RGD:11657180 Rat Genome Database

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Variant: RGD:11657180 -  Homo sapiens

RGD ID: 11657180
RS ID: rs886047954
ClinVar ID: CV325363
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: CDON  
Reference Nucleotide: -
Variant Nucleotide: TG
Position
Assembly Chr Position
GRCh37 11 125,828,456
GRCh38 11 125,958,561
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.109731_109732insCA
NC_000011.10:g.125958562_125958563insGT
NC_000011.9:g.125828457_125828458insGT
NM_016952.4:c.*2380_*2381insCA
More... 		06/14/2016 3 prime utr variant uncertain significance ARHINENCEPHALY; Holoprosencephaly; HOLOPROSENCEPHALY, FAMILIAL ALOBAR; HPE, FAMILIAL
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:CDON
Accession:NM_016952
Location:3UTRS;EXON

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

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

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

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

Gene Symbol:CDON
Accession:NM_001243597
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_017017873
Location:3UTRS;EXON

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

Gene Symbol:CDON
Accession:XM_047427063
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:XM_047427065
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000338907 CLINVAR
dbSNP (RS) rs886047954 CLINVAR
MedGen C0079541 CLINVAR
NCBI Gene CDON CLINVAR
OMIM 236100 CLINVAR
  608707 CLINVAR
SNOMED CT 30915001 CLINVAR