rs61758212 Rat Genome Database

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Variant: rs61758212 -  Homo sapiens

RGD ID: 150467575
RS ID: rs61758212
ClinVar ID: CV1269254
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC129931249  NRAS  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 115,259,217
GRCh38 1 114,716,596
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000001.11:g.114716596T>G
LRG_92:g.5299A>C
NC_000001.10:g.115259217T>G
NM_002524.5:c.-18+62A>C
More... 		06/23/2018 intron variant benign none provided

Gene Symbol:NRAS
Accession:NM_002524
Location:5UTRS;INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001694662 CLINVAR
dbSNP (RS) rs61758212 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC129931249 CLINVAR
  NRAS CLINVAR
OMIM 164790 CLINVAR