RGD:28892772 Rat Genome Database

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Variant: RGD:28892772 -  Homo sapiens

RGD ID: 28892772
RS ID: rs1201037392
ClinVar ID: CV861995
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRAS  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 115,248,387
GRCh38 1 114,705,766
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007572.1:g.16129G>A
NC_000001.11:g.114705766C>T
NM_002524.4:c.*2328G>A
NM_002524.5:c.*2328G>A
More... 		01/12/2018 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 RCV001100700 CLINVAR
dbSNP (RS) rs1201037392 CLINVAR
MedGen C2750732 CLINVAR
NCBI Gene NRAS CLINVAR
OMIM 164790 CLINVAR
  613224 CLINVAR