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)

29 records found for search term Nsfl1c
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15164950CV742264single nucleotide variantNM_016143.5(NSFL1C):c.180A>G (p.Ser60=)not provided [RCV000904115]benign2014643521464352Humanname
156282740CV2252430single nucleotide variantNM_016143.5(NSFL1C):c.70C>T (p.Arg24Cys)not specified [RCV004116268]uncertain significance2014667551466755Humanname
401760030CV2698716single nucleotide variantNM_016143.5(NSFL1C):c.85T>C (p.Ser29Pro)not specified [RCV004301174]uncertain significance2014667401466740Humanname
407517064CV3462056single nucleotide variantNM_016143.5(NSFL1C):c.37G>C (p.Val13Leu)not specified [RCV004650508]uncertain significance2014667881466788Humanname
156330597CV2224289single nucleotide variantNM_016143.5(NSFL1C):c.151G>C (p.Val51Leu)not specified [RCV004096110]uncertain significance2014643811464381Humanname
407476985CV3462055single nucleotide variantNM_016143.5(NSFL1C):c.191G>A (p.Gly64Asp)not specified [RCV004638741]uncertain significance2014643411464341Humanname
598220895CV3994743single nucleotide variantNM_016143.5(NSFL1C):c.235A>C (p.Ile79Leu)not specified [RCV005379577]uncertain significance2014582431458243Humanname
598220901CV3994744single nucleotide variantNM_016143.5(NSFL1C):c.172C>T (p.Pro58Ser)not specified [RCV005379578]uncertain significance2014643601464360Humanname
156325259CV2195263single nucleotide variantNM_016143.5(NSFL1C):c.348C>G (p.Asn116Lys)not specified [RCV004080197]uncertain significance2014550631455063Humanname
156170977CV2247417single nucleotide variantNM_016143.5(NSFL1C):c.439C>A (p.Pro147Thr)not specified [RCV004108748]uncertain significance2014549721454972Humanname
156291364CV2296632single nucleotide variantNM_016143.5(NSFL1C):c.968T>A (p.Leu323His)not specified [RCV004154689]uncertain significance2014438941443894Humanname
156299172CV2325983single nucleotide variantNM_016143.5(NSFL1C):c.433A>C (p.Ser145Arg)not specified [RCV004176195]uncertain significance2014549781454978Humanname
156264315CV2329432single nucleotide variantNM_016143.5(NSFL1C):c.920G>A (p.Arg307Lys)not specified [RCV004187437]uncertain significance2014456961445696Humanname
156065341CV2348784single nucleotide variantNM_016143.5(NSFL1C):c.641G>A (p.Arg214His)not specified [RCV004203231]uncertain significance2014530371453037Humanname
155934952CV2372580single nucleotide variantNM_016143.5(NSFL1C):c.679C>G (p.His227Asp)not specified [RCV004219372]uncertain significance2014525991452599Humanname
405710365CV3359411single nucleotide variantNM_016143.5(NSFL1C):c.349G>A (p.Glu117Lys)not specified [RCV004493759]uncertain significance2014550621455062Humanname
405710372CV3359412single nucleotide variantNM_016143.5(NSFL1C):c.407G>A (p.Arg136Gln)not specified [RCV004493760]uncertain significance2014550041455004Humanname
405710379CV3359413single nucleotide variantNM_016143.5(NSFL1C):c.421C>A (p.Pro141Thr)not specified [RCV004493761]uncertain significance2014549901454990Humanname
405710385CV3359414single nucleotide variantNM_016143.5(NSFL1C):c.440C>A (p.Pro147Gln)not specified [RCV004493762]uncertain significance2014549711454971Humanname
405710392CV3359415single nucleotide variantNM_016143.5(NSFL1C):c.616A>G (p.Asn206Asp)not specified [RCV004493763]uncertain significance2014530621453062Humanname
405710399CV3359416single nucleotide variantNM_016143.5(NSFL1C):c.682G>A (p.Gly228Ser)not specified [RCV004493764]uncertain significance2014525961452596Humanname
597707414CV3577029single nucleotide variantNM_016143.5(NSFL1C):c.679C>T (p.His227Tyr)not specified [RCV004840448]uncertain significance2014525991452599Humanname
597707425CV3577030single nucleotide variantNM_016143.5(NSFL1C):c.958G>A (p.Asp320Asn)not specified [RCV004840449]uncertain significance2014439041443904Humanname
597707433CV3577031single nucleotide variantNM_016143.5(NSFL1C):c.740A>G (p.Lys247Arg)not specified [RCV004840450]uncertain significance2014525381452538Humanname
597643197CV3577032single nucleotide variantNM_016143.5(NSFL1C):c.385C>T (p.His129Tyr)not specified [RCV004832569]uncertain significance2014550261455026Humanname
597707459CV3577035single nucleotide variantNM_016143.5(NSFL1C):c.395T>A (p.Val132Glu)not specified [RCV004840453]uncertain significance2014550161455016Humanname
15166423CV728545single nucleotide variantNM_016143.5(NSFL1C):c.664C>T (p.Leu222Phe)not provided [RCV000882629]likely benign2014526141452614Human3name
15166423CV728545single nucleotide variantNM_016143.5(NSFL1C):c.664C>T (p.Leu222Phe)not provided [RCV000882629]likely benign2014526141452615Human3name
405710359CV3359410single nucleotide variantNM_016143.5(NSFL1C):c.1085A>G (p.Asn362Ser)not specified [RCV004493758]uncertain significance2014437771443777Humanname