RGD:15185533 Rat Genome Database

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Variant: RGD:15185533 -  Homo sapiens

RGD ID: 15185533
RS ID: rs4648266
ClinVar ID: CV777036
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126805956  PTGS2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 186,647,384
GRCh38 1 186,678,252
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000963.4:c.457+9G>A
NG_028206.2:g.7176G>A
NC_000001.11:g.186678252C>T
NC_000001.10:g.186647384C>T
More... 		06/18/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PTGS2
Accession:NM_000963
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000953012 CLINVAR
dbSNP (RS) rs4648266 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126805956 CLINVAR
  PTGS2 CLINVAR
OMIM 600262 CLINVAR