RGD:8585768 Rat Genome Database

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Variant: RGD:8585768 -  Homo sapiens

RGD ID: 8585768
ClinVar ID: CV120357
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DCC  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 18 50,591,964
GRCh38 18 53,065,594
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005215.3:c.1141-452C>A
NG_013341.1:g.730423C>A
NC_000018.10:g.53065594C>A
NC_000018.9:g.50591964C>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:DCC
Accession:XM_017025569
Location:INTRON

Gene Symbol:DCC
Accession:XM_017025568
Location:INTRON

Gene Symbol:DCC
Accession:XM_047437311
Location:INTRON

Gene Symbol:DCC
Accession:XM_011525844
Location:INTRON

Gene Symbol:DCC
Accession:NM_005215
Location:INTRON

Variant Samples