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Variants search result for Homo sapiens
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46 records found for search term Cse1l
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156049956CV2242004single nucleotide variantNM_001316.4(CSE1L):c.283A>G (p.Asn95Asp)not specified [RCV004108950]uncertain significance204906624649066246Humanname
155993871CV2252404single nucleotide variantNM_001316.4(CSE1L):c.106G>A (p.Val36Ile)not specified [RCV004116245]uncertain significance204906322249063222Humanname
405677064CV3235962single nucleotide variantNM_001316.4(CSE1L):c.227T>G (p.Ile76Ser)not specified [RCV004370303]uncertain significance204906334349063343Humanname
597800017CV3657886single nucleotide variantNM_001316.4(CSE1L):c.230T>C (p.Val77Ala)not specified [RCV004905504]uncertain significance204906619349066193Humanname
598260714CV3963128single nucleotide variantNM_001316.4(CSE1L):c.1563C>T (p.Tyr521=)not specified [RCV005325029]likely benign204908410649084106Humanname
8628539CV83683single nucleotide variantNM_001316.3(CSE1L):c.2133C>T (p.Phe711=)Malignant melanoma [RCV000063764]not provided204908969849089698Humanname
156097209CV2253168single nucleotide variantNM_001316.4(CSE1L):c.920A>G (p.Glu307Gly)not specified [RCV004120936]uncertain significance204907243749072437Humanname
155927798CV2285253single nucleotide variantNM_001316.4(CSE1L):c.687A>T (p.Glu229Asp)not specified [RCV004145447]uncertain significance204907021649070216Humanname
156269987CV2305946single nucleotide variantNM_001316.4(CSE1L):c.535G>T (p.Ala179Ser)not specified [RCV004167724]uncertain significance204906724849067248Humanname
156391191CV2385161single nucleotide variantNM_001316.4(CSE1L):c.410G>A (p.Arg137His)not specified [RCV004228415]uncertain significance204906644449066444Humanname
329396745CV2455758single nucleotide variantNM_001316.4(CSE1L):c.717G>A (p.Met239Ile)not specified [RCV004279052]uncertain significance204907024649070246Humanname
401747369CV2688896single nucleotide variantNM_001316.4(CSE1L):c.883A>G (p.Thr295Ala)not specified [RCV004303904]uncertain significance204907240049072400Humanname
401773484CV2698230single nucleotide variantNM_001316.4(CSE1L):c.703A>G (p.Met235Val)not specified [RCV004304792]uncertain significance204907023249070232Humanname
401876076CV2777647single nucleotide variantNM_001316.4(CSE1L):c.569C>T (p.Ala190Val)not specified [RCV004343487]uncertain significance204906871649068716Humanname
405677071CV3235963single nucleotide variantNM_001316.4(CSE1L):c.533A>T (p.Asp178Val)not specified [RCV004370304]uncertain significance204906724649067246Humanname
407464775CV3429855single nucleotide variantNM_001316.4(CSE1L):c.947A>G (p.Asn316Ser)not specified [RCV004613542]uncertain significance204907257849072578Humanname
407464780CV3429856single nucleotide variantNM_001316.4(CSE1L):c.910A>G (p.Thr304Ala)not specified [RCV004613543]uncertain significance204907242749072427Humanname
407464784CV3429857single nucleotide variantNM_001316.4(CSE1L):c.689T>A (p.Phe230Tyr)not specified [RCV004613544]uncertain significance204907021849070218Humanname
597800022CV3657888single nucleotide variantNM_001316.4(CSE1L):c.898T>G (p.Leu300Val)not specified [RCV004905506]uncertain significance204907241549072415Humanname
597800024CV3657889single nucleotide variantNM_001316.4(CSE1L):c.974G>T (p.Cys325Phe)not specified [RCV004905507]uncertain significance204907260549072605Humanname
597800028CV3657891single nucleotide variantNM_001316.4(CSE1L):c.601G>A (p.Asp201Asn)not specified [RCV004905509]uncertain significance204906874849068748Humanname
597800030CV3657892single nucleotide variantNM_001316.4(CSE1L):c.871C>T (p.Pro291Ser)not specified [RCV004905510]uncertain significance204907238849072388Humanname
156085151CV2249309single nucleotide variantNM_001316.4(CSE1L):c.2078T>G (p.Val693Gly)not specified [RCV004118331]uncertain significance204908964349089643Humanname
156266350CV2275468single nucleotide variantNM_001316.4(CSE1L):c.1687C>A (p.Leu563Ile)not specified [RCV004137125]uncertain significance204908535049085350Humanname
156007977CV2288437single nucleotide variantNM_001316.4(CSE1L):c.1628C>T (p.Ala543Val)not specified [RCV004151984]uncertain significance204908529149085291Humanname
329361758CV2437897single nucleotide variantNM_001316.4(CSE1L):c.2345A>G (p.Lys782Arg)not specified [RCV004261184]uncertain significance204909100249091002Humanname
329397374CV2466095single nucleotide variantNM_001316.4(CSE1L):c.2318T>C (p.Leu773Pro)not specified [RCV004279762]uncertain significance204909097549090975Humanname
401748778CV2694500single nucleotide variantNM_001316.4(CSE1L):c.2810C>T (p.Thr937Ile)not specified [RCV004298639]uncertain significance204909494749094947Humanname
401737122CV2717958single nucleotide variantNM_001316.4(CSE1L):c.1987G>A (p.Val663Ile)not specified [RCV004321909]uncertain significance204908955249089552Humanname
401764267CV2725503single nucleotide variantNM_001316.4(CSE1L):c.1489A>G (p.Lys497Glu)not specified [RCV004320126]uncertain significance204908403249084032Humanname
401865281CV2768748single nucleotide variantNM_001316.4(CSE1L):c.1813G>A (p.Val605Ile)not specified [RCV004346588]uncertain significance204908809849088098Humanname
401891958CV2775847single nucleotide variantNM_001316.4(CSE1L):c.1582C>T (p.Arg528Trp)not specified [RCV004344883]uncertain significance204908412549084125Humanname
405677034CV3235956single nucleotide variantNM_001316.4(CSE1L):c.1054A>G (p.Met352Val)not specified [RCV004370297]uncertain significance204907268549072685Humanname
405677039CV3235957single nucleotide variantNM_001316.4(CSE1L):c.1184A>G (p.Lys395Arg)not specified [RCV004370298]uncertain significance204907536949075369Humanname
405677045CV3235958single nucleotide variantNM_001316.4(CSE1L):c.1249G>A (p.Ala417Thr)not specified [RCV004370299]uncertain significance204907543449075434Humanname
405677049CV3235959single nucleotide variantNM_001316.4(CSE1L):c.1508C>T (p.Ser503Leu)not specified [RCV004370300]uncertain significance204908405149084051Humanname
405677055CV3235960single nucleotide variantNM_001316.4(CSE1L):c.1585C>T (p.Leu529Phe)not specified [RCV004370301]uncertain significance204908412849084128Humanname
405677059CV3235961single nucleotide variantNM_001316.4(CSE1L):c.2155A>C (p.Ile719Leu)not specified [RCV004370302]uncertain significance204908972049089720Humanname
407464789CV3429858single nucleotide variantNM_001316.4(CSE1L):c.1120T>G (p.Leu374Val)not specified [RCV004613545]uncertain significance204907483849074838Humanname
597800020CV3657887single nucleotide variantNM_001316.4(CSE1L):c.1866A>G (p.Ile622Met)not specified [RCV004905505]uncertain significance204908929149089291Humanname
597800032CV3657893single nucleotide variantNM_001316.4(CSE1L):c.1598G>C (p.Arg533Pro)not specified [RCV004905511]uncertain significance204908414149084141Humanname
597800035CV3657894single nucleotide variantNM_001316.4(CSE1L):c.1504G>A (p.Val502Ile)not specified [RCV004905512]uncertain significance204908404749084047Humanname
598260691CV3963124single nucleotide variantNM_001316.4(CSE1L):c.1450G>A (p.Gly484Ser)not specified [RCV005325025]uncertain significance204907859049078590Humanname
598260703CV3963126single nucleotide variantNM_001316.4(CSE1L):c.2281G>C (p.Glu761Gln)not specified [RCV005325027]uncertain significance204909093849090938Humanname
598260709CV3963127single nucleotide variantNM_001316.4(CSE1L):c.2651T>C (p.Ile884Thr)not specified [RCV005325028]uncertain significance204909478849094788Humanname
598260719CV3963129single nucleotide variantNM_001316.4(CSE1L):c.2208G>C (p.Lys736Asn)not specified [RCV005325030]uncertain significance204909076849090768Humanname