WRAP53 WD repeat containing antisense to TP53

Information
Symbol
WRAP53
Type
protein-coding
Description
WD repeat containing antisense to TP53
Entrez Gene ID
55135
Genome
hg19
Position
chr17:7,589,619-7,606,820
Genome
hg38
Position
chr17:7,686,301-7,703,502
MIM
612661 OMIM
HGNC
HGNC:25522 HGNC
Ensembl
ENSG00000141499 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 6
Benign 0 64
Likely benign 0 370
Conflicting classifications of pathogenicity 0 34
not provided 2 0
Uncertain significance 0 508
Ranking
ClinVar
0
0
154
764
8
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM DKCB3
SYNONYM TCAB1
SYNONYM WDR79
MIM 612661 OMIM
HGNC HGNC:25522 HGNC
Ensembl ENSG00000141499 Ensembl
AllianceGenome HGNC:25522
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000316024.9 hg38 chr17 7,686,301 7,703,502 17,202
ENST00000457584.6 hg38 chr17 7,687,440 7,703,502 16,063
ENST00000396463.7 hg38 chr17 7,688,477 7,703,502 15,026
ENST00000698746.1 hg38 chr17 7,688,478 7,703,499 15,022
ENST00000431639.6 hg38 chr17 7,686,071 7,703,502 17,432
ENST00000698742.1 hg38 chr17 7,687,913 7,703,318 15,406
ENST00000534050.5 hg38 chr17 7,688,477 7,703,502 15,026
ENST00000431639.6 hg19 chr17 7,589,389 7,606,820 17,432
ENST00000316024.9 hg19 chr17 7,589,619 7,606,820 17,202
ENST00000457584.6 hg19 chr17 7,590,758 7,606,820 16,063
ENST00000698742.1 hg19 chr17 7,591,231 7,606,636 15,406
ENST00000396463.7 hg19 chr17 7,591,795 7,606,820 15,026
ENST00000534050.5 hg19 chr17 7,591,795 7,606,820 15,026
ENST00000698746.1 hg19 chr17 7,591,796 7,606,817 15,022
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