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)

72 records found for search term Pgm5
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150495171CV1266183single nucleotide variantNM_021965.4(PGM5):c.-32G>Anot provided [RCV001688505]benign96835709668357096Humanname
8651276CV127851single nucleotide variantNM_021965.3(PGM5):c.1615-2058A>GLung cancer [RCV000108338]uncertain significance96852750968527509Humanname
156234392CV2193304single nucleotide variantNM_021965.4(PGM5):c.40G>A (p.Ala14Thr)not specified [RCV004071609]uncertain significance96835716768357167Humanname
156334349CV2214752single nucleotide variantNM_021965.4(PGM5):c.76G>A (p.Gly26Ser)not specified [RCV004090561]uncertain significance96835720368357203Humanname
156175168CV2254639single nucleotide variantNM_021965.4(PGM5):c.52G>C (p.Asp18His)not specified [RCV004115127]uncertain significance96835717968357179Humanname
155935294CV2371766single nucleotide variantNM_021965.4(PGM5):c.49G>A (p.Glu17Lys)not specified [RCV004219430]uncertain significance96835717668357176Humanname
329376319CV2425071single nucleotide variantNM_021965.4(PGM5):c.94G>A (p.Gly32Ser)not specified [RCV004248967]uncertain significance96835722168357221Humanname
15101327CV701037single nucleotide variantNM_021965.4(PGM5):c.300G>A (p.Ser100=)not provided [RCV000959066]benign96837823768378237Humanname
15170992CV701038single nucleotide variantNM_021965.4(PGM5):c.366C>T (p.Ser122=)not provided [RCV000949752]likely benign96837830368378303Humanname
156306818CV2335285single nucleotide variantNM_021965.4(PGM5):c.202G>A (p.Gly68Ser)not specified [RCV004186851]uncertain significance96835732968357329Humanname
401717997CV2703658single nucleotide variantNM_021965.4(PGM5):c.186G>T (p.Met62Ile)not specified [RCV004315915]uncertain significance96835731368357313Humanname
401742719CV2715301single nucleotide variantNM_021965.4(PGM5):c.287A>C (p.Asn96Thr)not specified [RCV004324638]uncertain significance96837822468378224Humanname
401898477CV2787785single nucleotide variantNM_021965.4(PGM5):c.117C>G (p.Asn39Lys)not specified [RCV004356687]uncertain significance96835724468357244Humanname
405748186CV3364958single nucleotide variantNM_021965.4(PGM5):c.221C>A (p.Thr74Lys)not specified [RCV004498734]uncertain significance96835734868357348Humanname
407529038CV3466957single nucleotide variantNM_021965.4(PGM5):c.118T>C (p.Tyr40His)not specified [RCV004655842]uncertain significance96835724568357245Humanname
597675759CV3572154single nucleotide variantNM_021965.4(PGM5):c.164G>A (p.Arg55His)not specified [RCV004836853]uncertain significance96835729168357291Humanname
598197012CV3999923single nucleotide variantNM_021965.4(PGM5):c.232A>T (p.Ile78Phe)not specified [RCV005397809]uncertain significance96835735968357359Humanname
156239520CV2221264single nucleotide variantNM_021965.4(PGM5):c.676C>T (p.Arg226Cys)not specified [RCV004094697]uncertain significance96838756768387567Humanname
155989411CV2251314single nucleotide variantNM_021965.4(PGM5):c.613C>T (p.Arg205Trp)not specified [RCV004115525]uncertain significance96838750468387504Humanname
155943810CV2262372single nucleotide variantNM_021965.4(PGM5):c.365G>T (p.Ser122Ile)not specified [RCV004128554]uncertain significance96837830268378302Humanname
155922067CV2284261single nucleotide variantNM_021965.4(PGM5):c.721G>A (p.Val241Ile)not specified [RCV004146620]uncertain significance96839155768391557Humanname
156166406CV2315232single nucleotide variantNM_021965.4(PGM5):c.473C>T (p.Thr158Met)not specified [RCV004167225]uncertain significance96838444668384446Humanname
156167113CV2373657single nucleotide variantNM_021965.4(PGM5):c.565T>C (p.Phe189Leu)not specified [RCV004222745]uncertain significance96838453868384538Humanname
156392187CV2378364single nucleotide variantNM_021965.4(PGM5):c.679A>G (p.Ile227Val)not specified [RCV004226387]likely benign96838757068387570Humanname
156347684CV2382950single nucleotide variantNM_021965.4(PGM5):c.521G>A (p.Arg174Gln)not specified [RCV004217541]uncertain significance96838449468384494Humanname
156221891CV2392586single nucleotide variantNM_021965.4(PGM5):c.680T>C (p.Ile227Thr)not specified [RCV004245447]uncertain significance96838757168387571Humanname
155964727CV2395872single nucleotide variantNM_021965.4(PGM5):c.643G>A (p.Gly215Ser)not specified [RCV004237434]likely benign96838753468387534Humanname
329392095CV2445309single nucleotide variantNM_021965.4(PGM5):c.467G>A (p.Ser156Asn)not specified [RCV004263934]uncertain significance96838444068384440Humanname
329359577CV2461554single nucleotide variantNM_021965.4(PGM5):c.799C>G (p.Pro267Ala)not specified [RCV004269741]uncertain significance96839163568391635Humanname
329380480CV2466647single nucleotide variantNM_021965.4(PGM5):c.956C>T (p.Ala319Val)not specified [RCV004274166]uncertain significance96839238668392386Humanname
401734202CV2690510single nucleotide variantNM_021965.4(PGM5):c.580G>C (p.Val194Leu)not specified [RCV004304629]uncertain significance96838747168387471Humanname
401722969CV2703563single nucleotide variantNM_021965.4(PGM5):c.961A>G (p.Asn321Asp)not specified [RCV004317733]uncertain significance96839239168392391Humanname
401891384CV2769123single nucleotide variantNM_021965.4(PGM5):c.431C>T (p.Ala144Val)not specified [RCV004348972]uncertain significance96838440468384404Humanname
401869451CV2772404single nucleotide variantNM_021965.4(PGM5):c.515T>C (p.Leu172Pro)not specified [RCV004355199]uncertain significance96838448868384488Humanname
405748193CV3364959single nucleotide variantNM_021965.4(PGM5):c.499G>C (p.Asp167His)not specified [RCV004498735]uncertain significance96838447268384472Humanname
405748201CV3364960single nucleotide variantNM_021965.4(PGM5):c.577A>G (p.Ile193Val)not specified [RCV004498736]uncertain significance96838746868387468Humanname
405748207CV3364961single nucleotide variantNM_021965.4(PGM5):c.662G>T (p.Ser221Ile)not specified [RCV004498737]uncertain significance96838755368387553Humanname
405748212CV3364962single nucleotide variantNM_021965.4(PGM5):c.694G>A (p.Gly232Arg)not specified [RCV004498738]uncertain significance96838758568387585Humanname
405748218CV3364963single nucleotide variantNM_021965.4(PGM5):c.976C>T (p.Pro326Ser)not specified [RCV004498739]uncertain significance96839240668392406Humanname
407529031CV3466952single nucleotide variantNM_021965.4(PGM5):c.745C>T (p.Pro249Ser)not specified [RCV004655839]uncertain significance96839158168391581Humanname
407464379CV3466953single nucleotide variantNM_021965.4(PGM5):c.769G>T (p.Val257Phe)not specified [RCV004659937]uncertain significance96839160568391605Humanname
407464383CV3466954single nucleotide variantNM_021965.4(PGM5):c.506G>T (p.Arg169Leu)not specified [RCV004659938]uncertain significance96838447968384479Humanname
407529035CV3466956single nucleotide variantNM_021965.4(PGM5):c.878A>T (p.Asp293Val)not specified [RCV004655841]uncertain significance96839171468391714Humanname
597675997CV3572153single nucleotide variantNM_021965.4(PGM5):c.614G>A (p.Arg205Gln)not specified [RCV004836852]uncertain significance96838750568387505Humanname
597675796CV3572157single nucleotide variantNM_021965.4(PGM5):c.464T>C (p.Ile155Thr)not specified [RCV004836856]uncertain significance96838443768384437Humanname
597675834CV3572161single nucleotide variantNM_021965.4(PGM5):c.385G>A (p.Gly129Arg)not specified [RCV004836860]uncertain significance96837832268378322Humanname
598247676CV3999926single nucleotide variantNM_021965.4(PGM5):c.788G>A (p.Gly263Glu)not specified [RCV005384212]uncertain significance96839162468391624Humanname
156021401CV2226748single nucleotide variantNM_021965.4(PGM5):c.1286A>G (p.Tyr429Cys)not specified [RCV004101967]uncertain significance96847954468479544Humanname
156256019CV2307769single nucleotide variantNM_021965.4(PGM5):c.1330T>C (p.Tyr444His)not specified [RCV004168456]uncertain significance96848389968483899Humanname
156360774CV2329643single nucleotide variantNM_021965.4(PGM5):c.1079C>G (p.Thr360Ser)not specified [RCV004180755]uncertain significance96846512868465128Humanname
156131851CV2365621single nucleotide variantNM_021965.4(PGM5):c.1280G>A (p.Arg427His)not specified [RCV004214187]uncertain significance96847953868479538Humanname
156196889CV2367273single nucleotide variantNM_021965.4(PGM5):c.1379T>C (p.Ile460Thr)not specified [RCV004215693]uncertain significance96848394868483948Humanname
156147117CV2381834single nucleotide variantNM_021965.4(PGM5):c.1052A>G (p.Lys351Arg)not specified [RCV004232277]uncertain significance96846510168465101Humanname
156046859CV2390894single nucleotide variantNM_021965.4(PGM5):c.1679G>A (p.Arg560Gln)not specified [RCV004234909]uncertain significance96852963168529631Humanname
329386810CV2452553single nucleotide variantNM_021965.4(PGM5):c.1430A>T (p.Asp477Val)not specified [RCV004273141]uncertain significance96848399968483999Humanname
329367546CV2456904single nucleotide variantNM_021965.4(PGM5):c.1103C>T (p.Ser368Leu)not specified [RCV004270861]uncertain significance96846515268465152Humanname
401724535CV2677910single nucleotide variantNM_021965.4(PGM5):c.1646T>C (p.Leu549Pro)not specified [RCV004294398]uncertain significance96852959868529598Humanname
401893083CV2758458single nucleotide variantNM_021965.4(PGM5):c.1229G>A (p.Arg410Gln)not specified [RCV004335108]uncertain significance96847948768479487Humanname
405748160CV3364954single nucleotide variantNM_021965.4(PGM5):c.1384C>G (p.Gln462Glu)not specified [RCV004498730]uncertain significance96848395368483953Humanname
405748168CV3364955single nucleotide variantNM_021965.4(PGM5):c.1396G>A (p.Val466Met)not specified [RCV004498731]uncertain significance96848396568483965Humanname
405748174CV3364956single nucleotide variantNM_021965.4(PGM5):c.1501G>A (p.Asp501Asn)not specified [RCV004498732]uncertain significance96849924868499248Humanname
405748181CV3364957single nucleotide variantNM_021965.4(PGM5):c.1672A>G (p.Thr558Ala)not specified [RCV004498733]uncertain significance96852962468529624Humanname
407529033CV3466955single nucleotide variantNM_021965.4(PGM5):c.1124G>A (p.Arg375His)not specified [RCV004655840]uncertain significance96846517368465173Humanname
597766822CV3572152single nucleotide variantNM_021965.4(PGM5):c.1594G>A (p.Gly532Ser)not specified [RCV004850344]uncertain significance96849934168499341Humanname
597675772CV3572155single nucleotide variantNM_021965.4(PGM5):c.1523G>A (p.Arg508Gln)not specified [RCV004836854]uncertain significance96849927068499270Humanname
597675784CV3572156single nucleotide variantNM_021965.4(PGM5):c.1678C>G (p.Arg560Gly)not specified [RCV004836855]uncertain significance96852963068529630Humanname
597675816CV3572159single nucleotide variantNM_021965.4(PGM5):c.1314G>T (p.Leu438Phe)not specified [RCV004836858]uncertain significance96848388368483883Humanname
597675824CV3572160single nucleotide variantNM_021965.4(PGM5):c.1258G>T (p.Asp420Tyr)not specified [RCV004836859]uncertain significance96847951668479516Humanname
598247650CV3999921single nucleotide variantNM_021965.4(PGM5):c.1052A>T (p.Lys351Ile)not specified [RCV005384208]uncertain significance96846510168465101Humanname
598247657CV3999922single nucleotide variantNM_021965.4(PGM5):c.1204G>A (p.Val402Ile)not specified [RCV005384209]uncertain significance96847946268479462Humanname
598247663CV3999924single nucleotide variantNM_021965.4(PGM5):c.1586A>G (p.Asp529Gly)not specified [RCV005384210]uncertain significance96849933368499333Humanname
598247669CV3999925single nucleotide variantNM_021965.4(PGM5):c.1219A>G (p.Ile407Val)not specified [RCV005384211]uncertain significance96847947768479477Humanname