rs3737291 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: rs3737291 -  Homo sapiens

RGD ID: 150454359
RS ID: rs3737291
ClinVar ID: CV1219967
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTR  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 237,037,319
GRCh38 1 236,874,019
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001291940.2:c.1252+179C>T
NM_001291939.1:c.2320+179C>T
NM_000254.3:c.2473+179C>T
NG_008959.1:g.83739C>T
More... 		02/07/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MTR
Accession:XM_011544194
Location:INTRON

Gene Symbol:MTR
Accession:NM_000254
Location:INTRON

Gene Symbol:MTR
Accession:NM_001291939
Location:INTRON

Gene Symbol:MTR
Accession:NM_001410942
Location:INTRON

Gene Symbol:MTR
Accession:XM_047421185
Location:INTRON

Gene Symbol:MTR
Accession:XM_047421183
Location:INTRON

Gene Symbol:MTR
Accession:NM_001291940
Location:INTRON

Gene Symbol:MTR
Accession:XM_047421186
Location:INTRON

Gene Symbol:MTR
Accession:XM_047421182
Location:INTRON

Gene Symbol:MTR
Accession:XM_017001330
Location:INTRON

Gene Symbol:MTR
Accession:XM_017001329
Location:INTRON

Gene Symbol:MTR
Accession:XM_005273141
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MTR
Accession:XM_047421187
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001612349 CLINVAR
dbSNP (RS) rs3737291 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MTR CLINVAR
OMIM 156570 CLINVAR