RGD:8585763 Rat Genome Database

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Variant: RGD:8585763 -  Homo sapiens

RGD ID: 8585763
ClinVar ID: CV120352
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DCC  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 18 50,315,456
GRCh38 18 52,789,086
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.412+36712G>C
NG_013341.1:g.453915G>C
NC_000018.10:g.52789086G>C
NC_000018.9:g.50315456G>C
 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_047437311
Location:INTRON

Gene Symbol:DCC
Accession:NM_005215
Location:INTRON

Gene Symbol:DCC
Accession:XM_017025568
Location:INTRON

Gene Symbol:DCC
Accession:XM_011525844
Location:INTRON

Variant Samples