rs1555366010 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: rs1555366010 -  Homo sapiens

RGD ID: 13526270
RS ID: rs1555366010
ClinVar ID: CV504894
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: CALM1  
Reference Nucleotide: G
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 14 90,870,192
GRCh38 14 90,403,848
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006888.6:c.179-15del
NC_000014.9:g.90403847del
NC_000014.8:g.90870191del
NM_006888.4:c.179-15delG
More... 		04/20/2017 intron variant likely benign AllHighlyPenetrant

Gene Symbol:CALM1
Accession:NM_001363669
Location:INTRON

Gene Symbol:CALM1
Accession:NM_001363670
Location:INTRON

Gene Symbol:CALM1
Accession:NM_006888
Location:INTRON

.


Database
Acc Id
Source(s)
ClinVar RCV000603916 CLINVAR
dbSNP (RS) rs1555366010 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CALM1 CLINVAR
OMIM 114180 CLINVAR