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)

49 records found for search term Ido2
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329400567CV2438499single nucleotide variantNM_194294.5(IDO2):c.82C>A (p.Leu28Ile)not specified [RCV004259645]uncertain significance83994924739949247Humanname
401781125CV2726429single nucleotide variantNM_194294.5(IDO2):c.77G>C (p.Gly26Ala)not specified [RCV004328635]uncertain significance83994924239949242Humanname
401894258CV2780511single nucleotide variantNM_194294.5(IDO2):c.91G>C (p.Asp31His)not specified [RCV004358201]uncertain significance83994925639949256Humanname
155921383CV2276294single nucleotide variantNM_194294.5(IDO2):c.284T>C (p.Val95Ala)not specified [RCV004144046]uncertain significance83997915539979155Humanname
156195634CV2297250single nucleotide variantNM_194294.5(IDO2):c.121A>G (p.Arg41Gly)not specified [RCV004151130]uncertain significance83996362939963629Humanname
156349654CV2305676single nucleotide variantNM_194294.5(IDO2):c.242G>T (p.Arg81Leu)not specified [RCV004167503]uncertain significance83997911339979113Humanname
156190107CV2339507single nucleotide variantNM_194294.5(IDO2):c.192C>G (p.Asp64Glu)not specified [RCV004194173]uncertain significance83996370039963700Humanname
156154373CV2374927single nucleotide variantNM_194294.5(IDO2):c.232C>T (p.Arg78Trp)not specified [RCV004227948]uncertain significance83997910339979103Humanname
156228356CV2392954single nucleotide variantNM_194294.5(IDO2):c.109C>T (p.Pro37Ser)not specified [RCV004242809]uncertain significance83996361739963617Humanname
156005050CV2393947single nucleotide variantNM_194294.5(IDO2):c.181G>C (p.Ala61Pro)not specified [RCV004236178]uncertain significance83996368939963689Humanname
401759741CV2701697single nucleotide variantNM_194294.5(IDO2):c.160A>T (p.Ile54Phe)not specified [RCV004314105]uncertain significance83996366839963668Humanname
401895599CV2774476single nucleotide variantNM_194294.5(IDO2):c.143A>G (p.Asn48Ser)not specified [RCV004349968]uncertain significance83996365139963651Humanname
401923978CV2821052single nucleotide variantNM_194294.5(IDO2):c.1140G>A (p.Arg380=)not provided [RCV003435471]likely benign84001551840015518Humanname
407466813CV3444441single nucleotide variantNM_194294.5(IDO2):c.197T>A (p.Met66Lys)not specified [RCV004635513]uncertain significance83997906839979068Humanname
597762647CV3683097single nucleotide variantNM_194294.5(IDO2):c.272C>T (p.Thr91Ile)not specified [RCV004926171]uncertain significance83997914339979143Humanname
598257776CV3979085single nucleotide variantNM_194294.5(IDO2):c.232C>G (p.Arg78Gly)not specified [RCV005347059]uncertain significance83997910339979103Humanname
598257789CV3979087single nucleotide variantNM_194294.5(IDO2):c.280T>A (p.Tyr94Asn)not specified [RCV005347061]uncertain significance83997915139979151Humanname
150451564CV1254844single nucleotide variantNM_194294.5(IDO2):c.379A>G (p.Ile127Val)not provided [RCV001667903]benign83998271539982715Humanname
150443307CV1264578single nucleotide variantNM_194294.5(IDO2):c.703C>T (p.Arg235Trp)not provided [RCV001679562]benign84000536240005362Humanname
156274342CV2316368single nucleotide variantNM_194294.5(IDO2):c.690T>G (p.Phe230Leu)not specified [RCV004169871]uncertain significance84000534940005349Humanname
156263428CV2329370single nucleotide variantNM_194294.5(IDO2):c.438C>G (p.Phe146Leu)not specified [RCV004187386]uncertain significance83998551139985511Humanname
156330630CV2339509single nucleotide variantNM_194294.5(IDO2):c.683A>G (p.Asp228Gly)not specified [RCV004194175]uncertain significance84000534240005342Humanname
156288895CV2370712single nucleotide variantNM_194294.5(IDO2):c.652T>G (p.Leu218Val)not specified [RCV004209116]uncertain significance83998982339989823Humanname
156084953CV2390472single nucleotide variantNM_194294.5(IDO2):c.481G>A (p.Gly161Arg)not specified [RCV004239013]uncertain significance83998790239987902Humanname
156147492CV2394418single nucleotide variantNM_194294.5(IDO2):c.514G>T (p.Ala172Ser)not specified [RCV004240787]uncertain significance83998793539987935Humanname
156000159CV2396538single nucleotide variantNM_194294.5(IDO2):c.679C>A (p.Pro227Thr)not specified [RCV004242245]uncertain significance84000533840005338Humanname
329355553CV2434297single nucleotide variantNM_194294.5(IDO2):c.793G>A (p.Gly265Ser)not specified [RCV004251969]uncertain significance84001363840013638Humanname
401780448CV2674029single nucleotide variantNM_194294.5(IDO2):c.433G>A (p.Gly145Arg)not specified [RCV004293394]likely benign83998276939982769Humanname
401751284CV2708545single nucleotide variantNM_194294.5(IDO2):c.504A>G (p.Ile168Met)not specified [RCV004307541]uncertain significance83998792539987925Humanname
401862148CV2775171single nucleotide variantNM_194294.5(IDO2):c.366G>T (p.Leu122Phe)not specified [RCV004346521]uncertain significance83998270239982702Humanname
405791728CV3267322single nucleotide variantNM_194294.5(IDO2):c.439C>A (p.Leu147Met)not specified [RCV004399958]uncertain significance83998551239985512Humanname
405791731CV3267323single nucleotide variantNM_194294.5(IDO2):c.463A>G (p.Ile155Val)not specified [RCV004399959]uncertain significance83998788439987884Humanname
405791737CV3267325single nucleotide variantNM_194294.5(IDO2):c.640A>C (p.Ile214Leu)not specified [RCV004399961]uncertain significance83998981139989811Humanname
405791740CV3267326single nucleotide variantNM_194294.5(IDO2):c.734C>T (p.Pro245Leu)not specified [RCV004399962]uncertain significance84001357940013579Humanname
405791743CV3267327single nucleotide variantNM_194294.5(IDO2):c.925G>A (p.Glu309Lys)not specified [RCV004399963]uncertain significance84001530340015303Humanname
407466817CV3444440single nucleotide variantNM_194294.5(IDO2):c.796G>A (p.Gly266Arg)not specified [RCV004635512]uncertain significance84001364140013641Humanname
597762653CV3683098single nucleotide variantNM_194294.5(IDO2):c.432C>A (p.Asp144Glu)not specified [RCV004926172]likely benign83998276839982768Humanname
597762659CV3683099single nucleotide variantNM_194294.5(IDO2):c.826G>T (p.Ala276Ser)not specified [RCV004926173]uncertain significance84001367140013671Humanname
597762664CV3683100single nucleotide variantNM_194294.5(IDO2):c.827C>T (p.Ala276Val)not specified [RCV004926174]uncertain significance84001367240013672Humanname
598257783CV3979086single nucleotide variantNM_194294.5(IDO2):c.617G>A (p.Arg206Gln)not specified [RCV005347060]likely benign83998978839989788Humanname
598206396CV3979088single nucleotide variantNM_194294.5(IDO2):c.887T>C (p.Met296Thr)not specified [RCV005337773]uncertain significance84001526540015265Humanname
150436179CV1221799single nucleotide variantNM_194294.5(IDO2):c.1038T>A (p.Tyr346Ter)not provided [RCV001609491]benign84001541640015416Humanname
155966884CV2216766single nucleotide variantNM_194294.5(IDO2):c.1216C>T (p.Arg406Cys)not specified [RCV004083210]uncertain significance84001559440015594Humanname
156247212CV2306878single nucleotide variantNM_194294.5(IDO2):c.1015G>A (p.Ala339Thr)not specified [RCV004157408]uncertain significance84001539340015393Humanname
329370634CV2461788single nucleotide variantNM_194294.5(IDO2):c.1007G>A (p.Cys336Tyr)not specified [RCV004271714]uncertain significance84001538540015385Humanname
401857600CV2756136single nucleotide variantNM_194294.5(IDO2):c.1118C>T (p.Pro373Leu)not specified [RCV004338245]uncertain significance84001549640015496Humanname
401872263CV2793053single nucleotide variantNM_194294.5(IDO2):c.1181T>C (p.Val394Ala)not specified [RCV004360383]uncertain significance84001555940015559Humanname
405791722CV3267321single nucleotide variantNM_194294.5(IDO2):c.1142G>A (p.Gly381Asp)not specified [RCV004399957]uncertain significance84001552040015520Humanname
407511026CV3444442single nucleotide variantNM_194294.5(IDO2):c.1154C>T (p.Thr385Ile)not specified [RCV004626328]uncertain significance84001553240015532Humanname