RGD:11619523 Rat Genome Database

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Variant: RGD:11619523 -  Homo sapiens

RGD ID: 11619523
RS ID: rs185017679
ClinVar ID: CV326332
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDON  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 125,828,573
GRCh38 11 125,958,678
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_029776.1:g.109615C>T
NC_000011.10:g.125958678G>A
NC_000011.9:g.125828573G>A
NM_016952.4:c.*2264C>T
More... 		01/13/2018 3 prime utr variant benign|uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CDON
Accession:XM_017017873
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_047427061
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:NM_001378964
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_011542864
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_011542865
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:NM_001243597
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_047427063
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_047427062
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_011542863
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_047427064
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_011542862
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:NM_016952
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_047427060
Location:3UTRS;EXON

Gene Symbol:CDON
Accession:XM_047427065
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000326307 CLINVAR
dbSNP (RS) rs185017679 CLINVAR
MedGen C3280215 CLINVAR
NCBI Gene CDON CLINVAR
OMIM 608707 CLINVAR
  614226 CLINVAR