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Variants search result for Homo sapiens
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59 records found for search term Slco4c1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
402516482CV2936422microsatelliteNM_180991.5(SLCO4C1):c.1022-27AT[7]not provided [RCV003662988]likely benign5102260331102260332Humanname
156061947CV2263175single nucleotide variantNM_180991.5(SLCO4C1):c.50C>T (p.Pro17Leu)not specified [RCV004131408]uncertain significance5102296213102296213Humanname
156305647CV2314671single nucleotide variantNM_180991.5(SLCO4C1):c.56T>G (p.Ile19Ser)not specified [RCV004170823]uncertain significance5102296207102296207Humanname
15202885CV777489deletionNM_180991.5(SLCO4C1):c.1022-15_1022-10delnot provided [RCV000958090]likely benign5102260329102260334Humanname
156262289CV2201083single nucleotide variantNM_180991.5(SLCO4C1):c.115C>A (p.Pro39Thr)not specified [RCV004075206]likely benign5102296148102296148Humanname
597777433CV3603151single nucleotide variantNM_180991.5(SLCO4C1):c.182C>T (p.Pro61Leu)not specified [RCV004873034]uncertain significance5102296081102296081Humanname
597777441CV3603153single nucleotide variantNM_180991.5(SLCO4C1):c.249T>G (p.Phe83Leu)not specified [RCV004873036]uncertain significance5102296014102296014Humanname
156070003CV2316865single nucleotide variantNM_180991.5(SLCO4C1):c.316G>A (p.Gly106Ser)not specified [RCV004174393]uncertain significance5102295947102295947Humanname
156040647CV2387629single nucleotide variantNM_180991.5(SLCO4C1):c.889A>G (p.Met297Val)not specified [RCV004234177]likely benign5102263694102263694Humanname
156006408CV2401194single nucleotide variantNM_180991.5(SLCO4C1):c.539T>C (p.Phe180Ser)not specified [RCV004245748]uncertain significance5102291423102291423Humanname
329377830CV2436049single nucleotide variantNM_180991.5(SLCO4C1):c.796T>G (p.Tyr266Asp)not specified [RCV004255267]uncertain significance5102270630102270630Humanname
401717762CV2706903single nucleotide variantNM_180991.5(SLCO4C1):c.749G>C (p.Gly250Ala)not specified [RCV004321520]uncertain significance5102270677102270677Humanname
405772328CV3332940single nucleotide variantNM_180991.5(SLCO4C1):c.746T>A (p.Leu249Gln)not specified [RCV004457199]uncertain significance5102270680102270680Humanname
405772334CV3332941single nucleotide variantNM_180991.5(SLCO4C1):c.886G>C (p.Ala296Pro)not specified [RCV004457200]uncertain significance5102263697102263697Humanname
407493640CV3477351single nucleotide variantNM_180991.5(SLCO4C1):c.643A>T (p.Ser215Cys)not specified [RCV004667431]uncertain significance5102270783102270783Humanname
597777407CV3603144single nucleotide variantNM_180991.5(SLCO4C1):c.385A>T (p.Ser129Cys)not specified [RCV004873028]uncertain significance5102291577102291577Humanname
597725788CV3603148single nucleotide variantNM_180991.5(SLCO4C1):c.565T>C (p.Phe189Leu)not specified [RCV004862476]uncertain significance5102291397102291397Humanname
597777425CV3603149single nucleotide variantNM_180991.5(SLCO4C1):c.686T>C (p.Leu229Ser)not specified [RCV004873032]uncertain significance5102270740102270740Humanname
597777429CV3603150single nucleotide variantNM_180991.5(SLCO4C1):c.687G>T (p.Leu229Phe)not specified [RCV004873033]uncertain significance5102270739102270739Humanname
597777445CV3603154single nucleotide variantNM_180991.5(SLCO4C1):c.298C>A (p.Arg100Ser)not specified [RCV004873037]uncertain significance5102295965102295965Humanname
598261146CV3922243single nucleotide variantNM_180991.5(SLCO4C1):c.991C>T (p.Pro331Ser)not specified [RCV005279918]uncertain significance5102261942102261942Humanname
598261158CV3922245single nucleotide variantNM_180991.5(SLCO4C1):c.550C>G (p.Leu184Val)not specified [RCV005279920]uncertain significance5102291412102291412Humanname
156381364CV2214906single nucleotide variantNM_180991.5(SLCO4C1):c.1022G>C (p.Gly341Ala)not specified [RCV004084697]uncertain significance5102260319102260319Humanname
155948707CV2242546single nucleotide variantNM_180991.5(SLCO4C1):c.1984A>T (p.Ile662Phe)not specified [RCV004113615]uncertain significance5102239281102239281Humanname
156145094CV2265025single nucleotide variantNM_180991.5(SLCO4C1):c.2018T>C (p.Val673Ala)not specified [RCV004126184]uncertain significance5102237015102237015Humanname
156121179CV2275991single nucleotide variantNM_180991.5(SLCO4C1):c.1531T>C (p.Tyr511His)not specified [RCV004141671]uncertain significance5102249727102249727Humanname
155906932CV2302117single nucleotide variantNM_180991.5(SLCO4C1):c.2134T>G (p.Leu712Val)not specified [RCV004159137]uncertain significance5102236899102236899Humanname
155955252CV2302411single nucleotide variantNM_180991.5(SLCO4C1):c.1067G>A (p.Ser356Asn)not specified [RCV004161154]likely benign5102260274102260274Humanname
155967530CV2391354single nucleotide variantNM_180991.5(SLCO4C1):c.1510A>G (p.Asn504Asp)not specified [RCV004239761]uncertain significance5102249748102249748Humanname
156170781CV2400612single nucleotide variantNM_180991.5(SLCO4C1):c.1724C>T (p.Ala575Val)not specified [RCV004242300]uncertain significance5102247339102247339Humanname
329351829CV2455359single nucleotide variantNM_180991.5(SLCO4C1):c.1340G>T (p.Arg447Ile)not specified [RCV004274859]uncertain significance5102257244102257244Humanname
405772289CV3332934single nucleotide variantNM_180991.5(SLCO4C1):c.1168T>C (p.Ser390Pro)not specified [RCV004457193]uncertain significance5102258048102258048Humanname
405772294CV3332935single nucleotide variantNM_180991.5(SLCO4C1):c.1171A>G (p.Thr391Ala)not specified [RCV004457194]uncertain significance5102258045102258045Humanname
405772302CV3332936single nucleotide variantNM_180991.5(SLCO4C1):c.1459T>C (p.Ser487Pro)not specified [RCV004457195]uncertain significance5102257125102257125Humanname
405772310CV3332937single nucleotide variantNM_180991.5(SLCO4C1):c.1496C>A (p.Ala499Asp)not specified [RCV004457196]uncertain significance5102249762102249762Humanname
405772316CV3332938single nucleotide variantNM_180991.5(SLCO4C1):c.2030T>C (p.Val677Ala)not specified [RCV004457197]uncertain significance5102237003102237003Humanname
405772322CV3332939single nucleotide variantNM_180991.5(SLCO4C1):c.2084C>T (p.Ser695Leu)not specified [RCV004457198]likely benign5102236949102236949Humanname
407493611CV3477342single nucleotide variantNM_180991.5(SLCO4C1):c.1654A>C (p.Thr552Pro)not specified [RCV004667424]uncertain significance5102247409102247409Humanname
407493616CV3477343single nucleotide variantNM_180991.5(SLCO4C1):c.1993G>A (p.Ala665Thr)not specified [RCV004667425]uncertain significance5102239272102239272Humanname
407452154CV3477344single nucleotide variantNM_180991.5(SLCO4C1):c.1523C>T (p.Ser508Leu)not specified [RCV004683907]likely benign5102249735102249735Humanname
407493620CV3477345single nucleotide variantNM_180991.5(SLCO4C1):c.1514G>T (p.Cys505Phe)not specified [RCV004667426]uncertain significance5102249744102249744Humanname
407493628CV3477347single nucleotide variantNM_180991.5(SLCO4C1):c.1898T>C (p.Ile633Thr)not specified [RCV004667428]uncertain significance5102239367102239367Humanname
407493632CV3477348single nucleotide variantNM_180991.5(SLCO4C1):c.1406T>G (p.Phe469Cys)not specified [RCV004667429]uncertain significance5102257178102257178Humanname
407493636CV3477349single nucleotide variantNM_180991.5(SLCO4C1):c.1358C>G (p.Thr453Arg)not specified [RCV004667430]uncertain significance5102257226102257226Humanname
407452157CV3477350single nucleotide variantNM_180991.5(SLCO4C1):c.2160A>G (p.Ile720Met)not specified [RCV004683908]uncertain significance5102236873102236873Humanname
407493644CV3477352single nucleotide variantNM_180991.5(SLCO4C1):c.1976A>C (p.Tyr659Ser)not specified [RCV004667432]uncertain significance5102239289102239289Humanname
597725779CV3603143single nucleotide variantNM_180991.5(SLCO4C1):c.2062T>A (p.Phe688Ile)not specified [RCV004862475]uncertain significance5102236971102236971Humanname
597777411CV3603145single nucleotide variantNM_180991.5(SLCO4C1):c.1126A>G (p.Lys376Glu)not specified [RCV004873029]uncertain significance5102260215102260215Humanname
597777415CV3603146single nucleotide variantNM_180991.5(SLCO4C1):c.1025C>T (p.Thr342Ile)not specified [RCV004873030]uncertain significance5102260316102260316Humanname
597777419CV3603147single nucleotide variantNM_180991.5(SLCO4C1):c.2009C>A (p.Ala670Asp)not specified [RCV004873031]uncertain significance5102239256102239256Humanname
597777437CV3603152single nucleotide variantNM_180991.5(SLCO4C1):c.1707A>T (p.Lys569Asn)not specified [RCV004873035]uncertain significance5102247356102247356Humanname
597777449CV3603155single nucleotide variantNM_180991.5(SLCO4C1):c.1286T>A (p.Ile429Asn)not specified [RCV004873038]uncertain significance5102257298102257298Humanname
598261128CV3922240single nucleotide variantNM_180991.5(SLCO4C1):c.2168A>C (p.Glu723Ala)not specified [RCV005279915]uncertain significance5102236865102236865Humanname
598261134CV3922241single nucleotide variantNM_180991.5(SLCO4C1):c.1056G>C (p.Gln352His)not specified [RCV005279916]uncertain significance5102260285102260285Humanname
598261139CV3922242single nucleotide variantNM_180991.5(SLCO4C1):c.1961G>A (p.Gly654Glu)not specified [RCV005279917]uncertain significance5102239304102239304Humanname
598261152CV3922244single nucleotide variantNM_180991.5(SLCO4C1):c.1682T>C (p.Phe561Ser)not specified [RCV005279919]uncertain significance5102247381102247381Humanname
598261165CV3922246single nucleotide variantNM_180991.5(SLCO4C1):c.1090T>C (p.Phe364Leu)not specified [RCV005279921]uncertain significance5102260251102260251Humanname
15184276CV709543single nucleotide variantNM_180991.5(SLCO4C1):c.1032A>T (p.Glu344Asp)not provided [RCV000975074]benign5102260309102260309Humanname
15169436CV734785single nucleotide variantNM_180991.5(SLCO4C1):c.2173T>C (p.Ter725Arg)not provided [RCV000901816]likely benign5102236860102236860Humanname