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64 records found for search term Slc5a8
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15103363CV731492single nucleotide variantNM_145913.5(SLC5A8):c.351+7G>Cnot provided [RCV000892657]benign12101209491101209491Humanname
8647193CV107311single nucleotide variantNM_145913.3(SLC5A8):c.1527-1479C>ALung cancer [RCV000087796]uncertain significance12101163556101163556Humanname
15192095CV706486single nucleotide variantNM_145913.5(SLC5A8):c.84C>T (p.Ile28=)not provided [RCV000954967]benign12101209765101209765Humanname
405729400CV3325823single nucleotide variantNM_145913.5(SLC5A8):c.20T>C (p.Ile7Thr)not specified [RCV004464136]uncertain significance12101209829101209829Humanname
401932300CV2816773single nucleotide variantNM_145913.5(SLC5A8):c.771C>T (p.Tyr257=)not provided [RCV003391954]likely benign12101190530101190530Humanname
15187094CV706485single nucleotide variantNM_145913.5(SLC5A8):c.30C>A (p.Phe10Leu)not provided [RCV000953485]benign12101209819101209819Humanname
329396489CV2459560single nucleotide variantNM_145913.5(SLC5A8):c.112G>T (p.Gly38Cys)not specified [RCV004277013]uncertain significance12101209737101209737Humanname
407515414CV3480962single nucleotide variantNM_145913.5(SLC5A8):c.272C>T (p.Thr91Ile)not specified [RCV004674920]uncertain significance12101209577101209577Humanname
407515417CV3480963single nucleotide variantNM_145913.5(SLC5A8):c.197T>C (p.Met66Thr)not specified [RCV004674921]uncertain significance12101209652101209652Humanname
597776212CV3597035single nucleotide variantNM_145913.5(SLC5A8):c.295A>C (p.Ser99Arg)not specified [RCV004872739]uncertain significance12101209554101209554Humanname
156385800CV2228036single nucleotide variantNM_145913.5(SLC5A8):c.749C>A (p.Thr250Asn)not specified [RCV004096277]uncertain significance12101190552101190552Humanname
156360606CV2269070single nucleotide variantNM_145913.5(SLC5A8):c.665A>G (p.Tyr222Cys)not specified [RCV004130251]uncertain significance12101193652101193652Humanname
156028030CV2278489single nucleotide variantNM_145913.5(SLC5A8):c.533C>T (p.Thr178Ile)not specified [RCV004132931]uncertain significance12101195099101195099Humanname
155999456CV2373419single nucleotide variantNM_145913.5(SLC5A8):c.845T>C (p.Ile282Thr)not specified [RCV004220119]uncertain significance12101187504101187504Humanname
156263799CV2384493single nucleotide variantNM_145913.5(SLC5A8):c.710T>C (p.Leu237Ser)not specified [RCV004230289]uncertain significance12101190591101190591Humanname
329381062CV2440625single nucleotide variantNM_145913.5(SLC5A8):c.763A>G (p.Ser255Gly)not specified [RCV004256536]uncertain significance12101190538101190538Humanname
401781758CV2682183single nucleotide variantNM_145913.5(SLC5A8):c.746G>A (p.Gly249Glu)not specified [RCV004290229]uncertain significance12101190555101190555Humanname
401729592CV2683732single nucleotide variantNM_145913.5(SLC5A8):c.491G>T (p.Gly164Val)not specified [RCV004284473]uncertain significance12101195141101195141Humanname
401864911CV2757280single nucleotide variantNM_145913.5(SLC5A8):c.821T>G (p.Phe274Cys)not specified [RCV004338870]uncertain significance12101190480101190480Humanname
405729408CV3325824single nucleotide variantNM_145913.5(SLC5A8):c.314C>T (p.Pro105Leu)not specified [RCV004464137]uncertain significance12101209535101209535Humanname
405729416CV3325825single nucleotide variantNM_145913.5(SLC5A8):c.383G>A (p.Arg128His)not specified [RCV004464138]uncertain significance12101204534101204534Humanname
405729424CV3325826single nucleotide variantNM_145913.5(SLC5A8):c.403T>G (p.Phe135Val)not specified [RCV004464139]uncertain significance12101204514101204514Humanname
405729433CV3325827single nucleotide variantNM_145913.5(SLC5A8):c.632A>T (p.Gln211Leu)not specified [RCV004464140]uncertain significance12101193685101193685Humanname
407515423CV3480965single nucleotide variantNM_145913.5(SLC5A8):c.415A>G (p.Thr139Ala)not specified [RCV004674923]uncertain significance12101204502101204502Humanname
407451842CV3480966single nucleotide variantNM_145913.5(SLC5A8):c.427A>G (p.Thr143Ala)not specified [RCV004683819]uncertain significance12101202206101202206Humanname
407451845CV3480967single nucleotide variantNM_145913.5(SLC5A8):c.800A>C (p.Tyr267Ser)not specified [RCV004683820]uncertain significance12101190501101190501Humanname
597724347CV3597026single nucleotide variantNM_145913.5(SLC5A8):c.349G>C (p.Glu117Gln)not specified [RCV004862319]uncertain significance12101209500101209500Humanname
597776197CV3597028single nucleotide variantNM_145913.5(SLC5A8):c.434T>C (p.Ile145Thr)not specified [RCV004872735]uncertain significance12101202199101202199Humanname
597776201CV3597029single nucleotide variantNM_145913.5(SLC5A8):c.918T>G (p.His306Gln)not specified [RCV004872736]uncertain significance12101187431101187431Humanname
597724372CV3597032single nucleotide variantNM_145913.5(SLC5A8):c.443A>G (p.Tyr148Cys)not specified [RCV004862321]uncertain significance12101202190101202190Humanname
597724404CV3597036single nucleotide variantNM_145913.5(SLC5A8):c.380T>A (p.Val127Asp)not specified [RCV004862324]uncertain significance12101204537101204537Humanname
598259391CV3911487single nucleotide variantNM_145913.5(SLC5A8):c.512T>C (p.Val171Ala)not specified [RCV005279574]uncertain significance12101195120101195120Humanname
598259401CV3911489single nucleotide variantNM_145913.5(SLC5A8):c.551C>A (p.Ala184Glu)not specified [RCV005279576]uncertain significance12101193766101193766Humanname
598259411CV3911491single nucleotide variantNM_145913.5(SLC5A8):c.629T>C (p.Met210Thr)not specified [RCV005279578]uncertain significance12101193688101193688Humanname
598259415CV3911492single nucleotide variantNM_145913.5(SLC5A8):c.674G>A (p.Gly225Glu)not specified [RCV005279579]uncertain significance12101193643101193643Humanname
598259420CV3911493single nucleotide variantNM_145913.5(SLC5A8):c.848A>G (p.Asn283Ser)not specified [RCV005279580]uncertain significance12101187501101187501Humanname
598259435CV3911496single nucleotide variantNM_145913.5(SLC5A8):c.668A>G (p.Asp223Gly)not specified [RCV005279583]uncertain significance12101193649101193649Humanname
15184463CV729882single nucleotide variantNM_145913.5(SLC5A8):c.751T>G (p.Phe251Val)not provided [RCV000886453]benign12101190550101190550Humanname
156112811CV2267562single nucleotide variantNM_145913.5(SLC5A8):c.1433A>C (p.Gln478Pro)not specified [RCV004135975]uncertain significance12101166587101166587Humanname
155997276CV2287005single nucleotide variantNM_145913.5(SLC5A8):c.1787A>T (p.Glu596Val)not specified [RCV004144892]uncertain significance12101157325101157325Humanname
156254389CV2325628single nucleotide variantNM_145913.5(SLC5A8):c.1717C>A (p.His573Asn)not specified [RCV004180041]uncertain significance12101157395101157395Humanname
156084476CV2330899single nucleotide variantNM_145913.5(SLC5A8):c.1826G>A (p.Arg609His)not specified [RCV004185952]uncertain significance12101157286101157286Humanname
329368223CV2442661single nucleotide variantNM_145913.5(SLC5A8):c.1771G>C (p.Ala591Pro)not specified [RCV004265013]uncertain significance12101157341101157341Humanname
401751438CV2716387single nucleotide variantNM_145913.5(SLC5A8):c.1814G>A (p.Ser605Asn)not specified [RCV004325377]uncertain significance12101157298101157298Humanname
401887661CV2773582single nucleotide variantNM_145913.5(SLC5A8):c.1175A>G (p.Tyr392Cys)not specified [RCV004355988]uncertain significance12101180087101180087Humanname
401873513CV2776516single nucleotide variantNM_145913.5(SLC5A8):c.1006G>A (p.Gly336Arg)not specified [RCV004355617]uncertain significance12101184180101184180Humanname
405729362CV3325818single nucleotide variantNM_145913.5(SLC5A8):c.1111C>T (p.Pro371Ser)not specified [RCV004464131]uncertain significance12101182857101182857Humanname
405729371CV3325819single nucleotide variantNM_145913.5(SLC5A8):c.1223C>T (p.Ala408Val)not specified [RCV004464132]uncertain significance12101180039101180039Humanname
405729375CV3325820single nucleotide variantNM_145913.5(SLC5A8):c.1276G>A (p.Gly426Ser)not specified [RCV004464133]uncertain significance12101168140101168140Humanname
405729382CV3325821single nucleotide variantNM_145913.5(SLC5A8):c.1784T>G (p.Ile595Ser)not specified [RCV004464134]uncertain significance12101157328101157328Humanname
405729391CV3325822single nucleotide variantNM_145913.5(SLC5A8):c.1793A>T (p.Asn598Ile)not specified [RCV004464135]uncertain significance12101157319101157319Humanname
407451837CV3480961single nucleotide variantNM_145913.5(SLC5A8):c.1808G>A (p.Gly603Asp)not specified [RCV004683818]uncertain significance12101157304101157304Humanname
407515420CV3480964single nucleotide variantNM_145913.5(SLC5A8):c.1513T>C (p.Tyr505His)not specified [RCV004674922]likely benign12101166507101166507Humanname
597776193CV3597025single nucleotide variantNM_145913.5(SLC5A8):c.1468A>C (p.Met490Leu)not specified [RCV004872734]uncertain significance12101166552101166552Humanname
597724360CV3597027single nucleotide variantNM_145913.5(SLC5A8):c.1412T>G (p.Leu471Trp)not specified [RCV004862320]uncertain significance12101166608101166608Humanname
597776205CV3597030single nucleotide variantNM_145913.5(SLC5A8):c.1651G>T (p.Asp551Tyr)not specified [RCV004872737]uncertain significance12101158308101158308Humanname
597776208CV3597031single nucleotide variantNM_145913.5(SLC5A8):c.1031G>C (p.Cys344Ser)not specified [RCV004872738]uncertain significance12101184155101184155Humanname
597724381CV3597033single nucleotide variantNM_145913.5(SLC5A8):c.1122A>T (p.Arg374Ser)not specified [RCV004862322]uncertain significance12101182846101182846Humanname
597724393CV3597034single nucleotide variantNM_145913.5(SLC5A8):c.1187G>A (p.Cys396Tyr)not specified [RCV004862323]uncertain significance12101180075101180075Humanname
598259396CV3911488single nucleotide variantNM_145913.5(SLC5A8):c.1217T>C (p.Met406Thr)not specified [RCV005279575]uncertain significance12101180045101180045Humanname
598259406CV3911490single nucleotide variantNM_145913.5(SLC5A8):c.1498A>C (p.Ser500Arg)not specified [RCV005279577]uncertain significance12101166522101166522Humanname
598259425CV3911494single nucleotide variantNM_145913.5(SLC5A8):c.1240C>A (p.Leu414Ile)not specified [RCV005279581]uncertain significance12101168176101168176Humanname
598259430CV3911495single nucleotide variantNM_145913.5(SLC5A8):c.1234G>A (p.Ala412Thr)not specified [RCV005279582]uncertain significance12101168182101168182Humanname
15160424CV706484single nucleotide variantNM_145913.5(SLC5A8):c.1825C>T (p.Arg609Cys)not provided [RCV000947481]benign12101157287101157287Humanname