RGD:150470056 Rat Genome Database

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Variant: RGD:150470056 -  Homo sapiens

RGD ID: 150470056
RS ID: rs2004776
ClinVar ID: CV1247924
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AGT  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 230,848,702
GRCh38 1 230,712,956
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001384479.1:c.-31+1130G>A
NG_008836.2:g.6635G>A
NC_000001.11:g.230712956C>T
NC_000001.10:g.230848702C>T
More... 		02/17/2020 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:AGT
Accession:NM_001382817
Location:5UTRS;INTRON

Gene Symbol:AGT
Accession:NM_001384479
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001670960 CLINVAR
dbSNP (RS) rs2004776 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene AGT CLINVAR
OMIM 106150 CLINVAR