RGD:11649137 Rat Genome Database

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Variant: RGD:11649137 -  Homo sapiens

RGD ID: 11649137
RS ID: rs886061242
ClinVar ID: CV299617
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNASET2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 167,369,684
GRCh38 6 166,956,196
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.166956196G>T
NC_000006.11:g.167369684G>T
NM_003730.4:c.-14C>A
NG_016280.2:g.5394C>A
More... 		06/14/2016 5 prime utr variant uncertain significance 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 RCV000285738 CLINVAR
dbSNP (RS) rs886061242 CLINVAR
MedGen C2751843 CLINVAR
NCBI Gene RNASET2 CLINVAR
OMIM 612944 CLINVAR
  612951 CLINVAR