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)

31 records found for search term Taf1a
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150335328CV1170683single nucleotide variantNM_005681.4(TAF1A):c.1085+17G>Anot provided [RCV001540510]benign1222563156222563156Humanname
597781810CV3615475single nucleotide variantNM_005681.4(TAF1A):c.14G>A (p.Ser5Asn)not specified [RCV004874161]uncertain significance1222588550222588550Humanname
401742013CV2721892single nucleotide variantNM_005681.4(TAF1A):c.85C>G (p.His29Asp)not specified [RCV004326399]uncertain significance1222588479222588479Humanname
156330344CV2210604single nucleotide variantNM_005681.4(TAF1A):c.231G>A (p.Met77Ile)not specified [RCV004083755]uncertain significance1222584188222584188Humanname
156020145CV2270195single nucleotide variantNM_005681.4(TAF1A):c.280G>A (p.Ala94Thr)not specified [RCV004135421]uncertain significance1222584139222584139Humanname
156180576CV2288105single nucleotide variantNM_005681.4(TAF1A):c.185A>G (p.Gln62Arg)not specified [RCV004149638]uncertain significance1222584234222584234Humanname
156395090CV2325087single nucleotide variantNM_005681.4(TAF1A):c.167C>T (p.Ala56Val)not specified [RCV004175621]uncertain significance1222584252222584252Humanname
156072330CV2325318single nucleotide variantNM_005681.4(TAF1A):c.165T>A (p.Ser55Arg)not specified [RCV004177704]uncertain significance1222584254222584254Humanname
401890388CV2768730single nucleotide variantNM_005681.4(TAF1A):c.203A>T (p.His68Leu)not specified [RCV004346571]uncertain significance1222584216222584216Humanname
597781801CV3615473single nucleotide variantNM_005681.4(TAF1A):c.215A>C (p.Gln72Pro)not specified [RCV004874159]uncertain significance1222584204222584204Humanname
15150399CV707109single nucleotide variantNM_005681.4(TAF1A):c.294T>G (p.Ile98Met)not provided [RCV000967938]benign1222579870222579870Humanname
155265995CV1704870single nucleotide variantNM_005681.4(TAF1A):c.781A>C (p.Thr261Pro)Cardiomyopathy, familial restrictive, 6 [RCV002285115]uncertain significance1222569623222569623Human1name
156032421CV2259617single nucleotide variantNM_005681.4(TAF1A):c.605A>T (p.Asp202Val)not specified [RCV004116657]uncertain significance1222570665222570665Humanname
156068805CV2292620single nucleotide variantNM_005681.4(TAF1A):c.566A>T (p.Tyr189Phe)not specified [RCV004154310]uncertain significance1222577483222577483Humanname
156036821CV2332481single nucleotide variantNM_005681.4(TAF1A):c.515G>A (p.Arg172Gln)not specified [RCV004196206]likely benign1222577534222577534Humanname
329397960CV2467110single nucleotide variantNM_005681.4(TAF1A):c.838T>C (p.Tyr280His)not specified [RCV004282840]uncertain significance1222569566222569566Humanname
405745389CV3331400single nucleotide variantNM_005681.4(TAF1A):c.348G>C (p.Glu116Asp)not specified [RCV004466311]uncertain significance1222579816222579816Humanname
405745396CV3331401single nucleotide variantNM_005681.4(TAF1A):c.586A>G (p.Met196Val)not specified [RCV004466312]uncertain significance1222577463222577463Humanname
405745401CV3331402single nucleotide variantNM_005681.4(TAF1A):c.833A>G (p.Tyr278Cys)not specified [RCV004466313]uncertain significance1222569571222569571Humanname
407506347CV3478539single nucleotide variantNM_005681.4(TAF1A):c.602T>C (p.Leu201Pro)not specified [RCV004671091]uncertain significance1222577447222577447Humanname
597781793CV3615471single nucleotide variantNM_005681.4(TAF1A):c.736A>C (p.Met246Leu)not specified [RCV004874157]uncertain significance1222569668222569668Humanname
597781797CV3615472single nucleotide variantNM_005681.4(TAF1A):c.842A>G (p.Asn281Ser)not specified [RCV004874158]uncertain significance1222569562222569562Humanname
598182058CV3919878single nucleotide variantNM_005681.4(TAF1A):c.673A>G (p.Asn225Asp)not specified [RCV005286863]uncertain significance1222570597222570597Humanname
150430217CV1222289single nucleotide variantNM_005681.4(TAF1A):c.1021G>A (p.Gly341Arg)Cardiomyopathy, familial restrictive, 6 [RCV001615034]|Primary dilated cardiomyopathy [RCV002261375]|not provided [RCV003487538]uncertain significance1222563237222563237Human2name
156175720CV2331117single nucleotide variantNM_005681.4(TAF1A):c.1310A>G (p.Lys437Arg)not specified [RCV004181730]uncertain significance1222558703222558703Humanname
329385517CV2451513single nucleotide variantNM_005681.4(TAF1A):c.1193C>T (p.Ala398Val)not specified [RCV004272172]uncertain significance1222561411222561411Humanname
401889344CV2759783single nucleotide variantNM_005681.4(TAF1A):c.1097C>T (p.Ala366Val)not specified [RCV004342823]likely benign1222561507222561507Humanname
597781805CV3615474single nucleotide variantNM_005681.4(TAF1A):c.1216G>A (p.Val406Met)not specified [RCV004874160]uncertain significance1222561388222561388Humanname
597781813CV3615476single nucleotide variantNM_005681.4(TAF1A):c.1138C>G (p.Pro380Ala)not specified [RCV004874162]uncertain significance1222561466222561466Humanname
15160122CV707108single nucleotide variantNM_005681.4(TAF1A):c.1304G>A (p.Arg435Gln)not provided [RCV000969839]likely benign1222558709222558709Humanname
404994797CV2851252microsatelliteNM_005681.4(TAF1A):c.967GAA[1] (p.Glu324del)not provided [RCV003491663]uncertain significance1222563286222563288Humanname