RGD:28885777 Rat Genome Database

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Variant: RGD:28885777 -  Homo sapiens

RGD ID: 28885777
RS ID: rs553732498
ClinVar ID: CV863838
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AGT  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 230,838,599
GRCh38 1 230,702,853
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.230702853G>A
NC_000001.10:g.230838599G>A
NG_008836.2:g.16738C>T
NG_008836.1:g.16738C>T
 01/13/2018 3 prime utr variant uncertain significance Primitive renal tubule syndrome; Renotubular dysgenesis
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:AGT
Accession:NM_001384479
Location:3UTRS;EXON

Gene Symbol:AGT
Accession:NM_001382817
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001098248 CLINVAR
dbSNP (RS) rs553732498 CLINVAR
MedGen C0266313 CLINVAR
NCBI Gene AGT CLINVAR
OMIM 106150 CLINVAR
  267430 CLINVAR
SNOMED CT 702397002 CLINVAR