RGD:11600341 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:11600341 -  Homo sapiens

RGD ID: 11600341
ClinVar ID: CV319596
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: INSL6  JAK2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 5,128,142
GRCh38 9 5,128,142
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
LRG_612t1:c.*1351T>C
NM_004972.3:c.*1351T>C
LRG_612:g.147898T>C
NG_009904.1:g.147898T>C
More... 		06/14/2016 3 prime utr variant uncertain significance all ages 1-9 / 100 000
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:JAK2
Accession:NM_001322194
Location:3UTRS;EXON

Gene Symbol:JAK2
Accession:NM_001322199
Location:3UTRS;EXON

Gene Symbol:JAK2
Accession:NM_004972
Location:3UTRS;EXON

Gene Symbol:JAK2
Accession:NM_001322196
Location:3UTRS;EXON

Gene Symbol:JAK2
Accession:NM_001322198
Location:3UTRS;EXON

Gene Symbol:JAK2
Accession:NM_001322204
Location:3UTRS;EXON

Gene Symbol:JAK2
Accession:NM_001322195
Location:3UTRS;EXON

Gene Symbol:JAK2
Accession:NR_169763
Location:EXON;NON-CODING

Gene Symbol:JAK2
Accession:NR_169764
Location:EXON;NON-CODING

Gene Symbol:INSL6
Accession:XM_011517702
Location:INTRON

Gene Symbol:INSL6
Accession:NM_007179
Location:INTRON

Variant Samples