RGD:401727514 Rat Genome Database

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Variant: RGD:401727514 -  Homo sapiens

RGD ID: 401727514
ClinVar ID: CV2736345
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PTGS2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 186,643,058
GRCh38 1 186,673,926
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.186673926A>G
NC_000001.10:g.186643058A>G
NM_000963.4:c.*427T>C
NG_028206.2:g.11502T>C
 12/10/2022 3 prime utr variant other
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:PTGS2
Accession:NM_000963
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003312793 CLINVAR
MedGen C0206698 CLINVAR
NCBI Gene PTGS2 CLINVAR
OMIM 600262 CLINVAR