PWWP2B PWWP domain containing 2B

Information
Symbol
PWWP2B
Type
protein-coding
Description
PWWP domain containing 2B
Entrez Gene ID
170394
Genome
hg19
Position
chr10:134,210,704-134,231,363
Genome
hg38
Position
chr10:132,397,200-132,417,859
HGNC
HGNC:25150 HGNC
Ensembl
ENSG00000171813 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 112
Ranking
ClinVar
0
0
0
114
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 PWWP2
SYNONYM bA432J24.1
SYNONYM pp8607
HGNC HGNC:25150 HGNC
Ensembl ENSG00000171813 Ensembl
AllianceGenome HGNC:25150
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000305233.6 hg38 chr10 132,397,200 132,417,859 20,660
ENST00000631148.2 hg38 chr10 132,397,168 132,417,528 20,361
ENST00000631148.2 hg19 chr10 134,210,672 134,231,032 20,361
ENST00000305233.6 hg19 chr10 134,210,704 134,231,363 20,660
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