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)

45 records found for search term Fam83a
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8632831CV88046single nucleotide variantNM_032899.5(FAM83A):c.702G>A (p.Arg234=)Malignant melanoma [RCV000068138]not provided8123194077123194077Humanname
407454032CV3431910single nucleotide variantNM_001394396.1(FAM83A):c.7C>T (p.Arg3Trp)not specified [RCV004609285]uncertain significance8123182863123182863Humanname
8632830CV88045single nucleotide variantNM_032899.5(FAM83A):c.172G>A (p.Gly58Ser)Malignant melanoma [RCV000068137]not provided8123183028123183028Humanname
597750143CV3665743single nucleotide variantNM_001394396.1(FAM83A):c.22G>C (p.Gly8Arg)not specified [RCV004923494]uncertain significance8123182878123182878Humanname
156027851CV2195611single nucleotide variantNM_001394396.1(FAM83A):c.38G>A (p.Arg13His)not specified [RCV004082819]uncertain significance8123182894123182894Humanname
156256331CV2374055single nucleotide variantNM_001394396.1(FAM83A):c.84C>A (p.Asp28Glu)not specified [RCV004227178]uncertain significance8123182940123182940Humanname
329375861CV2431647single nucleotide variantNM_001394396.1(FAM83A):c.40C>G (p.Leu14Val)not specified [RCV004254792]uncertain significance8123182896123182896Humanname
405760798CV3256577single nucleotide variantNM_001394396.1(FAM83A):c.68G>A (p.Arg23Gln)not specified [RCV004383459]uncertain significance8123182924123182924Humanname
597750121CV3665738single nucleotide variantNM_001394396.1(FAM83A):c.94A>C (p.Asn32His)not specified [RCV004923489]uncertain significance8123182950123182950Humanname
598238227CV3962429single nucleotide variantNM_001394396.1(FAM83A):c.29T>A (p.Ile10Asn)not specified [RCV005343769]uncertain significance8123182885123182885Humanname
156389022CV2229853single nucleotide variantNM_001394396.1(FAM83A):c.263C>T (p.Ala88Val)not specified [RCV004105417]uncertain significance8123183119123183119Humanname
401762240CV2723369single nucleotide variantNM_001394396.1(FAM83A):c.168G>C (p.Gln56His)not specified [RCV004329578]uncertain significance8123183024123183024Humanname
405760776CV3256573single nucleotide variantNM_001394396.1(FAM83A):c.241C>G (p.Pro81Ala)not specified [RCV004383455]likely benign8123183097123183097Humanname
407509088CV3431909single nucleotide variantNM_001394396.1(FAM83A):c.212T>C (p.Ile71Thr)not specified [RCV004625608]uncertain significance8123183068123183068Humanname
597750126CV3665739single nucleotide variantNM_001394396.1(FAM83A):c.294C>A (p.Ser98Arg)not specified [RCV004923490]uncertain significance8123183150123183150Humanname
597750152CV3665745single nucleotide variantNM_001394396.1(FAM83A):c.124C>T (p.Leu42Phe)not specified [RCV004923496]uncertain significance8123182980123182980Humanname
597750268CV3665746single nucleotide variantNM_001394396.1(FAM83A):c.278A>C (p.Lys93Thr)not specified [RCV004923497]uncertain significance8123183134123183134Humanname
598195244CV3962425single nucleotide variantNM_001394396.1(FAM83A):c.209A>G (p.Tyr70Cys)not specified [RCV005335538]uncertain significance8123183065123183065Humanname
598195254CV3962428single nucleotide variantNM_001394396.1(FAM83A):c.107G>A (p.Arg36Gln)not specified [RCV005335540]uncertain significance8123182963123182963Humanname
156401569CV2207395single nucleotide variantNM_001394396.1(FAM83A):c.665G>A (p.Ser222Asn)not specified [RCV004088096]uncertain significance8123194040123194040Humanname
155951530CV2238808single nucleotide variantNM_001394396.1(FAM83A):c.318C>A (p.Phe106Leu)not specified [RCV004109727]uncertain significance8123183174123183174Humanname
156187833CV2258331single nucleotide variantNM_001394396.1(FAM83A):c.865C>T (p.Leu289Phe)not specified [RCV004121683]uncertain significance8123207248123207248Humanname
156058520CV2322936single nucleotide variantNM_001394396.1(FAM83A):c.755T>C (p.Val252Ala)not specified [RCV004185383]uncertain significance8123194130123194130Humanname
155910617CV2366524single nucleotide variantNM_001394396.1(FAM83A):c.481G>A (p.Val161Ile)not specified [RCV004208499]uncertain significance8123191803123191803Humanname
401735686CV2672716single nucleotide variantNM_001394396.1(FAM83A):c.353T>A (p.Leu118Gln)not specified [RCV004287729]uncertain significance8123183209123183209Humanname
401737744CV2718198single nucleotide variantNM_001394396.1(FAM83A):c.538G>C (p.Glu180Gln)not specified [RCV004315893]uncertain significance8123191860123191860Humanname
401870308CV2765827single nucleotide variantNM_001394396.1(FAM83A):c.850G>C (p.Glu284Gln)not specified [RCV004335820]uncertain significance8123207233123207233Humanname
405760783CV3256574single nucleotide variantNM_001394396.1(FAM83A):c.508A>T (p.Thr170Ser)not specified [RCV004383456]uncertain significance8123191830123191830Humanname
405760787CV3256575single nucleotide variantNM_001394396.1(FAM83A):c.520A>G (p.Ile174Val)not specified [RCV004383457]uncertain significance8123191842123191842Humanname
405760792CV3256576single nucleotide variantNM_001394396.1(FAM83A):c.652A>G (p.Ile218Val)not specified [RCV004383458]uncertain significance8123194027123194027Humanname
405760806CV3256578single nucleotide variantNM_001394396.1(FAM83A):c.869A>G (p.Tyr290Cys)not specified [RCV004383460]uncertain significance8123207252123207252Humanname
405760810CV3256579single nucleotide variantNM_001394396.1(FAM83A):c.893G>T (p.Gly298Val)not specified [RCV004383461]uncertain significance8123207276123207276Humanname
597750140CV3665742single nucleotide variantNM_001394396.1(FAM83A):c.755T>G (p.Val252Gly)not specified [RCV004923493]uncertain significance8123194130123194130Humanname
597750272CV3665747single nucleotide variantNM_001394396.1(FAM83A):c.307G>A (p.Gly103Ser)not specified [RCV004923498]uncertain significance8123183163123183163Humanname
598238205CV3962423single nucleotide variantNM_001394396.1(FAM83A):c.590G>A (p.Gly197Asp)not specified [RCV005343766]uncertain significance8123191912123191912Humanname
598195249CV3962427single nucleotide variantNM_001394396.1(FAM83A):c.490A>G (p.Ile164Val)not specified [RCV005335539]uncertain significance8123191812123191812Humanname
156365669CV2272155single nucleotide variantNM_001394396.1(FAM83A):c.1009G>T (p.Gly337Cys)not specified [RCV004124931]uncertain significance8123207392123207392Humanname
401894680CV2785172single nucleotide variantNM_001394396.1(FAM83A):c.1103G>T (p.Arg368Leu)not specified [RCV004355166]uncertain significance8123207486123207486Humanname
405760764CV3256571single nucleotide variantNM_001394396.1(FAM83A):c.1033G>C (p.Gly345Arg)not specified [RCV004383453]likely benign8123207416123207416Humanname
405760771CV3256572single nucleotide variantNM_001394396.1(FAM83A):c.1036A>G (p.Thr346Ala)not specified [RCV004383454]uncertain significance8123207419123207419Humanname
407509093CV3431911single nucleotide variantNM_001394396.1(FAM83A):c.1116C>A (p.His372Gln)not specified [RCV004625609]uncertain significance8123207499123207499Humanname
597750117CV3665737single nucleotide variantNM_001394396.1(FAM83A):c.1097C>T (p.Pro366Leu)not specified [RCV004923488]uncertain significance8123207480123207480Humanname
597750135CV3665741single nucleotide variantNM_001394396.1(FAM83A):c.1198A>T (p.Asn400Tyr)not specified [RCV004923492]uncertain significance8123207581123207581Humanname
597750148CV3665744single nucleotide variantNM_001394396.1(FAM83A):c.1099C>G (p.Pro367Ala)not specified [RCV004923495]uncertain significance8123207482123207482Humanname
598238221CV3962426single nucleotide variantNM_001394396.1(FAM83A):c.1082C>T (p.Pro361Leu)not specified [RCV005343768]uncertain significance8123207465123207465Humanname