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)

37 records found for search term Fip1l1
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401923295CV2822520single nucleotide variantNM_030917.4(FIP1L1):c.1500-8A>Cnot provided [RCV003435016]likely benign45345864553458645Humanname
15171841CV777475single nucleotide variantNM_030917.4(FIP1L1):c.1638-4C>Tnot provided [RCV000949905]likely benign45345929853459298Humanname
9689908CV173814single nucleotide variantNM_030917.4(FIP1L1):c.1285+11T>Gnot provided [RCV004715747]|not specified [RCV000155542]benign45344411453444114Humanname
597698757CV3669657single nucleotide variantNM_030917.4(FIP1L1):c.16G>T (p.Val6Phe)not specified [RCV004916164]uncertain significance45337785453377854Humanname
155989600CV2282804single nucleotide variantNM_030917.4(FIP1L1):c.55G>A (p.Gly19Arg)not specified [RCV004141652]uncertain significance45337789353377893Humanname
401928107CV2822519single nucleotide variantNM_030917.4(FIP1L1):c.810G>A (p.Pro270=)not provided [RCV003439309]likely benign45339983453399834Humanname
8687700CV138160single nucleotide variantNM_030917.4(FIP1L1):c.101A>G (p.His34Arg)not specified [RCV000121097]not provided45337908853379088Humanname
155920570CV2279618single nucleotide variantNM_030917.4(FIP1L1):c.260G>A (p.Ser87Asn)not specified [RCV004142118]uncertain significance45338380453383804Humanname
401728072CV2685810single nucleotide variantNM_030917.4(FIP1L1):c.1500C>T (p.Ser500=)not specified [RCV004294799]likely benign45345865353458653Humanname
598200512CV3955846single nucleotide variantNM_030917.4(FIP1L1):c.143T>C (p.Val48Ala)not specified [RCV005336665]uncertain significance45337923753379237Humanname
8631205CV86361single nucleotide variantNM_030917.3(FIP1L1):c.1071T>C (p.Pro357=)Malignant melanoma [RCV000066452]not provided45342808053428080Humanname
8687698CV138158single nucleotide variantNM_030917.4(FIP1L1):c.695A>G (p.Asn232Ser)not specified [RCV000121095]not provided45339148853391488Humanname
8687699CV138159single nucleotide variantNM_030917.4(FIP1L1):c.784T>C (p.Ser262Pro)not specified [RCV000121096]uncertain significance|not provided45339980853399808Humanname
156317738CV2204050single nucleotide variantNM_030917.4(FIP1L1):c.551C>A (p.Thr184Asn)not specified [RCV004076520]uncertain significance45339105453391054Humanname
156202322CV2256236single nucleotide variantNM_030917.4(FIP1L1):c.907G>A (p.Glu303Lys)not specified [RCV004116491]uncertain significance45341470653414706Humanname
156265061CV2275368single nucleotide variantNM_030917.4(FIP1L1):c.575A>T (p.Gln192Leu)not specified [RCV004135253]uncertain significance45339107853391078Humanname
156199502CV2365331single nucleotide variantNM_030917.4(FIP1L1):c.785C>G (p.Ser262Cys)not specified [RCV004209417]uncertain significance45339980953399809Humanname
329401283CV2442287single nucleotide variantNM_030917.4(FIP1L1):c.550A>G (p.Thr184Ala)not specified [RCV004264768]uncertain significance45339105353391053Humanname
329396948CV2468349single nucleotide variantNM_030917.4(FIP1L1):c.866A>G (p.Asn289Ser)not specified [RCV004275893]uncertain significance45341466553414665Humanname
401766973CV2680211single nucleotide variantNM_030917.4(FIP1L1):c.452C>T (p.Pro151Leu)not specified [RCV004286685]uncertain significance45339057553390575Humanname
405779794CV3260640single nucleotide variantNM_030917.4(FIP1L1):c.398G>T (p.Gly133Val)not specified [RCV004386575]uncertain significance45339052153390521Humanname
405779800CV3260641single nucleotide variantNM_030917.4(FIP1L1):c.601G>A (p.Val201Ile)not specified [RCV004386576]uncertain significance45339110453391104Humanname
405779808CV3260642single nucleotide variantNM_030917.4(FIP1L1):c.607C>G (p.Pro203Ala)not specified [RCV004386577]uncertain significance45339111053391110Humanname
407502707CV3435895single nucleotide variantNM_030917.4(FIP1L1):c.542A>T (p.Asn181Ile)not specified [RCV004623539]uncertain significance45339104553391045Humanname
407502718CV3435898single nucleotide variantNM_030917.4(FIP1L1):c.763G>A (p.Ala255Thr)not specified [RCV004623542]uncertain significance45339978753399787Humanname
597699612CV3669656single nucleotide variantNM_030917.4(FIP1L1):c.581G>A (p.Arg194Lys)not specified [RCV004916163]uncertain significance45339108453391084Humanname
598200518CV3955847single nucleotide variantNM_030917.4(FIP1L1):c.797C>T (p.Thr266Ile)not specified [RCV005336666]uncertain significance45339982153399821Humanname
155912408CV2245531single nucleotide variantNM_030917.4(FIP1L1):c.1380C>A (p.Asp460Glu)not specified [RCV004109623]uncertain significance45345301453453014Humanname
401856503CV2764829single nucleotide variantNM_030917.4(FIP1L1):c.1730C>T (p.Ala577Val)not provided [RCV003436022]|not specified [RCV004334929]uncertain significance45345939453459394Humanname
405867598CV2842327single nucleotide variantNM_030917.4(FIP1L1):c.1411C>T (p.Arg471Ter)EBV-positive nodal T- and NK-cell lymphoma [RCV004560276]likely benign45345304553453045Humanname
405867602CV2842328single nucleotide variantNM_030917.4(FIP1L1):c.1633C>T (p.Arg545Ter)EBV-positive nodal T- and NK-cell lymphoma [RCV004560277]likely benign45345878653458786Humanname
405779788CV3260639single nucleotide variantNM_030917.4(FIP1L1):c.1761C>G (p.Ser587Arg)not specified [RCV004386574]uncertain significance45345942553459425Humanname
407502703CV3435894single nucleotide variantNM_030917.4(FIP1L1):c.1470T>A (p.Asp490Glu)not specified [RCV004623538]uncertain significance45345310453453104Humanname
407502715CV3435897single nucleotide variantNM_030917.4(FIP1L1):c.1039A>G (p.Thr347Ala)not specified [RCV004623541]uncertain significance45342804853428048Humanname
597698741CV3669655single nucleotide variantNM_030917.4(FIP1L1):c.1073C>T (p.Pro358Leu)not specified [RCV004916162]uncertain significance45342808253428082Humanname
598200498CV3955844single nucleotide variantNM_030917.4(FIP1L1):c.1283A>G (p.Asn428Ser)not specified [RCV005336663]uncertain significance45344410153444101Humanname
598200504CV3955845single nucleotide variantNM_030917.4(FIP1L1):c.1147A>G (p.Thr383Ala)not specified [RCV005336664]uncertain significance45342815653428156Humanname