RGD:8579977 Rat Genome Database

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Variant: RGD:8579977 -  Homo sapiens

RGD ID: 8579977
ClinVar ID: CV114379
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF595  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 56,599
GRCh38 4 56,705
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_182524.3:c.4-2725A>G
NG_033822.1:g.8421A>G
NC_000004.12:g.56705A>G
NC_000004.11:g.56599A>G
 intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ZNF595
Accession:NM_001286054
Location:5UTRS;INTRON

Gene Symbol:ZNF595
Accession:NM_001286053
Location:5UTRS;INTRON

Gene Symbol:ZNF595
Accession:NM_001286052
Location:INTRON

Gene Symbol:ZNF595
Accession:NM_182524
Location:INTRON

Variant Samples