RGD:156166553 Rat Genome Database

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Variant: RGD:156166553 -  Homo sapiens

RGD ID: 156166553
ClinVar ID: CV2190055
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WRAP53  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 7,604,879
GRCh38 17 7,701,561
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_375t1:c.822+12C>G
NM_001143990.2:c.822+12C>G
NM_001143991.2:c.822+12C>G
NM_001143992.2:c.822+12C>G
More... 		05/04/2022 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 RCV003040896 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WRAP53 CLINVAR
OMIM 612661 CLINVAR