RGD:150500740 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:150500740 -  Homo sapiens

RGD ID: 150500740
RS ID: rs4812899
ClinVar ID: CV1256157
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIGT  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 20 44,050,342
GRCh38 20 45,421,702
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001184729.3:c.1033+1009T>C
NM_001184728.3:c.1066+119T>C
NM_015937.6:c.1234+119T>C
NM_001184730.3:c.928+119T>C
More... 		07/27/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIGT
Accession:NM_015937
Location:INTRON

Gene Symbol:PIGT
Accession:NM_001184728
Location:INTRON

Gene Symbol:PIGT
Accession:NM_001184729
Location:INTRON

Gene Symbol:PIGT
Accession:NM_001184730
Location:INTRON

Gene Symbol:PIGT
Accession:NR_047691
Location:INTRON;NON-CODING

Gene Symbol:PIGT
Accession:NR_047692
Location:INTRON;NON-CODING

Gene Symbol:PIGT
Accession:NR_047693
Location:INTRON;NON-CODING

Gene Symbol:PIGT
Accession:NR_047694
Location:INTRON;NON-CODING

Gene Symbol:PIGT
Accession:NR_047695
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001676781 CLINVAR
dbSNP (RS) rs4812899 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIGT CLINVAR
OMIM 610272 CLINVAR