WIPF2 WAS/WASL interacting protein family member 2

Information
Symbol
WIPF2
Type
protein-coding
Description
WAS/WASL interacting protein family member 2
Entrez Gene ID
147179
Genome
hg19
Position
chr17:38,375,556-38,440,388
Genome
hg38
Position
chr17:40,219,304-40,284,136
MIM
609692 OMIM
HGNC
HGNC:30923 HGNC
Ensembl
ENSG00000171475 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
50
0
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 WICH
SYNONYM WIRE
MIM 609692 OMIM
HGNC HGNC:30923 HGNC
Ensembl ENSG00000171475 Ensembl
AllianceGenome HGNC:30923
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000323571.9 hg38 chr17 40,219,304 40,284,136 64,833
ENST00000583130.5 hg38 chr17 40,219,790 40,278,231 58,442
ENST00000394103.7 hg38 chr17 40,219,357 40,279,849 60,493
ENST00000585043.5 hg38 chr17 40,219,349 40,279,357 60,009
ENST00000323571.9 hg19 chr17 38,375,556 38,440,388 64,833
ENST00000585043.5 hg19 chr17 38,375,601 38,435,609 60,009
ENST00000394103.7 hg19 chr17 38,375,609 38,436,101 60,493
ENST00000583130.5 hg19 chr17 38,376,042 38,434,483 58,442
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