rs34101444 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: rs34101444 -  Homo sapiens

RGD ID: 150488928
RS ID: rs34101444
ClinVar ID: CV1284125
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: C19orf12  LOC130064128  
Reference Nucleotide: AAA
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 19 30,196,311 - 30,196,314
GRCh38 19 29,705,404 - 29,705,407
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001282931.3:c.-153-11_-153-9del
NM_001282929.1:c.-32-2428_-32-2426del
NM_001282930.3:c.-32-2428_-32-2426del
NM_001031726.4:c.161-2428_161-2426del
More... 		04/13/2020 intron variant benign none provided

Gene Symbol:C19orf12
Accession:XM_047439497
Location:5UTRS;EXON

Gene Symbol:C19orf12
Accession:NM_001282929
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_001282930
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_001282931
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_031448
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_024451735
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_024451734
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001256046
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_047439496
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001256047
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001031726
Location:INTRON

.


Database
Acc Id
Source(s)
ClinVar RCV001716184 CLINVAR
dbSNP (RS) rs34101444 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C19orf12 CLINVAR
  LOC130064128 CLINVAR
OMIM 614297 CLINVAR