RGD:156262695 Rat Genome Database

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 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   new 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

Variant: RGD:156262695 -  Homo sapiens

RGD ID: 156262695
ClinVar ID: CV2368527
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOXN4  LOC127825000  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 109,723,315
GRCh38 12 109,285,510
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_213596.3:c.695C>T
NG_126513.1:g.631G>A
NC_000012.12:g.109285510G>A
NC_000012.11:g.109723315G>A
More... 		11/07/2022 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FOXN4
Accession:NM_213596
Location:EXON

Gene Symbol:FOXN4
Accession:XM_011537922
Location:EXON

Gene Symbol:FOXN4
Accession:XM_011537923
Location:EXON

Gene Symbol:FOXN4
Accession:XM_017018818
Location:EXON

Gene Symbol:FOXN4
Accession:XM_047428311
Location:EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002703123 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene FOXN4 CLINVAR
OMIM 609429 CLINVAR