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)

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

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15197735CV699949single nucleotide variantNM_144727.3(CRYGN):c.15G>A (p.Ser5=)not provided [RCV000956548]benign7151439903151439903Humanname
156047531CV2315701single nucleotide variantNM_144727.3(CRYGN):c.5C>T (p.Ala2Val)not specified [RCV004169721]uncertain significance7151439913151439913Humanname
156088671CV2259066single nucleotide variantNM_144727.3(CRYGN):c.22A>T (p.Ile8Phe)not specified [RCV004120328]uncertain significance7151438244151438244Humanname
8632482CV87690single nucleotide variantNM_144727.1(CRYGN):c.171C>T (p.Phe57=)Malignant melanoma [RCV000067782]not provided7151438095151438095Humanname
329393154CV2449527single nucleotide variantNM_144727.3(CRYGN):c.32A>G (p.Tyr11Cys)not specified [RCV004268463]uncertain significance7151438234151438234Humanname
598260487CV3963085single nucleotide variantNM_144727.3(CRYGN):c.74G>A (p.Gly25Glu)not specified [RCV005324989]uncertain significance7151438192151438192Humanname
598260503CV3963088single nucleotide variantNM_144727.3(CRYGN):c.77A>C (p.Asp26Ala)not specified [RCV005324992]uncertain significance7151438189151438189Humanname
156105646CV2257217single nucleotide variantNM_144727.3(CRYGN):c.172C>T (p.Arg58Trp)not specified [RCV004123425]uncertain significance7151438094151438094Humanname
156050014CV2315900single nucleotide variantNM_144727.3(CRYGN):c.166G>A (p.Asp56Asn)not specified [RCV004171674]uncertain significance7151438100151438100Humanname
329366565CV2441713single nucleotide variantNM_144727.3(CRYGN):c.256C>T (p.Arg86Trp)not specified [RCV004259882]uncertain significance7151438010151438010Humanname
405676638CV3239357single nucleotide variantNM_144727.3(CRYGN):c.221G>A (p.Arg74His)not specified [RCV004370239]uncertain significance7151438045151438045Humanname
597800228CV3657835single nucleotide variantNM_144727.3(CRYGN):c.290T>C (p.Leu97Pro)not specified [RCV004905461]uncertain significance7151436306151436306Humanname
598260492CV3963086single nucleotide variantNM_144727.3(CRYGN):c.173G>A (p.Arg58Gln)not specified [RCV005324990]uncertain significance7151438093151438093Humanname
598260498CV3963087single nucleotide variantNM_144727.3(CRYGN):c.100G>A (p.Gly34Ser)not specified [RCV005324991]uncertain significance7151438166151438166Humanname
598260509CV3963089single nucleotide variantNM_144727.3(CRYGN):c.216C>A (p.Phe72Leu)not specified [RCV005324993]uncertain significance7151438050151438050Humanname
155962062CV2254326single nucleotide variantNM_144727.3(CRYGN):c.436T>G (p.Phe146Val)not specified [RCV004123726]uncertain significance7151430161151430161Humanname
155919990CV2254970single nucleotide variantNM_144727.3(CRYGN):c.326G>A (p.Cys109Tyr)not specified [RCV004117202]uncertain significance7151436270151436270Humanname
156071470CV2295885single nucleotide variantNM_144727.3(CRYGN):c.399G>T (p.Lys133Asn)not specified [RCV004151792]uncertain significance7151436197151436197Humanname
329397975CV2467124single nucleotide variantNM_144727.3(CRYGN):c.324G>C (p.Gln108His)not specified [RCV004282853]uncertain significance7151436272151436272Humanname
405676641CV3239358single nucleotide variantNM_144727.3(CRYGN):c.450C>G (p.Asp150Glu)not specified [RCV004370240]uncertain significance7151430147151430147Humanname
407464690CV3429831single nucleotide variantNM_144727.3(CRYGN):c.370T>C (p.Trp124Arg)not specified [RCV004613518]uncertain significance7151436226151436226Humanname
597800221CV3657838single nucleotide variantNM_144727.3(CRYGN):c.419C>T (p.Ala140Val)not specified [RCV004905464]uncertain significance7151430178151430178Humanname
598260480CV3963084single nucleotide variantNM_144727.3(CRYGN):c.487C>T (p.Pro163Ser)not specified [RCV005324988]uncertain significance7151430110151430110Humanname
15166275CV699948single nucleotide variantNM_144727.3(CRYGN):c.301G>A (p.Glu101Lys)not provided [RCV000948796]benign7151436295151436295Humanname