RGD:11607171 Rat Genome Database

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Variant: RGD:11607171 -  Homo sapiens

RGD ID: 11607171
RS ID: rs567641975
ClinVar ID: CV319246
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EXOSC3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 37,780,274
GRCh38 9 37,780,277
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.9816C>T
NC_000009.12:g.37780277G>A
NC_000009.11:g.37780274G>A
NM_016042.4:c.*402C>T
More...
06/14/2016 3 prime utr variant uncertain significance
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 RCV000340374 CLINVAR
dbSNP (RS) rs567641975 CLINVAR
MedGen C3553449 CLINVAR
NCBI Gene EXOSC3 CLINVAR
OMIM 606489 CLINVAR
  614678 CLINVAR