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)

42 records found for search term Fcrl1
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8574931CV109270single nucleotide variantNM_001159397.1(FCRL1):c.32-4195A>GLung cancer [RCV000089795]uncertain significance1157811317157811317Humanname
598229672CV3959152single nucleotide variantNM_052938.5(FCRL1):c.77C>T (p.Ser26Phe)not specified [RCV005342114]uncertain significance1157804087157804087Humanname
155909035CV2350419single nucleotide variantNM_052938.5(FCRL1):c.248C>T (p.Ser83Leu)not specified [RCV004204796]uncertain significance1157803916157803916Humanname
156089371CV2359365single nucleotide variantNM_052938.5(FCRL1):c.209A>G (p.Lys70Arg)not specified [RCV004212644]uncertain significance1157803955157803955Humanname
405742322CV3256907single nucleotide variantNM_052938.5(FCRL1):c.110C>T (p.Thr37Met)not specified [RCV004391523]uncertain significance1157804054157804054Humanname
405742336CV3256909single nucleotide variantNM_052938.5(FCRL1):c.1224C>T (p.Ser408=)not specified [RCV004391525]likely benign1157796165157796165Humanname
405742341CV3256910single nucleotide variantNM_052938.5(FCRL1):c.171C>A (p.Asp57Glu)not specified [RCV004391526]uncertain significance1157803993157803993Humanname
407483151CV3438875single nucleotide variantNM_052938.5(FCRL1):c.265C>G (p.Gln89Glu)not specified [RCV004618518]uncertain significance1157803899157803899Humanname
597740006CV3676078single nucleotide variantNM_052938.5(FCRL1):c.188C>T (p.Pro63Leu)not specified [RCV004921373]likely benign1157803976157803976Humanname
598229655CV3959149single nucleotide variantNM_052938.5(FCRL1):c.224C>T (p.Ala75Val)not specified [RCV005342111]uncertain significance1157803940157803940Humanname
598229666CV3959151single nucleotide variantNM_052938.5(FCRL1):c.223G>C (p.Ala75Pro)not specified [RCV005342113]uncertain significance1157803941157803941Humanname
598229679CV3959153single nucleotide variantNM_052938.5(FCRL1):c.110C>G (p.Thr37Arg)not specified [RCV005342115]uncertain significance1157804054157804054Humanname
156102801CV2260455single nucleotide variantNM_052938.5(FCRL1):c.479C>T (p.Thr160Ile)not specified [RCV004123250]uncertain significance1157802505157802505Humanname
156291810CV2321156single nucleotide variantNM_052938.5(FCRL1):c.880T>C (p.Phe294Leu)not specified [RCV004175282]uncertain significance1157801921157801921Humanname
329356695CV2460482single nucleotide variantNM_052938.5(FCRL1):c.334G>A (p.Asp112Asn)not specified [RCV004268775]likely benign1157802650157802650Humanname
401772353CV2719615single nucleotide variantNM_052938.5(FCRL1):c.320G>C (p.Arg107Thr)not specified [RCV004327282]uncertain significance1157802664157802664Humanname
405742347CV3256911single nucleotide variantNM_052938.5(FCRL1):c.753C>G (p.Ser251Arg)not specified [RCV004391527]uncertain significance1157802048157802048Humanname
405742356CV3256912single nucleotide variantNM_052938.5(FCRL1):c.764C>A (p.Pro255His)not specified [RCV004391528]uncertain significance1157802037157802037Humanname
407483134CV3438872single nucleotide variantNM_052938.5(FCRL1):c.668A>G (p.Asp223Gly)not specified [RCV004618515]uncertain significance1157802133157802133Humanname
407483138CV3438873single nucleotide variantNM_052938.5(FCRL1):c.670G>A (p.Val224Met)not specified [RCV004618516]uncertain significance1157802131157802131Humanname
597739962CV3676069single nucleotide variantNM_052938.5(FCRL1):c.760G>C (p.Ala254Pro)not specified [RCV004921364]uncertain significance1157802041157802041Humanname
597739967CV3676070single nucleotide variantNM_052938.5(FCRL1):c.931G>A (p.Glu311Lys)not specified [RCV004921365]uncertain significance1157801533157801533Humanname
597739983CV3676073single nucleotide variantNM_052938.5(FCRL1):c.397A>G (p.Ile133Val)not specified [RCV004921368]likely benign1157802587157802587Humanname
597739988CV3676074single nucleotide variantNM_052938.5(FCRL1):c.508A>C (p.Ile170Leu)not specified [RCV004921369]uncertain significance1157802476157802476Humanname
597739992CV3676075single nucleotide variantNM_052938.5(FCRL1):c.766T>G (p.Ser256Ala)not specified [RCV004921370]uncertain significance1157802035157802035Humanname
597739997CV3676076single nucleotide variantNM_052938.5(FCRL1):c.691G>A (p.Ala231Thr)not specified [RCV004921371]uncertain significance1157802110157802110Humanname
597740002CV3676077single nucleotide variantNM_052938.5(FCRL1):c.856C>A (p.Arg286Ser)not specified [RCV004921372]uncertain significance1157801945157801945Humanname
598229649CV3959148single nucleotide variantNM_052938.5(FCRL1):c.967G>A (p.Ala323Thr)not specified [RCV005342110]uncertain significance1157801497157801497Humanname
598229661CV3959150single nucleotide variantNM_052938.5(FCRL1):c.737A>C (p.Asp246Ala)not specified [RCV005342112]uncertain significance1157802064157802064Humanname
156185472CV2292323single nucleotide variantNM_052938.5(FCRL1):c.1069C>A (p.Leu357Ile)not specified [RCV004150140]uncertain significance1157798206157798206Humanname
156340199CV2363198single nucleotide variantNM_052938.5(FCRL1):c.1004G>A (p.Gly335Glu)not specified [RCV004213765]uncertain significance1157800085157800085Humanname
329357713CV2453759single nucleotide variantNM_052938.5(FCRL1):c.1133A>G (p.Asp378Gly)not specified [RCV004269386]uncertain significance1157797921157797921Humanname
401773393CV2698197single nucleotide variantNM_052938.5(FCRL1):c.1079C>T (p.Pro360Leu)not specified [RCV004304764]uncertain significance1157798196157798196Humanname
401763623CV2714620single nucleotide variantNM_052938.5(FCRL1):c.1261A>G (p.Thr421Ala)not specified [RCV004318113]uncertain significance1157796128157796128Humanname
405742330CV3256908single nucleotide variantNM_052938.5(FCRL1):c.1201A>T (p.Thr401Ser)not specified [RCV004391524]uncertain significance1157797118157797118Humanname
597739973CV3676071single nucleotide variantNM_052938.5(FCRL1):c.1252G>A (p.Ala418Thr)not specified [RCV004921366]uncertain significance1157796137157796137Humanname
597739978CV3676072single nucleotide variantNM_052938.5(FCRL1):c.1160A>C (p.Asn387Thr)not specified [RCV004921367]uncertain significance1157797894157797894Humanname
8624741CV79855single nucleotide variantNM_001159397.1(FCRL1):c.741C>T (p.Ile247=)Malignant melanoma [RCV000059931]not provided1157802060157802060Humanname
8628994CV84137single nucleotide variantNM_001159397.1(FCRL1):c.945C>T (p.Phe315=)Malignant melanoma [RCV000064218]not provided1157798213157798213Humanname
8624740CV79854single nucleotide variantNM_001159397.1(FCRL1):c.841G>A (p.Gly281Ser)Malignant melanoma [RCV000059930]not provided1157801960157801960Humanname
8628995CV84138single nucleotide variantNM_001159397.1(FCRL1):c.904G>A (p.Asp302Asn)Malignant melanoma [RCV000064219]not provided1157800068157800068Humanname
8628996CV84139single nucleotide variantNM_001159397.1(FCRL1):c.556G>A (p.Glu186Lys)Malignant melanoma [RCV000064220]not provided1157802428157802428Humanname