rs267607662 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: rs267607662 -  Homo sapiens

RGD ID: 8622396
RS ID: rs267607662
ClinVar ID: CV77415
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KRT8  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 53,291,181
GRCh38 12 52,897,397
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000012.12:g.52897397G>A
NC_000012.11:g.53291181G>A
NG_008402.2:g.57470C>T
NM_001256282.2:c.*31C>T
More... 		3 prime utr variant|utr-3 not provided none provided

Gene Symbol:KRT8
Accession:NM_002273
Location:3UTRS;EXON

Gene Symbol:KRT8
Accession:NM_001256293
Location:3UTRS;EXON

Gene Symbol:KRT8
Accession:NM_001256282
Location:3UTRS;EXON

Gene Symbol:KRT8
Accession:NR_045962
Location:EXON;NON-CODING

.


Database
Acc Id
Source(s)
ClinVar RCV000056922 CLINVAR
dbSNP (RS) rs267607662 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene KRT8 CLINVAR
OMIM 148060 CLINVAR