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)

19 records found for search term Chic1
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597769294CV3653087single nucleotide variantNM_001039840.4(CHIC1):c.71A>C (p.Glu24Ala)not specified [RCV004896710]uncertain significanceX7356335573563355Humanname
329373827CV2434627single nucleotide variantNM_001039840.4(CHIC1):c.155A>C (p.Glu52Ala)not specified [RCV004248352]uncertain significanceX7356343973563439Humanname
329361874CV2448116single nucleotide variantNM_001039840.4(CHIC1):c.164A>G (p.Glu55Gly)not specified [RCV004263337]uncertain significanceX7356344873563448Humanname
401782251CV2686614single nucleotide variantNM_001039840.4(CHIC1):c.256C>T (p.Pro86Ser)not specified [RCV004300034]uncertain significanceX7356354073563540Humanname
401749315CV2694615single nucleotide variantNM_001039840.4(CHIC1):c.231C>G (p.Ser77Arg)not specified [RCV004298732]uncertain significanceX7356351573563515Humanname
401888545CV2757677single nucleotide variantNM_001039840.4(CHIC1):c.133G>A (p.Glu45Lys)not specified [RCV004334786]uncertain significanceX7356341773563417Humanname
405661608CV3297030single nucleotide variantNM_001039840.4(CHIC1):c.149A>G (p.Glu50Gly)not specified [RCV004439227]uncertain significanceX7356343373563433Humanname
405661611CV3297031single nucleotide variantNM_001039840.4(CHIC1):c.256C>G (p.Pro86Ala)not specified [RCV004439228]uncertain significanceX7356354073563540Humanname
597769301CV3653088single nucleotide variantNM_001039840.4(CHIC1):c.237G>C (p.Glu79Asp)not specified [RCV004896711]uncertain significanceX7356352173563521Humanname
598214421CV3951578single nucleotide variantNM_001039840.4(CHIC1):c.220C>T (p.Arg74Trp)not specified [RCV005316566]uncertain significanceX7356350473563504Humanname
150409667CV1196407single nucleotide variantNM_001039840.4(CHIC1):c.337G>A (p.Val113Ile)not provided [RCV001572754]|not specified [RCV004039382]likely benign|uncertain significanceX7357744773577447Humanname
10768654CV221038single nucleotide variantNM_001039840.4(CHIC1):c.331C>T (p.Pro111Ser)Prostate cancer [RCV000206759]uncertain significanceX7357744173577441Human2name
401874899CV2781351single nucleotide variantNM_001039840.4(CHIC1):c.397T>A (p.Cys133Ser)not specified [RCV004352360]uncertain significanceX7358446273584462Humanname
597769306CV3653089single nucleotide variantNM_001039840.4(CHIC1):c.509C>G (p.Thr170Ser)not specified [RCV004896712]uncertain significanceX7367932773679327Humanname
597769317CV3653091single nucleotide variantNM_001039840.4(CHIC1):c.416C>T (p.Pro139Leu)not specified [RCV004896714]uncertain significanceX7358448173584481Humanname
598214412CV3951576single nucleotide variantNM_001039840.4(CHIC1):c.630A>G (p.Ile210Met)not specified [RCV005316564]uncertain significanceX7368096073680960Humanname
598214416CV3951577single nucleotide variantNM_001039840.4(CHIC1):c.643T>G (p.Leu215Val)not specified [RCV005316565]uncertain significanceX7368097373680973Humanname
8637925CV93151single nucleotide variantNM_001039840.2(CHIC1):c.665G>A (p.Arg222Gln)Malignant melanoma [RCV000073249]not providedX7368099573680995Humanname
401928904CV2829316deletionNM_001039840.4(CHIC1):c.162_176del (p.Glu64_Glu68del)not provided [RCV003439652]uncertain significanceX7356343573563449Humanname