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45 records found for search term Nle1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401747994CV2716355single nucleotide variantNM_018096.5(NLE1):c.11C>T (p.Ala4Val)not specified [RCV004325351]uncertain significance173514226535142265Humanname
15154448CV715376single nucleotide variantNM_018096.5(NLE1):c.108C>T (p.Pro36=)not provided [RCV000968739]benign173514203335142033Humanname
401914519CV2811238single nucleotide variantNM_018096.5(NLE1):c.828C>T (p.Asp276=)not provided [RCV003428222]likely benign173513700135137001Humanname
405707245CV3362319single nucleotide variantNM_018096.5(NLE1):c.46C>T (p.Arg16Trp)not specified [RCV004493307]uncertain significance173514209535142095Humanname
156256960CV2322031single nucleotide variantNM_018096.5(NLE1):c.275A>G (p.Tyr92Cys)not specified [RCV004173782]uncertain significance173513995435139954Humanname
405707220CV3362316single nucleotide variantNM_018096.5(NLE1):c.181G>A (p.Ala61Thr)not specified [RCV004493304]uncertain significance173514004835140048Humanname
405707228CV3362317single nucleotide variantNM_018096.5(NLE1):c.208G>A (p.Val70Ile)not specified [RCV004493305]uncertain significance173514002135140021Humanname
598193916CV3994680single nucleotide variantNM_018096.5(NLE1):c.116T>C (p.Ile39Thr)not specified [RCV005374638]uncertain significance173514202535142025Humanname
156397505CV2200624single nucleotide variantNM_018096.5(NLE1):c.649C>A (p.Arg217Ser)not specified [RCV004078961]uncertain significance173513718035137180Humanname
156287039CV2229577single nucleotide variantNM_018096.5(NLE1):c.824A>T (p.His275Leu)not specified [RCV004103396]uncertain significance173513700535137005Humanname
156256305CV2374046single nucleotide variantNM_018096.5(NLE1):c.709C>T (p.Arg237Cys)not specified [RCV004227170]uncertain significance173513712035137120Humanname
329362650CV2438993single nucleotide variantNM_018096.5(NLE1):c.415C>T (p.Arg139Cys)not specified [RCV004264502]uncertain significance173513928035139280Humanname
329387336CV2463562single nucleotide variantNM_018096.5(NLE1):c.569A>G (p.Gln190Arg)not specified [RCV004277369]uncertain significance173513760935137609Humanname
401878982CV2781396single nucleotide variantNM_018096.5(NLE1):c.416G>A (p.Arg139His)not specified [RCV004352400]uncertain significance173513927935139279Humanname
405707237CV3362318single nucleotide variantNM_018096.5(NLE1):c.389C>T (p.Ala130Val)not specified [RCV004493306]uncertain significance173513930635139306Humanname
405707258CV3362320single nucleotide variantNM_018096.5(NLE1):c.485T>C (p.Ile162Thr)not specified [RCV004493308]uncertain significance173513786635137866Humanname
405707265CV3362321single nucleotide variantNM_018096.5(NLE1):c.904C>T (p.Arg302Cys)not specified [RCV004493309]uncertain significance173513642235136422Humanname
407508927CV3458669single nucleotide variantNM_018096.5(NLE1):c.455G>T (p.Cys152Phe)not specified [RCV004647273]uncertain significance173513924035139240Humanname
597651484CV3556394single nucleotide variantNM_018096.5(NLE1):c.503G>T (p.Gly168Val)not specified [RCV004826892]uncertain significance173513784835137848Humanname
597651491CV3556395single nucleotide variantNM_018096.5(NLE1):c.758G>A (p.Arg253Gln)not specified [RCV004826893]uncertain significance173513707135137071Humanname
597651501CV3556396single nucleotide variantNM_018096.5(NLE1):c.685C>T (p.Arg229Trp)not specified [RCV004826894]uncertain significance173513714435137144Humanname
598239277CV3994678single nucleotide variantNM_018096.5(NLE1):c.558C>G (p.Ser186Arg)not specified [RCV005382895]uncertain significance173513762035137620Humanname
598193910CV3994679single nucleotide variantNM_018096.5(NLE1):c.905G>A (p.Arg302His)not specified [RCV005374637]uncertain significance173513642135136421Humanname
598239283CV3994681single nucleotide variantNM_018096.5(NLE1):c.803C>T (p.Thr268Ile)not specified [RCV005382896]uncertain significance173513702635137026Humanname
156172731CV2194286single nucleotide variantNM_018096.5(NLE1):c.1058T>C (p.Leu353Ser)not specified [RCV004079403]uncertain significance173513540535135405Humanname
156020626CV2226531single nucleotide variantNM_018096.5(NLE1):c.1190A>T (p.Lys397Met)not specified [RCV004101793]uncertain significance173513527335135273Humanname
156246480CV2228304single nucleotide variantNM_018096.5(NLE1):c.1454G>A (p.Arg485Lys)not specified [RCV004098305]uncertain significance173513244135132441Humanname
156270901CV2237073single nucleotide variantNM_018096.5(NLE1):c.1127A>G (p.Asn376Ser)not specified [RCV004114834]uncertain significance173513533635135336Humanname
156075301CV2248233single nucleotide variantNM_018096.5(NLE1):c.1198G>C (p.Asp400His)not specified [RCV004117618]uncertain significance173513526535135265Humanname
155905976CV2357226single nucleotide variantNM_018096.5(NLE1):c.1060T>C (p.Phe354Leu)not specified [RCV004207008]uncertain significance173513540335135403Humanname
156213579CV2367105single nucleotide variantNM_018096.5(NLE1):c.1154G>A (p.Arg385His)not specified [RCV004215548]uncertain significance173513530935135309Humanname
155905340CV2385766single nucleotide variantNM_018096.5(NLE1):c.1327G>A (p.Val443Met)not specified [RCV004226516]uncertain significance173513338635133386Humanname
156004560CV2396953single nucleotide variantNM_018096.5(NLE1):c.1349T>C (p.Met450Thr)not specified [RCV004234065]likely benign173513336435133364Humanname
405707188CV3362312single nucleotide variantNM_018096.5(NLE1):c.1100G>A (p.Arg367Gln)not specified [RCV004493300]uncertain significance173513536335135363Humanname
405707197CV3362313single nucleotide variantNM_018096.5(NLE1):c.1159G>A (p.Val387Met)not specified [RCV004493301]uncertain significance173513530435135304Humanname
405707205CV3362314single nucleotide variantNM_018096.5(NLE1):c.1277G>A (p.Ser426Asn)not specified [RCV004493302]uncertain significance173513343635133436Humanname
405707213CV3362315single nucleotide variantNM_018096.5(NLE1):c.1350G>A (p.Met450Ile)not specified [RCV004493303]uncertain significance173513336335133363Humanname
407508920CV3458667single nucleotide variantNM_018096.5(NLE1):c.1208C>T (p.Thr403Met)not specified [RCV004647271]uncertain significance173513525535135255Humanname
407508923CV3458668single nucleotide variantNM_018096.5(NLE1):c.1153C>T (p.Arg385Cys)not specified [RCV004647272]uncertain significance173513531035135310Humanname
407497561CV3458670single nucleotide variantNM_018096.5(NLE1):c.1127A>T (p.Asn376Ile)not specified [RCV004643779]uncertain significance173513533635135336Humanname
597651473CV3556393single nucleotide variantNM_018096.5(NLE1):c.1099C>T (p.Arg367Trp)not specified [RCV004826891]uncertain significance173513536435135364Humanname
597651511CV3556397single nucleotide variantNM_018096.5(NLE1):c.1394G>C (p.Ser465Thr)not specified [RCV004826895]uncertain significance173513322235133222Humanname
597651521CV3556398single nucleotide variantNM_018096.5(NLE1):c.1151C>G (p.Ser384Cys)not specified [RCV004826896]uncertain significance173513531235135312Humanname
597651531CV3556399single nucleotide variantNM_018096.5(NLE1):c.1156A>T (p.Ile386Phe)not specified [RCV004826897]uncertain significance173513530735135307Humanname
597651540CV3556400single nucleotide variantNM_018096.5(NLE1):c.1120C>T (p.Leu374Phe)not specified [RCV004826898]uncertain significance173513534335135343Humanname