RGD:8579526 Rat Genome Database

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Variant: RGD:8579526 -  Homo sapiens

RGD ID: 8579526
ClinVar ID: CV113928
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IRF2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 185,349,168
GRCh38 4 184,428,014
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.184428014A>G
NC_000004.11:g.185349168A>G
NM_002199.3:c.87+964T>C
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:IRF2
Accession:NM_002199
Location:INTRON

Variant Samples