RGD:11657648 Rat Genome Database

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Variant: RGD:11657648 -  Homo sapiens

RGD ID: 11657648
RS ID: rs886045109
ClinVar ID: CV276131
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRAS  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 115,259,393
GRCh38 1 114,716,772
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.114716772G>A
NG_007572.1:g.5123C>T
NC_000001.10:g.115259393G>A
LRG_92:g.5123C>T
More... 		06/14/2016 5 prime utr variant uncertain significance Noonan's syndrome; Pseudo-Turner syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000342811 CLINVAR
dbSNP (RS) rs886045109 CLINVAR
MedGen C0028326 CLINVAR
NCBI Gene LOC129931249 CLINVAR
  NRAS CLINVAR
OMIM 164790 CLINVAR
SNOMED CT 205824006 CLINVAR