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)

32 records found for search term Tpst2
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407461272CV3492455single nucleotide variantNM_003595.5(TPST2):c.5G>A (p.Arg2His)not specified [RCV004687612]uncertain significance222654162626541626Humanname
598265154CV3924546single nucleotide variantNM_003595.5(TPST2):c.17G>A (p.Arg6Gln)not specified [RCV005281039]uncertain significance222654161426541614Humanname
405775512CV3344001single nucleotide variantNM_003595.5(TPST2):c.73G>A (p.Gly25Arg)not specified [RCV004471037]uncertain significance222654155826541558Humanname
598201386CV3924547single nucleotide variantNM_003595.5(TPST2):c.88G>C (p.Glu30Gln)not specified [RCV005290155]uncertain significance222654154326541543Humanname
156400071CV2198948single nucleotide variantNM_003595.5(TPST2):c.277G>C (p.Glu93Gln)not specified [RCV004080366]uncertain significance222654135426541354Humanname
329361848CV2448089single nucleotide variantNM_003595.5(TPST2):c.107C>T (p.Ala36Val)not specified [RCV004263312]uncertain significance222654152426541524Humanname
329395772CV2454550single nucleotide variantNM_003595.5(TPST2):c.130G>A (p.Ala44Thr)not specified [RCV004268034]uncertain significance222654150126541501Humanname
401735731CV2692185single nucleotide variantNM_003595.5(TPST2):c.124C>T (p.Arg42Trp)not specified [RCV004301883]uncertain significance222654150726541507Humanname
407521599CV3492452single nucleotide variantNM_003595.5(TPST2):c.188G>A (p.Arg63His)not specified [RCV004677367]uncertain significance222654144326541443Humanname
407521603CV3492453single nucleotide variantNM_003595.5(TPST2):c.125G>A (p.Arg42Gln)not specified [RCV004677368]uncertain significance222654150626541506Humanname
597795776CV3620937single nucleotide variantNM_003595.5(TPST2):c.157G>T (p.Val53Leu)not specified [RCV004878291]uncertain significance222654147426541474Humanname
598201379CV3924545single nucleotide variantNM_003595.5(TPST2):c.116G>A (p.Arg39Gln)not specified [RCV005290154]uncertain significance222654151526541515Humanname
598201392CV3924548single nucleotide variantNM_003595.5(TPST2):c.187C>T (p.Arg63Cys)not specified [RCV005290156]uncertain significance222654144426541444Humanname
156201149CV2234335single nucleotide variantNM_003595.5(TPST2):c.739C>T (p.Arg247Cys)not specified [RCV004100569]uncertain significance222654089226540892Humanname
156219624CV2254070single nucleotide variantNM_003595.5(TPST2):c.847G>A (p.Glu283Lys)not specified [RCV004129518]uncertain significance222653648226536482Humanname
156162103CV2311790single nucleotide variantNM_003595.5(TPST2):c.787G>T (p.Ala263Ser)not specified [RCV004170646]uncertain significance222654084426540844Humanname
156356108CV2320725single nucleotide variantNM_003595.5(TPST2):c.890C>T (p.Ala297Val)not specified [RCV004179077]uncertain significance222653643926536439Humanname
156335780CV2360551single nucleotide variantNM_003595.5(TPST2):c.898A>C (p.Lys300Gln)not specified [RCV004211311]uncertain significance222653643126536431Humanname
329391812CV2445073single nucleotide variantNM_003595.5(TPST2):c.854C>T (p.Ser285Phe)not specified [RCV004261678]uncertain significance222653647526536475Humanname
401893435CV2763408single nucleotide variantNM_003595.5(TPST2):c.868A>G (p.Ile290Val)not specified [RCV004349297]uncertain significance222653646126536461Humanname
405775506CV3344000single nucleotide variantNM_003595.5(TPST2):c.646A>G (p.Lys216Glu)not specified [RCV004471036]uncertain significance222654098526540985Humanname
405775524CV3344003single nucleotide variantNM_003595.5(TPST2):c.749A>G (p.Lys250Arg)not specified [RCV004471039]uncertain significance222654088226540882Humanname
405775531CV3344004single nucleotide variantNM_003595.5(TPST2):c.769G>A (p.Gly257Ser)not specified [RCV004471040]uncertain significance222654086226540862Humanname
405775537CV3344005single nucleotide variantNM_003595.5(TPST2):c.989A>T (p.Asn330Ile)not specified [RCV004471041]uncertain significance222653634026536340Humanname
407521611CV3492456single nucleotide variantNM_003595.5(TPST2):c.512G>A (p.Arg171His)not specified [RCV004677370]uncertain significance222654111926541119Humanname
597795773CV3620936single nucleotide variantNM_003595.5(TPST2):c.302G>T (p.Arg101Leu)not specified [RCV004878290]uncertain significance222654132926541329Humanname
597795779CV3620938single nucleotide variantNM_003595.5(TPST2):c.377C>T (p.Ala126Val)not specified [RCV004878292]uncertain significance222654125426541254Humanname
597795782CV3620939single nucleotide variantNM_003595.5(TPST2):c.485C>T (p.Thr162Met)not specified [RCV004878293]uncertain significance222654114626541146Humanname
598201398CV3924549single nucleotide variantNM_003595.5(TPST2):c.469A>G (p.Asn157Asp)not specified [RCV005290157]uncertain significance222654116226541162Humanname
155937120CV2376293single nucleotide variantNM_003595.5(TPST2):c.1039C>T (p.Arg347Trp)not specified [RCV004222557]uncertain significance222653629026536290Humanname
155991887CV2379254single nucleotide variantNM_003595.5(TPST2):c.1040G>A (p.Arg347Gln)not specified [RCV004223727]uncertain significance222653628926536289Humanname
407521613CV3492457single nucleotide variantNM_003595.5(TPST2):c.1070C>A (p.Ala357Asp)not specified [RCV004677371]uncertain significance222653271726532717Humanname