WWC3 WWC family member 3

Information
Symbol
WWC3
Type
protein-coding
Description
WWC family member 3
Entrez Gene ID
55841
Genome
hg19
Position
chrX:9,983,294-10,112,514
Genome
hg38
Position
chrX:10,015,254-10,144,474
MIM
301089 OMIM
HGNC
HGNC:29237 HGNC
Ensembl
ENSG00000047644 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 34
Conflicting classifications of pathogenicity 0 2
not provided 7 0
Uncertain significance 0 116
Ranking
ClinVar
0
0
2
160
4
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 BM042
MIM 301089 OMIM
HGNC HGNC:29237 HGNC
Ensembl ENSG00000047644 Ensembl
AllianceGenome HGNC:29237
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380861.10 hg38 chrX 10,015,254 10,144,474 129,221
ENST00000380861.10 hg19 chrX 9,983,294 10,112,514 129,221
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