RGD:151352992 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:151352992 -  Homo sapiens

RGD ID: 151352992
RS ID: rs1440811096
ClinVar ID: CV1326515
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MME  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 154,832,944
GRCh38 3 155,115,155
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000902.5:c.358G>A
NM_001354642.2:c.358G>A
NM_001354643.1:c.358G>A
NM_007287.4:c.358G>A
More... 		10/01/2021 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:MME
Accession:NM_000902
Location:INTRON

Gene Symbol:MME
Accession:NM_007289
Location:INTRON

Gene Symbol:MME
Accession:NM_001354644
Location:INTRON

Gene Symbol:MME
Accession:NM_007288
Location:INTRON

Gene Symbol:MME
Accession:XM_006713647
Location:INTRON

Gene Symbol:MME
Accession:NM_001354643
Location:INTRON

Gene Symbol:MME
Accession:NM_001354642
Location:INTRON

Gene Symbol:MME
Accession:XM_047448157
Location:INTRON

Gene Symbol:MME
Accession:NM_007287
Location:INTRON

Gene Symbol:MME
Accession:XM_011512857
Location:INTRON

Gene Symbol:MME
Accession:XM_011512856
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:25741868   PMID:28492532   PMID:33144514  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001815927 CLINVAR
  RCV003334400 CLINVAR
dbSNP (RS) rs1440811096 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MME CLINVAR
OMIM 120520 CLINVAR