RGD:11653434 Rat Genome Database

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Variant: RGD:11653434 -  Homo sapiens

RGD ID: 11653434
RS ID: rs886052007
ClinVar ID: CV325358
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: VPS35  
Reference Nucleotide: -
Variant Nucleotide: TG
Position
Assembly Chr Position
GRCh37 16 46,694,106
GRCh38 16 46,660,194
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_029970.1:g.34038_34039insCA
NM_018206.4:c.*277_*278insCA
NM_018206.6:c.*277_*278insCA
NC_000016.10:g.46660195_46660196insGT
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:VPS35
Accession:XM_011523227
Location:3UTRS;EXON

Gene Symbol:VPS35
Accession:XM_005256045
Location:3UTRS;EXON

Gene Symbol:VPS35
Accession:NM_018206
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000310783 CLINVAR
dbSNP (RS) rs886052007 CLINVAR
MedGen CN239359 CLINVAR
NCBI Gene VPS35 CLINVAR
OMIM 601501 CLINVAR