RGD:597647435 Rat Genome Database

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Variant: RGD:597647435 -  Homo sapiens

RGD ID: 597647435
ClinVar ID: CV3674193
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EGR1  LOC126807524  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 137,801,721
GRCh38 5 138,466,032
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001964.3:c.271G>A
NG_083838.2:g.1868G>A
NG_083838.3:g.2050G>A
NG_021374.1:g.5541G>A
More... 		11/07/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004910078 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene EGR1 CLINVAR
  LOC126807524 CLINVAR
OMIM 128990 CLINVAR