RGD:156448535 Rat Genome Database

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Variant: RGD:156448535 -  Homo sapiens

RGD ID: 156448535
ClinVar ID: CV1946534
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: WRAP53  
Reference Nucleotide: CTAA
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 17 7,593,034 - 7,593,038
GRCh38 17 7,689,716 - 7,689,720
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_375t1:c.642+16_642+19del
NM_001143990.2:c.642+16_642+19del
NM_001143991.2:c.642+16_642+19del
NM_001143992.2:c.642+16_642+19del
More... 		03/18/2022 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003120097 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WRAP53 CLINVAR
OMIM 612661 CLINVAR