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 Homo sapiens
(View Results for all Objects and Ontologies)

11 records found for search term Scrg1
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156184365CV2222497single nucleotide variantNM_007281.4(SCRG1):c.49G>A (p.Gly17Arg)not specified [RCV004099342]uncertain significance4173391366173391366Humanname
329399347CV2446821single nucleotide variantNM_007281.4(SCRG1):c.29T>C (p.Ile10Thr)not specified [RCV004257676]uncertain significance4173391386173391386Humanname
401741942CV2676560single nucleotide variantNM_007281.4(SCRG1):c.52G>T (p.Val18Phe)not specified [RCV004288747]uncertain significance4173391363173391363Humanname
407461794CV3480209single nucleotide variantNM_007281.4(SCRG1):c.89G>A (p.Arg30Lys)not specified [RCV004658842]uncertain significance4173391326173391326Humanname
401762332CV2723402single nucleotide variantNM_007281.4(SCRG1):c.247G>A (p.Val83Ile)not specified [RCV004329607]likely benign4173388391173388391Humanname
405759391CV3314016single nucleotide variantNM_007281.4(SCRG1):c.124C>T (p.Pro42Ser)not specified [RCV004455031]uncertain significance4173391291173391291Humanname
405759397CV3314017single nucleotide variantNM_007281.4(SCRG1):c.287A>G (p.Asn96Ser)not specified [RCV004455032]uncertain significance4173388351173388351Humanname
405759403CV3314018single nucleotide variantNM_007281.4(SCRG1):c.291T>G (p.Asn97Lys)not specified [RCV004455033]uncertain significance4173388347173388347Humanname
597692664CV3598325single nucleotide variantNM_007281.4(SCRG1):c.127G>C (p.Glu43Gln)not specified [RCV004859032]uncertain significance4173391288173391288Humanname
598235453CV3910561single nucleotide variantNM_007281.4(SCRG1):c.223G>A (p.Glu75Lys)not specified [RCV005275249]uncertain significance4173391192173391192Humanname
598235459CV3910562single nucleotide variantNM_007281.4(SCRG1):c.289A>C (p.Asn97His)not specified [RCV005275250]uncertain significance4173388349173388349Humanname