RGD:407507739 Rat Genome Database

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Variant: RGD:407507739 -  Homo sapiens

RGD ID: 407507739
ClinVar ID: CV3465487
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RETREG1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 16,475,178
GRCh38 5 16,475,069
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_363t1:c.1166A>C
NM_001034850.3:c.1166A>C
NM_019000.5:c.743A>C
LRG_363:g.146941A>C
More... 		06/03/2024 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004671849 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene RETREG1 CLINVAR
OMIM 613114 CLINVAR