RGD:11608490 Rat Genome Database

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Variant: RGD:11608490 -  Homo sapiens

RGD ID: 11608490
RS ID: rs1059059
ClinVar ID: CV319258
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EXOSC3  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 37,780,558
GRCh38 9 37,780,561
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_032780.1:g.9532G>T
NC_000009.12:g.37780561C>A
NC_000009.11:g.37780558C>A
NM_016042.4:c.*118G>T
More...
06/19/2018 3 prime utr variant benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:EXOSC3
Accession:NM_001002269
Location:3UTRS;EXON

Gene Symbol:EXOSC3
Accession:NM_016042
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000355923 CLINVAR
  RCV001613236 CLINVAR
dbSNP (RS) rs1059059 CLINVAR
MedGen C3553449 CLINVAR
  C3661900 CLINVAR
NCBI Gene EXOSC3 CLINVAR
OMIM 606489 CLINVAR
  614678 CLINVAR