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)

25 records found for search term Klrc2
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15164641CV702077single nucleotide variantNM_002260.4(KLRC2):c.5A>G (p.Asn2Ser)not provided [RCV000948395]benign121043598210435982Humanname
597797285CV3700950single nucleotide variantNM_002260.4(KLRC2):c.20C>T (p.Thr7Ile)not specified [RCV004935753]uncertain significance121043596710435967Humanname
15133795CV738407single nucleotide variantNM_002260.4(KLRC2):c.168T>C (p.Asp56=)not provided [RCV000898187]benign121043581910435819Humanname
15164638CV702076single nucleotide variantNM_002260.4(KLRC2):c.56G>C (p.Arg19Pro)not provided [RCV000948394]benign121043593110435931Humanname
156088261CV2337145single nucleotide variantNM_002260.4(KLRC2):c.166G>A (p.Asp56Asn)not specified [RCV004192904]uncertain significance121043582110435821Humanname
405814110CV3276475single nucleotide variantNM_002260.4(KLRC2):c.172A>G (p.Ile58Val)not specified [RCV004409711]uncertain significance121043581510435815Humanname
405814112CV3276476single nucleotide variantNM_002260.4(KLRC2):c.223G>T (p.Val75Phe)not specified [RCV004409712]uncertain significance121043537510435375Humanname
598161986CV3983872single nucleotide variantNM_002260.4(KLRC2):c.174A>G (p.Ile58Met)not specified [RCV005368545]uncertain significance121043581310435813Humanname
155924301CV2211513single nucleotide variantNM_002260.4(KLRC2):c.451A>C (p.Ser151Arg)not specified [RCV004084421]uncertain significance121043382310433823Humanname
156132806CV2216613single nucleotide variantNM_002260.4(KLRC2):c.380G>A (p.Ser127Asn)not specified [RCV004081025]likely benign121043389410433894Humanname
156334452CV2230925single nucleotide variantNM_002260.4(KLRC2):c.367A>G (p.Thr123Ala)not specified [RCV004092394]uncertain significance121043390710433907Humanname
156103943CV2310842single nucleotide variantNM_002260.4(KLRC2):c.662C>G (p.Ser221Cys)not specified [RCV004163888]uncertain significance121043115110431151Humanname
156170081CV2337413single nucleotide variantNM_002260.4(KLRC2):c.656G>A (p.Cys219Tyr)not specified [RCV004187854]uncertain significance121043115710431157Humanname
401890913CV2778510single nucleotide variantNM_002260.4(KLRC2):c.334C>T (p.Arg112Cys)not specified [RCV004344169]uncertain significance121043394010433940Humanname
405814114CV3276477single nucleotide variantNM_002260.4(KLRC2):c.335G>A (p.Arg112His)not specified [RCV004409713]uncertain significance121043393910433939Humanname
405814116CV3276478single nucleotide variantNM_002260.4(KLRC2):c.394G>A (p.Gly132Ser)not specified [RCV004409714]likely benign121043388010433880Humanname
405814118CV3276479single nucleotide variantNM_002260.4(KLRC2):c.608A>T (p.Glu203Val)not specified [RCV004409715]uncertain significance121043120510431205Humanname
407499131CV3448709single nucleotide variantNM_002260.4(KLRC2):c.640C>T (p.Leu214Phe)not specified [RCV004644234]uncertain significance121043117310431173Humanname
597797288CV3700951single nucleotide variantNM_002260.4(KLRC2):c.646T>A (p.Ser216Thr)not specified [RCV004935754]uncertain significance121043116710431167Humanname
597797291CV3700952single nucleotide variantNM_002260.4(KLRC2):c.530G>A (p.Arg177His)not specified [RCV004935755]uncertain significance121043216010432160Humanname
597797294CV3700953single nucleotide variantNM_002260.4(KLRC2):c.440C>T (p.Ser147Leu)not specified [RCV004935756]uncertain significance121043383410433834Humanname
597797301CV3700955single nucleotide variantNM_002260.4(KLRC2):c.474A>C (p.Glu158Asp)not specified [RCV004935758]uncertain significance121043380010433800Humanname
597797304CV3700956single nucleotide variantNM_002260.4(KLRC2):c.407G>C (p.Arg136Thr)not specified [RCV004935759]uncertain significance121043386710433867Humanname
598183222CV3983873single nucleotide variantNM_002260.4(KLRC2):c.617G>C (p.Cys206Ser)not specified [RCV005352862]uncertain significance121043119610431196Humanname
15160128CV702075single nucleotide variantNM_002260.4(KLRC2):c.305T>C (p.Phe102Ser)not provided [RCV000947422]benign121043451210434512Humanname