rs7136233 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 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)

Variant: rs7136233 -  Homo sapiens

RGD ID: 150499689
RS ID: rs7136233
ClinVar ID: CV1235772
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RACGAP1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 50,385,663
GRCh38 12 49,991,880
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001320007.2:c.1492+118A>G
NM_001320005.2:c.1540+118A>G
NM_001126103.3:c.1714+118A>G
NM_001126104.3:c.1714+118A>G
More... 		06/19/2021 intron variant benign none provided

Gene Symbol:RACGAP1
Accession:NM_001126103
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_013277
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001126104
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_006719359
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_011538238
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320004
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320005
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320003
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320007
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001319999
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320006
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320000
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320002
Location:INTRON

Gene Symbol:RACGAP1
Accession:NM_001320001
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019227
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019224
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019222
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019223
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019221
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019225
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_017019226
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_024448958
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428750
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428748
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428747
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428751
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428746
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428749
Location:INTRON

Gene Symbol:RACGAP1
Accession:XM_047428745
Location:INTRON

.


Database
Acc Id
Source(s)
ClinVar RCV001656455 CLINVAR
dbSNP (RS) rs7136233 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RACGAP1 CLINVAR
OMIM 604980 CLINVAR