RGD:150420835 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:150420835 -  Homo sapiens

RGD ID: 150420835
RS ID: rs71645982
ClinVar ID: CV1193895
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BRAF  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 140,477,170
GRCh38 7 140,777,370
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001378474.1:c.1518-282T>G
NM_004333.6:c.1518-282T>G
NM_001378467.1:c.1527-282T>G
NM_001374244.1:c.1638-282T>G
More... 		07/11/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:BRAF
Accession:NM_004333
Location:INTRON

Gene Symbol:BRAF
Accession:XM_017012559
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001354609
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001374258
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001374244
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378474
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378470
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378475
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378471
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378468
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378467
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378472
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378469
Location:INTRON

Gene Symbol:BRAF
Accession:NM_001378473
Location:INTRON

Gene Symbol:BRAF
Accession:XM_047420766
Location:INTRON

Gene Symbol:BRAF
Accession:XM_047420770
Location:INTRON

Gene Symbol:BRAF
Accession:XM_047420767
Location:INTRON

Gene Symbol:BRAF
Accession:XM_047420768
Location:INTRON

Gene Symbol:BRAF
Accession:XM_047420769
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001570292 CLINVAR
dbSNP (RS) rs71645982 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BRAF CLINVAR
OMIM 164757 CLINVAR