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 All species
(View Results for all Objects and Ontologies)

18 records found for search term Snrpa1
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597744982CV3607094single nucleotide variantNM_003090.4(SNRPA1):c.86A>G (p.Tyr29Cys)not specified [RCV004865578]uncertain significance15101293169101293169Humanname
597740861CV3607095single nucleotide variantNM_003090.4(SNRPA1):c.50A>G (p.Asn17Ser)not specified [RCV004864741]uncertain significance15101295129101295129Humanname
597740866CV3607099single nucleotide variantNM_003090.4(SNRPA1):c.97G>A (p.Val33Ile)not specified [RCV004864742]uncertain significance15101293158101293158Humanname
156146746CV2289263single nucleotide variantNM_003090.4(SNRPA1):c.268C>G (p.Leu90Val)not specified [RCV004152249]uncertain significance15101292003101292003Humanname
405731633CV3326288single nucleotide variantNM_003090.4(SNRPA1):c.201A>T (p.Lys67Asn)not specified [RCV004464412]uncertain significance15101293054101293054Humanname
407503689CV3474653single nucleotide variantNM_003090.4(SNRPA1):c.159G>C (p.Glu53Asp)not specified [RCV004670339]uncertain significance15101293096101293096Humanname
597744986CV3607096single nucleotide variantNM_003090.4(SNRPA1):c.127C>G (p.Gln43Glu)not specified [RCV004865579]uncertain significance15101293128101293128Humanname
597744990CV3607097single nucleotide variantNM_003090.4(SNRPA1):c.232C>T (p.Arg78Cys)not specified [RCV004865580]uncertain significance15101292039101292039Humanname
597744995CV3607098single nucleotide variantNM_003090.4(SNRPA1):c.173A>T (p.Asp58Val)not specified [RCV004865581]uncertain significance15101293082101293082Humanname
156382817CV2223651single nucleotide variantNM_003090.4(SNRPA1):c.700C>T (p.Arg234Cys)not specified [RCV004093775]uncertain significance15101284976101284976Humanname
156180857CV2327770single nucleotide variantNM_003090.4(SNRPA1):c.323C>G (p.Pro108Arg)not specified [RCV004179116]uncertain significance15101287689101287689Humanname
156018241CV2370248single nucleotide variantNM_003090.4(SNRPA1):c.584G>C (p.Gly195Ala)not specified [RCV004213168]uncertain significance15101285757101285757Humanname
156204597CV2385094single nucleotide variantNM_003090.4(SNRPA1):c.746A>G (p.Asp249Gly)not specified [RCV004228359]uncertain significance15101281746101281746Humanname
401858854CV2774955single nucleotide variantNM_003090.4(SNRPA1):c.301G>A (p.Val101Met)not specified [RCV004346357]uncertain significance15101291970101291970Humanname
401866504CV2782862single nucleotide variantNM_003090.4(SNRPA1):c.398T>C (p.Leu133Ser)not specified [RCV004361670]uncertain significance15101286969101286969Humanname
405731639CV3326289single nucleotide variantNM_003090.4(SNRPA1):c.698A>G (p.Glu233Gly)not specified [RCV004464413]uncertain significance15101284978101284978Humanname
597740853CV3607093single nucleotide variantNM_003090.4(SNRPA1):c.732A>T (p.Glu244Asp)not specified [RCV004864740]uncertain significance15101281760101281760Humanname
598171422CV3911597single nucleotide variantNM_003090.4(SNRPA1):c.701G>A (p.Arg234His)not specified [RCV005284838]uncertain significance15101284975101284975Humanname