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Variants search result for Homo sapiens
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52 records found for search term Slc23a1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405733761CV3325342single nucleotide variantNM_005847.5(SLC23A1):c.465+8T>Gnot specified [RCV004451366]uncertain significance5139380557139380557Humanname
15145237CV779269single nucleotide variantNM_005847.5(SLC23A1):c.1550-9C>Tnot provided [RCV000966962]benign5139372262139372262Humanname
15162267CV749256single nucleotide variantNM_005847.5(SLC23A1):c.22G>A (p.Glu8Lys)not provided [RCV000925855]benign5139383232139383232Humanname
329366141CV2438151single nucleotide variantNM_005847.5(SLC23A1):c.51G>C (p.Arg17Ser)not specified [RCV004256928]uncertain significance5139382591139382591Humanname
401751825CV2727420single nucleotide variantNM_005847.5(SLC23A1):c.34C>G (p.Gln12Glu)not specified [RCV004327510]uncertain significance5139383220139383220Humanname
401877504CV2769478single nucleotide variantNM_005847.5(SLC23A1):c.56C>G (p.Pro19Arg)not specified [RCV004357452]uncertain significance5139382586139382586Humanname
401925385CV2828026single nucleotide variantNM_005847.5(SLC23A1):c.558C>G (p.Leu186=)not provided [RCV003436452]likely benign5139380297139380297Humanname
598200269CV3918074single nucleotide variantNM_005847.5(SLC23A1):c.80C>T (p.Pro27Leu)not specified [RCV005268515]uncertain significance5139382562139382562Humanname
15099847CV698822single nucleotide variantNM_005847.5(SLC23A1):c.873T>C (p.Asp291=)not provided [RCV000958823]benign5139379730139379730Humanname
155912032CV2308603single nucleotide variantNM_005847.5(SLC23A1):c.250G>A (p.Gly84Ser)not specified [RCV004167162]uncertain significance5139381950139381950Humanname
401759237CV2712491single nucleotide variantNM_005847.5(SLC23A1):c.262A>G (p.Thr88Ala)not specified [RCV004313950]uncertain significance5139381938139381938Humanname
597699495CV3606158single nucleotide variantNM_005847.5(SLC23A1):c.146T>G (p.Phe49Cys)not specified [RCV004859755]uncertain significance5139382496139382496Humanname
598168123CV3918069single nucleotide variantNM_005847.5(SLC23A1):c.106G>A (p.Glu36Lys)not specified [RCV005284031]uncertain significance5139382536139382536Humanname
15156316CV721240single nucleotide variantNM_005847.5(SLC23A1):c.1077C>G (p.Gly359=)not provided [RCV000880601]benign5139378681139378681Humanname
8631397CV86558single nucleotide variantNM_005847.4(SLC23A1):c.1113G>A (p.Gly371=)Malignant melanoma [RCV000066649]not provided5139378645139378645Humanname
155994790CV2377650single nucleotide variantNM_005847.5(SLC23A1):c.493G>A (p.Val165Met)not specified [RCV004227829]likely benign5139380362139380362Humanname
401748878CV2692832single nucleotide variantNM_005847.5(SLC23A1):c.352G>A (p.Ala118Thr)not specified [RCV004306371]uncertain significance5139380843139380843Humanname
401758449CV2694108single nucleotide variantNM_005847.5(SLC23A1):c.944C>T (p.Thr315Met)not specified [RCV004302540]uncertain significance5139379336139379336Humanname
401762566CV2719977single nucleotide variantNM_005847.5(SLC23A1):c.314C>T (p.Pro105Leu)not specified [RCV004323562]uncertain significance5139380881139380881Humanname
401771959CV2723004single nucleotide variantNM_005847.5(SLC23A1):c.826G>A (p.Val276Met)not specified [RCV004327176]uncertain significance5139379777139379777Humanname
405733769CV3325343single nucleotide variantNM_005847.5(SLC23A1):c.574G>A (p.Val192Ile)not specified [RCV004451367]uncertain significance5139380281139380281Humanname
597699458CV3596648single nucleotide variantNM_005847.5(SLC23A1):c.998T>C (p.Ile333Thr)not specified [RCV004859751]uncertain significance5139379282139379282Humanname
597699467CV3606155single nucleotide variantNM_005847.5(SLC23A1):c.461G>A (p.Arg154Gln)not specified [RCV004859752]uncertain significance5139380569139380569Humanname
597699486CV3606157single nucleotide variantNM_005847.5(SLC23A1):c.805T>C (p.Tyr269His)not specified [RCV004859754]uncertain significance5139379798139379798Humanname
597699514CV3606160single nucleotide variantNM_005847.5(SLC23A1):c.827T>C (p.Val276Ala)not specified [RCV004859757]uncertain significance5139379776139379776Humanname
598168118CV3918068single nucleotide variantNM_005847.5(SLC23A1):c.685C>T (p.Arg229Cys)not specified [RCV005284030]uncertain significance5139380039139380039Humanname
598168128CV3918070single nucleotide variantNM_005847.5(SLC23A1):c.871G>A (p.Asp291Asn)not specified [RCV005284032]uncertain significance5139379732139379732Humanname
598168133CV3918071single nucleotide variantNM_005847.5(SLC23A1):c.409G>A (p.Gly137Ser)not specified [RCV005284033]uncertain significance5139380621139380621Humanname
598168138CV3918072single nucleotide variantNM_005847.5(SLC23A1):c.455G>A (p.Arg152Gln)not specified [RCV005284034]uncertain significance5139380575139380575Humanname
598168143CV3918073single nucleotide variantNM_005847.5(SLC23A1):c.305T>A (p.Ile102Asn)not specified [RCV005284035]uncertain significance5139381895139381895Humanname
598168159CV3918077single nucleotide variantNM_005847.5(SLC23A1):c.749A>T (p.Gln250Leu)not specified [RCV005284038]uncertain significance5139379975139379975Humanname
15145244CV709652single nucleotide variantNM_005847.5(SLC23A1):c.772A>G (p.Met258Val)not provided [RCV000966963]benign5139379831139379831Humanname
156368012CV2203636single nucleotide variantNM_005847.5(SLC23A1):c.1051C>A (p.Pro351Thr)not specified [RCV004073956]uncertain significance5139379229139379229Humanname
156261461CV2216455single nucleotide variantNM_005847.5(SLC23A1):c.1418A>G (p.Asn473Ser)not specified [RCV004097269]uncertain significance5139378010139378010Humanname
156292725CV2233480single nucleotide variantNM_005847.5(SLC23A1):c.1240G>A (p.Gly414Ser)not specified [RCV004106100]uncertain significance5139378291139378291Humanname
156348986CV2309209single nucleotide variantNM_005847.5(SLC23A1):c.1741A>G (p.Ile581Val)not specified [RCV004171553]likely benign5139372062139372062Humanname
156336285CV2360709single nucleotide variantNM_005847.5(SLC23A1):c.1610T>C (p.Met537Thr)not specified [RCV004213500]likely benign5139372193139372193Humanname
329392694CV2439124single nucleotide variantNM_005847.5(SLC23A1):c.1409C>T (p.Thr470Met)not specified [RCV004266411]uncertain significance5139378019139378019Humanname
329381259CV2464602single nucleotide variantNM_005847.5(SLC23A1):c.1649T>C (p.Met550Thr)not specified [RCV004278292]uncertain significance5139372154139372154Humanname
401773329CV2709247single nucleotide variantNM_005847.5(SLC23A1):c.1204T>G (p.Tyr402Asp)not specified [RCV004316413]uncertain significance5139378327139378327Humanname
405733742CV3325340single nucleotide variantNM_005847.5(SLC23A1):c.1346T>G (p.Phe449Cys)not specified [RCV004451364]uncertain significance5139378082139378082Humanname
405733749CV3325341single nucleotide variantNM_005847.5(SLC23A1):c.1750G>A (p.Asp584Asn)not specified [RCV004451365]uncertain significance5139372053139372053Humanname
407509143CV3473911single nucleotide variantNM_005847.5(SLC23A1):c.1729G>T (p.Asp577Tyr)not specified [RCV004672266]uncertain significance5139372074139372074Humanname
407509150CV3473913single nucleotide variantNM_005847.5(SLC23A1):c.1608C>A (p.Asp536Glu)not specified [RCV004672268]likely benign5139372195139372195Humanname
407519601CV3473914single nucleotide variantNM_005847.5(SLC23A1):c.1736T>C (p.Ile579Thr)not specified [RCV004676598]uncertain significance5139372067139372067Humanname
597699476CV3606156single nucleotide variantNM_005847.5(SLC23A1):c.1141T>A (p.Ser381Thr)not specified [RCV004859753]uncertain significance5139378617139378617Humanname
597699523CV3606161single nucleotide variantNM_005847.5(SLC23A1):c.1211C>T (p.Ala404Val)not specified [RCV004859758]uncertain significance5139378320139378320Humanname
597699532CV3606162single nucleotide variantNM_005847.5(SLC23A1):c.1316T>C (p.Ile439Thr)not specified [RCV004859759]uncertain significance5139378112139378112Humanname
597699541CV3606163single nucleotide variantNM_005847.5(SLC23A1):c.1654A>C (p.Ile552Leu)not specified [RCV004859760]uncertain significance5139372149139372149Humanname
598168148CV3918075single nucleotide variantNM_005847.5(SLC23A1):c.1108G>A (p.Ala370Thr)not specified [RCV005284036]uncertain significance5139378650139378650Humanname
598168153CV3918076single nucleotide variantNM_005847.5(SLC23A1):c.1054C>A (p.Pro352Thr)not specified [RCV005284037]uncertain significance5139379226139379226Humanname
598168169CV3918079single nucleotide variantNM_005847.5(SLC23A1):c.1231G>A (p.Gly411Ser)not specified [RCV005284040]uncertain significance5139378300139378300Humanname