RGD:28898479 Rat Genome Database

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Variant: RGD:28898479 -  Homo sapiens

RGD ID: 28898479
RS ID: rs1350996201
ClinVar ID: CV895667
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNASET2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 167,369,739
GRCh38 6 166,956,251
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.12:g.166956251G>A
NC_000006.11:g.167369739G>A
NM_003730.4:c.-69C>T
NG_016280.2:g.5339C>T
More... 		04/28/2017 5 prime utr variant uncertain significance
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 RCV001155447 CLINVAR
dbSNP (RS) rs1350996201 CLINVAR
MedGen C2751843 CLINVAR
NCBI Gene RNASET2 CLINVAR
OMIM 612944 CLINVAR
  612951 CLINVAR