PWWP3B PWWP domain containing 3B

Information
Symbol
PWWP3B
Type
protein-coding
Description
PWWP domain containing 3B
Entrez Gene ID
139221
Genome
hg19
Position
chrX:105,412,298-105,452,949
Genome
hg38
Position
chrX:106,168,305-106,208,956
HGNC
HGNC:26583 HGNC
Ensembl
ENSG00000157502 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 4
not provided 6 0
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
72
2
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 MUM1L1
HGNC HGNC:26583 HGNC
Ensembl ENSG00000157502 Ensembl
AllianceGenome HGNC:26583
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000337685.6 hg38 chrX 106,168,305 106,208,955 40,651
ENST00000372552.1 hg38 chrX 106,201,736 106,208,955 7,220
ENST00000357175.6 hg38 chrX 106,168,305 106,208,956 40,652
ENST00000337685.6 hg19 chrX 105,412,298 105,452,948 40,651
ENST00000357175.6 hg19 chrX 105,412,298 105,452,949 40,652
ENST00000372552.1 hg19 chrX 105,445,729 105,452,948 7,220
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