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)

21 records found for search term Cd164l2
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405758653CV3303536single nucleotide variantNM_001330448.1(CD164L2):c.19C>T (p.Arg7Cys)not specified [RCV004433222]uncertain significance12738322127383221Humanname
597738579CV3638609single nucleotide variantNM_001330448.1(CD164L2):c.228G>A (p.Val76=)not specified [RCV004890147]uncertain significance12738252827382528Humanname
405758665CV3303538single nucleotide variantNM_001330448.1(CD164L2):c.59T>C (p.Leu20Pro)not specified [RCV004433224]uncertain significance12738318127383181Humanname
405758671CV3303539single nucleotide variantNM_001330448.1(CD164L2):c.71C>T (p.Ala24Val)not specified [RCV004433225]uncertain significance12738316927383169Humanname
405758675CV3303540single nucleotide variantNM_001330448.1(CD164L2):c.75G>T (p.Gln25His)not specified [RCV004433226]uncertain significance12738316527383165Humanname
156060833CV2236037single nucleotide variantNM_001330448.1(CD164L2):c.245C>A (p.Pro82Gln)not specified [RCV004114202]uncertain significance12738251127382511Humanname
156335343CV2272833single nucleotide variantNM_001330448.1(CD164L2):c.157G>A (p.Ala53Thr)not specified [RCV004135739]uncertain significance12738259927382599Humanname
155929094CV2277960single nucleotide variantNM_001330448.1(CD164L2):c.170T>G (p.Leu57Arg)not specified [RCV004141206]uncertain significance12738258627382586Humanname
155972245CV2335769single nucleotide variantNM_001330448.1(CD164L2):c.250G>A (p.Glu84Lys)not specified [RCV004193961]uncertain significance12738250627382506Humanname
597777746CV3638610single nucleotide variantNM_001330448.1(CD164L2):c.176T>C (p.Val59Ala)not specified [RCV004898843]uncertain significance12738258027382580Humanname
597777750CV3638611single nucleotide variantNM_001330448.1(CD164L2):c.263G>A (p.Cys88Tyr)not specified [RCV004898844]uncertain significance12738239327382393Humanname
597738583CV3638612single nucleotide variantNM_001330448.1(CD164L2):c.293G>A (p.Gly98Asp)not specified [RCV004890148]uncertain significance12738236327382363Humanname
598206644CV3940076single nucleotide variantNM_001330448.1(CD164L2):c.116G>T (p.Gly39Val)not specified [RCV005315145]uncertain significance12738264027382640Humanname
155918890CV2360097single nucleotide variantNM_001330448.1(CD164L2):c.439G>A (p.Val147Met)not specified [RCV004215373]uncertain significance12738013027380130Humanname
156151573CV2377563single nucleotide variantNM_001330448.1(CD164L2):c.514A>G (p.Thr172Ala)not specified [RCV004227760]uncertain significance12738005527380055Humanname
405758661CV3303537single nucleotide variantNM_001330448.1(CD164L2):c.338A>G (p.His113Arg)not specified [RCV004433223]uncertain significance12738181527381815Humanname
407497850CV3424876single nucleotide variantNM_001330448.1(CD164L2):c.356C>G (p.Pro119Arg)not specified [RCV004606470]uncertain significance12738179727381797Humanname
597777756CV3638613single nucleotide variantNM_001330448.1(CD164L2):c.394G>A (p.Ala132Thr)not specified [RCV004898845]uncertain significance12738017527380175Humanname
598206639CV3940075single nucleotide variantNM_001330448.1(CD164L2):c.311G>T (p.Arg104Leu)not specified [RCV005315144]uncertain significance12738234527382345Humanname
598206649CV3940077single nucleotide variantNM_001330448.1(CD164L2):c.512A>G (p.Gln171Arg)not specified [RCV005315146]uncertain significance12738005727380057Humanname
598228763CV3940078single nucleotide variantNM_001330448.1(CD164L2):c.299C>T (p.Ser100Phe)not specified [RCV005319123]uncertain significance12738235727382357Humanname