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Variants search result for Homo sapiens
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84 records found for search term Adra1d
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597783379CV3658835single nucleotide variantNM_000678.4(ADRA1D):c.24C>G (p.Ser8Arg)not specified [RCV004900195]uncertain significance2042489344248934Humanname
597679280CV3662504single nucleotide variantNM_000678.4(ADRA1D):c.20T>A (p.Leu7Gln)not specified [RCV004914072]uncertain significance2042489384248938Humanname
329376738CV2428526single nucleotide variantNM_000678.4(ADRA1D):c.58G>A (p.Ala20Thr)not specified [RCV004253311]uncertain significance2042489004248900Humanname
329376739CV2428527single nucleotide variantNM_000678.4(ADRA1D):c.59C>G (p.Ala20Gly)not specified [RCV004253312]uncertain significance2042488994248899Humanname
329366491CV2445776single nucleotide variantNM_000678.4(ADRA1D):c.89G>T (p.Gly30Val)not specified [RCV004259835]uncertain significance2042488694248869Humanname
405758977CV3256067single nucleotide variantNM_000678.4(ADRA1D):c.65G>A (p.Gly22Asp)not specified [RCV004383132]uncertain significance2042488934248893Humanname
597801460CV3658784single nucleotide variantNM_000678.4(ADRA1D):c.64G>A (p.Gly22Ser)not specified [RCV004906211]uncertain significance2042488944248894Humanname
15121019CV773105single nucleotide variantNM_000678.4(ADRA1D):c.684C>G (p.Ser228=)not provided [RCV000940444]benign2042482744248274Humanname
156234288CV2193298single nucleotide variantNM_000678.4(ADRA1D):c.173G>A (p.Gly58Asp)not specified [RCV004071606]uncertain significance2042487854248785Humanname
156163167CV2305483single nucleotide variantNM_000678.4(ADRA1D):c.107C>G (p.Ala36Gly)not specified [RCV004165197]uncertain significance2042488514248851Humanname
401784154CV2721096single nucleotide variantNM_000678.4(ADRA1D):c.157G>A (p.Gly53Ser)not specified [RCV004330130]uncertain significance2042488014248801Humanname
405758631CV3256008single nucleotide variantNM_000678.4(ADRA1D):c.104C>G (p.Ala35Gly)not specified [RCV004383073]uncertain significance2042488544248854Humanname
405758806CV3256039single nucleotide variantNM_000678.4(ADRA1D):c.201C>A (p.Ser67Arg)not specified [RCV004383104]uncertain significance2042487574248757Humanname
405758818CV3256041single nucleotide variantNM_000678.4(ADRA1D):c.217G>A (p.Gly73Arg)not specified [RCV004383106]uncertain significance2042487414248741Humanname
407489254CV3434731single nucleotide variantNM_000678.4(ADRA1D):c.241G>C (p.Val81Leu)not specified [RCV004619882]uncertain significance2042487174248717Humanname
407489297CV3434739single nucleotide variantNM_000678.4(ADRA1D):c.124G>C (p.Ala42Pro)not specified [RCV004619890]uncertain significance2042488344248834Humanname
407489347CV3434750single nucleotide variantNM_000678.4(ADRA1D):c.125C>T (p.Ala42Val)not specified [RCV004619901]uncertain significance2042488334248833Humanname
597679807CV3662576single nucleotide variantNM_000678.4(ADRA1D):c.146G>A (p.Gly49Asp)not specified [RCV004914132]uncertain significance2042488124248812Humanname
598222494CV3956331single nucleotide variantNM_000678.4(ADRA1D):c.240C>G (p.Asp80Glu)not specified [RCV005317924]likely benign2042487184248718Humanname
598222664CV3956359single nucleotide variantNM_000678.4(ADRA1D):c.143G>A (p.Gly48Glu)not specified [RCV005317952]uncertain significance2042488154248815Humanname
156374063CV2198192single nucleotide variantNM_000678.4(ADRA1D):c.950G>A (p.Gly317Glu)not specified [RCV004079778]uncertain significance2042480084248008Humanname
156075768CV2281543single nucleotide variantNM_000678.4(ADRA1D):c.763G>C (p.Ala255Pro)not specified [RCV004153853]uncertain significance2042481954248195Humanname
156146146CV2289154single nucleotide variantNM_000678.4(ADRA1D):c.938C>A (p.Thr313Lys)not specified [RCV004150375]uncertain significance2042480204248020Humanname
156194991CV2297185single nucleotide variantNM_000678.4(ADRA1D):c.818T>C (p.Met273Thr)not specified [RCV004151076]uncertain significance2042481404248140Humanname
156044892CV2305977single nucleotide variantNM_000678.4(ADRA1D):c.568A>T (p.Ile190Phe)not specified [RCV004169536]uncertain significance2042483904248390Humanname
156276059CV2318456single nucleotide variantNM_000678.4(ADRA1D):c.370A>C (p.Asn124His)not specified [RCV004173103]uncertain significance2042485884248588Humanname
155968927CV2339365single nucleotide variantNM_000678.4(ADRA1D):c.844C>G (p.Arg282Gly)not specified [RCV004191590]uncertain significance2042481144248114Humanname
156329450CV2342405single nucleotide variantNM_000678.4(ADRA1D):c.722C>T (p.Pro241Leu)not specified [RCV004194017]uncertain significance2042482364248236Humanname
156125917CV2350239single nucleotide variantNM_000678.4(ADRA1D):c.957C>G (p.His319Gln)not specified [RCV004202196]uncertain significance2042480014248001Humanname
156200170CV2362924single nucleotide variantNM_000678.4(ADRA1D):c.778G>A (p.Val260Met)not specified [RCV004209028]uncertain significance2042481804248180Humanname
156267784CV2371884single nucleotide variantNM_000678.4(ADRA1D):c.331G>A (p.Val111Met)not specified [RCV004221573]uncertain significance2042486274248627Humanname
329402276CV2454118single nucleotide variantNM_000678.4(ADRA1D):c.568A>C (p.Ile190Leu)not specified [RCV004265615]uncertain significance2042483904248390Humanname
329392551CV2471314single nucleotide variantNM_000678.4(ADRA1D):c.496C>T (p.Arg166Cys)not specified [RCV004280328]uncertain significance2042484624248462Humanname
401728230CV2685958single nucleotide variantNM_000678.4(ADRA1D):c.739G>A (p.Gly247Ser)not specified [RCV004294928]uncertain significance2042482194248219Humanname
401769554CV2689824single nucleotide variantNM_000678.4(ADRA1D):c.458C>T (p.Ser153Leu)not specified [RCV004297726]uncertain significance2042485004248500Humanname
401761819CV2699424single nucleotide variantNM_000678.4(ADRA1D):c.628G>C (p.Glu210Gln)not specified [RCV004305995]uncertain significance2042483304248330Humanname
405758988CV3256069single nucleotide variantNM_000678.4(ADRA1D):c.721C>A (p.Pro241Thr)not specified [RCV004383134]uncertain significance2042482374248237Humanname
405759172CV3256099single nucleotide variantNM_000678.4(ADRA1D):c.926G>C (p.Arg309Pro)not specified [RCV004383164]uncertain significance2042480324248032Humanname
407489194CV3434719single nucleotide variantNM_000678.4(ADRA1D):c.322C>T (p.Leu108Phe)not specified [RCV004619870]uncertain significance2042486364248636Humanname
407489234CV3434726single nucleotide variantNM_000678.4(ADRA1D):c.799A>G (p.Met267Val)not specified [RCV004619877]uncertain significance2042481594248159Humanname
407489400CV3434763single nucleotide variantNM_000678.4(ADRA1D):c.949G>T (p.Gly317Trp)not specified [RCV004619914]uncertain significance2042480094248009Humanname
407489444CV3434771single nucleotide variantNM_000678.4(ADRA1D):c.523G>A (p.Val175Met)not specified [RCV004619922]uncertain significance2042484354248435Humanname
407489472CV3434777single nucleotide variantNM_000678.4(ADRA1D):c.496C>A (p.Arg166Ser)not specified [RCV004619928]uncertain significance2042484624248462Humanname
597801482CV3658794single nucleotide variantNM_000678.4(ADRA1D):c.758G>A (p.Gly253Asp)not specified [RCV004906221]uncertain significance2042482004248200Humanname
597801504CV3658804single nucleotide variantNM_000678.4(ADRA1D):c.949G>C (p.Gly317Arg)not specified [RCV004906231]uncertain significance2042480094248009Humanname
597801526CV3658814single nucleotide variantNM_000678.4(ADRA1D):c.992G>A (p.Ser331Asn)not specified [RCV004906241]uncertain significance2042479664247966Humanname
597679738CV3662568single nucleotide variantNM_000678.4(ADRA1D):c.928G>A (p.Gly310Ser)not specified [RCV004914124]uncertain significance2042480304248030Humanname
597679846CV3662586single nucleotide variantNM_000678.4(ADRA1D):c.521C>T (p.Ala174Val)not specified [RCV004914137]uncertain significance2042484374248437Humanname
597679930CV3662597single nucleotide variantNM_000678.4(ADRA1D):c.941G>T (p.Gly314Val)not specified [RCV004914147]uncertain significance2042480174248017Humanname
597801423CV3662655single nucleotide variantNM_000678.4(ADRA1D):c.959G>A (p.Gly320Asp)not specified [RCV004906193]uncertain significance2042479994247999Humanname
597783385CV3662663single nucleotide variantNM_000678.4(ADRA1D):c.631C>G (p.Arg211Gly)not specified [RCV004900194]uncertain significance2042483274248327Humanname
155915083CV2243664single nucleotide variantNM_000678.4(ADRA1D):c.1430C>G (p.Thr477Arg)not specified [RCV004114374]uncertain significance2042218124221812Humanname
155926558CV2258813single nucleotide variantNM_000678.4(ADRA1D):c.1231C>G (p.Arg411Gly)not specified [RCV004118034]uncertain significance2042220114222011Humanname
156269626CV2275713single nucleotide variantNM_000678.4(ADRA1D):c.1370C>T (p.Pro457Leu)not specified [RCV004137324]uncertain significance2042218724221872Humanname
156003818CV2290074single nucleotide variantNM_000678.4(ADRA1D):c.1427G>T (p.Gly476Val)not specified [RCV004152755]uncertain significance2042218154221815Humanname
156186570CV2302716single nucleotide variantNM_000678.4(ADRA1D):c.1432C>A (p.Pro478Thr)not specified [RCV004162647]uncertain significance2042218104221810Humanname
156291794CV2306126single nucleotide variantNM_000678.4(ADRA1D):c.1537A>G (p.Lys513Glu)not specified [RCV004162880]uncertain significance2042217054221705Humanname
401753739CV2685043single nucleotide variantNM_000678.4(ADRA1D):c.1309C>A (p.His437Asn)not specified [RCV004289623]uncertain significance2042219334221933Humanname
401760550CV2695080single nucleotide variantNM_000678.4(ADRA1D):c.1219C>A (p.Arg407Ser)not specified [RCV004303238]uncertain significance2042220234222023Humanname
401740711CV2702596single nucleotide variantNM_000678.4(ADRA1D):c.1707G>C (p.Glu569Asp)not specified [RCV004317078]uncertain significance2042215354221535Humanname
401782244CV2719248single nucleotide variantNM_000678.4(ADRA1D):c.1201A>G (p.Ile401Val)not specified [RCV004324897]uncertain significance2042220414222041Humanname
401866970CV2769925single nucleotide variantNM_000678.4(ADRA1D):c.1507T>C (p.Phe503Leu)not specified [RCV004353764]likely benign2042217354221735Humanname
405758792CV3256036single nucleotide variantNM_000678.4(ADRA1D):c.1541T>C (p.Val514Ala)not specified [RCV004383101]uncertain significance2042217014221701Humanname
407489142CV3434710single nucleotide variantNM_000678.4(ADRA1D):c.1072G>C (p.Val358Leu)not specified [RCV004619861]uncertain significance2042478864247886Humanname
407489231CV3434725single nucleotide variantNM_000678.4(ADRA1D):c.1247T>G (p.Leu416Arg)not specified [RCV004619876]uncertain significance2042219954221995Humanname
407489389CV3434761single nucleotide variantNM_000678.4(ADRA1D):c.1600G>A (p.Ala534Thr)not specified [RCV004619912]uncertain significance2042216424221642Humanname
407489530CV3434788single nucleotide variantNM_000678.4(ADRA1D):c.1511G>A (p.Arg504Gln)not specified [RCV004619939]uncertain significance2042217314221731Humanname
597801550CV3658825single nucleotide variantNM_000678.4(ADRA1D):c.1523C>G (p.Thr508Ser)not specified [RCV004906252]uncertain significance2042217194221719Humanname
597679183CV3662493single nucleotide variantNM_000678.4(ADRA1D):c.1032G>T (p.Lys344Asn)not specified [RCV004914061]uncertain significance2042479264247926Humanname
597679389CV3662515single nucleotide variantNM_000678.4(ADRA1D):c.1171G>A (p.Gly391Ser)not specified [RCV004914083]uncertain significance2042220714222071Humanname
597679429CV3662520single nucleotide variantNM_000678.4(ADRA1D):c.1661C>G (p.Ala554Gly)not specified [RCV004914087]uncertain significance2042215814221581Humanname
597679529CV3662532single nucleotide variantNM_000678.4(ADRA1D):c.1075C>T (p.Leu359Phe)not specified [RCV004914098]uncertain significance2042478834247883Humanname
597679603CV3662542single nucleotide variantNM_000678.4(ADRA1D):c.1063G>C (p.Gly355Arg)not specified [RCV004914106]uncertain significance2042478954247895Humanname
597679613CV3662550single nucleotide variantNM_000678.4(ADRA1D):c.1592C>T (p.Ala531Val)not specified [RCV004914107]uncertain significance2042216504221650Humanname
597679676CV3662558single nucleotide variantNM_000678.4(ADRA1D):c.1015A>C (p.Lys339Gln)not specified [RCV004914114]uncertain significance2042479434247943Humanname
597680008CV3662607single nucleotide variantNM_000678.4(ADRA1D):c.1316G>C (p.Arg439Pro)not specified [RCV004914157]uncertain significance2042219264221926Humanname
597801359CV3662618single nucleotide variantNM_000678.4(ADRA1D):c.1370C>G (p.Pro457Arg)not specified [RCV004906162]uncertain significance2042218724221872Humanname
597801378CV3662627single nucleotide variantNM_000678.4(ADRA1D):c.1685C>G (p.Ala562Gly)not specified [RCV004906171]uncertain significance2042215574221557Humanname
597801416CV3662647single nucleotide variantNM_000678.4(ADRA1D):c.1476C>A (p.Ser492Arg)not specified [RCV004906190]uncertain significance2042217664221766Humanname
598222546CV3956340single nucleotide variantNM_000678.4(ADRA1D):c.1283G>T (p.Arg428Leu)not specified [RCV005317933]uncertain significance2042219594221959Humanname
598222609CV3956350single nucleotide variantNM_000678.4(ADRA1D):c.1687G>A (p.Asp563Asn)not specified [RCV005317943]uncertain significance2042215554221555Humanname
598222725CV3956369single nucleotide variantNM_000678.4(ADRA1D):c.1504C>G (p.Pro502Ala)not specified [RCV005317962]uncertain significance2042217384221738Humanname
598222370CV3960247single nucleotide variantNM_000678.4(ADRA1D):c.1337G>A (p.Arg446His)not specified [RCV005317898]uncertain significance2042219054221905Humanname
598222448CV3960263single nucleotide variantNM_000678.4(ADRA1D):c.1264C>T (p.Arg422Cys)not specified [RCV005317914]uncertain significance2042219784221978Humanname