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)

27 records found for search term Igfbp1
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155741616CV1770431single nucleotide variantNM_000596.4(IGFBP1):c.80C>T (p.Pro27Leu)Hepatocellular carcinoma [RCV002302655]pathogenic74588873245888732Human1name
597764442CV3680149single nucleotide variantNM_000596.4(IGFBP1):c.52G>C (p.Val18Leu)not specified [RCV004926618]uncertain significance74588870445888704Humanname
155741743CV1770533single nucleotide variantNM_000596.4(IGFBP1):c.232T>G (p.Cys78Gly)Hepatocellular carcinoma [RCV002302758]pathogenic74588888445888884Human1name
156275739CV2316481single nucleotide variantNM_000596.4(IGFBP1):c.203G>A (p.Gly68Asp)not specified [RCV004169960]uncertain significance74588885545888855Humanname
156196291CV2337904single nucleotide variantNM_000596.4(IGFBP1):c.242G>T (p.Gly81Val)not specified [RCV004183911]uncertain significance74588889445888894Humanname
156105704CV2400389single nucleotide variantNM_000596.4(IGFBP1):c.118C>T (p.Leu40Phe)not specified [RCV004244439]uncertain significance74588877045888770Humanname
405799205CV3264032single nucleotide variantNM_000596.4(IGFBP1):c.177T>G (p.Cys59Trp)not specified [RCV004402484]uncertain significance74588882945888829Humanname
597764449CV3680151single nucleotide variantNM_000596.4(IGFBP1):c.163G>T (p.Ala55Ser)not specified [RCV004926620]uncertain significance74588881545888815Humanname
598269023CV3975695single nucleotide variantNM_000596.4(IGFBP1):c.253C>T (p.Arg85Cys)not specified [RCV005349822]uncertain significance74588890545888905Humanname
598269029CV3975696single nucleotide variantNM_000596.4(IGFBP1):c.140C>G (p.Ser47Trp)not specified [RCV005349823]uncertain significance74588879245888792Humanname
156220239CV2222236single nucleotide variantNM_000596.4(IGFBP1):c.727C>G (p.Pro243Ala)not specified [RCV004105263]uncertain significance74589303845893038Humanname
156296818CV2319175single nucleotide variantNM_000596.4(IGFBP1):c.482C>T (p.Ser161Leu)not specified [RCV004178237]uncertain significance74589068045890680Humanname
156289074CV2333052single nucleotide variantNM_000596.4(IGFBP1):c.317A>C (p.Gln106Pro)not specified [RCV004194347]likely benign74588896945888969Humanname
156054933CV2344671single nucleotide variantNM_000596.4(IGFBP1):c.388A>C (p.Thr130Pro)not specified [RCV004197438]uncertain significance74589058645890586Humanname
329391175CV2452118single nucleotide variantNM_000596.4(IGFBP1):c.662T>C (p.Met221Thr)not specified [RCV004278836]uncertain significance74589297345892973Humanname
405799208CV3264033single nucleotide variantNM_000596.4(IGFBP1):c.323C>T (p.Ser108Phe)not specified [RCV004402485]uncertain significance74588897545888975Humanname
405799211CV3264034single nucleotide variantNM_000596.4(IGFBP1):c.329C>A (p.Ala110Asp)not specified [RCV004402486]uncertain significance74588898145888981Humanname
405799214CV3264035single nucleotide variantNM_000596.4(IGFBP1):c.353C>A (p.Ala118Glu)not specified [RCV004402487]uncertain significance74589055145890551Humanname
405799217CV3264036single nucleotide variantNM_000596.4(IGFBP1):c.473A>G (p.Tyr158Cys)not specified [RCV004402488]uncertain significance74589067145890671Humanname
405799220CV3264037single nucleotide variantNM_000596.4(IGFBP1):c.550G>A (p.Val184Ile)not specified [RCV004402489]uncertain significance74589196245891962Humanname
405799222CV3264038single nucleotide variantNM_000596.4(IGFBP1):c.724T>A (p.Ser242Thr)not specified [RCV004402490]uncertain significance74589303545893035Humanname
405799229CV3264040single nucleotide variantNM_000596.4(IGFBP1):c.735C>G (p.Ile245Met)not specified [RCV004402492]uncertain significance74589304645893046Humanname
405799231CV3264041single nucleotide variantNM_000596.4(IGFBP1):c.740G>T (p.Gly247Val)not specified [RCV004402493]uncertain significance74589305145893051Humanname
407514834CV3440761single nucleotide variantNM_000596.4(IGFBP1):c.588A>T (p.Glu196Asp)not specified [RCV004627748]likely benign74589200045892000Humanname
597764451CV3680152single nucleotide variantNM_000596.4(IGFBP1):c.446C>A (p.Ser149Tyr)not specified [RCV004926621]uncertain significance74589064445890644Humanname
597764455CV3680153single nucleotide variantNM_000596.4(IGFBP1):c.373G>A (p.Glu125Lys)not specified [RCV004926622]uncertain significance74589057145890571Humanname
598269019CV3975694single nucleotide variantNM_000596.4(IGFBP1):c.524C>A (p.Pro175His)not specified [RCV005349821]uncertain significance74589193645891936Humanname