RGD:8586194 Rat Genome Database

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Variant: RGD:8586194 -  Homo sapiens

RGD ID: 8586194
ClinVar ID: CV120790
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF578  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 52,994,187
GRCh38 19 52,490,934
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000019.10:g.52490934T>C
NC_000019.9:g.52994187T>C
NM_001099694.1:c.-121-390T>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ZNF578
Accession:NM_001099694
Location:5UTRS;INTRON

Gene Symbol:ZNF578
Accession:NM_001366182
Location:5UTRS;INTRON

Gene Symbol:ZNF578
Accession:XM_047438189
Location:5UTRS;INTRON

Gene Symbol:ZNF578
Accession:XM_047438194
Location:5UTRS;INTRON

Gene Symbol:ZNF578
Accession:XM_047438191
Location:5UTRS;INTRON

Gene Symbol:ZNF578
Accession:XM_047438190
Location:5UTRS;INTRON

Gene Symbol:ZNF578
Accession:XM_047438192
Location:5UTRS;INTRON

Gene Symbol:ZNF578
Accession:XM_047438193
Location:INTRON

Variant Samples