RGD:11659000 Rat Genome Database

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Variant: RGD:11659000 -  Homo sapiens

RGD ID: 11659000
RS ID: rs886049888
ClinVar ID: CV318693
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DCN  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 91,539,392
GRCh38 12 91,145,615
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_011672.1:g.42415T>G
NC_000012.12:g.91145615A>C
NC_000012.11:g.91539392A>C
NM_001920.3:c.*443T>G
More... 		06/14/2016 3 prime utr variant uncertain significance all ages <1 / 1 000 000
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DCN
Accession:NM_133506
Location:3UTRS;EXON

Gene Symbol:DCN
Accession:NM_133504
Location:3UTRS;EXON

Gene Symbol:DCN
Accession:NM_001920
Location:3UTRS;EXON

Gene Symbol:DCN
Accession:NM_133507
Location:3UTRS;EXON

Gene Symbol:DCN
Accession:NM_133503
Location:3UTRS;EXON

Gene Symbol:DCN
Accession:NM_133505
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000353941 CLINVAR
dbSNP (RS) rs886049888 CLINVAR
MedGen C1864738 CLINVAR
NCBI Gene DCN CLINVAR
OMIM 125255 CLINVAR
  610048 CLINVAR