RGD:11599963 Rat Genome Database

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Variant: RGD:11599963 -  Homo sapiens

RGD ID: 11599963
RS ID: rs565362144
ClinVar ID: CV313266
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRAPPC9  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 140,743,123
GRCh38 8 139,730,880
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.139730880C>T
NC_000008.10:g.140743123C>T
NM_031466.5:c.*181G>A
NM_001160372.4:c.*181G>A
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TRAPPC9
Accession:NM_031466
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:XM_011517330
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:NM_001374684
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:XM_017013894
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:NM_001160372
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:XM_011517326
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:NM_001374683
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:NM_001374682
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:NM_001321646
Location:3UTRS;EXON

Gene Symbol:TRAPPC9
Accession:NR_164662
Location:EXON;NON-CODING

Gene Symbol:TRAPPC9
Accession:XM_011517328
Location:INTRON

Gene Symbol:TRAPPC9
Accession:XM_047422294
Location:INTRON

Gene Symbol:TRAPPC9
Accession:XM_047422299
Location:INTRON

Gene Symbol:TRAPPC9
Accession:XM_017013893
Location:INTRON

Gene Symbol:TRAPPC9
Accession:XM_047422296
Location:INTRON

Gene Symbol:TRAPPC9
Accession:XM_047422298
Location:INTRON

Gene Symbol:TRAPPC9
Accession:XM_047422295
Location:INTRON

Gene Symbol:TRAPPC9
Accession:XM_047422297
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000269789 CLINVAR
dbSNP (RS) rs565362144 CLINVAR
MedGen CN239290 CLINVAR
NCBI Gene TRAPPC9 CLINVAR
OMIM 611966 CLINVAR