RGD:11545398 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:11545398 -  Homo sapiens

RGD ID: 11545398
RS ID: rs376539910
ClinVar ID: CV251040
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MCCC1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 182,790,118
GRCh38 3 183,072,330
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008100.1:g.32248A>G
NC_000003.12:g.183072330T>C
NC_000003.11:g.182790118T>C
NM_020166.3:c.491+36A>G
More... 		intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:MCCC1
Accession:NM_001363880
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448588
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448587
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448590
Location:INTRON

Gene Symbol:MCCC1
Accession:NM_001293273
Location:INTRON

Gene Symbol:MCCC1
Accession:NM_020166
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448586
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_011512992
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448591
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448589
Location:INTRON

Gene Symbol:MCCC1
Accession:NR_120639
Location:INTRON;NON-CODING

Gene Symbol:MCCC1
Accession:NR_120640
Location:INTRON;NON-CODING

Gene Symbol:MCCC1
Accession:XR_007095707
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000245080 CLINVAR
dbSNP (RS) rs376539910 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MCCC1 CLINVAR
OMIM 609010 CLINVAR