RGD:11598829 Rat Genome Database

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Variant: RGD:11598829 -  Homo sapiens

RGD ID: 11598829
RS ID: rs2247325
ClinVar ID: CV306554
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC129997675  RNASET2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 167,369,992
GRCh38 6 166,956,504
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NC_000006.12:g.166956504A>G
NC_000006.11:g.167369992A>G
NG_016280.2:g.5086T>C
NG_016280.1:g.5086T>C
More... 		06/14/2016 5 prime utr variant benign infancy <1 / 1 000 000
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RNASET2
Accession:NM_003730
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000260374 CLINVAR
dbSNP (RS) rs2247325 CLINVAR
MedGen C2751843 CLINVAR
NCBI Gene LOC129997675 CLINVAR
  RNASET2 CLINVAR
OMIM 612944 CLINVAR
  612951 CLINVAR