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)

22 records found for search term Sult1b1
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401726679CV2738275single nucleotide variantNM_014465.4(SULT1B1):c.376-6044T>CLevothyroxine response [RCV003317016]other46974030869740308Humanname
329389215CV2467194single nucleotide variantNM_014465.4(SULT1B1):c.10C>T (p.Pro4Ser)not specified [RCV004285011]uncertain significance46975520869755208Humanname
15160338CV709432single nucleotide variantNM_014465.4(SULT1B1):c.192T>C (p.Asp64=)not provided [RCV000969882]benign46975475569754755Humanname
407530202CV3481864single nucleotide variantNM_014465.4(SULT1B1):c.78C>A (p.Ser26Arg)not specified [RCV004681747]uncertain significance46975514069755140Humanname
405705294CV3327400single nucleotide variantNM_014465.4(SULT1B1):c.272C>T (p.Thr91Ile)not specified [RCV004460992]likely benign46975467569754675Humanname
407497233CV3481865single nucleotide variantNM_014465.4(SULT1B1):c.286C>A (p.Gln96Lys)not specified [RCV004668335]uncertain significance46974981069749810Humanname
407497237CV3481867single nucleotide variantNM_014465.4(SULT1B1):c.278G>A (p.Gly93Asp)not specified [RCV004668336]uncertain significance46974981869749818Humanname
156297678CV2246900single nucleotide variantNM_014465.4(SULT1B1):c.628A>G (p.Arg210Gly)not specified [RCV004112702]uncertain significance46973065169730651Humanname
156174362CV2334529single nucleotide variantNM_014465.4(SULT1B1):c.665A>G (p.Asp222Gly)not specified [RCV004188490]uncertain significance46973061469730614Humanname
401723551CV2724943single nucleotide variantNM_014465.4(SULT1B1):c.569T>A (p.Leu190His)not specified [RCV004319707]uncertain significance46973344169733441Humanname
401869808CV2792187single nucleotide variantNM_014465.4(SULT1B1):c.392G>C (p.Arg131Pro)not specified [RCV004361394]uncertain significance46973424869734248Humanname
401923314CV2822555single nucleotide variantNM_014465.4(SULT1B1):c.782C>T (p.Thr261Met)not provided [RCV003435029]likely benign46972719769727197Humanname
405705302CV3327401single nucleotide variantNM_014465.4(SULT1B1):c.836C>T (p.Ala279Val)not specified [RCV004460993]uncertain significance46972714369727143Humanname
405705717CV3327402single nucleotide variantNM_014465.4(SULT1B1):c.838A>G (p.Ile280Val)not specified [RCV004460994]uncertain significance46972714169727141Humanname
405705722CV3327403single nucleotide variantNM_014465.4(SULT1B1):c.877C>T (p.Arg293Cys)not specified [RCV004460995]uncertain significance46972710269727102Humanname
407530203CV3481866single nucleotide variantNM_014465.4(SULT1B1):c.848C>T (p.Thr283Ile)not specified [RCV004681748]uncertain significance46972713169727131Humanname
597759654CV3611999single nucleotide variantNM_014465.4(SULT1B1):c.657G>C (p.Glu219Asp)not specified [RCV004869030]uncertain significance46973062269730622Humanname
597759658CV3612000single nucleotide variantNM_014465.4(SULT1B1):c.315T>G (p.Ile105Met)not specified [RCV004869031]uncertain significance46974978169749781Humanname
597759663CV3612001single nucleotide variantNM_014465.4(SULT1B1):c.630A>T (p.Arg210Ser)not specified [RCV004869032]uncertain significance46973064969730649Humanname
597759666CV3612002single nucleotide variantNM_014465.4(SULT1B1):c.677A>G (p.His226Arg)not specified [RCV004869033]uncertain significance46973060269730602Humanname
598221681CV3912441single nucleotide variantNM_014465.4(SULT1B1):c.569T>C (p.Leu190Pro)not specified [RCV005293658]uncertain significance46973344169733441Humanname
15196542CV698610single nucleotide variantNM_014465.4(SULT1B1):c.433T>G (p.Leu145Val)not provided [RCV000956218]benign46973420769734207Humanname