Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

57 records found for search term Il5
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15199684CV721213single nucleotide variantNM_000879.3(IL5):c.108G>T (p.Leu36=)not provided [RCV000890701]benign5132543371132543371Humanname
597775375CV3686579single nucleotide variantNM_000879.3(IL5):c.88G>A (p.Val30Met)not specified [RCV004929260]uncertain significance5132543391132543391Humanname
597775372CV3686580single nucleotide variantNM_000879.3(IL5):c.82G>A (p.Ala28Thr)not specified [RCV004929261]uncertain significance5132543397132543397Humanname
598180356CV3972328single nucleotide variantNM_000879.3(IL5):c.49G>A (p.Val17Met)not specified [RCV005352324]likely benign5132543430132543430Humanname
15164274CV698774single nucleotide variantNM_000879.3(IL5):c.384C>A (p.Thr128=)not provided [RCV000948300]benign5132541832132541832Humanname
15193573CV721212single nucleotide variantNM_000879.3(IL5):c.312G>A (p.Lys104=)not provided [RCV000888984]benign5132541904132541904Humanname
156345160CV2290937single nucleotide variantNM_000879.3(IL5):c.146C>T (p.Thr49Ile)not specified [RCV004151495]uncertain significance5132543125132543125Humanname
329392133CV2445352single nucleotide variantNM_000879.3(IL5):c.312G>C (p.Lys104Asn)not specified [RCV004263968]uncertain significance5132541904132541904Humanname
598207693CV3972329single nucleotide variantNM_000879.3(IL5):c.391A>G (p.Ile131Val)not specified [RCV005338013]uncertain significance5132541825132541825Humanname
15183806CV778971single nucleotide variantNM_175726.4(IL5RA):c.709+8C>Tnot provided [RCV000974961]benign330978623097862Humanname
405805077CV3271262single nucleotide variantNM_175726.4(IL5RA):c.10G>A (p.Val4Met)not specified [RCV004405323]likely benign331049753104975Humanname
405805084CV3271266single nucleotide variantNM_175726.4(IL5RA):c.41C>T (p.Ala14Val)not specified [RCV004405327]uncertain significance331049443104944Humanname
15143812CV734016single nucleotide variantNM_175726.4(IL5RA):c.432A>G (p.Ser144=)not provided [RCV000899899]benign330982263098226Humanname
156157415CV2235277single nucleotide variantNM_175726.4(IL5RA):c.257G>T (p.Cys86Phe)not specified [RCV004107318]uncertain significance331018023101802Humanname
156281918CV2288782single nucleotide variantNM_175726.4(IL5RA):c.238A>G (p.Arg80Gly)not specified [RCV004147996]uncertain significance331018213101821Humanname
156070158CV2355969single nucleotide variantNM_175726.4(IL5RA):c.296G>A (p.Arg99Gln)not specified [RCV004201348]likely benign331017633101763Humanname
401737929CV2676070single nucleotide variantNM_175726.4(IL5RA):c.224A>T (p.Asp75Val)not specified [RCV004284297]uncertain significance331026793102679Humanname
401719234CV2679463single nucleotide variantNM_175726.4(IL5RA):c.150G>C (p.Trp50Cys)not specified [RCV004285983]uncertain significance331027533102753Humanname
407516107CV3444640single nucleotide variantNM_175726.4(IL5RA):c.284C>T (p.Ser95Leu)not specified [RCV004628084]uncertain significance331017753101775Humanname
597775235CV3686584single nucleotide variantNM_175726.4(IL5RA):c.137T>C (p.Val46Ala)not specified [RCV004929265]uncertain significance331027663102766Humanname
15143933CV734017single nucleotide variantNM_175726.4(IL5RA):c.177G>T (p.Arg59Ser)not provided [RCV000899919]likely benign331027263102726Humanname
155935267CV2225541single nucleotide variantNM_175726.4(IL5RA):c.504G>C (p.Gln168His)not specified [RCV004100923]uncertain significance330981543098154Humanname
156335468CV2228397single nucleotide variantNM_175726.4(IL5RA):c.386T>C (p.Ile129Thr)not specified [RCV004098376]uncertain significance330982723098272Humanname
156384691CV2231160single nucleotide variantNM_175726.4(IL5RA):c.841A>C (p.Asn281His)not specified [RCV004094368]uncertain significance330953133095313Humanname
156276441CV2276798single nucleotide variantNM_175726.4(IL5RA):c.623G>C (p.Arg208Pro)not specified [RCV004140159]uncertain significance330979563097956Humanname
156035672CV2282998single nucleotide variantNM_175726.4(IL5RA):c.536C>A (p.Thr179Asn)not specified [RCV004143626]uncertain significance330980433098043Humanname
156289066CV2299287single nucleotide variantNM_175726.4(IL5RA):c.440G>A (p.Arg147Lys)not specified [RCV004152611]uncertain significance330982183098218Humanname
156267251CV2305631single nucleotide variantNM_175726.4(IL5RA):c.402C>G (p.Cys134Trp)not specified [RCV004165637]uncertain significance330982563098256Humanname
329398835CV2442944single nucleotide variantNM_175726.4(IL5RA):c.695C>G (p.Ala232Gly)not specified [RCV004253541]uncertain significance330978843097884Humanname
329391248CV2452187single nucleotide variantNM_175726.4(IL5RA):c.939C>G (p.Ser313Arg)not specified [RCV004278895]uncertain significance330922793092279Humanname
329358177CV2453928single nucleotide variantNM_175726.4(IL5RA):c.571G>T (p.Gly191Trp)not specified [RCV004271313]uncertain significance330980083098008Humanname
401720476CV2701915single nucleotide variantNM_175726.4(IL5RA):c.836C>A (p.Thr279Lys)not specified [RCV004320527]uncertain significance330953183095318Humanname
401781237CV2732338single nucleotide variantNM_175726.4(IL5RA):c.640C>A (p.Leu214Ile)not specified [RCV004331495]uncertain significance330979393097939Humanname
401886736CV2767888single nucleotide variantNM_175726.4(IL5RA):c.965G>T (p.Trp322Leu)not specified [RCV004348144]uncertain significance330922533092253Humanname
405805080CV3271264single nucleotide variantNM_175726.4(IL5RA):c.343T>G (p.Ser115Ala)not specified [RCV004405325]uncertain significance331017163101716Humanname
405805086CV3271267single nucleotide variantNM_175726.4(IL5RA):c.905C>G (p.Ser302Cys)not specified [RCV004405328]uncertain significance330923133092313Humanname
407516103CV3444639single nucleotide variantNM_175726.4(IL5RA):c.500C>T (p.Thr167Met)not specified [RCV004628083]uncertain significance330981583098158Humanname
407516110CV3444641single nucleotide variantNM_175726.4(IL5RA):c.923T>C (p.Val308Ala)not specified [RCV004628085]uncertain significance330922953092295Humanname
407516116CV3444643single nucleotide variantNM_175726.4(IL5RA):c.458T>A (p.Leu153His)not specified [RCV004628087]uncertain significance330982003098200Humanname
597775368CV3686581single nucleotide variantNM_175726.4(IL5RA):c.441G>T (p.Arg147Ser)not specified [RCV004929262]uncertain significance330982173098217Humanname
597775360CV3686583single nucleotide variantNM_175726.4(IL5RA):c.982C>A (p.Pro328Thr)not specified [RCV004929264]uncertain significance330922363092236Humanname
597775139CV3686585single nucleotide variantNM_175726.4(IL5RA):c.661C>T (p.His221Tyr)not specified [RCV004929266]uncertain significance330979183097918Humanname
597774990CV3686587single nucleotide variantNM_175726.4(IL5RA):c.368G>C (p.Gly123Ala)not specified [RCV004929268]uncertain significance330982903098290Humanname
598180362CV3972331single nucleotide variantNM_175726.4(IL5RA):c.875A>G (p.Asn292Ser)not specified [RCV005352325]uncertain significance330923433092343Humanname
598180368CV3972332single nucleotide variantNM_175726.4(IL5RA):c.434G>A (p.Arg145His)not specified [RCV005352326]likely benign330982243098224Humanname
598180376CV3972333single nucleotide variantNM_175726.4(IL5RA):c.630G>C (p.Trp210Cys)not specified [RCV005352327]uncertain significance330979493097949Humanname
598207707CV3972335single nucleotide variantNM_175726.4(IL5RA):c.370T>A (p.Ser124Thr)not specified [RCV005338015]uncertain significance330982883098288Humanname
155911153CV2362316single nucleotide variantNM_175726.4(IL5RA):c.1196C>T (p.Thr399Met)not specified [RCV004212951]uncertain significance330702923070292Humanname
405805071CV3271259single nucleotide variantNM_175726.4(IL5RA):c.1004A>C (p.Glu335Ala)not specified [RCV004405320]uncertain significance330766183076618Humanname
405805073CV3271260single nucleotide variantNM_175726.4(IL5RA):c.1034T>C (p.Ile345Thr)not specified [RCV004405321]uncertain significance330765883076588Humanname
405805075CV3271261single nucleotide variantNM_175726.4(IL5RA):c.1072C>G (p.Leu358Val)not specified [RCV004405322]uncertain significance330765503076550Humanname
405805078CV3271263single nucleotide variantNM_175726.4(IL5RA):c.1124T>C (p.Ile375Thr)not specified [RCV004405324]uncertain significance330748343074834Humanname
407516113CV3444642single nucleotide variantNM_175726.4(IL5RA):c.1202T>C (p.Ile401Thr)not specified [RCV004628086]uncertain significance330702863070286Humanname
407511222CV3444644single nucleotide variantNM_175726.4(IL5RA):c.1186T>C (p.Ser396Pro)not specified [RCV004626392]uncertain significance330703023070302Humanname
597775364CV3686582single nucleotide variantNM_175726.4(IL5RA):c.1130C>T (p.Ala377Val)not specified [RCV004929263]uncertain significance330748283074828Humanname
597775056CV3686586single nucleotide variantNM_175726.4(IL5RA):c.1199A>C (p.Glu400Ala)not specified [RCV004929267]uncertain significance330702893070289Humanname
598180381CV3972334single nucleotide variantNM_175726.4(IL5RA):c.1249G>T (p.Asp417Tyr)not specified [RCV005352328]uncertain significance330702393070239Humanname