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)

52 records found for search term Ehd2
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155911172CV2303764single nucleotide variantNM_014601.4(EHD2):c.88C>T (p.Arg30Cys)not specified [RCV004163614]uncertain significance194771670047716700Humanname
156083880CV2330781single nucleotide variantNM_014601.4(EHD2):c.43C>T (p.Pro15Ser)not specified [RCV004185841]uncertain significance194771665547716655Humanname
401743503CV2715497single nucleotide variantNM_014601.4(EHD2):c.31C>T (p.Arg11Trp)not specified [RCV004326591]uncertain significance194771664347716643Humanname
405717740CV3241864single nucleotide variantNM_014601.4(EHD2):c.59C>T (p.Thr20Met)not specified [RCV004377601]uncertain significance194771667147716671Humanname
597663450CV3674284single nucleotide variantNM_014601.4(EHD2):c.68C>T (p.Ser23Leu)not specified [RCV004912204]uncertain significance194771668047716680Humanname
598178381CV3961229single nucleotide variantNM_014601.4(EHD2):c.345C>T (p.Val115=)not specified [RCV005332331]likely benign194771695747716957Humanname
401744233CV2696962single nucleotide variantNM_014601.4(EHD2):c.122G>A (p.Arg41His)not specified [RCV004292955]uncertain significance194771673447716734Humanname
405717723CV3241862single nucleotide variantNM_014601.4(EHD2):c.173A>C (p.Lys58Thr)not specified [RCV004377599]uncertain significance194771678547716785Humanname
597663403CV3674277single nucleotide variantNM_014601.4(EHD2):c.262G>A (p.Val88Met)not specified [RCV004912198]uncertain significance194771687447716874Humanname
8628362CV83506single nucleotide variantNM_014601.3(EHD2):c.1011C>T (p.Val337=)Malignant melanoma [RCV000063587]not provided194773646447736464Humanname
155984386CV2241113single nucleotide variantNM_014601.4(EHD2):c.368G>A (p.Arg123His)not specified [RCV004104146]uncertain significance194771698047716980Humanname
155976084CV2324583single nucleotide variantNM_014601.4(EHD2):c.385G>A (p.Gly129Arg)not specified [RCV004179343]uncertain significance194771699747716997Humanname
156110107CV2387593single nucleotide variantNM_014601.4(EHD2):c.470T>C (p.Ile157Thr)not specified [RCV004234144]uncertain significance194771857447718574Humanname
156150968CV2394693single nucleotide variantNM_014601.4(EHD2):c.938A>G (p.Tyr313Cys)not specified [RCV004234374]uncertain significance194773639147736391Humanname
401772248CV2708223single nucleotide variantNM_014601.4(EHD2):c.625G>A (p.Gly209Ser)not specified [RCV004311575]uncertain significance194772593447725934Humanname
405717732CV3241863single nucleotide variantNM_014601.4(EHD2):c.298G>A (p.Val100Ile)not specified [RCV004377600]uncertain significance194771691047716910Humanname
405717747CV3241865single nucleotide variantNM_014601.4(EHD2):c.947A>G (p.Lys316Arg)not specified [RCV004377602]uncertain significance194773640047736400Humanname
405717755CV3241866single nucleotide variantNM_014601.4(EHD2):c.985A>C (p.Lys329Gln)not specified [RCV004377603]uncertain significance194773643847736438Humanname
407498563CV3438007single nucleotide variantNM_014601.4(EHD2):c.922G>A (p.Ala308Thr)not specified [RCV004622494]uncertain significance194773637547736375Humanname
407498572CV3438010single nucleotide variantNM_014601.4(EHD2):c.427A>G (p.Asn143Asp)not specified [RCV004622497]uncertain significance194771853147718531Humanname
407498575CV3438011single nucleotide variantNM_014601.4(EHD2):c.826C>G (p.Gln276Glu)not specified [RCV004622498]uncertain significance194772613547726135Humanname
407498577CV3438012single nucleotide variantNM_014601.4(EHD2):c.944A>G (p.Lys315Arg)not specified [RCV004622499]uncertain significance194773639747736397Humanname
597746469CV3674278single nucleotide variantNM_014601.4(EHD2):c.613G>C (p.Gly205Arg)not specified [RCV004922701]uncertain significance194772592247725922Humanname
597663416CV3674280single nucleotide variantNM_014601.4(EHD2):c.469A>G (p.Ile157Val)not specified [RCV004912200]uncertain significance194771857347718573Humanname
597663425CV3674281single nucleotide variantNM_014601.4(EHD2):c.728T>C (p.Val243Ala)not specified [RCV004912201]uncertain significance194772603747726037Humanname
597663433CV3674282single nucleotide variantNM_014601.4(EHD2):c.709A>T (p.Met237Leu)not specified [RCV004912202]uncertain significance194772601847726018Humanname
598178337CV3961223single nucleotide variantNM_014601.4(EHD2):c.817C>G (p.Leu273Val)not specified [RCV005332325]uncertain significance194772612647726126Humanname
598178344CV3961224single nucleotide variantNM_014601.4(EHD2):c.353C>T (p.Pro118Leu)not specified [RCV005332326]uncertain significance194771696547716965Humanname
598178367CV3961227single nucleotide variantNM_014601.4(EHD2):c.500G>A (p.Arg167His)not specified [RCV005332329]uncertain significance194771860447718604Humanname
156225284CV2203035single nucleotide variantNM_014601.4(EHD2):c.1177C>T (p.Leu393Phe)not specified [RCV004069287]uncertain significance194774097747740977Humanname
156212249CV2259939single nucleotide variantNM_014601.4(EHD2):c.1571C>A (p.Ala524Asp)not specified [RCV004118964]uncertain significance194774137147741371Humanname
156279875CV2325376single nucleotide variantNM_014601.4(EHD2):c.1171G>C (p.Ala391Pro)not specified [RCV004177748]uncertain significance194774097147740971Humanname
156167223CV2345275single nucleotide variantNM_014601.4(EHD2):c.1390G>A (p.Asp464Asn)not specified [RCV004196010]uncertain significance194774119047741190Humanname
156190510CV2356746single nucleotide variantNM_014601.4(EHD2):c.1382C>T (p.Ala461Val)not specified [RCV004202090]uncertain significance194774118247741182Humanname
156336368CV2360725single nucleotide variantNM_014601.4(EHD2):c.1070A>C (p.Gln357Pro)not specified [RCV004213512]uncertain significance194773652347736523Humanname
329355048CV2449240single nucleotide variantNM_014601.4(EHD2):c.1325C>A (p.Ala442Asp)not specified [RCV004257379]uncertain significance194774112547741125Humanname
401735616CV2672698single nucleotide variantNM_014601.4(EHD2):c.1258G>C (p.Gly420Arg)not specified [RCV004287711]uncertain significance194774105847741058Humanname
401733740CV2682627single nucleotide variantNM_014601.4(EHD2):c.1274G>A (p.Arg425Gln)not specified [RCV004292675]uncertain significance194774107447741074Humanname
401731002CV2686830single nucleotide variantNM_014601.4(EHD2):c.1151A>G (p.Glu384Gly)not specified [RCV004302010]uncertain significance194774095147740951Humanname
401730489CV2711349single nucleotide variantNM_014601.4(EHD2):c.1019C>A (p.Ala340Glu)not specified [RCV004313112]uncertain significance194773647247736472Humanname
401892854CV2758124single nucleotide variantNM_014601.4(EHD2):c.1094C>T (p.Ala365Val)not specified [RCV004341504]uncertain significance194774089447740894Humanname
407498566CV3438008single nucleotide variantNM_014601.4(EHD2):c.1046C>A (p.Ser349Tyr)not specified [RCV004622495]uncertain significance194773649947736499Humanname
407498580CV3438013single nucleotide variantNM_014601.4(EHD2):c.1553A>G (p.Glu518Gly)not specified [RCV004622500]uncertain significance194774135347741353Humanname
597663387CV3674275single nucleotide variantNM_014601.4(EHD2):c.1413G>T (p.Lys471Asn)not specified [RCV004912196]uncertain significance194774121347741213Humanname
597663396CV3674276single nucleotide variantNM_014601.4(EHD2):c.1237G>A (p.Ala413Thr)not specified [RCV004912197]uncertain significance194774103747741037Humanname
597663412CV3674279single nucleotide variantNM_014601.4(EHD2):c.1256T>C (p.Met419Thr)not specified [RCV004912199]uncertain significance194774105647741056Humanname
597663442CV3674283single nucleotide variantNM_014601.4(EHD2):c.1157T>G (p.Leu386Arg)not specified [RCV004912203]uncertain significance194774095747740957Humanname
597663457CV3674285single nucleotide variantNM_014601.4(EHD2):c.1262C>T (p.Pro421Leu)not specified [RCV004912205]uncertain significance194774106247741062Humanname
597746474CV3674286single nucleotide variantNM_014601.4(EHD2):c.1009G>A (p.Val337Ile)not specified [RCV004922702]uncertain significance194773646247736462Humanname
598178352CV3961225single nucleotide variantNM_014601.4(EHD2):c.1523T>C (p.Leu508Pro)not specified [RCV005332327]uncertain significance194774132347741323Humanname
598178359CV3961226single nucleotide variantNM_014601.4(EHD2):c.1300G>A (p.Gly434Ser)not specified [RCV005332328]uncertain significance194774110047741100Humanname
598178374CV3961228single nucleotide variantNM_014601.4(EHD2):c.1583G>C (p.Arg528Pro)not specified [RCV005332330]uncertain significance194774138347741383Humanname