RGD:150446514 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:150446514 -  Homo sapiens

RGD ID: 150446514
RS ID: rs10059957
ClinVar ID: CV1232115
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FYB1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 39,139,176
GRCh38 5 39,139,074
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_199335.5:c.1359+159T>C
NM_001243093.2:c.1389+159T>C
NM_018594.2:c.1389+159T>C
LRG_1351:g.136584T>C
More... 		11/11/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FYB1
Accession:NM_199335
Location:INTRON

Gene Symbol:FYB1
Accession:NM_001465
Location:INTRON

Gene Symbol:FYB1
Accession:NM_001243093
Location:INTRON

Gene Symbol:FYB1
Accession:XM_006714464
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514011
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514010
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514008
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514009
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514012
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514013
Location:INTRON

Gene Symbol:FYB1
Accession:NM_001349333
Location:INTRON

Gene Symbol:FYB1
Accession:NM_018594
Location:INTRON

Gene Symbol:FYB1
Accession:XM_047417073
Location:INTRON

Gene Symbol:FYB1
Accession:XM_047417072
Location:INTRON

Gene Symbol:FYB1
Accession:XM_047417074
Location:INTRON

Gene Symbol:FYB1
Accession:XM_047417071
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001646023 CLINVAR
dbSNP (RS) rs10059957 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FYB1 CLINVAR
OMIM 602731 CLINVAR