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)

19 records found for search term Grpel1
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405772137CV3258976single nucleotide variantNM_025196.4(GRPEL1):c.7G>C (p.Ala3Pro)not specified [RCV004396117]uncertain significance470680267068026Humanname
405772114CV3258972single nucleotide variantNM_025196.4(GRPEL1):c.26C>T (p.Ala9Val)not specified [RCV004396113]uncertain significance470680077068007Humanname
405772145CV3258977single nucleotide variantNM_025196.4(GRPEL1):c.92C>T (p.Thr31Met)not specified [RCV004396118]uncertain significance470641947064194Humanname
329364146CV2460356single nucleotide variantNM_025196.4(GRPEL1):c.119T>C (p.Leu40Pro)not specified [RCV004268674]uncertain significance470641677064167Humanname
329353421CV2469252single nucleotide variantNM_025196.4(GRPEL1):c.232T>C (p.Tyr78His)not specified [RCV004280593]uncertain significance470624607062460Humanname
401891053CV2778618single nucleotide variantNM_025196.4(GRPEL1):c.149A>G (p.Lys50Arg)not specified [RCV004344265]uncertain significance470641377064137Humanname
405772109CV3258971single nucleotide variantNM_025196.4(GRPEL1):c.265C>T (p.Arg89Trp)not specified [RCV004396112]uncertain significance470624277062427Humanname
407463855CV3433376single nucleotide variantNM_025196.4(GRPEL1):c.182T>C (p.Leu61Pro)not specified [RCV004634934]uncertain significance470641047064104Humanname
156232495CV2227687single nucleotide variantNM_025196.4(GRPEL1):c.453C>G (p.Ile151Met)not specified [RCV004094078]uncertain significance470610637061063Humanname
156047969CV2244987single nucleotide variantNM_025196.4(GRPEL1):c.365C>A (p.Thr122Lys)not specified [RCV004104721]uncertain significance470611517061151Humanname
156074326CV2281431single nucleotide variantNM_025196.4(GRPEL1):c.590T>C (p.Val197Ala)not specified [RCV004153762]uncertain significance470609267060926Humanname
155990222CV2374678single nucleotide variantNM_025196.4(GRPEL1):c.397G>A (p.Asp133Asn)not specified [RCV004225293]uncertain significance470611197061119Humanname
401733699CV2713184single nucleotide variantNM_025196.4(GRPEL1):c.422A>G (p.Tyr141Cys)not specified [RCV004316726]uncertain significance470610947061094Humanname
401927899CV2822397single nucleotide variantNM_025196.4(GRPEL1):c.349G>A (p.Val117Ile)not provided [RCV003439239]likely benign470611677061167Humanname
405772121CV3258973single nucleotide variantNM_025196.4(GRPEL1):c.372T>G (p.Cys124Trp)not specified [RCV004396114]uncertain significance470611447061144Humanname
405772132CV3258975single nucleotide variantNM_025196.4(GRPEL1):c.404C>G (p.Pro135Arg)not specified [RCV004396116]uncertain significance470611127061112Humanname
407463851CV3433375single nucleotide variantNM_025196.4(GRPEL1):c.406C>T (p.His136Tyr)not specified [RCV004634933]uncertain significance470611107061110Humanname
597771675CV3678903single nucleotide variantNM_025196.4(GRPEL1):c.365C>T (p.Thr122Ile)not specified [RCV004928423]uncertain significance470611517061151Humanname
597756145CV3678904single nucleotide variantNM_025196.4(GRPEL1):c.608G>A (p.Gly203Glu)not specified [RCV004924802]uncertain significance470609087060908Humanname