRNA9):c.442C>T (p.Pro148Ser)not specified [RCV004896950]uncertain significance44034895840348958Humanname
597770611CV3653379single nucleotide variantNM_017581.4(CHRNA9):c.637A>C (p.Asn213His)not specified [RCV004896952]uncertain significance44034915340349153Humanname
597770621CV3653381single nucleotide variantNM_017581.4(CHRNA9):c.742T>C (p.Cys248Arg)not specified [RCV004896954]uncertain significance44034925840349258Humanname
598215458CV3951776single nucleotide variantNM_017581.4(CHRNA9):c.347A>G (p.Asp116Gly)not specified [RCV005316755]uncertain significance44033734640337346Humanname
598215463CV3951777single nucleotide variantNM_017581.4(CHRNA9):c.707G>A (p.Arg236Lys)not specified [RCV005316756]uncertain significance44034922340349223Humanname
598215467CV3951778single nucleotide variantNM_017581.4(CHRNA9):c.650A>G (p.Tyr217Cys)not specified [RCV005316757]uncertain significance44034916640349166Humanname
598215471CV3951779single nucleotide variantNM_017581.4(CHRNA9):c.890C>T (p.Pro297Leu)not specified [RCV005316758]uncertain significance44034940640349406Humanname
598215475CV3951780single nucleotide variantNM_017581.4(CHRNA9):c.313A>G (p.Ile105Val)not specified [RCV005316759]uncertain significance44033731240337312Humanname
8625790CV80914single nucleotide variantNM_017581.3(CHRNA9):c.963G>A (p.Met321Ile)Malignant melanoma [RCV000060991]not provided44035404340354043Humanname
41405872CV981466single nucleotide variantNM_017581.4(CHRNA9):c.413G>A (p.Arg138Gln)not provided [RCV001810621]uncertain significance44034892940348929Humanname
156158536CV2262493single nucleotide variantNM_017581.4(CHRNA9):c.1416T>G (p.Ile472Met)not specified [RCV004128923]uncertain significance44035449640354496Humanname
155925941CV2287784single nucleotide variantNM_017581.4(CHRNA9):c.1298A>G (p.Lys433Arg)not specified [RCV004143232]uncertain significance44035437840354378Humanname
156058322CV2343614single nucleotide variantNM_017581.4(CHRNA9):c.1000C>T (p.Pro334Ser)not specified [RCV004190644]uncertain significance44035408040354080Humanname
156280081CV2348413single nucleotide variantNM_017581.4(CHRNA9):c.1037C>T (p.Ser346Phe)not specified [RCV004193605]uncertain significance44035411740354117Humanname
156009296CV2361984single nucleotide variantNM_017581.4(CHRNA9):c.1400T>C (p.Val467Ala)not specified [RCV004207750]uncertain significance44035448040354480Humanname
401729745CV2683783single nucleotide variantNM_017581.4(CHRNA9):c.1096G>C (p.Glu366Gln)not specified [RCV004284518]uncertain significance44035417640354176Humanname
401759877CV2707176single nucleotide variantNM_017581.4(CHRNA9):c.1214G>A (p.Gly405Asp)not specified [RCV004315539]uncertain significance44035429440354294Humanname
401887095CV2773150single nucleotide variantNM_017581.4(CHRNA9):c.1274C>T (p.Thr425Met)not specified [RCV004351878]uncertain significance44035435440354354Humanname
405672126CV3297315single nucleotide variantNM_017581.4(CHRNA9):c.1082C>T (p.Pro361Leu)not specified [RCV004441496]uncertain significance44035416240354162Humanname
405672132CV3297316single nucleotide variantNM_017581.4(CHRNA9):c.1100G>A (p.Arg367Gln)not specified [RCV004441497]uncertain significance44035418040354180Humanname
405672137CV3297317single nucleotide variantNM_017581.4(CHRNA9):c.1190A>G (p.Asn397Ser)not specified [RCV004441498]uncertain significance44035427040354270Humanname
407455880CV3422870single nucleotide variantNM_017581.4(CHRNA9):c.1252T>C (p.Cys418Arg)not specified [RCV004610499]uncertain significance44035433240354332Humanname
597770606CV3653378single nucleotide variantNM_017581.4(CHRNA9):c.1313A>G (p.His438Arg)not specified [RCV004896951]uncertain significance44035439340354393Humanname
597770616CV3653380single nucleotide variantNM_017581.4(CHRNA9):c.1114A>G (p.Lys372Glu)not specified [RCV004896953]uncertain significance44035419440354194Humanname
597770625CV3653382single nucleotide variantNM_017581.4(CHRNA9):c.1370G>A (p.Arg457Gln)not specified [RCV004896955]uncertain significance44035445040354450Humanname
598215453CV3951775single nucleotide variantNM_017581.4(CHRNA9):c.1252T>G (p.Cys418Gly)not specified [RCV005316754]uncertain significance44035433240354332Humanname
15150650CV748943single nucleotide variantNM_017581.4(CHRNA9):c.1418T>G (p.Leu473Trp)not provided [RCV000923517]likely benign44035449840354498Humanname
8631174CV86330single nucleotide variantNM_017581.3(CHRNA9):c.1226A>G (p.Lys409Arg)Malignant melanoma [RCV000066421]not provided44035430640354306Humanname