RGD:11587089 Rat Genome Database

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Variant: RGD:11587089 -  Homo sapiens

RGD ID: 11587089
RS ID: rs185234485
ClinVar ID: CV275941
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRAS  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 115,247,311
GRCh38 1 114,704,690
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_92:g.17205T>C
NG_007572.1:g.17205T>C
NC_000001.11:g.114704690A>G
NC_000001.10:g.115247311A>G
More... 		06/14/2016 3 prime utr variant uncertain significance NRAS gene related Noonan syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:NRAS
Accession:NM_002524
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000292737 CLINVAR
dbSNP (RS) rs185234485 CLINVAR
MedGen C2750732 CLINVAR
NCBI Gene NRAS CLINVAR
OMIM 164790 CLINVAR
  613224 CLINVAR