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)

43 records found for search term Frmd3
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597728399CV3670120single nucleotide variantNM_174938.6(FRMD3):c.6C>A (p.Phe2Leu)not specified [RCV004919568]uncertain significance98353822683538226Humanname
156162270CV2371681single nucleotide variantNM_174938.6(FRMD3):c.11C>T (p.Ser4Phe)not specified [RCV004216919]uncertain significance98353822183538221Humanname
405696643CV3226755single nucleotide variantNM_174938.6(FRMD3):c.516C>T (p.Tyr172=)not provided [RCV003993148]likely benign98333559683335596Humanname
156106276CV2217805single nucleotide variantNM_174938.6(FRMD3):c.109C>T (p.Arg37Trp)not specified [RCV004083979]uncertain significance98353812383538123Humanname
156298576CV2240971single nucleotide variantNM_174938.6(FRMD3):c.251G>C (p.Arg84Thr)not specified [RCV004102245]uncertain significance98338960583389605Humanname
156266870CV2296496single nucleotide variantNM_174938.6(FRMD3):c.213C>A (p.Asp71Glu)not specified [RCV004154577]uncertain significance98338964383389643Humanname
156097661CV2310285single nucleotide variantNM_174938.6(FRMD3):c.137G>C (p.Cys46Ser)not specified [RCV004157029]uncertain significance98353809583538095Humanname
598230751CV3970240single nucleotide variantNM_174938.6(FRMD3):c.291G>A (p.Met97Ile)not specified [RCV005342310]uncertain significance98337291783372917Humanname
156387487CV2221523single nucleotide variantNM_174938.6(FRMD3):c.755G>C (p.Arg252Thr)not specified [RCV004096793]uncertain significance98331190583311905Humanname
155957800CV2282113single nucleotide variantNM_174938.6(FRMD3):c.572T>G (p.Val191Gly)not specified [RCV004138852]uncertain significance98333554083335540Humanname
156255256CV2311592single nucleotide variantNM_174938.6(FRMD3):c.418C>T (p.Arg140Cys)not specified [RCV004168403]uncertain significance98334324483343244Humanname
329391478CV2452376single nucleotide variantNM_174938.6(FRMD3):c.853G>A (p.Ala285Thr)not specified [RCV004272697]uncertain significance98330960983309609Humanname
401738825CV2676381single nucleotide variantNM_174938.6(FRMD3):c.824G>A (p.Gly275Asp)not specified [RCV004286404]uncertain significance98331049883310498Humanname
401759227CV2701445single nucleotide variantNM_174938.6(FRMD3):c.487T>G (p.Tyr163Asp)not specified [RCV004312118]uncertain significance98333562583335625Humanname
405763935CV3251034single nucleotide variantNM_174938.6(FRMD3):c.341A>G (p.His114Arg)not specified [RCV004394740]uncertain significance98334971283349712Humanname
405763944CV3251035single nucleotide variantNM_174938.6(FRMD3):c.503A>G (p.His168Arg)not specified [RCV004394741]uncertain significance98333560983335609Humanname
405763950CV3251036single nucleotide variantNM_174938.6(FRMD3):c.517A>T (p.Ile173Phe)not specified [RCV004394742]uncertain significance98333559583335595Humanname
405763956CV3251037single nucleotide variantNM_174938.6(FRMD3):c.911A>G (p.Asn304Ser)not specified [RCV004394743]uncertain significance98330955183309551Humanname
407495046CV3442991single nucleotide variantNM_174938.6(FRMD3):c.592C>T (p.Leu198Phe)not specified [RCV004621483]uncertain significance98333552083335520Humanname
597728335CV3670112single nucleotide variantNM_174938.6(FRMD3):c.490G>A (p.Asp164Asn)not specified [RCV004919561]uncertain significance98333562283335622Humanname
597728345CV3670113single nucleotide variantNM_174938.6(FRMD3):c.551A>T (p.Gln184Leu)not specified [RCV004919562]uncertain significance98333556183335561Humanname
597728354CV3670114single nucleotide variantNM_174938.6(FRMD3):c.888T>A (p.His296Gln)not specified [RCV004919563]uncertain significance98330957483309574Humanname
598230744CV3970239single nucleotide variantNM_174938.6(FRMD3):c.861T>A (p.His287Gln)not specified [RCV005342309]uncertain significance98330960183309601Humanname
598230762CV3970242single nucleotide variantNM_174938.6(FRMD3):c.581A>G (p.His194Arg)not specified [RCV005342312]uncertain significance98333553183335531Humanname
156401160CV2213995single nucleotide variantNM_174938.6(FRMD3):c.1078A>G (p.Ile360Val)not specified [RCV004083712]uncertain significance98329072083290720Humanname
156286963CV2229566single nucleotide variantNM_174938.6(FRMD3):c.1027G>C (p.Glu343Gln)not specified [RCV004103388]uncertain significance98329879183298791Humanname
156117176CV2231809single nucleotide variantNM_174938.6(FRMD3):c.1748T>C (p.Val583Ala)not specified [RCV004098618]uncertain significance98324796483247964Humanname
156055018CV2243147single nucleotide variantNM_174938.6(FRMD3):c.1430G>A (p.Arg477Lys)not specified [RCV004110051]uncertain significance98324828283248282Humanname
156239879CV2286006single nucleotide variantNM_174938.6(FRMD3):c.1474G>A (p.Ala492Thr)not specified [RCV004143915]uncertain significance98324823883248238Humanname
329392930CV2469082single nucleotide variantNM_174938.6(FRMD3):c.1363C>T (p.Pro455Ser)not specified [RCV004274321]uncertain significance98324834983248349Humanname
401731924CV2690206single nucleotide variantNM_174938.6(FRMD3):c.1174G>A (p.Glu392Lys)not specified [RCV004302215]uncertain significance98329062483290624Humanname
401760286CV2694989single nucleotide variantNM_174938.6(FRMD3):c.1309G>A (p.Glu437Lys)not specified [RCV004301366]uncertain significance98324840383248403Humanname
401757970CV2708060single nucleotide variantNM_174938.6(FRMD3):c.1672T>C (p.Phe558Leu)not specified [RCV004309303]uncertain significance98324804083248040Humanname
405763923CV3251032single nucleotide variantNM_174938.6(FRMD3):c.1037C>T (p.Ser346Phe)not specified [RCV004394738]uncertain significance98329878183298781Humanname
405763928CV3251033single nucleotide variantNM_174938.6(FRMD3):c.1537G>A (p.Asp513Asn)not specified [RCV004394739]uncertain significance98324817583248175Humanname
407495037CV3442989single nucleotide variantNM_174938.6(FRMD3):c.1232C>T (p.Pro411Leu)not specified [RCV004621481]uncertain significance98324848083248480Humanname
597728365CV3670115single nucleotide variantNM_174938.6(FRMD3):c.1750G>C (p.Ala584Pro)not specified [RCV004919564]uncertain significance98324796283247962Humanname
597728373CV3670116single nucleotide variantNM_174938.6(FRMD3):c.1282C>T (p.Pro428Ser)not specified [RCV004919565]uncertain significance98324843083248430Humanname
597728383CV3670118single nucleotide variantNM_174938.6(FRMD3):c.1304T>C (p.Ile435Thr)not specified [RCV004919566]uncertain significance98324840883248408Humanname
597728391CV3670119single nucleotide variantNM_174938.6(FRMD3):c.1127A>G (p.Asn376Ser)not specified [RCV004919567]uncertain significance98329067183290671Humanname
597728407CV3670121single nucleotide variantNM_174938.6(FRMD3):c.1622T>C (p.Phe541Ser)not specified [RCV004919569]uncertain significance98324809083248090Humanname
598230756CV3970241single nucleotide variantNM_174938.6(FRMD3):c.1163G>C (p.Ser388Thr)not specified [RCV005342311]uncertain significance98329063583290635Humanname
8633414CV88629single nucleotide variantNM_174938.5(FRMD3):c.1540A>C (p.Ile514Leu)Malignant melanoma [RCV000068722]not provided98324817283248172Humanname