BRWD3 bromodomain and WD repeat domain containing 3

Information
Symbol
BRWD3
Type
protein-coding
Description
bromodomain and WD repeat domain containing 3
Entrez Gene ID
254065
Genome
hg19
Position
chrX:79,925,002-80,065,376
Genome
hg38
Position
chrX:80,669,503-80,809,877
MIM
300553 OMIM
HGNC
HGNC:17342 HGNC
Ensembl
ENSG00000165288 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 40
Likely pathogenic 0 36
Benign 0 274
Likely benign 0 308
Conflicting classifications of pathogenicity 0 40
not provided 6 0
Uncertain significance 0 550
Ranking
ClinVar
0
0
116
1,014
32
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 :
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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 BRODL
SYNONYM MRX93
SYNONYM XLID93
MIM 300553 OMIM
HGNC HGNC:17342 HGNC
Ensembl ENSG00000165288 Ensembl
AllianceGenome HGNC:17342
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000373275.5 hg38 chrX 80,669,503 80,809,877 140,375
ENST00000373275.5 hg19 chrX 79,925,002 80,065,376 140,375
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