rs1383288 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: rs1383288 -  Homo sapiens

RGD ID: 14721900
RS ID: rs1383288
ClinVar ID: CV669801
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DTNA  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 18 32,346,149
GRCh38 18 34,766,185
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_756t4:c.148+144G>T
NM_001386753.1:c.148+144G>T
NM_001386758.1:c.148+144G>T
NM_001386788.1:c.148+144G>T
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DTNA
Accession:NM_001198942
Location:INTRON

Gene Symbol:DTNA
Accession:NM_032981
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386754
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437333
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386763
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386771
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386776
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386762
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386755
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386764
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386795
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386767
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437326
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437328
Location:INTRON

Gene Symbol:DTNA
Accession:NM_032975
Location:INTRON

Gene Symbol:DTNA
Accession:NM_032979
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386770
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386753
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437321
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437324
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437320
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001128175
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001198944
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386768
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437323
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437322
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437331
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001198943
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386758
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386769
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437329
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001198938
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386777
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437332
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437319
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437334
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437325
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001392
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001390
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386775
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437316
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001391
Location:INTRON

Gene Symbol:DTNA
Accession:NM_032980
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386773
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386766
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437337
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001198941
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386765
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437336
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437338
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386761
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386756
Location:INTRON

Gene Symbol:DTNA
Accession:NM_032978
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386757
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437339
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437330
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001198940
Location:INTRON

Gene Symbol:DTNA
Accession:XM_017025575
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386760
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386788
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386774
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001198945
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001198939
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386772
Location:INTRON

Gene Symbol:DTNA
Accession:NM_001386759
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437318
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437340
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437317
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437327
Location:INTRON

Gene Symbol:DTNA
Accession:XM_047437335
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000831870 CLINVAR
dbSNP (RS) rs1383288 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DTNA CLINVAR
OMIM 601239 CLINVAR