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46 records found for search term Rgs14
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401741008CV2679854single nucleotide variantNM_006480.5(RGS14):c.41G>A (p.Arg14His)not specified [RCV004282308]uncertain significance5177358065177358065Humanname
405715550CV3309197single nucleotide variantNM_006480.5(RGS14):c.41G>T (p.Arg14Leu)not specified [RCV004449136]uncertain significance5177358065177358065Humanname
405715563CV3309199single nucleotide variantNM_006480.5(RGS14):c.94G>T (p.Gly32Cys)not specified [RCV004449138]uncertain significance5177366203177366203Humanname
597775751CV3586328single nucleotide variantNM_006480.5(RGS14):c.62A>G (p.Asp21Gly)not specified [RCV004852332]uncertain significance5177365979177365979Humanname
156360136CV2268987single nucleotide variantNM_006480.5(RGS14):c.103G>A (p.Glu35Lys)not specified [RCV004128385]uncertain significance5177366212177366212Humanname
405715525CV3309194single nucleotide variantNM_006480.5(RGS14):c.172G>A (p.Glu58Lys)not specified [RCV004449133]uncertain significance5177366281177366281Humanname
405715533CV3309195single nucleotide variantNM_006480.5(RGS14):c.173A>G (p.Glu58Gly)not specified [RCV004449134]uncertain significance5177366282177366282Humanname
329377736CV2436018single nucleotide variantNM_006480.5(RGS14):c.659C>T (p.Pro220Leu)not specified [RCV004255238]uncertain significance5177367745177367745Humanname
329389600CV2445230single nucleotide variantNM_006480.5(RGS14):c.658C>T (p.Pro220Ser)not specified [RCV004263863]uncertain significance5177367744177367744Humanname
329393441CV2453360single nucleotide variantNM_006480.5(RGS14):c.742C>G (p.Leu248Val)not specified [RCV004266982]uncertain significance5177368159177368159Humanname
329393442CV2453361single nucleotide variantNM_006480.5(RGS14):c.743T>G (p.Leu248Arg)not specified [RCV004266983]uncertain significance5177368160177368160Humanname
329397171CV2459982single nucleotide variantNM_006480.5(RGS14):c.880G>T (p.Gly294Cys)not specified [RCV004279458]uncertain significance5177368747177368747Humanname
329397867CV2464090single nucleotide variantNM_006480.5(RGS14):c.707G>A (p.Gly236Glu)not specified [RCV004273787]uncertain significance5177367793177367793Humanname
405715542CV3309196single nucleotide variantNM_006480.5(RGS14):c.418G>A (p.Ala140Thr)not specified [RCV004449135]uncertain significance5177366969177366969Humanname
405715555CV3309198single nucleotide variantNM_006480.5(RGS14):c.779C>T (p.Ser260Phe)not specified [RCV004449137]uncertain significance5177368196177368196Humanname
407474248CV3472811single nucleotide variantNM_006480.5(RGS14):c.546G>C (p.Glu182Asp)not specified [RCV004662950]uncertain significance5177367476177367476Humanname
407508103CV3472814single nucleotide variantNM_006480.5(RGS14):c.380C>G (p.Ser127Cys)not specified [RCV004671936]uncertain significance5177366931177366931Humanname
597775730CV3586323single nucleotide variantNM_006480.5(RGS14):c.665G>A (p.Gly222Asp)not specified [RCV004852327]uncertain significance5177367751177367751Humanname
597775742CV3586326single nucleotide variantNM_006480.5(RGS14):c.320C>G (p.Pro107Arg)not specified [RCV004852330]uncertain significance5177366781177366781Humanname
597775746CV3586327single nucleotide variantNM_006480.5(RGS14):c.448C>T (p.Pro150Ser)not specified [RCV004852331]uncertain significance5177366999177366999Humanname
597788048CV3586329single nucleotide variantNM_006480.5(RGS14):c.928G>C (p.Asp310His)not specified [RCV004855395]uncertain significance5177368795177368795Humanname
156374378CV2198427single nucleotide variantNM_006480.5(RGS14):c.1438A>G (p.Ser480Gly)not specified [RCV004081958]uncertain significance5177371529177371529Humanname
156112950CV2212629single nucleotide variantNM_006480.5(RGS14):c.1282G>A (p.Gly428Arg)not specified [RCV004085163]uncertain significance5177371192177371192Humanname
156401017CV2213736single nucleotide variantNM_006480.5(RGS14):c.1081G>A (p.Val361Met)not specified [RCV004089807]uncertain significance5177370618177370618Humanname
156342963CV2364037single nucleotide variantNM_006480.5(RGS14):c.1430C>T (p.Ala477Val)not specified [RCV004221426]likely benign5177371521177371521Humanname
155902767CV2386333single nucleotide variantNM_006480.5(RGS14):c.1604C>T (p.Ala535Val)not specified [RCV004228673]uncertain significance5177371978177371978Humanname
156110421CV2387644single nucleotide variantNM_006480.5(RGS14):c.1069C>G (p.Gln357Glu)not specified [RCV004234192]uncertain significance5177370606177370606Humanname
156221736CV2392556single nucleotide variantNM_006480.5(RGS14):c.1178C>G (p.Thr393Ser)not specified [RCV004245421]uncertain significance5177370955177370955Humanname
156002972CV2396666single nucleotide variantNM_006480.5(RGS14):c.1642A>G (p.Lys548Glu)not specified [RCV004240483]likely benign5177372016177372016Humanname
156003603CV2396767single nucleotide variantNM_006480.5(RGS14):c.1621G>C (p.Glu541Gln)not specified [RCV004233915]likely benign5177371995177371995Humanname
329391871CV2453204single nucleotide variantNM_006480.5(RGS14):c.1417C>T (p.His473Tyr)not specified [RCV004279576]uncertain significance5177371508177371508Humanname
401766608CV2676224single nucleotide variantNM_006480.5(RGS14):c.1175C>G (p.Pro392Arg)not specified [RCV004286269]uncertain significance5177370952177370952Humanname
401728658CV2729718single nucleotide variantNM_006480.5(RGS14):c.1685C>T (p.Thr562Ile)not specified [RCV004331973]uncertain significance5177372059177372059Humanname
405715479CV3309187single nucleotide variantNM_006480.5(RGS14):c.1013C>G (p.Ser338Cys)not specified [RCV004449126]uncertain significance5177368880177368880Humanname
405715492CV3309189single nucleotide variantNM_006480.5(RGS14):c.1117A>G (p.Ile373Val)not specified [RCV004449128]uncertain significance5177370654177370654Humanname
405715499CV3309190single nucleotide variantNM_006480.5(RGS14):c.1156G>A (p.Val386Ile)not specified [RCV004449129]uncertain significance5177370933177370933Humanname
405715507CV3309191single nucleotide variantNM_006480.5(RGS14):c.1213G>A (p.Glu405Lys)not specified [RCV004449130]uncertain significance5177370990177370990Humanname
405715513CV3309192single nucleotide variantNM_006480.5(RGS14):c.1283G>A (p.Gly428Glu)not specified [RCV004449131]likely benign5177371193177371193Humanname
405715519CV3309193single nucleotide variantNM_006480.5(RGS14):c.1364A>G (p.Lys455Arg)not specified [RCV004449132]uncertain significance5177371377177371377Humanname
407508095CV3472812single nucleotide variantNM_006480.5(RGS14):c.1172A>G (p.Lys391Arg)not specified [RCV004671934]uncertain significance5177370949177370949Humanname
407474253CV3472815single nucleotide variantNM_006480.5(RGS14):c.1004G>A (p.Arg335Gln)not specified [RCV004662951]uncertain significance5177368871177368871Humanname
597775726CV3586322single nucleotide variantNM_006480.5(RGS14):c.1151G>T (p.Arg384Leu)not specified [RCV004852326]uncertain significance5177370928177370928Humanname
597775734CV3586324single nucleotide variantNM_006480.5(RGS14):c.1468A>T (p.Thr490Ser)not specified [RCV004852328]uncertain significance5177371559177371559Humanname
597775738CV3586325single nucleotide variantNM_006480.5(RGS14):c.1394C>T (p.Pro465Leu)not specified [RCV004852329]uncertain significance5177371485177371485Humanname
598188904CV3902548single nucleotide variantNM_006480.5(RGS14):c.1664G>C (p.Gly555Ala)not specified [RCV005266642]uncertain significance5177372038177372038Humanname
15165982CV699022single nucleotide variantNM_006480.5(RGS14):c.1621G>A (p.Glu541Lys)not provided [RCV000948724]benign5177371995177371995Humanname