RGD:155917844 Rat Genome Database

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Variant: RGD:155917844 -  Homo sapiens

RGD ID: 155917844
ClinVar ID: CV2030018
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WRAP53  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 7,592,900
GRCh38 17 7,689,582
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_375:g.8512G>T
NG_017013.2:g.2969C>A
NG_028245.1:g.8512G>T
NC_000017.11:g.7689582G>T
More... 		03/12/2022 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:WRAP53
Accession:NM_001143990
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_001143991
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_018081
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_001143992
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002750556 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WRAP53 CLINVAR
OMIM 612661 CLINVAR