RGD:150424060 Rat Genome Database

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Variant: RGD:150424060 -  Homo sapiens

RGD ID: 150424060
RS ID: rs1421314
ClinVar ID: CV1185319
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WRAP53  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 7,591,540
GRCh38 17 7,688,222
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001143990.2:c.-1-426T>C
NM_001143991.2:c.-1-426T>C
LRG_321:g.4329A>G
LRG_375:g.7152T>C
More... 		02/04/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WRAP53
Accession:NM_001143990
Location:5UTRS;INTRON

Gene Symbol:WRAP53
Accession:NM_001143991
Location:5UTRS;INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_018081
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_001143992
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001556160 CLINVAR
dbSNP (RS) rs1421314 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WRAP53 CLINVAR
OMIM 612661 CLINVAR