RGD:152092788 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   new 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

Variant: RGD:152092788 -  Homo sapiens

RGD ID: 152092788
RS ID: rs185633123
ClinVar ID: CV1648474
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SULF1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 70,550,895
GRCh38 8 69,638,660
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001128204.2:c.2427+16T>A
NM_001128205.2:c.2427+16T>A
NM_001128206.2:c.2427+16T>A
NM_015170.3:c.2427+16T>A
More... 		04/17/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SULF1
Accession:NM_015170
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001128204
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001128205
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001128206
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:SULF1
Accession:XM_006716442
Location:INTRON

Gene Symbol:SULF1
Accession:XM_006716441
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412835
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412828
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412851
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412836
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412839
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412845
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412846
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412841
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412829
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412850
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412837
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412838
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412832
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412844
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412833
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412834
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412849
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412830
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412842
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412831
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412840
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412848
Location:INTRON

Gene Symbol:SULF1
Accession:NM_001412847
Location:INTRON

Gene Symbol:SULF1
Accession:NR_132437
Location:INTRON;NON-CODING

Gene Symbol:SULF1
Accession:NR_156415
Location:INTRON;NON-CODING

Gene Symbol:SULF1
Accession:NR_156414
Location:INTRON;NON-CODING

Gene Symbol:SULF1
Accession:NR_182051
Location:INTRON;NON-CODING

Gene Symbol:SULF1
Accession:NR_182053
Location:INTRON;NON-CODING

Gene Symbol:SULF1
Accession:NR_182050
Location:INTRON;NON-CODING

Gene Symbol:SULF1
Accession:NR_182055
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002077937 CLINVAR
dbSNP (RS) rs185633123 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SULF1 CLINVAR
OMIM 610012 CLINVAR