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)

27 records found for search term Arpc1a
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597729755CV3582990single nucleotide variantNM_006409.4(ARPC1A):c.63T>A (p.Thr21=)not specified [RCV004862958]likely benign79933341699333416Humanname
156177496CV2220444single nucleotide variantNM_006409.4(ARPC1A):c.199A>G (p.Ile67Val)not specified [RCV004095843]uncertain significance79934432299344322Humanname
156008436CV2365267single nucleotide variantNM_006409.4(ARPC1A):c.115G>A (p.Gly39Arg)not specified [RCV004209363]uncertain significance79933823199338231Humanname
156152227CV2394838single nucleotide variantNM_006409.4(ARPC1A):c.161A>G (p.His54Arg)not specified [RCV004234500]uncertain significance79933827799338277Humanname
597764725CV3582981single nucleotide variantNM_006409.4(ARPC1A):c.134C>T (p.Ala45Val)not specified [RCV004849847]uncertain significance79933825099338250Humanname
598174606CV3905198single nucleotide variantNM_006409.4(ARPC1A):c.250G>A (p.Gly84Ser)not specified [RCV005263882]uncertain significance79934437399344373Humanname
156251381CV2286839single nucleotide variantNM_006409.4(ARPC1A):c.461A>G (p.Asn154Ser)not specified [RCV004142641]uncertain significance79934892099348920Humanname
155999976CV2287331single nucleotide variantNM_006409.4(ARPC1A):c.682G>A (p.Val228Met)not specified [RCV004146954]uncertain significance79935409099354090Humanname
156229835CV2353021single nucleotide variantNM_006409.4(ARPC1A):c.308A>C (p.Lys103Thr)not specified [RCV004201050]uncertain significance79934443199344431Humanname
155924583CV2358176single nucleotide variantNM_006409.4(ARPC1A):c.599G>T (p.Gly200Val)not specified [RCV004211976]uncertain significance79935400799354007Humanname
156188052CV2395352single nucleotide variantNM_006409.4(ARPC1A):c.914A>G (p.Asn305Ser)not specified [RCV004239444]uncertain significance79935966999359669Humanname
329398167CV2464830single nucleotide variantNM_006409.4(ARPC1A):c.751A>T (p.Ser251Cys)not specified [RCV004284778]uncertain significance79935837799358377Humanname
401764129CV2717235single nucleotide variantNM_006409.4(ARPC1A):c.581T>C (p.Leu194Pro)not specified [RCV004324068]uncertain significance79935398999353989Humanname
401870024CV2765567single nucleotide variantNM_006409.4(ARPC1A):c.643A>G (p.Ser215Gly)not specified [RCV004335585]uncertain significance79935405199354051Humanname
407468891CV3473317single nucleotide variantNM_006409.4(ARPC1A):c.830G>A (p.Arg277His)not specified [RCV004661281]uncertain significance79935958599359585Humanname
597764684CV3582960single nucleotide variantNM_006409.4(ARPC1A):c.829C>T (p.Arg277Cys)not specified [RCV004849836]uncertain significance79935958499359584Humanname
597764698CV3582971single nucleotide variantNM_006409.4(ARPC1A):c.887A>G (p.Asn296Ser)not specified [RCV004849840]uncertain significance79935964299359642Humanname
597764746CV3583000single nucleotide variantNM_006409.4(ARPC1A):c.604G>A (p.Gly202Ser)not specified [RCV004849852]uncertain significance79935401299354012Humanname
598174532CV3905187single nucleotide variantNM_006409.4(ARPC1A):c.439A>G (p.Ser147Gly)not specified [RCV005263871]uncertain significance79934889899348898Humanname
598174681CV3905209single nucleotide variantNM_006409.4(ARPC1A):c.659C>G (p.Ala220Gly)not specified [RCV005263893]uncertain significance79935406799354067Humanname
598174734CV3905219single nucleotide variantNM_006409.4(ARPC1A):c.829C>G (p.Arg277Gly)not specified [RCV005263903]uncertain significance79935958499359584Humanname
156069777CV2203835single nucleotide variantNM_006409.4(ARPC1A):c.1054A>C (p.Met352Leu)not specified [RCV004069898]uncertain significance79936361399363613Humanname
156285788CV2360838single nucleotide variantNM_006409.4(ARPC1A):c.1060A>G (p.Ile354Val)not specified [RCV004213610]uncertain significance79936361999363619Humanname
405663827CV3290316single nucleotide variantNM_006409.4(ARPC1A):c.1022G>A (p.Arg341His)not specified [RCV004418089]uncertain significance79936358199363581Humanname
405664719CV3290317single nucleotide variantNM_006409.4(ARPC1A):c.1102C>T (p.Arg368Trp)not specified [RCV004418090]uncertain significance79936591899365918Humanname
407514354CV3473326single nucleotide variantNM_006409.4(ARPC1A):c.1103G>A (p.Arg368Gln)not specified [RCV004674410]uncertain significance79936591999365919Humanname
597764663CV3582950single nucleotide variantNM_006409.4(ARPC1A):c.1088C>T (p.Ser363Phe)not specified [RCV004849831]uncertain significance79936590499365904Humanname